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9.7: Hominin Charts

  • Page ID
    70786
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    Hominin

    Sahelanthropus tchadensis

    Dates

    7 mya to 6 mya

    Region(s)

    Chad

    Famous discoveries

    The initial discovery, made in 2001.

    Brain size

    360 cc average

    Dentition

    Smaller than in extant great apes, larger and pointier than in humans. Canines worn at the tips.

    Cranial features

    A short cranial base and a foramen magnum (hole in which the spinal cord enters the cranium) that is more humanlike in positioning, has been argued to indicate upright walking.

    Postcranial features

    Currently little published postcranial material.

    Culture

    N/A

    Other

    The extent to which this hominin was bipedal is currently heavily debated. If so, it would indicate an arboreal bipedal ancestor of hominins, not a knuckle-walker like chimpanzees.

       

    Hominin

    Orrorin tugenensis

    Dates

    6 mya to 5.7 mya

    Region(s)

    Tugen Hills (Kenya)

    Famous discoveries

    Original discovery in 2000.

    Brain size

    N/A

    Dentition

    Smaller cheek teeth (molars and premolars) than even more recent hominins (i.e., derived), thick enamel, and reduced, but apelike, canines.

    Cranial features

    Not many found

    Postcranial features

    Fragmentary leg, arm, and finger bones have been found. Indicates bipedal locomotion.

    Culture

    Potential toolmaking capability based on hand morphology, but nothing found directly.

    Other

    This is the earliest species that clearly indicates adaptations for bipedal locomotion.

       

    Hominin

    Ardipithecus ramidus

    Dates

    4.4 mya

    Region(s)

    Middle Awash region and Gona (Ethiopia)

    Famous discoveries

    A partial female skeleton nicknamed “Ardi” (ARA-VP-6/500).

    Brain size

    300 cc to 350 cc

    Dentition

    Little differences between the canines of males and females (small sexual dimorphism).

    Cranial features

    Midfacial projection, slightly prognathic. Cheekbones less flared and robust than in later hominins.

    Postcranial features

    Ardi demonstrates a mosaic of ancestral and derived characteristics in the postcrania. For instance, an opposable big toe similar to chimpanzees (i.e., “primitive” or more ancestral), which could have aided in climbing trees effectively. However, the pelvis and hip show that she could walk upright (i.e., it is derived), supporting her hominin status.

    Culture

    None directly associated

    Other

    Over 110 specimens from Aramis

       

    Hominin

    Ardipithecus kadabba

    Dates

    5.2 mya to 5.8 mya

    Region(s)

    Middle Awash (Ethiopia)

    Famous discoveries

    This species discovery in 1997 by Yohannes Haile-Selassie.

    Brain size

    N/A

    Dentition

    Larger hind dentition than in modern chimpanzees. Thick enamel and larger canines than in later hominins.

    Cranial features

    N/A

    Postcranial features

    A large hallux (big toe) bone indicates a bipedal “push off.”

    Culture

    N/A

    Other

    Faunal evidence indicates a mixed grassland/woodland environment.

       

    Hominin

    Australopithecus anamensis

    Dates

    4.2 mya to 3.8 mya

    Region(s)

    Turkana region (Kenya), Middle Awash (Ethiopia)

    Famous discoveries

    A 2019 find from Ethiopia, named MRD.

    Brain size

    370 cc

    Dentition

    Relatively large canines compared with more recent Australopithecines.

    Cranial features

    Projecting cheekbones and primitive earholes.

    Postcranial features

    Lower limb bones (tibia and femur) indicate bipedality; arboreal features in upper limb bones (humerus) found.

    Culture

    N/A

    Other

    Almost 100 specimens, representing over 20 individuals, have been found to date.

       

    Hominin

    Australopithecus afarensis

    Dates

    2.9 mya to 3.9 mya

    Region(s)

    Afar Region, Omo, Maka, Fejej, and Belohdelie (Ethiopia); Laetoli (Tanzania); Koobi Fora (Kenya).

    Famous discoveries

    Lucy, Selam (Dikika Child), Laetoli Footprints.

    Brain size

    380 cc to 430 cc

    Dentition

    Reduced canines and molars relative to great apes, but larger than in modern humans.

    Cranial features

    Prognathic face, facial features indicate relatively strong chewing musculature (compared with Homo), but less extreme than in Paranthropus.

    Postcranial features

    Clear evidence for bipedalism from lower limb postcranial bones. Laetoli Footprints indicate humanlike walking. Dikika Child bones indicate retained primitive arboreal traits in the postcrania.

    Culture

    None directly; but close in age and proximity to controversial cut marks at Dikika and early tools in Lomekwi.

