Biomedical subjects

Masaki Tomonaga

Publications and source records attributed to Masaki Tomonaga.

At least 19 recordsLinked to original sources

PubMed2006

Visual search for orientation of faces by a chimpanzee (Pan troglodytes): face-specific upright superiority and the role of facial configural properties.

A previous experiment showed that a chimpanzee performed better in searching for a target human face that differed in orientation from distractors when the target had an upright orientation than when targets had inverted or horizontal orientation [Tomonaga (1999a) Primate Res 15:215-229]. This upright superiority effect was also seen when using chimpanzee faces as targets but not when using photographs of a house. The present study sought to extend these results and explore factors affecting the face-specific upright superiority effect. Upright superiority was shown in a visual search for orientation when caricaturized human faces and dog faces were used as stimuli for the chimpanzee but not when shapes of a hand and chairs were presented. Thus, the configural properties of facial features, which cause an inversion effect in face recognition in humans and chimpanzees, were thought to be a source of the upright superiority effect in the visual search process. To examine this possibility, various stimuli manipulations were introduced in subsequent experiments. The results clearly show that the configuration of facial features plays a critical role in the upright superiority effect, and strongly suggest similarity in face processing in humans and chimpanzees.

Animals↗

PubMed2006

Visual search for moving and stationary items in chimpanzees (Pan troglodytes) and humans (Homo sapiens).

Four visual search experiments were conducted using human and chimpanzee subjects to investigate attentional processing of movement, and perceptual organization based on movement of items. In the first experiment, subjects performed visual searches for a moving target among stationary items, and for a stationary target among moving items. Subjects of both species displayed an advantage in detecting the moving item compared to the stationary one, suggesting the priority of movement in the attentional processing. A second experiment assessed the effect of the coherent movement of items in the search for a stationary target. Facilitative effects of motion coherence were observed only in the performance of human subjects. In the third and fourth experiments, the effect of coherent movement of the reference frame on the search for moving and stationary targets was tested. Related target movements significantly influenced the search performance of both species. The results of the second, third, and fourth experiments suggest that perceptual organization based on coherent movements is partially shared by chimpanzees and humans, and is more highly developed in humans.

Adolescent↗

PubMed2006

Japanese macaques form a cross-modal representation of their own species in their first year of life.

We tested whether infant Japanese macaques (Macaca fuscata) have a cross-modal representation of their own species. We presented monkeys with a photograph of either a monkey or a human face on an LCD monitor after playing back a vocalization of one of those two species. The subjects looked at the monitor longer when a human face was presented after the monkey vocalization than when the same face was presented after human vocalization. This suggests that monkeys recall and expect a monkey's face upon hearing a monkey's voice.

Animals↗

PubMed2005

Origins of smile and laughter: a preliminary study.

To present fundamental data, spontaneous smiles and spontaneous laughs (smiles accompanied by vocal sounds) were cross-sectionally observed in 10 newborn infants and longitudinally observed in six infants. Unilateral spontaneous smiles were more common than bilateral smiles in neonates, but by 2 months almost all spontaneous smiles were bilateral. All spontaneous laughs were bilateral. "Spontaneous smile" and "Spontaneous laugh" might be different behaviors from the beginning.

Cross-Sectional Studies↗

PubMed2005

Perception of motion trajectory of object from the moving cast shadow in infants.

A moving cast shadow of the object affects the perception of the object's trajectory in adults [Kersten, D., Mamassian, P., & Knill, D. C. (1997). Moving cast shadow induce apparent motion in depth. Perception, 26, 171-192]. In the present study, we investigated by using a habituation-dishabituation procedure whether infants at 4- to 7-months old discriminate the motion trajectory of a ball from the moving shadow it casts. In Experiment 1, 4- to 5-month-old and 6- to 7-month-old were tested for ability to discriminate between a "depth" display containing a ball and a cast shadow with a diagonal trajectory and an "up" display containing a ball with a diagonal trajectory and a cast shadow with a horizontal trajectory. Six- and 7-month-old, but not 4- and 5-month-old, infants looked significantly longer at the "up" display than at the "depth" display. In Experiment 2, we tested whether 4- to 5-month-old and 6- to 7-month-old infants would perceive "up" motion as categorically different from "depth" depending on the object's 3-D trajectory. We used displays containing a ball and a cast shadow with the same trajectories as those in Experiment 1 except that the cast shadows appeared above the ball. These displays did not produce 3-D impressions in adults. Neither age group of infants exhibited significant differences between "up" and "depth" displays. When the results from the two experiments are considered, 6- and 7-month-old infants discriminated the motion trajectory of the ball from the moving cast shadows. This developmental emergence of depth perception from a moving cast shadow at 6 months of age is consistent with that of other pictorial depth cues.

