Dominance Turnover Between an Alpha and a Beta Male and Dynamics of Social Relationships in Japanese Macaques

We report a case of turnover between an alpha (GN) and a beta male (R7) and its effects in a troop of provisioned Japanese macaques (Macaca fuscata fuscata) in Shiga-Heights, Nagano Prefecture, Japan. The aggression between the 2 males was caused by the intrusion of GN towards the consort of R7. R7 received support from his brother and mother, and consequently defeated GN. After the turnover, R7 attacked GN frequently, which may have functioned to stabilize the dominance relationship between them. Also, R7 selectively attacked females friendly to GN soon after the turnover. Although we never observed polyadic aggression among males during the stable dominance period, 20 cases of polyadic aggression occurred among the 6 highest-ranked males in the 2 days following the turnover, and one case occurred on the fourth day. R7 and GN formed stable conservative alliances for attacking subordinate males. Males that did not participate in the turnover began to form revolutionary coalitions to attack higher-ranking males, but they were thwarted by the conservative coalitions between the dominants. Mutualism was a plausible explanation for the patterns of coalition formation because most of them were conservative with little associated cost. Seven females had a high proximity index (C-score) to GN before the turnover, but a significantly lower proximity index after the turnover. On the day of the turnover, 6 non-lactating females suddenly became receptive, suggesting that the turnover induced immediate receptivity in the females.     

Dominance, aggression and physiological stress in wild male Assamese macaques (Macaca assamensis)

In group-living animals relative rank positions are often associated with differences in glucocorticoid output. During phases of social stability, when dominance positions are clear and unchallenged, subordinates often face higher costs in terms of social stress than dominant individuals. In this study we test this prediction and examine additional potential correlates of stress, such as reproductive season, age and amount of aggression received in wild, seasonally breeding Assamese macaques (Macaca assamensis). During a mating and a non-mating season we collected 394 h of focal observational data and 440 fecal samples of six adult and six large subadult males living in a multimale–multifemale group in their natural habitat in northeastern Thailand. The mating season was characterized by a general increase in aggressive behavior and glucocorticoid excretion across all males compared to the non-mating season. Among adult males, mating season glucocorticoid levels were significantly negatively related with dominance rank and positively with the amount of aggression received. Both relationships were non-significant among large subadult males. Thus, our results suggest that in adult Assamese macaques a high dominance position is not associated with high costs. Low costs of dominance might be induced by strong social bonds among top-ranking males, which exchange frequent affiliative interactions and serve as allies in coalitionary aggression against potentially rank-challenging subordinate males.     

Dominance,aggression and physiological stress in wild male Assamese macaques (Macaca assamensis)

In group-living animals relative rank positions are often associated with differences in glucocorticoid output. During phases of social stability, when dominance positions are clear and unchallenged, subordinates often face higher costs in terms of social stress than dominant individuals. In this study we test this prediction and examine additional potential correlates of stress, such as reproductive season, age and amount of aggression received in wild, seasonally breeding Assamese macaques (Macaca assamensis). During a mating and a non-mating season we collected 394 h of focal observational data and 440 fecal samples of six adult and six large subadult males living in a multimale–multifemale group in their natural habitat in northeastern Thailand. The mating season was characterized by a general increase in aggressive behavior and glucocorticoid excretion across all males compared to the non-mating season. Among adult males, mating season glucocorticoid levels were significantly negatively related with dominance rank and positively with the amount of aggression received. Both relationships were non-significant among large subadult males. Thus, our results suggest that in adult Assamese macaques a high dominance position is not associated with high costs. Low costs of dominance might be induced by strong social bonds among top-ranking males, which exchange frequent affiliative interactions and serve as allies in coalitionary aggression against potentially rank-challenging subordinate males.     

