Perception

Pictorial relief was measured for a series of pictures of a smooth solid object. The scene was geometrically identical for all pictures, but the rendering was different. Whereas all pictures were monochrome full-scale photographs, they were taken under different illuminations of the scene, the source being frontal and displaced towards either the upper left, the upper right, the lower right, or the lower left. It was found that different illuminations led to significantly different, systematic alterations of pictorial relief. It is concluded that though shape constancy under changes in illumination might be said to rule in the first rough approximation, the deviations from true constancy are indeed both significant and systematic. Different from either stimulus-reduction or cue-conflict paradigms, this ‘perturbation analysis’ shows that shading is used as an important source of information even if the particular illumination appears to be ignored at first blush. For all subjects, brighter parts in the stimulus were consistently interpreted as being nearer in pictorial space, both for the global layout and for the subsidiary relief.

Eye movements are an important aid in active visual exploration of the environment and in performing behavioural tasks. Eye movements might also play a role in human perception of three-dimensional (3-D) objects. Eye-movement strategies were investigated when humans inspected and memorised 3-D objects. Subjects were instructed to memorise the 3-D structure of parts of statues of human figures placed on a turntable free to rotate through 360°. Eye movements and turning behaviour were recorded. Different turning and eye-movement strategies could be observed. Subjects showed individual turning behaviours that were reproducible between trials. Turning strategies ranged from focusing on only a limited number of perspective views to almost continuously rotating the object with only short stops. On average twelve–thirteen views were inspected during memorising. Eye movements also revealed individual strategies. Fixation locations within each inspection view ranged from either closely spaced on isolated parts of the object to distributed over the whole view with large saccades in between. Eye movements were often directed to the same details from different perspectives. The differences in turning and viewing strategy also resulted in differences in the ability to recognise parts of the object later on. In general, successful later recognition required that the subject actually fixated the part to be recognised. A strategy of thoroughly inspecting the object with a series of closely spaced fixations from only a limited number of viewpoints led to best recognition rates. This was especially true for two subjects trained in fine arts with prior experiences in modelling. The results support models of viewpoint-dependent object recognition with viewer-centred, two-dimensional representations of 3-D objects.

It has often been noted that with repeated exposure to random-dot stereograms the time required to perceived depth decreases. Further, with extensive practice, stereoacuity thresholds have been shown to decrease. For both types of learning some researchers have reported specificity of the improvements to retinal location, and have thus suggested that the learning may be localised at early levels of visual processing, such as in primary visual cortex. However, these studies have not adequately ruled out the possibility that the specificity shown may be due to the operation of selective-spatial-attention mechanisms. In the present study this possibility was examined by training observers to judge the relative depth of a pair of stereograms presented equally often in two spatial locations, but stimuli were only presented with one direction of disparity (ie crossed or uncrossed) in any one location. Results indicated that, as expected, observers' judgments improved with practice. However, this improvement transferred completely to stimuli presented with the other direction of disparity in each location. Thus, it is argued that previous findings of retinal-location-specific improvements in stereoacuity may well be due to selective-spatial-attention mechanisms, rather than to learning localised at an early level of visual processing.

The threshold for detecting a change in orientation away from the vertical of a briefly presented foveal line target is raised when there are immediately following visual presentations. This masking effect was examined by measuring the capacity of a variety of patterns to act as masks. When patterns were made of exactly the same number of light pixels, masking was least when they formed random dots and progressively became stronger as they formed lines of decreasing curvature from full circles to straight lines. The longer the lines, the stronger the masking. Threshold elevation was highest when the masking pattern was spatially superimposed on the line and was lessened when a large surround area was included, but there was still considerable masking when the interfering patterns were confined to the surround. By placing masks and test lines in different eyes, or by giving them opposite contrast polarity, almost complete interocular and interpolarity transfer was demonstrated. Relating these results to anatomical and electrophysiological findings about neurons in the primary visual cortex leads to the conclusion that the masking effects could have their substrates in interaction between cells in V1.

