The waning of dependence in infant free-ranging yellow baboons (Papio cynocephalus) of Mikumi National Park

Development toward independence during the early years of baboon life is reflected in the infant's transition from riding on its mother to walking on its own during progressions from one location to another. This transition was studied during the first year of life in 55 infants from two differently sized troops living in Mikumi National Park, Tanzania. There was a nearly linear transition in the first year from almost 100% ventral riding to almost 100% walking. The amount of dorsal riding started near zero, reached a plateau lasting from about the 15th to the 26th wk of life, and then gradually declined to zero. Dorsal riding did not replace ventral; rather, dorsal riding increased in frequency until it occurred about as often as ventral riding. Prolonged ventral riding by infants of the smaller of the two troops may have been due to spacing differences or to greater nervousness among members of the smaller troop. There were no significant differences in riding or walking associated with the time of day or the infant's sex. The rate of transition from riding to walking was greatest from about the fifth to the seventh months, which may be especially significant time in the early development of independence.     

Reactions to fear as a proximate factor in the sociospatial organization of baboon progressions

The objective of this study was to test the hypothesis that fearfulness is a key proximate factor determining the nonrandom order repeatedly reported for baboon troops progressing from one location to another. According to this hypothesis, the most vulnerable troop members, the walking immatures, are expected in most circumstances to be cautious and to keep others between themselves and potential danger. The more confident adults, especially large powerful males, should tend toward the front and rear of progressing troops. The fear hypothesis predicts that in progressions toward a fear source, adult males should be near the front of the troop; on the other hand, when the troop is retreating from a frightening or tense situation, adult males should be found more toward the rear. Progressions of chacma baboons away from the location of a severe fright or in retreat from another troop were compared with other progressions. Adult males tended to be more rearward in these situations. The number of adults of either sex interposed between a fear source and the first walking immature was greater for retreating troops than for others. Some adult males continued to be near the front of the troop when retreating from tense situations.     

Movement patterns of yellow baboons (Papio cynocephalus): Sex differences in juvenile development toward adult patterns

Age-sex differences in the sociospatial positioning of progressing baboon troops have been postulated as an important, protective aspect of baboon adaptation to a terrestrial existence. The protection theory is an ultimate hypothesis which can be disproven by showing that the postulated age-sex positioning fails to occur. Alternatively, confidence in the protection theory can be increased if the postulated positioning persists across several troops despite significant opportunities for variation, and if progression order is shown to be linked to biological phenomena such as sex differences in physical maturation. Data from 73 individually identified, free-ranging juveniles of both sexes were compared with previous findings. Small juveniles of several troops were more centrally located than large juveniles. Large juveniles males were more toward the front than were large juvenile females. As male walking infants and juveniles aged, a change in positioning (i.e., location) occurred: males were located increasingly toward the front of progressions. Comparable data from females suggest that the adult female pattern had begun to form among large juveniles. Data are consistent with an ultimate protection theory.     

Progressions of adult male chacma baboons (Papio ursinus) in the moremi wildlife reserve

It has been suggested that the sociospatial organization of baboon progressions has a protective function in which the most physically powerful troop members, the adult males, play a key role. This theory implies regularities in adult male progression order for different species of savannah baboons with similar social systems. Quantitative progression data are available from two such similar baboon species, olive and yellow, but not from the third, chacma. The order of movement of 15 adult male chacma baboons was determined from 40 progressions observed at the Moremi Wildlife Reserve, Botswana. The chacma males were most often found in the front sixth of progressions, next most often in the second sixth, and about equally often from there to the rear. As expected from the protection theory, this frontal positioning is consistent with available quantitative data from other species of savannah baboons.     

