The streaming of the endoplasm is the most conspicuous feature of ameboid movement. It is even more noticeable than the movement of the pseudopods themselves, because of its greater speed and because it occurs in all parts of the ameba. Its importance in movement is essential, for no continued locomotion can be observed unless accompanied by streaming. It may be profitable therefore to enquire into the general features of streaming, and to observe some of the necessary consequences streaming imposes upon such an animal as the ameba.

Let us take as an example an Amoeba proteus (Pallas, ’66, emend. Leidy, ’79, emend. Schaeffer, ’16) in characteristic movement (see Figure 11, p. 37). The main streams of endoplasm are in the same direction as that in which the ameba moves. In the withdrawing pseudopods the current is, of course, toward the main mass of the ameba. The endoplasmic stream is continuous from the posterior end to the tips of the advancing pseudopods. The retracting pseudopods flow into the main stream as tributaries. If, as often happens, the ameba is without pseudopods, there is then a single stream arising in the posterior end and flowing to the anterior end. In such a case it is readily observed how absolutely dependent locomotion is upon endoplasmic streaming.

It often happens, such as when the ameba is receiving a strong stimulus, that streaming is arrested and brought to a stop for a few seconds, more or less. Presently however the endoplasm begins to flow as before. At what point, in such a case, is the first movement of endoplasm detectible? Is it at the free end of the pseudopod, at its middle region, at its base, or at the posterior end of the ameba? BÜtschli (’80, p. 116) observed that in a withdrawing pseudopod the streaming begins at the free end of the pseudopod; but his (’92, p. 201) later explanation of ameboid movement seems to require that the endoplasm must begin to move at the base of the withdrawing pseudopod. Jennings (’04, p. 157) observed that in a withdrawing pseudopod the current of endoplasm begins at the base of the pseudopod.

From numerous observations directed toward this point, it appears that the conditions under which streaming is resumed after a pause, whether in the same or in the reverse direction, are of great variety. The shape, size, slenderness, and the position on the ameba of the pseudopod, as well as the strength and character of the stimulus, are among the factors capable of changing in whole or in part the flow of endoplasm in a pseudopod. In an ameba that has been moving along a homogeneous flat surface, as nearly unstimulated as may be, the endoplasm first begins to flow out of the lower half of the retracting pseudopod, if the pseudopod is more or less uniformly conical in shape and rather slender. In such a case it may be said that the retracting pseudopod was withdrawn “by the ameba,” and that it did not itself receive an external stimulus producing retraction. If, however, the tip of a pseudopod as described receives a strong negative stimulus, the endoplasm frequently flows back from the tip while it is still flowing into the pseudopod at the base. But very soon thereafter, in such an event, the streaming becomes unified and the pseudopod is withdrawn. In broad pseudopods about to be withdrawn, the endoplasm may begin to move anywhere along its length. This is undoubtedly due to the continuous local changes in the walls of the pseudopod, which are characteristic of this species of ameba (see p. 20).

In an ameba which has been brought to a standstill, as by a sudden flash of light, the first sign of recurring streaming is in the anterior half, whether the original direction of streaming is resumed or reversed. If the direction is reversed, the active pseudopods retract for a considerable distance before a new one is projected. The endoplasmic stream in a slender withdrawing pseudopod may not reach to the tip for from several seconds to a minute, if the tip is slightly positively stimulated. One may then observe ectoplasm streaming toward the tip and toward the base, in the respective regions, at the same time, with considerable fluctuation back and forth of the neutral zone separating the two streams. The fate of such a pseudopod depends on its size, on its position on the ameba, and the strength of the stimulus affecting it and the rest of the ameba. That is, if the pseudopod is small or on the posterior half of the ameba, or only slightly stimulated, it will be retracted; but if it is large, or on the anterior end of the ameba, or more strongly stimulated than the rest of the ameba, it may again become active.

The fact that protoplasm is practically incompressible makes it clear that if streaming can be observed to begin after a pause at some point after it begins at others, the ectoplasmic walls of the ameba must give way in the region where streaming begins. Since it has been established by observation that the ectoplasm may give way at any point, it follows that one of the principal factors affecting streaming is the elasticity and liquefiability of the ectoplasm.

The streaming in an ameba is coordinated. The direction in which the endoplasm flows in the several pseudopods, when there are no stimuli received externally that produce visible changes in behavior, gives one the impression that there is a “centre” controlling movement. The several pseudopods do not act at all capriciously. The ameba seems to move the pseudopods, not the pseudopods the ameba. If this impression of coordination is correct, it is of the first importance in a study of ameboid movement. Further on, this point will be taken up at length in connection with the character of the path an externally unstimulated ameba describes (p. 109); but there are certain observations which aid in the analysis of the problem of coÖrdination from the point of view of the pseudopod, instead of that of the ameba as a whole, and to these observations we may now direct our attention.

