New evidence for Late Pleistocene human exploitation of Jefferson's Ground Sloth (Megalonyx jeffersonii) from northern Ohio, USA

2012 ◽  
Vol 44 (1) ◽  
pp. 75-101 ◽  
Author(s):  
Brian G. Redmond ◽  
H Gregory McDonald ◽  
Haskel J. Greenfield ◽  
Matthew L. Burr
Author(s):  
Gaspar Morcote-Ríos ◽  
Francisco Javier Aceituno ◽  
José Iriarte ◽  
Mark Robinson ◽  
Jeison L. Chaparro-Cárdenas

Paleobiology ◽  
1984 ◽  
Vol 10 (3) ◽  
pp. 338-357 ◽  
Author(s):  
Daniel C. Fisher

Taphonomic analysis of several late Pleistocene mastodon (Mammut americanum) skeletons excavated in southern Michigan provides compelling evidence of mastodon butchery by Paleo-Indians. The occurrence of butchery and details of butchering technique are inferred primarily from patterns of bone modification. An important aspect of butchering practice was production and use of tools fashioned from bones of the animal being butchered. Evidence for butchery and bone tool use includes matching marks on the conarticular surfaces of disarticulated pairs of bones; cutmarks on bones; green bone fracturing; use wear, secondary flaking, and impact features on bone fragments; and burned bone. Interpretation of these features is facilitated by information on patterns of bone distribution and disarticulation preserved in a primary depositional context. Preliminary comparisons among nine sites indicate that putative butchering sites differ consistently and in a variety of ways from sites that appear to record no human involvement. Although based on a small sample of sites, the apparent frequency of butchered individuals relative to those that were not butchered is unexpectedly high. These findings provide new evidence of a well-developed “bone technology” employed by the late Pleistocene human inhabitants of eastern North America. In addition, these data offer circumstantial support for the hypothesis that human hunting was an important factor in the late Pleistocene extinction of mastodons.


Author(s):  
A.M. Klementiev ◽  
◽  
A.M. Khatsenovich ◽  
E.P. Rybin ◽  
D. Bazargur ◽  
...  

2009 ◽  
Vol 8 (6) ◽  
pp. 551-558 ◽  
Author(s):  
Juan Manuel López-García ◽  
Paloma Sevilla ◽  
Gloria Cuenca-Bescós

2012 ◽  
Vol 77 (3) ◽  
pp. 418-423 ◽  
Author(s):  
Tom D. Dillehay ◽  
Duccio Bonavia ◽  
Steve L. Goodbred ◽  
Mario Pino ◽  
Victor Vásquez ◽  
...  

Archaeological excavations in deep pre-mound levels at Huaca Prieta in northern Peru have yielded new evidence of late Pleistocene cultural deposits that shed insights into the early human occupation of the Pacific coast of South America. Radiocarbon dates place this occupation between ~ 14,200 and 13,300 cal yr BP. The cultural evidence shares certain basic technological and subsistence traits, including maritime resources and simple flake tools, with previously discovered late Pleistocene sites along the Pacific coast of Peru and Chile. The results help to expand our knowledge of early maritime societies and human adaption to changing coastal environments.


2018 ◽  
Vol 366 ◽  
pp. 47-66 ◽  
Author(s):  
Carlos Sancho ◽  
Concha Arenas ◽  
Gonzalo Pardo ◽  
José Luis Peña-Monné ◽  
Edward J. Rhodes ◽  
...  

2020 ◽  
Vol 76 (1) ◽  
pp. 1-16
Author(s):  
Luciano Varela ◽  
P. Sebastián Tambusso ◽  
Richard A. Fariña

The inhibitory cascade (IC) represents a developmental model that explains the evolution of molar relative sizes, originally described in rodents but later validated in several mammalian groups. The IC comprises signalling molecules produced by the first molar buds that inhibit the development of subsequent molars and molecules from surrounding tissues that have opposite effects. Sloths, as xenarthrans, present many peculiarities in their dentition, like tooth and enamel loss, homodonty, and changes in the typically mammalian dental formula. Here, we test the existence of an IC and explore the evolution of the lower dentition in sloths. We studied the variability of molariform proportions in 20 specimens of the Late Pleistocene ground sloth Lestodon armatus. We also analysed molariforms proportions in 53 sloth genera to explore evolutionary trends. Our results show that the lower dentition of most sloths complies with the IC model, despite the difficulties of assessing dental homologies with other mammals. Furthermore, we tested the existence of different patterns among families, obtaining support for models taking mylodontids and orophodontids separately from the rest of sloths. Also, members of Mylodontidae show a unique IC pattern, with a slope considerably higher than 2 and an mf1 ≤ mf2 << mf3 configuration. This pattern could be related to the morphological adaptations to grazing showed by mylodontids during most of their evolutionary history.


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