The Story of Evolution

by Joseph McCabe

In view of the innumerable and infinitely varied forms of "instinct" in the insect world we must restrict ourselves to a single illustration—say, the social life of the ants and the bees. We are not without indications of the gradual development of this social life. In the case of the ant we find that the Tertiary specimens—and about a hundred species are found in Switzerland alone, whereas there are only fifty species in the whole of Europe to-day—all have wings and are, apparently, of the two sexes, not neutral. This seems to indicate that even in the mid-Tertiary some millions of years after the first appearance of the ant, the social life which we admire in the ants today had not yet been developed. The Tertiary bees, on the other hand, are said to show some traces of the division of labour (and modification of structure) which make the bees so interesting; but in this case the living bees, rising from a solitary life through increasing stages of social co-operation, give us some idea of the gradual development of this remarkable citizenship.

It seems to me that the great selective agency which has brought about these, and many other remarkable activities of the insects (such as the storing of food with their eggs by wasps), was probably the occurrence of periods of cold, and especially the beginning of a winter season in the Cretaceous or Tertiary age. In the periods of luxuriant life (the Carboniferous, the Jurassic, or the Oligocene), when insects swarmed and varied in every direction, some would vary in the direction of a more effective placing of the eggs; and the supervening period of cold and scarcity would favour them. When a regular winter season set in, this tendency would be enormously increased. It is a parallel case to the evolution of the birds and mammals from the reptiles. Those that varied most in the direction of care for the egg and the young would have the largest share in the next generation. When we further reflect that since the Tertiary the insect world has passed through the drastic disturbance of the climate in the great Ice-Age, we seem to have an illuminating clue to one of the most remarkable features of higher insect life.

The origin of the colour marks' and patterns on so many of the higher insects, with which we may join the origin of the stick-insects, leaf-insects, etc., is a subject of lively controversy in science to-day. The protective value of the appearance of insects which look almost exactly like dried twigs or decaying leaves, and of an arrangement of the colours of the wings of butterflies which makes them almost invisible when at rest, is so obvious that natural selection was confidently invoked to explain them. In other cases certain colours or marks seemed to have a value as "warning colours," advertising the nauseousness of their possessors to the bird, which had learned to recognise them; in other cases these colours and marks seemed to be borrowed by palatable species, whose unconscious "mimicry" led to their survival; in other cases, again, the patterns and spots were regarded as "recognition marks," by which the male could find his mate.

Science is just now passing through a phase of acute criticism—as the reader will have realised by this time—and many of the positions confidently adopted in the earlier constructive stage are challenged. This applies to the protective colours, warning colours, mimicry, etc., of insects. Probably some of the affirmations of the older generation of evolutionists were too rigid and extensive; and probably the denials of the new generation are equally exaggerated. When all sound criticism has been met, there remains a vast amount of protective colouring, shaping, and marking in the insect world of which natural selection gives us the one plausible explanation. But the doctrine of natural selection does not mean that every feature of an animal shall have a certain utility. It will destroy animals with injurious variations and favour animals with useful variations; but there may be a large amount of variation, especially in colour, to which it is quite indifferent. In this way much colour-marking may develop, either from ordinary embryonic variations or (as experiment on butterflies shows) from the direct influence of surroundings which has no vital significance. In this way, too, small variations of no selective value may gradually increase until they chance to have a value to the animal. [*]

* For a strong statement of the new critical position see
Dewar and Finn's "Making of Species," 1909, ch. vi.

The origin of the metamorphosis, or pupa-stage, of the higher insects, with all its wonderful protective devices, is so obscure and controverted that we must pass over it. Some authorities think that the sleep-stage has been evolved for the protection of the helpless transforming insect; some believe that it occurs because movement would be injurious to the insect in that stage; some say that the muscular system is actually dissolved in its connections; and some recent experts suggest that it is a reminiscence of the fact that the ancestors of the metamorphosing insects were addicted to internal parasitism in their youth. It is one of the problems of the future. At present we have no fossil pupa-remains (though we have one caterpillar) to guide us. We must leave these fascinating but difficult problems of insect life, and glance at the evolution of the birds.

To the student of nature whose interest is confined to one branch of science the record of life is a mysterious Succession of waves. A comprehensive view of nature, living and non-living, past and present, discovers scores of illuminating connections, and even sees at times the inevitable sequence of events. Thus if the rise of the Angiospermous vegetation on the ruins of the Mesozoic world is understood in the light of geological and climatic changes, and the consequent deploying of the insects, especially the suctorial insects, is a natural result, the simultaneous triumph of the birds is not unintelligible. The grains and fruits of the Angiosperms and the vast swarms of insects provided immense stores of food; the annihilation of the Pterosaurs left a whole stratum of the earth free for their occupation.

We saw that a primitive bird, with very striking reptilian features, was found in the Jurassic rocks, suggesting very clearly the evolution of the bird from the reptile in the cold of the Permian or Triassic period. In the Cretaceous we found the birds distributed in a number of genera, but of two leading types. The Ichthyornis type was a tern-like flying bird, with socketed teeth and biconcave vertebrae like the reptile, but otherwise fully evolved into a bird. Its line is believed to survive in the gannets, cormorants, pelicans, and frigate-birds of to-day. The less numerous Hesperornis group were large and powerful divers. Then there is a blank in the record, representing the Cretaceous upheaval, and it unfortunately conceals the first great ramification of the bird world. When the light falls again on the Eocene period we find great numbers of our familiar types quite developed. Primitive types of gulls, herons, pelicans, quails, ibises, flamingoes, albatrosses, buzzards, hornbills, falcons, eagles, owls, plovers, and woodcocks are found in the Eocene beds; the Oligocene beds add parrots, trogons, cranes, marabouts, secretary-birds, grouse, swallows, and woodpeckers. We cannot suppose that every type has been preserved, but we see that our bird-world was virtually created in the early part of the Tertiary Era.

With these more or less familiar types were large ostrich-like survivors of the older order. In the bed of the sea which covered the site of London in the Eocene are found the remains of a toothed bird (Odontopteryx), though the teeth are merely sharp outgrowths of the edge of the bill. Another bird of the same period and region (Gastornis) stood about ten feet high, and must have looked something like a wading ostrich. Other large waders, even more ostrich-like in structure, lived in North America; and in Patagonia the remains have been found of a massive bird, about eight feet high, with a head larger than that of any living animal except the elephant, rhinoceros, and hippopotamus (Chamberlin).

The absence of early Eocene remains prevents us from tracing the lines of our vast and varied bird-kingdom to their Mesozoic beginnings. And when we appeal to the zoologist to supply the missing links of relationship, by a comparison of the structures of living birds, we receive only uncertain and very general suggestions. [*] He tells us that the ostrich-group (especially the emus and cassowaries) are one of the most primitive stocks of the bird world, and that the ancient Dinornis group and the recently extinct moas seem to be offshoots of that stock. The remaining many thousand species of Carinate birds (or flying birds with a keel [carina]-shaped breast-bone for the attachment of the flying muscles) are then gathered into two great branches, which are "traceable to a common stock" (Pycraft), and branch in their turn along the later lines of development. One of these lines—the pelicans, cormorants, etc.—seems to be a continuation of the Ichthyornis type of the Cretaceous, with the Odontopteryx as an Eocene offshoot; the divers, penguins, grebes, and petrels represent another ancient stock, which may be related to the Hesperornis group of the Cretaceous. Dr. Chalmers Mitchell thinks that the "screamers" of South America are the nearest representatives of the common ancestor of the keel-breasted birds. But even to give the broader divisions of the 19,000 species of living birds would be of little interest to the general reader.