Among the Euglenaceae, Euglena viridis is a very common form, giving the green colour to stagnant or slow-flowing ditches and puddles in light places, especially when contaminated by a fair amount of dung, as by the overflow of a pig-sty, in company with a few hardy Rotifers, such as Hydatina senta (Vol. II. Fig. 106, p. 199) and Brachionus. Euglena is about 0.1 mm. in length when fully extended, oval, pointed behind, obliquely truncate in front, with a flagellum arising from the pharyngeal pit. It shows a peculiar wriggling motion, waves of transverse constriction passing along the body from end to end, as well as flexures in different meridians. Such motions are termed "euglenoid." The front part is colourless, but under a low power the rest of the cell is green, owing to the numerous chlorophyll bodies or chloroplasts. The outermost layer of the cytoplasm shows a somewhat spiral longitudinal striation, possibly due to muscular fibrils. The interior contains many laminated plates of paramylum, and a large single nucleus. At the front of the body at the base of the flagellum is a red "eye-spot" on the dorsal side of the pharynx-tube or pit, from which the flagellum protrudes. Wager has shown that this tube receives, also on its dorsal side, the opening of a large vacuole, sometimes called the reservoir, for into it discharges the contractile vacuole (or vacuoles). The eye-spot is composed of numerous granules, containing the vegetal colouring matter "haematochrome." It embraces the lower or posterior side of the communication between the tube and the reservoir. The flagellum has been traced by Wager through the tube into the reservoir, branching into two roots where it enters the aperture of communication, and these are inserted on the wall of the reservoir at the side opposite the eye-spot. But on one of the roots near the bifurcation is a dilatation which lies close against the eye-spot, so that it can receive the light reaction. Euglena is an extremely phototactic organism. It shows various wrigglings along the longitudinal axis, and transverse waves of contraction and expansion may pass from pole to pole.[[138]]

Among the Chrysomonadaceae the genus Zooxanthella, Brandt, has already been described under the Radiolaria (p. [86]), in the jelly of which it is symbiotic. It also occurs in similar union in the marine Ciliates, Vorticella sertulariae and Scyphidia scorpaenae, and in Millepora (p. [261]) and many Anthozoa (pp. [373] f., [396]).

Of the Chlamydomonadidae, Sphaerella (Haematococcus, Ag.) pluvialis (Fig. 43), and S. nivalis, in which the green is masked by red pigment, give rise to the phenomena of "red snow" and "bloody rain." The type genus, Chlamydomonas, is remarkable for the variations from species to species in the character and behaviour of the gametes. Sometimes they are equal, at other times of two sizes. In some species they fuse immediately on approximation, in the naked active state; in others, they encyst on approaching, and unite by the emission of a fertilising tube, as in the Algal Conjugatae. Zoochlorella is symbiotic in green Ciliata (pp. [153] f., [158]), Sponges (p. [175]), Hydra (p. [256]), and Turbellaria (Vol. II. p. 43).

Fig. 43.—Sphaerella pluvialis. A, motile stage; B, resting stage; C, D, two modes of fission; E, Sphaerella lacustris, motile stage. chr, Chromatophores; c.vac, contractile vacuole; c.w, cell-wall; fl, flagella; nu, nucleus; nu', nucleolus; pyr, pyrenoids. (From Parker's Biology.)

Of the Volvocidae, Volvox (Fig. 44) is the largest and most conspicuous genus. Its colony forms a globe the size of a pin's head, floating on the surface of ponds, drains, or even puddles or water-barrels freely open to the light. It has what may be called a skeleton of gelatinous matter,[[139]] condensed towards the surface into a denser layer in which the minute cells are scattered. These have each an eye-spot, a contractile vacuole, and two flagella, by the combined action of which the colony is propelled. Delicate boundary lines in the colonial wall mark out the proper investment of each cell. The cells give off delicate plasmic threads which meet those of their neighbours, and form a bond between them. In that half of the hemisphere which is posterior in swimming, a few (five to eight) larger cells ("macrogonidia" of older writers) are evenly distributed, protruding as they increase in size into the central jelly. These as they grow segment to form a new colony.

Fig. 44.—Volvox globator. A, entire colony, enclosing several daughter-colonies; B, the same during sexual maturity; C, four zooids in optical section; D1-D5, development of parthenogonidium; E, ripe spermogonium; F, sperm; G, ovum; H, oosperm. a, Parthenogonidia; fl, flagellum; ov, ovum; ovy, ovaries; pg, pigment spot; sp, sperms; Spy, spermogonia dividing to form sperms. (From Parker's Biology, after Cohn and Kirchner.)

The divisions are only in two planes at right angles, so that the young colony is at first a plate, but as the cells multiply the plate bends up (as in the gastrulation of the double cellular plate of the Nematode Cucullanus, Vol. II. p. 136), and finally forms a hollow sphere bounded by a single layer of cells: the site of the original orifice may be traced even in the adult as a blank space larger than exists elsewhere. Among the cells of the young colony some cease to divide, but continue to grow at an early period, and these are destined to become in turn the mothers ("parthenogonidia") of a new colony; they begin segmenting before the colony of which they are cells is freed. The young colonies are ultimately liberated by the rupture of the sphere as small-sized spheres, which henceforth only grow by enlargement of the sphere as a whole, and the wider separation of the vegetative cells. Thus the vegetative cells soon cease to grow; all the supply of food material due to their living activities goes to the nourishment of the parthenogonidia, or the young colonies, as the case may be. These vegetative cells have therefore surrendered the power of fission elsewhere inherent in the Protist cell. Moreover, when the sphere ruptures for the liberation of the young colonies, it sinks and is doomed to death, whether because its light-loving cells are submerged in the ooze of the bottom, or because they have no further capacity for life. When conjugation is about to take place, it is the cells that otherwise would be parthenogonidia that either act as oospheres or divide as "spermogonia" to form a flat brood of minute yellow male cells ("sperms"). These resemble vegetative cells, in the possession of an eye-spot and two contractile vacuoles, but differ in the enormously enlarged nucleus which determines a beaked process in front. After one of these has fused with the female cell ("oosphere") the product ("oosperm") encysts, passes into a stage of profound rest, and finally gives rise to a new colony. The oospheres and sperm-broods may arise in the same colony or in distinct ones, according to the species.

Before we consider the bearings of the syngamic processes of Volvox, we will study those presented by its nearer allies, which have the same habitat, but are much more minute. Three of these are well known, Stephanosphaera, Pandorina, and Eudorina, all of which have spherical colonies of from eight to thirty-two cells embedded at the surface of a sphere, and no differentiation into vegetative cells and parthenogonidia (or reproductive cells).