Part 4

Under the present limitations, it is impossible to give this subject the further discussion it deserves. It is not our purpose to review the origin of life in times past, and the origin of living matter from inorganic constituents, though the subject is one of the most important in the field of cosmic evolution. We must begin with the living organism; and how the first one arose must be of less importance to us than the knowledge of its mechanical constitution and of its mechanical operation. Of far greater value is the realization that a living creature is not an independent thing, but that, on the contrary, it must hold the closest possible relations with the world of materials and energies constituting its environment. We must again insist upon the importance of that mechanical adjustment to the conditions of life which is the universal characteristic of plants and animals. It is the history of these creatures and the origin of their adapted conditions that we are called upon to study. We must scrutinize the nature of to-day to see if we can find evidence that evolution is true, and if we can discern the forces which, acting upon the living mechanism as man has dealt with machines, might bring the various species of the present day to their modern forms.

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We have now learned that evolution means a common ancestry of living forms that have come to differ in the course of time; our common reason has shown us also that organisms are in a true sense complicated chemical mechanisms adapted to meet the conditions under which they must operate. We come now to the evidences offered by the organic world that evolution is true and that natural forces control its workings. Clearly the examination of the matter of fact is independent of the question of method. For just as the chemist may experiment with various substances to see if they will dissolve in water and not in alcohol before it is necessary or desirable for him to take up the further studies of the laws of solution, so reasonable grounds must be found for regarding evolution as true before passing to its method of accomplishment. And in the following discussions, the animals will be used almost exclusively, not because the study of plants fails to discover the same relations and principles, but because the better known animal series is more varied and extensive, and above all for the reason that the human organism arrays itself as the highest term of the animal series.

In the complete scheme adopted by most naturalists, five categories include the evidences bearing upon the fact of evolution. These are Classification; Comparative Anatomy, or Morphology; Comparative Development, or Embryology; Palaeontology, which comprises the facts provided by fossil relics of animals and plants of earlier geological ages; and Geographical Distribution_. Each of these divisions includes a descriptive and analytical series of facts, whose characteristics are "explained" or summarized in the form of the general principles of the respective divisions. Such principles, taken singly and collectively, constitute the evidences of evolution.

The particular nature of any one of these categories, evolved in the development of science practically in the order stated, depends upon the special quality of an animal which it selects for comparison and organization in connection with other similar facts, and also in its own mode of viewing its facts. One and the same organism may present materials for two, three, or even all five of these divisions, for they are by no means mutually exclusive. For example, a common cat possesses certain definite characteristics which give it a particular place when animals more or less like it are grouped or classified according to their degrees of resemblance and difference, in small genera of very similar forms, in larger tribes or orders of similar genera, and in more and more inclusive groups of these lesser divisions, such as the classes and phyla, or main branches of the animal tree. The common cat and its relatives are even earlier to be regarded as anatomical subjects, and their thorough analysis belongs to comparative anatomy,--a name which explains itself. The purpose of this department of natural history is to explore the entire range of animal forms and animal structures, and to determine the degree of resemblance and difference exhibited by the general characters of entire organisms and by the special qualities of their several systems of organs. It provides the data from which classification selects those which indicate mutual affinities with greatest precision and surety. But its materials are all the facts of animal structure, and because each and every known organism can be and must be studied, the investigator engaged in formulating the evidence of evolution has at his disposal all the data referring to the entire realm of animals. The data of embryology are likewise coextensive with the territory of the animal world, for we do not know of any form which does not change in the course of its life history. An adult cat is the product of a kitten which is itself the result of a long series of changes from earlier and simpler conditions. In so far as it deals with structures in the making, embryology is a study of anatomy, but as it is concerned primarily with all of the plastic remodeling which animals undergo during the production of their final forms, it is an independent study. Nevertheless we shall learn how intimate are the relations of these two divisions of zooelogy and how the evolutionary teachings of each body of fact support and supplement those of the other.