Post-conflict Social Events in Wild Mountain Gorillas. II. Redirection,Side Direction,and Consolation

Inevitably, members of primate groups sometimes have aggressive contests with each other. Targets of aggression can engage in several types of interaction with third parties to ameliorate its adverse effects. They can redirect aggression, which may reduce the risk of further aggression from the initial opponents and reduce tension, or they can initiate affinitive interactions with third parties, in order to seek protection or reassurance. They can also receive reassuring acts from them (‘consolation’). Researchers have documented high levels of redirection in many primate species, but consolation is thus far known only in chimpanzees. Data on post-conflict social interactions between targets of aggression and third parties in two groups of wild mountain gorillas (Gorilla gorilla beringei) show that immatures and subordinate males, but not females, redirect aggression at high rates. Furthermore, immatures seek affinitive interactions with their mothers, and adult females seek them with adult males, at elevated rates. Affinitive interactions between females and males seem mainly to have a protective function and are associated with decreased risks of further aggression between female opponents. Redirection by females after female-female conflicts may be uncommon because targets commonly retaliate against aggressors. Males may offer females protection and consolation as services, and the results support the argument that such services are important when dominance relationships between females are often undecided and retaliation between opponents is common.     

Serum testosterone, male dominance, and aggression in captive groups of vervet monkeys (Cercopithecus aethiops sabaeus)

The relationship of serum testosterone concentration to male dominance rank and frequency of aggression was investigated in stable vervet monkey social groups, each containing two or three adult males, several adult females, and their offspring. Dominance relationships were determined by noting an animal's success in intermale aggressive encounters. A striking finding was the marked within-subject variation in testosterone concentration: 5- to 10-fold fluctuations were often observed on successive days. When all 15 groups were considered together, testosterone concentration was unrelated to dominance rank. Although mean testosterone concentration for all dominant males was higher than the mean for all subordinate males, this difference was not significant. In a subset of 4 groups, the rate of aggression initiated was significantly correlated with same-day testosterone in dominant but not in subordinate males.     

Modification of aggression through socialization and the special case of adult and adolescent male rhesus monkeys (Macaca mulatta)

Significant differences exist in the frequencies with which age-sex classes of rhesus macaques engage in agonistic interactions with other age-sex classes. In the study reported here, individuals engaged in significantly more agonistic interactions within their own age-sex classes, but, adult females also showed significantly more aggression toward infants and young females whereas adult males directed significantly more aggression toward adolescent males. Infants directed aggression toward infants of both sexes, but adults showed significantly less aggression toward adults of the opposite sex. These findings are hypothesized to reflect (1) competitive conflict among those individuals in the group most similar to each other (members of the same age-sex class); (2) the protection and socialization of offspring by adult females; and (3) the modification of adolescent male aggressive expression by the selective interference of adult males. As a consequence of adult response to the agonistic behavior of adolescent males, maturing males (1) selectively target other older males, avoid aggression against females and immatures; (2) form alliances with other males; and (3) become progressively isolated from their matrilines.     

Aggression in adult male primates: A comparison of confined Japanese macaques and free-ranging olive baboons

The frequencies and types of adult male aggressive behavior of confined Japanese macaques (Macaca fuscata)and free-ranging olive baboons (Papio anubis)were compared. The baboons, which do not have a mating season, were more aggressive to conspecific males than were the macaques during their nonmating season. The baboons also solicited aid during aggressive encounters more frequently than the macaques. However, during their mating season, the macaques were more aggressive to conspecific females than were the baboons. The macaques were also involved in more triadic sequences of aggression, and the frequency of occurrence of these patterns supported Chase’s theory of dominance hierarchy formation and maintenance. The differences in aggressive behavior appeared to be related to the seasonal reproductive cycle of the macaques.     

Social relationships in a herd of Sorraia horses Part I. Correlates of social dominance and contexts of aggression

Factors related to dominance rank and the functions of aggression were studied in a herd of Sorraia horses, Equus caballus, under extensive management. Subjects were 10 adult mares 5-18 years old and a stallion introduced into the group for breeding. Dominance relationships among mares were clear, irrespective of rank difference, and remained stable after introduction of the stallion. The dominance hierarchy was significantly linear and rank was positively correlated with age and total aggressiveness. Higher-ranking mares received lower frequency and intensity of agonistic interactions. Nevertheless, higher-ranking dominants were not more likely to elicit submission from their subordinates than lower-ranking dominants. Neither close-ranking mares nor mares with less clear dominance relationships were more aggressive towards each other. Agonistic interactions seemed to be used more importantly in regulation of space than to obtain access to food or to reassert dominance relationships. Contexts of aggression were related to mare rank. The results suggest that dominance relationships based on age as a conventional criterion were established to reduce aggressiveness in a herd where the costs of aggression are likely to outweigh the benefits.     

