Intragroup Social Relationships of Male Alouatta palliata on Barro Colorado Island,Republic of Panama

We examined social and spatial relations of adult males in one group of mantled howling monkeys (Alouatta palliata) on Barro Colorado Island (BCI) in central Panama to document patterns of association. Beyond the existence of an alpha male, we could not distinguish any linear dominance hierarchy among the 6 study males. All males copulated with estrous females. Our findings contrast with reports of intragroup male behavior in Costa Rican howlers. Study males engaged in little or no affiliative or agonistic behavior with one another, but engaged in significantly more such interactions with females. The alpha male, the oldest male and a younger male were most frequently in association with females. Of group males, the oldest male associated significantly more with other males. Overall, male behavior in mantled howling monkeys on BCI generally followed the van Hooff and van Schaik (1994) model of male relationships. The low incidence of intragroup social interactions of any type in the focal males may reflect the energetic costs of social behavior. We suggest that intragroup social relationships among mantled howler males are structured by more subtle means than overt physical interactions, possibly including vocal communication, relationships with individual group females, and kinship.     

Agonistic Interactions and Matrifocal Dominance Rank of Wild Bonobos (Pan paniscus) at Wamba

I studied dominance relations in a wild group of bonobos at Wamba, Democratic Republic of Congo. Although agonistic interactions between males occurred frequently, most of them consisted only of display, and physical attacks were infrequent. Dominance rank order seemed to exist among males, but its linearity is unclear. Dominant males rarely disturbed copulatory behavior by subordinate males. However, high-ranking males usually stayed in the central position of the mixed party and, so, would have more chance of access to estrous females. Among females, older individuals tended to be dominant over younger individuals. However, agonistic interactions between females occurred rather infrequently, and most consisted of displacement without any overt aggressive behavior. Dominance between males and females is unclear, but females tended to have priority of access to food. The close social status between males and females may be related to the prolonged estrus of females and their close aggregation during ranging. Existence of a male's mother in the group and her dominance status among females seemed to influence his dominance rank among males. Young adult males whose mothers were alive in the group tended to have high status. In some cases, change in dominance between high-ranking males was preceded by a corresponding change in dominance between their mothers. As the dominance status of females is similar to that of males, mothers may be able to support their sons to achieve high status, stay in the center of the mixed party, and so have greater access to females, which may maximize the number of descendants of the mothers.     

Hierarchy and social status in Budongo chimpanzees

The status hierarchy is fundamental in the lives of male chimpanzees. This study describes the dominance interactions and social status among adult male chimpanzees of the Sonso community in the Budongo Forest Reserve, Uganda, during the period that they were first studied (1994 and 1995). Social dominance is typically measured using the behaviour of either the subordinate or the dominant individual, but a relationship is dependent on the behaviour of both parties and this study explicitly used both subordinate and dominant behaviours to investigate the status hierarchy. Among adult males of the Sonso community, agonistic interactions occurred at a low rate and pant-grunts were rare, but males could be ranked into separate hierarchies of agonistic dominance and pant-grunting (labelled respect) using ratios of behaviour performed/behaviour received. These hierarchies were combined to form a single hierarchy of social status that divided the males among five distinct status levels. The highest status level was held by an alliance between two males who replaced the previous alpha male during the first part of the study. Neither male in this alliance partnership pant-grunted to the other, although the reason for cooperative behaviour was unclear. Although the nominally beta male was treated as such by other adult males, he achieved surprisingly little mating success. Budongo Forest chimpanzees do not warrant the sometimes-expressed view that they are non-aggressive and peaceable and the broad pattern of their status interactions matches with that seen in other chimpanzee populations.     

