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This study investigated the difference in the McGurk effect between own-race-face and other-race-face stimuli among Japanese infants from 5 to 9 months of age. The McGurk effect results from infants using information from a speaker’s face in audiovisual speech integration. We hypothesized that the McGurk effect varies with the speaker’s race because of the other-race effect, which indicates an advantage for own-race faces in our face processing system. Experiment 1 demonstrated the other-race effect on audiovisual speech integration such that the infants ages 5–6 months and 8–9 months are likely to perceive the McGurk effect when observing an own-race-face speaker, but not when observing an other-race-face speaker. Experiment 2 found the other-race effect on audiovisual speech integration regardless of irrelevant speech identity cues. Experiment 3 confirmed the infants’ ability to differentiate two auditory syllables. These results showed that infants are likely to integrate voice with an own-race-face, but not with an other-race-face. This implies the role of experiences with own-race-faces in the development of audiovisual speech integration. Our findings also contribute to the discussion of whether perceptual narrowing is a modality-general, pan-sensory process.

This study examined whether 8-month-old infants’ hemodynamic responses in the temporal region were modulated by repeated presentation of “Peekaboo” by using functional near-infrared spectroscopy (fNIRS). Previous studies have shown that infants’ temporal region responds to faces (e.g., Otsuka et al., 2007). A recent electroencephalography study showed that the neural activity of infants was modulated by repeated presentation of “Peekaboo.” Some fNIRS studies also revealed that the movie of “Peekaboo” activated the hemodynamic response of the temporal region in infancy. However, no studies have shown the hemodynamic modulation of the temporal region according to the repeated presentation of “Peekaboo” in infants. In order to examine whether the hemodynamic responses of the temporal region were modulated by repeated presentation of “Peekaboo,” we compared the activity of the temporal region between the early and late trials. We set long and short delays before face-presentation. The results showed that the concentration of oxy-hemoglobin in the right occipitotemporal region (Ch 21) in both conditions increased after the presentation of “Peekaboo” relative to the baseline. Moreover, in the long delay condition, the hemodynamic modulation of the right occipitotemporal region was induced according to the repeated presentation of “Peekaboo” in infants.

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.

Primary cognitive processes, such as spatial attention, are essential to our higher cognitive abilities and develop dramatically in the first year of life. The spatial aspect of infants' working memory is equivalent to that of adults. However, it is unclear whether this is true for the temporal domain. Thus, we investigated the temporal aspect of infants' working memory using an attentionally demanding task by focusing on the attentional blink effect, in which the identification of the second of the two brief targets is impaired when inter-target lags are short. We argue that finding a similar pattern of the attentional blink in preverbal infants and adults indicates that infants can complete the consolidation of the first target into working memory at a similar temporal scale as adults. In this experiment, we presented 7- to 8-month-old infants with rapid serial visual streams at a rate of 100 ms/item, including two female faces as targets, and examined whether they could identify the targets by measuring their preference to novel faces compared to targets. The temporal separation between the two targets was 200 or 800 ms. We found that the infants could identify both targets under the longer lag, but they failed to identify the second target under the shorter lag. The adult experiment using the same temporal separation as in the infant experiment revealed the attentional blink effect. These results suggest that 7- to 8-month-old infants can consolidate two items into working memory by 800 ms but not by 200 ms.

Sound symbolism, which is the systematic and non-arbitrary link between a word and its meaning, has been suggested to bootstrap language acquisition in infants. However, it is unclear how sound symbolism is processed in the infants’ brain. To address this issue, we investigated the cortical response in 11-month-old infants in relation to sound-symbolic correspondences using near-infrared spectroscopy (NIRS). Two types of stimuli were presented: a novel visual stimulus (e.g., a round shape) followed by a novel auditory stimulus that either sound-symbolically matched (moma) or mismatched (kipi) the shape. We found a significant hemodynamic increase in the right temporal area, when the sound and the referent sound were symbolically matched, but this effect was limited to the moma stimulus. The anatomical locus corresponds to the right posterior superior temporal sulcus (rSTS), which is thought to process sound symbolism in adults. These findings suggest that prelinguistic infants have the biological basis to detect cross-modal correspondences between word sounds and visual referents.

