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Hadza Hunting, Butchering, and Bone Transport and Their Archaeological Implications
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inferred← citeshttps://doi.org/10.1006/jasc.2001.0768openalex-snapshot
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inferred← citeshttps://doi.org/10.1006/jasc.2001.0797openalex-snapshot
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inferred← citeshttps://doi.org/10.1006/jfca.2000.0960openalex-snapshot
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inferred← citeshttps://doi.org/10.1006/jhev.1996.0103openalex-snapshot
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Central-place foraging by humans: transport and processing
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inferred← citeshttps://doi.org/10.1007/s10437-018-9319-xopenalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s10745-020-00162-4openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s10745-021-00260-xopenalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s10745-024-00519-zopenalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s10814-006-9003-6openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s10814-007-9011-1openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s10814-025-09217-wopenalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s10816-026-09777-1openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s12110-013-9173-0openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/0033-5894(92)90085-wopenalex-snapshot
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inferred← citeshttps://doi.org/10.1016/0278-4165(91)90019-topenalex-snapshot
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inferred← citeshttps://doi.org/10.1016/0305-4403(89)90012-5openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/0305-4403(89)90014-9openalex-snapshot
Analysis of kangaroo body part transport among the alyawara of central Australia
inferred← citeshttps://doi.org/10.1016/0305-4403(89)90028-9openalex-snapshot
Bone transport, bone destruction, and reverse utility curves
inferred← citeshttps://doi.org/10.1016/0305-4403(90)90025-zopenalex-snapshot
Reanalysis of large mammal body part transport among the Hadza
inferred← citeshttps://doi.org/10.1016/0305-4403(91)90038-qopenalex-snapshot
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inferred← citeshttps://doi.org/10.1016/0305-4403(91)90044-popenalex-snapshot
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inferred← citeshttps://doi.org/10.1016/0305-4403(92)90003-lopenalex-snapshot
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inferred← citeshttps://doi.org/10.1016/0305-4403(92)90009-ropenalex-snapshot
Captive hyaena bone choice and destruction, the Schlepp effect and olduvai archaeofaunas
inferred← citeshttps://doi.org/10.1016/0305-4403(92)90020-4openalex-snapshot
Patterns in the distribution, site structure and assemblage composition of Hadza kill-butchering sites
inferred← citeshttps://doi.org/10.1016/0305-4403(92)90027-zopenalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-0-443-27380-3.00027-0openalex-snapshot
Life history evolution explains so many features of humanity
inferred← citeshttps://doi.org/10.1016/j.anthro.2021.102976openalex-snapshot
New Oldowan localities at high level within Kilombe Caldera, Kenya
inferred← citeshttps://doi.org/10.1016/j.crpv.2009.06.003openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.crpv.2010.05.004openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.crpv.2015.09.012openalex-snapshot
Neanderthal mobility and technological change in the northeastern of the Iberian Peninsula: The patterns of chert exploitation at the Abric Romaní rock-shelter
inferred← citeshttps://doi.org/10.1016/j.crpv.2015.11.006openalex-snapshot
Ungulate carcass transport strategies at the Middle Palaeolithic site of Abric Romaní (Capellades, Spain)
inferred← citeshttps://doi.org/10.1016/j.jaa.2004.09.001openalex-snapshot
Upper Paleolithic raw material economies at Üçağızlı cave, Turkey
inferred← citeshttps://doi.org/10.1016/j.jaa.2006.03.009openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.jaa.2008.11.001openalex-snapshot
The use of optimal foraging theory to estimate Late Glacial site catchment areas from a central place: The case of eastern Cantabria, Spain
inferred← citeshttps://doi.org/10.1016/j.jaa.2009.10.002openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.jaa.2011.04.002openalex-snapshot
The evolution of human culture during the later Pleistocene: Using fauna to test models on the emergence and nature of “modern” human behavior
inferred← citeshttps://doi.org/10.1016/j.jaa.2012.03.003openalex-snapshot
The Broad Spectrum Revolution at 40: Resource diversity, intensification, and an alternative to optimal foraging explanations
inferred← citeshttps://doi.org/10.1016/j.jaa.2014.06.005openalex-snapshot
Subsistence economy and social life: A zooarchaeological view from the 300 kya central hearth at Qesem Cave, Israel
inferred← citeshttps://doi.org/10.1016/j.jaa.2016.05.005openalex-snapshot
Holocene cold storage practices on the eastern Snake River Plain: A risk-mitigation strategy for lean times
inferred← citeshttps://doi.org/10.1016/j.jaa.2016.07.005openalex-snapshot
Ethnoarchaeology and Plio-Pleistocene sites: Some lessons from the Hadza
inferred← citeshttps://doi.org/10.1016/j.jaa.2016.07.006openalex-snapshot
Are we missing the “sweet spot” between optimality theory and niche construction theory in archaeology?
