Darwin and Modern Science Part 16

In addition to the main stem of equine descent, briefly considered in the foregoing paragraphs, several side-branches were given off at successive levels of the stem. Most of these branches were short-lived, but some of them flourished for a considerable period and ramified into many species.

Apparently related to the horses and derived from the same root-stock is the family of the Palaeotheres, confined to the Eocene and Oligocene of Europe, dying out without descendants. In the earlier attempts to work out the history of the horses, as in the famous essay of Kowalevsky ("Sur l'Anchitherium aurelianense Cuv. et sur l'histoire paleontologique des Chevaux", "Mem. de l'Acad. Imp. des Sc. de St Petersbourg", XX. no.

5, 1873.), the Palaeotheres were placed in the direct line, because the number of adequately known Eocene mammals was then so small, that Cuvier's types were forced into various incongruous positions, to serve as ancestors for unrelated series.

The American family of the t.i.tanotheres may also be distantly related to the horses, but pa.s.sed through an entirely different course of development. From the lower Eocene to the lower sub-stage of the middle Oligocene the series is complete, beginning with small and rather lightly built animals. Gradually the stature and ma.s.siveness increase, a transverse pair of nasal horns make their appearance and, as these increase in size, the canine tusks and incisors diminish correspondingly. Already in the oldest known genus the number of digits had been reduced to four in the fore-foot and three in the hind, but there the reduction stops, for the increasing body-weight made necessary the development of broad and heavy feet. The final members of the series comprise only large, almost elephantine animals, with immensely developed and very various nasal horns, huge and ma.s.sive heads, and altogether a grotesque appearance. The growth of the brain did not at all keep pace with the increase of the head and body, and the ludicrously small brain may will have been one of the factors which determined the startlingly sudden disappearance and extinction of the group.

Less completely known, but of unusual interest, is the genealogy of the rhinoceros family, which probably, though not certainly, was likewise of American origin. The group in North America at least, comprised three divisions, or sub-families, of very different proportions, appearance and habits, representing three divergent lines from the same stem.

Though the relations.h.i.+p between the three lines seems hardly open to question, yet the form ancestral to all of them has not yet been identified. This is because of our still very incomplete knowledge of several perissodactyl genera of the Eocene, any one of which may eventually prove to be the ancestor sought for.

The first sub-family is the entirely extinct group of Hyracodonts, which may be traced in successive modifications through the upper Eocene, lower and middle Oligocene, then disappearing altogether. As yet, the hyracodonts have been found only in North America, and the last genus of the series, Hyracodon, was a cursorial animal. Very briefly stated, the modifications consist in a gradual increase in size, with greater slenderness of proportions, accompanied by elongation of the neck, limbs, and feet, which become tridactyl and very narrow. The grinding teeth have a.s.sumed the rhinoceros-like pattern and the premolars resemble the molars in form; on the other hand, the front teeth, incisors and canines, have become very small and are useless as weapons.

As the animal had no horns, it was quite defenceless and must have found its safety in its swift running, for Hyracodon displays many superficial resemblances to the contemporary Oligocene horses, and was evidently adapted for speed. It may well have been the compet.i.tion of the horses which led to the extinction of these cursorial rhinoceroses.

The second sub-family, that of the Amynodonts, followed a totally different course of development, becoming short-legged and short-footed, ma.s.sive animals, the proportions of which suggest aquatic habits; they retained four digits in the front foot. The animal was well provided with weapons in the large canine tusks, but was without horns. Some members of this group extended their range to the Old World, but they all died out in the middle Oligocene, leaving no successors.

The sub-family of the true rhinoceroses cannot yet be certainly traced farther back than to the base of the middle Oligocene, though some fragmentary remains found in the lower Oligocene are probably also referable to it. The most ancient and most primitive member of this series yet discovered, the genus Trigonias, is unmistakably a rhinoceros, yet much less ma.s.sive, having more the proportions of a tapir; it had four toes in the front foot, three in the hind, and had a full complement of teeth, except for the lower canines, though the upper canines are about to disappear, and the peculiar modification of the incisors, characteristic of the true rhinoceroses, is already apparent; the skull is hornless. Representatives of this sub-family continue through the Oligocene and Miocene of North America, becoming rare and localised in the Pliocene and then disappearing altogether. In the Old World, on the other hand, where the line appeared almost as early as it did in America, this group underwent a great expansion and ramification, giving rise not only to the Asiatic and African forms, but also to several extinct series.

