The Story of the Living Machine

direct bleaching effect of the northern climate upon a skin which otherwise would have been dark. In other words, a conclusive answer can not here be given. It is not our purpose, however, to attempt to distinguish between these two kinds of variations, but simply to recognize that they occur. Our next problem must be to search for an explanation of these variations. With the acquired variations we have no particular trouble, for they are easily explained as due to the direct action of the environment upon animals. One of the fundamental characters of the living protoplasm (using the word now in its widest sense) is its extreme instability. So unstable is it that any disturbing influence will affect it. If two similar unicellular organisms are placed under different conditions they become unlike, since their unstable protoplasm is directly affected by the surrounding conditions. With higher animals the process is naturally a little more complicated; but here, too, they are easily understood as part of the function of the machine. One of the adjustments of the machine is such that when any organ is used more than usual the whole machine reacts in such a way as to send more blood to this special organ. The result is a change in the nutrition of the organ and a corresponding variation in the individual. Thus acquired variations are simply functions of the action of the machine. Congenital variations, however, can not receive such an explanation. Being born with the individual, they can not be produced by conditions affecting him, but rather to something affecting the germ plasm from which he sprung. The nature of the germ plasm controls the nature of the individual, and congenital variations must consequently be due to its variations. But it is not so easy to see how this germ plasm can undergo variation. The conditions which surround the individual would affect its body, but it is not easy to believe that they would affect the germinal substance. Indeed, it is not easy to see how any external conditions can have influence upon this germinal material if it is not an active part of the body, but is simply stored within it for future use in reproduction. How could any changes in the environment of the individual have any effect upon this dormant material stored within it? But if we are correct in regarding this germ material in the reproductive bodies as the basis of heredity and the guiding force in development, then it follows that the only way in which congenital variations can occur is by some variations in the germ plasm. If a child developed from germ plasm identical with that from which its parents developed, it would inherit identical characters; and if there are any congenital variations from its parents, they must be due to some variations in the germ plasm. In other words, in order to explain congenital variations we must account for variations in the germ plasm. Now, there are two methods by which we may suppose that these variations in the germ may arise. The first is by the direct influence upon the germ plasm of certain unknown external conditions. The life substance of organisms is always very unstable, and, as we have seen, acquired variations are caused by external influences directly affecting it. Now, the hereditary material is also life substance, and it is plainly a possibility for us to imagine that this germ material is also subject to influences from the conditions surrounding it. That such variations do occur appears to be hardly doubtful, although we do not know what sort of influences can produce them. If the germ plasm is wholly stored within the reproductive gland, it is certainly in a position to be only slightly affected by surrounding conditions which affect the animal. We can readily understand that the use of an organ like the arm will affect it in such a way as to produce changes in its protoplasm, but we can hardly imagine that such use of the arm would produce any change in the hereditary substance which is stored in the reproductive organs. External conditions may thus readily affect the body, but not so readily the germ material. Even if such material is distributed more or less over the body instead of being confined to the reproductive glands, as some believe, the difficulty is hardly lessened. This difficulty of understanding how the germ plasm can be affected by external conditions has led one school of biologists to deny that it is subject to any variation by external conditions, and hence that all modification of the germ plasm must come from some other source. Probably no one, however, holds this position to-day, and it is the general belief that the germ plasm may be to some slight extent modified by external conditions. Of course, if such variations do occur in the germ plasm they will become congenital variations of the next generation, since the next generation is the unfolding of the germ plasm. The second method by which the variations of germ plasm may arise is apparently of more importance. It is based upon the fact that, with all higher animals and plants at least, each individual has two parents instead of one. In our study of cells we have seen that the machinery of the cell is such that it requires in the ordinary process of reproduction the union of germinal material from two different individuals to produce a cell which can develop into a new individual. As we have seen, the egg gets rid of half its chromosomes in order to receive an equal number from a male parent; and thus the fertilized egg contains chromosomes, and hence hereditary material, from two different individuals. Now, this sexual reproduction occurs very widely in the organic world. Among some of the lowest forms of unicellular organisms it is not known, but in most others some form of such union is universal. Now, here is plainly an abundant opportunity for congenital variations; for it is seen that each individual does not come from germ material identical with that from which either parent came, but from some of this material mixed with a similar amount from a different parent. Now, the two parents are never exactly alike, and hence the germ plasm which each contributes to the offspring will not be exactly alike. The offspring will thus be the result of the unfolding of a bit of germ plasm which will be different from that from which either of its parents developed, and these differences will result in congenital variations. Sexual reproduction thus results in congenital variations; and if congenital variations are necessary for the evolution of the living machine—and we shall soon see reason for believing that they are—we find that sexual reproduction is a device adopted for bringing out such congenital variations. Inheritance of Variations.