Aging↗

PubMed2005

Group differences in the mutual gaze of chimpanzees (Pan troglodytes).

A comparative developmental framework was used to determine whether mutual gaze is unique to humans and, if not, whether common mechanisms support the development of mutual gaze in chimpanzees and humans. Mother-infant chimpanzees engaged in approximately 17 instances of mutual gaze per hour. Mutual gaze occurred in positive, nonagonistic contexts. Mother-infant chimpanzees at a Japanese center exhibited significantly more mutual gaze than those at a center in the United States. Cradling and motor stimulation varied across groups. Time spent cradling infants was inversely related to mutual gaze. It is suggested that in primates, mutual engagement is supported via an interchangeability of tactile and visual modalities. The importance of mutual gaze is best understood within a perspective that embraces both cross-species and cross-cultural data.

Agonistic Behavior↗

PubMed2005

Can chimpanzee infants (Pan troglodytes) form categorical representations in the same manner as human infants (Homo sapiens)?

We directly compared chimpanzee infants and human infants for categorical representations of three global-like categories (mammals, furniture and vehicles), using the familiarization-novelty preference technique. Neither species received any training during the experiments. We used the time that participants spent looking at the stimulus object while touching it as a measure. During the familiarization phase, participants were presented with four familiarization objects from one of three categories (e.g. mammals). Then, they were tested with a pair of novel objects, one was a familiar-category object and another was a novel-category object (e.g. vehicle) in the test phase. The chimpanzee infants did not show significant habituation, whereas human infants did. However, most important, both species showed significant novelty-preference in the test phase. This indicates that not only human infants, but also chimpanzee infants formed categorical representations of a global-like level. Implications for the shared origins and species-specificity of categorization abilities, and the cognitive operations underlying categorization, are discussed.

Age Factors↗

PubMed2004

Facial responses to four basic tastes in newborn rhesus macaques (Macaca mulatta) and chimpanzees (Pan troglodytes).

Newborn humans are known to show specific facial expressions in response to various kinds of taste stimuli and are presumed to be able to discriminate those kinds of tastes from just after birth. As the closest relatives to humans, the taste reactivity (threshold, preference and taste-elicited facial expression) of non-human primates has long been of great interest. To date, however, there have been few investigations in newborn non-human primates. In the present study, we investigated the facial expressions elicited in response to four basic taste stimuli, sweet, salty, sour and bitter, in the newborns of two non-human primate species, rhesus macaques and chimpanzees. The taste-elicited facial expressions were compared among the kinds of taste stimuli and between the two species. Rhesus macaques of less than 7 days old showed different patterns of facial expressions for water/sweet than for bitter, and chimpanzees less than 30 days old did so for sweet and bitter. The differences between these two species were evident in the presence and absence of certain facial expressions and the emerging patterns of certain components for each stimulus. In particular, chimpanzee response patterns to the bitter stimulus resembled to those of humans rather than rhesus macaques. Overall, rhesus macaques and chimpanzees responded differently to the same kinds of tastes, presumably reflecting differences in their evolutionary backgrounds.

Animals↗

PubMed2004

Fetal habituation correlates with functional brain development.

In this study, we divided 26 fetuses at 32-37 weeks of gestation into three groups using combined criteria of gestational age and behavioral indicators. We investigated fetal habituation to vibroacoustic stimulation (VAS). Fetuses showed habituation from at least 32 weeks of gestation. Furthermore, fetuses less developed from behavioral standpoint took significantly more trials to achieve habituation than developed fetuses even in the same gestational age. Taken together with these data, it was proved that there was a relationship between aspects of behavioral development and habituation.

