Premolar in the context of "Carpolestidae"

Human teeth function to mechanically break down items of food by cutting and crushing them in preparation for swallowing and digesting. As such, they are considered part of the human digestive system. Humans have four types of teeth: incisors, canines, premolars, and molars, which each have a specific function. The incisors cut the food, the canines tear the food and the molars and premolars crush the food. The roots of teeth are embedded in the maxilla (upper jaw) or the mandible (lower jaw) and are covered by gums. Teeth are made of multiple tissues of varying density and hardness.

Humans, like most other mammals, are diphyodont, meaning that they develop two sets of teeth. The first set, deciduous teeth, also called "primary teeth", "baby teeth", or "milk teeth", normally eventually contains 20 teeth. Primary teeth typically start to appear ("erupt") around six months of age and this may be distracting and/or painful for the infant. However, some babies are born with one or more visible teeth, known as neonatal teeth or "natal teeth".

Dentition pertains to the development of teeth and their arrangement in the mouth. In particular, it is the characteristic arrangement, type, and number of teeth in a given species at a given age, as well as the morpho-physiology (that is, the relationship between the shape and form of the tooth in question and its inferred function) of the animal's teeth.

In dentistry, the crown is the visible part of the tooth above the gingival margin and is an essential component of dental anatomy. Covered by enamel, the crown plays a crucial role in cutting, tearing, and grinding food. Its shape and structure vary depending on the type and function of the tooth (incisors, canines, premolars, or molars), and differ between primary dentition and permanent dentition. The crown also contributes to facial aesthetics, speech, and oral health.

Australopithecus garhi is a species of australopithecine from the Bouri Formation in the Afar Region of Ethiopia 2.6–2.5 million years ago (mya) during the Early Pleistocene. The first remains were described in 1999 based on several skeletal elements uncovered in the three years preceding. A. garhi was originally considered to have been a direct ancestor to Homo and the human line, but is now thought to have been an offshoot. Like other australopithecines, A. garhi had a brain volume of 450 cc (27 cu in); a jaw which jutted out (prognathism); relatively large molars and premolars; adaptations for both walking on two legs (bipedalism) and grasping while climbing (arboreality); and it is possible that, though unclear if, males were larger than females (exhibited sexual dimorphism). One individual, presumed female based on size, may have been 140 cm (4 ft 7 in) tall.

A. garhi is the first pre-Homo hominin postulated to have manufactured tools—using them in butchering—and may be counted among a growing body of evidence for pre-Homo stone tool industries (the ability to manufacture tools was previously believed to have separated Homo from predecessors). A. garhi possibly produced the Oldowan industry which was previously considered to have been invented by the later H. habilis, though this may have instead been produced by contemporary Homo.

Australopithecus bahrelghazali is an extinct species of australopithecine discovered in 1995 at Koro Toro, Bahr el Gazel, Chad, existing around 3.5 million years ago in the Pliocene. It is the first and only australopithecine known from Central Africa, and demonstrates that this group was widely distributed across Africa as opposed to being restricted to East and southern Africa as previously thought. The validity of A. bahrelghazali has not been widely accepted, in favour of classifying the specimens as A. afarensis, a better known Pliocene australopithecine from East Africa, because of the anatomical similarity and the fact that A. bahrelghazali is known only from 3 partial jawbones and an isolated premolar. The specimens inhabited a lakeside grassland environment with sparse tree cover, possibly similar to the modern Okavango Delta, and similarly predominantly ate C₄ savanna foods—such as grasses, sedges, storage organs, or rhizomes—and to a lesser degree also C₃ forest foods—such as fruits, flowers, pods, or insects. However, the teeth seem ill-equipped to process C₄ plants, so its true diet is unclear.

Paranthropus robustus is a species of robust australopithecine from the Early and possibly Middle Pleistocene of the Cradle of Humankind, South Africa, about 2.27 to 0.87 (or, more conservatively, 2 to 1) million years ago. It has been identified in Kromdraai, Swartkrans, Sterkfontein, Gondolin, Cooper's, and Drimolen Caves. Discovered in 1938, it was among the first early hominins described, and became the type species for the genus Paranthropus. However, it has been argued by some that Paranthropus is an invalid grouping and synonymous with Australopithecus, so the species is also often classified as Australopithecus robustus.

Robust australopithecines—as opposed to gracile australopithecines—are characterised by heavily built skulls capable of producing high stresses and bite forces, as well as inflated cheek teeth (molars and premolars). Males had more heavily built skulls than females. P. robustus may have had a genetic susceptibility for pitting enamel hypoplasia on the teeth, and seems to have had a dental cavity rate similar to non-agricultural modern humans. The species is thought to have exhibited marked sexual dimorphism, with males substantially larger and more robust than females. Based on 3 specimens, males may have been 132 cm (4 ft 4 in) tall and females 110 cm (3 ft 7 in). Based on 4 specimens, males averaged 40 kg (88 lb) in weight and females 30 kg (66 lb). The brain volume of the specimen SK 1585 is estimated to have been 476 cc, and of DNH 155 about 450 cc (for comparison, the brain volume of contemporary Homo varied from 500 to 900 cc). P. robustus limb anatomy is similar to that of other australopithecines, which may indicate a less efficient walking ability than modern humans, and perhaps some degree of arboreality (movement in the trees).

Cheek teeth or postcanines comprise the molar and premolar teeth in mammals. Cheek teeth are multicuspidate (having many folds or tubercles). Mammals have multicuspidate molars (three in placentals, four in marsupials, in each jaw quadrant) and premolars situated between canines and molars whose shape and number varies considerably among particular groups. For example, many modern Carnivora possess carnassials, or secodont teeth. This scissor-like pairing of the last upper premolar and first lower molar is adapted for shearing meat. In contrast, the cheek teeth of deer and cattle are selenodont. Viewed from the side, these teeth have a series of triangular cusps or ridges, enabling the ruminants' sideways jaw motions to break down tough vegetable matter. Cheek teeth are sometimes separated from the incisors by a gap called a diastema.

Cheek teeth in reptiles are much simpler as compared to mammals.

Permanent teeth or adult teeth are the second set of teeth formed in diphyodont mammals. In humans and old world simians, there are thirty-two permanent teeth, consisting of six maxillary and six mandibular molars, four maxillary and four mandibular premolars, two maxillary and two mandibular canines, four maxillary and four mandibular incisors.