Troop Histories and Range Inertia of Lemur catta at Berenty,Madagascar: A 33-year Perspective

Lemur catta troops in a 1-km ² study area at Berenty Reserve have maintained fidelity to core areas since Budnitz and Dainis' study of 1972–1973, and for two troops possibly since 1963. Population in 1 km ² fluctuated from 155 to 105 to 282 individuals (excluding infants), and the number of troops increased from 12 to 21. Most troops retain the same core areas from year to year (170 observed troop-years). Ten troops derived from known fissions have settled in parts of their parent troop range or an adjacent neighbor's range. Five more troops may derive from similar matrilocal fissioning, inferred from behavior and ranging patterns. One has remained unchanged. Five have unknown parentage, in the ranges of four previously censused troops. Once a fissioned troop completely replaced another, one troop permanently extended its range, three times females joined a different troop, once a female remained nomadic for two years without stable home range. No fissioned troop has been seen to leapfrog others: to settle discontiuously from its parent. Intertroop antagonism may reflect benefits of long-term core area control.     

Intertroop relationships among Japanese monkeys

Intertroop relationships among Japanese monkeys, which have been paid only scant attention for the past 20 years, are examined from several points of view. Japanese monkey troops are generally distributed in such a way as to concentrate locally, that is, to form a local concentration of troops (LCT). About 20% of the nomadic ranges of the troops within LCT's overlap; but in their natural state, they seldom approach but rather to avoid one another. From observations of intertroop encounters at Takasakiyama, where three troops are provisionized and use the same feeding place, it has been found that there exists a dominant-subordinate relationship among troops, that monkeys of each troop have a clear consciousness of belonging to their troop, and that monkeys of different troops rate one another on the basis of their capability. The frequency of male transfer between troops within LCT's is by far higher than between LCT's. In Japanese monkey society, a troop only is a social unit and a social order higher than a troop is not seen; however, it is not impossible to consider an LCT a consanguineally connected group by reason of the transfer of males among the troops within it.     

Radio tracking of a male Japanese macaque emigrated from its group

A male Japanese macaque's ranging behavior before and after emigration from its group was investigated by using radiotelemetry techniques. The male's locations before leaving the troop were regarded as those of the troop, while those after leaving were regarded as those of a solitary male. Monthly home range sizes of the male with the troop were larger than those of the male moving alone, while the whole home range of the male with the troop for three months was much smaller than that of the male moving alone for five months. Overlaps between the male's home ranges with the troop between months were much greater than those between the ranges of the male moving alone. One neighboring troop's home range overlapped the male's range in August and September, and another neighboring troop's range overlapped the male's in October. The mean travel distance and speed of the male with the troop per day did not differ significantly from those of the male moving alone. The results suggest that emigrated males of Japanese macaques may visit home ranges of some troops and stay for a while without interacting troop monkeys before they decide to visit or join the troops.     

The order of movement of yellow baboons (Papio cynocephalus).

The spatial organization of progressing baboons is thought to serve a protective function considered important in their adaptation to a terrestrial existence. Progression positions of identified black infants, adult males, and other yellow baboons were determined from repeated samples of troop movements. Spatial positioning by demographic class was similar to that previously found for three troops of anubis baboons living in two different habitats. Such consistency across species and habitats seems unlikely unless it arises from a common genetic background or common ontogenetic stabilizing mechanism.     

Troop-specific responses to long calls of isolated tamarins (Saguinus mystax)

Recently captured moustached tamarins (Saguinus mystax) were briefly separated from other members of their troop. Most separated animals emitted long calls that were, in general, similar in acoustic structure to those of sympatric tamarin species while retaining species distinctiveness. Individual differences also appeared in call structure. The long calls of a separated animal were responded to almost entirely by members of the animal's own troop rather than by other troops, and reciprocal calling occurred among troop members significantly more often than expected by chance. Although there was no evidence of troop-specific call structure or dialect, there were troop-specific responses to the calls of separated tamarins. This response implies the existence of a stable and integrated troop structure that allows troop members to learn and to respond to the individual specific features of each troop member's calls.     

