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 COGNAC sub-class in question. The mesogloea is in itself an inert non-cellular secretion, but the immigration of muscular and other cells into its substance, both from ectoderm and endoderm, gives it in many cases a strong resemblance to the mesoderm of Triploblastica,—a resemblance which, while probably superficial, may yet serve to indicate the path of evolution of the mesoderm. The Ccelentera may thus be briefly defined as Metazoa which exhibit two embryonic cell-layers only,—the ectoderm and endoderm,—their body-cavities being referable to a single cavity or ccelenteron in the endoderm. Their position in the Animal Kingdom and their main subdivisions may be expressed in the following table :— I. Protozoa. II. Parazoa. III. Metazoa. Coelentera = Diploblastica. Hydroniedusae. Scyphomedusse.

Triploblastica (including Coelomata). Scypbozoa.

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The Anthozoa differ from the Scyphomedusae in having no medusoid form; they all more or less resemble a seaanemone, and may be termed actinioid. They are (with rare exceptions, probably secondarily acquired) hypogenetic, the offspring resembling the parent, and both being sexual. The sexual cells are borne on the mesenteries in positions irrespective of obvious developmental radii. The Ctenophora are so aberrant in structure that it has been proposed to separate them from the Coelentera altogether: they are, however, theoretically deducible from an ancestor common to other Coelentera, but their extreme specialization precludes the idea of any close relationship with the rest (see Ctenophora). As regards the other three groups, however, it is easy to conceive of them as derived from an ancestor, represented to-day to some extent by the planula-larva {Ency. Brit., Hydrozoa, vol. xii. p. 548), which was Coelenterate in so far as it was composed of an ectoderm and endoderm, and had an internal digestive cavity (I. of the table).

Ctenophora. Anthozoa.

On a comparison of these subdivisions with those adopted by Professor Lankester in the article Hydrozoa (Ency. Brit. vol. xii.), it will be noticed that the Scyphomedusse then included with the Hydromedusse as Hydrozoa are here placed nearer to the Anthozoa than to their old pendants. The reasons for this may be stated briefly. The Hydromedus^s are distinguished from the Scyphozoa chiefly by negative characters; they have no stomodseum, that is, no ingrowth of ectoderm at the mouth to form an oesophagus ; they have no mesenteries (radiating partitions) which incompletely subdivide the coelenteron ; and they have no concentration of digestive cells into special organs. Their ectodermal muscles are mainly longitudinal, their endodermal muscles are circularly arranged on the body-wall. Their sexual cells are (probably in all cases) produced from the ectoderm, and lie in those radii which are first accentuated in development. They typically present two structural forms, the non-sexual hydroid, and the sexual medusoid; in such a case there is an alternation of generations (metagensis), the hydroid giving rise to the medusoid by a sexual gemmation, the medusoid bearing sexual cells which develop into a hydroid. In some other cases medusoid develops directly from medusoid (hypogenesis), whether by sexual cells or by gemmation. The medusoids have a muscular velum of ectoderm and mesogloea only. The Scyphozoa have the following features in common:— They typically exhibit an ectodermal stomodseum; partitions or mesenteries project into their coelenteron from the body-wall, and on these are generally concentrated digestive cells (to form mesenterial filaments, phaceuse, etc.); the external musculature of the body-wall is circular (except in Cerianthus); the internal, longitudinal; and the sexual cells probably always arise in the endoderm. The Scyphomedusje, like the Hydromedusae, typically present a metagenesis, the non-sexual scyphistomoid (corresponding to the hydroid) alternating with the sexual medusoid. In other cases the medusoid is hypogenetic, medusoid producing medusoid. The sexual cells of the medusoid lie in the endoderm on interradii, that is, on the second set of radii accentuated in the course of development. The medusoids have no true velum ; in some cases a structure more or less resembling this organ, termed a velarium, is present, permeated by endodermal canals.

At the point of divergence between Scyphozoa and Hydromedusae (II. of the table of hypothetical descent), we may conceive of its descendant as tentaculate, capable of either floating (swimming) or fixation at will like Lucernaria to-day; and exhibiting incipient differentiation of myoepithial cells (neuro-muscular cells of Hydrozoa, loc. cit. p. 549). At the parting of the ways which led, on the one hand, to modern Scyphomedusae, on the other to Anthozoa (III.), it is probable that the common ancestor was marked by incipient mesenteries and by the limitation of the sexual cells to endoderm. The lines of descent— II. to Hydromedusae, and III. to Scyphomedusae—represent periods during which the hypothetical ancestors II. and III., capable of either locomotion or fixation at will, were either differentiated into alternating generations of fixed sterile nutritive hydroids (scyphistomoids) and locomotor sexual medusoids, or abandoned the power of fixation in hypogenetic cases. During the period represented by the line of descent—III. to Anthozoa—this group abandoned its power of adult locomotion by swimming. During these periods were also attained those less important structural characters which these three groups present to-day. (o. h. fo.) Cognac, chief town of arrondissement, department of Charente, France, 32 miles west by north of Angouleme, by rail. Large quantities of brandy and wine are exported to England, America, and Australia, and the total trade in alcoholic liquors of Cognac alone has a mean annual value of £1,200,000. Population (1881), 13,096; (1896), 18,932.