Male-male Interactions in Heterosexual and All-male Wild Mountain Gorilla Groups

Variation in male dispersal and behavior patterns are components of intraspecific differences in social systems. A comparison of male behavior in different social settings can be useful for determining which behavioral mechanisms contribute to variability in social systems. Two heterosexual multimale groups and one all-male group of mountain gorillas (Gorilla gorilla beringei) were observed for over 1100 h at the Karisoke Research Centre, Rwanda. Data on proximity patterns, dominance relationships, aggression, agonistic interventions, affiliation, and homosexual behavior were compared among the males in these groups to examine the influence of female presence, sex ratio, group size, and kinship on male—male interactions. Males in the all-male group stayed closer together, affiliated more, exhibited more homosexual behavior, and were more aggressive toward each other than males in heterosexual groups. However, the males in heterosexual groups showed more wounding and more consistent dominance relationships. Kinship did not influence male-male relationships in the all-male group. The males in the heterosexual groups rarely interacted with one another; they may actively avoid close proximity to reduce aggression. Results suggest that the variable social system of mountain gorillas may be more strongly influenced by demographic factors, male-female social relationships, and male-male competition for mates than by any benefits of male-male relationships.     

Dominance status reversal based on pair-bond formation in the convict cichlid (Amatitlania nigrofasciata)

Dominant individuals have access to higher-quality resource; thus, reversing their dominance status would be important for subordinate individuals. Using the convict cichlid fish (Amatitlania nigrofasciata), this study examines whether forming a pair bond can reverse dominance status. Furthermore, I hypothesize that female convict cichlids will incur more dominance reversals from pair-bond formation than males. Dyadic, same-sex contests were conducted to determine dominant and subordinate individuals. Forced pairing of these individuals based on status was followed by polyadic, between-pair contests. The results indicate that individual dominance status does carry over into between-pair competition. Furthermore, dominance reversals do occur in convict cichlids and occur more frequently in females than in males. In addition, dominant males assist their mates during aggressive encounters, and these assists may account for subordinate females winning against dominant females during polyadic contests.     

Social parameters and urinary testosterone level in male chimpanzees (Pan troglodytes)

Studies investigating relationships between social parameters (such as dominance rank, rates of aggressive and sexual behaviors) and androgen (particularly, testosterone) levels in male primates have yielded inconsistent results. In the present study, we address the relationship between androgens, male dominance rank and rank-associated behaviors in two groups of captive chimpanzees, a species characterized by a pronounced dominance hierarchy between adult males. By combining behavioral observations with urinary testosterone (T) measurements, we found that the differences in T concentrations between males were small and not obviously related to their dominance rank. T levels were not related to the rates of initiated aggression and copulatory behavior, but a significant negative relationship between male T level and the rates of strong aggression received was apparent. Our findings, combined with those of others, suggest that any relationship between dominance rank and T depends upon the extent to which individual rank-associated behaviors (e.g. aggressive/sexual) are themselves related to T.     

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.     

Sex-Specific Aggression and Antipredator Behaviour in Young Brown Trout

Sex differences in adult behaviour are often interpreted as consequences of sexual selection and/or different reproductive roles in males and females. Sex-specific juvenile behaviour, however, has received less attention. Adult brown trout males are more aggressive than females during spawning and juvenile aggression may be genetically correlated with adult aggression in fish. We therefore tested the prediction that immature brown trout males are more aggressive and bolder than immature females. Because previous work has suggested that precocious maturation increases dominance in salmonids, we included precocious males in the study to test the prediction that early sexual maturation increase male aggression and boldness. Aggression and dominance relations were estimated in dyadic contests, whereas boldness was measured as a response to simulated predation risk using a model heron. Independent of maturity state, males initiated more than twice as many agonistic interactions as females in intersexual contests. However, males were not significantly more likely to win these contests than females. The response to a first predator attack did not differ between sex categories, but males reacted less to a second predator attack than females. Sexual maturity did not affect the antipredator response in males. Since there is no evidence from field studies that stream-living immature male and female salmonids differ in growth rate, it appears unlikely that the sex differences demonstrated are behavioural consequences of sex-specific investment in growth. It seems more likely that sex-specific behaviour arises as a correlated response to sexually selected gene actions promoting differential behaviour in adult males and females during reproduction. Alternatively, sex differences may develop gradually during juvenile life, because a gradual developmental program should be less costly than a sudden behavioural change at the onset of sexual maturity.     