Intra-troop affiliative relationships of females with newborn infants in wild ring-tailed lemurs (Lemur catta)

To determine how the birth and development of infants influence their mothers' social relationships with other adult troop members, we observed two free-ranging troops of ring-tailed lemurs (Lemur catta) at the Berenty Reserve, Madagascar. The number of acts of affiliative contact that the mothers received from other adult troop members during the first and second months of infant life were significantly higher than those before they gave birth, and the values during the third month were as low as that before giving birth. Two mothers received acts of affiliative contact less frequently after their infants died, compared with the values while the infants were alive. On the other hand, more than 95% of all acts of licking of infants by adult troop members other than their mothers occurred when the infants were in contact with their mothers. These findings suggest that infants per se and mothers per se were not attractive, but rather the mother-infant pair was attractive to other troop members. Acts of infant-licking were observed in almost all mother-mother pairs and mother-non-mother adult female pairs, and in two thirds of mother-adult male pairs. Moreover, the frequency of infant-licking was not affected by female parity, female and male dominance rank, or infant sex. Therefore, acts of infant-licking, which are widespread among troop members, may function to make or maintain stable social relationships.     

Troop history,female reproductive strategies and timing of male change in Hanuman langurs,Presbytis entellus

Female reproductive data are presented from 9 years of longitudinal observations on two troops of Hanuman langurs (Presbytis entellus) living around Jodhpur, India. On the basis of 89 live births interbirth intervals were calculated to examine the effect of demographic factors on reproductive behaviour and troop composition. Sex of an infant seems to influence the length of intervals which are longer after the birth of female infants at an average of 1.7 months. It is suggested that this may be an outcome of differential maternal investment by allocating more time and energy towards female infants who run a higher mortality risk than male infants, at least up to an age of 27 months. Troopspecific interbirth intervals are influenced by social events. If the last infant is still alive when the next one is conceived, the intervals are significantly longer than after the premature loss of an infant (Bijolai troop: 15.6 vs. 12.1 months; Kailana-1 troop: 16.7 vs. 11.4 months). During undisturbed male tenureship intervals are shorter than after a male change (Bijolai troop: 14.3 vs. 16.0 months; Kailana-I troop: 15.6 vs. 17.5 months). Thus the frequency of male changes can influence the demography of a troop. Furthermore, the data suggest that take-overs are optimally timed by males. New males tend to take over a troop when most of the females are cycling.     

Socio-sexual factors of troop fission in wild Japanese monkeys (Macaca fuscata yakui) on Yakushima Island,Japan

The troop fissions which occurred in a wild population of Japanese monkeys (Macaca fuscata yakui) were observed from 1977 to 1979 on Yakushima Island. The fissions were initiated in the breeding season by non-troop males who established a consort relation with estrous females. In order to analyze the socio-sexual factors which accelerated the fissions, the male emigrations and immigrations before and after two successive fissions, and the copulation frequencies, competition among males and preferences of mating partners in both sexes in the 1977–78 breeding season after the first fission were examined. The results indicated that three factors (a large number of non-troop males, a shortage of troop males and the females' choice of mating partners) effectively influenced on the establishment of consort relationships between non-troop males and estrous females. It is suggested that these factors may exert different effects on the troop disorganization in relation to troop size. In small-sized troops, a large number of non-troop males and a shortage of troop males may lead to stronger competition between them, and the females' choice affected by prolonged intimate relations with the dominant TMs may reduce their priority of access to estrous females. This situation possibly stimulates fission or male emigration in small-sized troops under the natural conditions on Yakushima Island. In contrast, in large-sized troops under isolated conditions, a surplus rather than a shortage of troop males may contribute to troop disorganization, as most former studies have suggested. A higher socionomic sex ratio may decrease the mating activities of subordinate troop males and increase the competition among them. This situation possibly accelerates the fission of large-sized troops through prolonged interactions between females and subordinate or peripheral troop males. A lower ratio and the females' choice, however, raise the mating chances of subordinate troop males and may not promote the fission of large-sized troops under isolated conditions. This study was financed in part by a Grant-in-Aid for Special Project Research on Biological Aspects of Optimal Strategy and Social Structure from the Japan Ministry of Education, Science and Culture, and by the Cooperative Research Fund of the Primate Research Institute, Kyoto University.     