Palaeontology searches everywhere among the deposits of earlier ages for links to be fitted into their proper sequence of time, from which it constructs the chain of diverse types leading down to the species of the present. A cat of to-day is therefore viewed in an entirely different connection, as the last term in a consecutive series of species. Forming alliances with geology, and even with physics and chemistry, this department of zooelogy endeavors to reconstruct the past from what it learns to-day about organisms and the conditions under which they live. Finally the observations that cats of various kinds do not occur everywhere in the world, but only in certain more or less restricted localities, belong to the subject of geographical distribution, and illustrate its nature.

Our task is to learn the teachings of these several divisions by recalling and putting together what we know already about the commonest animals, or noting what can be observed in a visit to a zooelogical garden and aquarium. On account of the present limitations of time, the subject of classification will be combined with comparative anatomy; embryology will be taken up together with these subjects; palaeontology will be the main subject of the next discussion, which will include also a brief statement of the meaning of distribution. Then we will be prepared to study nature to see how evolution works.

THE STRUCTURE AND DEVELOPMENT OF ANIMALS AS EVIDENCE OF EVOLUTION

In order to become acquainted with the way the structures of animals provide evidences of evolution, it is by no means necessary to review the entire range of their forms, because research has discovered that the principles of relationship are universal among animals, and that any group of examples will demonstrate what is taught by comparative anatomy as a whole. The commonest creatures may serve us best in order that we may come to view evolution as a process that involves each and every living thing that we know, and not as something which belongs only to the remote and unknown past.

Let us begin with the common cat and the group of carnivora or flesh-eating animals to which it belongs. As we pass along the streets of the city, we will see many cats which differ in some details, though they resemble one another closely. While they vary somewhat in form, the range in this quality is not so noticeable as in the matter of color; some of them will be gray, some maltese, while others will be yellowish or black, and they will differ in the striped or spotted character of their coloration. We readily classify them all as "cats" in spite of their differences, because they are alike in so many ways that we have learned to associate as the distinguishing characteristics of these animals, and to label--"cat." The animals which we might see in a walk of several blocks may reasonably be regarded as offspring of the same pair of ancestors of a few years back, even though they are dissimilar. We all know that the kittens of one and the same litter vary: no two of them are ever exactly alike in color or disposition or voice or size, nor is any one identical with either of its parents, although it may be necessary to employ exact means of measuring them in order to demonstrate their variation. The fact of difference, then, is surely not inconsistent with even the closest ties of blood, and we do not need to go beyond the scope of daily observation to find that this is true in nature wherever we look.

Should we extend our observations so as to include the cats of Boston and Philadelphia and San Francisco, the animals would probably vary over a wider range, but they would be so similar to New York cats in their make-up that we would have no difficulty in regarding them and all the others of the United States as the descendants of a single pairs of ancestors, perhaps brought over in the "Mayflower." But why does this view seem justified? Because experience has taught us that the living things which resemble each other most closely are those which are most intimately bound by ties of blood and common heritage. It is "natural" for relatives to resemble one another more than persons not related, and for brothers and sisters to be more alike than cousins. Science does not refer to something outside everyday observation when it states that the possession by two animals of a great body of similar characters beneath their minor differences is an indication of their common ancestry.

Thus at the very outset our simple illustration establishes the most fundamental principle of comparative anatomy. Let us see how it works further. The Manx cat possesses an abbreviated tail, although in other respects it is practically the same as the familiar long-tailed form; the Angora and the Persian differ in having long hair. All of these animals are so much alike in so many respects, and so closely resemble the wild cats, that it is not unreasonable to regard them all as the descendants of the same original wild ancestors, and as the varying products of lines which branched out from the same stock in different directions and at different times. It is, in a word, their "cat-ness" which demonstrates their relationships. But common sense need not stop here. Guided by the facts of anatomical similarity, it convinces us that the dun-colored lion and puma, the striped tiger and the spotted leopard are simply cats of a larger growth whose remoter ancestry is one with that of the previously cited forms. Not until we explore and compare their several systems do we see how thoroughgoing is their uniformity in structural plan. And because reason justifies the view regarding the origin of domestic cats from wild ancestors, the evolution of all the various members of the cat tribe must be acknowledged. These animals exhibit a fundamental likeness, which, to employ a musical analogy, is the "theme" of "cat-ness," and they are so many variations of this theme.

