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Significance Recent studies in neuroscience suggest that visual perception is not processed by the purely feed-forward system but by the interaction of forward, horizontal, and feedback processing called recurrent loops. The present study examined the development of recurrent processing using visual backward masking, a perceptual phenomenon in which a visual stimulus is rendered invisible by a mask that follows the stimulus, possibly because of the disruption of recurrent processing. We showed that backward masking is ineffective for infants under 7 mo of age and that they can perceive masked objects that older infants cannot see because of masking. These results suggest that recurrent processing is immature in early infancy and that the mechanisms of visual perception drastically change around this age., Recurrent loops in the visual cortex play a critical role in visual perception, which is likely not mediated by purely feed-forward pathways. However, the development of recurrent loops is poorly understood. The role of recurrent processing has been studied using visual backward masking, a perceptual phenomenon in which a visual stimulus is rendered invisible by a following mask, possibly because of the disruption of recurrent processing. Anatomical studies have reported that recurrent pathways are immature in early infancy. This raises the possibility that younger infants process visual information mainly in a feed-forward manner, and thus, they might be able to perceive visual stimuli that adults cannot see because of backward masking. Here, we show that infants under 7 mo of age are immune to visual backward masking and that masked stimuli remain visible to younger infants while older infants cannot perceive them. These results suggest that recurrent processing is immature in infants under 7 mo and that they are able to perceive objects even without recurrent processing. Our findings indicate that the algorithm for visual perception drastically changes in the second half of the first year of life.

Little is known about the time of development of binocular suppression. In the present study, we evaluated the emergence of binocular suppression in infants by using continuous flash suppression (CFS, Tsuchiya and Koch, 2005). In our experiment, one eye of infants was presented with a static face image at one side of the screen, while another eye was presented with dynamic Mondrian patterns in full screen. Adult observers confirmed that the static face image was consciously repressed by the changing Mondrian patterns. If binocular suppression was functional, the infants would not perceive the face and thus would not show any preference in the experiment. However, if binocular suppression in the infants was not yet acquired, they would perceive the face and the Mondrian patterns at the same time and would thus show preference for the side where the face was presented. The results showed that infants aged 2-3 months, but not those aged 4-5 months, detected the position of the face. Furthermore, this detection was not due to weak contrast sensitivity to the dynamic Mondrian mask. These results indicated that the immature binocular visual system may perceive different images from different eyes simultaneously and that infants may lose this ability after establishing binocular suppression at 4-5 months of age.

Infants less than 1 year old are known to preferentially look at pictures of motion illusion induced by luminance gradation. However, the mechanisms underlying infant’s perception of motion illusion remain unclear. The current study analyzed the eye movement patterns of infants perceiving a motion illusion induced by stationary luminance gradations (a derivative of the Fraser-Wilcox illusion). Infants produced the same movement patterns that increase the magnitude of illusory motion in adults. We conclude that infants and adults similarly perceive motion illusion.

Summary Motion direction of a large high-contrast pattern is more difficult to perceive than that of a small one [ 1 ]. This counterintuitive perceptual phenomenon is considered to reflect surround suppression, a receptive field property observed in the visual cortex [ 2 , 3 , 4 , 5 ]. Here, we demonstrate that this phenomenon can be observed in human infants. Infants at 7 to 8 months of age showed higher sensitivity for a small motion stimulus than for a large one. However, infants under 6 months showed the opposite result; motion sensitivity was higher for a large stimulus. These results suggest that suppressive surround regions beyond classical receptive fields develop in the second half of the first year. Moreover, we examined the size of spatial summation in infants and found that the spatial summation area shrinks from 3 to 8 months of age. Our findings suggest that the summation area for motion is broad with no surround suppression in early infancy and that it narrows and acquires suppressive surround regions in the first year of life, which might reflect the developmental changes in the receptive field structure.

Shadows are powerful cues in the perception of shapes. We can perceive shading and cast shadow implicitly. We investigated infants' ability to detect a single discrepant figure that was depicted by shading or cast shadow and examined the influence of the contrast polarity of shadows on this process. In Experiment 1, we manipulated the blur direction of a shadow to create stimuli that appeared either to be partially shaded or to cast a shadow and then used a preference to test whether this difference would allow 5- to 8-month-old infants to discriminate the figures that adults were able to perceive as different shapes. Only 7- to-8-month-old infants could differentiate one shading figure from cast shadow figures, and vice versa. In Experiment 2, we reversed the contrast polarity of the figure (dark object with a light shadow) and tested whether discrimination was affected. As has been found with adults, infants exposed to this condition were unable to discriminate the contrast-reversed shading and cast shadow figures. Our results suggested that an age of around 7 months is important for development of the ability to perceive shape differences from shading and cast shadows.

Perceptual color space is continuous; however, we tend to divide it into only a small number of categories. It is unclear whether categorical color perception is obtained solely through the development of the visual system or whether it is affected by language acquisition. To address this issue, we recruited prelinguistic infants (5- to 7-mo-olds) to measure changes in brain activity in relation to categorical color differences by using near-infrared spectroscopy (NIRS). We presented two sets of geometric figures to infants: One set altered in color between green and blue, and the other set altered between two different shades of green. We found a significant increase in hemodynamic responses during the between-category alternations, but not during the within-category alternations. These differences in hemodynamic response based on categorical relationship were observed only in the bilateral occipitotemporal regions, and not in the occipital region. We confirmed that categorical color differences yield behavioral differences in infants. We also observed comparable hemodynamic responses to categorical color differences in adults. The present study provided the first evidence, to our knowledge, that colors of different categories are represented differently in the visual cortex of prelinguistic infants, which implies that color categories may develop independently before language acquisition.

