The principal points which have been brought out in this paper may be summarised as follows : (1) The early development of Ophiothrix fragilis varies with the condition of the egg at the moment of fertilisation, and the development of the unripe egg resembles in certain features that of Ophiura brevis. (2) The cœlom originates as a single vesicle from the apex of the archenteron, and this appears to be true for all classes of Echinoderms. (3) The segmentation of the cœlom proceeds along the same lines as those already elucidated for Asteroidea and Echinoidea, viz. into three somites on each side, but the middle somite on the right side is not shifted dorsally as it is in Asteroidea and Echinoidea. This somite occasionally assumes a five-lobed form, proving beyond doubt that it is a right antimere of the water-vascular system. (4) The left hydrocœle is budded from the anterior division of the left cœlom, not from the posterior division as Bury supposed (5), and its persistent connection with the left anterior cœlom constitutes the stone-caual; this opens into the hydrocœle between lobes 1 and 2, as in Asteroidea, not between lobes 4 and 5 as Bury asserted. (5) The metamorphosis is initiated by a preponderant growth of the organs of the left side, which affects the larval arms and the sides of the œsophagus, aud which not only carries the hydrocœle round the œsophagus but also the madreporic pore and the left anterior cœlom, so that these come to be near the right hydrocœle. (6) The perihæmal system of canals originates as a series of five hollow evaginations, the cavities being small and the walls thick. The first Originates from the left anterior cœlom, the other four from the left posterior cœlom. From their walls originate the motor ganglion cells and in all probability the ventral inter-vertebral muscles. (7) The left posterior cœlom gives rise to a dorsal and a ventral horn, which eventually meet, causing it to assume a ring-shape. From it five evaginations give rise to the arm rudiments and the first of these comes to overlie hydrocœle lobe No. 2. (8) A peri-oral cœlom closely surrounding the adult œsophagus originates from the left posterior cœlom. (9) A series of epineural ridges, the tops of which grow out so as to form arch-like folds, are formed inter-radially alternating with the primary tentacles. By the union of adjacent arches the basal portions of the tentacles are covered, exactly as occurs in. the Echinoid larva. (10) The adult œsophagus is formed from the left inner portion of the larval one: its covering is made of the adoral ciliated baud, chiefly of the left half thereof, which grows pari passu with the left hydrocœle. The outer part of the larval œsophagus opens out in consequence of the shrinkage of the forehead to form an atrium into which the primary hydrocœle lobes project. (11) The larval intestine slowly diminishes in size and degenerates, this process being accompanied by a vacuolisation of its cells. The larval stomach becomes pushed over to the right--a process which leads to the same result as the moving of the larval mouth to the left in Holothuroidea, or the formation of the adult mouth on the left in Asteroidea and Echinoidea. (12) The primitive germ-cells originate from the left posterior cœlom covering the stone-canal. In conclusion, I have to express my thanks, first to the University of Cambridge and to the British Association, who granted me the use of their tables at Plymouth; next to Dr. E. J. Allen, Director of the Marine Biological Laboratory at Plymouth, who in the most whole-hearted and generous manner placed the resources of the laboratory at my disposal; then to my friend and colleague, Mr. J. Simpson, B.Sc., Demonstrator of Zoology in McGill University, to whoso skill I owe a large proportion of the drawings which illustrate this paper; and lastly to my wife, who also assisted with the more complicated drawings, with the text-figures, and with the general revision of the text.
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