All Stories

  1. The use of canid tooth marks on bone for the identification of livestock predation
  2. Level U3.1, a new archaeological level discovered at BK (upper bed II, Olduvai Gorge) with evidence of megafaunal exploitation
  3. Assessing functionality during the early Acheulean in level TKSF at Thiongo Korongo site (Olduvai Gorge, Tanzania)
  4. Cut marks and raw material exploitation in the lower pleistocene site of Bell's Korongo (BK, Olduvai Gorge, Tanzania): A geometric morphometric analysis
  5. Middle Pleistocene human occupation in the interior of the Iberian Peninsula during cold climate conditions: Zooarchaeology and taphonomy of ETB-H02 site in the Manzanares valley (Madrid, Spain)
  6. Neanderthal diet in fluvial environments at the end of the Middle Pleistocene/early Late Pleistocene of PRERESA site in the Manzanares Valley (Madrid, Spain)
  7. The Middle to Late Pleistocene herpetofaunal assemblages from the Jarama and Manzanares valleys (Madrid, central Spain): An ecological synthesis
  8. Hominins and Proboscideans in the Lower and Middle Palaeolithic in the Central Iberian Peninsula
  9. A geometric-morphometric assessment of three-dimensional models of experimental cut-marks using flint and quartzite flakes and handaxes
  10. Application of geometric morphometrics to the analysis of cut mark morphology on different bones of differently sized animals. Does size really matter?
  11. Applying new technologies to the taphonomic study of La Lluera (Asturias, Spain). Geometric morphometrics and the study of bone surface modifications (BSM)
  12. Approaching raw material functionality in the Upper Magdalenian of Coímbre cave (Asturias, Spain) through geometric morphometrics
  13. Combining machine learning algorithms and geometric morphometrics: A study of carnivore tooth marks
  14. First assessments of the taphonomic behaviour of jaguar (Panthera onca)
  15. Geometric-morphometric analysis of tooth pits and the identification of felid and hyenid agency in bone modification
  16. New taphonomic advances in 3D digital microscopy: A morphological characterisation of trampling marks
  17. New technologies applied to modelling taphonomic alterations
  18. Who ate OH80 (Olduvai Gorge, Tanzania)? A geometric-morphometric analysis of surface bone modifications of a Paranthropus boisei skeleton
  19. Characterising leopard as taphonomic agent through the use of micro-photogrammetric reconstruction of tooth marks and pit to score ratio
  20. Classifying agency in bone breakage: an experimental analysis of fracture planes to differentiate between hominin and carnivore dynamic and static loading using machine learning (ML) algorithms
  21. Automated identification and deep classification of cut marks on bones and its paleoanthropological implications
  22. Lagomorph exploitation during the Upper Palaeolithic in the Northern Iberian Peninsula. New evidence from Coímbre Cave (Asturias, Spain)
  23. Spilled ink blots the mind: A reply to Merrit et al. (2018) on subjectivity and bone surface modifications
  24. The exploitation of hunted resources during the Magdalenian in the Cantabrian region. Systematization of butchery processes at Coímbre cave (Asturias, Spain)
  25. Striped hyenas as bone modifiers in dual human-to-carnivore experimental models
  26. Testing accuracy in 2D and 3D geometric morphometric methods for cut mark identification and classification
  27. Differentiating percussion pits and carnivore tooth pits using 3D reconstructions and geometric morphometrics
  28. Recurrent Magdalenian occupation in the interior of the Iberian Peninsula: new insights from the archaeological site of La Peña de Estebanvela (Segovia, Spain)
  29. Economic implications of livestock management strategies in the center of the Iberian Peninsula, Tagus Basin, and Mancha Alta region between the VIII and XI centuries AD
  30. Biotic and abiotic processes affecting the formation of BK Level 4c (Bed II, Olduvai Gorge) and their bearing on hominin behavior at the site
  31. Discerning carnivore agency through the three-dimensional study of tooth pits: Revisiting crocodile feeding behaviour at FLK- Zinj and FLK NN3 (Olduvai Gorge, Tanzania)