Affiliative relationships and reciprocity among adult male bonnet macaques (Macaca radiata) at Arunachala Hill, India

In captivity, male bonnet macaques (Macaca radiata) frequently express "friendship" toward one another, including affiliative behavior such as huddling, grooming, coalitionary support, and sitting in close proximity. The purpose of this study was to determine whether wild adult male bonnet macaques also express "friendship" by investigating whether or not (1) adult male bonnet macaques have affiliative social relationships with other males, (2) the strength of social relationships varies among dyads, (3) there is time-matched reciprocity in allogrooming among dyads, and if so, whether the level of reciprocity occurs within a bout of grooming, a day, or over 2 months (the limit of this study), and (4) a correlation exists between the strength of social relationships and dominance ranks among adult males. Focal samples totaling 150 hr on all seven adult males in one study group were conducted to record both agonistic and affiliative interactions. Agonistic interactions were used to construct a dominance hierarchy, whereas affiliative interactions (sitting in proximity to within 1 m with and without grooming) were used to quantify the existence and strength of social bonds within dyads. Results show that adult male bonnet macaques had differentiated affiliative relationships with other males in their group. There was little reciprocity of grooming within a bout of grooming or within a day, but greater reciprocity over the study period of 2 months. There was no correlation between dominance ranking distance and the strength of affiliative relationship within dyads; however, within dyads lower-ranking males groomed higher-ranking males more than vice versa. This study suggests that friendships in male bonnet macaques are characterized not by immediate tit-for-tat reciprocal altruism, but by reciprocity over a longer time span, and that affiliative social relationships may be less constrained by agonistic relationships than is the case in more despotic species of macaques.     

Ontogenetic changes and the stability of rhesus monkey dominance relationships

Dominance relationships were studied in a rhesus monkey group during five consecutive years. The group consisted of eight stable matriarchies and an adult male class which was replaced at the start, and again at the midpoint, of the study. Immature males were selectively harvested to maintain a sex ratio typical of natural troops. Maximum group size during the study was 77 animals.Dominance relationships were remarkably stable, with only 4.4% of dyads failing to show unidirectional relationships. Despite this stability, a linear ranking of all group members was not possible. Male dominance relationships with other males were among the most stable, following the fighting which ensued on male introductions. Male introductions did not disrupt female dominance relationships.Adult female dominance relationships were also quite stable, but immature females slowly achieved dominance over older sisters and females subordinate to their mothers. Such reversals were the result of processes lasting over many months. Many dominance assertions occurred prior to puberty but a significant number occurred following sexual maturity. Maturing females did not reverse dominance relationships according to any particular hierarchial order and, as a consequence, many were subordinate to animals that were dominated by others that they dominated.Although there was an alpha male that was dominant to all animals in the group, adult females dominated most adult males. Adult males, however, often reciprocated aggression directed at them. They almost invariably threatened or countercharged aggressive immature animals regardless of matriarchial membership. Adult males dominated some adult and most young females, even in families containing matriarchs and adult females to which the adult males always submitted.The dominance relationships of young males were similar to those of their sisters, until puberty. Young males did not necessarily bypass adult males that their mothers outranked, and often failed to win against adult females that their mothers dominated. Adolescent female aggression against females is seldom interfered with by adult males, and females may actively aid one another against males. In contrast, the aggression of young males often elicits interference by adult males, and young males often become the targets of redirected aggression in the group. As a consequence, whereas young females rise in rank to positions adjacent to their mothers, adolescent males often suffer losses to animals that they had dominated as juveniles.     