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.

Our visual system can rapidly process stimuli relevant to our current behavioral goal within various irrelevant stimuli in natural scenes. This ability to detect and identify target stimuli during non target stimuli has been mainly studied in adults, so that the development of this high-level visual function has been unknown among infants, although it has been shown that 15-month-olds' temporal thresholds of face visibility are close to those of adults. However, we demonstrate here that infants younger than 15 months can identify a target face among nontarget but meaningful scene images. In the current study, we investigated infants' ability to detect and identify a face in a rapid serial visual presentation. Experiment 1 examined whether 5- to 8-month-olds could discriminate the difference in the presentation duration of visual streams (100 vs. 11 ms). Results showed that 7- and 8-month olds successfully discriminated between the presentation durations. In Experiment 2, we examined whether 5- to 8-month-olds could detect the face presented for 100 ms and found that 7- and 8-month-olds could detect the face embedded in rapid serial visual streams. To further clarify the face processing at this age of infants, we tested whether infants could identify upright and inverted faces in rapid visual streams in Experiments 3a and 3b. The results showed that 7- and 8-month-olds identified upright faces, but not inverted faces, during the visual stream, which reflected face inversion effects. Overall, we suggest that the temporal speed of face processing at 7 and 8 months of age would be comparable to that of adults. (C) 2019 The Authors. Published by Elsevier Inc. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).

This study examined the development of ability to recognize familiar face in drawings in infants aged 6-8 months. In Experiment 1, we investigated infants' recognition of their mothers' faces by testing their visual preference for their mother's face over a stranger's face under three conditions: photographs, cartoons produced by online software that simplifies and enhances the contours of facial features of line drawings, and veridical line drawings. We found that 7- and 8-month-old infants showed a significant preference for their mother's face in photographs and cartoons, but not in veridical line drawings. In contrast, 6-month-old infants preferred their mother's face only in photographs. In Experiment 2, we investigated a visual preference for an upright face over an inverted face for cartoons and veridical line drawings in 6- to 8-month-old infants, finding that infants aged older than 6 months showed the inversion effect in face preference in both cartoons and veridical line drawings. Our results imply that the ability to utilize the enhanced information of a face to recognize familiar faces may develop aged around 7 months of age.

View-invariant face processing emerges early in life. A previous study (Nakato et al., 2009) measured infant hemodynamic responses to faces from the frontal and profile views in the bilateral temporal areas, which have been reported to be involved in face processing using near-infrared spectroscopy. It was reported that 5-month-old infants showed increased oxyhemoglobin (oxy-Hb) responses to frontal faces, but not to profile faces. In contrast, 8-month-old infants displayed increased oxy-Hb responses to profile faces as well as to frontal faces. In this study, we used the experimental method developed in the previous study to investigate the development of view-invariant face processing, every month for 5 months (from the first 3–8 months of life). We longitudinally measured hemodynamic responses to faces from the frontal and profile views in 14 infants. The longitudinal measurements allowed us to investigate individual differences in each participant. We modeled each infant's hemodynamic oxy-Hb responses to frontal and profile faces using linear regression analysis. Processing of profile faces emerged later and underwent larger improvements than that of frontal faces. We also found an anticorrelation between the speed of improvement in face processing and the hemodynamic response to faces at the age of 3- months. Group analysis of the averaged hemodynamic data from the 14 infants using linear regression revealed that the processing of profile faces emerged between 5 and 6 months of age. Infant view-invariant face processing developed first for frontal faces. This was followed by the emergence of processing of profile faces.