  32. On applications of micro-photogrammetry and geometric morphometrics to studies of tooth mark morphology: The modern Olduvai Carnivore Site (Tanzania)
  33. The paleoecology and taphonomy of AMK (Bed I, Olduvai Gorge) and its contributions to the understanding of the “Zinj” paleolandscape
  34. 3D analysis of cut marks using a new geometric morphometric methodological approach
  35. Hominin and carnivore interactions during the Early Pleistocene in Western Europe
  36. New evidences of exploitation of faunal remains in the Upper Palaeolithic in N Spain
  37. Use and abuse of cut mark analyses: The Rorschach effect
  38. Site function and lithic technology in the Acheulean technocomplex: a case study from Thiongo Korongo (TK), Bed II, Olduvai Gorge, Tanzania
  39. Flint and Quartzite: Distinguishing Raw Material Through Bone Cut Marks
  40. Statistical Comparison between Low-Cost Methods for 3D Characterization of Cut-Marks on Bones
  41. The use of Micro-Photogrammetry and Geometric Morphometrics for identifying carnivore agency in bone assemblages
  42. Subsistencia, movilidad y adaptación al medio de los cazadores-recolectores gravetienses en el sector occidental de la región cantábrica: la cueva de Coímbre (Asturias)
  43. A context for the last Neandertals of interior Iberia: Los Casares cave revisited
  44. Pandora : A new morphometric and statistical software for analysing and distinguishing cut marks on bones
  45. Assessment of statistical agreement of three techniques for the study of cut marks: 3D digital microscope, laser scanning confocal microscopy and micro-photogrammetry
  46. Fluvial spatial taphonomy: a new method for the study of post-depositional processes
  47. Spatial simulation and modelling of the early Pleistocene site of DS (Bed I, Olduvai Gorge, Tanzania): a powerful tool for predicting potential archaeological information from unexcavated areas
  48. SHK Extension: a new archaeological window in the SHK fluvial landscape of Middle Bed II (Olduvai Gorge, Tanzania)
  49. FLK West (Lower Bed II, Olduvai Gorge, Tanzania): a new early Acheulean site with evidence for human exploitation of fauna
  50. A new approach to raw material use in the exploitation of animal carcasses at BK (Upper Bed II, Olduvai Gorge, Tanzania): a micro-photogrammetric and geometric morphometric analysis of fossil cut marks
  51. Micro-photogrammetric and morphometric differentiation of cut marks on bones using metal knives, quartzite, and flint flakes
  52. The larger mammal palimpsest from TK (Thiongo Korongo), Bed II, Olduvai Gorge, Tanzania
  53. On the use of space at La Peña de Estebanvela (Ayllón, Segovia, Spain): An approach to economic and social behaviour in the Upper Magdalenian
  54. Hominin-Carnivore Adaptive Strategies in Western Europe During the Early Pleistocene
  55. Lions as Bone Accumulators? Paleontological and Ecological Implications of a Modern Bone Assemblage from Olduvai Gorge
  56. Not so deserted…paleoecology and human subsistence in Central Iberia (Guadalajara, Spain) around the Last Glacial Maximum
  57. The Magdalenian sequence at Coímbre cave (Asturias, Northern Iberian Peninsula): Adaptive strategies of hunter–gatherer groups in montane environments
  58. New evidence of use of bones as fuel
  59. An experimental lion-to-hammerstone model and its relevance to understand hominin-carnivore interactions in the archeological record
  60. The Origin of The Acheulean: The 1.7 Million-Year-Old Site of FLK West, Olduvai Gorge (Tanzania)
  61. Vegetation, climate and human settlement interactions at the late Mesolithic site of Cueva Blanca (Hellín, Albacete, SE Spain)
  62. Micro-photogrammetric characterization of cut marks on bones
  63. Another window to the subsistence of Middle Pleistocene hominins in Europe: A taphonomic study of Cuesta de la Bajada (Teruel, Spain)
  64. A new methodological approach to the taphonomic study of paleontological and archaeological faunal assemblages: a preliminary case study from Olduvai Gorge (Tanzania)
  65. Campaniforme no funerario en la provincia de Toledo: el yacimiento de Las Vegas. De nuevo el Valle de Huecas