The mass of endoplasm within a pseudopod moves practically always in one direction. In any cross-section of a pseudopod that is more or less cylindrical in shape, the endoplasm in the center moves most rapidly, that near to it less rapidly, while that near the ectoplasm moves very slowly. One never observes a forward stream on one side of the pseudopod and a backward stream on the other. Nor does one observe parallel streams of endoplasm flowing in opposite directions within the same

ectoplasmic tube, in an ameba of several pseudopods, excepting where there is a wide zone of stationary endoplasm between the streams (Figure 1, v, w). But in “fountain currents,” such as Rhumbler (’98, p. 190) described and figured for Amoeba blattae BÜtschli, and which may readily be observed in most species of amebas if immersed in a solution of gelatin thick enough to keep the amebas from sinking, there is a central stream of endoplasm flowing forward, and a peripheral stream of ectoplasm flowing backward, with a thin neutral zone between (Figure 29, d). As we shall see further on, however, these fountain currents are in principle the same as the currents observed in ordinary locomotion, the apparent difference being due to the fact that there is no locomotion. It is true, then, that within the same pseudopod at any cross section the endoplasm always streams in one direction, and the streaming is unified.

When new pseudopods are formed, or when old ones are retracted, and especially when both these phenomena occur at the same time and close together on a part of an older pseudopod, some of the details of coordination in streaming are readily made out. In Figure 1 are shown a number of observed cases of pseudopod formation and retraction, with the direction of endoplasmic streams indicated at a given instant. For the purpose of illustration, several (presumably) possible but unobserved cases, m and r, are sketched, and also two cases, u and v, which have not been observed and which probably do not occur. The general conclusion to be drawn from these observations is that, while the endoplasm in the body of an ameba as a whole may be streaming in several different directions at any given instant, that is almost never the case with an individual pseudopod, especially if the pseudopod is of small or medium size and not too flat or otherwise irregular in shape. The pseudopod is therefore the unit of coordinated protoplasmic streaming.

Another general observation which undoubtedly is connected in some way with the problem of coordinated streaming is the following. In externally unstimulated amebas, the new pseudopods are almost without exception directed 60° or less from the direction in which the parent pseudopods are moving.

It is a matter of common observation that an ameba may throw out a pseudopod in any direction whatsoever when stimulated. The ameba may reverse its direction of movement completely, or it may move in scores of different directions at one time for awhile, if properly stimulated. There is no restraint or limit imposed upon the ameba insofar as the direction of movement is concerned. Why then should a great majority of new pseudopods in an unstimulated ameba be projected at an angle of approximately 60° to the parent pseudopod? It might seem at first sight as if the merely physical aspect of the streaming would be a sufficient explanation, in that less resistance would be met with in sending a stream off at a small angle than at a large. But it is probable that inertia plays no part in maintaining the direction of streaming (see p. 123, footnote, for further discussion). It requires perhaps more energy for a pseudopod to flow off from the main stream at an angle of 120° than at an angle of 30°. But it is plain that as many pseudopods are withdrawn as are thrown out, and they are withdrawn at an angle against the main stream of endoplasm in the ameba that is the complement of the angle at which they were projected. Whatever energy might be saved therefore in the projection of a new pseudopod at a small angle with the main stream is lost in withdrawing the pseudopod against the stream at a correspondingly large angle. It is clear therefore that the physics of moving viscous fluids cannot solve the problem. It is probable that the mechanism which controls the direction of locomotion as exemplified in the wavy path of the ameba (see p. 109) is also involved in the direction in which pseudopods are projected.

Some very interesting special cases of endoplasmic streaming are observed during the process of feeding. As is well known, amebas capture their food by the protoplasm flowing around it and engulfing it. If the object is large the protoplasm may flow around it, in contact with it, so that the shape of the object determines the direction in which the enveloping protoplasm flows. If the object is small, particularly if it is a live organism, the behavior of the ameba is quite different (Kepner and Taliaferro, ’13, Schaeffer, ’16). To capture such a food object a cup of protoplasm is gradually formed over it so as to imprison it (Figure 2). If the food organism lies against some flat object, the food cup is brought down to the surface of the object all around, thus making escape impossible, before the protoplasm comes into contact with the food organism. Schaeffer (’16, ’18) by experimental methods has shown that the stimulus calling forth the formation of food cups as just described, is the mechanical vibration of the water. At least the same response was produced on the part

of the ameba when the ameba was carefully stimulated by means of very fine clean glass needles. The conclusion is unavoidable therefore that the shape of the food cup and the method of its formation is a racial characteristic and is hereditary. The streaming endoplasm therefore, upon suitable stimulation, takes on a definite form, that of a food cup. This indicates again that the endoplasm is something more than the ordinary fluids of physics, for out of an apparently structureless fluid, organization is effected.

