Visual movement discrimination

Data are presented which support a mathematical model for visual movement perception. An observer’s ability to judge the relative position of two successively presented points of light in an otherwise dark room is shown to diminish as the inter-stimulus interval is increased. However, a measure of visual position memory appears to remain invariant a5 this interval is varied. Neither the degree of head stabilization nor whether viewing is monocular or binocular appreciably alters this measure.     

Visual discrimination of texture

Julesz (1975) proposed a theory of texture discrimination, based on an order statistics principle, which states that no two textures can be perceptually discriminated if they have identical second-order statistics. The experiments reported here demonstrate that this principle is not adequate to predict visual texture discriminability. Both letter and dot micropatterns were used to create texture pairs that either differed or were identical with respect to secondorder statistics. The subject’s task was to decide which quadrant of an array contained a disparate texture. In Experiments 1, 2, and 3, when controlling for spatial overlap, texture pairs having identical second-order statistics were discriminated more quickly than similar texture pairs having different second-order statistics, in contradiction to the principle. Although a significant effect in the direction predicted by the order statistics principle was found in Experiment 4 for texture pairs created from the dot micropatterns, other factors, such as spatial overlap, border differences, and goodness of pattern, must also be considered in predicting texture discriminability.     

Visual discrimination of spectral distributions

Human observers seem to be able to use different features that classify materials with a large degree of accuracy. In this paper, we look at human perception of statistical properties of the spectral distribution in a scene. We investigated whether human observers can discriminate just as accurately between coloured textures that have a spectral distribution due either to shading only or to both shading and specular reflectance as between uniform colours. Thresholds for the discrimination of coloured textures are about 15 times as high as thresholds for the discrimination of uniform colours, provided there is a sharp transition between the two colours. However, the coloured texture thresholds are only 1.5 times higher when we introduce a gradual transition between the two colours. There are also distinct qualitative differences in discrimination thresholds for different base colours. These differences cannot be predicted from discrimination thresholds for uniform colours. Human observers are surprisingly good at discriminating between a material edge and a shadow edge in complex scenes. Statistical differences in the orientation of the colour distributions in colour space might be used to accomplish this. In a second experiment we investigated how well observers can discriminate between two linear distributions in colour space that have the same base colour but different orientations. When we vary the line-length in R, G, B space, thresholds cannot be predicted completely by the conservation of the average distance between the two distributions. This means that observers use not only the maximum colour difference in the stimulus to do the task, but other cues are also involved.     

Visual discrimination of vowel duration

Discrimination of vowel duration was explored with regard to discrimination threshold, error bias, and effects of modality and consonant context. A total of 122 normal-hearing participants were presented with disyllabic-like items such as /lal-lal/ or /mam-mam/ in which the lengths of the vowels were systematically varied and were asked to judge whether the first or second vowel was longer. Presentation was either visual, auditory, or audiovisual. Vowel duration differences varied in 24 steps: 12 with a longer first /a/ and 12 with a longer last /a/ (range: ±33–400 ms). Results: 50% JNDs were smaller than the lowest tested step size (33 ms); 75% JNDs were in the 33–66 ms range for all conditions but V /lal/, with a 75% JND at 66–100 ms. Errors were greatest for visual presentation and for /lal-lal/ tokens. There was an error bias towards reporting the first vowel as longer, and this was strongest for /mam-mam/ and when both vowels were short, possibly reflecting a sublinguistic processing strategy.     

