The Origin of Species, Chapters 11, 12 & 13

BY CHARLES DARWIN 

On the Geological Succession of Organic Beings 

On the slow and successive appearance of new species — On their different rates of change — Species once lost do not reappear — Groups of species follow the same general rules in their appearance and disappearance as do single species — On extinction — On simultaneous changes in the forms of life throughout the world — On the affinities of extinct species to each other and to living species — On the state of development of ancient forms — On the succession of the same types within the same areas — Summary of preceding and present chapter.

LET US now see whether the several facts and laws relat. ing to the geological succession of organic beings ^ accord best with the common view of the immutability of species, or with that of their slow and gradual modification, through variation and natural selection.

New species have appeared very slowly, one after another, both on the land and in the waters. Lyell has shown that it is hardly possible to resist the evidence on this head in the case of the several tertiary stages ; and every year tends to fill up the blanks between the stages, and to make the proportion between the lost and existing forms more gradual. In some of the most recent beds, though undoubtedly of high antiquity if measured by years, only one or two species are extinct, and only one or two are new, having appeared there for the first time, either locally, or, as far as we know, on the face of the earth. The secondary formations are more broken; but, as Bronn has remarked, neither the appearance nor disappearance of the many species embedded in each formation has been simultaneous.

Species belonging to different genera and classes have not changed at the same rate, or in the same degree. In the older tertiary beds a few living shells may still be found in the midst of a multitude of extinct forms. Falconer has given a striking instance of a similar fact, for an existing crocodile is associated with many lost mammals and reptiles in the suh-Himalayan deposits. The Silurian Lingula differs but little from the living species of this genus ; whereas most of the other Silurian Molluscs and all the Crustaceans have changed greatly. The productions of the land seem to have changed at a quicker rate than those of the sea, of which a striking instance has been observed in Switzerland. There is some reason to believe that organisms high in the scale, change more quickly than those that are low: though there are exceptions to this rule. The amount of organic change, as Pictet has remarked, is not the same in each successive so-called formation. Yet if we compare any but the most closely related formations, all the species will be found to have undergone some change. When a species has once disappeared from the face of the earth, we have no reason to believe that the same identical form ever reappears. The strongest apparent exception to this latter rule is that of the so-called "colonies" of M. Barrande, which intrude for a period in the midst of an older formation, and then allow the pre-existing fauna to reappear; but Lyell's explanation, namely, that it is a case of temporary migration from a distinct geographical province, seems satisfactory.

These several facts accord well with our theory, which includes no fixed law of development, causing all the inhabitants of an area to change abruptly, or simultaneously, or to an equal degree. The process of modification must be slow, and will generally affect only a few species at the same time ; for the variability of each species is independent of that of all others. Whether such variations or individual differences as may arise will be accumulated through natural selection in a greater or less degree, thus causing a greater or less amount of permanent modification, will depend on many complex contingencies — on the variations being of a beneficial nature, on the freedom of intercrossing, on the slowly changing physical conditions of the country, on the immigration of new colonists, and on the nature of the other inhabitants with which the varying species come into competition. Hence it is by no means surprising that one species should retain the same identical form much longer than others; or, if changing, should change in a less degree. We find similar relations between the existing inhabitants of distinct countries ; for instance, the land-shells and coleopterous insects of Madeira have come to differ considerably from their nearest allies on the continent of Europe, whereas the marine shells and birds have remained unaltered. We can perhaps understand the apparently quicker rate of change in terrestrial and in more highly organised productions compared with marine and lower productions, by the more complex relations of the higher beings to their organic and inorganic conditions of life, as explained in a former chapter. When many of the inhabitants of any area have become modified and improved, we can understand, on the principle of competition, and from the all-important relations of organism to organism in the struggle for life, that any form which did not become in some degree modified and improved, would be liable to extermination. Hence we see why all the species in the same region do at last, if we look to long enough intervals of time, become modified, for otherwise they would become extinct.

In members of the same class the average amount of change during long and equal periods of time, may, perhaps, be nearly the same; but as the accumulation of enduring formation, rich in fossils, depends on great masses of sediment being deposited on subsiding areas, our formations have been almost necessarily accumulated at wide and irregularly intermittent intervals of time; consequently the amount of organic change exhibited by the fossils embedded in consecutive formations is not equal. Each formation, on this view, does not mark a new and complete act of creation, but only an occasional scene, taken almost at hazard in an ever slowly changing drama.

We can clearly understand why a species when once lost should never reappear, even if the very same conditions of life, organic and inorganic, should recur. For though the offspring of one species might be adapted (and no doubt this has occurred in innumerable instances) to fill the place of another species in the economy of nature, and thus supplant it; yet the two forms — the old and the new — would not be identically the same; for both would almost certainly inherit different characters from their distinct progenitors; and organisms already differing would vary in a different manner. For instance, it is possible, if all our fantail pigeons were destroyed, that fanciers might make a new breed hardly distinguishable from the present breed ; but if the parent rock-pigeon were likewise destroyed, and under nature we have every reason to believe that parent-forms are generally supplanted and exterminated by their improved offspring, it is incredible that a fantail, identical with the existing breed, could be raised from any other species of pigeon, or even from any other well-established race of the domestic pigeon, for the successive variations would almost certainly be in some degree different, and the newly-formed variety would probably inherit from its progenitor some characteristic differences.

Groups of species, that is, genera and families, follow the same general rules in their appearance and disappearance as do single species, changing more or less quickly, and in a greater or lesser degree. A group, when it has once disappeared, never reappears ; that is, its existence, as long as it lasts, is continuous. I am aware that there are some apparent exceptions to this rule, but the exceptions are surprisingly few, so few that E. Forbes, Pictet, and Woodward (though all strongly opposed to such views as I maintain) admit its truth ; and the rule strictly accords with the theory. For all the species of the same group, however long it may have lasted, are the modified descendants one from the other, and all from a common progenitor. In the genus Lingula, for instance, the species which have successively appeared at all ages must have been connected by an unbroken series of generations, from the lowest Silurian stratum to the present day.

We have seen in the last chapter that whole groups of species sometimes falsely appear to have been abruptly developed; and I have attempted to give an explanation of this fact, which if true would be fatal to my views. But such cases are certainly exceptional ; the general rule being a gradual increase in number, until the group reaches its maximum, and then, sooner or later, a gradual decrease. If the number of the species included within a genus, or the number of the genera within a family, be represented by a vertical line of varying thickness, ascending through the successive geological formations, in which the species are found, the line will sometimes falsely appear to begin at its lower end, not in a sharp point, but abruptly ; it then gradually thickens upwards, often keeping of equal thickness for a space, and ultimately thins out in the upper beds, marking the decrease and final extinction of the species. This gradual increase in number of the species of a group is strictly conformable with the theory, for the species of the same genus, and the genera of the same family, can increase only slowly and progressively ; the process of modification and the production of a number of allied forms necessarily being a slow and gradual process, — one species first giving rise to two or three varieties, these being slowly converted into species, •which in their turn produce by equally slow steps other varieties and species, and so on, like the branching of a great tree from a single stem, till the group becomes large.

ON EXTINCTION

We have as yet only spoken incidentally of the disappearance of species and of groups of species. On the theory of natural selection, the extinction of old forms and the production of new and improved forms are intimately connected together. The old notion of all the inhabitants of the earth having been swept away by catastrophes at successive periods is very generally given up, even by those geologists, as Elie de Beaumont, Murchison, Barrande, &c., whose general views would naturally lead them to this conclusion. On the contrary, we have every reason to believe, from the study of the tertiary formations, that species and groups of species gradually disappear, one after another, first from one spot, then from another, and finally from the world. In some few cases, however, as by the breaking of an isthmus and the consequent irruption of a multitude of new inhabitants into an adjoining sea, or by the final subsidence of an island, the process of extinction may have been rapid. Both single species and whole groups of species last for very unequal periods; some groups, as we have seen, have endured from the earliest known dawn of life to the present day; some have disappeared before the close of the palaeozoic period. No fixed law seems to determine the length of time during which any single species or any single genus endures. There is reason to believe that the extinction of a whole group of species is generally a slower process than their production: if their appearance and disappearance be represented, as before, by a vertical line of varying thickness the line is found to taper more gradually at its upper end, which marks the progress of extermination, than at its lower end, which marks the first appearance and the early increase in number of the species. In some cases, however, the extermination of whole groups, as of ammonites, towards the close of the secondary period, has been wonderfully sudden.

