Attentional blink in infants under 7 months.

Attentional blink manifests in infants at 7 months of age, indicating that the working memory capacity of 7-month-olds is comparable to that of adults. However, attentional blink in infants under 7 months is not well understood. In this study, we conducted two experiments to investigate attentional blink in 5- and 6-month-old infants. The results of Experiment 1 demonstrated that attentional blinks were not observed with either a short lag (200 ms) or a long lag (800 ms). This suggests that 5- and 6-month-olds are unable to consolidate both targets regardless of the temporal distance between the two. We then split the infants into two groups by their age and conducted Experiment 2 with infants aged younger and older than 180 days to compare their consolidating ability to observe whether they could recognize a single item at 100-ms speed by presenting the same visual stream that was used in Experiment 1 except that one target was eliminated. The results showed that infants over 180 days of age could identify a single target in the visual stream at 100-ms presentation speed, whereas infants under 180 days could not. The findings of the current study indicate that the limitation of working memory capacity in infants under 7 months of age is a possible reason for the lack of attentional blink.

Emotional response in babies' pupil contagion.

In this study, it was investigated whether an emotional response would occur in pupil contagion by using skin conductance response (SCR) in 5- and 6-month-old infants. In the experiment, emotional responses to pupil diameter change (dilating/constricting) between the face and eyes regions were compared by using pupil diameter response and SCR. The results showed that pupil diameter responses to pupil diameter changes did not differ between face and eyes regions. The emotional response indicated by the SCR significantly increased when participants looked at dilating pupils of face stimuli compared with when participants looked at constricted pupils of face stimuli. In addition, we found a significant correlation between SCR and pupil dilation in the face. This means that pupil diameter expansion significantly increases emotional response in pupil dilation of the face region.

Perception of invisible masked objects in early infancy.

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.

Infants' visual perception without feature-binding.

We reveal a unique visual perception before feature-integration of colour and motion in infants. Visual perception is established by the integration of multiple features, such as colour and motion direction. The mechanism of feature integration benefits from the ongoing interplay between feedforward and feedback loops, yet our comprehension of this causal connection remains incomplete. Researchers have explored the role of recurrent processing in feature integration by studying a visual illusion called 'misbinding', wherein visual characteristics are erroneously merged, resulting in a perception distinct from the originally presented stimuli. Anatomical investigations have revealed that the neural pathways responsible for recurrent connections are underdeveloped in early infants. Therefore, there is a possibility that younger infants could potentially perceive the physically presented visual information that adults miss due to misbinding. Here, we demonstrate that infants less than half a year old showed no misbinding; thus, they perceived the physically presented visual information, while infants more than half a year old perceived incorrectly integrated visual information, showing misbinding. Our findings indicate that recurrent processing barely functions in infants younger than six months of age and that visual information that should have been originally integrated is perceived as it is without being integrated.

Development of upper visual field bias for faces in infants.

The spatial location of the face and body seen in daily life influences human perception and recognition. This contextual effect of spatial locations suggests that daily experience affects how humans visually process the face and body. However, it remains unclear whether this effect is caused by experience, or innate neural pathways. To address this issue, we examined the development of visual field asymmetry for face processing, in which faces in the upper visual field were processed preferentially compared to the lower visual field. We found that a developmental change occurred between 6 and 7 months. Older infants aged 7-8 months showed bias toward faces in the upper visual field, similar to adults, but younger infants of 5-6 months showed no such visual field bias. Furthermore, older infants preferentially memorized faces in the upper visual field, rather than in the lower visual field. These results suggest that visual field asymmetry is acquired through development, and might be caused by the learning of spatial location in daily experience.

Infants' anticipatory eye movements: feature-based attention guides infants' visual attention.

When looking for an object, we identify it by selectively focusing our attention to a specific feature, known as feature-based attention. This basic attentional system has been reported in young children; however, little is known of whether infants could use feature-based attention. We have introduced a newly developed anticipation-looking task, where infants learned to direct their attention endogenously to a specific feature based on the learned feature (color or orientation), in 60 preverbal infants aged 7-8 months. We found that preverbal infants aged 7-8 months can direct their attention endogenously to the specific target feature among irrelevant features, thus showing the feature-based attentional selection. Experiment 2 bolstered this finding by demonstrating that infants directed their attention depending on the familiarized feature that belongs to a never-experienced object. These results that infants can form anticipation by color and orientation reflect they could drive their attention through feature-based selection.