The members of another tribe of the familiar carnivora display in their own way the same kind of evidences of relationship. The varieties of domesticated dogs differ far more widely among themselves than do common cats, yet their community of ancestry is demonstrated not only by structural resemblances, but also by the striking fact that forms as diverse as the greyhound and the fox terrier can be crossed. Here again there are wild forms, like the wolf and fox and jackal, so like the domesticated members of the dog tribe that we cannot fail to recognize a common "dog-ness" and its significance as evidence of the relationship in ancestry of all these animals.

Extending our survey so as to include the other tribes of flesh-eaters, identical principles come to light. One is compelled to regard the polar and grizzly bears as obvious blood relatives of the brown bear, and even of the raccoon of our own territory. Instead of walking upon their toes like cats and dogs, these animals plant their feet flat upon the ground; and they agree in many other details of structure that place them together, but somewhat apart from the other tribes. The many kinds of seals and walruses and sea elephants form still another group displaying similar bodily characters, but differing more widely from the "cat theme" in these differences. They are all true carnivora, but in the course of their evolution they have progressively changed so as to be adapted to life in the water where they find their prey. The bones of the limbs are the same in number and arrangement as in the cat's limb, but the seal's anterior appendage or "arm" has altered in numerous ways so as to become an efficient flexible paddle, while the hind limbs have shifted posteriorly, very much as screw propellers have evolved in the history of steam vessels. How the members of the seal tribe have changed in their descent from purely terrestrial ancestors is partly explained by such intermediate animals as the otter. This form is adapted by its slender body and partly webbed feet to a semi-aquatic life; it seems to have halted at a point beyond which all of the seals have passed in their evolution.

Each one of these tribes by itself provides conclusive evidence of evolution, for it is most reasonable to regard the "theme" in every case as a product of common inheritance, while the variations of any theme are best understood as the results of adaptive changes in various directions. But the examples have disclosed a larger relation and a principle of wider scope, as indeed the assignment of all these tribes to the single natural group of the carnivora implies. These tribes are put together because comparative anatomy finds that the common characters of all cats are fundamentally like those of all dogs and bears and seals, and in these common qualities the carnivora differ from all other mammalia. Does this mean that the branches which bear respectively the various members of the several tribes are outgrowths of a single limb of the evolving animal tree? Science does not hesitate to give an affirmative answer, because, as in the case of the similar but varying domestic cats, no other explanation of tribal resemblance in structure seems so reasonable and natural.

So far the examples have been taken from one order of the highest class of backboned animals, called mammalia. When our survey is extended to other divisions of this class, additional laws of organic relationship are discovered. If in a series of evolving generations the line of modification proceeding from a terrestrial animal like a cat to semi-aquatic and marine types substantially like an otter and a seal should be carried further, it will inevitably lead to forms possessing characters such as those displayed by whales and the related porpoises, dolphins, and narwhals of the order cetacea. In their make-up all of these animals clearly possess the general characteristics of mammals, and they constitute collectively another limb which has sprung from the same stock as the carnivora, although at an earlier time. This we believe because of their plan of body and because their peculiar organization fits them even more perfectly than the seals for aquatic existence that is their only possible mode of life. In the case of the whales the bony framework of the fore limb is again like that of the cat's leg, although the whole structure is a flexible finlike paddle. The hind limb has disappeared as an efficient organ, but the significant fact is that small rudiments of hind limbs are present just where corresponding structures are placed in the seal. These vestiges cannot be reasonably accounted for, unless they are the degenerate hinder limbs of a remote four-footed ancestor. Furthermore the unborn whale possesses a complete coat of hair, which is afterwards replaced by blubber; but hair is a thatchlike coat to shed rain, as the way the hairs lie on a terrestrial mammal indicates. We are therefore forced to conclude that whales have originated from four-footed animals walking about on land, because no opposed explanation gives so reasonable an interpretation of the observed facts.