The extinction of species has been involved in the most gratuitous mystery. Some authors have even supposed that, as the individual has a definite length of life, so have species a definite duration. No one can have marvelled more than I have done at the extinction of species. When I found in La Plata the tooth of a horse embedded with the remains of Mastodon, Megatherium, Toxodon, and other extinct monsters, which all co-existed with still living shells at a very late geological period, I was filled with astonishment; for, seeing that the horse, since its introduction by the Spaniards into South America, has run wild over the whole country and has increased in numbers at an unparalleled rate, I asked myself what could so recently have exterminated the former horse under conditions of life apparently so favourable. But my astonishment was groundless. Professor Owen soon perceived that the tooth, though so like that of the existing horse, belonged to an extinct species. Had this horse been still living, but in some degree rare, no naturalist would have felt the least surprise at its rarity; for rarity is the attribute of a vast number of species of all classes, in all countries. If we ask ourselves why this or that species is rare, we answer that something is unfavourable in its conditions of life; but what that something is we can hardly ever tell. On the supposition of the fossil horse still existing as a rare species, we might have felt certain, from the analogy of all other mammals, even of the slow-breeding elephant, and from the history of the naturalisation of the domestic horse in South America, that under more favourable conditions it would in a very few years have stocked the whole continent. But we could not have told what the unfavourable conditions were which checked its increase, whether some one or several contingencies, and at what period of the horse's life, and in what degree they severally acted. If the conditions had gone on, however slowly, becoming less and less favourable, we assuredly should not have perceived the fact, yet the fossil horse would certainly have become rarer and rarer, and finally extinct; — its place being seized on by some more successful competitor.

It is most difficult always to remember that the increase of every creature is constantly being checked by unperceived hostile agencies; and that these same unperceived agencies are amply sufficient to cause rarity, and finally extinction. So little is this subject understood, that I have heard surprise repeatedly expressed at such great monsters as the Mastodon and the more ancient Dinosaurians having become extinct; as if mere bodily strength gave victory in the battle of life. Mere size, on the contrary, would in some cases determine, as has been remarked by Owen, quicker extermination from the greater amount of requisite food. Before man inhabited India or Africa, some cause must have checked the continued increase of the existing elephant. A highly capable judge, Dr. Falconer, believes that it is chiefly insects which, from incessantly harassing and weakening the elephant in India, check its increase; and this was Bruce's conclusion with respect to the African elephant in Abyssinia. It is certain that insects and bloodsucking bats determine the existence of the larger naturalized quadrupeds in several parts of S. America. ^ We see in many cases in the more recent tertiary formations, that rarity precedes extinction ; and we know that this has been the progress of events with those animals which have been exterminated, either locally or wholly, through man's agency. I may repeat what I published in 1845, namely, that to admit that species generally become rare before they become extinct — to feel no surprise at the rarity of a species, and yet to marvel greatly when the species ceases to exist, is much the same as to admit that sickness in the individual is the forerunner of death — to feel no surprise at sickness, but, when the sick man dies, to wonder and to suspect that he died by some deed of violence.

The theory of natural selection is grounded on the belief that each new variety and ultimately each new species, is produced and maintained by having some advantage over those with which it comes into competition; and the consequent extinction of the less favoured forms almost inevitably follows. It is the same with our domestic productions ; when a new and slightly improved variety has been raised, it at first supplants the less improved varieties in the same neighbourhood; when much improved it is transported far and near, like our short-horn cattle, and takes the place of other breeds in other countries. Thus the appearance of new forms and the disappearance of old forms, both those naturally and those artificially produced, are bound together. In flourishing groups, the number of new specific forms which have been produced within a given time has at some periods probably been greater than the number of the old specific forms which have been exterminated ; but we know that species have not gone on indefinitely increasing, at least during the later geological epochs, so that, looking to later times, we may believe that the production of new forms has caused the extinction of about the same number of old forms.

The competition will generally be most severe, as formerly explained and illustrated by examples, between the forms which are most like each other in all respects. Hence the improved and modified descendants of a species will generally cause the extermination of the parent species; and if many new forms have been developed from any one species, the nearest allies of that species, i.e., the species of the same genus, will be the most liable to extermination. Thus, as I believe, a number of new species descended from one species, that is a new genus, comes to supplant an old genus, belonging to the same family. But it must often have happened that a new species belonging to some one group has seized on the place occupied by a species belonging to a distinct group, and thus have caused its extermination. If many allied forms be developed from the successful intruder, many will have to yield their places; and it will generally be the allied forms, which will suffer from some inherited inferiority in common. But whether it be species belonging to the same or to a distinct class, which have yielded their places to other modified and improved species, a few of the sufferers may often be preserved for a long time, from being fitted to some peculiar line of life, or from inhabiting some distant and isolated station, where they will have escaped severe competition. For instance, some species of Trigonia, a great genus of shells in the secondary formations, survive in the Australian seas; and a few members of the great and almost extinct group of Ganoid fishes still inhabit our fresh waters. Therefore the utter extinction of a group is generally, as we have seen, a slower process than its production.

With respect to the apparently sudden extermination of whole families or orders, as of Trilobites at the close of the palaeozoic period and of Ammonites at the close of the secondary period, we must remember what has been already said on the probable wide intervals of time between our consecutive formations; and in these intervals there may have been much slow extermination. Moreover, when, by sudden immigration or by unusually rapid development, many species of a new group have taken possession of an area, many of the older species will have been exterminated in a correspondingly rapid manner; and the forms which thus yield their places will commonly be allied, for they will partake of the same inferiority in common.

Thus, as it seems to me, the manner in which single species and whole groups of species become extinct accord well with the theory of natural selection. We need not marvel at extinction ; if we must marvel, let it be at our own presumption in imagining for a moment that we understand the many complex contingencies on which the existence of each species depends. If we forget for an instant that each species tends to increase inordinately, and that some check is always in action, yet seldom perceived by us, the whole economy of nature will be utterly obscured. Whenever we can precisely say why this species is more abundant in individuals than that; why this species and not another can be naturalised in a given country; then, and not until then, we may justly feci surprise why we cannot account for the extinction of any particular species or group of species.

ON THE FORMS OF LIFE CHANGING ALMOST SIMULTANEOUSLY THROUGHOUT THE WORLD

Scarcely any paleontological discovery is more striking than the fact that the forms of life change almost simultaneously throughout the world. Thus our European Chalk formation can be recognised in many distinct regions, under the most different climates, where not a fragment of the mineral chalk itself can be found; namely in North America, in equatorial South America, in Ticrra del Fuego, at the Cape of Good Hope, and in the peninsula of India. For at these distant points, the organic remains in certain beds present an unmistakeable resemblance to those of the Chalk. It is not that the same species are met with ; for in some cases not one species is identically the same, but they belong to the same families, genera, and sections of genera, and sometimes are similarly characterised in such trifling points as mere superficial sculpture. Moreover, other forms, which are not found in the Chalk of Europe, but which occur in the formations either above or below, occur in the same order at these distant points of the world. In the several successive palaeozoic formations of Russia, Western Europe, and North America, a similar parallelism in the forms of life has been observed by several authors; so it is, according to Lyell, with the European and North American tertiary deposits. Even if the few fossil species which are common to the Old and New Worlds were kept wholly out of view, the general parallelism in the successive forms of life, in the palaeozoic and tertiary stages, would still be manifest, and the several formations could be easily correlated.

These observations, however, relate to the marine inhabitants of the world: we have not sufficient data to judge whether the productions of the land and of fresh water at distant points change in the same parallel manner. We may doubt whether they have thus changed: if the Megatherium, Mylodon, Macrauchenia, and Toxodon had been brought to Europe from La Plata, without any information in regard to their geological position, no one would have suspected that they had co-existed with sea-shells all still living; but as these anomalous monsters co-existed with the Mastodon and Horse, it might at least have been inferred that they had lived during one of the later tertiary stages.

When the marine forms of life are spoken of as having changed simultaneously throughout the world, it must not be supposed that this expression relates to the same year, or to the same country, or even that it has a very strict geological sense; for if all the marine animals now living in Europe, and all those that lived in Europe during the pleistocene period (a very remote period as measured by years, including the whole glacial epoch) were compared with those now existing in South America or in Australia, the most skilful naturalist would hardly be able to say whether the present or the pleistocene inhabitants of Europe resembled most closely those of the southern hemisphere. So, again, several highly competent observers maintain that the existing productions of the United States are more closely related to those which lived in Europe during certain late tertiary stages, than to the present inhabitants of Europe; and if this be so, it is evident that fossiliferous beds now deposited on the shores of North America would hereafter be liable to be classed with somewhat older European beds. Nevertheless, looking to a remotely future epoch, there can be little doubt that all the more modern marine formations, namely, the upper pliocene, the pleistocene and strictly modern beds of Europe, North and South America, and Australia, from containing fossil remains in some degree allied, and from not including those forms which are found only in the older underlying deposits, would be correctly ranked as simultaneous in a geological sense.

The fact of the forms of life changing simultaneously, in the above large sense, at distant parts of the world, has greatly struck those admirable observers, MM. de Verneuil and d'Archiac. After referring to the parallelism of the palaeozoic forms of life in various parts of Europe, they add, "If, struck by this strange sequence, we turn our attention to North America, and there discover a series of analogous phenomena, it will appear certain that all these modifications of species, their extinction, and the introduction of new ones, cannot be owing to mere changes in marine currents or other causes more or less local and temporary, but depend on general laws which govern the whole animal kingdom." M. Barrande has made forcible remarks to precisely the same effect. It is, indeed, quite futile to look to changes of currents, climate, or other physical conditions, as the cause of these great mutations in the forms of life throughout the world, under the most different climates. We must, as Barrande has remarked, look to some special law. We shall see this more clearly when we treat of the present distribution of organic beings, and find how slight is the relation between the physical conditions of various countries and the nature of their inhabitants.

