The thumb is the first finger of the hand, next to the index finger. When a person is standing in the medical anatomical position (where the palm is facing to the front), the thumb is the outermost finger. The Medical Latin English noun for thumb is pollex (compare hallux for big toe), and the corresponding adjective for thumb is pollical.
The first finger of the hand
Thumb and fingers
The English word "finger" has two senses, even in the context of appendages of a single typical human hand:
Any of the five terminal members of the hand.
Any of the four terminal members of the hand, other than the thumb
Linguistically, it appears that the original sense was the first of these two: penkwe-ros (also rendered as penqrós) was, in the inferred Proto-Indo-European language, a suffixed form of penkwe (or penqe), which has given rise to many Indo-European-family words (tens of them defined in English dictionaries) that involve, or stem from, concepts of fiveness.
The thumb shares the following with each of the other four fingers:
Having a skeleton of phalanges, joined by hinge-like joints that provide flexion toward the palm of the hand
Having a dorsal surface that features hair and a nail, and a hairless palmar aspect with fingerprint ridges
The thumb contrasts with each of the other four by being the only finger that:
Is opposable to the other four fingers
Has two phalanges rather than three
Has greater breadth in the distal phalanx than in the proximal phalanx
Is attached to such a mobile metacarpus (which produces most of the opposability)
and hence the etymology of the word: "tum" is Proto-Indo-European for "swelling" (cf "tumour" and "thigh") since the thumb is the stoutest of the fingers.
Opposition and apposition
Anatomists and other researchers focused on human anatomy have hundreds of definitions of opposition. Some anatomists restrict opposition to when the thumb is approximated to the fifth finger (little finger) and refer to other approximations between the thumb and other fingers as apposition. To anatomists, this makes sense as two intrinsic hand muscles are named for this specific movement (the opponens pollicis and opponens digiti minimi respectively).
Other researchers use another definition, referring to opposition-apposition as the transition between flexion-abduction and extension-adduction; the side of the distal thumb phalanx thus approximated to the palm or the hand's radial side (side of index finger) during apposition and the pulp or "palmar" side of the distal thumb phalanx approximated to either the palm or other fingers during opposition.
Moving a limb back to its neutral position is called reposition and a rotary movement is referred to as circumduction.
Primatologists and hand research pioneers John and Prudence Napier defined opposition as: "A movement by which the pulp surface of the thumb is placed squarely in contact with - or diametrically opposite to - the terminal pads of one or all of the remaining fingers." For this true, pulp-to-pulp opposition to be possible, the thumb must rotate about its long axis (at the carpometacarpal joint). Arguably, this definition was chosen to underline what is unique to the human thumb.
A bonobo "fishing" for termites, an example of incomplete/"untrue" opposition
Opposable with comparatively long thumbs: gibbons (or lesser apes)
Yet to be classified: other New World monkeys (tamarins, Aotidae: night or owl monkeys, Pitheciidae: titis, sakis and uakaris, Atelidae: howler and woolly monkeys)
The spider monkey compensates for being virtually thumbless by using the hairless part of its long, prehensile tail for grabbing objects. In apes and Old World monkeys, the thumb can be rotated around its axis, but the extensive area of contact between the pulps of the thumb and index finger is a human characteristic.
Left: Opposable toes of the Sulawesi bear cuscus forelimb Right: Opposable thumb on rear foot of an opossum
In most phalangeridmarsupials (a family of possums) except species Trichosurus and Wyulda the first and second toes of the forefoot are opposable to the other three. In the hind foot, the first toe is clawless but opposable and provides firm grip on branches. The second and third toes are partly syndactylous, united by skin at the top joint while the two separate nails serve as hair combs. The fourth and fifth toes are the largest of the hind foot.
Similar to phalangerids though in a different order, koalas have five toes on their fore and hind feet with sharp curved claws except for the first toe of the hind foot. The first and second toes of the forefeet are opposable to the other three, which enables the koala to grip smaller branches and search for fresh leaves in the outer canopy. Similar to the phalangerids, the second and third toes of the hind foot are fused but have separate claws.
Opossums are New World marsupials with opposable thumbs in the hind feet giving these animals their characteristic grasping capability (with the exception of the water opossum, the webbed feet of which restrict opposability).
The mouse-like microbiotheres were a group of South American marsupials most closely related to Australian marsupials. The only extant member, Dromiciops gliroides, is not closely related to opossums but has paws similar to these animals, each having opposable toes adapted for gripping.
The front feet of chameleons are organized into a medial bundle of toes 1, 2 and 3, and a lateral bundle of toes 4 and 5, and the hind feet are organized into a medial bundle of toes 1 and 2, and a lateral bundle of toes 3, 4 and 5.
The bird-like dinosaur Troodon had a partially opposable finger. It is possible that this adaptation was used to better manipulate ground objects or moving undergrowth branches when searching for prey.
The small predatory dinosaur Bambiraptor may have had mutually opposable first and third fingers and a forelimb maneouverability that would allow the hand to reach its mouth. Its forelimb morphology and range of motion enabled two-handed prehension, one-handed clutching of objects to the chest, and use of the hand as a hook.