Visual discrimination and response programming

Summary Choice reaction time (RT) depends on the relationship between responses, and these dependencies are usually interpreted in terms of the advance-specification assumption. According to this assumption characteristics that are the same for the choice responses can be specified in advance of the response signal, thus allowing faster RTs. Since the advance-specification assumption is called into question by some of the available data, an alternative interpretation is suggested and formalized in terms of an accumulator model. According to the programming-interactions assumption, stimulus processing is tightly linked to response programming, so that both the possible responses are programmed as long as there is uncertainty with regard to stimulus identity. This gives rise to interactions between simultaneous processes of motor programming. Predictions of this assumption for the joint effects of signal similarity and the relationship between responses are tested and confirmed.This research was supported by grant no. He 1187/3–1 from the Deutsche Forschungsgemeinschaft     

Visual discrimination in the toad

Using a method of successive discrimination, 10 toads (Bufo bufo), were trained to discriminate between horizontal and vertical rectangles each 5.0 ± 7.5 cm. After training, one optic nerve was severed in certain animals and the stumps pushed well apart to delay regeneration. The non-operated animals retained their learning over the rest-period of 10 weeks at a level similar to training. The animals with one eye showed considerably less retention than the non-operated animals.     

Visual discrimination of shape by humans

Reaction times to tachistoscopic exposure and a card-sorting task are the two methods by which visual discrimination of shape is studied. The results of experiments using both methods tally, i.e. the order of difficulty of the following shapes was: (1) (easiest) circle vs. triangle; (2) circle vs. square; (3) square vs. triangle; (4) (most difficult) triangle vs. diamond. These results are compared with those obtained by Sutherland, using octopus, and it is concluded that it should be possible to establish to what extent the system of visual analysis in humans differs from that postulated for both octopus and rat.     

Visual form discrimination: Multidimensional analyses

Nonmetric multidimensional scaling techniques were used to evaluate discrimination latency as a similarity measure. A three dimensional Euclidian solution was found for a sample of random polygons. The dimensions were labeled compactness, jaggedness, and elongation. The spatial configuration was highly similar to results obtained from similarity estimates and the dimensions were systematically related to physical shape measures.     

Size invariance in visual number discrimination

Summary This study deals with the observer's ability to discriminate the numerosity of two random dot-patterns irrespective of their relative size. One of these two patterns was a reference one that was always composed of 32 dots randomly distributed within aK ×K invisible square window (K = 1.92°). The second one was the test pattern with one of the five magnifications (K = 0.64°, 1.28°, 1.92°, 2.56°, 3.20°) and the relative number of dots varied on 11 levels (N = –15, –12, –9, –6, –3, 0, 3, 6, 9, 12, or 15 dots). The observer's task was to indicate which of the two patterns contained more dots. The results show that the stimulus size, as an irrelevant stimulus attribute, can be ignored in the judgements about relative numerosity. This means that the perceived numerosity is size invariant, at least for a 1.6-times magnification and a 3-times reduction of the test pattern. The size invariance observed constrains the range of potential models, since the perceived numerosity can be identified only by means of a feature of the stimulus that will remain invariant after any change in the absolute stimulus size.     

Visual sensing without seeing

Abstract— It has often been assumed that when we use vision to become aware of an object or event in our surroundings, this must be accompanied by a corresponding visual experience (i.e., seeing). The studies reported here show that this assumption is incorrect. When observers view a sequence of displays alternating between an image of a scene and the same image changed in some way, they often feel (or sense) the change even though they have no visual experience of it. The subjective difference between sensing and seeing is mirrored in several behavioral differences, suggesting that these are two distinct modes of conscious visual perception.     

Visual discrimination between rectangular and nonrectangular parallelopipeds

Twenty-seven university students judged whether each of 128 drawings of parallelopipeds appeared to represent three-dimensional rectangular boxes. Half the pictures could not geometrically have been projections of rectangular boxes. The null hypothesis that Ss’ judgments were unrelated to geometry was rejected at the .001 level of significance, and the correlation between Ss’ judgments and perfect discrimination averaged .86 over three variations of the experiment. The results support a general hypothesis about the perception of simple space forms according to which viewers impose geometric constraints, such as rectangularity and symmetry, but only when the constraints are projectively possible.     