Another group of familiar animals materially reinforces the results already established. After what has been said, it will not be difficult to perceive the meaning of the resemblances among mice of the house and field, and of rats and rabbits and squirrels. All of them possess heavy curved gnawing teeth, or incisors, and lack the flesh-tearing or canine teeth. They agree in many other respects which distinguish them as a separate natural order of the mammals called the rodentia. Again we find a highly aberrant form in the flying squirrel, which leads toward an order with another plan of body. This animal is a true rodent, which lengthens its leap from branch to branch by means of a fold of skin stretching between its fore and its hind limbs. It is an animated aeroplane, and it shows in part how bats have originated. The wing of a bat is an elastic membrane stretching not only between the two legs of one side, but also between the greatly lengthened "fingers" of the fore limb. But the bones of arm, wrist, and fingers are almost precisely the same in number and relation as in walking forms. The fact that this peculiar wing adheres to a plan belonging to the anterior legs of walking or climbing types has no reasonable explanation save that of evolution.

The well-known group of hoofed animals, including horses and cattle, is also valuable for our present purposes, as well as in a later connection when the evidence of fossils is described. The elephant possesses five toes armed with well-developed nails or hoofs. A tapir has four or three toes, and it would seem that its ancestor had had five toes, of which one or two had been lost. A rhinoceros possesses three toes, and its foot is constructed internally like the elephant's with the outer elements absent. The horse comes last with one large toe and hoof, but on either side of the main bones of this digit are vestiges of what must have been toes in its ancestors. Among the even-toed forms the hippopotamus has four which reach the ground, with a vestige of a fifth, so this animal has apparently descended from a typical mammal with the full number along a different line from that taken by the odd-toed forms. A pig has a cloven hoof, made up of what we may call the third and fourth members of a series of five digits, but the second and fifth fingers and toes are present, though they are withdrawn from the ground so as to be no longer functional; this animal seems to have proceeded further along the same line taken by the hippopotamus. A deer, with still smaller rudiments at the sides of its double foot, leads in the comparative series to the camel with a cloven hoof devoid of any such relics.

We must pass with only brief mention the lower orders of mammalia, like the insect-eating forms to which armadillos and ant-bears belong. Of greater interest are the pouched mammals like the kangaroo and opossums, which live almost exclusively in the Australian realm. The kangaroo is endowed with a head somewhat like that of a goat, and well-developed hind legs that enable it to make leaps of astonishing length. Some of its relatives, such as the bandicoot, are like rats, or like bears, as in the case of the wombat. The Tasmanian wolf is another true marsupial, even though divergent adaptation has brought it to resemble the carnivora of the dog tribe in general appearance and in special structures like the teeth. Finally at the very bottom of the mammalian scale are two small forms living in the Australian faunal region. The duckbill or Ornithorhynchus is the better known animal, with its close fur, webbed feet, and flattened ducklike beak, while its only other near relative, the Echidna, is somewhat similar to the spiny hedgehog in external appearance. A unique peculiarity of these two forms is that they produce eggs much like those of reptiles and birds, and this fact, together with others of a structural nature, brings the whole group of mammals near to the lower classes of the Vertebrata.

Looking back on the several orders of mammals, it will be seen that the last mentioned are much less differentiated or specialized in their general organization. Above the level of the egg-layers and the pouched mammals, the higher orders branch out in different directions and reach up to various levels of the scale of animal organization.

The foregoing structural evidences of organic transformation in the past histories of cats and seals and whales insistently recall the analogies of the locomotive and the ship employed at the outset. All these animals, like the mechanical examples, have come to differ in their derivation from the same original parents, and their lines of descent have diverged so as to fit the products of evolutionary modification to diverse circumstances. Even the vestigial organs of animals have their counterparts in the machines. The cowcatcher was a large and important structure in the early days of railroading, but it has become relatively useless with the decrease of grade crossings and the construction of more complete lines of fence. The structure still persists, sometimes in a greatly reduced form. Even more obvious is the change of structure in the case of masts of vessels, which originally bore the sails for propelling the ship. When steam engines were employed to give motive power, masts did not disappear. They now provide the derrick supports of trading steamers; in battleships their function is changed to that of fighting tops and signal yards. Even the poles carried by canal boats to bear windmills must be regarded as the reduced vestiges of masts originally constructed to carry sails; and their adaptive evolution, like that of countless structures in animals, has been accomplished by degeneration.