Cortical processing of dynamic bodies in the superior occipito-temporal regions of the infants' brain: Difference from dynamic faces and inversion effect.

Previous functional neuroimaging studies imply a crucial role of the superior temporal regions (e.g., superior temporal sulcus: STS) for processing of dynamic faces and bodies. However, little is known about the cortical processing of moving faces and bodies in infancy. The current study used functional near-infrared spectroscopy (fNIRS) to directly compare cortical hemodynamic responses to dynamic faces (videos of approaching people with blurred bodies) and dynamic bodies (videos of approaching people with blurred faces) in infants' brain. We also examined the body-inversion effect in 5- to 8-month-old infants using hemodynamic responses as a measure. We found significant brain activity for the dynamic faces and bodies in the superior area of bilateral temporal cortices in both 5- to 6-month-old and 7- to 8-month-old infants. The hemodynamic responses to dynamic faces occurred across a broader area of cortex in 7- to 8-month-olds than in 5- to 6-month-olds, but we did not find a developmental change for dynamic bodies. There was no significant activation when the stimuli were presented upside down, indicating that these activation patterns did not result from the low-level visual properties of dynamic faces and bodies. Additionally, we found that the superior temporal regions showed a body inversion effect in infants aged over 5 months: the upright dynamic body stimuli induced stronger activation compared to the inverted stimuli. The most important contribution of the present study is that we identified cortical areas responsive to dynamic bodies and faces in two groups of infants (5-6-months and 7-8-months of age) and we found different developmental trends for the processing of bodies and faces.

Infants' recognition of their mothers' faces in facial drawings.

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.

Development of the multisensory perception of water in infancy.

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.

A longitudinal study of infant view-invariant face processing during the first 3-8 months of life.

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.

Rapid identification of the face in infants.

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 nontarget 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.

Cortical response to categorical color perception in infants investigated by near-infrared spectroscopy.

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.

Perceptual narrowing towards adult faces is a cross-cultural phenomenon in infancy: a behavioral and near-infrared spectroscopy study with Japanese infants.

Recent data showed that, in Caucasian infants, perceptual narrowing occurs for own-race adult faces between 3 and 9 months of age, possibly as a consequence of the extensive amount of social and perceptual experience accumulated with caregivers and/or other adult individuals of the same race of the caregiver. The neural correlates of this developmental process remain unexplored, and it is currently unknown whether perceptual tuning towards adult faces can be extended to other cultures. To this end, in the current study we tested the ability of 3- and 9-month-old Japanese infants to discriminate among adult and infant Asian faces in a visual familiarization task (Experiment 1), and compared 9-month-olds' cerebral hemodynamic responses to adult and infant faces as measured by near-infrared spectroscopy (NIRS) (Experiment 2). Results showed that 3-month-olds exhibit above-chance discrimination of adult and infant faces, whereas 9-month-olds discriminate adult faces but not infant faces (Experiment 1). Moreover, adult faces, but not infant faces, induced significant increases in hemodynamic responses in the right temporal areas of 9-month-old infants. Overall, our data suggest that perceptual narrowing towards adult faces is a cross-cultural phenomenon occurring between 3 and 9 months of age, and translates by 9 months of age into a right-hemispheric specialization in the processing of adult faces.

Wollaston's effect in infants: Do infants integrate eye and head information in gaze perception?

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.

Infants' visual system nonretinotopically integrates color signals along a motion trajectory.

Whereas early visual processing has been considered primarily retinotopic, recent studies have revealed significant contributions of nonretinotopic processing to the human perception of fundamental visual features. For adult vision, it has been shown that information about color, shape, and size is nonretinotipically integrated along the motion trajectory, which could bring about clear and unblurred perception of a moving object. Since this nonretinotopic processing presumably includes tight and elaborated cooperation among functional cortical modules for different visual attributes, how this processing matures in the course of brain development is an important unexplored question. Here we show that the nonretinotopic integration of color signals is fully developed in infants at five months of age. Using preferential looking, we found significantly better temporal segregation of colors for moving patterns than for flickering patterns, even when the retinal color alternation rate was the same. This effect could be ascribed to the integration of color signals along a motion trajectory. Furthermore, the infants' color segmentation performance was comparable to that of human adults. Given that both the motion processing and color vision of 5-month-old infants are still under development, our findings suggest that nonretinotopic color processing develops concurrently with basic color and motion processing. Our findings not only support the notion of an early presence of cross-modal interactions in the brain, but also indicate the early development of a purposive cross-module interaction for elegant visual computation.