Adolescent male chimpanzees do not form a dominance hierarchy with their peers

Dominance hierarchies are a prominent feature of the lives of many primate species. These hierarchies have important fitness consequences, as high rank is often positively correlated with reproduction. Although adult male chimpanzees strive for status to gain fitness benefits, the development of dominance relationships is not well understood. While two prior studies found that adolescent males do not display dominance relationships with peers, additional research at Ngogo in Kibale National Park, Uganda, indicates that adolescents there form a linear dominance hierarchy. These conflicting findings could reflect different patterns of rank acquisition across sites. An alternate possibility arises from a recent re-evaluation of age estimates at Ngogo and suggests that the report describing decided dominance relationships between adolescent males may have been due to the accidental inclusion of young adult males in the sample. To investigate these issues, we conducted a study of 23 adolescent male chimpanzees of known age during 12 months at Ngogo. Adolescent male chimpanzees exchanged pant grunts, a formal signal of submission, only 21 times. Recipients of pant grunts were late adolescent males, ranging between 14 and 16 years old. In contrast, younger adolescent males never received pant grunts from other males. Aggression between adolescent males was also rare. Analysis of pant grunts and aggressive interactions did not produce a linear dominance hierarchy among adolescent males. These data indicate that adolescent male chimpanzees do not form decided dominance relationships with their peers and are consistent with the hypothesis that the hierarchy described previously at Ngogo resulted from inaccurate age estimates of male chimpanzees. Because dominance relationships develop before adulthood in other primates, our finding that adolescent male chimpanzees do not do so is surprising. We offer possible explanations for why this is the case and suggest future studies that may help clarify the matter.     

Age differences in social interactions of young males in a chimpanzee unit-group at the Mahale Mountains National Park,Tanzania

The behavior and social interactions of young male chimpanzees were studied in relation to their age change. The data were obtained at the Mahale Mountains National Park, during a four-month period in 1986. Early adolescent males, becoming independent of their mothers, spend a long time near adults of both sexes. Late adolescent males are not tolerated by the senior males. Although such animals do not stop traveling together with their seniors, they are separated from the other members including the males of their own age class, and each of them lives a relatively lonely life. Where seniors are not nearby, they perform charging displays in front of estrous females. Young adult males tend to remain in the proximity of the alpha male, and can associate with their seniors without pant-grunting. Although some young adult males dominate over some senior males, increasingly performing charging displays, they do not appear to be permitted to associate intimately with their seniors; they are not yet considered to have attained social maturity. Prime and senior males are strongly bonded with one another, being able to associate intimately with those of their own or senior age classes including the alpha male. A young adult male's rise in rank is not connected with joining the “adult male-cluster,” nor does a senior male's decline necessarily means his dropping out from the cluster: the social position of male chimpanzees cannot be understood solely from their agonistic dominance rank. The alpha male plays a leading part in integrating the males of the unit-group. Young adult males and their seniors tend to associate most frequently with him, and all the males of the early adolescent or senior age classes pay attention to his movements.     

Male-male relationships among wild bonobos (Pan paniscus) at Wamba,Republic of Zaire

Male-male relationships among wild bonobos (Pan paniscus) in two adjacent unitgroups (E1 and E2 groups), which were formed by division of the E group, were studied at Wamba, in the Central Zaire Basin, by analyzing the proximity and social interactions among males. Dominant-subordinate relationships between a male-male dyad were easily recognized from the directions of individual agonistic interactions. Male bonobos rarely joined forces in aggression. Clear differences in social status existed between adult and adolescent male bonobos in both groups, as reported in the case of chimpanzees (Pan troglodytes). The presence of mothers in the unit-group greatly influenced the dominant-subordinate relationships among males through strong mother-son bonds in both groups. However, the extent of the mother-son bonds differed between the groups. Males in the E2 group participated more frequently in agonistic or affinitive interactions than did males in the E1 group. Males in the E1 group were divided spatially into several clusters, while there were cohesive relationships among the adult males in the E2 group. The difference in intensities of mother-son bonds between the groups may be explained by the distribution of males at the time of the division of the E group. Differences in male-male relationships between bonobos and chimpanzees seem to be related to differences in intra- and inter-unit-group competition among males between the two species. Male chimpanzees may achieve coexistence by manipulating ambivalent relationships that are caused by intra- and inter-unit-group competition among them, while male bonobos may achieve coexistence by decreasing intra- and inter-unit-group competition among them.     