The fact that food cups are formed by amebas implies of course that stimuli are received whose effect cannot be explained as a direct physical reaction. Rhumbler (’10) has attempted to explain the formation of food cups as the direct physical result of the stimulation by the food body; but in recent experiments Schaeffer (’16) has shown that food cups are formed over diffusing solutions of tyrosin, where the solutions were quite as concentrated outside as inside the cup. These results prove convincingly that the shape and size of the food cup are not determined by direct action of the stimulating agent, but by hereditary factors within the protoplasm of the ameba.

Other stimuli also affect streaming characteristically, though not so strikingly perhaps as food stimuli. One of the most widely observed effects on streaming is the momentary pause following stimulation of many sorts. If an ameba that is moving along unstimulated externally, suddenly comes near a food object, it frequently stops forward streaming for about a second, and then begins again, usually at increased speed. The ameba behaves as if it were startled. A similar reaction is observed if a small perpendicular beam of light is flashed near the anterior end of the ameba. Here also streaming is resumed with accelerated speed toward the beam of light. Harrington and Leaming (’00) showed that if strong light, especially at the blue end of the spectrum, is suddenly thrown on the ameba, movement is arrested for a short time. Miss Hyman (’17) has shown recently that if an ameba is strongly stimulated with a glass needle, streaming is arrested momentarily, but the direction of streaming when resumed subsequently, depends partly upon the former direction of streaming and partly upon the location of the stimulus. All of these cases of temporarily arrested movement are strikingly similar to what is observed in the higher animals under similar conditions.

The ingestion of a large food mass produces usually a marked change in streaming. A more or less spherical form is assumed, and if the food mass be a live organism such as a large ciliate, the ameba frequently remains quiet for a considerable interval. If a large amount of food is eaten, as for example a dozen or two colpidia, the ameba may suspend concerted streaming for an hour or more. During this time small pseudopods are projected here and there, but there is no locomotion. But if an ameba eats large masses of carmine, there is usually no pause following ingestion, and the same thing is true when the ameba is induced to eat bits of glass and other indigestible substances. It follows therefore that the interrupted streaming of the endoplasm due to feeding is not caused by the act of ingestion as such, but rather by the onset and continuance of the normal digestive processes on a large scale. These reactions are again strikingly similar to what is observed in many vertebrates, in which a more or less definite body sense, whose sense organs are in the splanchnic region, is supposed to be involved; but what the explanation of similar behavior in ameba is, is not at all clear.

Another factor of great importance in endoplasmic streaming is the nucleus. It was observed by Hofer (’90) that amebas lacking nuclei did not move in a coordinated manner. Štolc (’10) however records a number of observations in which characteristic movement was observed in enucleate amebas ten or more days after the enucleate ameba had been cut off from a normal ameba. Hofer’s amebas died after nine or ten days, while Štolc’s remained alive, some of them for over thirty days. Recently Willis (’16) confirmed Hofer’s findings, but does not discuss Štolc’s results.

The cutting of an ameba into two pieces, one with and the other without a nucleus, is a very simple operation. It is also very easy to observe that within an hour or so the enucleate ameba does not move normally, and that there is no concerted endoplasmic streaming while the nucleate ameba seems to behave normally. But Štolc’s contention that enucleate amebas move characteristically (l. c., p. 159, 160, 167) is not necessarily contradicted by these observations, for Štolc’s observations refer to amebas that lived much longer than the enucleate amebas of Hofer and of Willis. Even if an enucleate ameba is able to recover, after many days, its power of concerted movement, there can be no doubt that enucleate amebas do not move characteristically for a short time after the operation, and that this effect is due to the lack of a nucleus.

Very likely the action of the nucleus on the locomotory processes is neither direct nor specific. The metabolic balance must be disturbed by so fundamental an operation as the removal of the nucleus, and all fundamental activities must in consequence be affected. That food organisms (chilomonas and coleps) may be eaten and digested as Štolc (’10) states, indicates however that the metabolic balance may after a time be regained in some degree, for feeding undoubtedly calls for concerted streaming, and digestion for the formation and transfer of enzymes. Until this point receives further attention therefore, it remains unknown in what way the removal of the nucleus disturbs streaming for some time after the operation; but of the fact that streaming is disorganized for some time, there can be no doubt.