This great fact of the parallel succession of the forms of life throughout the world, is explicable on the theory of natural selection. New species arc formed by having some advantage over older forms ; and the forms, which are already dominant, or have some advantage over the other forms in their own country, give birth to the greatest number of new varieties or incipient species. We have distinct evidence on this head, in the plants which are dominant, that is, which are commonest and most widely diffused, producing the greatest number of new varieties. It is also natural that the dominant, varying, and far-spreading species, which have already invaded to a certain extent the territories of other species, should be those which would have the best chance of spreading still further, and of giving rise in new countries to other new varieties and species The process of diffusion would often be very slow, depending on climatal and geographical changes, on strange accidents, and on the gradual acclimatisation of new species to the various climates through which they might have to pass, but in the course of time the dominant forms would generally succeed in spreading and would ultimately prevail. The diffusion would, it is probable, be slower with the terrestrial inhabitants of the distinct continents than with the marine inhabitants of the continuous sea. We might therefore expect to find, as we do find, a less strict degree of parallelism in the succession of the productions of the land than with those of the sea.

Thus, as it seems to me, the parallel, and, taken in a large sense, simultaneous, succession of the same forms of life throughout the world, accords well with the principle of new species having been formed by dominant species spreading widely and varying; the new species thus produced being themselves dominant, owing to their having had some advantage over their already dominant parents, as well as over other species, and again spreading, varying, and producing new forms. The old forms which are beaten and which yield their places to the new and victorious forms, will generally be allied in groups, from inheriting some inferiority in common; and therefore, as new and improved groups spread throughout the world, old groups disappear from the world; and the succession of forms everywhere tends to correspond both in their first appearance and final disappearance.

There is one other remark connected with this subject worth making. I have given my reasons for believing that most of our great formations, rich in fossils, were deposited during periods of subsidence; and that blank intervals of vast duration, as far as fossils are concerned, occurred during the periods when the bed of the sea was either stationary or rising, and likewise when sediment was not thrown down quickly enough to embed and preserve organic remains. During these long and blank intervals I suppose that the inhabitants of each region underwent a considerable amount of modification and extinction, and that there was much migration from other parts of the world. As we have reason to believe that large areas are affected by the same movement, it is probable that strictly contemporaneous formations have often been accumulated over very wide spaces in the same quarter of the world ; but we are very far from having any right to conclude that this has invariably been the case, and that large areas have invariably been affected by the same movements. When two formations have been deposited in two regions during nearly, but not exactly, the sarne period, we should find in both, from the causes explained in the foregoing paragraphs, the same general succession in the forms of life; but the species would not exactly correspond ; for there will have been a little more time in the one region than in the other for modification, extinction, and immigration.

I suspect that cases of this nature occur in Europe. Mr. Prestwich, in his admirable Memoirs on the eocene deposits of England and France, is able to draw a close general parallelism between the successive stages in the two countries; but when he compares certain stages in England with those in France, although he finds in both a curious accordance in the numbers of the species belonging to the same genera, yet the species themselves differ in a manner very difficult to account for considering the proximity of the two areas, — ■ unless, indeed, it be assumed that an isthmus separated two seas inhabited by distinct, but contemporaneous, faunas. Lyell has made similar observations on some of the later tertiary formations. Barrande, also, shows that there is a striking general parallelism in the successive Silurian deposits of Bohemia and Scandinavia; nevertheless he finds a surprising amount of difference in the species. If the several formations in these regions have not been deposited during the same exact periods, — a formation in one region often corresponding with a blank interval in the other, — and if in both regions the species have gone on slowly changing during the accumulation of the several formations and during the long intervals of time between them; in this case the several formations in the two regions could be arranged in the same order, in accordance with the general succession of the forms of life, and the order would falsely appear to be strictly parallel ; nevertheless the species would not be all the same in the apparently corresponding stages in the two regions.

ON THE AFFINITIES OF EXTINCT SPECIES TO EACH OTHER AND TO LIVING FORMS

Let us now look to the mutual affinities of extinct and living species. All fall into a few grand classes; and this fact is at once explained on the principle of descent. The more ancient any form is, the more, as a general rule, it differs from living forms. But, as Buckland long ago remarked, extinct species can all be classed either in still existing groups, or between them. That the extinct forms of life help to fill up the intervals between existing genera, families, and orders, is certainly true; but as this statement has often been ignored or even denied, it may be well to make some remarks on this subject, and to give some instances. If we confine our attention either to the living or to the extinct species of the same class, the series is far less perfect that if we combine both into one general system. In the writings of Professor Owen we continually meet with the expression of generalised forms, as applied to extinct animals; and in the writings of Agassiz, of prophetic or synthetic types; and these terms imply that such forms are in fact intermediate or connecting links. Another distinguished palaeontologist, M. Gaudry, has shown in the most striking manner that many of the fossil mammals discovered by him in Attica serve to break down the intervals between existing genera. Cuvier ranked the Ruminants and Pachyderms, as two of the most distinct orders of mammals: but so many fossil links have been disentombed that Owen has had to alter the whole classification, and has placed certain pachyderms in the same sub-order with ruminants ; for example, he dissolves by gradations the apparently wide interval between the pig and the camel. The Ungulata or hoofed quadrupeds are now divided into the even-toed or odd-toed divisions; but the Macrauchenia of S. America connects to a certain extent these two grand divisions. No one will deny that the Hipparion is intermediate between the existing horse and certain older ungulate forms. What a wonderful connecting link in the chain of mammals is the Typotherium from S. America, as the name given to it by Professor Gervais expresses, and which cannot be placed in any existing order. The Sirenia form a very distinct group of mammals, and one of the most remarkable peculiarities in the existing dugong and lamentin is the entire absence of hind limbs without even a rudiment being left; but the extinct Halitherium had, according to Professor Flower, an ossified thigh-bone "articulated to a well-defined acetabulum in the pelvis," and it thus makes some approach to ordinary hoofed quadrupeds, to which the Sirenia are in other respects allied. I'he cetaceans or whales are widely different from all other mammals, but the tertiary Zeuglodon and Squalodon, which have been placed by some naturalists in an order by themselves, are considered by Professor Huxley to be undoubtedly cetaceans, ''and to constitute connecting links with the aquatic carnivora."

Even the wide interval between birds and reptiles has been shown by the naturalist just quoted to be partially bridged over in the most unexpected manner, on the one hand, by the ostrich and extinct Archeopteryx, and on the other hand, by the Compsognathus, one of the Dinosaurians — that group which includes the most gigantic of all terrestrial reptiles. Turning to the Invertebrata, Barrande asserts, a higher authority could not be named, that he is every day taught that, although palaeozoic animals can certainly be classed under existing groups, yet that at this ancient period the groups were not so distinctly separated from each other as they now are.

Some writers have objected to any extinct species, or group of species, being considered as intermediate between any two living species, or groups of species. If by this term Jt is meant that an extinct form is directly intermediate in all its characters between two living forms or groups, the objection is probably valid. But in a natural classification many fossil species certainly stand between living species, and some extinct genera between living genera, even between genera belonging to distinct families. The most common case, especially with respect to very distinct groups, such as fish and reptiles, seems to be, that, supposing them to be distinguished at the present day by a score of characters, the ancient members are separated by a somewhat lesser number of characters; so that the two groups formerly made a somewhat nearer approach to each other than they now do.

It is a common belief that the more ancient a form is, by so much the more it tends to connect by some of its characters groups now widely separated from each other. This remark no doubt must be restricted to those groups which have undergone much change in the course of geological ages ; and it would be difficult to prove the truth of the proposition, for every now and then a living animal, as the Lepidosiren, is discovered having affinities directed towards very distinct groups. Yet if we compare the older Reptiles and Batrachians, the older Fish, the older Cephalopods, and the eocene Mammals, with the more recent members of the same classes, we must admit that there is truth in the remark.

Let us see how far these several facts and inferences accord with the theory of descent with modification. As the subject is somewhat complex, I must request the reader to turn to the diagram in the fourth chapter. We may suppose that the numbered letters in italics represent genera, and the dotted lines diverging from them the species in each genus. The diagram is much too simple, too few genera and too few species being given, but this is unimportant for us. The horizontal lines may represent successive geological formations, and all the forms beneath the uppermost line may be considered as extinct. The three existing genera o" q^\ p^\ will form a small family; t" and /" a closely allied family or sub-family; and o'\ e'\ m" a third family. These three families, together with the many extinct genera on the several lines of descent diverging from the parent-form (A) will form an order, for all will have inherited something in common from their ancient progenitor. On the principle of the continued tendency to divergence of character, which was formerly illustrated by this diagram, the more recent any form is, the more it will generally differ from its ancient progenitor. Hence we can understand the rule that the most ancient fossils differ most from existing forms. We must not, however, assume that divergence of character is a necessary contingency; it depends solely on the descendants from a species being thus enabled to seize on many and different places in the economy of nature. Therefore it is quite possible, as we have seen in the case of some Silurian forms, that a species might go on being slightly modified in relation to its slightly altered conditions of life, and yet retain throughout a vast period the same general characteristics. This is represented in the diagram by the letter.

