The Architecture of Leg Muscles

Each of the four muscles shown in Figure 36.1 (a to d) consists of muscle fascicles (bundles of muscle fibers) connected at either end to tendons, but they show striking differences of architecture. Most authors would describe (a) and (c) as pen- nate, but (b) and (d) as parallel-fibered. It often seems convenient to use these adjectives, but the distinction that they make is not a sharp one: it is easy to imagine a continuous series of intermediates between (a) and (b) or between (c) and (d). It is sometimes suggested that the diagnostic feature of a pennate muscle is that its fascicles attach obliquely to the tendons. However, the cross- sectional areas of the tendons are always much less than the total of the cross-sectional areas of the muscle fascicles, so geometry requires that the attachment be oblique even in muscles such as (b) and (d) that would generally be described as parallel-fibered. Muscle (e) has fascicles that attach at one end directly to a bone rather than to a tendon.

[1]  Charles Lewis Camp,et al.  Phylogeny and functions of the digital ligaments of the horse , 1942 .

[2]  G. E. Goslow,et al.  The cat step cycle: Hind limb joint angles and muscle lengths during unrestrained locomotion , 1973, Journal of morphology.

[3]  C. R. Taylor,et al.  Running in cheetahs, gazelles, and goats: energy cost and limb configuration. , 1974, The American journal of physiology.

[4]  U. Proske,et al.  Measurements of muscle stiffness and the mechanism of elastic storage of energy in hopping kangaroos. , 1978, The Journal of physiology.

[5]  R. Alexander,et al.  Allometry of the leg muscles of mammals , 1981 .

[6]  P. Rack,et al.  Forces generated at the thumb interphalangeal joint during imposed sinusoidal movements , 1982, The Journal of physiology.

[7]  P. Rack,et al.  Elastic properties of the cat soleus tendon and their functional importance. , 1984, The Journal of physiology.

[8]  P. Rack,et al.  The tendon of flexor pollicis longus: its effects on the muscular control of force and position at the human thumb. , 1984, The Journal of physiology.

[9]  N. Curtin,et al.  Energetic aspects of muscle contraction. , 1985, Monographs of the Physiological Society.

[10]  A. Cutts Sarcomere length changes in the wing muscles during the wing beat cycle of two bird species , 1986 .

[11]  R. F. Ker,et al.  Mechanical properties of various mammalian tendons , 1986 .

[12]  C. M. Chanaud,et al.  Distribution and innervation of short, interdigitated muscle fibers in parallel‐fibered muscles of the cat hindlimb , 1987, Journal of morphology.

[13]  R. F. Ker,et al.  The spring in the arch of the human foot , 1987, Nature.

[14]  G. Cavagna,et al.  Mechanical work, oxygen consumption, and efficiency in isolated frog and rat muscle. , 1987, The American journal of physiology.

[15]  R. F. Ker,et al.  Why are mammalian tendons so thick , 1988 .

[16]  R. M. Alexander,et al.  Elastic mechanisms in animal movement , 1988 .

[17]  Lawrence C. Rome,et al.  Why animals have different muscle fibre types , 1988, Nature.

[18]  R. Griffiths,et al.  The Mechanics of the Medial Gastrocnemius Muscle in the Freely Hopping Wallaby (Thylogale Billardierii) , 1989 .

[19]  R. Griffiths,et al.  Roles of muscle activity and load on the relationship between muscle spindle length and whole muscle length in the freely walking cat. , 1989, Progress in brain research.