Mirror guided behavior in Japanese monkeys (Macaca fuscata fuscata)

Two male Japanese monkeys were trained to use a mirror to reach an object that could not be seen directly. Training to use a mirror in this way proceeded, step-by-step, from reaching a piece of apple to key-tracking. In Experiment 1 the monkeys were trained to use the mirror to locate a desired object, a piece of apple in a box facing the mirror, which could be seen only by looking into the mirror. The apple, once located, however, could be grasped without further reference to the mirror. This behavior is referred to as mirror mediated object discrimination. In subsequent experiments the monkeys could not reach the goal object except by observing it and his hand movement in the mirror. In Experiment 2 the target was a piece of apple visible in the mirror, in Experiment 3 an illuminated key and in Experiment 4 a series of keys which were illuminated sequentially. Mirror guided behavior such as shown in Experiment 2, 3, and 4 has not previously been demonstrated in monkeys.     

Intra-group variations in the dental eruption sequence of Macaca fuscata fuscata

The purpose of this investigation was to establish general trends of intra-group variations in the dental eruption sequence of a semi-wild troop of Maca fuscata fuscata. Dental impressions were taken on 128 animals of varying ages. The analysis of the dental casts revealed sexual dimorphism in sequence and timing of eruption.     

Self-wrist biting in Arashiyama-B troop of Japanese monkeys (Macaca fuscata fuscata)

Self-wrist biting in the Arashiyama-B troop of Japanese monkeys was observed during a nearly 4-year study. In all, six monkeys were seen performing this behavioural pattern. Medium ranking monkeys belonging to the age class 2–7 years performed this behavioural pattern most frequently. A slight tendency for the diffusion of this behaviour along kinship lines was also observed.     

Annual changes in hair length of the Japanese monkey (Macaca fuscata fuscata)

The hair length of Japanese monkeys was investigated for a period of one year and the molting phenomenon was clarified. Nine monkeys were employed in the study. The molting of the Japanese monkey was found to be of a seasonal type and occurred once during the year. The molting continued for one to four months in each monkey. The hair of the Japanese monkeys was wholly replaced during the period from April to August. The hair length was thus short in summer, and long in winter. Hair replacement in pregnant females began after parturition and was generally later than that in other individuals. During molting, both new and old hairs could be observed simultaneously in the same region of the body. The hair replacement ended around summer when the hair became the shortest. The new hairs continued to grow after molting and became the longest towards autumn or winter. Thus, the summer coat and the winter coat were essentially the same in the Japanese monkey. Such annual changes in the hair of the Japanese monkey were considered to be suitable for the climate of Japan.     

Aspiration pneumonia with adenovirus infection in a Japanese macaque (Macaca fuscata fuscata)

Pneumonia with aspiration of foreign bodies and adenovirus infection was identified in a wild Japanese macaque which died 1 month after capture. The adenovirus infection was considered to be secondary in importance to the pneumonia.     

Development of co-feeding relationships in immature free-ranging Japanese monkeys (Macaca fuscata fuscata)

The co-feeding relationships of immature Japanese monkeys in the provisioned situation were studied. The most frequent co-feeders for immature females were diversified as compared to those for immature males. The number of immature females who showed strong co-feeding relationships with their mothers gradually decreased with age in both high- and middle/low-ranking matrilines, but the percent decrease was greater for middle/low-ranking immatures. Almost all immature females who displayed strong co-feeding relationships with adult males were from middle/low-ranking matrilines. Strong co-feeding relationships with mothers among immature males from high-ranking matrilines remained until 4 years of age. In contrast, strong co-feeding relationships with mothers among middle/low-ranking immature males decreased rapidly in the first year of life, and most 1- to 4-year-olds showed no strong co-feeding relationships with other group members. It is considered that middle/low-ranking mothers may not provide their immatures with a secure base for obtaining food in the provisioned situation.     

Habitat utilization by wintering Japanese monkeys (macaca fuscata fuscata) in the Shiga heights

The detailed habitat utilization of the Shiga B₂ troop was studied in winter. The following results were obtained. (1) The roosting site distribution was limited to the Yokoyugawa valley. (2) The measured home range size was 1.99 km², which was greater than the 1.23 km² of larger population size of the Shiga C troop. (3) The daily travel distance ranged from 0 to 1,825 m (mean 646 m). (4) The pendulum cycle of troop movement is composed of two types: wandering and tripping. The daily travel distance in tripping was much longer than that in wandering. (5) The utilization rate of the home range was assessed according to the total length of the travelling course per grid square. Highly utilized areas in the home range were found along the Yokoyugawa valley without using areas far from the valley. (6) Diurnal activity was influenced by climate, although it was difficult to establish any clear daily rhythm. (7) The food items amounted to 39 species. (8) Distribution of densely utilized sites of food resources almost coincided with those of resting sites. (9) The reasons for the use of the complete home range by the B₂ were also discussed.     