—The reason why congenital variations are needed for the evolution of the living machine is clear enough. Evanescent variations can have no effect upon this machine, for they would disappear with the individual in which they appeared. In order that they should have any influence in the process of machine building they must be permanent ones; or, in other words, they must be inherited from generation to generation. Only as such variations are transmitted by heredity can they be added to the structure of the developing machine. Therefore we must ask whether the variations are inherited. In regard to the congenital variations there can be no difficulty. The very fact that they are congenital shows us that they have been produced by variations in the germ plasm, and as such they must be transmitted, not only to the next generation, but to all following generations, until the germ plasm becomes again modified. This germ plasm is handed on from generation to generation with all its variations, and hence the variations will be added permanently to the machine. Congenital variations are thus a means for permanently modifying the organism, and by their agency must we in large measure believe that evolution through the ages has taken place. With the acquired variations the matter stands quite differently. We can readily understand how influences surrounding an animal may affect its organs. The increase in the size of the muscles of the blacksmith's arm by use we understand readily enough. But with our understanding of the machinery of heredity we can not see how such an effect can extend to the next generation. It is only the organ directly affected that is modified by external conditions. Acquired variations will appear in the part of the body influenced by the changed conditions. But the germ plasm within the reproductive glands is not, so far as we can see, subject to the influence of an increased use, for example, in the arm muscles. The germ material is derived from the parents, and, if it is simply stored in the individual, how could an acquired variation affect it? If an individual lose a limb his offspring will not be without a corresponding limb, for the hereditary material is in the reproductive organs, and it is impossible to believe that the loss of the limb can remove from the hereditary material in the reproductive glands just that part of the germ plasm which was designed for the production of the limb. So, too, if the germ plasm is simply stored in the individual, it is impossible to conceive any way that it can be affected by the conditions around the individual in such a way as to explain the inheritance of acquired variations. If acquired variations do not affect the germ plasm they cannot be inherited, and if the germ plasm is only a bit of protoplasmic substance handed down from generation to generation, we can not believe that acquired variations can influence it. From such considerations as these have arisen two quite different views among biologists; and, while it is not our purpose to deal with disputed points, these views are so essential to our subject that they must be briefly referred to. One class of biologists adhere closely to the view already outlined, and insist for this reason that acquired variations can not under any conditions be inherited. They insist that all inherited variations are congenital, and due therefore to direct variations in the germ plasm, and that all instances of seeming inheritance of acquired variations are capable of other explanation. The other school is equally insistent that there are abundant instances of the inheritance of acquired characters, claiming that these proofs are so strong as to demand their acceptance. Hence this class of biologists insist that the explanation of heredity given as a simple handing down from generation to generation of a germ plasm is not complete, and that while it is doubtless the foundation of heredity, it must be modified in some way so as to admit of the inheritance of acquired characters. There is no question that has excited such a wide interest in the biological world during the last fifteen years as this one of the inheritance of acquired characters. Until about 1884 the question was not seriously raised. Heredity was known to be a fact, and it was believed that while congenital characters are more commonly inherited, acquired characters may also frequently be handed down from generation to generation. The facts which we have noted of the continuity of germ plasm have during the last fifteen years led many biologists to deny the possibility of the latter. The debate which arose has continued vigorously, and can not be regarded as settled at the present time. One result of this debate is clear. It has been shown beyond question that while the inheritance of congenital characters is the rule, the inheritance of acquired characters is at all events unusual. At the present time many naturalists would be inclined to think that the balance of evidence indicates that under certain conditions certain