Material perception is facilitated by multisensory interactions that enable us to associate the visual properties of a material with its auditory properties. Such interactions develop during infancy and are assumed to depend on the familiarity of materials. Here, we aimed to pinpoint the age at which infants acquire multisensory interactions for the perception of water, which is a familiar material to them. We presented two side-by-side movies of pouring water and ice while providing the corresponding sounds of water and ice, as well as silence. We found that infants older than 5 months of age looked longer at the water movie when they heard the sound of water. Conversely, they did not look at the ice movie when they heard the sound of ice. These results indicate that at approximately 5 months of age, infants develop multisensory interactions between auditory and visual properties of water, but not of ice. The contrasting results between water and ice suggest that the development of multisensory material perception depends on the frequency of interactions with materials during infancy.

Motion direction of a large high-contrast pattern is more difficult to perceive than that of a small one [1]. This counterintuitive perceptual phenomenon is considered to reflect surround suppression, a receptive field property observed in the visual cortex [2-5]. Here, we demonstrate that this phenomenon can be observed in human infants. Infants at 7-8 months of age showed higher sensitivity for a small motion stimulus than for a large one. However, infants under 6 months showed the opposite result; motion sensitivity was higher for a large stimulus. These results suggest that suppressive surround regions beyond classical receptive fields develop in the second half of the first year. Moreover, we examined the size of receptive fields in infants using this phenomenon and found that the center region of receptive fields shrinks from 3 months to 8 months. Our findings suggest that receptive fields related to motion processing are broad and do not have extra-classical receptive fields in early infancy, and that they become narrower and acquire suppressive surround regions in the first year of life.

Our visual system can easily estimate the constant color and material of external objects despite dynamic changes in the retinal image across viewpoints and illuminations in natural scenes. It is commonly believed that this high-level visual function, called "perceptual constancy," is acquired through postnatal learning [1], building upon low-level functions that have developed earlier, such as image discrimination. However, we demonstrate here that before developing perceptual constancy, 3- to 4-month-old infants have a striking ability to discriminate slight image changes due to illumination that are not salient for adults. These young infants lose this ability after 5 months of age and then develop an ability to perceive distal surface properties (glossy or matte) at 7-8 months of age. Moreover, we identify the transition period between these two functions at 5-6 months of age, wherein infants show difficulty in both image and surface discrimination. These findings support the notion that acquiring perceptual constancy leads to a loss of sensitivity to variant information, which is negligible for constant surface material perception. We suggest that the immature visual system may initially directly access local image features and then develops a complementary constant neural representation of the properties of an object.

When humans perceive the lightness of an object's surface in shadows there is an implicit assumption that cast shadows dim the surface. In two experiments, we investigated whether 5- to 8-month-old infants make this assumption about shadows. According to this shadow assumption, the apparent change in lightness produced by shadows on an object's surface are attributed to blocked light sources. If infants can use the shadow assumption to perceive the object's lightness in shadows, they will also be able to detect unnatural lightness changes in shadows. We compared the infants' looking times to the unnatural and the natural lightness changes in the shadow when an object (duck) goes through the cast shadow. In Experiment 1, we examined whether infants could detect the unnatural lightness changes of the object's surface in shadows. We created computer-graphic movies of unnatural and natural lightness changes to the duck's surface. Our results showed that 7- to 8-month-olds but not 5- to 6-month-olds significantly preferred the movie with the unnatural changes in lightness, indicating that only the older infants could detect these changes. In Experiment 2, we confirmed that the infants' preference was based on the detection of unnatural lightness changes according to the shadow assumption. The natural and the unnatural lightness changes of Experiment 1 were presented without cast shadows. Under these conditions, neither younger nor older infants showed a significant preference. Taken together, the experiments showed that 7- to 8-month-old infants could detect the unnaturalness of a surface's lightness changes produced by shadows. In conclusion, our findings suggest that 7- to 8-month-old infants can perceive an object's lightness in shadows by using an assumption that cast shadows dim the surface of an object.

Infants' ability to recognize uncanny human faces increases during the first year of life. In turn, their ability to recognize faces of other species declines at almost the same period (perceptual narrowing). In the current study, we aimed to clarify the relationship between the perception of uncanniness of faces and perceptual narrowing in infants and adults. We used the “uncanny valley task,” in which the participants were required to discriminate the faces of humans and monkeys by different eye size. Results showed that 3- to 5-month-old infants could not discriminate either monkey or human faces by eye size, whereas 6- to 8-month olds could. Adults showed higher discrimination performance for human than monkey faces and perceived the human faces with extremely large or small eyes as exceedingly eerie. Our results suggest that perception of uncanniness of faces is formed after perceptual narrowing.