Seasonal changes in the spermatogenic epithelium of adult Japanese macaques (Macaca fuscata fuscata)

A histological study was undertaken to clarify seasonal changes in the spermatogenic epithelium of Japanese macaques. Testicular tissue samples were excised by biopsies from five adult laboratory-maintained males in mating and non-mating seasons. The samples were fixed with Bouin's solution, embedded in paraffin, and stained with PAS and hematoxylin. Microscopic observations on cross-sections of seminiferous tubules revealed that the seminiferous epithelium in the mating season was thicker than in the non-mating season. PAS-stained granules were found in some of the dark A-type spermatogonia, which significantly increased in the non-mating season. Spermatids of the steps preceding the appearance of the acrosomic cap in stages I to III were observed significantly more often than those in the step coinciding with the formation of the acrosomic cap in stage IV. In stage I, the ratio of mature spermatids or spermatozoa to immature spermatids in the mating season was higher than that in the non-mating season. These findings suggest that spermiogenesis, as well as spermatocytogenesis, is inhibited in the non-mating season.     

Morphological studies ofMacaca fuscata

Dermatoglyphics of the foot of two groups of Japanese monkey (Macaca fuscata fuscata of Takasakiyama, Oita Prefecture andMacaca fuscata yakui of Yakushima, Kagoshima Prefecture) were examined. All the fingerprints of the foot consist of a whorl type. Concerning plantar patterns and ridge directions in the sole, there are some differences between both groups. Common to both groups, we find that three kinds of interdigital pattern (II, III, and IV) and proximal thenar pattern (Th^p) are usually of the non-whirling type. This comparatively low frequency of occurrence of a whirling type may be regarded as a characteristic of this species (Macaca fuscata).     

A preliminary study on hair length in the Japanese monkey (Macaca fuscata fuscata)

The hair length of Japanese monkeys was investigated. The hair of the Japanese monkey is long on the back and the lateral side of the upper arm and short on the back of the hand. There was variation in the length of hairs in the same region of the body. The distribution of hair length approximated to a normal curve and did not display any marked bias or skewness. The increase in length of hairs was remarkable from 0 to 1 year of age, and then continued at a constant rate. Sex differences in hair length were not so remarkable at any age.     

Psycholinguistic analyses of alarm calls of Japanese monkeys (Macaca fuscata fuscata)

Alarm and estrous calls emitted by Japanese macaques were recorded and analyzed in the Arashiyama West and East groups. Their responses to natural calls as well as to synthesized versions varying in the acoustic parameters that defined the vocalizations were studied. The response patterns shown by Arashiyama West group members, which were subject to a distinct change with only a slight difference of a single parameter, appeared to reflect strict underlying perceptual boundaries. This was analogous to the categorical perception that humans show with speech sounds. In contrast, continuous perception was exhibited by Arashiyama East group individuals. When several sounds were played back in combination to the former group, following stimuli were recognized by quite different cues from those by which the first sound was perceived. The groups' differences in vocal perception are discussed in terms of the ecological differences of the environments they inhabit.     

Age-related changes in ovarian morphology from birth to menopause in the Japanese monkey,Macaca fuscata fuscata

Age-related changes in ovarian morphology were studied in female Japanese monkeys,Macaca fuscata fuscata. A total of 47 nonlactating females of various ages ranging from new-born to >28 yr old were used. Ovarian size increased during the first decade of life, reached a plateau at around 10 yr. This was followed by a gradual decline throughout the remaining life span. The ovarian cortex of new-born animals consisted of numerous clusters of mitotic primordial germ cells. Such mitotic germ cells were observed even in the ovary of 28-day-old animal, but were not found in any animal after 1.5 yr of age. Numbers of primordial follicles decreased exponentially with the advance of age, and only a few primordial follicles were observed after about 16 yr of age. The numbers of primary and tertiary follicles increased from ages 4 to 16 yr, with a peak at 8 to 10 yr, and then decreased gradually. Developing tertiary follicles were observed as early as 1.5 yr of age. About 40% of tertiary follicles were atretic follicles throughout life, and their size was similar to that of developing tertiary follicles. Corpora lutea or corpora albicantia were found in ovaries more than 4 yr old. Remnants of corpora lutea and corpora albicantia, together with thick-walled blood vessels and fibrosis, became apparent in ovaries after 16 yr, and were observed characteristically in ovaries over 26 yr of age. There was no significant difference in the number or in the size of tertiary follicles between the breeding and nonbreeding seasons.     

Differences in hair density of Japanese monkeys (Macaca fuscata fuscata) with locality and age

The hair density of free-ranging Japanese monkeys (Macaca fuscata fuscata) living in three different areas was investigated. The Japanese monkeys had thicker hair than other macaques. The hair density in the Japanese monkeys varied with locality: the northern monkeys had thicker hair than the southern ones. The density did not vary markedly with age up to 3 years of age, but then decreased gradually up to adult age (≧7 years old). The remarkable growth of the trunk suggested that the total number of hairs increased with age, especially during the period as a juvenile.     

Use of a mirror to direct their responses in Japanese monkeys (Macaca fuscata fuscata)

Two male Japanese monkeys used a mirror to inspect an object attached to their bodies but not directly visible. These monkeys had been trained previously to use a mirror to guide their hand to a target. In Experiment 1 their behavior in the presence of a mirror was observed. In Experiment 2 the monkeys used the mirror to locate a picture projected on a screen to the left or right rear side of the cage. In Experiment 3 the monkeys used a mirror to observe and finally grasp an object attached behind their heads. Two monkeys who were not trained to use a mirror to obtain an otherwise hidden object did not show such behavior.