Turning now to the Artiodactyla, we find still another group of mammals, that of the camels and llamas, which has long vanished from North America, yet took its rise and ran the greater part of its course in that continent. From the lower Eocene onward the history of this series is substantially complete, though much remains to be learned concerning the earlier members of the family. The story is very like that of the horses, to which in many respects it runs curiously parallel. Beginning with very small, five-toed animals, we observe in the successive genera a gradual transformation in all parts of the skeleton, an elongation of the neck, limbs and feet, a reduction of the digits from five to two, and eventually the coalescence of the remaining two digits into a "cannon-bone." The grinding teeth, by equally gradual steps, take on the ruminant pattern. In the upper Miocene the line divides into the two branches of the camels and llamas, the former migrating to Eurasia and the latter to South America, though representatives of both lines persisted in North America until a very late period. Interesting side-branches of this line have also been found, one of which ended in the upper Miocene in animals which had almost the proportions of the giraffes and must have resembled them in appearance.

The American Tertiary has yielded several other groups of ruminant-like animals, some of which form beautifully complete evolutionary series, but s.p.a.ce forbids more than this pa.s.sing mention of them.

It was in Europe that the Artiodactyla had their princ.i.p.al development, and the upper Eocene, Oligocene and Miocene are crowded with such an overwhelming number and variety of forms that it is hardly possible to marshal them in orderly array and determine their mutual relations.h.i.+ps.

Yet in this chaotic exuberance of life, certain important facts stand out clearly, among these none is of greater interest and importance than the genealogy of the true Ruminants, or Pecora, which may be traced from the upper Eocene onward. The steps of modification and change are very similar to those through which the camel phylum pa.s.sed in North America, but it is instructive to note that, despite their many resemblances, the two series can be connected only in their far distant beginnings. The pecoran stock became vastly more expanded and diversified than did the camel line and was evidently more plastic and adaptable, spreading eventually over all the continents except Australia, and forming to-day one of the dominant types of mammals, while the camels are on the decline and not far from extinction. The Pecora successively ramified into the deer, antelopes, sheep, goats and oxen, and did not reach North America till the Miocene, when they were already far advanced in specialisation. To this invasion of the Pecora, or true ruminants, it seems probable that the decline and eventual disappearance of the camels is to be ascribed.

Recent discoveries in Egypt have thrown much light upon a problem which long baffled the palaeontologist, namely, the origin of the elephants.

(C.W. Andrews, "On the Evolution of the Proboscidea", "Phil. Trans. Roy.

Soc." London, Vol. 196, 1904, page 99.) Early representatives of this order, Mastodons, had appeared almost simultaneously (in the geological sense of that word) in the upper Miocene of Europe and North America, but in neither continent was any more ancient type known which could plausibly be regarded as ancestral to them. Evidently, these problematical animals had reached the northern continents by migrating from some other region, but no one could say where that region lay. The Eocene and Oligocene beds of the Fayoum show us that the region sought for is Africa, and that the elephants form just such a series of gradual modifications as we have found among other hoofed animals. The later steps of the transformation, by which the mastodons lost their lower tusks, and their relatively small and simple grinding teeth acquired the great size and highly complex structure of the true elephants, may be followed in the uppermost Miocene and Pliocene fossils of India and southern Europe.

Egypt has also of late furnished some very welcome material which contributes to the solution of another unsolved problem which had quite eluded research, the origin of the whales. The toothed-whales may be traced back in several more or less parallel lines as far as the lower Miocene, but their predecessors in the Oligocene are still so incompletely known that safe conclusions can hardly be drawn from them. In the middle Eocene of Egypt, however, has been found a small, whale-like animal (Protocetus), which shows what the ancestral toothed-whale was like, and at the same time seems to connect these thoroughly marine mammals with land-animals. Though already entirely adapted to an aquatic mode of life, the teeth, skull and backbone of Protocetus display so many differences from those of the later whales and so many approximations to those of primitive, carnivorous land-mammals, as, in a large degree, to bridge over the gap between the two groups. Thus one of the most puzzling of palaeontological questions is in a fair way to receive a satisfactory answer. The origin of the whalebone-whales and their relations to the toothed-whales cannot yet be determined, since the necessary fossils have not been discovered.

