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contrast between the two animals may be that we have here an instance of an interesting gradation in evolution. From serving primitively as the essential organ of the cleft the tongue-bar may have undergone reduction and modification, becoming a secondary bar in _Amphioxus_, subordinate to the primary bars in size, vascularity and development; finally, in the craniate vertebrates it would then have completed its involution, the suggestion having been made that the tongue-bars are represented by the thymus-primordia. _Gill-pouches and Gill-pores_.--Only rarely do the gill-slits open freely and directly to the exterior (fig. 1). In most species of _Balanoglossus_ each gill-slit may be said to open into its own atrial chamber or gill-pouch; this in its turn opens to the exterior by a minute gill-pore. There are, therefore, as many gill-pouches as there are gill-slits and as many gill-pores as pouches. The gill-pores occur on each side of the dorsal aspect of the worm in a longitudinal series at the base of a shallow groove, the branchial groove. The respiratory current of water is therefore conducted to the exterior by different means from that adopted by _Amphioxus_, and this difference is so great that the theory which seeks to explain it has to postulate radical changes of structure, function and topography. _Excretory and Vascular Systems_.--It seems likely that the coelomic pore-canals were originally excretory organs, but in the existing Enteropneusta the pore-canals (especially the collar canals) have, as we have seen, acquired new functions or become vestigial, and the function of excretion is now mainly accomplished by a structure peculiar to the Enteropneusta called the glomerulus, a vascular complex placed on either side of the anterior portion of the stomochord, projecting into the proboscis-coelom. The vascular system itself is quite peculiar, consisting of lacunae and channels destitute of endothelium, situated within the thickness of the basement-membrane of the body-wall, of the gut-wall and of the mesenteries. The blood, which is a non-corpuscular fluid, is propelled forwards by the contractile dorsal vessel and collected into the central blood-sinus; this lies over the stomochord, and is surrounded on three sides by a closed vesicle, with contractile walls, called the pericardium (_Herzblase_). By the pulsation of the pericardial vesicle (best observed in the larva) the blood is driven into the glomeru
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