Facial movement facilitates the recognition of facial expressions. While an intense expression is expressive enough to be recognized in a still image, a subtle expression can be recognized only in motion (Ambadar, Schooler, & Cohn, 2005, Psychological Science, 16, 403–410). The present study investigated whether infants recognize a subtle expression, and whether facial movement facilitates infants' recognition of a subtle expression. In experiment 1 4- to 7-month-old infants were tested for their spontaneous preference for a happy subtle expression rather than a neutral face, but they did not show a spontaneous preference. To confirm that infants did not recognize the static subtle expression, we conducted experiment 2 using the familiarization-novelty procedure. Infants were first familiarized with a static subtle happy expression. Following familiarization, they were presented with a pair of peak expressions of happiness and anger, but showed no significant novelty preference. In experiment 3 we presented the subtle expression dynamically. Infants were familiarized with a dynamic subtle expression and were tested for their novelty preference. The 6- to 7-month-olds showed a significant novelty preference, while 4- to 5-month-olds did not. These results suggest that infants can recognize the subtle expression only in dynamic presentation and that facial movement facilitates infants' recognition of facial expression.

Human can easily detect other's eyes and gaze from early in life. Such sensitivity is supported by the contrast polarity of human eyes, which have a white sclera contrasting with the darker colored iris (Kobayashi & Kohshima, (1997). Nature, 387, 767-768; Kobayashi & Kohshima, (2001). Journal of Human Evolution, 40, 419-435). Recent studies suggest that the contrast polarity around the eyes plays an important role in infants' face processing. Newborns preferred upright face images to inverted ones in contrast-preserved faces, but not in contrast-reversed faces (Farroni et al., (2005). Proceedings of National Academy of Sciences of the United States of America, 102, p. 17245-17250). Seven- to 8-month-old infants failed to discriminate between faces when the contrast polarity of eyes was reversed (Otsuka et al., (2013). Journal of Experimental Child Psychology, 115, 598-606). Neuroimaging study with adults revealed that full-negative faces induced less activation in the right fusiform gyrus than either full-positive faces or negative faces with contrast-preserved eyes (Gilad et al., (2009). Proceedings of National Academy of Sciences of the United States of America, 106, p. 5353-5358). In the present study, we investigated whether contrast-reversed eyes diminish infants' brain activity related to face processing. We measured hemodynamic responses in the bilateral temporal area of 5- to 6-month-old infants. Their hemodynamic responses to faces with positive eyes and those with negative eyes were compared against the baseline activation during the presentation of object images. We found that the presentation of faces with positive eyes increased the concentration of oxy-Hb in the right temporal area and those of total-Hb in the bilateral temporal areas. No such change occurred for faces with negative eyes. Our results suggest the importance of contrast polarity of the eyes in the face-selective neural responses from early development.

Just as faces share the same basic arrangement of features, with two eyes above a nose above a mouth, human eyes all share the same basic contrast polarity relations, with a sclera lighter than an iris and a pupil, and this is unique among primates. The current study examined whether this bright–dark relationship of sclera to iris plays a critical role in face recognition from early in development. Specifically, we tested face discrimination in 7- and 8-month-old infants while independently manipulating the contrast polarity of the eye region and of the rest of the face. This gave four face contrast polarity conditions: fully positive condition, fully negative condition, positive face with negated eyes (“negative eyes”) condition, and negated face with positive eyes (“positive eyes”) condition. In a familiarization and novelty preference procedure, we found that 7- and 8-month-olds could discriminate between faces only when the contrast polarity of the eyes was preserved (positive) and that this did not depend on the contrast polarity of the rest of the face. This demonstrates the critical role of eye contrast polarity for face recognition in 7- and 8-month-olds and is consistent with previous findings for adults.

Infants’ recognition of facial expressions develops during postnatal life. Previous studies have showed that infants learned to discriminate the facial expression of basic emotions such as happy or angry expressions by approximately 7 months of age. Although infants’ recognition of intense expressions has been demonstrated, their recognition of subtle expressions is unclear. The present study examined whether 6- to 7-month-old infants recognize the subtle anger expression. We presented the subtle expressions either as static or as dynamic displays. In static presentations, infants recognized the subtle anger expression. This result suggests that the infants have high sensitivity to angry expressions which signal a dangerous situation. In dynamic presentations, infants did not recognize the subtle anger expression. Infants around this age rarely see the dynamic anger expression in their daily lives. Their limited experience with dynamic expressions of anger might make it hard to recognize a dynamic subtle expression. Infants could learn to utilize facial motions in the development of recognition of facial expressions.

We investigated illusory motion perception in 6-to-8-month-old infants using a static figure which produces strong illusory motion. In experiment 1 we prepared a control figure, which was physically similar to the illusory motion figure but which did not produce illusory motion. We presented the illusory figure and the control figure side-by-side, and measured infants' looking time at the target illusory figure. Results showed that the infants' looking time at the illusory figure was significantly longer than that for the control. In experiment 2 we made another set of stimuli consisting of the same local pattern used in experiment 1, but which did not produce illusory motion. The results showed that no preferences were observed in experiment 2. These results suggest that 6-to-8-month-old infants perceive illusory motion in static figures.

To examine young infants' sensitivity to a pictorial depth cue, we compared monocular and binocular preferential looking to objects of which depth was specified by height-in-the-picture-plane. For adults, this cue generates the perception that a lower object is closer than a higher object. This study showed that 4- and 5-month-old infants fixated the lower, apparently closer, figure more often under the monocular than binocular presentation providing evidence of their sensitivity to the pictorial depth cue. Because the displays were identical in the two conditions except for binocular information for depth, the difference in looking-behavior indicated sensitivity to depth information, excluding a possibility that they responded to 2D characteristics. This study also confirmed the usefulness of the method, preferential looking with a monocular and binocular comparison, to examine sensitivity to a pictorial depth cue in young infants, who are too immature to reach reliably for the closer of two objects.

