Though most of my readers, I do not doubt, know how imperfect and erroneous a conception this is, yet I shall not, I think, be wasting time in stating what the Darwinian theory really is. In fact, it is so continuously misrepresented and misunderstood, that no opportunity should be lost of calling attention to its real character. Bit by bit, naturalists had succeeded in discovering the order of nature—so far that all the great facts of the universe, the constitution and movements of the heavenly bodies, the form of our earth, and all the peculiarities of its crust, had been successfully assigned to one set of causes—the properties of matter, which are set forth in what we know by the name of the “laws of physics and chemistry.” Whilst geologists, led by Lyell, had shown that the strata of the earth’s crust and its mountains, rivers, and seas were due to the long-continued operation of the very same general causes—the physico-chemical causes—which at this moment are in operation and are continuing their work of change, yet the living matter on the crust of the earth had to be excluded from the grand uniformity which was elsewhere complete.

The first hypothesis, then, which was present to Mr. Darwin’s mind, as it had been to that of other earlier naturalists, was this: “Have not all the varieties or species of living things (man, of course, included) been produced by the continuous operation of the same set of physico-chemical causes which alone we can discover, and which alone have been proved sufficient to produce everything else?” “If this be so,” Mr. Darwin must have argued (and here it was that he boldly stepped beyond the speculations of Lamarck and adopted the method by which Lyell had triumphantly established Geology as a science), “these causes must still be able to produce new forms, and are doing so wherever they have opportunity.” He had accordingly to bring the matter to the test of observation by seeking for some case of the production of new forms of plants, or of animals, by natural causes at the present day. Such cases he found in the production of new forms or varieties of plants and animals, by breeders. Breeders (the persons who make it their business to produce new varieties of flowers, of pigeons, of sheep, or what not) make use of two fundamental properties of living things in order to accomplish their purpose. These two properties are, firstly, that no two animals or plants, even when born of the same parents, are exactly alike; this is known as Variation: secondly, that an organism, as a rule, inherits, that is to say, is born with the peculiarities of its parents; this is known as Transmission, and is simply dependent on the fact that the offspring of any plant or animal is only a detached portion of the parent—a chip of the old block, as the saying is. The breeder selects from a number of specimens of a plant or animal a variety which comes nearest to the form he wishes to produce. Supposing he wished to produce a race of oxen with short horns, he would select from his herd bulls and cows with the shortest horns, and allow these only to breed; they would transmit their relatively short horns to their offspring, and from these again the cattle with the shortest horns would be selected by the breeder for propagation, and so on through several generations. In the end a very short-horned generation would be obtained, differing greatly in appearance from the cattle with which the breeder started.

Now we know of no facts which forbid us to suppose that could a breeder continue his operations indefinitely for any length of time—say for a few million years—he could convert the short-horned breed into a hornless breed; that he could go on and thicken the tail, could shorten the legs, get rid of the hind limbs altogether by a series of insensible gradations, and convert the race into forms like the Sirenia, or sea-cows. But if he could do this, you have only to give him a longer time still and there is no obstacle remaining to the conversion, by the same kind of process, of a polyp into a worm, or of a worm into a fish, or even of a monkey into a man.[3]

So far we have supposed the interference of a breeder who selects and determines the varieties which shall propagate themselves; so far we have not got a complete explanation, for we must find a substitute in nature for the human selection exercised by the breeder. The question arises, then, “Is there any necessary selective process in nature which could have operated through untold ages, and so have represented the selective action of the breeder, during an immense period of time?” Strangely enough, Mr. Darwin was led to the discovery of such a cause existing necessarily in the mechanical arrangements of nature, by reading the celebrated book of an English clergyman, the Rev. Mr. Malthus, On Population. On happening to read this book, Mr. Darwin himself tells us that the idea of “natural selection” flashed upon him. That idea is as follows. Not only among mankind, but far more largely among other kinds of animals and of plants, the number of offspring produced by every pair is immensely in excess of the available amount of the food appropriate to the particular species in question. Accordingly, there is necessarily a struggle for existence—a struggle among all those born for the possession of the small quantum of food. The result of this struggle is to pick out, or select, a few who survive and propagate the species, whilst the majority perish before reaching maturity. The fact that no two members of a species are alike has already been shown to be the starting-point which enables the breeder to make his selection. So, too, with natural selection in the struggle for existence; the fact that all the young born of one species are not exactly alike—but some larger, some smaller, some lighter, some darker, some short-legged, some big-eyed, some long-tongued, some sharp-toothed, and so on—furnishes the opportunity for a selection. Those varieties which are best fitted to obtain food and to baffle their competitors, gain the food and survive, the rest perish.