  66. Neanderthal and Homo sapiens subsistence strategies in the Cantabrian region of northern Spain
  67. Biocronología de la Terraza Compleja de Butarque del río Manzanares en el Estanque de Tormentas al sur de Madrid (España)
  68. Neanderthal exploitation of ibex and chamois in southwestern Europe
  69. The Middle Paleolithic site of Cuesta de la Bajada (Teruel, Spain): a perspective on the Acheulean and Middle Paleolithic technocomplexes in Europe
  70. Taphonomic implications for the Late Mousterian of South-West Europe at Esquilleu Cave (Spain)
  71. Manzanares Valley (Madrid, Spain): A good country for Proboscideans and Neanderthals
  72. Neanderthal and Mammuthus interactions at EDAR Culebro 1 (Madrid, Spain)
  73. A critical re-evaluation of bone surface modification models for inferring fossil hominin and carnivore interactions through a multivariate approach: Application to the FLK Zinj archaeofaunal assemblage (Olduvai Gorge, Tanzania)
  74. On meat eating and human evolution: A taphonomic analysis of BK4b (Upper Bed II, Olduvai Gorge, Tanzania), and its bearing on hominin megafaunal consumption
  75. Study of the SHK Main Site faunal assemblage, Olduvai Gorge, Tanzania: Implications for Bed II taphonomy, paleoecology, and hominin utilization of megafauna
  76. Autochthonous anisotropy of archaeological materials by the action of water: experimental and archaeological reassessment of the orientation patterns at the Olduvai sites
  77. Zooarqueología de los macrovertebrados del yacimiento fenicio del Teatro Cómico (Cádiz)
  78. First Partial Skeleton of a 1.34-Million-Year-Old Paranthropus boisei from Bed II, Olduvai Gorge, Tanzania
  79. A taphonomic study of the African wild dog (Lycaon pictus)
  80. Los orígenes del Solutrense y la ocupación pleniglaciar del interior de la Península Ibérica: implicaciones del nivel 3 de Peña Capón (valle del Sorbe, Guadalajara)
  81. The deliberate use of bones for fuel or for systematic disposal of organic waste
  82. A cautionary note on the use of captive carnivores to model wild predator behavior: a comparison of bone modification patterns on long bones by captive and wild lions
  83. Taphonomy of ungulate ribs and the consumption of meat and bone by 1.2-million-year-old hominins at Olduvai Gorge, Tanzania
  84. New Contributions on Subsistence Practices during the Middle-Upper Paleolithic in Northern Spain
  85. Earliest Porotic Hyperostosis on a 1.5-Million-Year-Old Hominin, Olduvai Gorge, Tanzania
  86. Human landscapes of the Late Glacial Period in the interior of the Iberian Peninsula: La Peña de Estebanvela (Segovia, Spain)
  87. Autochthony and orientation patterns in Olduvai Bed I: a re-examination of the status of post-depositional biasing of archaeological assemblages from FLK North (FLKN)
  88. A study of dimensional differences of tooth marks (pits and scores) on bones modified by small and large carnivores
  89. Elephants and subsistence. Evidence of the human exploitation of extremely large mammal bones from the Middle Palaeolithic site of PRERESA (Madrid, Spain)
  90. Human behaviour and adaptations to MIS 3 palaeoecological trends in northern Spain
  91. Disentangling hominin and carnivore activities near a spring at FLK North (Olduvai Gorge, Tanzania)
  92. New excavations at the FLK Zinjanthropus site and its surrounding landscape and their behavioral implications
  93. Was FLK North levels 1–2 a classic “living floor” of Oldowan hominins or a taphonomically complex palimpsest dominated by large carnivore feeding behavior?
  94. Cut marks on the Middle Pleistocene elephant carcass of Áridos 2 (Madrid, Spain)
  95. Unraveling hominin behavior at another anthropogenic site from Olduvai Gorge (Tanzania): new archaeological and taphonomic research at BK, Upper Bed II
  96. Why are cut mark frequencies in archaeofaunal assemblages so variable? A multivariate analysis
  97. The shaft-based methodological approach to the quantification of long limb bones and its relevance to understanding hominid subsistence in the Pleistocene: application to four Palaeolithic sites
  98. Determination of the fracture processes of fresh bone: an analytical system of the angles of fracture planes as an indicator of biotic agents