Sexual competition in a group of captive bonobos (Pan paniscus)

We describe the occurrence of sexual competition, expressed as harassment of sexual interactions in a captive group of bonobos. We monitored all aggressive and pestering interventions during sexual interactions of three captive adult females, one adolescent, and three adult males. The study period covered two complete menstrual cycles for each female, with continuous daily observations. There was relatively little overt sexual competition by the males, in analogy with other studies. Most male interventions occurred towards interactions with the alfa female. The alfa female performed the most intense and the highest number of interventions towards the sexual interactions of the other females. The data provide evidence for female intra-sexual competition in this female dominant species.     

The orangutan long call and snag crashing at Tanjung Puting Reserve

The long call, which is only given by adult males, is the most frequently uttered orangutan vocalization and the only one which can be heard over long distances. At the Orangutan Research and Conservation Project study area in the Tanjung Puting Reserve, Central Indonesian Borneo, adult males were calling more regularly and frequently than reported from other areas in Borneo. Adult males also exhibited a behavior, not reported elsewhere, sometimes associated with the vocalization of long calls: the pushing over of large snags (branchless dead trees) to the ground. At Tanjung Puting long calls functioned primarily to mediate dominance relationships among adult males who rarely came into direct contact with one another. In addition, long calls may have been helping sexually receptive females locate males.     

Inter-male associations in a wild Japanese macaque troop on Yakushima Island,Japan

Adult male association and its annual change were studied in a wild population of Japanese macaques (Macaca fuscata yakui) on Yakushima Island, Japan. Unlike many other Japanese macaque troops, adult troop males frequently maintained proximity and exchanged grooming with one another in both the mating and non-mating seasons, and the dominance relationship rarely appeared in such inter-male associations. The few cases of agonistic interactions occurred mostly when estrous females or food resources were immediately concerned. Although troop males were very intolerant to newly appeared solitary males (new males) during the mating season, close associations were formed between troop males and new males as soon as the mating season terminated. The consort of new males and lower-ranking troop males with estrous females was frequently disturbed, but these males could copulate no less frequently than higher-ranking males. A comparison among macaque species suggests the existence of two forms of inter-male association: (1) the frequent association based on the symmetrical exchange of social behaviors; and (2) the infrequent and asymmetrical association related to the dominance relationship. The form of inter-male association seems to be influenced by whether or not males can keep close associations with females throughout the year.     

Social Relationships Among Ring-Tailed Lemurs (Lemur catta) in Two Free-Ranging Troops at Berenty Reserve, Madagascar

We observed two free-ranging troops of ring-tailed lemurs at the Berenty Reserve, Madagascar. Kinship affinities in these troops are known only for mothers and their offspring 4 years of age. We attempted to quantify social relationships. Almost all agonistic interactions were dyadic, and triadic agonistic interactions, such as alliances, were very rare. Dominance hierarchies in both sexes in the two troops were not linear. As in cercopithecine monkeys, mothers were dominant over their adult daughters. However, the daughters were not ranked immediately below their mothers. Close proximity and social grooming occurred more frequently between closely related females, such as mother–daughter and sister–sister dyads, than between unrelated females. Frequent-proximity relations also occurred between adult males that had emigrated from another troop and entered the present troop together, even though they did not rank closely to one another. Subordinates were likely to groom and to greet dominants more frequently than vice versa. During group encounters, particular females were involved in agonistic interactions with animals of other troops, regardless of dominance rank. Adult males, regardless of their dominance rank, but not adult females, constantly tried to drive solitary males away.     

