Hormonal and social factors affecting evoked sexual behavior in Rhesus monkeys

Male rhesus monkey sexual behavior occurring spontaneously or evoked by remotely-controlled hypothalamic stimulation was studied in dominant and subdominant males with both dominant and subdominant, estrogen-treated or untreated, ovariectomized females. The behavior was quantified in terms of number and duration of ejaculatory sequences, number of thrusts, and number of mounts per sequence. Little or no spontaneous sexual behavior was observed with an untreated ovariectomized female. However, evoked sexual behavior with the exception of evoked ejaculation could be obtained whether the females were treated or untreated. Spontaneous and evoked sexual behavior was directed towards both dominant and subdominant females. The female chosen by the male was in part determined by the dominance status of the female. Evoked sexual behavior differed from spontaneous behavior in terms of an increased number of thrusts per mount, an increased number of ejaculations per session, and a decrease in latency between ejaculatory sequences.     

The timing of fission among free-ranging Rhesus monkeys

Behavioral observations were carried out on a large group of free-ranging rhesus monkeys (Macaca mulatta) on Cayo Santiago from January 1968 to December 1969 and from October through December 1970. During this period, social group A divided. The 24-month study period can be classified into five stages which represent the different phases in the process of group fission. Two criteria for fission were established: the cessation of grooming between adult females of different sub-groups of the main group and the stabilization of the adult female population. The criteria were based on established information on group dynamics and inter-group behavior on Cayo Santiago. Several points became clear from the chronological analysis. Group fission is a long process. The duration of the process of fission and the specification of the season in which fission begins and is completed depends upon the definition applied. For purposes of this analysis, fission was defined as beginning with the onset of spatial fragmentation and corresponded to the initial part of the breeding season. The fission was completed during the breeding season. The duration of the process of fission was 18 months.     

Cardiac allograft pathology in Rhesus monkeys

Orthotopic, allogeneic heart transplantations were performed in 26 randomly selected rhesus monkeys to study the effect of immunosuppressive treatment on survival and cardiac morphology. The histological picture of the acute and chronically rejected hearts was similar to that described for acute and chronic cardiac allograft rejection in man. As seems to be the case in man, an obliterative arteritis of the coronary arteries appears to be the limiting factor in cardiac allograft survival in the rhesus monkey. Immunosuppressive treatment with either Imuran and ALS or Imuran, ALS, and Prednisone could not prevent the occurrence of obliterative arteritis of the coronary arteries. Contrary to the observation in man, no atherosclerotic changes were found in the affected parts of the coronary arteries or in the non-diseased parts.     

Night observations of free-ranging Rhesus monkeys

The nocturnal distribution and behavior of individually marked Macaca mulatta were studied at the La Parguera, Puerto Rico, colony of the Caribbean Primate Research Center. The new image intensifier was used successfully to identify 399 monkeys in 185 sleeping clusters. Monkeys moved into mangrove trees close to favorite feeding areas usually 35 minutes after sunset. The group condensed to less than one-half the daytime spread, vocalizations increased and grooming ceased. Movements and vocalizations ceased several hours after sunset, although bursts of activity occurred throughout the night. Activity resumed 40 minutes before sunrise. Activity was higher during full moon, when I observed feeding, play and sexual behavior. Fights at night were twice as frequent during the breeding season. Monkeys slept in clusters of one to four, 58% of which were of two. Sixty-three percent were composed of maternal relatives, 33% were mother-infant pairs. Mature males clustered with non-related males, slept alone or with females (in the breeding season). Yearlings slept with their mothers or with older siblings. Distribution of monkeys in a group at night reflects daytime associations.     

Social dominance and reproductive behavior in male rhesus monkeys

Altmann's model describing the relationship of social dominance to breeding behavior in some non-human primate species has been tested using data from the Cayo Santiago rhesus colony. Although some of the model's assumptions are clearly not met by field observations, a good fit is often found for groups containing relatively few sexually mature, non-pregnant females. It is suggested that genetic change could be rapid under conditions described by this model. It is estimated that a “beneficial mutation” could spread through all the breeding males in as little as six generations regardless of group size. The speed at which an allele can spread through the group is discussed in terms of the mean length of female receptivity.     

Behavior of an all-juvenile group of Rhesus monkeys

The behavior and organization of a group of 33 juvenile rhesus monkeys removed from a single free-ranging group were found to parallel closely intact rhesus social groups. Dominance ranking among the juveniles was 95% predictable from prior knowledge of mothers' ranks. Grooming, sitting close together, sitting touching, and play were found to occur much more frequently between matrilineal kin than expected from random selection of partner. Some estrous behavior was observed, including two instances of peri-menstrual estrus. One lengthy homosexual interaction between two two-year-old females was observed. The basis of much of the behavior and organization shown by the juveniles was found to be the matrilineal kin bonds brought from their natal group.     

The influence of male dominance on social interactions in black ducks and mallards

The influence of male dominance on male-female social interactions was examined in black ducks, Anas rubripes, and mallards, A. platyrhynchos, that were raised from hatch in four different groups (male and female mallards; male and female black ducks; male mallards and female black ducks; male black ducks and female mallards). The mate preference of females, independent of the influence of male dominance, was determined by exposing females to four caged, isolated males, one from each different group. All females preferred the type of male they had been raised with since hatch. Females were then exposed to the same four males, now free-swimming, to determine how male dominance influenced the initial preference. Under these conditions, each female associated primarily with the most dominant of the four males, regardless of her initial mate preference. Mallards were the most dominant males in all tests. These results demonstrate that male dominance influences social interactions and is one factor contributing to hybridization between these two species.     

An assessment of dominance and kinship among patas monkeys

Kaplan andZucker (1980) argued that dominance and kinship do not function as important organizing features for intragroup behavior and social structure among patas monkeys (Erythrocebus patas). This paper reviews the available data pertinent to this argument and concludes that dominance probably is not a reliable structural variable for captive patas, despite its clear development in most groups. In contrast, kinship is a major organizing feature that strongly affects allogrooming and other affiliative interactions, and socialization.