The ectoplasmic tube is not as thick as in proteus, though it appears to be more solid than in that species. It is thrown into folds at the posterior end as it is liquified to form endoplasm, which indicates a firm texture of the ectoplasm. As to the endoplasmic stream, it presents no visible characteristics which set it apart from the fluids of physics; it moves most rapidly in the middle, and gradually less rapidly as the ectoplasm is approached. There is no backward movement of the ectoplasm against the sides of the pseudopod at the anterior end—nothing approaching a “fountain current”—which indicates that the transformation of endoplasm into ectoplasm is rapid and complete. That is, all the endoplasm which reaches the anterior end is turned into ectoplasm. Typically this would result in an ameba of average size, in a layer of ectoplasm of a thickness of about one-seventh of the diameter of the pseudopod (for the area of the cut ectoplasmic tube would equal the area of the endoplasmic stream). But because of friction against the sides of the ectoplasmic tube, there is a layer of endoplasm of appreciable thickness that is practically motionless. This layer of endoplasm therefore makes the diameter of the endoplasmic stream appear smaller than it actually is, and the ectoplasmic tube larger than it is. The actual thickness of the tube of ectoplasm, as distinguished from the flowing endoplasm, is difficult to measure, but it seems to be about one-tenth the diameter of the pseudopod. (Kite (’13) found ameboid ectoplasm to be from eight to twelve microns thick, but he does not state from what part of the ameba nor from what species the ectoplasm was taken.) This would indicate that if the transformation of endoplasm into ectoplasm is as complete as the conditions permit, the thickness of the friction layer would be about one-twenty-third of the diameter of the pseudopod. These observations therefore point to the conclusion that the tendency in laureata is for all the endoplasm to be transformed into ectoplasm at the anterior end, and for the reverse process to occur at the posterior end.

Several of the pelomyxas also move in much the same manner as Amoeba laureata, that is, in clavate form and more or less cylindrical in shape. This is especially the case with Pelomyxa palustris and P. belevskii. But in these species the endoplasm is not completely converted into ectoplasm at the anterior end, as is shown by the fact that there is a slight backward current of endoplasm at the sides near the anterior end (Schultze, ’75). Observation indicates also that the ectoplasmic tube is thinner than would be the case were there complete transformation of endoplasm into ectoplasm at the anterior end. The origin of pseudopods in these pelomyxas is not steady and under control as in laureata, but sudden and eruptive, indicating a less coherent ectoplasm.

The nearest approach to the conditions of streaming as found in Amoeba laureata is found in A. discoides ([Figure 11], B) a species often confounded with proteus. This species is frequently found in clavate form, and the conversion of endoplasm into ectoplasm is complete at the anterior end. In other respects of streaming and pseudopod formation, the two species are also similar.

In another very common species of ameba, Amoeba dubia ([Figure 11], C) the clavate stage of locomotion is comparatively rare, but when it is found it is observed that the transformation of endoplasm into ectoplasm at the anterior end is incomplete, and the endoplasm seems to be of very liquid consistency. This ameba is characterized by the possession, usually, of numerous pseudopods extending from a central mass of protoplasm. In this stage it possesses no main pseudopod as does proteus, discoides, laureata and other species, but there are three or four pseudopods extending actively in the general direction of locomotion. The physical characteristics of these pseudopods, in so far as streaming is affected, are different from those of the clavate amebas. The ectoplasmic tubes are relatively thicker, the endoplasm is less fluid, and new pseudopods are not formed so readily. It appears therefore that an increase of surface in the ameba serves to increase the amount of ectoplasm that is formed during locomotion.

Figure 5. Amoeba limicola, after Penard. Figures a, b, e, illustrate the “eruptive pseudopods” by means of which this ameba moves. f, a variety or separate species whose ectoplasm is somewhat firmer, and whose posterior end possesses a conspicuous uroid. c, the nucleus found in a, b, e. d, the nucleus found in f.

There is another group of amebas in which the endoplasm is much more fluid than in dubia. To this group belong Amoeba limicola ([Figure 5]) and Pelomyxa schiedti ([Figure 6]). The latter never forms pseudopods, and the former does so very seldom. A. limicola is extremely fluid, and in locomotion the flow of the endoplasm can hardly be called streaming, for it rushes about in the body as if it were only partially under control. The ectoplasm does not give way steadily at the anterior end during locomotion, allowing a steady forward flow of the endoplasm, but it breaks away suddenly here or there, allowing the endoplasm to rush through as if it were under considerable pressure. When the endoplasm rushes through these breaches in the ectoplasm, it is usually deflected back along the side of the ameba for a considerable distance, thus leaving a part of the old ectoplasmic wall stand for a few seconds between the reflected wave of ectoplasm and the main body of the ameba. It is then that one can observe especially well the very thin ectoplasm covering the ameba, the thickness of which is about one-fortieth the diameter of the ameba. This ameba is somewhat dorso-ventrally flattened and generally oblong in shape during locomotion.