All the many forms, extinct and recent, descended from (A), make, as before remarked, one order; and this order. from the continued effects of extinction and divergence of character, has become divided into several sub-families and families, some of which are supposed to have perished at different periods, and some to have endured to the present day.

By looking at the diagram we can see that if many of the extinct forms supposed to be imbedded in the successive formations, were discovered at several points low down in the series, the three existing families on the uppermost line would be rendered less distinct from each other. If, for instance, the genera a\ d" , a", /", »^^ »»", 7n', were disinterred, these three families would be so closely linked together that they probably would have to be united into one great family, in nearly the same manner as has occurred with ruminants and certain pachyderms. Yet he who objected to consider as intermediate the extinct genera, which thus link together the living genera of three families, would be partly justified, for they are intermediate, not directly, but only by a long and circuitous course through many widely dift'ercnt forms. If many extinct forms were to be discovered above one of the horizontal lines or geological formations — for instance, above No. VI. — but none from beneath this line, then only two of the families (those on the left hand, a\ &c., and fc," &c.) would have to be united into one; and there would remain two families, which would be less distinct from each other than they were before the discovery of the fossils. So again if the three families formed of eight genera (a" to *»"), on the uppermost line, be supposed to differ from each other by half-a-dozen important characters, then the families which existed at the period marked VI. would certainly have differed from each other by a less number of characters; for they would at this early stage of descent have diverged in a less degree from their common progenitor. Thus it comes that ancient and extinct genera are often in a greater or less degree intermediate in character between their modified descendants, or between their collateral relations.

Under nature the process will be far more complicated than is represented in the diagram; for the groups will have been more numerous; they will have endured for extremely unequal lengths of time, and will have been modified in various degrees. As we possess only the last volume of the geological record, and that in a very broken condition, we have no right to expect, except in rare cases, to fill up the wide intervals in the natural system, and thus to unite distinct families or orders. All that we have a right to expect is, that those groups which have, within known geological periods, undergone much modification, should in the older formations make some slight approach to each other; so that the older members should differ less from each other in some of their characters than do the existing members of the same groups; and this by the concurrent evidence of our best palaeontologists is frequently the case.

Thus, on the theory of descent with modification, the main facts with respect to the mutual affinities of the extinct forms of life to each other and to living forms, are explained in a satisfactory manner. And they are wholly inexplicable on any other view.

On this same theory, it is evident that the fauna during any one great period in the earth's history will be intermediate in general character between that which preceded and that which succeeded it. Thus the species which lived at the sixth great stage of descent in the diagram are the modified offspring of those which lived at the fifth stage, and are the parents of those which became still more modified at the seventh stage; hence they could hardly fail to be nearly intermediate in character between the forms of life above and below. We must, however, allow for the entire extinction of some preceding forms, and in any one region for the immigration of new forms from other regions, and for a large amount of modification during the long and blank interval between the successive formations. Subject to these allowances, the fauna of each geological period undoubtedly is intermediate in character, between the preceding and succeeding faunas. I need give only one instance, namely, the manner in which the fossils of the Devonian system, when this system was first discovered, were at once recognised by palaeontologists as intermediate in character between those of the overlying carboniferous, and underlying Silurian systems. But each fauna is not necessarily exactly intermediate, as unequal intervals of time have elapsed between consecutive formations.

It is no real objection to the truth of the statement that the fauna of each period as a whole is nearly intermediate in character between the preceding and succeeding faunas, that certain genera offer exceptions to the rule. For instance, the species of mastodons and elephants, when arranged by Dr. Falconer in two series, — in the first place according to their mutual affinities, and in the second place according to their periods of existence, — do not accord in arrangement. The species extreme in character are not the oldest or the most recent; nor are those which are intermediate in character, intermediate in age. But supposing for an instant, in this and other such cases, that the record of the first appearance and disappearance of the species was complete, which is far from the case, we have no reason to believe that forms successively produced necessarily endure for corresponding lengths of time. A very ancient form may occasionally have lasted much longer than a form elsewhere subsequently produced, especially in the case of terrestrial productions inhabiting separated districts. To compare small things with great; if the principal living and extinct races of the domestic pigeon were arranged in serial affinity, this arrangement would not closely accord with the order in time of their production, and even less with the order of their disappearance; for the parent, rock-pigeon still lives; and many varieties between the rock-pigeon and the carrier have become extinct; and carriers which are extreme in the important character of length of back originated earlier than short-beaked tumblers, which are at the opposite end of the series in this respect.

Closely connected with the statement, that the organic remains from an intermediate formation are in some degree intermediate in character, is the fact, insisted on by all palaeontologists, that fossils from two consecutive formations are far more closely related to each other, than are the fossils from two remote formations. Pictet gives as a wellknown instance, the general resemblance of the organic remains from the several stages of the Chalk formation, though the species arc distinct in each stage. This fact alone, from. its generality, seems to have shaken Professor Pictet in his belief in the immutability of species. He who is acquainted with the distribution of existing species over the globe, will not attempt to account for the close resemblance of distinct species in closely consecutive formations, by the physical conditions of the ancient areas having remained nearly the same. Let it be remembered that the forms of life, at least those inhabiting the sea, have changed almost simultaneously throughout the world, and therefore 'under the most different climates and conditions. Consider the prodigious vicissitudes of climate during the pleistocene period, which includes the whole glacial epoch, and note how little the specific forms of the inhabitants of the sea have been affected.

On the theory of descent, the full meaning of the fossil remains from closely consecutive formations being closely related, though ranked as distinct species, is obvious. As the accumulation of each formation has often been interrupted, and as long blank intervals have intervened between successive formations, we ought not to expect to find, as I attempted to show in the last chapter, in any one or in any two formations, all the intermediate varieties between the species which appeared at the commencement and close of these periods : but we ought to find after intervals, very long as measured by years, but only moderately long as measured geologically, closely allied forms, or, as they have been called by some authors, representative species; and these assuredly we do find. We find, in short, such evidence of the slow and scarcely sensible mutations of specific forms, as we have the right to expect.

ON THE STATE OF DEVELOPMENT OF ANCIENT COMPARED WITH LIVING FORMS

We have seen in the fourth chapter that the degree of differentiation and specialisation of the parts in organic beings, when arrived at maturity, is the best standard, as yet suggested, of their degree of perfection or highness. We have also seen that, as the specialisation of parts is an advantage to each being, so natural selection will tend to render the organisation of each being more specialised and perfect, and in this sense higher; not but that it may leave many creatures with simple and unimproved structures fitted for simple conditions of life, and in some cases will even degrade or simplify the organisation, yet leaving such degraded beings better fitted for their new walks of life. In another and more general manner, new species become superior to their predecessors; for they have to beat in the struggle for life all the older forms, with which they come into close competition. We may therefore conclude that if under a nearly similar climate the eocene inhabitants of the world could be put into competition with the existing inhabitants, the former would be beaten and exterminated by the latter, as would the secondary by the eocene, and the palaeozoic by the secondary forms. So that by this fundamental test of victory in the battle for life, as well as by the standard of the specialisation of organs, modern forms ought, on the theory of natural selection, to stand higher than ancient forms. Is this the case? A large majority of palaeontologists would answer in the affirmative; and it seems that this answer must be admitted as true, though difficult of proof.

It is no valid objection to this conclusion, that certain Brachiopods have been but slightly modified from an extremely remote geological epoch; and that certain land and fresh-water shells have remained nearly the same, from the time when, as far as is known, they first appeared. It is not an insuperable difficulty that Foraminifera have not, as insisted on by Dr. Carpenter, progressed in organisation since even the I.aurentian epoch ; for some organisms would have to remain fitted for simple conditions of life, and what could be better fitted for this end than these lowly organised Protozoa? Such objections as the above would be fatal to my view, if it included advance in organisation as a necessary contingent. They would likewise be fatal, if the above Foraminifera, for instance, could be proved to have first come into existence during the Laurentian epoch, or the above Brachiopods during the Cambrian formation ; for in this case, there would not have been time sufficient for the development of these organisms up to the standard which they had then reached. When advanced up to any given point, there is no necessity, on the theory of natural selection, for ) their further continued progress; though they will, during each successive age, have to be slightly modified, so as to hold their places in relation to slight changes in their conditions. The foregoing objections hinge on the question whether we really know how old the world is, and at what period the various forms of life first appeared; and this may well be disputed.

