The Vertebrate Skeleton

by Sidney H. Reynolds

In Bony Ganoids the skeletogenous layer becomes calcified ectochondrally in such a way that the notochord is pinched in at intervals, and distinct vertebrae are produced. Ossification of the calcified cartilage rapidly follows. In Amia the vertebrae are biconcave, in Lepidosteus they are opisthocoelous, cup and ball joints being developed between the vertebrae in a manner unique among fishes. The notochord entirely disappears in the adult Lepidosteus, but at one stage in larval life it is expanded vertebrally and constricted intervertebrally in the manner usual in the higher vertebrata, but unknown elsewhere among fishes.

The tail of Amia is remarkable from the fact that as a rule to each neuromere, as determined by the exit of the spinal nerves, there are two centra, a posterior one which bears nothing, and an anterior one which bears the neural and haemal arches, these being throughout the vertebral column connected with the centra by cartilaginous discs.

In most Teleosteans but not in the Plectognathi the neural arches are continuous with the centra, which are nearly always deeply biconcave.

In some cases many of the anterior vertebrae are ankylosed together and to the skull. The vertebrae often articulate with one another by means of obliquely placed flattened surfaces, the zygapophyses. The centrum in early stages of development is partially cartilaginous, but the neural arches and spines in the trunk at any rate, pass directly from the membranous to the osseous condition.

Fins.

The most primitive fins are undoubtedly the unpaired ones, which probably originally arose as ridges or folds of skin along the mid-dorsal line of the body, and passed thence round the posterior end on to the ventral surface, partially corresponding in position and function to the keel of a ship.

In long 'fish' which pass through the water with an undulating motion such simple continuous fins may be the only ones found, as in Myxine. To support these median fins skeletal structures came to be developed; these show two very distinct forms, viz. cartilaginous endoskeletal pieces, the radiale, and horny exoskeletal fibres, the fin-rays. Mechanical reasons caused the fin to become concentrated at certain points and reduced at intervening regions. Thus a terminal caudal fin arose and became the chief organ of propulsion, and the dorsal and ventral fins became specialised to act as balancing organs.

In some of the earlier Elasmobranchs, the Pleuracanthidae, the endoskeletal cartilaginous radiale are directly continuous with outgrowths from the dorsal and ventral arches of the vertebrae, and form the main part of the fin. In later types of Elasmobranchs the horny exoskeletal fin-rays have comparatively greater prominence. In bony fish, as has been already stated, the horny fibres are replaced by bony rays of dermal origin, and at the same time complete reduction and disappearance of the cartilaginous radiale takes place.

The Caudal fin.

The caudal region of the spinal column in fishes is of special importance. It is distinctly marked off from the rest of the spinal column by the fact that the ventral or haemal arches meet one another and are commonly prolonged into spines, while in the trunk region they do not meet but commonly diverge from one another.