The human perceptual system enables us to extract visual properties of an object’s material from auditory information. In monkeys, the neural basis underlying such multisensory association develops through experience of exposure to a material; material information could be processed in the posterior inferior temporal cortex, progressively from the high-order visual areas. In humans, however, the development of this neural representation remains poorly understood. Here, we demonstrated for the first time the presence of a mapping of the auditory material property with visual material (“Metal” and “Wood”) in the right temporal region in preverbal 4- to 8-month-old infants, using near-infrared spectroscopy (NIRS). Furthermore, we found that infants acquired the audio-visual mapping for a property of the “Metal” material later than for the “Wood” material, since infants form the visual property of “Metal” material after approximately 6 months of age. These findings indicate that multisensory processing of material information induces the activation of brain areas related to sound symbolism. Our findings also indicate that the material’s familiarity might facilitate the development of multisensory processing during 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.

Objective: We aimed to clarify the validity of fNIRS measurement for assessing the methylphenidate (MPH) induced neuropharmacological effect in medication-naive children with attention deficit hyperactivity disorder (ADHD) with or without comorbid autism spectrum disorder (ASD), thereby providing the first evidence for differing neurofunctional pathology between the two groups. Methods: We monitored the effects of a single acute clinical dose of MPH on the cortical hemodynamics of 32 medication-naive ADHD children (ADHD with ASD n=11 and ADHD without ASD n=21) performing a go/no-go task before and 1.5 h after MPH or placebo administration, using a randomized, double-blind, placebo-controlled, crossover design. In addition, all subjects’ symptoms were monitored using the Japanese version of the ADHD Rating Scale-IV (ADHDRS- IV-J) before and one month after MPH administration. Results: Medication-naive ADHD children without ASD exhibited reduced right prefrontal activation. MPH medication elicited significant right prefrontal activation except in comparative conditions associated with the placebo effect. Medication-naive ADHD children with ASD exhibited marginal activation before the first day of medication and reduced activation after MPH medication in the right prefrontal area. While the neuropharmacological effects of MPH were different, ADHD-RS-IV-J scores were significantly improved one month after MPH administration in ADHD groups both with and without ASD. Conclusion: Taken together, these results suggest that ADHD with ASD is characterized by a different underlying neurofunctional pathology for inhibition control than that without ASD. To our knowledge, this is the first comparative neuroimaging study between ADHD patients with and without comorbid ASD.

To examine sensitivity to pictorial depth cues in young infants (4 and 5 months-of-age), we compared monocular and binocular preferential looking to a display on which two faces were equidistantly presented and one was larger than the other, depicting depth from the size of human faces. Because human faces vary little in size, the correlation between retinal size and distance can provide depth information. As a result, adults perceive a larger face as closer than a smaller one. Although binocular information for depth provided information that the faces in our display were equidistant, under monocular viewing, no such information was provided. Rather, the size of the faces indicated that one was closer than the other. Infants are known to look longer at apparently closer objects. Therefore, we hypothesized that infants would look longer at a larger face in the monocular than in the binocular condition if they perceived depth from the size of human faces. Because the displays were identical in the two conditions, any difference in looking-behavior between monocular and binocular viewing indicated sensitivity to depth information. Results showed that 5-month-old infants preferred the larger, apparently closer, face in the monocular condition compared to the binocular condition when static displays were presented. In addition, when presented with a dynamic display, 4-month-old infants showed a stronger ‘closer’ preference in the monocular condition compared to the binocular condition. This was not the case when the faces were inverted. These results suggest that even 4-month-old infants respond to depth information from a depth cue that may require learning, the size of faces.

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.

We aimed to verify painters' empirical rules in painting portraits from the perspective of face perception. In particular, we examined the effects of lighting on perceiving impressions and facial expressions of a depicted person by using portrait paintings with various lighting conditions of contrast (high, low) and position (left, right). Viewers rated their impressions of the people in the portraits and those people's expressions using 7-point scales. Impressions regarding likability or attractiveness were stable regardless of the lighting conditions, while the other impressions differed among the lighting conditions. Positive emotions were perceived more strongly in paintings with low contrast, whereas negative emotions were perceived more strongly in paintings with high contrast. Overall, these results suggest that lighting has a systematic effect on face perception even in portrait paintings. We propose that the current study provides empirical evidence of painters' implicit knowledge.

