The venous blood is returned to the heart by the pair of pre caval, and single postcaval veins which open into the sinus ve nosus. The branches of the precavals come from the head and fore limb, the subclavian often receiving an azygous vein from the anterior part of the body wall which represents part of the embry onic posterior cardinal. Nearly the whole of the blood which Urodela structure. The systemic arches unite to form the dorsal aorta; from one or both of them arise coronary arteries to the heart. From the right come off both subclavians, and the left usually gives off a coelic branch. The carotids may arise inde pendently from the right systemico-carotid, or may be formed by the branching of a single primary carotid. In snakes the right carotid is usually much reduced or absent.
The renal portal system drains the tail, and part of the hind limbs, the afferent renals arising from the bifurcated anterior end of the caudal vein and the iliacs. The efferent renals open into the postcaval, whose hinder end is formed by them. The supra renal portal system consists of a series of afferent veins which come from the body wall; the efferents discharge with the gonadial veins into the postcaval.
The hepatic portal system includes the series of veins from the gut, which form the true hepatic portal vein and also the median anterior abdominal vein, which is originally formed by a fusion in the middle line of pelvic veins, themselves built up from the iliacs and a series of vessels from the hinder part of the body wall of the abdomen. The anterior abdominal passes along in a mesenteric sheet in the ventral part of the body cavity to enter the liver and there receive the hepatic portal or a branch from it. Finally, the whole of the blood in the liver passes by the
hepatic veins into the posterior cardinal.
There are two pairs of thymuses in Sphenodon and lizards, derived from the second and third pharyngeal pouches in the latter. In snakes there are usually two pairs derived from the mammals. The nasal cavity finally opens to the palate by the internal nostril, which may be carried far back by the formation of a secondary palate.
Jacobsen's organ is, in Chelonia, a mere diverticulum of the ventral part of the nasal cavity. In Squamata it becomes an independent chamber, separated from the nasal cavity by the septomaxillary bone; it then has a special opening to the palate and may be very highly developed, receiving a large proportion of the olfactory nerve fibres. Its function is clearly to smell food after it has been taken into the mouth.
Jacobsen's organ soon vanishes in crocodiles. A special nasal gland is developed in the concha of reptiles, and the naso-lachri mal duct opens on the lateral wall of the nasal cavity.