Cat-like carnivorans are a textbook example of convergent evolution, with distinct morphological differences between taxa with short or elongated upper canines, the latter often being interpreted as an adaptation to bite at large angles and subdue large prey. This interpretation of the sabre-tooth condition is reinforced by a reduced taxonomic sampling in some studies, often focusing on highly derived taxa or using simplified morphological models. Moreover, most biomechanical analyses focus on biting scenarios at small gapes, ideal for modern carnivora but ill-suited to test for subduction of large prey by sabre-toothed taxa. In this contribution, we present the largest three-dimensional collection-based muscle-induced biting simulations on cat-like carnivorans by running a total of 1074 analyses on 17 different taxa at three different biting angles (30°, 60° and 90°) including both morphologies. While our results show a clear adaptation of extreme sabre-toothed taxa to bite at larger angles in terms of stress distribution, other performance variables display surprising similarities between all forms at the different angles tested, highlighting a continuous rather than bipolar spectrum of hunting methods in cat-like carnivorans and demonstrating a wide functional disparity and nuances of the sabre-tooth condition that cannot simply be characterized by specialized feeding biomechanics.

How sabertoothed felids have evolved their iconic morphology remains unclear because of the patchy fossil record of early machairodontines. Batallones localities in the Madrid region (Spain) have the potential to clarify this as two sites have yielded hundreds of fossils of the early machairodontines Promegantereon ogygia and Machairodus aphanistus. Previous analyses suggested that these two sites are not contemporaneous and a morphological drift between cavities was described for these two species; characterizing intraspecific variability is thus important to better understand the evolution of machairodontines. To tackle this issue, we modelled 62 felid mandibles in 3D using a laser scanner. We applied 3D geometric morphometrics (3D GM) and linear morphometrics on these models to test for differences in populations and to better characterize the morphology of early machairodontines. Both linear measurements and 3D data reveal an absence of morphological changes in mandible shape between the two sites. Batallones machairodontines are closer to felines than to other, more derived machairodontines in mandibular morphology, suggesting the existence of rapid shift in the mandibular shape between primitive and derived members of the clade. Our analysis did not reveal any allometric relationship between the overall shape of the mandible when studied with 3D GM and body size. Finally, we reveal a previously overlooked diversity in felid mandibular condyles, with machairodontines having much larger and medially inclined condyles.

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