The processing of faces across non-rigid facial transformation develops at 7 month of age: a fNIRS-adaptation study.

BACKGROUND: Using near-infrared spectroscopy (NIRS), our previous neural adaptation studies found that infants' bilateral temporal regions process facial identity (FiHN 5:153, 2011). In addition, we revealed that size-invariant processing of facial identity develops by 5 months of age (NR 23:984-988, 2012), while view-invariant processing develops around 7 months of age (FiHN 5:153, 2011). The aim in the current study was to examine whether infants' brains process facial identity across the non-rigid transformation of facial features by using the neural adaptation paradigm. We used NIRS to compare hemodynamic changes in the bilateral temporal areas of 5- to 6-month-olds and 7- to 8-month-olds during presentations of an identical face and of different faces. RESULTS: We found that (1) the oxyhemoglobin concentration around the T5 and T6 positions increased significantly during the presentation of different faces only in 7- to 8-month-olds and (2) 7- to 8-month-olds, but not 5- to 6-month-olds, showed attenuation in these channels to the presentation of the same face rather than to the presentation of different faces, regardless of non-rigid changes in facial features. CONCLUSIONS: Our results suggest that the processing of facial identity with non-rigid facial transformation develops around 7 months after birth.

Measuring young infants' sensitivity to height-in-the-picture-plane by contrasting monocular and binocular preferential-looking.

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.

Three-quarter view preference for three-dimensional objects in 8-month-old infants.

This study examined infants' visual perception of three-dimensional common objects. It has been reported that human adults perceive object images in a view-dependent manner: three-quarter views are often preferred to other views, and the sensitivity to object orientation is lower for three-quarter views than for other views. We tested whether such characteristics were observed in 6- to 8-month-old infants by measuring their preferential looking behavior. In Experiment 1 we examined 190- to 240-day-olds' sensitivity to orientation change and in Experiment 2 we examined these infants' preferential looking for the three-quarter view. The 240-day-old infants showed a pattern of results similar to adults for some objects, while the 190-day-old infants did not. The 240-day-old infants' perception of object view is (partly) similar to that of adults. These results suggest that human visual perception of three-dimensional objects develops at 6 to 8 months of age.

The other-race effect of pupil contagion in infancy.

Pupil contagion refers to the observer's pupil-diameter changes in response to changes in the pupil diameter of others. Recent studies on the other-race effect on pupil contagion have mainly focused on using eye region images as stimuli, revealing the effect in adults but not in infants. To address this research gap, the current study used whole-face images as stimuli to assess the pupil-diameter response of 5-6-month-old and 7-8-month-old infants to changes in the pupil-diameter of both upright and inverted unfamiliar-race faces. The study initially hypothesized that there would be no pupil contagion in either upright or inverted unfamiliar-race faces, based on our previous finding of pupil contagion occurring only in familiar-race faces among 5-6-month-old infants. Notably, the current results indicated that 5-6-month-old infants exhibited pupil contagion in both upright and inverted unfamiliar-race faces, while 7-8-month-old infants showed this effect only in upright unfamiliar-race faces. These results demonstrate that the face inversion effect of pupil contagion does not occur in 5-6-month-old infants, thereby suggesting the presence of the other-race effect in pupil contagion among this age group. Overall, this study provides the first evidence of the other-race effect on infants' pupil contagion using face stimuli.

Metacontrast masking is ineffective in the first 6 months of life.

Metacontrast masking is one of the most widely studied types of visual masking, in which a visual stimulus is rendered invisible by a subsequent mask that does not spatially overlap with the target. Metacontrast has been used for many decades as a tool to study visual processing and conscious perception in adults. However, there are so far no infant studies on metacontrast and it remains unknown even whether it occurs in infants. The present study examined metacontrast masking in 3- to 8-month-old infants (N = 168) using a habituation paradigm. We found that metacontrast is ineffective for infants under 7 months and that younger infants can perceive a masked stimulus that older infants cannot. Our results suggest that metacontrast is distinct from other simple types of masking that occur in early infancy, and would be consistent with the idea that metacontrast results from the disruption of recurrent processing.