The Blood-system in the Serpulimorpha (Annelida, Polychaeta) : 1. The Anatomy of the Blood-system in the Serpulidae

Abstract

ABSTRACT 1. An account will be given of the anatomy of the blood-system of Pomatoceros triqueter, and of comparative observations on the following serpulids: Serpula vermi- cularis, S. lo-biancoi, Hydroides norvegica, Vermiliopsis infundibulum, Salmacina incrustans, Protula intestinum, P. tubularia, Apomatus ampulliferus, A. similis, Spirorbis militaris, and S. corrugatus. 2. In all species there is a central blood-system of large vessels in which blood circulates in the usual manner, and a peripheral system of small blind-ending vessels which are alternately full and empty, receiving their blood from the central system, then returning it along the same channels to the central system. 3. The central blood-system is as follows: Blood moves from the tip of the abdomen to the front of the thorax through a sinus enveloping the alimentary canal. Anteriorly it passes through dorsal, transverse, and circum-oesophageal vessels to a ventral vessel in which it moves backwards to the tip of the abdomen. A pair of ring vessels connects the ventral vessel with the sinus at the posterior end of each segment. 4. The anterior end of the dorsal vessel in Pomatoceros triqueter, Serpula vermi- cularis, Hydroides norvegica, and Vermiliopsis infundibulum is surrounded by a sphincter muscle of unknown function, and contains a muscular valve which probably obstructs the back-flow of blood from the transverse vessel. Protula intestinum possesses the valve but lacks the sphincter. Salmacina incrustans and Spirorbis militaris have neither valve nor sphincter. 5. The peripheral blood-system has the following components: the branchial vessels with branches in the crown; the vessels of the collar and lips; the peri-oesophageal plexuses; the trans-septal vessels supplying the body-wall, parapodia, and thoracic membrane. 6. In Pomatoceros triqueter the opercular vessel is spirally coiled, but in other serpulids it is characteristically branched. 7. When Pomatoceros withdraws into its tube, movement of blood in the crown ceases. The operculum is therefore not used as a special respiratory organ when the crown is retracted. 8. The oesophagus of Pomatoceros is surrounded by two independent blind-ending vascular plexuses, an outer plexus communicating with the gut sinus and an inner plexus with the circum-oesophageal vessels. Serpula vermicularis is probably the same. Hydroides norvegica and Protula intestinum lack the outer plexus. Salmacina and Spirorbis have neither plexus. 9. The body-wall of each segment derives its blood-supply from trans-septal branches of the ring vessels of the preceding segment. In Salmacina and Spirorbis these trans-septal vessels are unbranched. In larger serpulids they have numerous [Quarterly Journal of Microscopical Science, Vol. 91, part 2, June 1950.] branches under the epidermis, in the parapodia, and in some cases on the coelomic surface of the body-wall. Branches of the thoracic trans-septal vessels supply the thoracic membrane. In all species except Salmacina, Spirorbis, and Protula intestinum the thoracic trans-septal vessels end ventrally in two superficial ventro-lateral longitudinal vessels which communicate either with the circum-oesophageal vessels or with the ventral vessel. In P. intestinum the thoracic trans-septal vessels enter the ventral vessel directly. The pattern of superficial vessels on the ventral surface of the thorax is useful for identifying specimens. 10. Lateral vessels, such as are found in Sabella, are absent in all serpulids.