Effects of previous experience on the agonistic behaviour of male crickets, Gryllus bimaculatus

Male solitary animals frequently enter aggressive interactions with conspecific individuals to protect their territory or to gain access to females. After an agonistic encounter, the loser (subordinate individual) changes its behaviour from aggression to avoidance. We investigated agonistic interactions between pairs of male crickets to understand how dominance is established and maintained. Two na?ve males readily entered into agonistic interactions. Fights escalated in a stereotyped manner and were concluded with the establishment of dominance. If individuals were isolated after the first encounter and placed together 15 minutes later, subordinate crickets tended to avoid any further contact with the former dominant opponent. Moreover, subordinate males also avoided unfamiliar dominant and na?ve opponents. They displayed aggressive behaviour only towards unfamiliar subordinate opponents. This suggests that the subordinate male change their behaviour depending on the dominance status of the opponent. Dominant crickets, in contrast, displayed aggressive behaviour towards familiar as well as unfamiliar opponents. If the interval between the first and second encounter was longer than 30 minutes, the former subordinate male showed aggressive behaviour again. However, if the subordinate cricket was paired with the same opponent three consecutive times within 45 minutes, it avoided the former dominant opponent for up to 6 hours following the third encounter. Our results suggest that the maintenance of dominance in male crickets depends largely on the behavioural change of subordinate individuals. Possible mechanisms to maintain dominance are discussed.     

Rank,relationships, and responses to intruders among adult male vervet monkeys

We examined the influences of dyadic relationships among captive adult male vervet monkeys (Cercopithecus aethiops sabaeus) on behavior directed toward caged “intruder” males placed inside subjects' enclosures. Subjects were all 9 adult male residents from three stable social groups, each of which contained 3 adult males, at least 3 adult females, and their immature offspring. Every male was observed in two 3-hour sessions, each time with one of the 2 other adult males from his group. Observation sessions consisted of six consecutive 30-min stages in which group composition and the presence of the intruder were manipulated. All groups exhibited a stable, linear male dominance hierarchy prior to and throughout the study. In each group, there was one pair of males, when together, in which each member exhibited higher rates of intruder-directed approach and aggressive behaviors than when either animal was paired with the third male of his social group. Such pairs were also distinguished by high levels of within-pair agonistic interactions. The higher-ranking member of each dyad was the most aggressive male toward the intruder in his social group, although only one of these animals was the dominant male of his group. Mutual facilitation of aggression against intruding males is interpreted as cooperative behavior benefitting both males by increasing the likelihood of repelling a potential competitor for resident females. Such cooperation provides further evidence in nonhuman primates for cohesive male-male dyads between animals whose social interactions are characterized by agonism. © 1993 Wiley-Liss, Inc.     

Information on Resource Quality Mediates Aggression between Male Madagascar Hissing Cockroaches, Gromphadorhina portentosa (Dictyoptera: Blaberidae)

Male Madagascar hissing cockroaches, Gromphadorhina portentosa Schaum (Dictyoptera: Blaberidae) have a well‐defined dominance hierarchy that has been assumed to explain the outcome of most competitive interactions. We studied whether males of this species would alter their level of aggression towards unfamiliar rivals as a function of changing resource availability and value – two factors that are key to aggression levels in non‐hierarchical species. We quantified male aggression as three variables (aggressive state – behaviours measured by their duration; aggressive act – behaviours measured by their frequency of occurrence; aggressive latency – the latency to first aggressive behaviour, either state or act) and tested for any context‐specific variation within each by manipulating both territorial status (males were either residents or intruders) and access to mates (female present or absent). Both the presence of a female and territorial status affected male aggression towards rivals as measured by duration of aggressive state. Highest levels of aggression were displayed by residents when a female was present. These results show that inter‐male aggression in G. portentosa is tuned to the immediate expected payoff from fighting, and not exclusively aimed at establishing dominance relationships (which can affect future payoffs).     