    Other

    Au. afarensis is one of the oldest and most well-known australopithecine species and consists of a large number of fossil remains.

       

    Hominin

    Australopithecus bahrelghazali

    Dates

    3.6 mya

    Region(s)

    Chad

    Famous discoveries

    “Abel,” the holotype.

    Brain size

    N/A

    Dentition

    N/A

    Cranial features

    N/A

    Postcranial features

    N/A

    Culture

    N/A

    Other

    Arguably within range of variation of Au. afarensis

       

    Hominin

    Australopithecus deyiremada

    Dates

    3.5 mya to 3.3 mya

    Region(s)

    Woranso-Mille (Afar region, Ethiopia)

    Famous discoveries

    First fossil mandible bones were discovered in 2011 in the Afar region of Ethiopia by Yohannes Haile-Selassie.

    Brain size

    N/A

    Dentition

    Smaller teeth with thicker enamel than seen in Au. afarensis, with a potentially hardier diet.

    Cranial features

    Larger mandible and more projecting cheekbones than in Au. afarensis.

    Postcranial features

    N/A

    Culture

    N/A

    Other

    Contested species designation; arguably a member of Au. afarensis.

       

    Hominin

    Australopithecus garhi

    Dates

    2.5 mya

    Region(s)

    Middle Awash (Ethiopia)

    Famous discoveries

    N/A

    Brain size

    450 cc

    Dentition

    Larger hind dentition than seen in other gracile Australopithecines.

    Cranial features

    N/A

    Postcranial features

    A femur of a fragmentary partial skeleton, argued to belong to Au. garhi, indicates this species may be longer-limbed than Au. afarensis, although still able to move arboreally.

    Culture

    Crude/primitive stone tools resembling Oldowan (described later) have been found in association with Au. garhi.

    Other

    This species is not well documented or understood and is based on only a few fossil specimens.

       

    Hominin

    Australopithecus africanus

    Dates

    3.3 mya to 2.1 mya

    Region(s)

    Sterkfontein, Taung, Makapansgat, Gladysvale (South Africa)

    Famous discoveries

    Taung Child, “Mrs. Ples,” Little Foot (?).

    Brain size

    400 cc to 500 cc

    Dentition

    Smaller teeth (derived) relative to Au. afarensis. Small canines with no diastema.

    Cranial features

    A rounder skull compared with Au. afarensis in East Africa. A sloping face (primitive).

    Postcranial features

    Similar postcranial evidence for bipedal locomotion (derived pelvis) with retained arboreal locomotion (e.g., curved phalanges—fingers), as seen in Au. afarensis.

    Culture

    None with direct evidence.

    Other

    A 2015 study noted that the trabecular bone morphology of the hand was consistent with forceful tool manufacture and use, suggesting potential early tool abilities.

       

    Hominin

    Australopithecus sediba

    Dates

    1.97 mya

    Region(s)

    Malapa Fossil Site (South Africa)

    Famous discoveries

    Karabo (MH1)

    Brain size

    420 cc to 450 cc

    Dentition

    Small dentition with Australopithecine cusp-spacing.

    Cranial features

    Small brain size (Australopithecus-like), but gracile mandible (Homo-like).

    Postcranial features

    Scientists have interpreted this mixture of traits (such as a robust ankle but evidence for an arch in the foot) as a transitional phase between a body previously adapted to arborealism (tree climbing, particularly in evidence from the bones of the wrist) to one that adapted to bipedal ground walking.

    Culture

    None of direct association, but some have argued that a modern hand morphology (shorter fingers and a longer thumb) means that adaptations to tool manufacture and use may be present in this species.

    Other

    It was first discovered through a clavicle bone in 2008 by nine-year-old Matthew Berger, son of paleoanthropologist Lee Berger.

       

    Hominin

    Australopithecus prometheus

    Dates

    3.7 mya (debated)

    Region(s)

    Sterkfontein (South Africa)

    Famous discoveries

    “Little Foot” (StW 573)

    Brain size

    408 cc (Little Foot estimate)

    Dentition

    Heavy anterior dental wear patterns, relatively large anterior dentition and smaller hind dentition, similar to Au. afarensis.

    Cranial features

    Relatively larger brain size, robust zygomatic arch, and a flatter midface.

    Postcranial features

    The initial discovery of four ankle bones indicated bipedality.

    Culture

    N/A

    Other

    Highly debated new species designation.