Among the carnivorous mammals, phylogenetic series are not so clear and distinct as among the hoofed animals, chiefly because the carnivores are individually much less abundant, and well-preserved skeletons are among the prizes of the collector. Nevertheless, much has already been learned concerning the mutual relations of the carnivorous families, and several phylogenetic series, notably that of the dogs, are quite complete. It has been made extremely probable that the primitive dogs of the Eocene represent the central stock, from which nearly or quite all the other families branched off, though the origin and descent of the cats have not yet been determined.

It should be clearly understood that the foregoing account of mammalian descent is merely a selection of a few representative cases and might be almost indefinitely extended. Nothing has been said, for example, of the wonderful museum of ancient mammalian life which is entombed in the rocks of South America, especially of Patagonia, and which opens a world so entirely different from that of the northern continents, yet exemplifying the same laws of "descent with modification." Very beautiful phylogenetic series have already been established among these most interesting and marvellously preserved fossils, but lack of s.p.a.ce forbids a consideration of them.

The origin of the mammalia, as a cla.s.s, offers a problem of which palaeontology can as yet present no definitive solution. Many morphologists regard the early amphibia as the ancestral group from which the mammals were derived, while most palaeontologists believe that the mammals are descended from the reptiles. The most ancient known mammals, those from the upper Tria.s.sic of Europe and North America, are so extremely rare and so very imperfectly known, that they give little help in determining the descent of the cla.s.s, but, on the other hand, certain reptilian orders of the Permian period, especially well represented in South Africa, display so many and such close approximations to mammalian structure, as strongly to suggest a genetic relations.h.i.+p. It is difficult to believe that all those likenesses should have been independently acquired and are without phylogenetic significance.

Birds are comparatively rare as fossils and we should therefore look in vain among them for any such long and closely knit series as the mammals display in abundance. Nevertheless, a few extremely fortunate discoveries have made it practically certain that birds are descended from reptiles, of which they represent a highly specialised branch. The most ancient representative of this cla.s.s is the extraordinary genus Archaeopteryx from the upper Jura.s.sic of Bavaria, which, though an unmistakable bird, retains so many reptilian structures and characteristics as to make its derivation plain. Not to linger over anatomical minutiae, it may suffice to mention the absence of a h.o.r.n.y beak, which is replaced by numerous true teeth, and the long lizard-like tail, which is made up of numerous distinct vertebrae, each with a pair of quill-like feathers attached to it. Birds with teeth are also found in the Cretaceous, though in most other respects the birds of that period had attained a substantially modern structure. Concerning the interrelations of the various orders and families of birds, palaeontology has as yet little to tell us.

The life of the Mesozoic era was characterised by an astonis.h.i.+ng number and variety of reptiles, which were adapted to every mode of life, and dominated the air, the sea and the land, and many of which were of colossal proportions. Owing to the conditions of preservation which obtained during the Mesozoic period, the history of the reptiles is a broken and interrupted one, so that we can make out many short series, rather than any one of considerable length. While the relations of several reptilian orders can be satisfactorily determined, others still baffle us entirely, making their first known appearance in a fully differentiated state. We can trace the descent of the sea-dragons, the Ichthyosaurs and Plesiosaurs, from terrestrial ancestors, but the most ancient turtles yet discovered show us no closer approximation to any other order than do the recent turtles; and the oldest known Pterosaurs, the flying dragons of the Jura.s.sic, are already fully differentiated.

There is, however, no ground for discouragement in this, for the progress of discovery has been so rapid of late years, and our knowledge of Mesozoic life has increased with such leaps and bounds, that there is every reason to expect a solution of many of the outstanding problems in the near future.

Pa.s.sing over the lower vertebrates, for lack of s.p.a.ce to give them any adequate consideration, we may briefly take up the record of invertebrate life. From the overwhelming ma.s.s of material it is difficult to make a representative selection and even more difficult to state the facts intelligibly without the use of unduly technical language and without the aid of ill.u.s.trations.