The muscles of the thumb can be compared to guy-wires supporting a flagpole; tension from these muscular guy-wires must be provided in all directions to maintain stability in the articulated column formed by the bones of the thumb. Because this stability is actively maintained by muscles rather than by articular constraints, most muscles attached to the thumb tend to be active during most thumb motions.
The muscles acting on the thumb can be divided into two groups: The extrinsic hand muscles, with their muscle bellies located in the forearm, and the intrinsic hand muscles, with their muscle bellies located in the hand proper.
Flexor pollicis longus (left) and deep muscles of dorsal forearm (right)
The abductor pollicis longus (APL) originates on the dorsal sides of both the ulna and the radius, and from the interosseous membrane. Passing through the first tendon compartment, it inserts to the base of the first metacarpal bone. A part of the tendon reaches the trapezium, while another fuses with the tendons of the extensor pollicis brevis and the abductor pollicis brevis. Except for abducting the hand, it flexes the hand towards the palm and abducts it radially. It is innervated by the deep branch of the radial nerve (C7-C8).
The extensor pollicis longus (EPL) originates on the dorsal side of the ulna and the interosseous membrane. Passing through the third tendon compartment, it is inserted onto the base of the distal phalanx of the thumb. It uses the dorsal tubercle on the lower extremity of the radius as a fulcrum to extend the thumb and also dorsiflexes and abducts the hand at the wrist. It is innervated by the deep branch of the radial nerve (C7-C8).
The extensor pollicis brevis (EPB) originates on the ulna distal to the abductor pollicis longus, from the interosseus membrane, and from the dorsal side of the radius. Passing through the first tendon compartment together with the abductor pollicis longus, it is attached to the base of the proximal phalanx of the thumb. It extends the thumb and, because of its close relationship to the long abductor, also abducts the thumb. It is innervated by the deep branch of the radial nerve (C7-T1).
The tendons of the extensor pollicis longus and extensor pollicis brevis form what is known as the anatomical snuff box (an indentation on the lateral aspect of the thumb at its base) The radial artery can be palpated anteriorly at the wrist(not in the snuffbox).
Thenar (left) and dorsal interossei (right) muscles
The flexor pollicis brevis (FPB) has two heads. The superficial head arises on the flexor retinaculum, while the deep head originates on three carpal bones: the trapezium, trapezoid, and capitate. The muscle is inserted onto the radial sesamoid bone of the metacarpophalangeal joint. It acts to flex, adduct, and abduct the thumb, and is therefore also able to oppose the thumb. The superficial head is innervated by the median nerve, while the deep head is innervated by the ulnar nerve (C8-T1).
The opponens pollicis originates on the tubercle of the trapezium and the flexor retinaculum. It is inserted onto the radial side of the first metacarpal. It opposes the thumb and assists in adduction. It is innervated by the median nerve.
Other muscles involved are:
The adductor pollicis also has two heads. The transversal head originates along the entire third metacarpal bone, while the oblique head originates on the carpal bones proximal to the third metacarpal. The muscle is inserted onto the ulnar sesamoid bone of the metacarpophalangeal joint. It adducts the thumb, and assists in opposition and flexion. It is innervated by the deep branch of the ulnar nerve (C8-T1).
The first dorsal interosseous, one of the central muscles of the hand, extends from the base of the thumb metacarpal to the radial side of the proximal phalanx of the index finger.
There is a variation of the human thumb where the angle between the first and second phalanges varies between 0° and almost 90° when the thumb is in a thumbs-up gesture.
It has been suggested that the variation is an autosomal recessive trait, called a "Hitchhiker's thumb", with homozygous carriers having an angle close to 90°. However this theory has been disputed, since the variation in thumb angle is known to fall on a continuum and shows little evidence of the bi-modality seen in other recessive genetic traits.
Left: In a power grip the object is in contact with the palm. Right: Cricketer Jack Iverson's "bent finger grip", an unusual pad-to-side precision grip designed to confuse batsmen.
One of the earlier significant contributors to the study of hand grips was orthopedic primatologist and paleoanthropologist John Napier, who proposed organizing the movements of the hand by their anatomical basis as opposed to work done earlier that had only used arbitrary classification. Most of this early work on hand grips had a pragmatic basis as it was intended to narrowly define compensable injuries to the hand, which required an understanding of the anatomical basis of hand movement. Napier proposed two primary prehensile grips: the precision grip and the power grip. The precision and power grip are defined by the position of the thumb and fingers where:
The power grip is when the fingers (and sometimes palm) clamp down on an object with the thumb making counter pressure. Examples of the power grip are gripping a hammer, opening a jar using both your palm and fingers, and during pullups.
The precision grip is when the intermediate and distal phalanges ("fingertips") and the thumb press against each other. Examples of a precision grip are writing with a pencil, opening a jar with the fingertips alone, and gripping a ball (only if the ball is not tight against the palm).
Thumb and index finger during pad-to-pad precision grasping.
Opposability of the thumb should not be confused with a precision grip as some animals possess semi-opposable thumbs yet are known to have extensive precision grips (Tufted Capuchins for example). Nevertheless, precision grips are usually only found in higher apes, and only in degrees significantly more restricted than in humans.