       

    Hominin

    Paranthropus aethiopicus

    Dates

    2.7 mya to 2.3 mya

    Region(s)

    West Turkana (Kenya), Laetoli (Tanzania), Omo River Basin (Ethiopia)

    Famous discoveries

    The ‘Black Skull” (KNM–WT 17000)

    Brain Size

    410 cc

    Dentition

    P. aethiopicus has the shared derived traits of large flat premolars and molars, although few teeth have been found.

    Cranial features

    Large flaring zygomatic arches for accommodating large chewing muscles (the temporalis muscle), a sagittal crest for increased muscle attachment of the chewing muscles to the skull, and a robust mandible and supraorbital torus (brow ridge).

    Postcranial features

    A proximal tibia indicates bipedality, and similar size to Au. afarensis.

    Culture

    N/A

    Other

    The “Black Skull” is so called because of the mineral manganese that stained it black during fossilization.

       

    Hominin

    Paranthropus boisei

    Dates

    2.4 mya to 1.4 mya

    Region(s)

    Koobi Fora, West Turkana, and Chesowanja (Kenya), Malema-Chiwondo (Malawi), Olduvai Gorge and Peninj (Tanzania), and Omo River basin and Konso (Ethiopia)

    Famous discoveries

    “Zinj,” or sometimes “Nutcracker Man” (OH5), in 1959 by Mary Leakey. The Peninj mandible from Tanzania, found in 1964 by Kimoya Kimeu.

    Brain size

    500 cc to 550 cc

    Dentition

    Very large, flat posterior dentition (largest of all hominins currently known). Much smaller anterior dentition. Very thick dental enamel.

    Cranial features

    Indications of very large chewing muscles (e.g., flaring zygomatic arches and a large sagittal crest).

    Postcranial features

    Evidence for high variability and sexual dimorphism, with estimates of males at 1.37 meters tall and females at 1.24 meters.

    Culture

    Richard Leakey and Bernard Wood have both suggested that P. boisei could have made and used stone tools. Tools dated to 2.5 mya in Ethiopia have been argued to possibly belong to this species.

    Other

    Despite the cranial features of P. boisei indicating a tough diet of tubers, nuts, and seeds, isotopes indicate a diet high in C4 foods (e.g., grasses, such as sedges). This differs from what is seen in P. robustus.

       

    Hominin

    Paranthropus robustus

    Dates

    2.3 mya to 1 mya

    Region(s)

    Kromdraai B, Swartkrans, Gondolin, Drimolen, and Coopers Cave (South Africa)

    Famous discoveries

    SK48 (original skull)

    Brain size

    410 cc to 530 cc

    Dentition

    Large posterior teeth with thick enamel, consistent with other Robust Australopithecines. Enamel hypoplasia is also common in this species, possibly because of instability in the development of large, thick enameled dentition.

    Cranial features

    P. robustus features are neither as “hyper-robust” as P. boisei or as primitive as P. aethiopicus, but have been described as less derived more general features that are shared with both East African species, e.g., the sagittal crest and zygomatic flaring.

    Postcranial features

    Reconstructions indicate sexual dimorphism.

    Culture

    N/A

    Other

    Several of these fossils are fragmentary in nature, distorted, and not well preserved, because they have been recovered from quarry breccia using explosives.

       

    Hominin

    Kenyanthopus platyops

    Dates

    3.5 mya to 3.2 mya

    Region(s)

    Lake Turkana (Kenya)

    Famous discoveries

    KNM–WT 40000

    Brain size

    Difficult to determine, but appears within the range of Australopithecus afarensis.

    Dentition

    Small molars/dentition (Homo-like characteristic)

    Cranial features

    Flatter (i.e., orthognathic) face

    Postcranial features

    N/A

    Culture

    Some have associated the earliest tool finds from Lomekwi, Kenya, temporally (3.3 mya) and in close geographic proximity to this species/specimen.

    Other

    Taxonomic placing of this species is quite divided. The discoverers have argued that this species is ancestral to Homo, in particular to Homo ruldolfensis.

       

    Review Questions

    • What is the difference between a “derived” versus a “primitive” trait? Give an example of both, seen in Au. afarensis.
    • Which of the paleoenvironment hypotheses have been used to describe early hominin diversity, and which have been used to describe bipedalism?
    • Which anatomical features for bipedalism do we see in early hominins? Are these primarily obligate bipeds? Explain.
    • Describe the dentition of gracile and robust australopithecines. What might these tell us about their relative diets?
    • List the hominin species argued to be associated with stone tool technologies. Are you convinced of these associations? Why/why not?

    This page titled 9.7: Hominin Charts is shared under a CC BY-NC 4.0 license and was authored, remixed, and/or curated by Beth Shook, Katie Nelson, Kelsie Aguilera, & Lara Braff, Eds. (Society for Anthropology in Community Colleges) via source content that was edited to the style and standards of the LibreTexts platform; a detailed edit history is available upon request.