Newborn infants prefer face-like patterns over non-face-like patterns. This preference is explained by newborns' preference for a “top-heavy” configuration, that is, for geometric patterns that have more elements in the upper part than in the lower part of the configuration (Simion, Valenza, Macchi Cassia, Turati, & Umilta, 2002). However, for 3-month-old infants, face preference cannot be explained only by a preference for “top-heaviness” because they prefer veridical face images over top-heavy images. The present study used geometric patterns to investigate whether 2- to 3-month-old infants' preference for face patterns exceeds their preference for top-heavy configurations. In Experiment 1, we revealed that the infants preferred the face pattern to the top-heavy pattern only when the internal elements of the patterns were presented with face-like movements. This facilitative effect of internal movement was observed again in Experiment 2, in which the patterns were presented with non-face-like movements. These results suggest that 2- to 3-month-olds' preference for geometric face patterns is greater than their preference for top-heavy patterns only when aided by the movement of internal elements.

We examined the ability of young infants (3- and 4-month-olds) to detect faces in the two-tone images often referred to as Mooney faces. In Experiment 1, this performance was examined in conditions of high and low visibility of local features and with either the presence or absence of the outer head contour. We found that regardless of the presence of the outer head contour, infants preferred upright over inverted two-tone face images only when local features were highly visible (Experiment 1a). We showed that this upright preference disappeared when the contrast polarity of two-tone images was reversed (Experiment 1b), reflecting operation of face-specific mechanisms. In Experiment 2, we investigated whether motion affects infants’ perception of faces in Mooney faces. We found that when the faces appeared to be rigidly moving, infants did show an upright preference in conditions of low visibility of local features (Experiment 2a). Again the preference disappeared when the contrast polarity of the image was reversed (Experiment 2b). Together, these results suggest that young infants have the ability to integrate fragmented image features to perceive faces from two-tone face images, especially if they are moving. This suggests that an interaction between motion and form rather than a purely motion-based process (e.g., structure from motion) facilitates infants’ perception of faces in ambiguous two-tone images.

We examined glossiness perception in infants using a preferential looking paradigm. In experiment 1, the images of two doll-shaped objects with matte and glossy surfaces were presented to infants aged 5 to 6 and 7 to 8 months. The results showed that the 7 to 8 month olds, but not the 5 to 6 month olds, looked significantly longer at the glossy object than at the matte object. In experiment 2, we additionally employed an object that was matte and covered with textures of white paint splashes, whose luminance histogram was almost identical to that of the glossy object. The results showed that the 7 to 8 month old infants could discriminate between the glossy object and the textured object even though both had similar luminance histograms. Qualitatively similar results were obtained for simple spheres that did not contain facial features. Therefore, the results of experiments 1 and 2 were not due to differences in the visibility of the dolls' facial features. These findings suggest that 7 to 8 month old infants perceive difference between glossy objects and matte objects on the basis of surface representations.

We investigated whether infants experience the hollow-face illusion using a screen-based presentation of a rotating hollow mask. In experiment 1 we examined preferential looking between rotating convex and concave faces. Adults looked more at the concave—illusory convex—face which appears to counter rotate. Infants of 7- to 8-month-old infants preferred the convex face, and 5- to 6-month-olds showed no preference. While older infants discriminate, their preference differed from that of adults possibly because they don't experience the illusion or counter rotation. In experiment 2 we tested preference in 7- to 8-month-olds for angled convex and concave static faces both before and after habituation to the stimuli shown in experiment 1. The infants showed a novelty preference for the static shape opposite to the habituation stimulus, together with a general preference for the static convex face. This shows that they discriminate between convex and concave faces and that habituation to either transfers across a change in view. Seven- to eight-month-olds have been shown to discriminate direction of rigid rotation on the basis of perspective changes. Our results suggest that this, perhaps together with a weaker bias to perceive faces as convex, allows these infants to see the screen-based hollow face as hollow even though adults perceive it as convex.

We investigated the effect of the regular sequence of different views and the three-quarter view effect on the learning of unfamiliar faces by infants. 3–8-month-old infants were familiarized with unfamiliar female faces in either the regular condition (presenting 11 different face views from the frontal view to the left-side profile view in regular order) or the random condition (presenting the same 11 different face views in random order). Following the familiarization, infants were tested with a pair of a familiarized and a novel female face either in a three-quarter (Experiment 1) or in a profile view (Experiment 2). Results showed that only 6–8-month-old infants could identify a familiarized face in the regular condition when they were tested in three-quarter views. In contrast, 6–8-month-old infants showed no significant novelty preference in profile views. The results suggest that the regular sequence of different face views promotes the learning of unfamiliar faces by infants over 6 months old. Moreover, our findings imply that the three-quarter view effect appears in infants.

We examined two hypotheses about infants' perception of orientation. The first is that infants develop an expectation that the human body is normally vertical. To examine this hypothesis, we compared the preferential looking to vertical and oblique versions of a silhouette of a human body, to an inverted body, and to a grating. Our second hypothesis is that presenting a figure inside a frame affects the perception of orientation. To examine the second hypothesis, we placed the figure inside a surrounding square that was oriented normally or at an oblique angle. Four- to seven-month-old infants (N = 78) participated. The results showed that 6–7-month-old infants preferred the oblique human body presented upright; no such preference was observed for the inverted body or the grating. For all types of displays, the surrounding square influenced preferences. Our results suggest that (a) 6–7-month-old infants have specific expectations about the orientation of the human body, and (b) surrounding displays with a square could influence the perception of the orientation of the human body, as well as that of a grating.

