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HYENA

Anthozoa respectively. In the hydropolyp the body is typically elongated, the height of the column being far greater than the diameter. The peristome is relatively small and the mouth is generally raised on a projecting spout or hypostome. The ectoderm loses entirely the ciliation which it had in the planula and actinula stages and commonly secretes on its external surface a protective or supporting investment, the perisarc. Contrasting with this, the anthopolyp is generally of squat form, the diameter often exceeding the height; the peristome is wide, a hypostome is lacking, and the ectoderm, or so much of it as is exposed, i.e. not covered by secretion of skeletal or other investment, retains its ciliation throughout life. The internal structural differences are even more characteristic. In the hydropolyp the blastopore of the embryo forms the adult mouth situated at the extremity of the hypostome, and the ectoderm and endoderm meet at this point. In the anthopolyp the blastopore is carried inwards by an in-pushing of the body-wall of the region of the peristome, so that the adult mouth is an opening leading into a short ectodermal oesophagus or stomodaeum, at the bottom of which is the blastopore. Further, in the hydropolyp the digestive cavity either remains simple and undivided and circular in transverse section, or may show ridges projecting internally, which in this case are formed of endoderm alone, without any participation of the mesogloea. In the anthopolyp, on the other hand, the digestive cavity is always subdivided by so-called mesenteries, in-growths of the endoderm containing vertical lamellae of mesogloea (see Anthozoa). In short, the hydropolyp is characterized by a more simple type of organization than the anthopolyp, and is in most respects less modified from the actinula type of structure.

Fig. 4.—Diagram showing the change of the Actinula into a Medusa . A, Vertical section of the actinula; a-b and c-d as in fig. 3, B, transitional stage, showing preponderating growth in the horizontal plane. (C,C’, D,D’, two types of medusa organization; C and D are composite sections, showing a radius (R) on one side, an interradius (IR) on the other; C’ and D’ are plans; the mouth and manubrium are indicated at the centre, leading into the gastral cavity subdivided by the four areas of concrescence in each interradius (IR). t, tentacle; g.p, gastric pouch; r.c, radial canal not present in C and C’; c.c, circular or ring-canal; e.l, endoderm-lamella formed by concrescence. For a more detailed diagram of medusa-structure see article Medusa.

Returning now to the actinula, this form may, as already stated, develop into a medusa, a type of individual found only in the Hydrozoa, as here understood. To become a medusa, the actinula grows scarcely at all in the direction of the principal axis, but greatly along a plane at right angles to it. Thus the body becomes umbrella-shaped, the concave side representing the peristome, and the convex side the column, of the polyp. Hence the tentacles are found at the edge of the umbrella, and the hypostome forms usually a projecting tube, with the mouth at the extremity, forming the manubrium or handle of the umbrella. The medusa has a pronounced radial symmetry, and the positions of the primary tentacles, usually four in number, mark out the so-called radii, alternating with which are four interradii. The ectoderm retains its ciliation only in the sensory organs. The mesogloea becomes enormously increased in quantity (hence the popular name "jelly-fish"), and in correlation with this the endoderm-layer lining the coelenteron becomes pressed together in the interradial areas and undergoes concrescence, forming a more or less complicated gastrovascular system (see Medusa). It is sufficient to state here that the medusa is usually a free-swimming animal, floating mouth downwards on the open seas, but in some cases it may be attached by its aboral pole, like a polyp, to some firm basis, either temporarily or permanently.

Thus the development of the two types of individual seen in the Hydrozoa may be summarized as follows:—

 ${\displaystyle \scriptstyle {\left\{{\begin{matrix}\ \\\\\ \\\ \\\ \\\ \\\ \ \end{matrix}}\right.}}$ Egg | Free Blastula | .mw-parser-output .nowrap,.mw-parser-output .nowrap a:before,.mw-parser-output .nowrap .selflink:before{white-space:nowrap}⁠"Planula"⁠ Parenchymula | Stage Gastrula | Actinula /⁠\ Polyp⁠Medusa

This development, though probably representing the primitive sequence of events, is never actually found in its full extent, but is always abbreviated by omission or elimination of one or more of the stages. We have already seen that the parenchymula stage is passed over when the gastrulation is of the invaginate type. On the other hand, the parenchymula may develop directly into the actinula or even into the polyp, with suppression of the intervening steps. Great apparent differences may also be brought about by variations in the period at which the embryo is set free as a larva, and since two free-swimming stages, planula and actinula, are unnecessary, one or other of them is always suppressed. A good example of this is seen in two common genera of British hydroids, Cordylophora and Tabularia. In Cordylophora the embryo is set free at the parenchymula stage as a planula which fixes itself and develops into a polyp, both gastrula and actinula stages being suppressed. In Tubularia, on the other hand, the parenchymula develops into an actinula within the maternal tissues, and is then set free, creeps about for a time, and after fixing itself, changes into a polyp; hence in this case the planula-stage, as a free larva, is entirely suppressed.

The Hydrozoa may be defined, therefore, as Cnidaria in which two types of individual, the polyp and the medusa, may be present, each type developed along divergent lines from the primitive actinula form. The polyp (hydropolyp) is of simple structure and never has an ectodernal oesophagus or mesenteries.[1] The general ectoderm loses its cilia, which persist only in the sensory cells, and it frequently secretes external protective or supporting structures. An internal mesogloeal skeleton is not found.

The class is divisible into two main divisions or sub-classes, Hydromedusae and Scyphomedusae, of which definitions and detailed systematic accounts will be found under these headings.

General Works on Hydrozoa.—C. Chun, “Coelenterata (Hohlthiere),” Bronn's Klassen und Ordnungen des Thier-Reichs ii. 2 (1889 et seq.); Y. Delage, and E. Hérouard, Traité de zoologie concrète, ii. part 2, Les Coelentérés (1901); G. H. Fowler, “The Hydromedusae and Scyphomedusae” in E. R. Lankester's Treatise on Zoology, ii. chapters iv. and v. (1900); S. J. Hickson, “Coelenterata and Ctenophora,” Cambridge Natural History, i. chapters x.-xv. (1906).

(E. A. M.)

HYENA, a name applicable to all the representatives of the mammalian family Hyaenidae, a group of Carnivora (q.v.) allied to the civets. From all other large Carnivora except the African hunting-dog, hyenas are distinguished by having only four toes on each foot, and are further characterized by the length of the fore-legs as compared with the hind pair, the non-retractile claws, and the enormous strength of the jaws and teeth, which enables them to break the hardest bones and to retain what they have seized with unrelaxing grip.

1. See further under Scyphomedusae.