Journal
ZOOLOGICAL JOURNAL OF THE LINNEAN SOCIETY
Volume 140, Issue 2, Pages 207-221Publisher
WILEY-BLACKWELL
DOI: 10.1111/j.1096-3642.2003.00093.x
Keywords
basicranial morphology; Felinae; hunting behaviour; Machairodontinae; neck muscles; skull
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Muscle attachments in the mastoid region of the skull of extant felids are studied through dissection of two adult tigers Panthera tigris (Linnaeus, 1758) Pocock, 1930, a lion Panthera leo (Linnaeus, 1758) Pocock, 1930 and a puma Puma concolor (Linnaeus, 1771) Jardine, 1834, providing for the first time an adequate reference for the study of the evolution of that region in sabretoothed felids. Our study supports the inference by W Akersten that the main muscles inserting in the mastoid process in sabretooths were those originating in the atlas, rather than those from the posterior neck, sternum and forelimb. Those inferences were based on the anatomy of the giant panda, Ailuropoda melanoleuca (David, 1869) Milne-Edwards, 1870, raising uncertainties about homology, which were founded, as revealed by our results. The mastoid muscle insertions in extant felids differ in important details from those described for Ailuropoda, but agree with those described for domestic cats, hyenas and dogs. The large, anteroventrally projected mastoid process of pantherines allows a moderate implication of the in. obliquus capitis anterior in head-flexion. This contradicts the widespread notion that the function of this muscle in carnivores is to extend the atlanto-cranial joint and to flex it laterally, but supports previous inferences about the head-flexing function of atlanto-mastoid muscles in machairodontines. Sabretooth mastoid morphology implies larger and longer-fibred atlanto-mastoid muscles than in pantherines, and that most of their fibres ran inferior to the axis of rotation of the atlanto-occipital joint, emphasizing head-flexing action. (C) 2004 The Linnean Society of London.
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