Several groups of the Mollusca, or sh.e.l.l-fish, yield very full and convincing evidence of their descent from earlier and simpler forms, and of these none is of greater interest than the Ammonites, an extinct order of the cephalopoda. The nearest living ally of the ammonites is the pearly nautilus, the other existing cephalopods, such as the squids, cuttle-fish, octopus, etc., are much more distantly related. Like the nautilus, the ammonites all possess a coiled and chambered sh.e.l.l, but their especial characteristic is the complexity of the "sutures." By sutures is meant the edges of the transverse part.i.tions, or septa, where these join the sh.e.l.l-wall, and their complexity in the fully developed genera is extraordinary, forming patterns like the most elaborate oak-leaf embroidery, while in the nautiloids the sutures form simple curves. In the rocks of the Mesozoic era, wherever conditions of preservation are favourable, these beautiful sh.e.l.ls are stored in countless mult.i.tudes, of an incredible variety of form, size and ornamentation, as is shown by the fact that nearly 5000 species have already been described. The ammonites are particularly well adapted for phylogenetic studies, because, by removing the successive whorls of the coiled sh.e.l.l, the individual development may be followed back in inverse order, to the microscopic "protoconch," or embryonic sh.e.l.l, which lies concealed in the middle of the coil. Thus the valuable aid of embryology is obtained in determining relations.h.i.+ps.

The descent of the ammonites, taken as a group, is simple and clear; they arose as a branch of the nautiloids in the lower Devonian, the sh.e.l.ls known as goniat.i.tes having zigzag, angulated sutures. Late in the succeeding Carboniferous period appear sh.e.l.ls with a truly ammonoid complexity of sutures, and in the Permian their number and variety cause them to form a striking element of the marine faunas. It is in the Mesozoic era, however, that these sh.e.l.ls attain their full development; increasing enormously in the Tria.s.sic, they culminate in the Jura.s.sic in the number of families, genera and species, in the complexity of the sutures, and in the variety of sh.e.l.l-ornamentation. A slow decline begins in the Cretaceous, ending in the complete extinction of the whole group at the end of that period. As a final phase in the history of the ammonites, there appear many so-called "abnormal" genera, in which the sh.e.l.l is irregularly coiled, or more or less uncoiled, in some forms becoming actually straight. It is interesting to observe that some of these genera are not natural groups, but are "polyphyletic," i.e.

are each derived from several distinct ancestral genera, which have undergone a similar kind of degeneration.

In the huge a.s.sembly of ammonites it is not yet possible to arrange all the forms in a truly natural cla.s.sification, which shall express the various interrelations of the genera, yet several beautiful series have already been determined. In these series the individual development of the later general shows transitory stages which are permanent in antecedent genera. To give a mere catalogue of names without figures would not make these series more intelligible.

The Brachiopoda, or "lamp-sh.e.l.ls," are a phylum of which comparatively few survive to the present day; their sh.e.l.ls have a superficial likeness to those of the bivalved Mollusca, but are not h.o.m.ologous with the latter, and the phylum is really very distinct from the molluscs. While greatly reduced now, these animals were incredibly abundant throughout the Palaeozoic era, great ma.s.ses of limestone being often composed almost exclusively of their sh.e.l.ls, and their variety is in keeping with their individual abundance. As in the case of the ammonites, the problem is to arrange this great mult.i.tude of forms in an orderly array that shall express the ramifications of the group according to a genetic system. For many brachiopods, both recent and fossil, the individual development, or ontogeny, has been worked out and has proved to be of great a.s.sistance in the problems of cla.s.sification and phylogeny.

Already very encouraging progress has been made in the solution of these problems. All brachiopods form first a tiny, embryonic sh.e.l.l, called the protegulum, which is believed to represent the ancestral form of the whole group, and in the more advanced genera the developmental stages clearly indicate the ancestral genera of the series, the succession of adult forms in time corresponding to the order of the ontogenetic stages. The transformation of the delicate calcareous supports of the arms, often exquisitely preserved, are extremely interesting. Many of the Palaeozoic genera had these supports coiled like a pair of spiral springs, and it has been shown that these genera were derived from types in which the supports were simply sh.e.l.ly loops.