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The birds are another class of backboned animals which exhibit identical principles of relationship. A heron has long legs and wide-spreading toes, which keep its body out of the water as it stalks about the marshes where it seeks its food; its bill is a long slender pincers. Compare it with an eagle; the latter has a short and heavily hooked beak to tear flesh, while its stout legs bear strongly curved talons to hold its struggling prey. Swimming birds like the swan and duck and loon possess feet which are constructed in general like those of the former examples, but they are webbed and shortened to serve as paddles. In the penguin we find a counterpart of the seal among mammals; its feathers are much reduced and its fore limbs are no longer wings enabling the animal to fly, but they are paddles which it uses when it swims in pursuit of fish. Finally the ostrich and wingless bird of New Zealand--the Apteryx--have wings that are useless vestiges, which, in the latter case, are hidden under the brushlike feathers covering the body. It is unnecessary to add more examples, for even these few illustrations establish exactly the same principles of relationship and evidences of evolution that are to be found in the series of mammalia.

Reptiles also are grouped, like the mammals and birds, as variations about a central theme. An ordinary lizard is perhaps the nearest in form to the remote ancestor from which all have sprung. Some lizards are long and very slender, with all four limbs of greatly reduced size. Others, which are still true lizards, have lost the hind limbs, or even all the legs, as in the "blind worms" of England. One step more, and an animal which has progressed further along a similar line of descent would be a snake. Just as whales as a group are derivable from forms which resemble types belonging to another order, so snakes as an order are to be regarded as more radically altered derivatives of some four-footed lizardlike creature. Alligators are very much like lizards in general form, and their order is a diverging branch from the same limb. Finally the evolution of turtles from the same ancestors is intelligible if we begin with a short stout animal like the so-called "horned toad" of Arizona, and proceed to the soft-shelled tortoise of the Mississippi River system; the establishment of a bony armor completes the evolution of the familiar and more characteristic turtle.

Frogs and salamanders constitute another lower class, called the amphibia, whose members are gilled during the earlier stages of development. An adult frog is essentially a salamander without a tail and with highly developed hinder limbs. The salamanders differ as regards the number of fishlike gill clefts that they all possess in their young stages, but which disappear entirely or in part during later life. In comparison with the lizard as a typical reptile, a salamander is more primitive in all of its inner organic systems, while in its nearly continuous body, with head and tail gradually merging into the trunk, it also displays a somewhat simpler form of body.

The fishes are the lowest among the common vertebrates, and they offer an abundance of independent testimony as to the truth of the principles of comparative anatomy. The common shark is perhaps the most fundamental form, with a hull-like body undivided into head, trunk, and tail, and from it have originated such peculiar variations as the hammerhead and skate. Among fishes with true bones, a cod or trout is the most typical in general features. Without ceasing to be true bony fishes, the trunk-fish and cow-fish are adapted by their peculiar characters of spine and armor plate to repel many enemies. The puff fish can take in a great amount of water, when disturbed, so as to become too large to be swallowed by some of its foes, illustrating another adaptive modification for self-defense. The wonderful colors and color patterns of the tropical fish of the reef, or of the open water forms like the mouse-fish of the Sargossa Sea, often render them more or less completely hidden from the foraging enemy. A flounder looks like a fish which was originally symmetrical, but which had come to lie flat on its side upon the bottom, whereupon the eye underneath had left its original place to appear on the upper surface. The difficult and unusual conditions of deep-sea existence have been met by fishes in two ways; some forms possess luminous frilled and weedlike fins, which lure their prey to within easy reach of their jaws, while others have enormous eyes, so as to make use of all possible rays of light in their pursuit of food organisms. But all of these diverse forms are true fishes, possessing a common heritage of structure which demonstrates their unity of origin.

The brief review of backboned animals has shown how comprehensive are the principles of relationship. The families and tribes of each order, such as the carnivora, are like branches arising from a single limb; the orders in their turn exhibit common qualities of structure which mean that they have grown from the same antecedents, while even the larger divisions or classes of mammals, birds, reptiles, amphibia, and fishes, possess a deep underlying theme whose dominant motif is the backbone, which proves their ultimate unity in ancestry. The greater and lesser branches have reached different levels, for the fish is clearly simpler in its make-up than the highly specialized bird. But the great fact is that structural evidences demonstrating the reality of genealogical affinities are displayed by the entire series of vertebrates; although they differ much or little in many or fewer respects they have one and the same ground-plan.

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