Fig. 361—Merocytes of a shark-embryo, rhizopod-like yelk-cells underneath the embryonic cavity (B). (From Ruckert.) z two embryonic cells, k nuclei of the merocytes, which wander about in the yelk and eat small yelk-plates (d), k smaller, more superficial, lighter nuclei, k′ a deeper nucleus, in the act of cleavage, k* chromatin-filled border-nucleus, freed from the surrounding yelk in order to show the numerous pseudopodia of the protoplasmic cell-body.
Half of the twelve stems of the animal world have no blood-vessels. They make their first appearance in the Vermalia. Their earliest source is the primary body-cavity, the simple space between the two primary germinal layers, which is either a relic of the segmentation-cavity, or is a subsequent formation. Amoeboid planocytes, which migrate from the entoderm and reach this fluid-filled primary cavity, live and multiply there, and form the first colourless blood-cells. We find the vascular system in this very simple form to-day in the Bryozoa, Rotatoria, Nematoda, and other lower Vermalia.
The first step in the improvement of this primitive vascular system is the formation of larger canals or blood-conducting tubes. The spaces filled with blood, the relics of the primary body-cavity, receive a special wall. “Blood-vessels” of this kind (in the narrower sense) are found among the higher worms in various forms, sometimes very simple, at other times very complex. The form that was probably the incipient structure of the elaborate vascular system of the Vertebrates (and of the Articulates) is found in two primordial principal vessels—a dorsal vessel in the middle line of the dorsal wall of the gut, and a ventral vessel that runs from front to rear in the middle line of its ventral wall. From the dorsal vessel is evolved the aorta (or principal artery), from the ventral vessel the principal or subintestinal vein. The two vessels are connected in front and behind by a loop that runs round the gut. The blood contained in the two tubes is propelled by their peristaltic contractions.
Fig. 362—Vascular system of an Annelid (Sænuris), foremost section. d dorsal vessel, v ventral vessel, c transverse connection of two (enlarged in shape of heart). The arrows indicate the direction of the flow of blood. (From Gegenbaur.
The earliest Vermalia in which we first find this independent vascular system are the Nemertina (Fig. 244). As a rule, they have three parallel longitudinal vessels connected by loops, a single dorsal vessel above the gut and a pair of lateral vessels to the right and left. In some of the Nemertina the blood is already coloured, and the red colouring matter is real hæmoglobin, connected with elliptical discoid cells, as in the Vertebrates. The further evolution of this rudimentary vascular system can be gathered from the class of the Annelids in which we find it at various stages of development. First, a number of transverse connections are formed between the dorsal and ventral vessels, which pass round the gut ring-wise (Fig. 362). Other vessels grow into the body-wall and ramify in order to convey blood to it. In addition to the two large vessels of the middle plane there are often two lateral vessels, one to the right and one to the left; as, for instance, in the leech. There are four of these parallel longitudinal vessels in the Enteropneusts (Balanoglossus, Fig. 245). In these important Vermalia the foremost section of the gut has already been converted into a gill-crate, and the vascular arches that rise in the wall of this from the ventral to the dorsal vessel have become branchial vessels.