A comparison of aggressive play and aggression in free-living baboons, Papio anubis.

A quantitative comparison is given of aggressive play and aggression in terms of the duration and type of movement patterns employed, and the relationships between individuals. The mean length of contact in play was greater than in aggression, whereas chases tended to be longer in adult male aggression than in play, Linear hierarchies describing the overall direction of interactions between individuals were divisible into two sorts, according to the frequency with which roles were reversed. The regions of the body bitten and the proportions in which six types of movement pattern were used were related to the type of hierarchy involved. The results are discussed with reference to the possible functions of social play in the development of movement patterns and individual relationships.     

Patterns of female dominance in Propithecus diadema edwardsi of Ranomafana National Park, Madagascar

Many lemur species are characterized by some form of female dominance, ranging from female feeding priority to complete female dominance, although this is a rare trait in primates and other mammals. The status of the Milne-Edwards' sifaka (Propithecus diadema edwardsi), a diurnal lemur, is ambiguous. Some short-term studies have found little or no aggression. The aim of the current, long-term study was to quantify the intersexual-dominance patterns of this sifaka. The distribution, outcome, and context of aggressive interactions were studied in four groups of wild sifakas. The majority of intersexual aggressive interactions were decided, with the loser expressing submissive behavior. Intersexual aggressive interactions occurred in all social contexts, and within all social contexts the females won the vast majority (92.7-96.0%) of aggressive interactions. While aggression rates were low (0.22/hr), this evidence suggests female dominance. We propose that female dominance exists because it provides a fitness advantage to both males and females.     

Dominance,Age and Aggression among Female Pronghorn,Antilocapra americana (Family: Antilocapridae)

The relationships among dominance, age and aggressive behaviour of marked, female pronghorn (Antilocapra americana; Family Antilocapridae) were studied in north central Colorado. Females formed dominance hierarchies with few circular relationships. Unlike other female ungulates, dominance rank was not correlated with age. Dominance rank was negatively correlated with rate of aggression initiated in summer and winter; however, aggressiveness as an individual trait was not related to dominance. Older females received higher rates of aggression than younger females in summer and winter. During the rut, dominance rank was correlated with rate of aggression received but not with rate of aggression initiated. Patterns of aggression that differ by season within a given hierarchy of dominance relationships suggest a different cause or function of aggressive behaviour in different seasons.     

Testing Functional Hypotheses for the Behavior of Resident Pine Voles, Microtus pinetorum, Toward Non-Residents

Members of a social group should attempt to maximize their fitness by maintaining an optimal group composition. Allowing an immigrant into the group may be beneficial or costly depending on the characteristics of the immigrant as well as the composition of the group. Therefore, we examined behavioral interactions between pine voles to test three functional hypotheses proposed to explain behavior of residents toward non‐residents: the resource defense, mate defense, and benefit of extra‐pair copulation hypotheses. To test these, we examined the effects of age, sexual experience and sex of non‐residents as well as the effects of sex of residents on the behavior of residents. Neither male nor female residents showed affiliative behavior toward non‐residents. Residents were more aggressive toward non‐residents than vice versa. The frequency of same‐sex aggression was greater than opposite‐sex aggression for male residents and this aggression was directed at adult male non‐residents to a greater degree than at subadult males. Resident males were least aggressive toward adult females. We found no differences in the behavior of females toward subadults, sexually naive adult non‐residents or sexually experienced adult non‐residents. Females also displayed similar amounts of aggression toward male and female non‐residents. Therefore, for males, aggression may function in defense of a mate while for females, aggression functions in resource defense. For both sexes, aggression is likely to play a role in the regulation of group composition.