Dominance relationships among male hamadryas baboons (Papio hamadryas)

The concept of dominance has been shown to be useful in describing and predicting social interactions in group-living animals. However, the dominance relationships among adult hamadryas males (Papio hamadryas) are poorly understood, and systematic data are missing from the literature. This study investigated dominance relationships among male hamadryas baboons by applying novel statistical techniques to systematic detailed data on agonistic interactions. We also analyzed the dominance relationship with male age and evaluated the association between dominance and access to mating partners (i.e. the number of adult females per one-male unit (OMU)), food resources (i.e. monopolization of feeding areas), and greeting interactions. The derived dominance indexes showed that, in general, leader males were dominant over followers, and that dominance ability did not correlate with male age. Individual dominance values were very close to each other, suggesting that dominance relationships among hamadryas males were not very rigid. In addition, dominance values were positively correlated with number of adult females per OMU but not with feeding priority. Finally, greeting interactions occurred more frequently between individuals with similar dominance values and with low levels of dominance decidedness. We suggest the need of further studies, especially in wild populations, to confirm our findings.     

Social interactions and reproductive tactics in red–necked wallabies (Macropus rufogriseus banksianus)

Male red–necked wallabies established dominance relationships by fighting, and dominance rankings among males were positively correlated with body size. Females became outstandingly attractive to males during the week preceding mating, and males, who normally ranged widely and solitarily in search of mates, gathered in groups around such females. It is suggested that females, by prolonging their advertisement of oestrus, and thereby inciting sustained competitive interactions among the males who were attracted to them, contributed to a bias in the distribution of male mating success in favour of very large dominant individuals. High–ranking males mated within discrete but undefended areas of absolute dominance ('dominions'). Direct interactions between dominion–holding males were rare, but males just below dominion–holding status often fought with one another, and were frequently harassed by dominional males.     

Male–Male Relationships in Lion-tailed Macaques (<Emphasis Type="Italic">Macaca silenus</Emphasis>) and Bonnet Macaques (<Emphasis Type="Italic">Macaca radiata</Emphasis>)

Socioecology suggests that female distribution in space is determined by the distribution of food resources and the male distribution is influenced by female distribution. Though studies have traditionally focused on females, males have received increasing attention in recent years. We compared male–male relationships in lion-tailed macaques and bonnet macaques. Because bonnet macaques have a high adult male:female sex ratio and are seasonal breeders whereas lion-tailed macaques have a low adult male:female sex ratio and are largely aseasonal breeders, we predicted that bonnet macaque males would be spatially and socially more tolerant of each other and would have less linear dominance relationships than lion-tailed macaques. We recorded male–male and male–female relationships in 1 group of wild macaques of each species via scan sampling and 1–0 sampling. The results revealed that lion-tailed macaque males largely remained at a distance from each other whereas bonnet macaque males remained in close proximity to one another. Lion-tailed macaque males were more agonistic toward each other whereas bonnet macaque males showed more affiliative interactions. The dominance hierarchy among lion-tailed macaque males was more linear than among bonnet macaque males. Our data support the hypothesis that the study of spatial structuring, temporality of interactions, and linearity of social relationships may contribute to a better understanding of macaque social systems.     

Social relationships and ritualized greetings in adult male baboons (Papio cynocephalus anubis)

Greetings involving exchanges of ritualized sexual gestures are a common form of interaction among adult male baboons, although relatively little attention has been paid to them. In this study, we investigate how greetings reflect important aspects of the male's social relationships, including dominance rank, age/residence status, and cooperative tendencies. The results are based on over 600 greetings among 12 adult males recorded during a 4-month study of a troop of wild olive baboons near Gilgil, Kenya. Four of the adult males were older, lower-ranking, long-term residents, which frequently formed coalitions to take estrous females away from the eight young, higher-ranking males. Virtually all dyads greeted: greetings occurred more than twice as often as other types of male-male interactions; and nearly all greetings occurred in a neutral context, in which there was no resource at stake. The percentage of greetings completed, the frequency with which different gestures were employed, and the roles adopted by each male varied significantly across old-old, old-young, and young-young dyads. Greetings between young adult males were often interrupted or actively resisted, consistent with their unstable and ambiguous dominance relationships. Greetings between old-old dyads were usually completed and appeared consistent with their cooperative relationships. One pair of old males formed a stable, reciprocal coalition against young males, and this pair's greetings showed remarkable symmetry of roles. Greetings, we hypothesize, function to allow males to negotiate important aspects of their relationships, including cooperation.     