Radial optic flow is one of the crucial cues for the perception of motion-in-depth and contributes to our daily adaptive actions such as locomotion or postural control. Although many researchers have examined the development of radial motion perception and that of adaptive motor actions, no valid developmental model for visuo-motor coordination has been proposed. In the present study, we tried to propose a developmental framework for the interactive process between visual radial motion perception and the adaptive motor actions in infancy, with a brief review of the previous psychophysical, psychophysiological, and neurophysiological studies. The effect of the functional development of the posterior parietal cortex, which might be induced by the experiences of ego motion in particular developmental periods, on visuo-motor coordination was discussed.

This study examined the perception of the rotating Kanizsa square by using a fixed-trial familiarization method. If the Kanizsa square is rotated across the pacmen, adult observers perceive not only a rotating illusory square, but also an illusory expansion/contraction motion of this square. The phenomenon is called a "rotational dynamic illusion". In experiments 1 and 2, we investigated whether infants perceived the rotational dynamic illusion, finding that 3-8-month-old infants perceived the rotational dynamic illusion as a simple rotation of the Kanizsa square. In experiment 3, we investigated whether infants perceived the rotational dynamic illusion as a rotation of the Kanizsa square or as a deformation of shape, finding that 3-4-month-old infants did perceive the rotational dynamic illusion as a rotation of the Kanizsa square. Our results show that while 3-8-month-old infants perceive the rotating Kanizsa square, however, it is difficult for the infants to extract expansion/contraction motion from the rotational dynamic illusion.

The Ebbinghaus illusion is a geometric illusion based on a size-contrast between a central circle and surrounding circles. A central circle surrounded by small inducing circles is perceived as being larger than a central circle surrounded by large inducing circles. In the present study we investigated 5- to 8-month-old infants' perception of the Ebbinghaus illusion using a preferential-looking paradigm. We measured the preference between a central circle surrounded by small inducing circles (overestimated figure) and a central circle surrounded by large inducing circles (underestimated figure). Infants showed a significant preference for the overestimated figure when the central circle was flashing, but not when it was static. Furthermore, there was no preference between the two figures when the central circles were removed. These results suggest that infants' preference reflects their perception of the size illusion of the central circle. There is a possibility that 5- to 8-month-old infants perceive the Ebbinghaus illusion.

We explored infants' ability to recognize the canonical colors of daily objects, including two color-specific objects (human face and fruit) and a non-color-specific object (flower), by using a preferential looking technique. A total of 58 infants between 5 and 8 months of age were tested with a stimulus composed of two color pictures of an object placed side by side: a correctly colored picture (e.g., red strawberry) and an inappropriately colored picture (e.g., green-blue strawberry). The results showed that, overall, the 6- to 8-month-olds showed preference for the correctly colored pictures for color-specific objects, whereas they did not show preference for the correctly colored pictures for the non-color-specific object. The 5-month-olds showed no significant preference for the correctly colored pictures for all object conditions. These findings imply that the recognition of canonical color for objects emerges at 6 months of age.

Using near-infrared spectroscopy (NIRS), we recorded changes of oxy-Hb, deoxy-Hb, and total-Hb in 7- to 8-month-old infants' and adults' brains in response to canonical face and scrambled face stimuli. Using a newly developed probe for NIRS recording, which was light and soft enough to be tolerated by infants, we were able to acquire data from the very young even in the awake state. Total-Hb in response to a canonical face stimulus was greater than for scrambled face stimuli only in the right hemisphere in infants. This indicates the presence of right hemisphere dominance of brain activity in response to face images in 7- to 8-month-old infants. In adults, oxy-Hb and total-Hb were significantly increased from baseline only for the canonical face in the right hemisphere. There were greater numbers of channels showing significantly increased activity for the canonical face in the right than in the left hemisphere. These data indicate that the right hemisphere is more dominant for canonical face perception in both infants and adults. However, overall, the increase of total-Hb and oxy-Hb in adults was modest compared to infants. Although the reason for the difference between infants and adults is unclear, in addition to developmental changes influencing face perception, some methodological problems may be present. Thus, because we recorded NIRS signals in infants and adults using the same method, anatomical and physiological problems might affect the results to some degree. Although comparing the results between infants and adults is not simple, the present study is the first to indicate how 7- to 8-month-old infants perceive scrambled face stimuli and to compare such results with those of adults in order to understand developmental changes in face perception.

Visual radial expansion/contraction motion provides important visual information that is used to control several adaptive actions. We investigated radial motion perception in infant Japanese macaque monkeys using an experimental procedure previously developed for human infants. We found that the infant monkeys' visual preference for the radial expansion pattern was greater than that for the radial contraction pattern. This trend towards an "expansion bias" is similar to that observed in human infants. These results suggest that asymmetrical radial motion processing is a basic visual function common to primates, and that it emerges early in life.