A motion aftereffect (MAE) can be induced by stimuli moving in surrounding areas. This suggests the relevance of mechanisms for relative motion, rather than early-level motion detectors, which are considered to work locally. Experiments are reported in which the role of local adaptation in the MAE with a stimulus configuration comprising relative motion has been discussed. Sinusoidal gratings were presented in three rectangular windows: a centre window, and two windows one above and one below the central one. The surrounding top and bottom windows, which were divided into left and right halves, had gratings presented in only one of the two halves. The MAE duration was measured after adaptation to motion either in the central or in the surrounding windows, by controlling the regions with the gratings. From this, the regions of surrounding gratings were found not to have a significant effect with adaptation in the centre window. With adaptation in the surrounds, however, these regions did affect the MAE; the MAE duration was reduced when the adapted region had no gratings in the test phase. Thus, for an MAE it is necessary for the adapted area to be covered with stimuli in the test phase, which indicates the dominance of local adaptation for the MAE even when relative motion is relevant in producing the MAE.

Synaesthesia is a condition in which a mixing of the senses occurs; for example, sounds trigger the experience of colour. Previous reports suggest this may be familial, but no systematic studies exist. In addition, there are no reliable prevalence or sex-ratio figures for the condition, which is essential for establishing if the reported sex ratio (female bias) is reliable, and if this implicates a sex-linked genetic mechanism. Two independent population studies were conducted in the city of Cambridge, England (studies 1 and 2 here), as necessary background to the family genetic study of synaesthesia (study 3). Studies 1 and 2 arrived at an almost identical prevalence rate for synaesthesia: approximately 1 case in 2000. The sex ratio found was 6:1 (female:male). A third of cases also reported familial aggregation. In study 3 six families were examined, and first-degree relatives were tested for genuineness of the condition. All six families were indeed multiplex for synaesthesia. Alternative modes of inheritance are discussed.

The literature contains numerous claims that 90% of all the information used in driving is visual. This article presents a theoretical discussion, a citation search, and a review of evidence concerning such claims. The findings indicate that not only do we lack data from which to derive an accurate numerical estimate, but we lack a measurement system within which any numerical estimate would be meaningful. Consequently, although the information relevant to driving is likely to be predominantly visual, any claims about the precise percentage attributable to vision are premature. The proliferation of such claims in the absence of direct evidence is a reminder that researchers should be careful about assuring the validity of the claims they are passing on.

It is widely reported that a picture of an angry face seems to figuratively pop out of an array of happy faces, although all of these reports are based on a single experiment by Hansen and Hansen. Pop out, when it occurs, indicates that an observer has located the target by means of a preattentive, parallel search. Hansen and Hansen concluded that it was the affect displayed by the face which caused it to pop out from its surrounding distracters. However, Hansen and Hansen's angry faces contained extraneous dark areas which were introduced when they transformed Ekman and Friesen's photographs of angry and happy faces into black-on-white sketches. When the original artifact-free gray-scaled versions of angry and happy faces were used no evidence for pop out was found. All target faces were found during a serial, self-terminating search regardless of their expression. The angry face in Hansen and Hansen's experiments may have popped out from a crowd of happy faces because of a contrast artifact inadvertently introduced when they created their stimuli.

One of the most common obstacles to object perception is the fact that objects often occlude parts of themselves and parts of other objects. Perceptual completion has been studied extensively in humans, and researchers have shown that humans do complete partly occluded objects. In an effort to understand more about the mechanisms underlying completion, recent research has extended the study of perceptual completion to other mammalian species. Monkeys and mice also seem to complete two-dimensional representations of partly occluded objects. The present study addresses the question of whether this capacity generalizes to a nonmammalian species, the pigeon (Columba livia). The results point to a limit of the generalizability of perceptual completion: pigeons do not complete partly occluded figures.

In an attempt to demonstrate whether horses could make use of pictorial cues to depth, two were trained initially to make a relative-line-length discrimination between two lines placed one above the other. Psychophysical measurement of their discrimination thresholds showed that from a viewing distance of approximately 160 cm they could reliably distinguish a lower line of 10 cm from an upper one of 14 cm. In the second phase of the experiment, two lines of equal length were superimposed on a photograph of a set of railway tracks with many pictorial cues to depth, or a photograph of a pastoral scene with fewer obvious depth cues. To humans, the railway tracks created a Ponzo illusion, making the upper line appear longer. When the horses were allowed to choose between the photographs, they overwhelmingly chose the display containing the converging railway tracks. Control experiments ruled out alternative explanations, leading to the conclusion that horses are susceptible to a Ponzo illusion created by depth cues in photographs.