Acoustic Stimulation↗

PubMed2004

Associative learning and memory in a chimpanzee fetus: Learning and long-lasting memory before birth.

We tested whether a chimpanzee fetus could form an association between an extrauterine tone and vibroacoustic stimulation (VAS) using classical conditioning treatment. Two kinds of pure tone were used as the conditioned stimuli, one where a 500-Hz tone was always followed by a VAS of 80 Hz (110 gal), the unconditioned stimulus (US), and another where a 1000-Hz tone was never followed by a VAS. This treatment was repeated 156 times in total until natural labor at 233 days of gestational age. Behavioral tests on the 33rd and 58th days after birth revealed a differential response to the tones: The infant displayed an exaggerated response to the 500-Hz tone, but not to the 1000-Hz tone. Other naïve chimpanzee infants did not show any response to either tone, which suggests that a chimpanzee fetus can distinguish between tones and form an association, and that it retains such information for at least 2 months after birth.

Animals↗

PubMed2004

Imitation in neonatal chimpanzees (Pan troglodytes).

This paper provides evidence for imitative abilities in neonatal chimpanzees (Pan troglodytes), our closest relatives. Two chimpanzees were reared from birth by their biological mothers. At less than 7 days of age the chimpanzees could discriminate between, and imitate, human facial gestures (tongue protrusion and mouth opening). By the time they were 2 months old, however, the chimpanzees no longer imitated the gestures. They began to perform mouth opening frequently in response to any of the three facial gestures presented to them. These findings suggest that neonatal facial imitation is most likely an innate ability, developed through natural selection in humans and in chimpanzees. The relationship between the disappearance of neonatal imitation and the development of social communicative behavior is discussed from an evolutionary perspective.

Age Factors↗

PubMed2003

Perception of depth from shading in infant chimpanzees ( Pan troglodytes).

We investigated the ability to perceive depth from shading, one of the pictorial depth cues, in three chimpanzee infants aged 4-10 months old, using a preferential reaching task commonly used to study pictorial depth perception in human infants. The chimpanzee infants reached significantly more to three-dimensional toys than to pictures thereof and more to the three-dimensional convex than to the concave. Furthermore, two of the three infants reached significantly more to the photographic convex than to the photographic concave. These infants also looked longer at the photographic convex than the concave. Our results suggest that chimpanzees perceive, at least as early as the latter half of the first year of life, pictorial depth defined by shading information. Photographic convexes contain richer information about pictorial depth (e.g., attached shadow, cast shadow, highlighted area, and global difference in brightness) than simple computer-graphic graded patterns. These cues together might facilitate the infants' perception of depth from shading.

Age Factors↗

PubMed2003

Finger drawing by infant chimpanzees ( Pan troglodytes).

We introduced a new technique to investigate the development of scribbling in very young infants. We tested three infant chimpanzees to compare the developmental processes of scribbling between humans and chimpanzees. While human infants start to scribble on paper at around the age of 18 months, our 13- to 23-month-old infant chimpanzees had never been observed scribbling prior to this study. We used a notebook computer with a touch-sensitive screen. This apparatus was able to record the location of the subjects' touches on the screen. Each touch generated a fingertip-sized dot at the corresponding on-screen location. During spontaneous interactions with this apparatus, all three infants and two mother chimpanzees left scribbles with their fingers on the screen. The scribbles contained not only simple dots or short lines, but also curves and hook-like lines or loops, most of which were observed in the instrumental drawings of adult chimpanzees. The results suggest that perceptual-motor control for finger drawing develops in infant chimpanzees. Two of the infants performed their first scribble with a marker on paper at the age of 20-23 months. Just prior to this, they showed a rapid increase in combinatory manipulation of objects. These findings suggest that the development of combinatory manipulation of objects as well as that of perceptual-motor control may be necessary for the emergence of instrumental drawing on paper.

Animals↗

PubMed2003

Do infant Japanese macaques ( Macaca fuscata) categorize objects without specific training?

