In this article, hypotheses about the origin, evolution and dispersal of Megantereon are reviewed using the fossil specimens included in previous comparative studies as well as the remains identified in the late Pliocene site of Fonelas (Spain) and the early Pleistocene localities of Lantian, Lingyi, Longdan, Renzidong (China), and Untermassfeld (Germany). The validity of the two species proposed by Martínez-Navarro and Palmqvist (1995), Megantereon cultridens and M. whitei, is evaluated using tooth measurements and multivariate statistical methods. The hypothesis of sexual dimorphism as an explanation for the morphological variability of Megantereon is tested with a large sample of sexed individuals of Panthera pardus and Panthera leo. Results obtained indicate similar or even smaller differences in tooth dimensions between M. cultridens and M. whitei than between sexes in both leopards and lions, except in the case of the lower fourth premolar. However, in spite of a substantial overlap between...
The relative importance of the two main cranial complexes, the neurocranium and the splanchnocranium, has been examined in the five species of extant hominoids and in a huge sample of extinct hominins using six standard craniometric variables that measure the length, width and height of each cranial module. Factor analysis and two-block partial least squares were used for establishing the major patterns of developmental and evolutionary integration between both cranial modules. The results obtained show that all extant hominoids (including the anatomically modern humans) share a conserved pattern of developmental integration, a result that agrees with previous studies. The pattern of evolutionary integration between both cranial modules in australopiths runs in parallel to developmental integration. In contrast, the pattern of evolutionary and developmental integration of the species of the genus Homo is the opposite, which is probably the consequence of distinctive selective regimes for both hominin groups.
The late Early Pleistocene archaeological site of Fuente Nueva 3 (Orce, Guadix-Baza Depression, SE Spain), dated to ~1.4 Ma, provides evidence on the subsistence strategies of the first hominin population that dispersed in Western Europe. The site preserves Oldowan tool assemblages associated with abundant remains of large mammals. A small proportion of these remains show cut marks and percussion marks resulting from defleshing and bone fracturing, and a small proportion of bones also show tooth marks. Previous taphonomic studies of FN3 suggested that the hominins had secondary access to the prey leftovers abandoned by sabretooth cats and other primary predators. However, a recent analysis by Yravedra et al. (2021) of the frequency of anthropogenic marks and tooth marks has concluded that the hominins had primary access to the carcasses of a wide variety of ungulate prey, even though the frequency of evisceration marks is strikingly low. In this rebuttal, we analyse the patterns of bone preservation in FN3, which show that the exploitation of bone marrow by the hominins after hammerstone breakage was a usual activity at the site. Our study also reviews the evidence available on the lesser abilities of sabretooth cats for carcass processing compared to pantherine felids. This reinforces the hypothesis that primary predators provided the hominins the opportunity to scavenge sizeable chunks of meat and bone marrow of their prey carcasses before the arrival of hyaenas. Finally, we also provide new inferences on resource availability and competition intensity among the members of the carnivore guild in FN3, which reinforce our interpretation that a secondary access by the Oldowan hominins to the prey leftovers of sabretooth cats was an optimal foraging strategy in the Guadix-Baza Depression.
We analyzed the lower and upper dentition of the family Hyaenidae along its evolutionary history from a multivariate point of view. A total of 13,103 individual measurements of the lengths and widths of canines and the main post-canine teeth (lower third and fourth premolar, lower first molar, and upper second, third, and fourth premolars) were collected for 39 extinct and extant species of this family. We analyzed these measurements using principal component analyses. The multivariate structure characterized the main groups of previously defined hyaenid ecomorphs. Strikingly, our analyses also detected differences between social hunting durophages (such asCrocuta crocuta) and solitary scavengers (such asHyaena hyaenaorParahyaena brunnea). Concerning the hyaenid bauplan, social hunters have large carnassials and smaller canines, whereas solitary scavengers show the exact opposite morphological adaptations. Additionally, scavengers exhibited upper canines larger than lower ones, whereas hunters have upper and lower canines of similar size. It is hypothesized that sociality has led to an increase in carnassial length for hunting durophages via scramble competition at feeding. Such competition also penalizes adults from bringing food to cubs, which are consequently breastfed. On the other hand, it is also hypothesized that natural selection has led to solitary scavengers having large canines to transport carcasses to cubs. Our results indicate that these functional aspects are also better reflected by lower teeth than the upper dentition, which leads to a mosaic evolution.