Detection of others' gaze direction is an essential tool in everyday communication. As the gaze direction is analyzed rapidly and automatically, we hardly notice how we are performing this task. Wollaston's illusion [Wollaston, W. H. (1824). On the apparent direction of eye in a portrait. Philosophical Transactions of the Royal Society of London Series B, 114, 247-256] provides us the chance to understand an aspect of this problem, in which the change in orientation of the face results in the shift of the perceived gaze direction. This illusion suggests that we analyze others' gaze directions by integrating information from eyes and that from face. By using Wollaston's illusion, we examined how 6- to 8-month-old infants process gaze direction in upright and inverted faces. Our results suggest that 8-month-olds process gaze direction in terms of the orientation of the face, and perceive an illusory shift of the gaze direction in Wollaston's illusion when the face was shown in an upright orientation.

This study compared 3- to 4-month-olds' recognition of previously unfamiliar faces learned in a moving or a static condition. Infants in the moving condition showed successful recognition with only 30 s familiarization, even when different images of a face were used in the familiarization and test phase (Experiment 1). In contrast, infants in the static condition showed successful recognition only when the familiarization duration was lengthened to 90 s and when the same image was used between the familiarization and test phase (Experiments 2 and 3). Furthermore, presentation of multiple static images of a face did not yield the same level of performance as the moving condition (Experiment 4). These results suggest that facial motion promotes young infants' recognition of unfamiliar faces.

We investigated 3- and 4-month-old infants’ sensitivity to differences defined by shading using a paired-comparison familiarity/novelty preference procedure. Infants were familiarized with a pair of displays consisting of homogeneous shaded disks, and then were tested with two displays: the familiar display and a novel one containing shaded disks with reversed polarity (defined as the target). Experiment 1 examined two assumptions on discerning shapes from shading in infants by manipulating the orientations in the shading gradient of stimuli. When the orientation of the shading gradient was vertical, 4-month-old infants looked at the novel display for a longer time during the test trial. However, they failed to detect differences when the orientation of shading gradients was horizontal. Three-month-old infants did not detect differences in either orientation of the shading gradient. Experiment 2 examined asymmetry in the detection of convex versus concave shapes. Four-month-old infants failed to detect the target when the orientation of the shading grating was vertical and the target was convex. Taken with the results of Experiment 1, concave shapes were much easier to detect than convex shapes for 4-month-olds. This asymmetry suggests that 4-month-old infants process shading information in the same manner as adults.

The perception of colour in an embedded field is affected by the surround colour. This phenomenon is known as chromatic induction. In the present study we investigated whether the colour perception by infants aged 5–7 months could be affected by the surround colour. In Experiments 1 and 2 each stimulus was composed of an array of six squares in tandem. The colour appearance of the array in the familiarization stimulus was established by chromatic induction. In Experiment 1 we used familiarization stimuli that were perceived as two-colour array with a two-colour surround. In Experiment 2 we used a familiarization stimulus that was perceived as a uniform-colour array with a two-colour surround. In the test phase, the uniform-colour array and the two-colour array were presented on a white uniform-colour surround in both experiments. The results showed that in Experiment 1 the 5- and 7-month-old infants had novelty preference for the uniform-colour test array. This suggested that the infants' colour perception could be affected by surround colour. The results of Experiment 2 showed that the 7-month-olds showed a novelty preference for the two-colour test array, but the 5-month-olds showed no novelty preference. This suggested that 7-month-olds' colour perception could be affected by surround colour, but that of 5-month-olds could not. We discuss the contradiction of the results between Experiments 1 and 2. Copyright © 2007 John Wiley & Sons, Ltd.

We investigated the perceptual development of motion transparency in 3- to 5-month-old infants. In two experiments we tested a total of 55 infants and examined their preferential looking behaviour. In experiment 1, we presented transparent motion as a target, and uniform motion as a non-target consisting of random-dot motions. We measured the time during which infants looked at the target and non-target stimuli. In experiment 2, we used paired-dot motions (Qian et al, 1994 Journal of Neuroscience14 7357 – 7366) as non-targets and also measured target looking time. We calculated the ratio of the target looking time to the total target and no-target looking time. In both experiments we controlled the dot size, speed, the horizontal travel distance of the dots, and the motion pattern of the dots. The results demonstrated that 5-month-old infants showed a statistically significant preference for motion transparency in almost all stimulus conditions, whereas the preference in 3- and 4-month-old infants depended on stimulus conditions. These results suggest that the sensitivity to motion transparency was robust in 5-month-olds, but not in 3- and 4-month-olds.

We examined perceptual transparency in infants. In a previous study, Johnson and Aslin (2000 Developmental Psychology36 808 – 816) found that 4-month-olds could perceive transparency in a moving chromatic display, but not in an achromatic display. In this study, we further examined perceptual transparency in infants using a static achromatic display. Considering the development of figural organisation and contrast sensitivity, we assumed that 3- to 4-month-olds would perceive transparency even in a static achromatic display. We created a transparency and a non-transparent display composed of a partially overlapping circle and square, by switching the colours. Infants aged 3 to 4 months ( n = 24) were familiarised with the transparency display (experiment 1) or with the non-transparent display (experiment 2). Then, they were confronted with a uniform colour and a two-colour figure. Infants showed novelty preference for the two-colour figure after they had been familiarised with the transparency display (experiment 1), but not after they had been familiarised with the non-transparent display (experiment 2). These results suggest that 3- to 4-month-old infants can perceive transparency in a static achromatic display.