inferred← citeshttps://doi.org/10.1016/j.jaa.2016.07.012openalex-snapshot
When bigger is not better: The economics of hunting megafauna and its implications for Plio-Pleistocene hunter-gatherers
inferred← citeshttps://doi.org/10.1016/j.jaa.2016.07.013openalex-snapshot
The roots of the question: Surprise Valley, Alyawarra, and the early development of James F. O’Connell’s ethnoarchaeology
inferred← citeshttps://doi.org/10.1016/j.jaa.2016.12.002openalex-snapshot
Efficiency of gathering and its archaeological implications for an European Early Palaeolithic population
inferred← citeshttps://doi.org/10.1016/j.jaa.2023.101565openalex-snapshot
Actualistic butchery studies in zooarchaeology: Where we’ve been, where we are now, and where we want to go
inferred← citeshttps://doi.org/10.1016/j.jaa.2025.101656openalex-snapshot
Short-distance hunting strategies of Late Quaternary foragers in the miombo woodlands of Malawi
inferred← citeshttps://doi.org/10.1016/j.jaa.2025.101742openalex-snapshot
Diversified human dietary strategies and settlement patterns in the core of the Atacama Desert during the late Pleistocene-Holocene transition (∼12.8 – 11.2 ka)
inferred← citeshttps://doi.org/10.1016/j.jas.2004.08.007openalex-snapshot
Gazelle bone fat processing in the Levantine Epipalaeolithic
inferred← citeshttps://doi.org/10.1016/j.jas.2005.04.004openalex-snapshot
Declining foraging efficiency and moa carcass exploitation in southern New Zealand
inferred← citeshttps://doi.org/10.1016/j.jas.2005.05.003openalex-snapshot
Should we expect large game specialization in the late Pleistocene? An optimal foraging perspective on early Paleoindian prey choice
inferred← citeshttps://doi.org/10.1016/j.jas.2006.08.007openalex-snapshot
Skeletal element abundances in archaeofaunal assemblages: economic utility, sample size, and assessment of carcass transport strategies
inferred← citeshttps://doi.org/10.1016/j.jas.2007.01.014openalex-snapshot
Changes in reindeer body part representation at Grotte XVI, Dordogne, France
inferred← citeshttps://doi.org/10.1016/j.jas.2010.05.009openalex-snapshot
Overdone overkill – the archaeological perspective on Tasmanian megafaunal extinctions
inferred← citeshttps://doi.org/10.1016/j.jas.2010.07.020openalex-snapshot
Interpreting abundance indices: some zooarchaeological implications of Martu foraging
inferred← citeshttps://doi.org/10.1016/j.jas.2011.03.013openalex-snapshot
Split phalanges from archaeological sites: evidence of nutritional stress?
inferred← citeshttps://doi.org/10.1016/j.jas.2013.12.003openalex-snapshot
Early Upper Paleolithic bone processing and insights into small-scale storage of fats at Vale Boi, southern Iberia
inferred← citeshttps://doi.org/10.1016/j.jas.2014.03.024openalex-snapshot
Quantifying the energetic returns for pronghorn: a food utility index of meat and marrow
inferred← citeshttps://doi.org/10.1016/j.jas.2014.08.026openalex-snapshot
Optimal foraging, dietary change, and site use during the Paleolithic at Klissoura Cave 1 (southern Greece)
inferred← citeshttps://doi.org/10.1016/j.jas.2014.09.002openalex-snapshot
Development of a metric technique for identification of rib number (position) in white-tailed deer (Odocoileus virginianus): an initial attempt
inferred← citeshttps://doi.org/10.1016/j.jas.2015.02.009openalex-snapshot
Revisiting Paleoindian exploitation of extinct North American mammals
inferred← citeshttps://doi.org/10.1016/j.jas.2015.02.027openalex-snapshot
Behavioral ecology and the future of archaeological science
inferred← citeshttps://doi.org/10.1016/j.jas.2015.12.004openalex-snapshot
An experimental lion-to-hammerstone model and its relevance to understand hominin-carnivore interactions in the archeological record
inferred← citeshttps://doi.org/10.1016/j.jas.2017.06.009openalex-snapshot
Diagnostic properties of hammerstone-broken long bone fragments, specimen identifiability, and Early Stone Age butchered assemblage interpretation
inferred← citeshttps://doi.org/10.1016/j.jas.2021.105518openalex-snapshot
A stone in the hand is worth how many in the bush? Applying the marginal value theorem to understand optimal toolstone transportation, processing, and discard decisions
inferred← citeshttps://doi.org/10.1016/j.jas.2023.105725openalex-snapshot
Can transport costs explain the near absence of marmot bones at shoreline archaeological sites on Vancouver Island? Finding input values for central place modelling with biological scaling
inferred← citeshttps://doi.org/10.1016/j.jas.2024.106024openalex-snapshot
Experimental assessment of the impact of food processing on δ15N values in dietary meat – Implications for paleodietary reconstruction
inferred← citeshttps://doi.org/10.1016/j.jasrep.2015.09.025openalex-snapshot
Tropical forager gastrophagy and its implications for extinct hominin diets
inferred← citeshttps://doi.org/10.1016/j.jasrep.2015.10.035openalex-snapshot
Foraging strategies during the final Middle Stone Age occupation at Sibudu Cave, South Africa
inferred← citeshttps://doi.org/10.1016/j.jasrep.2021.102863openalex-snapshot
Coast-proximal inland archaeology and the Vancouver Island marmot (Marmota vancouverensis)
inferred← citeshttps://doi.org/10.1016/j.jasrep.2022.103601openalex-snapshot
Not just for proboscidean hunting: On the efficacy and functions of Clovis fluted points
inferred← citeshttps://doi.org/10.1016/j.jasrep.2025.105222openalex-snapshot
Strontium (87Sr/86Sr) evidence for the geography of Indigenous deer hunting in the North Carolina Piedmont
inferred← citeshttps://doi.org/10.1016/j.jasrep.2026.105896openalex-snapshot
Did Clovis foragers hunt megafauna, scavenge their carrion, or both – And can we tell the difference?