The problem whether organisation on the whole has advanced is in many ways excessively intricate. The geological record, at all times imperfect, does not extend far enough back, to show with unmistakeable 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 the 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, whilst 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 the 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 naturalised 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 formerlymore 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 first appearance of new forms in any one area and formation ; that widely ranging species are those which have varied most frequently, and have oftenest given rise to new species; that varieties have at first been local; and lastly, although each species must have passed through numerous transitional stages, it is probable that the periods, during which each underwent modification, though many and long as measured by years, have been short in comparison with the periods during which each remained in an unchanged condition. These causes, taken conjointly, will to a large extent explain why — though we do find many links — we do not find interminable varieties, connecting together all extinct and existing forms by the finest graduated steps. It should also be constantly borne in mind that any linking variety between two forms, which might be found, would be ranked, unless the whole chain could be perfectly restored, as a new and distinct species; for it is not pretended that we have any sure criterion by which species and varieties can be discriminated.

He who rejects this view of the imperfection of the geological record, will rightly reject the whole theory. For he may ask in vain where are the nmnberless transitional links which must formerly have connected the closely allied or representative species, found in the successive stages of the same great formation? He may disbelieve in the immense intervals of time which must have elapsed between our consecutive formations ; he may overlook how important a part migration has played, when the formations of any one great region, as those of Europe, are considered; he may urge the apparent, but often falsely apparent, sudden coming in of whole groups of species. He may ask where are the remains of those infinitely numerous organisms which must have existed long before the Cambrian system was deposited? We now know that at least one animal did then exist; but I can answer this last question only by supposing that where our oceans now extend they have extended for an enormous period, and where our oscillating continents now stand they have stood since the commencement of the Cambrian system; but that, long before that epoch, the world presented a widely different aspect; and that the older continents, formed of formations older than any known to us, exist now only as remnants in a metamorphosed condition, or lie still buried under the ocean.

Passing from these difficulties, the other great leading facts in palaeontology agree admirably with the theory of descent with modification through variation and natural selection. We can thus understand how it is that new species come in slowly and successively; how species of different classes do not necessarily change together, or at the same rate, or in the same degree ; yet in the long run that all undergo modification to some extent. The extinction of old forms is the almost inevitable consequence of the production of new forms. We can understand why, when a species has once disappeared, it never reappears. Groups of species increase in numbers slowly, and endure for unequal periods of time; for the process of modification is necessarily slow, and depends on many complex contingencies. The dominant species belonging to large and dominant groups tend to leave many modified descendants, which form new sub-groups and groups. As these are formed, the species of the less vigorous groups, from their inferiority inherited from a common progenitor, tend to become extinct together, and to leave no modified offspring on the face of the earth. But the utter extinction of a whole group of species has sometimes been a slow process, from the survival of a few descendants, lingering in protected and isolated situations. When a group has once wholly disappeared, it does not reappear; for the link of generation has been broken.

We can understand how it is that dominant forms which spread widely and yield the greatest number of varieties tend to people the world with allied, but modified, descendants; and these will generally succeed in displacing the groups which are their inferiors in the struggle for existence. Hence, after long intervals of time, the productions of the world appear to have changed simultaneously.

We can understand how it is that all the forms of life, ancient and recent, make together a few grand classes. We can understand, from the continued tendency to divergence of character, why the more ancient a form is, the more it generally differs from those now living; why ancient and extinct forms often tend to fill up gaps between existing forms, sometimes blending two groups, previously classed as distinct, into one; but more commonly bringing them only a little closer together. The more ancient a form is, the more often it stands in some degree intermediate between groups now distinct ; for the more ancient a form is, the more nearly it will be related to, and consequently resemble, the common progenitor of groups, since become widely divergent. Extinct forms are seldom directly intermediate between existing forms ; but are intermediate only by a long and circuitous course through other extinct and different forms. We can clearly see why the organic remains of closely consecutive formations are closely allied; for they are closely linked together by generation. We can clearly see why the remains of an intermediate formation arc intermediate in character.

The inhabitants of the world at each successive period in its histor> have beaten their predecessors in the race for life, and are, in so far, higher in the scale, and their structure has generally become more specialised; and this may account foi the common belief lield by so many palaeontologists, that organisation on the whole has progressed. Extinct and ancient animals resemble to a certain extent the embryos of the more recent animals belonging to the same classes, and this wonderful fact receives a simple explanation according to our views. The succession of the same types of structure within the same areas during the later geological periods ceases to be mysterious, and is intelligible on the principle of inheritance.

If then the geological record be as imperfect as many believe, and it may at least be asserted that the record cannot be proved to be much more perfect, the main objections to the theory of natural selection are greatly diminished or disappear. On the other hand, all the chief laws of palaeontology plainly proclaim, as it seems to me, that species have been produced by ordinary generation : old forms having been supplanted by new and improved forms of life, the products of Variation and the Survival of the Fittest.



Present distribution cannot be accounted for by differences in physical conditions — Importance of barriers — Affinity of the productions of the same continent — Centres of creation — Means of dispersal, by changes of climate and of the level of the land, and by occasional means — Dispersal during the Glacial period — Alternate Glacial periods in the North and South.

IN considering the distribution of organic beings over the face of the globe, the first great fact which strikes us is, that neither the similarity nor the dissimilarity of the inhabitants of various regions can be wholly accounted for by climatal and other physical conditions. Of late, almost every author who has studied the subject has come to this conclusion. The case of America alone would almost suffice to prove its truth; for if we exclude the arctic and northern temperate parts, all authors agree that one of the most fundamental divisions in geographical distribution is that between the New and Old Worlds; yet if we travel over the vast American continent, from the central parts of the United States to its extreme southern point, we meet with the most diversified conditions ; humid districts, arid deserts, lofty mountains, grassy plains, forests, marshes, lakes, and great rivers, under almost every temperature. There is hardly a climate or condition in the Old World which cannot be paralleled in the New — at least as closely as the same species generally require. No doubt small areas can be pointed out in the Old World hotter than any in the New World; but these are not inhabited by a fauna different from that of the surrounding districts; for it is rare to find a group of organisms confined to a small area, of which the conditions are peculiar in only a slight degree. Notwithstanding this general parallelism in the conditions of the Old and New Worlds, how widely different are their living productions !

In the southern hemisphere, if we compare large tracts of land in Australia, South Africa, and western South America, between latitudes 25° and 35°, we shall find parts extremely similar in all their conditions, yet it would not be possible to point out three faunas and floras more utterly dissimilar. Or, again, we may compare the productions of South America south of lat. 35° with those north of 25°, which consequently are separated by a space of ten degrees of latitude, and are exposed to considerably different conditions ; yet they are incomparably more closely related to each other than they are to the productions of Australia or Africa under nearly the same climate. Analogous facts could be given with respect to the inhabitants of the sea.

A second great fact which strikes us in our general review is, that barriers of any kind, or obstacles to free migration, are related in a close and important manner to the differences between the productions of various regions. We see this in the great differences in nearly all the terrestrial productions of the New and Old Worlds, excepting in the northern parts, where the land almost joins, and where, under a slightly different climate, there might have been free migration for the northern temperate forms, as there now is for the strictly arctic productions. We see the same fact in the great difference between the inhabitants of Australia, Africa, and South America under the same latitude; for these countries are almost as much isolated from each other as is possible. On each continent, also, we see the same fact; for on the opposite sides of lofty and continuous mountain-ranges, of great deserts and even of large rivers, we find different productions; though as mountain-chains, deserts, &c., are not as impassable, or likely to have endured so long, as the oceans separating continents, the differences are very inferior in degree to those characteristic of distinct continents.

Turning to the sea, we find the same law. The marine inhabitants of the eastern and western shores of South America are very distinct, with extremely few shells, Crustacea, or echinodermata in common; but Dr. Giinther has recently shown that about thirty per cent, of the fishes are the same on the opposite sides of the isthmus of Panama; and this fact has led naturaHsts to believe that the isthmus was formerly open. Westward of the shores of America, a wide space of open ocean extends, with not an island as a haltinj^-place for emigrants ; here we have a barrier of another kind, and as soon as this is passed we meet in the eastern islands of the Pacific with another and totally distinct fauna. So that three marine faunas range far northward and southward in parallel lines not far from each other, under corresponding climates ; but from being separated from each other by impassable barriers, either of land or open sea, they are almost wholly distinct. On the other hand, proceeding still farther westward from the eastern islands of the tropical parts of the Pacific, we encounter no impassable barriers, and we have innumerable islands as halting-places, or continuous coasts, until, after travelling over a hemisphere, we come to the shores of Africa; and over this vast space we meet with no well-defined and distinct marine faunas. Although so few marine animals are common to the abovenamed three approximate faunas of Eastern and Western America and the eastern Pacific islands, yet many fishes range from the Pacific into the Indian Ocean, and many shells are common to the eastern islands of the Pacific and the eastern shores of Africa on almost exactly opposite meridians of longitude.

