Department Biology, University of Antwerp, Antwerpen, Belgium.
Department of Movement and Sports Sciences, University of Ghent, Ghent, Belgium.
Proc Biol Sci. 2018 Jun 13;285(1880). doi: 10.1098/rspb.2018.0859.
The well-developed Achilles tendon in humans is generally interpreted as an adaptation for mechanical energy storage and reuse during cyclic locomotion. All other extant great apes have a short tendon and long-fibred triceps surae, which is thought to be beneficial for locomotion in a complex arboreal habitat as this morphology enables a large range of motion. Surprisingly, highly arboreal gibbons show a more human-like triceps surae with a long Achilles tendon. Evidence for a spring-like function similar to humans is not conclusive. We revisit and integrate our anatomical and biomechanical data to calculate the energy that can be recovered from the recoiling Achilles tendon during ankle plantar flexion in bipedal gibbons. Only 7.5% of the required external positive work in a stride can come from tendon recoil, yet it is delivered at an instant when the whole-body energy level drops. Consequently, an additional similar amount of mechanical energy must simultaneously dissipate elsewhere in the system. Altogether, this challenges the concept of an energy-saving function in the gibbon's Achilles tendon. Cercopithecids, sister group of the apes, also have a human-like triceps surae. Therefore, a well-developed Achilles tendon, present in the last common 'Cercopithecoidea-Hominoidea' ancestor, seems plausible. If so, the gibbon's anatomy represents an evolutionary relict (no harm-no benefit), and the large Achilles tendon is not the premised key adaptation in humans (although the spring-like function may have further improved during evolution). Moreover, the triceps surae anatomy of extant non-human great apes must be a convergence, related to muscle control and range of motion. This perspective accords with the suggestions put forward in the literature that the last common hominoid ancestor was not necessarily great ape-like, but might have been more similar to the small-bodied catarrhines.
人类高度发达的跟腱通常被解释为在循环运动中储存和再利用机械能的适应。所有其他现存的大型猿类都有短的跟腱和长纤维的三頭肌后群,这被认为有利于在复杂的树栖栖息地中运动,因为这种形态使运动范围更大。令人惊讶的是,高度树栖的长臂猿表现出更类似于人类的三頭肌后群,跟腱较长。类似于人类的弹簧样功能的证据并不确凿。我们重新审视和整合我们的解剖学和生物力学数据,以计算在双足长臂猿的踝关节跖屈过程中,回弹的跟腱可以从反冲中恢复多少能量。在一个步幅中,只有 7.5%的外部正功可以来自跟腱的回弹,但它是在整个身体能量水平下降的瞬间产生的。因此,必须在系统的其他地方同时消耗类似数量的机械能。总的来说,这挑战了在长臂猿跟腱中具有节能功能的概念。与猿类是姐妹群的猴科动物也有类似人类的三頭肌后群。因此,一个高度发达的跟腱,存在于最后共同的“猴科动物-人科动物”祖先中,似乎是合理的。如果是这样,那么长臂猿的解剖结构代表了一种进化遗迹(没有伤害-没有好处),而发达的跟腱不是人类的前提关键适应(尽管弹簧样功能可能在进化过程中进一步改善)。此外,现存非人类大型猿类的三頭肌后群解剖结构必须是一种趋同现象,与肌肉控制和运动范围有关。这种观点与文献中提出的建议一致,即最后的共同原始人祖先不一定像大型猿类,而可能更类似于小型的贫齿类。