Visual completion has been divided into two types: modal and amodal. While psychophysical studies with adults provided several common properties between modal and amodal completion, studies with infants showed differential trends in the development of these perceptual abilities. In the present study, we further examined the development of these two kinds of visual completion in infants aged 3 to 6 months. We created a display composed of a partially overlapping circle and square. The display induced either modal or amodal completion depending on the colour. Infants were familiarised with either the modal or the amodal display. After this familiarisation, the infants were tested on their discrimination between the complete figure and the broken figure. If the infants could perceptually complete the figures in the familiarisation display, they were expected to show a novelty preference for the broken figure. A total of thirty-two infants participated in the present study. Our results suggest that modal completion develops by 3 – 4 months of age, whereas amodal completion develops by 5 – 6 months of age.

We conducted four experiments on the development of motion perception in a total of 109 3- to 5-month-old infants using motion stimuli consisting of opposite-moving dots. A psychophysical study showed that adult subjects perceived two global planes with opposite-moving dots, but this global perception collapsed when paired opposite-moving dots were located within 0.4deg of one another (Qian, Andersen, & Adelson, 1994). We used this paired-dot stimulus as a non-target and the opponent motion stimulus as a target and examined target preference using methods based on forced-choice-preferential looking (Teller, 1979). In Experiment 1, we used 90 moving dots as stimuli. The results showed that 5-month-old infants had a significant preference for the targets but 4- and 3-month-olds did not. In Experiment 2, we used a small number of dots, and the results showed that 5-month-old infants did not prefer the target significantly. These results suggest that the preference for a target decreases according to the number of dots. In Experiment 3, we used opponent motion with long traveling length of the dots, and the results showed that all age groups, including 3-month-olds, had a preference for the moving targets. We showed that the preference observed in Experiment 3 was dependent not on local traveling length but on the global opponency. These results suggest that the perception of motion opponency based on a global motion cue emerges at 5 months of age (Experiments 1 and 2) and that the traveling length of the dots promote this perception (Experiments 3 and 4).

We examined the developmental process of the sensitivity to expansion and contraction with two separate experiments. In the present study, 121 2–8-month-old-infants were participated. In the expansion search condition, 58 infants were exposed to a display consisted of an expansion (target) and 11 contractions (distractors). In the contraction search condition, the other 63 infants were exposed to a display consisted of a contraction (target) and 11 expansions (distractors). The results showed that in the expansion search condition the infants except for 2-month-olds show significant preference for the target. The sensitivity (or insensitivity) to expansion (or contraction) over 3 months of age observed in the present study is similar to the asymmetry for the perception of expansion/contraction [T. Takeuchi, Visual search of expansion and contraction, Vision Res. 37 (1997) 2083–2090]. The relation between the development of the asymmetric perception of expansion/contraction and that of the cortical pathway was discussed.

In this paper, we summarize a series of studies on the developmental changes in social cognition in mother-raised infant chimpanzees from birth to around 2 years old. The infants preferentially tracked a photograph of their mother's face at 1 month but showed indifferent preferences to faces at 2 months old. This change in facial recognition was correlated with a decrease in neonatal spontaneous smiling, increase in social smiling and a decline in neonatal imitation of facial expressions. Also at around 2 months, the infants began to show preferences for directed-gaze faces over averted gazes, and the amount of mutual gaze time between mother and infant chimpanzees increased. Thus, by 2 months of age, abilities required for dyadic interactions are already developed in chimpanzees as is the case in humans. The development of triadic interactions, however, is rather different between these two species. The infant chimpanzee can follow another's pointing or gaze at around 1 year, but even by 2 years old, does not “share” attention with the others.

Emotional facial expressions are considered adaptive universal signals that emerged through phylogenetic evolution because of their crucial role for the survival of social species. From infancy humans develop dedicated neural circuits to exhibit and recognize a variety of facial expressions. However increasing evidence has shown instead that culture not only specifies when and how certain emotions can be expressed – i.e. social norms – but the mature perceptual mechanisms used to transmit and decode the visual information from emotional signals also differ between Western and Eastern adults. Specifically the mouth is more informative for transmitting emotional signals in Westerners and the eye region for Easterners engendering culture specific fixation biases towards these features. During development it is recognized that cultural differences can be observed at the level of emotional reactivity and regulation and to the culturally dominant modes of attention. Nonetheless no study has ever explored whether culture shapes the processing of facial emotional signals early in development. Our data show that by 7 months infants from both cultures visually discriminate facial expressions of emotion by relying on culturally distinct fixation strategies resembling those used by the adults from the environment in which they develop.

We investigated 3-8-month-olds' (N=62) perception of illusory contours in a Kanizsa figure by using a preferential looking technique. Previous studies suggest that this ability develops around 8 months of age. However, we hypothesized that even 3-4-month-olds could perceive illusory contours in a moving figure. To check our hypothesis, we created an illusory contour figure in which the illusory square underwent lateral movement. By rotating the elements of this figure, we created non-illusory contour figures. We found that: (1) infants preferred moving illusory contours to non-illusory contours by 3-4 months of age, and (2) only 7-8-month-olds preferred static illusory contours. Our findings demonstrate that motion information promotes infants' perception of illusory contours. Our results parallel those reported in the study of partly occluded objects ().

