Some observations on the solitary male among Japanese monkeys

The social behavior pattern of a solitary male at Koshima was studied by means of radio-telemetry. The relationship between the solitary males and the troop was estimated from radio-tracking data of the former's location and movement, and by direct observation of the latter at each corresponding hour.For most of day, the solitary male stayed within a distance of about 20 to 150 m from the central part of the troop, occasionally approaching it. His movement also was synchronized with that of the troop. For two nights, the solitary male slept at places which were about 200 m from the sleeping sites of the troop and faced them across the beach. The relationship between the solitary male and the troop did not seem to be strongly antagonistic.It can be assumed that the solitary male was moving according to certain pre-determined relationships or social contacts with the troop. The example of this solitary male shows the existence of the solitary male that follows and maintains contact with the troop, even outside the copulatory season.This study was sponsored by Scientific Research Grant No. 91620 of the Ministry of Education to the Japan Monkey Centre.     

Standing and climbing a pole by members of a captive group of Japanese monkeys

In a captive group of Japanese monkeys, a juvenile female spontaneously began standing poles against a concrete wall and climbing up them in 1983. By 1987, 3 juvenile females out of 39 monkeys had acquired the behavior. They stood rather heavy poles, weighing 2.6 kg, against the wall and climbed up them without training. At the top of the poles, they often explored the smooth wall by licking or touching it.     

Food aversion learning in Japanese monkeys (Macaca fuscata). A strategy to avoid a noxious food

Japanese monkeys consumed two kinds of food, the novel almonds and the familiar sweet potatoes, simultaneously, and then received a cyclophosphamide injection (20 mg/kg) intravenously. As the food-poison pairing was repeated, they first avoided the novel food completely, and then came to suppress eating the familiar one. During the subsequent extinction tests, the aversion to the familiar food was extinguished rapidly, whereas the aversion to the novel one was retained more than 2 months. In food aversion learning in a mixed situation, monkeys have a strategy to avoid a noxious food on the basis of the novelty of the food.     

Population differences and learning effects in walnut feeding technique by the Japanese squirrel

Feeding efficiency is an important factor explaining diet selection in seed-eating animals. Behavioral adaptation to process and consume the seed is advantageous to improve their feeding rate. The Japanese walnut (Juglans ailanthifolia), which has a nutritious kernel surrounded by a hard shell, is an important food for the Japanese squirrel (Sciurus lis) in lowland mixed-species forests in Japan. In the present study, population differences in feeding technique were examined. In all squirrels captured from the Takao population (with wild Japanese walnuts in their habitat), the optimal feeding technique for quickly opening the walnut shell was observed. However, only 8% of the squirrels from the Fuji population (without walnuts in their habitat) processed the walnuts by the optimal feeding technique. By a repetitive provision of walnuts for 50 days, 14% of squirrels from the Fuji population acquired the optimal feeding technique. Learning effects did not differ significantly between solitary (without a demonstrator) and social conditions (with a demonstrator). The effects of age on learning the feeding technique were examined using individuals from a zoo population that had been naïve for Japanese walnuts. All five individuals aged 6 months old, and half the individuals aged 1–2 years old, ate walnuts by the optimal feeding technique after a 2-month learning period, but none of the individuals older than 3 years did. Consequently, the walnut feeding techniques of the Japanese squirrel are not entirely genetically fixed behavior and can be improved by learning at a young age.     

Behavioral compensations in a positional learning and memory task by aged monkeys

The present experiment assessed learning and memory of a positional task by evaluating behavioral strategies as well as accuracy of a task in four young and four aged monkeys. They were tested in a delayed response (DR) task that has been widely used to study animal models of aging. The task consisted of two phases; an acquisition of the task and a positional memory test with five delay times (1-30 s). There was no clear difference between age groups in the number of trials needed for acquisition of the task. However, an analysis of behavior revealed differences in behavioral characteristics displayed during testing. The young monkeys showed various irrelevant behaviors during the execution of the task. In contrast, the aged monkeys consistently concentrated on the task exhibiting no behaviors irrelevant to the task. These results showed than the aged monkeys' performance was supported by a different behavioral strategy from the young monkeys. The results of the memory test were similar to those of the acquisition on the accuracy and the behavior. The aged monkeys depended on behavioral cues to preserve their positional memory, especially during the task. The present study suggests that cognitive impairments in aged monkeys can be compensated for by employing behavioral strategies.     

Threat calls in alliance formation by members of a captive group of Japanese monkeys

The vocal behavior of threat calls was investigated in a captive group of Japanese monkeys (Macaca fuscata fuscata). The vocalizations were heard most often when they undertook winner-support during triadic agonistic interactions. The likelihood of call emission in support of the winner was affected by the attributes of the participants, and not by the types of agonistic behavior. The calls were emitted by intermediate ranking animals frequently in support of high ranking animals and in support of females. The calling behavior of winner-supporters appears to advertise the partner and distant group members of their support for reciprocation in the near future.     