A third great fact, partly included in the foregoing statement, is the affinity of the productions of the same continent or of the same sea, though the species themselves are distinct at dififerent points and stations. It is a law of the widest generality, and every continent offers innumerable instances. Nevertheless, the naturalist, in travelling, for instance, from north to south, never fails to be struck by the manner in which successive groups of beings, specifically distinct, though nearly related, replace each other. Pie hears from closely allied, yet distinct kinds of birds, notes nearly similar, and sees their nests similarly constructed, but not quite alike, with eggs coloured in nearly the same manner. The plains near the Straits of Magellan are inhabited by one species of Rhea (American ostrich), and northward the plains of La Plata by another species of the same genus ; and not by a true ostrich or emu, like those inhabiting Africa and Australia under the same latitude. On these same plains of La Plata we see the agouti and bizcacha, animals having nearly the same habits as our hares and rabbits, and belonging to the same order of Rodents, but they plainly display an American type of structure. We ascend the lofty peaks of the Cordillera, and we find an alpine species of bizcacha; we look to the waters, and we do not find the beaver or musk-rat, but the coypu and capybara, rodents of the S. American type. Innumerable other instances could be given. If we look to the islands off the American shore, however much they may differ in geological structure, the inhabitants are essentially American, though they may be all peculiar species. We may look back to past ages, as shown in the last chapter, and we find American types then prevailing dn the American continent and in the American seas. We see in these facts some deep organic bond, throughout space and time, over the same areas of land and water, independently of physical conditions. The naturalist must be dull who is not led to inquire what this bond is.

The bond is simply inheritance, that cause which alone, as far as we positively know, produces organisms quite like each other, or, as we see in the case of varieties, nearly alike. The dissimilarity of the inhabitants of different regions may be attributed to modification through variation and natural selection, and probably in a subordinate degree to the definite influence of different physical conditions. The degrees of dissimilarity will depend on the migration of the more dominant forms of life from one region into another having been more or less effectually prevented, at periods more or less remote; — on the nature and number of the former immigrants; — and on the action of the inhabitants on each other in leading to the preservation of different modifications; the relation of organism to organism in the struggle for life being, as I have already often remarked, the most important of all relations. Thus the high importance of barriers comes into play by checking migration ; as does time for the slow process of modification through natural selection. Widely-ranging species, abounding in individuals, which have already triumphed over many competitors in their own widely-extended homes, will have the best chance of seizing on new places, when they spread into new countries. In their new homes they will be exposed to new conditions, and will frequently undergo further modification and improvement; and thus they will become still further victorious, and will produce groups of modified descendants. Or. this principle of inheritance with modification we can understand how it is that sections of genera, whole genera, and even families, are confined to the same areas, as is so commonly and notoriously the case.

There is no evidence, as was remarked in the last chapter, of the existence of any law of necessary development. As the variability of each species is an independent property, and will be taken advantage of by natural selection, only so far as it profits each individual in its complex struggle for life, so the amount of modification in different species will be no uniform quantity. If a number of species, after having long competed with each other in their old home, were to migrate in a body into a new and afterwards isolated country, they would be little liable to modification ; for neither migration nor isolation in themselves effect anything. These principles come into play only by bringing organisms into new relations with each other and in a lesser degree with the surrounding physical conditions. As we have seen in the last chapter that some forms have retained nearly the same character from an enormously remote geological period, so certain species have migrated over vast spaces, and have not become greatly or at all modified.

According to these views, it is obvious that the several species of the same genus, though inhabiting the most distant quarters of the world, must originally have proceeded from the same source, as they are descended from the same progenitor. In the case of those species which have undergone during whole geological periods little modification, there is not much difficulty in believing that they have migrated from the same region ; for during the vast geographical and climatal changes which have supervened since ancient times, almost any amount of migration is possible. But in many other cases, in which we have reason to believe that the species of a genus have been produced within comparatively recent times, there is great difficulty on this head. It is also obvious that the individuals of the same species, though now inhabiting distant and isolated regions, must have proceeded from one spot, where their parents were first produced : for, as has been explained, it is incredible that individuals identically the same should have been produced from parents specifically distinct.

Single Centres of supposed Creation. — We are thus brought to the question which has been largely discussed by naturalists, namely, whether species have been created at one or more points of the earth's surface. Undoubtedly there are many cases of extreme difficulty in understanding how the same species could possibly have migrated from some one point to the several distant and isolated points, where now found. Nevertheless the simplicity of the view that each species was first produced within a single region captivates the mind. He who rejects it, rejects the vera causa of ordinary generation with subsequent migration, and calls in the agency of a miracle. It is universally admitted, that in most cases the area inhabited by a species is continuous ; and that when a plant or animal inhabits two points so distant from each other, or with an interval of such a nature, that the space could not have been easily passed over by migration, the fact is given as something remarkable and exceptional. The incapacity of migrating across a wide sea is more clear in the case of terrestrial mammals than perhaps with any other organic beings; and, accordingly, we find no inexplicable instances of the same mammals inhabiting distant points of the world. No geologist feels any difficulty in Great Britain possessing the same quadrupeds with the rest of Europe, for they were no doubt once united. But if the same species can be produced at two separate points, why do we not find a single mammal common to Europe and Australia or South America? The conditions of life are nearly the same, so that a multitude of European animals and plants have become naturalised in America and Australia; and some of the aboriginal plants are identically the same at these distant points of the northern and southern hemispheres. The answer, as I believe, is, that mammals have not been able to migrate, whereas some plants, from their varied means of dispersal, have migrated across the wide and broken interspaces. The great and striking influence of barriers of all kinds, is intelligible only on the view that the great majority of species have been produced on one side, and have not been able to migrate to the opposite side. Some few families, many sub-families, very many genera, and a still greater number of sections of genera, are confined to a single region; and it has been observed by several naturalists that the most natural genera, or those genera in which the species are most closely related to each other, are generally confined to the same country, or if they have a wide range that their range is continuous. What a strange anomaly it would be, if a directly opposite rule were to prevail, when we go down one step lower in the series, namely, to the individuals of the same species, and these had not been, at least at first, confined to some one region!

Hence it seems to me, as it has to many other naturalists, that the view of each species having been produced in one area alone, and having subsequently migrated from that area as far as its powers of migration and subsistence under past and present conditions permitted, is the most probable. Undoubtedly many cases occur, in which we cannot explain how the same species could have passed from one point to the other. But the geographical and climatal changes which have certainly occurred within recent geological times, must have rendered discontinuous the formerly continuous range of many species. So that we are reduced to consider whether the exceptions to continuity of range are so numerous and of so grave a nature, that we ought to give up the belief, rendered probable by general considerations, that each species has been produced within one area, and has migrated thence as far as it could. It would be hopelessly tedious to discuss all the exceptional cases of the same species, now living at distant and separated points, nor do I for a moment pretend that any explanation could be offered of many instances. But, after some preliminary remarks, I will discuss a few of the most striking classes of facts; namely, the existence of the same species on the summits of distant mountain ranges, and at distant points in the arctic and antarctic regions; and secondly (in the following chapter), the wide distribution of fresh-water productions; and thirdly, the occurrence of the same terrestrial species on islands and on the nearest mainland, though separated by hundreds of miles of open sea. If the existence of the same species at distant and isolated points of the earth's surface, can in many instances be explained on the view of each species having migrated from a single birthplace; then, considering our ignorance with respect to former climatal and geographical changes and to the various occasional means of transport, the belief that a single birthplace is the law, seems to me incomparably the safest.

In discussing this subject, we shall be enabled at the same time to consider a point equally important for us, namely, whether the several species of a genus which must on our theory all be descended from a common progenitor, can have migrated, undergoing modification during their migration, from some one area. If, when most of the species inhabiting one region are different from those of another region, though closely allied to them, it can be shown that migration from the one region to the other has probably occurred at some former period, our general view will be much strengthened* for the explanation is obvious on the principle of descent with modification. A volcanic island, for instance, upheaved and formed at the distance of a few hundreds of miles from a continent, would probably receive from it in the course of time a few colonists, and their descendants, though modified, would still be related by inheritance to the inhabitants of that continent. Cases of this nature are common, and are, as we shall hereafter see, inexplicable on the theory of independent creation. This view of the relation of the species of one region to those of another, does not differ much from that advanced by Mr. Wallace, who concludes that "every species has come into existence coincident both in space and time with a pre-existing closely allied species." And it is now well known that he attributes this coincidence to descent with modification.

The question of single or multiple centres of creation differs from another though allied question, — namely, whether all the individuals of the same species are descended from a single pair, or single hermaphrodite, or whether, as some authors suppose, from many individuals simultaneously ereated. With organic beings which never intercross, if such exist, each species must be descended from a succession of modified varieties, that have supplanted each other, but have never blended with other individuals or varieties of the same species; so that, at each successive stage of modification, all the individuals of the same form will be descended from a single parent. But in the great majority of cases, namely, with all organisms which habitually unite for each birth, or which occasionally intercross, the individuals of the same species inhabiting the same area will be kept nearly uniform by intercrossing; so that many individuals will go on simultaneously changing, and the whole amount of modification at each stage will not be due to descent from a single parent. To illustrate what I mean: our English race-horses dififer from the horses of every other breed; but they do not owe their difference and superiority to descent from any single pair, but to continued care in the selecting and training of many individuals during each generation.

Before discussing the three classes of facts, which I have selected as presenting the greatest amount of difficulty on the theory of "single centres of creation," I must say a few words on the means of dispersal.

