Living primates
There are about six hundred varieties of living non-human primates, divided into some fifty genera and two hundred species. Because of this extraordinary diversity, ranging from such forms as the small, insectivore-like tree shrews and âmouse lemursâ to the great apes and man, it is sometimes assumed that the behavior of living primates can be arranged along an evolutionary scale of increasing behavioral similarity to man. However, no living primate is the ancestor of any other, and many varieties have had separate evolutionary histories for tens of millions of years. Every living species has survived by specialized adaptations, and while it is possible to make some broad generalizations about the physical characteristics of prosimians, monkeys and apes (Clark, 1960), behavioral comparisons are more difficult. Washburn and Hamburg (1965) have recently discussed the classification of the primate order from a behavioral point of view.
The many varieties of monkeys alone range in size from creatures weighing less than a pound to others weighing more than one hundred pounds. They have exploited a wide variety of jungle and open woodland habitats, frequently achieving population densities of one hundred or more individuals per square mile. The Old-World monkeys (Cercopithecidae) are divided into two subfamilies, the Cercopithecinae and the Colobinae; the latter group is distinguished by a specialized stomach capable of digesting large quantities of mature leaves. Brief observations have been made of several species of Colobinae, but the only form studied in detail is the common langur of India and Ceylon Presbytis spp (Jay, 1965). Among the Cercopithecinae, numerous studies have been made of the two closely related ground-adapted forms, the African baboon (Papio) and the Asian macaques (Macaca). Of the other two basic groups of Cercopithecinae, the mangabeys (Cercocebus) and the guenons, or vervets (Cercopithecus), a long-term field study has been made of only one, a ground-adapted species, Cercopithecus aethiops (Struhsaker, 1965).
The four apes, the Pongidae, are the gibbon (including the siamang), the orangutan, the gorilla and the chimpanzee. All of the apes differ from the monkeys in that the trunk is âshort, wide and shallow ⌠the lumbar region is short⌠and the shoulder and arm muscles are especially adapted to abduction, flexion, and rotationâ (Washburn and Hamburg, 1965, p. 9). Because of this adaptation to climbing and the ability to hang or swing from branches, to brachiate, apes have a âverticalâ posture, thus differing from the horizontal, quadrupedal monkeys, and it is no surprise that in their structure and bodily movements the apes closely resemble man. Physically, and to some extent behaviorally, man is most like the African great apes â the gorilla and the chimpanzee. But apes are confined to heavily wooded areas, and some of the behavioral patterns which have enabled man to travel long distances in open country are more closely paralleled in the behavior of terrestrial monkeys, such as baboons and macaques. In fundamental senses such as hearing, eyesight and smell and in the organization of the brain, the viscera and the reproductive organs, man, the apes and the Old-World monkeys share a basic biological pattern which distinguishes them from all other mammals, including New World monkeys and other primates.
Field studies of primates
Although attempts were made to study the African apes soon after their discovery in the nineteenth century, most reports of monkey and ape behavior in the wild remained anecdotal until Carpenter observed the howler monkeys of Panama in 1931. In succeeding years, other field studies were attempted, but these were usually brief; then, in the 1950s, investigators in Japan, the United States and Europe independently initiated a variety of field studies emphasizing long-term, systematic observation of primates living in natural habitats.
Most field studies have been made on monkey species that spend large amounts of time on the ground, where observation conditions are easiest. Because of their similarity to man, all the living apes except the orangutan have been the subject of at least one major field study. Long-term studies of free-ranging groups in monkey colonies have also contributed valuable data. The Japan Monkey Center has kept records of individual monkeys in its colonies since the early 1950s. Beginning with Altmann in 1958 (see Buettner-Janusch et al., 1962), various investigators have restudied the rhesus monkey colony established on Cayo Santiago by Carpenter in 1938; in fact, since 1958 almost all the members of this free-ranging colony have been tattooed for identification. Because the life cycle of primates is so long, field workers cannot ordinarily ascertain sibling or mother-offspring bonds between adults, and yet these relationships are proving to be very important in some species. (For a more complete history of field studies see Southwick, 1963, pp. 1â6; and Washburn, Jay and Lancaster, 1965.)
Laboratory studies of primates, especially of the common Indian rhesus monkeys, have continued without interruption since the 1930s. Contemporary views of such topics as discrimination, operant conditioning, perception, and learning have been summarized by Schrier, Harlow and Stollnitz (1965). Recent studies of hemoglobins, blood serums, chromosomes, the nervous system, and the skin have been reported by Buettner-Janusch (1963â4). There are two journals devoted entirely to primate studies, Primates and Folia primatologica, and there are many films of primate behavior.
The formerly facile generalizations about monkey and ape behavior are no longer tenable. Although only about a dozen of the several hundred varieties of living primates have been studied to date, it is already clear that primates exploit a wide variety of ecological niches, that they live in different kinds of social groups, and that different species display quite different temperaments. Some species are distributed over large geographical areas, and group structure and behavior have been found to vary significantly between different populations of the same species (Jay, 1965). The unique life history of every individual produces distinctive patterns of temperament and social behavior among the members of a single group. All of these variables make it inevitable that there will be important exceptions to many of the following generalizations.