The reproductive biology of a free-ranging troop of Japanese monkeys

Quantitative data on the reproductive biology of Japanese monkeys (Macaca fuscata), especially of females, are reported here. Arashiyama B troop shows stable annual breeding periodicity, and has mating seasons between October and March. In mating seasons, females show estrus with rather consistent cyclicity, and are in estrus for a total of 35 days on an average. The mean length of estrous cycle is 34 days. Although most females show estrus inter-menstrually, some show peri-menstrually; i.e., estrus does not always synchronize strictly with ovulation. Pubescent females between 3.5 and 6.5 years show estrus, but with low sexual activity. Middle-aged females between 7.5 and 16.5 years show high sexual activity with high conception rate. Old-aged females over 17.5 years show low sexual activity. Females with surviving infants have lower sexual activity than those without infants. There is found no significant correlation between female's ranking and sexual activity. This study was financed partly by the Cooperative Research Fund of the Primate Research Institute, Kyoto University.     

On the handedness of Japanese monkeys

Forty-one monkeys living on the Koshima Island were tested for handedness by throwing a peanut 10 or 20 times toward each subject and recording which hand was used to pick it up. Handedness was judged at the 5% level of confidence. Animals showing no preference for the left or right hand after 20 trials were considered to be ambidextrous. The following distribution of handedness was found: left-handed, 17 (41%); right-handed, 8 (20%); ambidextrous, 16 (39%). These findings were compared with other studies on the handedness of Japanese monkeys. Handed monkeys outnumber the ambidextrous ones and the left-handed monkeys outnumber the right-handed ones. The characteristic distribution of handedness was shown to be irrespective of troop. By looking over the data from these different sources, the proportions of the left-handed, the ambidextrous, and the right-handed in Japanese monkeys were estimated at 39%, 33%, and 28% respectively. The method used in this study was compared withKawai's catching behavior and reasons for disagreement between judgments of handedness were discussed.     

Effect of a learning trial on self-selected resistance training load

Previous research has shown that individuals self-select loads for resistance training that falls below the accepted threshold for overload and do not lift to volitional fatigue. The purpose of this study was to determine the effects of a resistance training learning trial on self-selected resistance training load. A control group (5 women, 3 men) and a learning group of (4 women, 4 men) novice lifters were recruited. The control group (CG) received an orientation to selected strength machines (seated bench, leg extension, back row, biceps curl, triceps extension, shoulder press). On a subsequent training day, CG self-selected a training load, while blinded to the actual loads. The learning group (LG) received an initial orientation and also was tested for estimated 1 repetition maximum (1RM) for the seated bench press. On a subsequent day, the LG completed 2 sets of the seated bench press at 75% of estimated 1RM and were encouraged to lift until failure. On a third day, LG subjects completed a self-selected trial identical to that of the CG. Both groups were assessed for estimated 1RM for each exercise on a separate day following all trials. Comparisons between CG and LG were made using independent-means t tests and adjusted using Bonferroni's equation (p < 0.01). While subjects selected a bench press load that was 21% greater for LG (63.4 +/- 6.4% 1RM) compared to the CG (50.3 +/- 12.0%), there was no statistical significance. There were no significant differences in self-selected load for any of the other exercises. There were also no significant differences for number of repetitions or rate of perceived exertion between groups. We conclude that a learning trial of the bench press exercise to increase self-selected workload is not enough to change load self-selection.     

Behavioural correlate of choice confidence in a discrete trial paradigm

How animals make choices in a changing and often uncertain environment is a central theme in the behavioural sciences. There is a substantial literature on how animals make choices in various experimental paradigms but less is known about the way they assess a choice after it has been made in terms of the expected outcome. Here, we used a discrete trial paradigm to characterise how the reward history shaped the behaviour on a trial by trial basis. Rats initiated each trial which consisted of a choice between two drinking spouts that differed in their probability of delivering a sucrose solution. Critically, sucrose was delivered after a delay from the first lick at the spouts--this allowed us to characterise the behavioural profile during the window between the time of choice and its outcome. Rats' behaviour converged to optimum choice, both during the acquisition phase and after the reversal of contingencies. We monitored the post-choice behaviour at a temporal precision of 1 millisecond; lick-response profiles revealed that rats spent more time at the spout with the higher reward probability and exhibited a sparser lick pattern. This was the case when we exclusively examined the unrewarded trials, where the outcome was identical. The differential licking profiles preceded the differential choice ratios and could thus predict the changes in choice behaviour.