Brachiation (from "brachium", Latin for "arm"), or arm swinging, is a form of arboreal locomotion in which swing from tree limb to tree limb using only their arms. During brachiation, the body is alternately supported under each forelimb. This form of locomotion is the primary means of locomotion for the small and of southeast Asia. Gibbons in particular use brachiation for as much as 80% of their locomotor activities. Some New World monkeys, such as Spider monkey and Muriqui, were initially classified as semibrachiators and move through the trees with a combination of leaping and brachiation. Some New World species also practice suspensory behaviors by using their prehensile tail, which acts as a fifth grasping hand. Evidence has shown that the extinct ape Proconsul from the Miocene of East Africa developed an early form of suspensory behaviour, and was therefore referred to as a probrachiator.
Upon further observations and more in depth understandings of the anatomy and behaviour of primates, the terms semibrachiator and probrachiator have largely fallen out of favour within the scientific community. Currently, researchers classify gibbons and siamangs as the only true brachiators and classify the great apes as modified brachiators. All other brachiation behaviours that do not meet either of these classifications are referred to as forearm suspensory postures and locomotion.
Some traits that allow primates to brachiate include a short spine (particularity the lumbar vertebrae), short fingernails (instead of claws), long curved fingers, reduced thumbs, long forelimbs and freely rotating wrists. Modern humans retain many physical characteristics that suggest a brachiator ancestor, including flexible shoulder joints and fingers well-suited for grasping. In lesser apes, these characteristics were adaptations for brachiation. Although great apes do not normally brachiate (with the exception of ), human anatomy suggests that brachiation may be an exaptation to bipedalism, and healthy modern humans are still capable of brachiating.
As well as shaping the evolution of gibbon body structure, brachiation has influenced the style and order of their behaviour. For example, unlike other primates who carry infants on their back, gibbons will carry young ventrally. It also affects their play activities, copulation, and fighting. It is thought that gibbons gain evolutionary advantages through brachiation and being suspended by both hands ( bimanual suspension) when feeding. While smaller primates cannot hold themselves by both hands for long periods, and larger primates are too heavy to exploit food resources on the ends of branches, gibbons can remain suspended for a significant period and use their long arms to reach food in terminal branches more easily. Another theory postulates that brachiation is a quieter and less obvious mode of locomotion than quadrupedal jumping and climbing thereby more successfully avoiding predators.
The amount of energy transferred from potential to kinetic during pendulum-like movement is known as energy recovery. Maintaining a higher energy recovery during brachiation costs less energy and allows the animal to move to its destination quickly, however, this type of movement is also harder to control. Therefore, since the risk of missing a handhold can result in injury or death, the benefit of moving slower with a lower energy recovery and more control likely outweighs the cost of extra energy expenditure.
Specialized locomotor behaviours, such as brachiating, are thought to have evolved from arboreal quadrupedalism. This behaviour is the ancestral and most common locomotor mechanism among primates. This would explain why living apes and humans share many unusual morphological aspects of the upper limb and thorax. The transition to brachiation is regarded as a major shift during primate evolution and is thought to be a possible precursor to the adaptation of bipedal walking in early Hominidae. Specialized suspensory behaviour was shown to have evolved independently between hominid groups.
There are several hypotheses for how early brachiating primates may have transitioned into bipedalism. The most generally accepted of these is the vertical climbing hypothesis, which states that vertical climbing is the biomechanical link between brachiation and bipedalism.Fleagle, JG, Stern, JT, Jungers, WL, Susman, RL, Vangor, AK and Wells, JP. (1981). "Climbing: a biomechanical link with brachiation and with bipedalism". Symp. Zool. Soc. Lond. 48: 359-375. Many climbing adaptations have been found in early Homininae and some of these adaptations can still be seen in present day humans. The distinctive body posture, limb proportions and trunk design identified in living apes are better explained by the previous adaptation of climbing behaviours.
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