The gastraea probably lived in the sea during the Laurentian period, swimming about in the water by means of its ciliary coat much as free ciliated gastrulae do to-day. Probably it differed from the existing gastrula only in one essential point, though extinct millions of years ago. We have reason, from comparative anatomy and ontogeny, to believe that it multiplied by sexual generation, not merely asexually (by cleavage, gemmation, and spores), as was no doubt the case with the earlier ancestors. Some of the cells of the primary germ-layers probably became ova and others fertilising sperm. We base these hypotheses on the fact that we do to-day find the simplest form of sexual reproduction in some of the living gastraeads and other lower animals, especially the sponges. The fact that there are still in existence various kinds of gastraeads, or lower Metazoa with an organisation little higher than that of the hypothetical gastraea, is a strong point in favour of our theory. There are not very many species of these living gastraeads; but their morphological and phylogenetic interest is so great, and their intermediate position between the Protozoa and Metazoa so instructive, that I proposed long ago (1876) to make a special class of them. I distinguished three orders in this class--the Gastremaria, Physemaria, and Cyemaria (or Dicyemida). But we might also regard these three orders as so many independent classes in a primitive gastraead stem. The Gastremaria and Cyemaria, the chief of these living gastraeads, are small Metazoa that live parasitically inside other Metazoa, and are, as a rule, 1/50 to 1/25 of an inch long, often much less (Figure 2.233, 1 to 15). Their soft body, devoid of skeleton, consists of two simple strata of cells, the primary germinal layers; the outer of these is thickly clothed with long hair-like lashes, by which the parasites swim about in the various cavities of their host. The inner germinal layer furnishes the sexual products. The pure type of the original gastrula (or archigastrula, Figure 1.29 I) is seen in the Pemmatodiscus gastrulaceus, which Monticelli discovered in the umbrella of a large medusa (Pilema pulmo) in 1895; the convex surface of this gelatinous umbrella was covered with numbers of clear vesicles, of 1/25 to 1/8 inch in diameter, in the fluid contents of which the little parasites were swimming. The cup-shaped body of the Pemmatodiscus (Figure 2.233, 1) is sometimes rather flat, and shaped like a hat or cone, at other times almost curved into a semi-circle. The simple hollow of the cup, the primitive gut (g), has a narrow opening (o). The skin layer (e) consists of long slender cylindrical cells, which bear long vibratory hairs; it is separated by a thin structureless, gelatinous plate (f) from the visceral or gut layer (i), the prismatic cells of which are much smaller and have no cilia. Pemmatodiscus propagates asexually, by simple longitudinal cleavage;