The pad-to-pad pinch between the thumb and index finger is made possible because of the human ability to passively hyperextend the distal phalanx of the index finger. Most non-human primates have to flex their long fingers in order for the small thumb to reach them.
In humans, the distal pads are wider than in other primates because the soft tissues of the finger tip are attached to a horseshoe-shaped edge on the underlying bone, and, in the grasping hand, the distal pads can therefore conform to uneven surfaces while pressure is distributed more evenly in the finger tips. The distal pad of the human thumb is divided into a proximal and a distal compartment, the former more deformable than the latter, which allows the thumb pad to mold around an object.
In robotics, almost all robotic hands have a long and strong opposable thumb. Like human hands, the thumb of a robotic hand also plays a key role in gripping an object. One inspiring approach of robotic grip planning is to mimic human thumb placement.
 In a sense, human thumb placement indicates which surface or part of the object is good for grip. Then the robot places its thumb to the same location and plans the other fingers based on the thumb placement.
The function of the thumb declines physiologically with aging. This can be demonstrated by assessing the motor sequencing of the thumb.
A primitive autonomization of the first carpometacarpal joint (CMC) may have occurred in dinosaurs. A real differentiation appeared perhaps 70 mya in early primates, while the shape of the human thumb CMC finally appears about 5 mya. The result of this evolutionary process is a human CMC joint positioned at 80° of pronation, 40 of abduction, and 50° of flexion in relation to an axis passing through the second and third CMC joints.
Opposable thumbs are shared by some primates, including most catarrhines. The climbing and suspensory behaviour in orthograde apes, such as chimpanzees, has resulted in elongated hands while the thumb has remained short. As a result, these primates are unable to perform the pad-to-pad grip associated with opposability. However, in pronograde monkeys such as baboons, an adaptation to a terrestrial lifestyle has led to reduced finger length and thus hand proportions similar to those of humans. Consequently, these primates have dexterous hands and are able to grasp objects using a pad-to-pad grip. It can thus be difficult to identify hand adaptations to manipulation-related tasks based solely on thumb proportions.
The evolution of the fully opposable thumb is usually associated with Homo habilis, a forerunner of Homo sapiens. This, however, is the suggested result of evolution from Homo erectus (around 1 mya) via a series of intermediate anthropoid stages, and is therefore a much more complicated link.
Modern humans are unique in the musculature of their forearm and hand. Yet, they remain autapomorphic, meaning each muscle is found in one or more non-human primates. The extensor pollicis brevis and flexor pollicis longus allow modern humans to have great manipulative skills and strong flexion in the thumb.
However, a more likely scenario may be that the specialized precision gripping hand (equipped with opposable thumb) of Homo habilis preceded walking, with the specialized adaptation of the spine, pelvis, and lower extremities preceding a more advanced hand. And, it is logical that a conservative, highly functional adaptation be followed by a series of more complex ones that complement it. With Homo habilis, an advanced grasping-capable hand was accompanied by facultative bipedalism, possibly implying, assuming a co-opted evolutionary relationship exists, that the latter resulted from the former as obligate bipedalism was yet to follow. Walking may have been a by-product of busy hands and not vice versa.
^"The Thumb is the Hero". The New York Times. January 11, 1981. Retrieved 2010. The "fishing rod" a chimp strips of leaves and pokes into a termite nest to bring up a snack is as far as he'll ever get toward orbiting the planets.
^Grzimek, Bernhard (2003). Hutchins, Michael; Kleiman, Devra G.; Geist, Valerius; et al. (eds.). Grzimek's Animal Life Encyclopedia, Vol 16, Mammals V (2nd ed.). Farmington Hills, MI: Gale Group. p. 293. ISBN978-0-7876-7750-3.
^Anderson, Christopher V. & Higham, Timothy E. (2014). "Chameleon anatomy". In Tolley, Krystal A. & Herrel, Anthony (eds.). The Biology of Chameleons. Berkeley: University of California Press. pp. 7-55. ISBN9780520276055.
^Leakey, Tobias & Napier 1964: "[In Homo habilis] the pollex is well developed and fully opposable and the hand is capable not only of a power grip but of, at least, a simple and usually well developed precision grip."
^Diogo, R.; Richmond, B. G.; Wood, B. (2012). "Evolution and homologies of primate and modern human hand and forearm muscles, with notes on thumb movements and tool use". Journal of Human Evolution. 63 (1): 64-78. doi:10.1016/j.jhevol.2012.04.001. PMID22640954.
Austin, Noelle M. (2005). "Chapter 9: The Wrist and Hand Complex". In Levangie, Pamela K.; Norkin, Cynthia C. (eds.). Joint Structure and Function: A Comprehensive Analysis (4th ed.). Philadelphia: F. A. Davis Company. ISBN978-0-8036-1191-7.
Diogo, R; Richmond, BG; Wood, B (2012). "Evolution and homologies of primate and modern human hand and forearm muscles, with notes on thumb movements and tool use". Journal of Human Evolution. 63 (1): 64-78. doi:10.1016/j.jhevol.2012.04.001. PMID22640954.