MEANS OF DISPERSAL

Sir C. Lyell and other authors have ably treated this subject. I can give here only the briefest abstract of the more important facts. Change of climate must have had a powerful influence on migration. A region now impassable to certain organisms from the nature of its climate, might have been a high road for migration, when the climate was different. I shall, however, presently have to discuss this branch of the subject in some detail. Changes of level in the land must also have been highly influential: a narrow isthmus now separates two marine faunas; submerge it, or let it formerly have been submerged, and the two faunas will now blend together, or may formerly have blended. Where the sea now extends, land may at a former period have connected islands or possibly even continents together, and thus have allowed terrestrial productions to pass from one to the other. No geologist disputes that great mutations of level have occurred within the period of existing organisms. Edward Forbes insisted that all the islands in the Atlantic must have been recently connected with Europe or Africa, and Europe likewise with America. Other authors have thus hypothetically bridged over every ocean, and united almost every island with some mainland. If indeed the arguments used by Forbes are to be trusted, it must be admitted that scarcely a single island exists which has not recently been united to some continent. This view cuts the Gordian knot of the dispersal of the same species to the most distant points, and removes many a difficulty; but to the best of my judgment we are not authorised in admitting such enormous geographical changes within the period of existing species. It seems to me that we have abundant evidence of great oscillations in the level of the land or sea; but not of such vast changes in the position and extension of our continents, as to have united them within the recent period to each other and to the several intervening oceanic islands. I freely admit the former existence of many islands, now buried beneath the sea, which may have served as haltingplaces for plants and for many animals during their migration. In the coral-producing oceans such sunken islands are now marked by rings of coral or atolls standing over them. Whenever it is fully admitted, as it will some day be, that each species has proceeded from a single birthplace, and when in the course of time we know something definite about the means of distribution, we shall be enabled to speculate with security on the former extension of the land. But I do not believe that it will ever be proved that within the recent period most of our continents which now stand quite separate, have been continuously, or almost continuously united with each other, and with the many existing oceanic islands. Several facts in distribution — such as the great difference in the marine faunas on the opposite sides of almost every continent, — the close relation of the tertiary inhabitants of several lands and even seas to their present inhabitants, — the degree of affinity between the mammals inhabiting islands with those of the nearest continent, being in part determined (as we shall hereafter see) by the depth of the intervening ocean, — these and other such facts are opposed to the admission of such prodigious geographical revolutions within the recent period, as arc necessary on the view advanced by Forbes and admitted by his followers. The nature and relative proportions of the inhabitants of oceanic islands are likewise opposed to the belief of their former continuity with continents. Nor does the almost universally volcanic composition of such islands favour the admission that they are the wrecks of sunken continents; — if they had originally existed as continental mountain ranges, some at least of the islands would have been formed, like other mountain summits, of granite, mctamorphic schists, old fossiliferous and other rocks, instead of consisting of mere piles of volcanic matter.

I must now say a few words on what are called accidental means, but which more properly should be called occasional means of distribution. I shall here confine myself to plants. In botanical works, this or that plant is often stated to be ill adapted for wide dissemination ; but the greater or less facilities for transport across the sea may be said to be almost wholly unknown. Until I tried, with Mr. Berkeley's aid. a few experiments, it was not even known how far seeds could resist the injurious action of sea-water. To my surprise I found that out of 87 kinds, 64 germinated after an immersion of 28 days, and a few survived an immersion of 137 davs. It deserves notice that certain orders were far more injured than others: nine Leguminosae were tried, and, with one exception, they resisted the salt-water badly ; seven species of the allied orders, Hydrophyllacede and Polemoniacere, were all killed by a month's immersion. For convenience' sake I chiefly tried small seeds without the capsule or fruit; and as all of these sank in a few days they could not have been floated across wide spaces of the sea, whether or not they were injured by the salt-water. Afterwards I tried some larger fruits, capsules, &c., and some of these floated for a long time. It is well known what a difference there is in the buoyancy of green and seasoned timber ; and it occurred to me that floods would often wash into the sea dried plants or branches with seed-capsules or fruit attached to them. Hence I was led to dry the stems and branches of 94 plants with ripe fruit, and to place them on sea-water. The majority sank quickly, but some which, whilst green, floated for a very short time, when dried floated much longer ; for instance, ripe hazel-nuts sank immediately, but when dried they floated for 90 days, and afterwards when planted germinated; an asparagus-plant with ripe berries floated for 23 days, when dried it floated for 85 days, and the seeds afterwards germinated ; the ripe seeds of Helosciadium sank in two days, when dried they floated for above 90 days, and afterwards germinated. Altogether, out of the 94 dried plants, 18 floated for above 28 days ; and some of the 18 floated for a very much longer period. So that as |^ kinds of seeds germinated after an immersion of 28 days; and as -^f distinct species with ripe fruit (but not all the same species as in the foregoing experiment) floated, after being dried, for above 28 days, we may conclude, as far as anything can be inferred from these scanty facts, that the seeds of -^^-^ kinds of plants of any country might be floated by sea-currents during 28 days, and would retain their power of germination. In Johnston's Physical Atlas, the average rate of the several Atlantic currents is 33 miles per diem (some currents running at the rate of 60 miles per diem) ; on this average, the seeds of ^-^ plants belonging to one country might be floated across 924 miles of sea to another country, and when stranded, if blown by an inland gale to a favourable spot, would germinate.

Subsequently to my experiments, M. Martens tried similar ones, but in a much better manner, for he placed the seeds in a box in the actual sea, so that they were alternately wet and exposed to the air like really floating plants. He tried 98 seeds, mostly different from mine; but he chose many large fruits and likewise seeds from plants which live near the sea: and this would have favoured both the average length of their flotation and their resistance to the injurious action of the salt-water. On the other hand, he did not previously dry the plants or branches with the fruit; and this, as we have seen, would have caused some of them to have floated much longer. The result was that -^f of his seeds of different kinds floated for 42 days, and were then capable of germination. But I do not doubt that plants exposed to the waves would float for a less time than those protected from violent movement as in our experiments. Therefore it would perhaps be safer to assume that the seeds of about ^% plants of a flora, after having been dried, could be floated across a space of sea 900 miles in width, and would then germinate. The fact of the larger fruits often floating longer than the small, is interesting; as plants with large seeds or fruit which, as Alph. de Candolle has shown, generally have restricted ranges, could hardly be transported by any other means.

Seeds may be occasionally transported in another manner. Drift timber is thrown up on most islands, even on those in the midst of the widest oceans ; and the natives of the coralislands in the Pacific procure stones for their tools, solely from the roots of drifted trees, these stones being a valuable royal tax. I find that when irregularly shaped stones are embedded in the roots of trees, small parcels of earth are frequently enclosed in their interstices and behind them, — so perfectly that not a particle could be washed away during the longest transport: out of one small portion of earth thus completely enclosed by the roots of an oak about 50 years old, three dicotyledonous plants germinated; I am certain of the accuracy of this observation. Again, I can show that the carcases of birds, when floating on the sea, sometimes escape being immediately devoured : and many kinds of seeds in the crops of floating birds long retain their vitality: peas and vetches, for instance, are killed by even a few days' immersion in sea-water; but some taken out of the crop of a pigeon, which had floated on artificial sea-water for 30 days, to my surprise nearly all germinated.

Living birds can hardly fail to be highly effective agents in the transportation of seeds. I cpuld give many facts showing how frequently birds of many kinds are blown by gales to vast distances across the ocean. We may safely assume that under such circumstances their rate of flight would often be 25 miles an hour; and some authors have given a far higher estimate. I have never seen an instance of nutritious seeds passing through the intestines of a bird; but hard seeds of fruit pass uninjured through even the digestive organs of a turkey. In the course of two months, I picked up in my garden 12 kinds of seeds, out of the excrement of small birds, and these seemed perfect, and some of them, which were tried, germinated. But the following fact is more important: the crops of birds do not secrete gastric juice, and do not, as I know by trial, injure in the least the germination of seeds; now, after a bird has found and devoured a large supply of food, it is positively asserted that all the grains do not pass into the gizzard for twelve or even eighteen hours. A bird in this interval might easily be blown to the distance of 500 miles, and hawks are known to look out for tired birds, and the contents of their torn crops might thus readily get scattered. Some hawks and owls bolt their prey whole, and, after an interval of from twelve to twenty hours, disgorge pellets, which, as I know from experiments made in the Zoological Gardens, include seeds capable of germination. Some seeds of the oat, wheat, millet, canary, hemp, clover, and beet germinated after having been from twelve to twenty-one hours in the stomachs of different birds of prey ; and two seeds of beet grew after having been thus retained for two days and fourteen hours. Fresh-water fish, I find, eat seeds of many land and water plants; fish are frequently devoured by birds, and thus the seeds might be transported from place to place. I forced many kinds of seeds into the stomachs of dead fish, and then gave their bodies to fishing-eagles, storks, and pelicans; these birds, after an interval of many hours, either rejected the seeds in pellets or passed them in their excrement; and several of these seeds retained the power of germination. Certain seeds, however, were always killed by this process. Locusts are sometimes blown to great distances from the land ; I myself caught one 370 miles from the coast of Africa, and have heard of others caught at greater distances. The Rev. R. T. Lowe informed Sir C. Lyell that in November 1844 swarms of locusts visted the island of Madeira. They were in countless numbers, as thick as the flakes of snow in the heaviest snowstorm, and extended upwards as far as could be seen with a telescope. During two or three days they slowly careered round and round in an immense ellipse, at least five or six miles in diameter, and at night alighted on the taller trees, which were completely coated with them. They then disappeared over the sea, as suddenly as they had appeared, and have not since visited the island. Now, in parts of Natal it is believed by some farmers, though on insufficient evidence, that injurious seeds are introduced into their grassland in the dung left by the great flights of locusts v^'hich often visit that country. In consequence of this belief Mr. Weale sent me in a letter a small packet of the dried pellets, out of which I extracted under the microscope several seeds, and raised from them seven grass plants, belonging to two species, of two genera. Hence a swarm of locusts, such as that which visited Madeira, might readily be the means of introducing several kinds of plants into an island lying far from the mainland.