The long extinct cla.s.s of crustacea known as the Trilobites are likewise very favourable subjects for phylogenetic studies. So far as the known record can inform us, the trilobites are exclusively Palaeozoic in distribution, but their course must have begun long before that era, as is shown by the number of distinct types among the genera of the lower Cambrian. The group reached the acme of abundance and relative importance in the Cambrian and Ordovician; then followed a long, slow decline, ending in complete and final disappearance before the end of the Permian. The newly-hatched and tiny trilobite larva, known as the protaspis, is very near to the primitive larval form of all the crustacea. By the aid of the correlated ontogenetic stages and the succession of the adult forms in the rocks, many phylogenetic series have been established and a basis for the natural arrangement of the whole cla.s.s has been laid.

Very instructive series may also be observed among the Echinoderms and, what is very rare, we are able in this sub-kingdom to demonstrate the derivation of one cla.s.s from another. Indeed, there is much reason to believe that the extinct cla.s.s Cystidea of the Cambrian is the ancestral group, from which all the other Echinoderms, star-fishes, brittle-stars, sea-urchins, feather-stars, etc., are descended.

The foregoing sketch of the palaeontological record is, of necessity, extremely meagre, and does not represent even an outline of the evidence, but merely a few ill.u.s.trative examples, selected almost at random from an immense body of material. However, it will perhaps suffice to show that the geological record is not so hopelessly incomplete as Darwin believed it to be. Since "The Origin of Species"

was written, our knowledge of that record has been enormously extended and we now possess, no complete volumes, it is true, but some remarkably full and illuminating chapters. The main significance of the whole lies in the fact, that JUST IN PROPORTION TO THE COMPLETENESS OF THE RECORD IS THE UNEQUIVOCAL CHARACTER OF ITS TESTIMONY TO THE TRUTH OF THE EVOLUTIONARY THEORY.

The test of a true, as distinguished from a false, theory is the manner in which newly discovered and unantic.i.p.ated facts arrange themselves under it. No more striking ill.u.s.tration of this can be found than in the contrasted fates of Cuvier's theory and of that of Darwin. Even before Cuvier's death his views had been undermined and the progress of discovery soon laid them in irreparable ruin, while the activity of half-a-century in many different lines of inquiry has established the theory of evolution upon a foundation of ever growing solidity. It is Darwin's imperishable glory that he prescribed the lines along which all the biological sciences were to advance to conquests not dreamed of when he wrote.

XII. THE PALAEONTOLOGICAL RECORD. By D.H. Scott, F.R.S.

President of the Linnean Society.

II. PLANTS.

There are several points of view from which the subject of the present essay may be regarded. We may consider the fossil record of plants in its bearing: I. on the truth of the doctrine of Evolution; II. on Phylogeny, or the course of Evolution; III. on the theory of Natural Selection. The remarks which follow, ill.u.s.trating certain aspects only of an extensive subject, may conveniently be grouped under these three headings.

I. THE TRUTH OF EVOLUTION.

When "The Origin of Species" was written, it was necessary to show that the Geological Record was favourable to, or at least consistent with, the Theory of Descent. The point is argued, closely and fully, in Chapter X. "On the Imperfection of the Geological Record," and Chapter XI. "On the Geological Succession of Organic Beings"; there is, however, little about plants in these chapters. At the present time the truth of Evolution is no longer seriously disputed, though there are writers, like Reinke, who insist, and rightly so, that the doctrine is still only a belief, rather than an established fact of science. (J. Reinke, "Kritische Abstammungslehre", "Wiesner-Festschrift", page 11, Vienna, 1908.) Evidently, then, however little the Theory of Descent may be questioned in our own day, it is desirable to a.s.sure ourselves how the case stands, and in particular how far the evidence from fossil plants has grown stronger with time.

As regards direct evidence for the derivation of one species from another, there has probably been little advance since Darwin wrote, at least so we must infer from the emphasis laid on the discontinuity of successive fossil species by great systematic authorities like Grand'Eury and Zeiller in their most recent writings. We must either adopt the mutationist views of those authors (referred to in the last section of this essay) or must still rely on Darwin's explanation of the absence of numerous intermediate varieties. The attempts which have been made to trace, in the Tertiary rocks, the evolution of recent species, cannot, owing to the imperfect character of the evidence, be regarded as wholly satisfactory.

When we come to groups of a somewhat higher order we have an interesting history of the evolution of a recent family in the work, not yet completed, of Kidston and Gwynne-Vaughan on the fossil Osmundaceae.

