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or reniform bodies which are more or less amoeboid, and capable of active movement at certain temperatures. They appear to be naked, and consist of finely granular protoplasm, containing a single nucleus and one or two vacuoles. The chlamydospores, or true spores, occur in S. tenella of sheep (fig. 13), and have been described by Laveran and Mesnil (26). They also are falciform, but one extremity is rounded, the other pointed. There is a very thin, delicate membrane, most unlike a typical, resistant spore-wall; and the spores themselves are extremely fragile and easily acted upon and deformed by reagents, even by distilled water. The rounded end of the spore contains a large nucleus, while at the other end is an oval, clear space, which, in the fresh condition, shows a distinct spiral striation. The exact significance of this structure has been much debated. In position and appearance it recalls the polar-capsule of a Myxosporidian spore. The proof of this interpretation would be the expulsion of a filament on suitably stimulating the spore; while, however, some investigators have asserted that such a filament is extruded, this cannot be regarded as at all certain. Hence it is still doubtful whether this striated body really corresponds to a polar-capsule.

	From Wasielewski’s Sporozoenkunde.
	Fig. 12.—A, Sarcocystis miescheriana (Kühn) from the pig: late stage in which the body has become divided up into numerous chambers or alveoli, each containing a number of germs.
B, Sarcocystis of the ox: section of a stage similar to fig. 12. a, Substance of muscle-fibre; b, envelope of parasite; c, nuclei of the muscle; d, parasitic germs (gymnospores); e, walls of the alveoli. In the peripheral alveoli are seen immature germs.

(After Laveran and Mesnil, from Lankester’s Treatise on Zoology, vol. Protozoa.)

Fig. 13.—Spores of Sarcocystis tenella, Raill., from the sheep.

a, Spore in the fresh condition, showing a clear nucleus (n) and a striated body or capsule (c).

b, Stained spore; the nucleus (n) shows a central karyosome; the striations of the polar capsule (c) are not visible.

Nothing whatever is known as to the natural means by which infection with Sarcosporidia is brought about. Smith (39) showed that mice can be infected with Sarcocystis muris by simply feeding them on the flesh of infected mice. It is not very likely, however, that this represents the natural mode, even in the case of mice; and it certainly cannot do so in the case of Herbivora. The difficulty in the way is the delicacy of the spores, which seem totally unfitted to withstand external conditions. It may be that some alternative (intermediate) host is concerned in dispersal; but this has yet to be ascertained.

All known Sarcosporidia are included in a single genus Sarcocystis, Lank. (= Miescheria + Balbiania, Blanchard.) Some of the principal species are: S. miescheriana, from pigs; S. tenella, from sheep; S. bertrami, from horses; S. blanchardi, from Bovines; S. muris, from mice; S. platydactyli, from the gecko; and lastly, S. lindemanni, described from man.

4. Order—Haplosporidia. The Sporozoa included in this order are characterized by the general simplicity of their development, and by the undifferentiated character of their spores. The order includes a good many forms, whose arrangement and classification have been recently undertaken by Caullery and Mesnil (15), to whom, indeed, most of our knowledge relating to the Haplosporidia is due. The habitat of the parasites is sufficiently varied; Rotifers, Crustacea, Annelids and fishes furnishing most of the hosts. A recent addition to the list of Protozoa causing injury to man, a Haplosporidian, has been described by Minchin and Fantham (29d), who have termed the parasite Rhinosporidium, from its habitat in the nasal septum, where it produces pedunculate tumours.

From Minchin, in Lankester’s Treatise on Zoology, vol. Protozoa.

Fig. 14.—Bertramia Asperospora (Fritsch) from the body-cavity of Brachionus. × 1040.

a, Young form with opaque, evenly-granulated protoplasm and few refringent granules; the nuclei (n) are small, and appear to be surrounded each by a clear space.

b and c, Full-grown specimens with large nuclei and clearer protoplasm, containing numerous refringent granules (r. gr.).

d and e, Morula stages, derived from b and c by division of the body into segments centred round the nuclei, each cell so formed being a spore. Between the spores a certain amount of intercellular substance or residual protoplasm is left, in which the refringent granules seem to be embedded. The morula may break up forthwith and scatter the spores, or may first round itself off and form a spherical cyst with a tough, fairly thick wall.

f, Empty, slightly shrunken cyst, from which the spores have escaped.

g, Free spore or youngest unicellular trophozoite.

h, i, j, Commencing growth of the trophozoite, with multiplication of the nuclei, which results ultimately in forms such as a and b.

Bertramia, a well-known parasite of the body-cavity of Rotifers, will serve very well to give a general idea of the life-cycle so far as it has yet been made out (fig. 14). The trophozoite begins life as a small, rounded uninucleate corpuscle, which as it grows, becomes multinucleate. The multinuclear body generally assumes a definite shape, often that of a sausage. Later, the protoplasm becomes segregated around each of the nuclei, giving the parasite a mulberry-like aspect; hence this stage is frequently known as a morula. The uninuclear cellules thus formed are the spores, which are ultimately liberated by the break-up of the parent body. Each is of quite simple, undifferentiated structure, possesses a large, easily-visible nucleus, and gives rise in due course to another young trophozoite. In some instances, as described by