inferred← citeshttps://doi.org/10.1016/j.jhevol.2006.01.004openalex-snapshot
Faunal remains from Porc-Epic: Paleoecological and zooarchaeological investigations from a Middle Stone Age site in southeastern Ethiopia
inferred← citeshttps://doi.org/10.1016/j.jhevol.2007.01.012openalex-snapshot
The endurance running hypothesis and hunting and scavenging in savanna-woodlands
inferred← citeshttps://doi.org/10.1016/j.jhevol.2007.05.006openalex-snapshot
From carcass to cave: Large mammal exploitation during the Aurignacian at Vogelherd, Germany
inferred← citeshttps://doi.org/10.1016/j.jhevol.2007.05.008openalex-snapshot
Modern hunting behavior in the early Middle Paleolithic: Faunal remains from Misliya Cave, Mount Carmel, Israel
inferred← citeshttps://doi.org/10.1016/j.jhevol.2007.07.008openalex-snapshot
Scavenging by chimpanzees at Ngogo and the relevance of chimpanzee scavenging to early hominin behavioral ecology
inferred← citeshttps://doi.org/10.1016/j.jhevol.2008.02.001openalex-snapshot
New evidence for hominin carcass processing strategies at 1.5Ma, Koobi Fora, Kenya
inferred← citeshttps://doi.org/10.1016/j.jhevol.2008.12.008openalex-snapshot
Long-distance carcass transport at Olduvai Gorge? A quantitative examination of Bed I skeletal element abundances
inferred← citeshttps://doi.org/10.1016/j.jhevol.2011.05.012openalex-snapshot
Carcass transport decisions in Homo antecessor subsistence strategies
inferred← citeshttps://doi.org/10.1016/j.jhevol.2014.06.004openalex-snapshot
A model of hunter-gatherer skeletal element transport: The effect of prey body size, carriers, and distance
inferred← citeshttps://doi.org/10.1016/j.jhevol.2015.03.013openalex-snapshot
The significance of cooking for early hominin scavenging
inferred← citeshttps://doi.org/10.1016/j.jhevol.2015.05.011openalex-snapshot
Humeral torsion does not dictate shoulder position, but does influence throwing speed
inferred← citeshttps://doi.org/10.1016/j.jhevol.2016.03.009openalex-snapshot
Climate-mediated shifts in Neandertal subsistence behaviors at Pech de l'Azé IV and Roc de Marsal (Dordogne Valley, France)
inferred← citeshttps://doi.org/10.1016/j.jhevol.2016.09.010openalex-snapshot
Small mammal utilization by Middle Stone Age humans at Die Kelders Cave 1 and Pinnacle Point Site 5-6, Western Cape Province, South Africa
inferred← citeshttps://doi.org/10.1016/j.jhevol.2017.01.007openalex-snapshot
Human predatory behavior and the social implications of communal hunting based on evidence from the TD10.2 bison bone bed at Gran Dolina (Atapuerca, Spain)
inferred← citeshttps://doi.org/10.1016/j.jhevol.2017.04.003openalex-snapshot
Subsistence strategies during the Late Pleistocene in the southern Cape of South Africa: Comparing the Still Bay of Blombos Cave with the Howiesons Poort of Klipdrift Shelter
inferred← citeshttps://doi.org/10.1016/j.jhevol.2017.04.005openalex-snapshot
Paleolithic subsistence strategies and changes in site use at Klissoura Cave 1 (Peloponnese, Greece)
inferred← citeshttps://doi.org/10.1016/j.jhevol.2018.11.001openalex-snapshot
The meta-group social network of early humans: A temporal–spatial assessment of group size at FLK Zinj (Olduvai Gorge, Tanzania)
inferred← citeshttps://doi.org/10.1016/j.jhevol.2019.01.005openalex-snapshot
The hunters or the hunters: Human and hyena prey choice divergence in the Late Pleistocene Levant
inferred← citeshttps://doi.org/10.1016/j.jhevol.2019.02.005openalex-snapshot
Relative fibular strength and locomotor behavior in KNM-WT 15000 and OH 35
inferred← citeshttps://doi.org/10.1016/j.jhevol.2019.05.007openalex-snapshot
Early Upper Paleolithic subsistence in the Levant: Zooarchaeology of the Ahmarian–Aurignacian sequence at Manot Cave, Israel
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