The Origin of Species by means of Natural Selection (6th ed) by Charles Darwin (ebook reader below 3000 .TXT) 📕

ways excessively intricate. The geological record, at all times imperfect, does not extend far enough back to show with unmistakable clearness that within the known history of the world organisation has largely advanced. Even at the present day, looking to members of the same class, naturalists are not unanimous which forms ought to be ranked as highest: thus, some look at the selaceans or sharks, from their approach in some important points of structure to reptiles, as the highest fish; others look at the teleosteans as the highest. The ganoids stand intermediate between the selaceans and teleosteans; the latter at the present day are largely preponderant in number; but formerly selaceans and ganoids alone existed; and in this case, according to the standard of highness chosen, so will it be said that fishes have advanced or retrograded in organisation. To attempt to compare members of distinct types in the scale of highness seems hopeless; who will decide whether a cuttle-fish be higher than a bee—that insect which the great Von Baer believed to be “in fact more highly organised than a fish, although upon another type?” In the complex struggle for life it is quite credible that crustaceans, not very high in their own class, might beat cephalopods, the highest molluscs; and such crustaceans, though not highly developed, would stand very high in the scale of invertebrate animals, if judged by the most decisive of all trials—the law of battle. Beside these inherent difficulties in deciding which forms are the most advanced in organisation, we ought not solely to compare the highest members of a class at any two periods—though undoubtedly this is one and perhaps the most important element in striking a balance—but we ought to compare all the members, high and low, at two periods. At an ancient epoch the highest and lowest molluscoidal animals, namely, cephalopods and brachiopods, swarmed in numbers; at the present time both groups are greatly reduced, while others, intermediate in organisation, have largely increased; consequently some naturalists maintain that molluscs were formerly more highly developed than at present; but a stronger case can be made out on the opposite side, by considering the vast reduction of brachiopods, and the fact that our existing cephalopods, though few in number, are more highly organised than their ancient representatives. We ought also to compare the relative proportional numbers, at any two periods, of the high and low classes throughout the world: if, for instance, at the present day fifty thousand kinds of vertebrate animals exist, and if we knew that at some former period only ten thousand kinds existed, we ought to look at this increase in number in the highest class, which implies a great displacement of lower forms, as a decided advance in the organisation of the world. We thus see how hopelessly difficult it is to compare with perfect fairness, under such extremely complex relations, the standard of organisation of the imperfectly-known faunas of successive periods.

We shall appreciate this difficulty more clearly by looking to certain existing faunas and floras. From the extraordinary manner in which European productions have recently spread over New Zealand, and have seized on places which must have been previously occupied by the indigenes, we must believe, that if all the animals and plants of Great Britain were set free in New Zealand, a multitude of British forms would in the course of time become thoroughly naturalized there, and would exterminate many of the natives. On the other hand, from the fact that hardly a single inhabitant of the southern hemisphere has become wild in any part of Europe, we may well doubt whether, if all the productions of New Zealand were set free in Great Britain, any considerable number would be enabled to seize on places now occupied by our native plants and animals. Under this point of view, the productions of Great Britain stand much higher in the scale than those of New Zealand. Yet the most skilful naturalist, from an examination of the species of the two countries, could not have foreseen this result.

Agassiz and several other highly competent judges insist that ancient animals resemble to a certain extent the embryos of recent animals belonging to the same classes; and that the geological succession of extinct forms is nearly parallel with the embryological development of existing forms. This view accords admirably well with our theory. In a future chapter I shall attempt to show that the adult differs from its embryo, owing to variations having supervened at a not early age, and having been inherited at a corresponding age. This process, whilst it leaves the embryo almost unaltered, continually adds, in the course of successive generations, more and more difference to the adult. Thus the embryo comes to be left as a sort of picture, preserved by nature, of the former and less modified condition of the species. This view may be true, and yet may never be capable of proof. Seeing, for instance, that the oldest known mammals, reptiles, and fishes strictly belong to their proper classes, though some of these old forms are in a slight degree less distinct from each other than are the typical members of the same groups at the present day, it would be vain to look for animals having the common embryological character of the Vertebrata, until beds rich in fossils are discovered far beneath the lowest Cambrian strata—a discovery of which the chance is small.

ON THE SUCCESSION OF THE SAME TYPES WITHIN THE SAME AREAS, DURING THE LATER

TERTIARY PERIODS.