We have, then, to note that the hypothesis that there must be a selection—which was framed or deduced as a “test hypothesis” from the earlier hypothesis that species have arisen by the action of causes still competent to produce new forms—led Mr. Darwin to the discovery of this great cause—the “natural selection,” or “survival of the fittest,” in the struggle for existence. Just as the breeder can slowly change the proportions of the animals or plants on which he operates, so in inconceivably long periods of time has this struggling of varieties, and the consequent natural selection of the fittest, led to the production, from shapeless primitive living matter, of all the endless varieties of complicated plants and animals which now people the world. Countless varieties have died out, leaving only their modified descendants to puzzle the ingenuity of the biologist.

Of the tens and hundreds of thousands of intermediate forms we know nothing by direct observation. They have perished as better fitted forms ousted them in the never-ending conflict. But we feel sure that they once were in existence, and can infer what was their structure, and what were their peculiarities, by the study of the structure and attributes of their now living descendants.

If all the forms of life at present living are the modified offspring of a smaller number of ancestral forms which have died out, and if these again were the modified descendants produced by ordinary parentage of a single original living thing—then the whole series of forms that have ever lived could, if we had them before us, be arranged in the form of a great family-tree—the various branches presenting a perfect gradation of forms arranged one after another, leading down from the terminal twigs (which would represent the latest forms produced) to larger and larger branches, until the common trunk representing the original ancestor would be reached. Our actual means of observing the genealogical affinities of different kinds of animals and plants may be understood by a further use of the metaphor of a genealogical tree in shape like an elm or an oak. Suppose the genealogical tree completely written out—a perfect record—to be sunk in muddy water so that only its topmost branches and twigs are here and there visible—then you have a fair notion of the present condition of the great family of organisms. Only the topmost twigs remain visible, the rest of the great family-tree of living beings is hidden from view, submerged beneath the muddy waters of time. Naturalists have, however, undertaken to reconstruct this great genealogical tree. It is a main object now in the study both of zoology and of botany to find out what are the cousinships, what the exact genetic relationships of all the various species of plants and animals, and so to show, even to the minutest detail, in what particular ways physico-chemical causes have brought about and modified the forms of living things.

The task is not quite so difficult as the comparison to a submerged forest-tree would lead one to expect; at the same time it is more difficult than those who have boldly attempted it appear to believe. We have one great help in the carefully worked out systematic classification of animals and plants according to their structure. We are justified in assuming as a general law that animals or plants of like structure have descended from common ancestors—that is to say, that the same kind of organisation (especially where a number of elaborate details of structure are involved) has not been twice produced by natural selection. Thus we are entitled to conclude that all the animals which have a backbone and pharyngeal gill-slits combined—the Vertebrates, as we call them—have descended from a common parent; that all the animals with a muscular foot-like belly and lateral gill filaments, the Molluscs, have also had a common parent, and so on.

A classification according to structure goes then a long way towards mapping out the main lines of the family-tree of organisms. We are further assisted in the task by the fossil remains of extinct organisms which sometimes give to us the actual ancestors of forms now living. But the most remarkable aid to the correct building-up of the pedigree of animals at least (and the remarks which follow are confined to that division of the organic world), is afforded by the changes—the phases of development—which every animal exhibits in passing from the small shapeless egg to the adult condition. The aid which we here obtain depends on the following facts. Just as we suppose any one animal—say a dog—to have developed by slow change through an immense series of ancestors which become simpler and simpler as we recede into the past until we reach a small shapeless lump of living matter devoid of structure, so do we find actually as a matter of fact, which any one can see for himself, that every individual animal begins its individual life as a structureless particle which is thrown off from its parent, and is known as the egg-cell (Fig. 1). Gradually passing through a series of more and more elaborated conditions of structure, that egg grows into the adult dog. The changes which have taken countless ages in the one case, are accomplished in a few weeks in the other.

And now we have to note the important fact which makes this process of development so intensely interesting in relation to the pedigree of the animal kingdom. There is very strong reason to believe that it is a general law of transmission or inheritance, that structural characteristics appear in the growth of a young organism in the order in which those characteristics have been acquired by its ancestors. At first the egg of a dog represents (imperfectly, it is true,) in form and structure the earliest ancestors of the dog; a few days later it has the form and structure of somewhat later ancestors; later still the embryo dog resembles less remote ancestors; until at last it reaches the degree of elaboration proper to its immediate forefathers.