Humans have the tendency to perceive a face even in a non-living object. Previous studies report that people perceive facial features and even interpret a personality in a car front. Following these findings, we investigated whether the perception of a face in a face-like object is mediated by human face processing, which involves both featural and configural processing. In our experiment, participants were presented with 30 face-like objects and were asked about the existence of facial features, the intensity of typicality/distinctiveness, and the intensity of facial expression. Using multiple regression analysis, which predicts the perception of a face in a face-like object, we found that the existence of eyes was a significant predictor of variance in perceiving a face in a face-like object.

A cast shadow occurs when an object blocks the light from an illumination and projects a dark region onto a surface. Previous studies have reported that adults are slower to identify an object when the object has an incongruent cast shadow than when it has a congruent cast shadow ( Castiello, 2001 ). Here, we used the familiarization-novelty preference procedure to examine whether 5- to 8-month-old infants could detect the relationship between object shapes and cast shadows. In Experiment 1, we examined the infants' ability to detect incongruency between objects and cast shadows. Results showed that 7- to 8-month olds could detect incongruence between the object shapes and the cast shadows, whereas 5- to 6-month olds did not. Yet, our control experiment showed that infants could not detect this incongruence from stimuli in which a white outline had been added to the original cast shadow to decrease the possibility of it being perceived as a cast shadow (Experiment 2). The results of these experiments demonstrate that 7- to 8-month olds responded to the congruence of cast shadows and to consistent contrast polarity between the cast shadow and its background.

The current study examined the temporal dynamics of coarse and fine spatial information processing in 7- to 8-month-old infants. The ability to discriminate between spatially filtered images was assessed by measuring infants' spontaneous preference for a changing over no-changing image sequences. In Experiments 1 and 2, we found that infants were able to discriminate between low spatial frequency (LSF) image sequences at shorter durations (150 ms) than was the case with high spatial frequency (HSF) images (300 ms). When the LSF and HSF changes were pitted against each other in hybrid images containing both spatial frequencies (Experiment 3), the 7- to 8-month-old infants showed a preference for the LSF change across all tested durations (150 ms to 600 ms). However, infants' processing of hybrid image sequences was modulated both by changes in the relative contrast energy between LSFs and HSFs (Experiment 4), and image duration (Experiment 5). Finally, we found that in 12- to 13-month-old infants, the shift toward HSF dominance occurred at shorter duration than in 7- to 8-month-old infants (Experiment 6). Our findings are among the first to provide a temporal characterization of coarse-to-fine processing in infants' perception. Possible links to the development of specialized visual pathways are discussed.

This article presents two studies investigating the relationships between physical measurements and psychological judgments of human faces. The first study is concerned with gender and age classification, the second with femininity-masculinity and childlike-adultlike judgments of Japanese faces. The results indicate that (1) faces can be accurately classified into age categories based on physical measurements, (2) whereas age classification depends on the global information of a face, gender classification depends on its local information and (3) the femininity-masculinity judgment of male faces tends to be made on the basis of age information. The authors relate these results to the processing of KANSEI-information of, or subjective feelings about, a biological stimulus.

BackgroundIt is known that subjective contours are perceived even when a figure involves motion. However, whether this includes the perception of rigidity or deformation of an illusory surface remains unknown. In particular, since most visual stimuli used in previous studies were generated in order to induce illusory rigid objects, the potential perception of material properties such as rigidity or elasticity in these illusory surfaces has not been examined. Here, we elucidate whether the magnitude of phase difference in oscillation influences the visual impressions of an object's elasticity (Experiment 1) and identify whether such elasticity perceptions are accompanied by the shape of the subjective contours, which can be assumed to be strongly correlated with the perception of rigidity (Experiment 2).Methodology/principal findingsIn Experiment 1, the phase differences in the oscillating motion of inducers were controlled to investigate whether they influenced the visual impression of an illusory object's elasticity. The results demonstrated that the impression of the elasticity of an illusory surface with subjective contours was systematically flipped with the degree of phase difference. In Experiment 2, we examined whether the subjective contours of a perceived object appeared linear or curved using multi-dimensional scaling analysis. The results indicated that the contours of a moving illusory object were perceived as more curved than linear in all phase-difference conditions.Conclusions/significanceThese findings suggest that the phase difference in an object's motion is a significant factor in the material perception of motion-related elasticity.

A radially expanding flow with a linear positive speed gradient is perceived as a rigid object approaching the observer, whereas such a flow having no or a reduced speed gradient is perceived as a non-rigid, two-dimensionally deforming object (De Bruyn & Orban, 1990). We tested elementary school-aged children (younger children, 6–9 years, and older children, 9–11 years) and adults (20–22 years) to examine the development of the perception of rigidity. The results suggest that the perception of rigidity in response to a radial flow pattern with a speed gradient is similar in older (but not younger) children and adults. The development of rigidity perception from a radial flow pattern may be related to the maturation of the dorsal and ventral visual pathways during the elementary school years. Copyright © 2016 John Wiley & Sons, Ltd.

The current study examined infants' sensitivity to Wollaston's effect: When identical eyes are placed in differently angled faces, the perceived gaze direction shifts toward the orientation of the face such that physically, the direct gaze is perceived as averted toward the orientation of the face. Consistent with Wollaston's effect, we found that looking toward direct and averted gaze by 4- to 5- and 7- to 8-month-olds (n = 40) was affected by the head orientation context. These results demonstrate that infants aged 4 to 5 and 7 to 8 months integrate eye and head information to perceive another's gaze direction. In light of recent psychophysical findings, the current results suggest that the visual function supporting constant gaze perception across head rotation is already at work by 4 to 5 months of age.