Population and social dynamics changes in ring-tailed lemur troops at Berenty,Madagascar between 1989 - 1999

In the present study, we recorded all births, immigrations, deaths, and emigrations for a population of ring-tailed lemurs at Berenty Reserve, Madagascar, between September 1989 and August 1999. In September 1989, three troops (C, B, and T) inhabited the study area of 14.2 ha. During the 10-year period, eight troop divisions, six evictions of females, and three troop takeovers of ranges by other troops occurred in and around the study area. Consequently, in August 1999, the number of troops in the same area increased to six (CX, C1, C2A, C2B, T1, and T2). The number of lemurs aged >1 year increased from 63 to 82, which resulted from 204 births, 58 immigrations, 125 deaths, and 118 emigrations. Of the 204 newborn lemurs during the study period, 103 died, 44 emigrated outside the study area, and 57 remained within the study area. The total number of lemurs that emigrated from natal troops was 69 (54 males and 15 females). Natal males left their troops around the age of 3. Non-natal males changed troops after a tenure varying from 1 to 7 years. Survival curves showed a fall in survival rates of both sexes to < 0.5 between the ages of 2 and 3. For females, the survival rate gradually decreased to < 0.2 at the age of 9. On the other hand, due to emigration, the survival rate of males could not be determined after the age of 5 yr. Since some males attained high-rank at the age of 6 – 10 yr, the prime age for male ring-tailed lemurs is thought to be around 7 – 10 yr. Ring-tailed lemurs are essentially female philopatric, because all cases of females leaving natal troops resulted from troop divisions or forced evictions. Such social changes may have resulted from competition among females. All cases of troop divisions or evictions occurred in larger troops consisting of ≥20 lemurs, and only a few females could rejoin their troops. When males joined such a female-group, a new troop was formed. Although promoted by an increase in population, frequent emigrations of females from original troops are the characteristics of ring-tailed lemurs at Berenty.     

Survey and census of howler monkeys (Alouatta palliata) in the rain forest of “Los Tuxtlas,” Veracruz,Mexico

Howler monkey troops were censused at the biological reserve “Los Tuxtlas” in Veracruz, Mexico. The reserve includes 700 ha of rain forest. Twenty howler monkeys were also trapped, measured, marked, and released. Censuses were conducted for a period of 26 months, and they indicated the existence of 17 troops. The mean troop size was 9.12 (SD ± 2.93), and mean troop composition was 3.0 adult males, 4.12 females, 1.56 juveniles, and 1.54 infants. Ecological density was 0.23 howlers/ha or 23.29 howlers/km². The male to female ratio was 1:1.37. No discrete seasonality in births was noted. Howler monkeys in this locality inhabit the northernmost limit of the neotropical rain forest. The population parameters fall within those reported for Alouatta palliata at other sites.     

Birth-season variation in Japanese macaques,<Emphasis Type="Italic"> Macaca fuscata</Emphasis>

Japanese macaques, Macaca fuscata, exhibit an annual reproductive cycle that apparently is maintained intrinsically. Translocation of nine troops to new latitudes within the northern hemisphere has had minimal effect on the timing of birth seasonality in these troops; translocation of one troop to the southern hemisphere has resulted in a 6-month forward displacement of birth seasonality in this troop. Limited available evidence indicates that, in the latitudinal zone between Toimisaki (31°22′N) and Kinkazan (38°17′N), mean birth date in in-situ troops becomes earlier as latitude of troop localities increases; the same relationship between mean birth date and latitude apparently does not apply to in-situ troops south and north of the Toimisaki–Kinkazan latitudinal zone. Within the Toimisaki–Kinkazan latitudinal zone, earlier mean birth dates at higher latitudes may permit infants to achieve an adequate level of development before the earlier onset of poor winter food conditions. South of the Toimisaki–Kinkazan latitudinal zone, winters are relatively mild and may be less of a factor in infant survival; north of this zone, poor winter food conditions persist so long that earlier infant births may be maladaptive. Electronic Publication     

Social interactions among adult male langurs (Presbytis entellus) at Rajaji Wildlife Sanctuary