("Trans. Royal Soc. Edinburgh", Vol. 45, Part III. 1907, Vol. 46, Part II. 1908, Vol. 46, Part III. 1909.) The authors are able, mainly on anatomical evidence, to trace back this now limited group of Ferns, through the Tertiary and Mesozoic to the Permian, and to show, with great probability, how their structure has been derived from that of early Palaeozoic types.

The history of the Ginkgoaceae, now represented only by the isolated maidenhair tree, scarcely known in a wild state, offers another striking example of a family which can be traced with certainty to the older Mesozoic and perhaps further back still. (See Seward and Gowan, "The Maidenhair Tree (Gingko biloba)", "Annals of Botany", Vol. XIV. 1900, page 109; also A. Sprecher "Le Ginkgo biloba", L., Geneva, 1907.)

On the wider question of the derivation of the great groups of plants, a very considerable advance has been made, and, so far as the higher plants are concerned, we are now able to form a far better conception than before of the probable course of evolution. This is a matter of phylogeny, and the facts will be considered under that head; our immediate point is that the new knowledge of the relations between the cla.s.ses of plants in question materially strengthens the case for the theory of descent. The discoveries of the last few years throw light especially on the relation of the Angiosperms to the Gymnosperms, on that of the Seed-plants generally to the Ferns, and on the interrelations between the various cla.s.ses of the higher Cryptogams.

That the fossil record has not done still more for Evolution is due to the fact that it begins too late--a point on which Darwin laid stress ("Origin of Species" (6th edition), page 286.) and which has more recently been elaborated by Poulton. ("Essays on Evolution", pages 46 et seq., Oxford, 1908.) An immense proportion of the whole evolutionary history lies behind the lowest fossiliferous rocks, and the case is worse for plants than for animals, as the record for the former begins, for all practical purposes, much higher up in the rocks.

It may be well here to call attention to a question, often overlooked, which has lately been revived by Reinke. (Reinke, loc. cit. page 13.) As all admit, we know nothing of the origin of life; consequently, for all we can tell, it is as probable that life began, on this planet, with many living things, as with one. If the first organic beings were many, they may have been heterogeneous, or at least exposed to different conditions, from their origin; in either case there would have been a number of distinct series from the beginning, and if so we should not be justified in a.s.suming that all organisms are related to one another.

There may conceivably be several of the original lines of descent still surviving, or represented among extinct forms--to reverse the remark of a distinguished botanist, there may be several Vegetable Kingdoms!

However improbable this may sound, the possibility is one to be borne in mind.

That all VASCULAR plants really belong to one stock seems certain, and here the palaeontological record has materially strengthened the case for a monophyletic history. The Bryophyta are not likely to be absolutely distinct, for their s.e.xual organs, and the stomata of the Mosses strongly suggest community of descent with the higher plants; if this be so it no doubt establishes a certain presumption in favour of a common origin for plants generally, for the gap between "Mosses and Ferns" has been regarded as the widest in the Vegetable Kingdom. The direct evidence of consanguinity is however much weaker when we come to the Algae, and it is conceivable (even if improbable) that the higher plants may have had a distinct ancestry (now wholly lost) from the beginning. The question had been raised in Darwin's time, and he referred to it in these words: "No doubt it is possible, as Mr G.H.

Lewes has urged, that at the first commencement of life many different forms were evolved; but if so, we may conclude that only a very few have left modified descendants." ("Origin of Species", page 425.) This question, though it deserves attention, does not immediately affect the subject of the palaeontological record of plants, for there can be no reasonable doubt as to the interrelations.h.i.+p of those groups on which the record at present throws light.

The past history of plants by no means shows a regular progression from the simple to the complex, but often the contrary. This apparent anomaly is due to two causes.

1. The palaeobotanical record is essentially the story of the successive ascendancy of a series of dominant families, each of which attained its maximum, in organisation as well as in extent, and then sank into comparative obscurity, giving place to other families, which under new conditions were better able to take a leading place. As each family ran its downward course, either its members underwent an actual reduction in structure as they became relegated to herbaceous or perhaps aquatic life (this may have happened with the Horsetails and with Isoetes if derived from Lepidodendreae), or the higher branches of the family were crowded out altogether and only the "poor relations" were able to maintain their position by evading the compet.i.tion of the ascendant races; this is also ill.u.s.trated by the history of the Lycopod phylum. In either case there would result a lowering of the type of organisation within the group.