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.

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.

Arcimboldo images induce the perception of faces when shown upright despite the fact that only nonfacial objects such as vegetables and fruits are painted. In the current study, we examined whether infants recognize a face in the Arcimboldo images by using the preferential looking technique and near-infrared spectroscopy (NIRS). In the first experiment, we measured looking preference between upright and inverted Arcimboldo images among 5- and 6-month-olds and 7- and 8-month-olds. We hypothesized that if infants perceive the Arcimboldo images as faces, they would prefer the upright images to the inverted ones. We found that only 7- and 8-month-olds significantly preferred upright images, suggesting that they could perceive the Arcimboldo images as faces. In the second experiment, we measured hemodynamic responses using NIRS. Based on the behavioral data, we hypothesized that 7- and 8-month-olds would show different neural activity for upright and inverted Arcimboldo images, as do adults. Therefore, we measured hemodynamic responses in 7- and 8-month-olds while they were looking at upright and inverted Arcimboldo images. Their responses were then compared with the baseline activation during the presentation of individual vegetables. We found that the concentration of oxyhemoglobin increased in the left temporal area during the presentation of the upright images compared with the baseline during the presentation of vegetables. The results of the two experiments suggest that (a) the ability to recognize the upright Arcimboldo images as faces develops at around 7 or 8 months of age and (b) processing of the upright Arcimboldo images is related to the left temporal area of the brain.

A visual pattern's orientation influences how adults amodally complete that pattern. We examined whether this is also the case with infants using Markovich's pattern, consisting of a black polygon partially occluded by a gray disc, which is completed as either a vertically symmetrical hexagon or as a pentagon, depending on the pattern's orientation. Our experiment consisted of two prefamiliarization test trials, six familiarization trials, and two postfamiliarization test trials. In the familiarization trials, two identical Markovich patterns, upright or slanted, were presented to 7–8-month-old infants (N = 28) side by side on a CRT monitor. In the pre- and postfamiliarization test trials, a pentagon and a hexagon were presented side by side. Infants looked longer at the hexagon than at the pentagon in the postfamiliarization test trials. This suggests that infants completed the pattern as a pentagon regardless of the pattern's orientation. This lack of an orientation effect suggests that infants do not use the figure's symmetry as a guiding principle for amodal completion.

Recognition of other people's facial expressions of emotion plays an important role in social communication in infants as well as adults. Evidence from behavioral studies has demonstrated that the ability to recognize facial expressions develops by 6 to 7 months of age. Although the regions of the infant brain involved in processing facial expressions have not been investigated, neuroimaging studies in adults have revealed that several areas including the superior temporal sulcus (STS) participate in the processing of facial expressions. To examine whether the temporal area overlying the STS is responsible for the processing of facial expressions in infants, near-infrared spectroscopy (NIRS) was used to measure the neural activity in the temporal area overlying the STS as infants looked at happy and angry faces. NIRS provides a non-invasive means of estimating cerebral blood flow in the human brain and does not require severe constraints of head-movement. According to the International 10-20 system for EEG electrode placement, the measurement area was located in the bilateral temporal area centered at positions T5 and T6, which correspond to the STS. The time-course of the average change in total-Hb concentration revealed a clear difference in the pattern of hemodynamic responses to happy and angry faces. The hemodynamic response increased gradually when infants looked at happy faces and was activated continuously even after the disappearance of the face. In contrast, the hemodynamic responses for angry faces increased during the presentation of angry faces, then decreased rapidly after the face disappeared. Moreover, the left temporal area was significantly activated relative to the baseline when infants looked at happy faces, while the right temporal area was significantly activated for angry faces. These findings suggest hemispheric differences in temporal areas during the processing of positive and negative facial expressions in infants.

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.

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.

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.

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).

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.