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Corrigendum to “The effect of bi-iliac breadth on core body temperature” [J. Hum. Evol. 195 (2024) 103580]
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Humanlike manual activities in Australopithecus
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The dentition of a new adult Neanderthal individual from Grotte Mandrin, France
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Craniomandibular variation in the endemic Hispaniolan primate, Antillothrix bernensis
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Persistent predators: Zooarchaeological evidence for specialized horse hunting at Schöningen 13II-4
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Additional isolated hominin canine tooth from Kanapoi, Kenya
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An assessment of puberty status in adolescents from the European Upper Paleolithic
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Molar enamel–dentine junction shape of Pliobates cataloniae and other Iberian pliopithecoids
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Adhesive technology based on biomass tar documents engineering capabilities in the African Middle Stone Age
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A 4.3-million-year-old Australopithecus anamensis mandible from Ileret, East Turkana, Kenya, and its paleoenvironmental context
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The archaeological visibility of chimpanzee (Pan troglodytes) nut-cracking
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The effect of bi-iliac breadth on core body temperature
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Reduced limb integration characterizes primate clades with diverse locomotor adaptations
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Diverse bone-calcium isotope compositions in Neandertals suggest different dietary strategies
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New hominin dental remains from Olduvai Gorge (Tanzania)
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Dental microwear and diets of mainland fossil Pongo from the Mid-Pleistocene of southern China
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Dental remains of Plio–Pleistocene Cercopithecidae (Mammalia: Primates) from Romania
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Postcranial evidence does not support habitual bipedalism in Sahelanthropus tchadensis: A reply to Daver et al. (2022)
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Consumption of underground storage organs is associated with improved energetic status in a graminivorous primate
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An ape partial postcranial skeleton (KNM-NP 64631) from the Middle Miocene of Napudet, northern Kenya
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Hominin turnover at Laetoli is associated with vegetation change: Multiproxy evidence from the large herbivore community
Hominin turnover at Laetoli is associated with vegetation change: Multiproxy evidence from the large herbivore community
The emergence in eastern Africa of the Homo and Paranthropus lineages as well as the extinction of Australopithecus afaren...
Estimating ancestral ranges and biogeographical processes in early hominins
Estimating ancestral ranges and biogeographical processes in early hominins
Biogeographical analyses are critical to understanding hominin evolutionary history, and the importance of biogeographic p...
Enamel thickness in the deciduous postcanine dentition of fossil and extant Pongo
Enamel thickness in the deciduous postcanine dentition of fossil and extant Pongo
Among extant great apes, Pongo is the only genus represented by a substantial Pleistocene fossil record that is distribute...
Description and taxonomic assessment of fossil Cercopithecidae from the Pliocene Galili Formation (Ethiopia)
Description and taxonomic assessment of fossil Cercopithecidae from the Pliocene Galili Formation (Ethiopia)
Cercopithecids became diverse in the African Plio–Pleistocene (Jablonski, 2002; Jablonski and Frost, 2010). They also comp...
New Oldowan locality Sare-Abururu (ca. 1.7 Ma) provides evidence of diverse hominin behaviors on the Homa Peninsula, Kenya
New Oldowan locality Sare-Abururu (ca. 1.7 Ma) provides evidence of diverse hominin behaviors on the Homa Peninsula, Kenya
Volume 190, May 2024, 103498Author links open overlay panel, , , , , , , , , , , , , , , , , , , …AbstractThe Homa Peninsu...
Conserved patterns and locomotor-related evolutionary constraints in the hominoid vertebral column
Conserved patterns and locomotor-related evolutionary constraints in the hominoid vertebral column
Humans and other hominins are characterized by a shared reliance on upright, hind limb-dominated positional behaviors. Alt...
Trabecular bone volume fraction in Holocene and Late Pleistocene humans
Trabecular bone volume fraction in Holocene and Late Pleistocene humans
Extensive evidence exists from experimental and observational research showing that trabecular bone is labile and thus res...