A population of langurs (Presbytis entellus)at the Rajaji Wildlife Sanctuary in northern India was investigated for 1820 hr throughout a 10-month period in 1978. Data were collected from four bisexual troops and the adult males that ranged outside of bisexual troops. Most (60%) of the observation hours occurred with a main study troop from which social and ecological data were collected. The langur population at Rajaji shows pronounced birth and mating seasons. The population density is high (ca. 80/km ²), with about 75% of the adult males living outside of bisexual troops, which typically are large and multimale. Males outside of bisexual troops occur in small all-male bands or as isolates. Relations between bisexual troops and all-male bands are characterized by relatively low levels of aggression, and members of all-male bands are able to associate with bisexual troops for prolonged periods during the mating season. As a result of these associations, nontroop males are about as successful as troop males in achieving reproductive access to troop females. These associations between bisexual troops and all-male bands occurred with a minimal amount of agonistic behavior and without mortality or injury to troop females or immatures.     

Comparative study of grooming relationships among wild Japanese macaques in Kinkazan A troop and Yakushima M troop

The influences of socionomic sex ratio (SSR; adult males/adult female) and troop size upon male-male, female-female, and male-female grooming relationships were examined and compared between two wild Japanese macaque troops (Kinkazan A and Yakushima M troops) in Japan. The Yakushima M troop was smaller and had a higher-SSR than the Kinkazan A troop. Between the troops, (1) the male-male grooming frequency and number of partners were greater in the Yakushima M troop than in the Kinkazan A troop; (2) the female-female grooming frequency and number of partners were not different; and (3) the male-female grooming frequency and number of partners were not different. Based on these features, the patterns of female-female and male-female grooming relationships appear to be independent of SSR and troop size variations. In contrast, male-male grooming relationships are influenced by both factors, especially SSR. Frequent grooming interactions among males may be useful for the continued coexistence of relatively many males especially in a higher-SSR troop.     

Changes in dominance rank and division of a wild Japanese monkey troop in Arashiyama

This article forms the second report on the Arashiyama troop of Japanese monkeys and concerns a troop division which took place in June, 1966, and various problems of rank and consanguinity which accelerated the division. (1) The hypothesis advanced in the first report has been verified; (2) at the time of troop division, several consanguineal groups formed one unit; (3) among 16 consanguineal groups, those from 1st to 7th in rank joined the A troop, while those from 8th to 16th joined the B troop; (4) dominance relation between the two division troops was B troop>A troop, reflecting the former ranking between the leader males of the two troops; (5) shifting of monkeys from one troop to the other after division occurred frequently, but males began to make their own movements when they attained 4 or 5 years of age and rarely moved together with their mothers or other consanguineous-relatives; (6) monkeys which were continuously in the same troop after division almost always obtained higher ranks than did monkeys who frequently shifted from one troop to the other; (7) after division, some males joined neither of the two division troops but formed a group, a so-called all-male group or male party, and moved about independently.     

Intertroop Transfer and Dominance Rank Structure of Nonnatal Male Japanese Macaques in Yakushima, Japan

We examined the interaction between intertroop transfer and male dominance ranks in a wild population of Japanese macaques (Macaca fuscata yakui) in Yakushima using data collected over 15 years. Intertroop transfer tended to maintain a linear, stable, and age-graded dominance rank order among nonnatal males irrespective of variation in troop size or composition. All males that joined a troop at the top of the rank order were prime adults. Among males joining at lower ranks, entry at the most subordinate position in the hierarchy was common. Males joining at lower ranks tended to join troops in which all other resident males were the same age or older. Adult males tended to join troops with few or no males. Young males tended to join troops with many resident males, and in which a relatively large proportion of males was other young ones. Intertroop transfer was responsible for most rank changes of resident males. The most common cause of males rising in rank was the emigration or death of a higher-ranking male. Males fell in rank most frequently as a result of a new male joining the troop at the top of the hierarchy. Rank reversals among resident males were rare. The cumulative effects of male transfers produce sociodemographic variation within a troop over time and sociodemographic diversity among troops in a local population. A key feature of intertroop diversity is that larger troops have a significantly greater proportion of young males than smaller troops. This diversity also creates the potential for intertroop variation in the severity of male competition and provides a range of options for transferring males.