Mr. Clift many years ago showed that the fossil mammals from the Australian caves were closely allied to the living marsupials of that continent. In South America, a similar relationship is manifest, even to an uneducated eye, in the gigantic pieces of armour, like those of the armadillo, found in several parts of La Plata; and Professor Owen has shown in the most striking manner that most of the fossil mammals, buried there in such numbers, are related to South American types. This relationship is even more clearly seen in the wonderful collection of fossil bones made by MM.

Lund and Clausen in the caves of Brazil. I was so much impressed with these facts that I strongly insisted, in 1839 and 1845, on this “law of the succession of types,”—on “this wonderful relationship in the same continent between the dead and the living.” Professor Owen has subsequently extended the same generalisation to the mammals of the Old World. We see the same law in this author’s restorations of the extinct and gigantic birds of New Zealand. We see it also in the birds of the caves of Brazil. Mr. Woodward has shown that the same law holds good with sea-shells, but, from the wide distribution of most molluscs, it is not well displayed by them. Other cases could be added, as the relation between the extinct and living land-shells of Madeira; and between the extinct and living brackish water-shells of the Aralo-Caspian Sea.

Now, what does this remarkable law of the succession of the same types within the same areas mean? He would be a bold man who, after comparing the present climate of Australia and of parts of South America, under the same latitude, would attempt to account, on the one hand through dissimilar physical conditions, for the dissimilarity of the inhabitants of these two continents; and, on the other hand through similarity of conditions, for the uniformity of the same types in each continent during the later tertiary periods. Nor can it be pretended that it is an immutable law that marsupials should have been chiefly or solely produced in Australia; or that Edentata and other American types should have been solely produced in South America. For we know that Europe in ancient times was peopled by numerous marsupials; and I have shown in the publications above alluded to, that in America the law of distribution of terrestrial mammals was formerly different from what it now is. North America formerly partook strongly of the present character of the southern half of the continent; and the southern half was formerly more closely allied, than it is at present, to the northern half. In a similar manner we know, from Falconer and Cautley’s discoveries, that Northern India was formerly more closely related in its mammals to Africa than it is at the present time. Analogous facts could be given in relation to the distribution of marine animals.

On the theory of descent with modification, the great law of the long enduring, but not immutable, succession of the same types within the same areas, is at once explained; for the inhabitants of each quarter of the world will obviously tend to leave in that quarter, during the next succeeding period of time, closely allied though in some degree modified descendants. If the inhabitants of one continent formerly differed greatly from those of another continent, so will their modified descendants still differ in nearly the same manner and degree. But after very long intervals of time, and after great geographical changes, permitting much intermigration, the feebler will yield to the more dominant forms, and there will be nothing immutable in the distribution of organic beings.

It may be asked in ridicule whether I suppose that the megatherium and other allied huge monsters, which formerly lived in South America, have left behind them the sloth, armadillo, and anteater, as their degenerate descendants. This cannot for an instant be admitted. These huge animals have become wholly extinct, and have left no progeny. But in the caves of Brazil there are many extinct species which are closely allied in size and in all other characters to the species still living in South America; and some of these fossils may have been the actual progenitors of the living species. It must not be forgotten that, on our theory, all the species of the same genus are the descendants of some one species; so that, if six genera, each having eight species, be found in one geological formation, and in a succeeding formation there be six other allied or representative genera, each with the same number of species, then we may conclude that generally only one species of each of the older genera has left modified descendants, which constitute the new genera containing the several species; the other seven species of each old genus having died out and left no progeny. Or, and this will be a far commoner case, two or three species in two or three alone of the six older genera will be the parents of the new genera: the other species and the other old genera having become utterly extinct. In failing orders, with the genera and species decreasing in numbers as is the case with the Edentata of South America, still fewer genera and species will leave modified blood-descendants.

SUMMARY OF THE PRECEDING AND PRESENT CHAPTERS.

I have attempted to show that the geological record is extremely imperfect; that only a small portion of the globe has been geologically explored with care; that only certain classes of organic beings have been largely preserved in a fossil state; that the number both of specimens and of species, preserved in our museums, is absolutely as nothing compared with the number of generations which must have passed away even during a single formation; that, owing to subsidence being almost necessary for the accumulation of deposits rich in fossil species of many kinds, and thick enough to outlast future degradation, great intervals of time must have elapsed between most of our successive formations; that there has probably been more extinction during the periods of subsidence, and more variation during the periods of elevation, and during the latter the record will have been least perfectly kept; that each single formation has not been continuously deposited; that the duration of each formation is probably short compared with the average duration of specific forms; that migration has played an important part in the