Matrilineal overthrows in rhesus monkey groups

Between January 1976 and February 1983, there were four overthrows of the highest-ranking matriline in a group of rhesus monkeys. The overthrows were the result of members of multiple mainlines jointly attacking the adult female and adolescent members of the ranking matrilines. In three cases, the next-ranking matriline assumed highest position, while the surviving members of the deposed matrilines fell to the bottom of the hierarchy. Dominance relationships among other group members remained stable. High-ranking adult males vigorously defended the victims, but their efforts were ineffective. Unlike other members of the matrilines, adolescent males were not cohesive with their relatives during the overthrows and did not defend them. These young males were attacked by some adult and adolescent males. These incidents demonstrate the aggressive potential of females and underscore the importance of baboon and macaque females as the enduring and stable core of their social organization. The lack of effective participation by adult males demonstrates the independent functioning of this female core. These overthrows were similar in structure to incidents reported for other captive rhesus colonies and feral baboons, but no explanatory hypothesis posed accounts for all the data. Overthrows may be examples of opportunistic female behavior producing rapid changes in the normally stable female dominance system. Even if such events are rare, the deaths and reproductive failures within deposed matrilines may drastically affect inclusive fitness, counteracting the reproductive advantages of several years of dominance for a matriline.     

定量评估豢养长江江豚个体间的优势关系

2000年1—4月和2000年4月—2002年4月,分别连续3个月和2年观察了中国科学院水生生物研究所白鱀豚馆6头长江江豚（3雌3雄,8个不同组合群）个体间发生的3种交互关系,即接近—逃开、接近—接触和接近—尾鳍击打。在累计8,162min的观察时间内,共观察到这些交互关系1,685次。本研究将江豚个体间发生的这3种交互关系作为个体间优势关系的指示,并分别给交互双方赋予不同的分值,采用优势比分矩阵方法定量分析了江豚个体之间的优势关系。结果表明江豚群体内存在优势关系。同性别个体之间,优势关系与年龄和饲养时间有关,年龄大的个体比年龄小的个体具有优势,饲养时间短的个体比饲养时间长的个体具有优势。但是,异性成年个体之间,优势关系通常是可变的。     

Functional analysis of social staring behavior in an all-male group of mountain gorillas

A total 202 social staring episodes (prolonged gazing by one individual toward another within a short distance) were observed in various social contexts among six unrelated, adult, and subadult male mountain gorillas. Staring was not accompanied by distinct facial expressions by actors or recipients, irrespective of their age or dominance rank. Younger, subordinate animals tended to stare at elder, dominant animals more frequently than vice versa. Staring may have multiple functions depending on the social context. In the initiation of non-agonistic interactions, staring rarely occurred, but was very successful for younger males in eliciting play or homosexual interactions from older animals. Staring was also directed by younger males to older males for greeting or appeasement. It may possibly play a role in reducing the increased social tension that occurs during or after conflict and in averting the potential conflict among older males. Younger males occasionally supplanted older males by staring at feeding spots. This slow supplantation is similar to the phenomenon of food sharing achieved through begging behavior in chimpanzees and bonobos. A prolonged gaze including staring by subordinates towards dominants may characterize the frequent and prolonged face-to-face interactions in the African great apes, and contrasts with a frequent gaze aversion by subordinates towards dominants in macaques or baboons. A difference between gorillas and other apes is that, chimpanzees and bonobos make positive contact with each other through eye contact, while gorillas simply stare at another without physical contact in greeting or appeasement process. Staring may serve an effective strategy for younger male gorillas to intervene safely in olders' conflict and sometimes to suppress or inhibit olders' performance, but their non-agonistic contacts or supporting attacks may not contribute to the establishment or support of social bonds between them. It is possible that staring may be common among the African great apes and man, and that it has evolved as a tactics to mask the dominant/subordinate relationships between individuals with multiple functions.