Visual discrimination thresholds for time to arrival

In a seminal article, Todd (Journal of Experimental Psychology: Human Perception and Performance 7:795-810, 1981) reported a difference threshold of about 50 ms to discriminate the times of arrival of two differently sized objects that simultaneously approached head-on at constant but different velocities. Subsequent investigators, however, have often found much higher thresholds. We did one complete replication of Todd’s experiment, and then modified his stimuli and experimental regime, which we hypothesized may have been responsible for some of the discrepancies reported in the literature. Unlike Todd and most other researchers, we exclusively used untrained observers. Several of our participants performed almost as well as the trained observers used by Todd and others, but the performance of most of our participants fell short of this standard. Furthermore, thresholds were affected by the experimental regimes, with large differences between objects’ sizes and speeds compromising performance. Analyses of the response patterns revealed that the responses were driven mainly by the objects’ relative apparent sizes.     

Small and large number discrimination in guppies

Non-verbal numerical behavior in human infants, human adults, and non-human primates appears to be rooted in two distinct mechanisms: a precise system for tracking and comparing small numbers of items simultaneously (up to 3 or 4 items) and an approximate system for estimating numerical magnitude of a group of objects. The most striking evidence that these two mechanisms are distinct comes from the apparent inability of young human infants and non-human primates to compare quantites across the small (<3 or 4)/large (>4) number boundary. We ask whether this distinction is present in lower animal species more distantly related to humans, guppies (Poecilia reticulata). We found that, like human infants and non-human primates, fish succeed at comparisons between large numbers only (5 vs. 10), succeed at comparisons between small numbers only (3 vs. 4), but systematically fail at comparisons that closely span the small/large boundary (3 vs. 5). Furthermore, increasing the distance between the small and large number resulted in successful discriminations (3 vs. 6, 3 vs. 7, and 3 vs. 9). This pattern of successes and failures is similar to those observed in human infants and non-human primates to suggest that the two systems are present and functionally distinct across a wide variety of animal species.     

Visual field differences in spatial frequency discrimination

Subjects discriminated between sine-wave gratings that differed by either +/-0.125 octaves (small difference) or +/-1.0 octaves (large difference). Baseline stimuli consisted of either 1.0 or 4.0 cycles per degree gratings. A left visual field advantage was obtained for the small difference in frequency, with no visual field advantages for the large difference in frequency. Similarly, moderate support for right versus left visual field advantages in processing high versus low spatial frequencies was found, although these interactions were not statistically significant. The results are discussed in light of Kosslyn's (1987) categorical and coordinate framework.     

Large number discrimination in 6-month-old infants

Two experiments with the Stroop paradigm were conducted to investigate the role of phonological codes in access to the meaning of Chinese characters. Subjects named the ink color of viewed characters or color patches. Key items were color characters, their homophones with the same tone, homophones with different tones, and semantic associates. Apart from finding the usual Stroop interference effect, homophones produced significant interference in the incongruent condition, provided that they had the same tone as the color characters. The interference effect from homophones, however, was significantly smaller than that from color characters. Semantic associates generated an interference effect in the incongruent condition, an effect of the same magnitude as the effect from the same-tone homophones. Finally, in the congruent conditions, all the key items yielded facilitations compared to neutral controls, though the facilitation from color characters was larger than the facilitations from other types of characters. These findings suggest that phonological codes in Chinese are activated obligatorily and provide early sources of constraint in access to meaning.     

Temporal integration in duration and number discrimination

Temporal integration in duration and number discrimination by rats was investigated with the use of a psychophysical choice procedure. A response on one lever ("short" response) following a 1-s white-noise signal was followed by food reinforcement, and a response on the other lever ("long" response) following a 2-s white-noise signal was also followed by food reinforcement. Either response following a signal of one of five intermediate durations was unreinforced. This led to a psychophysical function in which the probability of a long response was related to signal duration in an ogival manner. On 2 test days, a white-noise signal with 5, 6, 7, 8, or 10 segments of either 0.5-s on and 0.5-s off or 1-s on and 1-s off was presented, and a choice response following these signals was unreinforced. The probability of a long response was the same function of a segmented signal and a continuous signal if each segment was considered equivalent to 200 ms. A quantitative fit of a scalar estimation theory suggested that the latencies to initiate temporal integration and to terminate the process are both about 200 ms, and that the same internal accumulation process can be used for counting and timing.