In the present study, we examined whether infant Japanese macaques categorize objects without any training, using a similar technique also used with human infants (the paired-preference method). During the familiarization phase, subjects were presented twice with two pairs of different objects from one global-level category. During the test phase, they were presented twice with a pair consisting of a novel familiar-category object and a novel global-level category object. The subjects were tested with three global-level categories (animal, furniture, and vehicle). It was found that they showed significant novelty preferences as a whole, indicating that they processed similarities between familiarization objects and novel familiar-category objects. These results suggest that subjects responded distinctively to objects without training, indicating the possibility that infant macaques possess the capacity for categorization.

Analysis of Variance↗

PubMed2003

Preference for human direct gaze in infant chimpanzees (Pan troglodytes).

We studied gaze perception in three infant chimpanzees (Pan troglodytes), aged 10-32 weeks, using a two-choice preferential-looking paradigm. The infants were presented with two photographs of a human face: (a) with the eyes open or closed, and (b) with a direct or an averted gaze. We found that the chimpanzees preferred looking at the direct-gaze face. However, in the context of scrambled faces, the infants showed no difference in gaze discrimination between direct and averted gazes. These findings suggest that gaze perception by chimpanzees may be influenced by the surrounding facial context. The relationship between gaze perception, face processing, and the adaptive significance of gaze perception are discussed from an evolutionary perspective.

Animals↗

PubMed2003

Urinary steroids, FSH and CG measurements for monitoring the ovarian cycle and pregnancy in the chimpanzee.

Non-invasive methods for monitoring reproductive status of chimpanzee based on the measurement of urinary steroids and gonadotropins were examined. A typical pre-ovulatory urinary estrone conjugate (E1C) surge and post-ovulatory increase in pregnandiol glucuronide (PdG) were seen during the menstrual cycle. Urinary follicle stimulating hormone (FSH) showed two peaks over the infertile menstrual cycle. The earliest changes indicating pregnancy were a coincident rise in E1C and chorionic gonadotropin (CG) levels and a concomitant fall in FSH levels. Urinary PdG levels showed a prolonged rise. Urinary E1C in the pregnant chimpanzee was higher than during the menstrual cycle and increased with advancing gestation, with maximum levels occurring near term. In the case of stillbirth, E1C and CG levels from mid- through late-pregnancy were low and the prepartum progressive increase in E1C was not shown. The data presented here are of great practical value in captive breeding management of chimpanzees.

Animals↗

PubMed2002

The calming effect of stimuli presentation on infant Japanese Macaques (Macaca fuscata) under stress situation: a preliminary study.

In human newborns, presentation of sounds and odors under stress situations had a calming effect on behavioral and cortisol responses (Kawakami et al., 1996, 1997). These calming effects were examined with 10-day- and 15-day-old Japanese macaques. In Study 1, white noise presentation (Experimental conditions) at the blood sampling was compared with no sound presentation (Control conditions) at the blood sampling. White noise presentation has a calming effect on coded behavioral responses. In Study 2, lavender scent presentation (Experimental conditions) at the blood sampling was compared with no odor presentation (Control conditions) at the blood sampling. Lavender presentation has a calming effect on cortisol responses in the marginal level. From the data of these studies, the salivary cortisol levels were related to the cortisol levels in plasma. Our results may suggest the different effects of sound and odor on infant Japanese macaques.

Animals↗

PubMed2002

An infant chimpanzee (Pan troglodytes) follows human gaze.

The ability of non-human primates to follow the gaze of other individuals has recently received much attention in comparative cognition. The aim of the present study was to investigate the emergence of this ability in a chimpanzee infant. The infant was trained to look at one of two objects, which an experimenter indicated by one of four different cue conditions: (1) tapping on the target object with a finger; (2) pointing to the target object with a finger; (3) gazing at the target object with head orientation; or (4) glancing at the target object without head orientation. The subject was given food rewards independently of its responses under the first three conditions, so that its responses to the objects were not influenced by the rewards. The glancing condition was tested occasionally, without any reinforcement. By the age of 13 months, the subject showed reliable following responses to the object that was indicated by the various cues, including glancing alone. Furthermore, additional tests clearly showed that the subject's performance was controlled by the "social" properties of the experimenter-given cues but not by the non-social, local-enhancing peripheral properties.

Animals↗