Hylander W L
J Morphol. 1979 May;160(2):223-40. doi: 10.1002/jmor.1051600208.
A stress analysis of the primate mandible suggests that vertically deep jaws in the molar region are usually an adaptation to counter increased sagittal bending stress about the balancing-side mandibular corpus during unilateral mastication. This increased bending stress about the balancing side is caused by an increase in the amount of balancing-side muscle force. Furthermore, this increased muscle force will also cause an increase in dorso-ventral shear stress along the mandibular symphysis. Since increased symphyseal stress can be countered by symphyseal fusion and as increased bending stress can be countered by a deeper jaw, deep jaws and symphyseal fusion are often part of the same functional pattern. In some primates (e.g., Cercocebus albigena), deep jaws are an adaptation to counter bending in the sagittal plane during powerful incisor biting, rather than during unilateral mastication. The stress analysis of the primate mandible also suggests that jaws which are transversely thick in the molar region are an adaptation to counter increased torsion about the long axis of the working-side mandibular corpus during unilateral mastication. Increased torsion of the mandibular corpus can be caused by an increase in masticatory muscle force, an increase in the transverse component of the postcanine bite force and/or an increase in premolar use during mastication. Patterns of masticatory muscle force were estimated for galagos and macaques, demonstrating that the ratio of working-side muscle force to balancing-side muscle force is approximately 1.5:1 in macaques and 3.5:1 in galagos during unilateral isometric molar biting. These data support the hypothesis that mandibular symphyseal fusion is an adaptative response to maximize unilateral molar bite force by utilizing a greater percentage of balancing-side muscle force.
对灵长类动物下颌骨的应力分析表明,磨牙区域垂直深度较大的颌骨通常是一种适应性特征,用于应对单侧咀嚼时平衡侧下颌体矢状面弯曲应力的增加。平衡侧弯曲应力的增加是由平衡侧肌肉力量的增加引起的。此外,这种增加的肌肉力量还会导致下颌联合处背腹剪切应力的增加。由于联合处应力的增加可以通过联合融合来抵消,而弯曲应力的增加可以通过更深的颌骨来抵消,因此深颌骨和联合融合往往是同一功能模式的一部分。在一些灵长类动物(如白颈白眉猴)中,深颌骨是一种适应性特征,用于在强力切牙咬合时,而不是在单侧咀嚼时,应对矢状面的弯曲。对灵长类动物下颌骨的应力分析还表明,磨牙区域横向较厚的颌骨是一种适应性特征,用于应对单侧咀嚼时工作侧下颌体围绕长轴的扭转增加。下颌体扭转的增加可能是由咀嚼肌力量的增加、犬齿后咬合力横向分量的增加和/或咀嚼时前磨牙使用的增加引起的。对婴猴和猕猴的咀嚼肌力量模式进行了估计,结果表明,在单侧等长磨牙咬合时,猕猴工作侧肌肉力量与平衡侧肌肉力量的比例约为1.5:1,婴猴为3.5:1。这些数据支持了以下假设:下颌联合融合是一种适应性反应,通过利用更大比例的平衡侧肌肉力量来最大化单侧磨牙咬合力。