Auditory evoked potentials in the Japanese monkey.

Auditory sensitivity based on auditory brain stem response (ABR), whole nerve action potential (AP), and cochlear microphonics (CM) to tone bursts of 0.5-8 kHz were compared with behavioral audiometry in the Japanese monkeys. Although sensitivity loss at 4-6 kHz was observed in these potentials, an increase in sensitivity at 8 kHz was obtained only in the ABR. Thus the sensitivity loss at 4-6 kHz originates at the peripheral system and the increased sensitivity at 8 kHz originates at the central.     

The bronchial tree and blood vessels of the Japanese monkey lung

The author injected various colored celluloid solutions into the bronchial tree and blood vessels of the lungs of five adult Japanese monkeys (Macaca fuscata) in order to prepare cast specimens. These specimens were investigated from the comparative anatomical viewpoint to determine whether the bronchial ramification theory of the mammalian lung (Nakakuki, 1975, 1980) can be applied to the Japanese monkey lung or not. The bronchioles are arranged stereotaxically like those of other mammalian lungs. The four bronchiole systems, dorsal, ventral, medial, and lateral, arise from both bronchi, respectively, although some bronchioles are lacking. In the right lung, the bronchioles form the upper, middle, accessory, and lower lobes, while in the left lung, the upper and accessory lobes are lacking and bi-lobed middle and lower lobes are formed. In the right lung, the upper lobe is formed by the first branch of the dorsal bronchiole system. The middle lobe is the first branch of the lateral bronchiole system. The accessory lobe is the first branch of the ventral bronchiole system. The lower lobe is formed by the remaining bronchioles of the four bronchiole systems. In the left lung, the middle lobe is formed by the first branch of the lateral bronchiole system. The lower lobe is formed by the remaining bronchioles. Thus, the bronchial ramification theory of the mammalian lung applied well to the Japanese monkey lung. The right pulmonary artery runs across the ventral side of the right upper lobe bronchiole. It then runs along the dorso-lateral side of the right bronchus between the dorsal bronchiole system and the lateral bronchiole system. On its way, it gives off branches of the pulmonary artery which run along the dorsal or lateral side of each bronchiole except in the ventral bronchiole system. In the ventral bronchiole system, the branches run along the ventral side of the bronchioles. The distributions of the pulmonary artery in the left lung are the same as those in the right lung. The pulmonary veins do not always run along the bronchioles. Most of them run on the medial or ventral side of the bronchioles. Some of them run between the pulmonary segments. In the right lung, these pulmonary veins finally form the right upper lobe vein, right middle lobe vein and the right lower lobe pulmonary venous trunk before entering the left atrium. However, the right accessory lobe vein runs on the dorsal side of the bronchiole and pours into the right lower lobe pulmonary venous trunk. In four cases out of the five examples, part of the right lower lobe veins pour into the right middle lobe vein, while the others enter the right lower lobe pulmonary venous trunk. In the left lung, the branches of the pulmonary veins finally form the left middle lobe vein and the left lower lobe pulmonary venous trunk.     

Accumulation of calcium in the arteries of Japanese monkey

To examine whether the calcium accumulation in the arteries is related to the way of walk or not, the calcium contents were determined in various arteries of Japanese monkeys of quadrupedal walk by inductively coupled plasma-atomic emission spectrometry. Japanese monkeys consisted of five males and four females, ranging in age from 2 to 29 yr. Age-related changes of the calcium content were examined in various monkey arteries. Significant relationships between age and calcium content were found in the arteries, such as the axillary, brachial, radial, subclavian, common carotid, common iliac, and femoral arteries, but not statistically in the thoracic and abdominal aortas, ulnar, external iliac, internal iliac, popliteal, and tibial arteries. The average contents of calcium were compared between the two groups of the monkeys below 14 yr and over 24 yr of age. Below 14 yr, the calcium content was a little higher in the arteries, such as the common, external and internal iliac, and femoral arteries than that of the other ones. Over 24 yr, the calcium content increased remarkably in the arteries, such as the thoracic aorta, common, internal and external iliac, common carotid, and subclavian arteries. The calcium contents of the thoracic aorta, common, internal and external iliac, common carotid, and subclavian arteries increased by more than two times over 24 yr compared with those below 14 yr. In a comparison between the calcium contents of the arteries in the anatomically corresponding regions of the upper and lower limbs, no statistically significant differences were found in the subjects over 24 yr as well as the subjects 2–29 yr of age. The calcium accumulation in the arteries of monkeys with aging was different from those in the arteries of humans, because in the case of human, a very high accumulation of calcium occurred in the arteries of the lower limb with aging in comparison with those in the upper limbs. Therefore, it is likely that different ways of walk or different species are partly affected in the calcium accumulation in the arteries with aging.     

The daily activity rhythm in a troop of wild Japanese monkey

An assessment of the daily activity rhythm of wild Japanese monkeys was tried both from the calculation of the proportion that each activity occupied in the total activities and the “nomadograph,” representing temporary change in the pace of the daily movement. Seasonal and day-to-day changes are recognized in the daily activity rhythm of the troop of wild Japanese monkeys. It seems that seasonal change in the daily activity rhythm corresponds to the seasonal fluctuation of food supply and atmospheric temperature. From autumn to early winter, when much food is available, a clear-cut pattern of activity emerges; namely, three intensive feeding periods are recognized in a day. Moreover, day-to-day variation in the activity rhythm is fairly small and the activity pattern thus becomes standardized. In winter, when least food is available, activity of monkeys drops to the lowest level of the year. Day-to-day variation in the activity rhythm is great. Two to four intensive feeding periods in a day are recognized. In early spring and summer, when food supply is rather scarce, there exist two to three intensive feeding periods in a day. During the heat of the day in summer, activity of monkeys is conspicuously low.     

Senile features in the skeleton of an aged Japanese monkey

The senile features in the skeleton of a male Japanese monkey, who is presumed to be about 40 years old, were examined in comparison with younger individuals. As for the skull, every part is constructed solidly, and the sutures around the temporal and parietal bones are for the most part closed. In the dentition many of the front teeth are destroyed or lost, and the cheek teeth are severely worn. In the vertebrae, the annular epiphyseal discs unite completely with the body at its anterior and posterior surfaces, and the porosity and deformation of the bodies are remarkable. The hip bones, in the pelvis, unite with each other by solid ossification of the pubic symphysis. The long bones of the anterior and posterior limbs are marked by their general thickness, the rugged increase of bone around the joints, especially in the arms, and the complete union of each epiphysis with the shaft through the ossification of the epiphyseal cartilage. These senile features furnish a clue as to the establishment of a criterion for age estimation in Japanese monkeys.This observation was briefly reported inMonkey Vol. 13, No. 1, 1969, and Fig. 9 was used there.     

Playmate relationships among individuals of the Japanese monkey troop in arashiyama

Observations of play behavior were made on a troop of Japanese monkeys for five months. The troop consisted of 125 animals during the study period. Only 104 animals were observed playing with the troop members while the other 21 animals were never observed playing with other individuals. Two-member play was the most frequent. On the average, a monkey played with 20.7 individuals. A total of 6,068 play bouts were observed. The frequency of play appeared to be affected by age, sex, and degree of relatedness. One-year-old infant males played most with other members and the frequency of play decreased with age. Between monkeys whose disparity of age was less than two years, 5,763 bouts (95.0% of the total) were observed. Moreover, among sameaged monkeys who comprised 10.6% of the possible pair combinations, 2,739 play bouts (45.1%) were observed. Juvenile males played with same-sexed peers more than with opposite-sexed peers, whereas older juvenile females appeared to play with infants of both sexes. Individuals who were related and similarly-ranked tended to play together. There was no apparent preference for animals to play with the offspring of the highest-ranking female. Dominance rank of infnats and juveniles was primarily affected by rank of their mothers and to a lesser extent by play partners. Dominance rank of older juvenile males is more likely to be affected by play partners than females. It may be a critical time for males when they leave their natal troop and join a new troop. The timing of troop shifting by males seemed to be affected by the presence or absence of play-mates. For male Japanese monkeys, play is very important in developing social bonds. Play may act to perpetuate social bonds, enhance the chance of survival, and may contribute to their future reproductive success.     

Morphological observations on the congenital malformation of limbs in the Japanese monkey

Congenital malformation of limbs is found in many troops of the Japanese monkey. The author morphologically examined more than ten monkeys with such malformations by means of palpation and Röntgenographing. Anatomical dissection was performed on two of these monkeys. Malformation manifests a considerable variety of forms, from the reduction or absence of fingers to almost total lack of limbs, and is prone to occur in the region of the third finger, the center of malformation, occasionally showing a “split” or “cleft” hand or foot. The latter tendency is more conspicuous in the hand than in the foot. In a word, most of the malformations are characterized by congenital amputation, though the degree varies considerably. The occurrence of supernumerary digits was not found and fusion between fingers was rare. One of the most interesting anatomical results found may be the continuation or fusion between muscles which are normally opposed to each other in action. The occurrence of malformation is more frequent in the male than in the female, and in the hand than in the foot. Little is known about the causes of such malformations, except that they do not occur, at least, according to dominant inheritance.     

Peripheral neuropathy associated with osteosarcoma in a Japanese monkey

Peripheral neuropathy associated with osteosarcoma of the humerus was reported in a Japanese monkey (Macaca fuscata). The monkey developed osteosarcoma in the right humerus. Postmortem morphometric analyses on lower limb nerves revealed loss and size reduction of myelinated nerve fibers. Pathological findings including various demyelinative processes were found with electron microscopy. These findings were more predominant in the distal part than in the proximal part of the nerves, which is compatible with axonal degeneration of peripheral nerve fibers. This is the first case found in a monkey of dying-back neuropathy associated with malignancy, which is not infrequent in humans.