Although the beaks and feet of birds are generally clean, earth sometimes adheres to them : in one case I removed sixty-one grains, and in another case twenty-two grains of dry argillaceous earth from the foot of a partridge, and in the earth there was a pebble as large as the seed of a vetch. Here is a better case : the leg of a woodcock was sent to me by a friend, with a little cake of dry eartli attached to the shank, weighing only nine grains ; and this contained a seed of the toad-rush (Juncus bufonius) which germinated and flowered. Mr. Swaysland, of Brighton, who during the last forty years has paid close attention to our migratory birds, informs me that he has often shot wagtails (Motacillae), wheatears, and whincats (Saxicolse), on their first arrival on our shores, before they had alighted ; and he has several times noticed little cakes of earth attached to their feet. Many facts could be given showing how generally soil is charged with seeds. For instance. Prof. Newton sent nie the leg of a red-legged partridge (Caccabis rufa) which had been wounded and could not fly, with a ball of hard earth adhering to it, and weighing six and a half ounces. The earth had been kept for three years, but when broken, watered and placed under a bell-glass, no less than 82 plants sprung from it: these consisted of 12 monocotyledons, including the common oat, and at least one kind of grass, and of 70 dicotyledons, which consisted, judging from the young leaves, of at least three distinct species. With such facts before us, can we doubt that the many birds which are annually blown by gales across great spaces of ocean, and which annually migrate— for instance, the millions of quails across the Mediterranean — must occasionally transport a few seeds embedded in dirt adhering to their feet or beaks? But I shall have to recur to this subject.

As icebergs are known to be sometimes loaded with earth and stones, and have even carried brushwood, bones, and the nest of a land-bird, it can hardly be doubted that they must occasionally, as suggested by Lyell, have transported seeds form one part to another of the arctic and antarctic regions ; and during the Glacial period from one part of the now temperate regions to another. In the Azores, from the large number of plants common to Europe, in comparison with the species on the other islands of the Atlantic, which stand nearer to the mainland, and (as remarked by Mr. H. C. Watson) from their somewhat northern character in comparison with the latitude, I suspected that these islands had been partly stocked by ice-borne seeds, during the Glacial epoch. At my request Sir C. Lyell wrote to M. Hartung to inquire whether he had observed erratic boulders on these islands, and he answered that he had found large fragments of granite and other rocks, which do not occur in the archipelago. Hence we may safely infer that icebergs formerly landed their rocky burthens on the shores of these mid-ocean islands, and it is at least possible that they may have brought thither some few seeds of northern plants.

Considering that these several means of transport, and that other means, which without doubt remain to be discovered, have been in action year after year for tens of thousands of years, it would, I think, be a marvellous fact if many plants had not thus become widely transported. These means of transport are sometimes called accidental, but this is not strictly correct: the currents of the sea are not accidental, nor is the direction of prevalent gales of wind. It should be observed that scarcely any means of transport would carry seeds for very great distances: for seeds do not retain their vitality when exposed for a great length of time to the action of sea-water; nor could they be long carried in the crops or intestines of birds. These means, however, would suffice for occasional transport across tracts of sea some hundred miles in breadth, or from island to island, or from a continent to a neighbouring island, but not from one distant continent to another. The floras of distant continents would not by such means become mingled ; but would remain as distinct as they now are. The currents, from their course, would never bring seeds from North America to Britain, though they might and do bring seeds from the West Indies to our western shores, where, if not killed by their long immersion in salt-water, they could not endure our climate. Almost every year, one or two land-birds are blown across the whole Atlantic Ocean, from North America to the western shores of Ireland and England; but seeds could be transported by these rare wanderers only by one means, namely, by dirt adhering to their feet or beaks, which is in itself a rare accident. Even in this case, how small would be the chance of a seed falling on favourable soil, and coming to maturity ! But it would be a great error to argue that because a well-stocked island, like Great Britain, has not, as far as is known (and it would be very difficult to prove this), received within the last few centuries, through occasional means of transport, immigrants from Europe or any other continent, that a poorly-stocked island, though standing more remote from the mainland, would not receive colonists by similar means. Out of a hundred kinds of seeds or animals transported to an island, even if far less well-stocked than Britain, perhaps not more than one would be so well fitted to its new home, as to become naturalised. But this is no valid argument against what would be effected by occasional means of transport, during the long lapse of geological time, whilst the island was being upheaved, and before it had become fully stocked with inhabitants. On almost bare land, with few or no destructive insects or birds living there, nearly every seed which chanced to arrive, if fitted for the climate, would germinate and survive.

DISPERSAL DURING THE GLACIAL PERIOD

The identity of many plants and animals, on mountainsummits, separated from each other by hundreds of miles of lowlands, where Alpine species could not possibly exist, is one of the most striking cases known of the same species living at distant points, without the apparent possibility of their having migrated from one point to the other. It is indeed a remarkable fact to see so many plants of the same species living on the snowy regions of the Alps or Pyrenees, and in the extreme northern parts of Europe; but it is far more remarkable, that the plants on the White Mountains, in the United States of America, are all the same with those of Labrador, and nearly all the same, as we hear from Asa Gray, with those on the loftiest mountains of Europe. Even as long ago as 1747, such facts led Gmelin to conclude that the same species must have been independently created at many distinct points ; and we might have remained in this same belief, had not Agassiz and others called vivid attention to the Glacial period, which, as we shall immediately see, affords a simple explanation of these facts. We have evidence of almost every conceivable kind, organic and inorganic, that, within a very recent geological period, central Europe and North America suffered under an arctic climate. The ruins of a house burnt by fire do not tell their tale more plainly than do the mountains of Scotland and Wales, with their scored flanks, polished surfaces, and perched boulders, of the icy streams with which their valleys were lately filled. So greatly has the climate of Europe changed, that in Northern Italy, gigantic moraines, left by old glaciers, are now clothed by the vine and maize. Throughout a large part of the United States, erratic boulders and scored rocks plainly reveal a former cold period.

The former influence of the glacial climate on the distribution of the inhabitants of Europe, as explained by Edward Forbes, is substantially as follows. But we shall follow the changes more readily, by supposing a new glacial period slowly to come on, and then pass away, as formerly occurred. As the cold came on, and as each more southern zone became fitted for the inhabitants of the north, these would take the places of the former inhabitants of the temperate regions. The latter, at the same time, would travel further and further southward, unless they were stopped by barriers, in which case they would perish. The mountains would become covered with snow and ice, and their former Alpine inhabitants would descend to the plains. By the time that the cold had reached its maximum, wc should have an arctic fauna and flora, covering the central parts of Europe, as far south as the Alps and Pyrenees, and even stretching into Spain. The now temperate regions of the United States would likewise be covered by arctic plants and animals and these would be nearly the same with those of Europe ; for the present circumpolar inhabitants, which we suppose to have everywhere travelled southward, are remarkably uniform round the world.

As the warmth returned, the arctic forms would retreat northward, closely followed up in their retreat by the productions of the more temperate regions. And as the snow melted from the bases of the mountains, the arctic forms would seize on the cleared and thawed ground, always ascending, as the warmth increased and the snow still further disappeared, higher and higher, whilst their brethren were pursuing their northern journey. Hence, when the warmth had fully returned, the same species, which had lately lived together on the European and North American lowlands, would again be found in the arctic regions of the Old and New Worlds, and on many isolated mountain-summits far distant from each other.

Thus we can understand the identity of many plants at points so immensely remote as the mountains of the United States and those of Europe. We can thus also understand the fact that the Alpine plants of each mountain-range are more especially related to the arctic forms living due north or nearly due north of them : for the first migration when the cold came on, and the re-migration on the returning warmth, would generally have been due south and north. The Alpine plants, for example, of Scotland, as remarked by Mr. H. C. Watson, and those of the Pyrenees, as remarked by Ramond, are more especially allied to the plants of northern Scandinavia ; those of the United States to Labrador; those of the mountains of Siberia to the arctic regions of that country. These views, grounded as they are on the perfectly well-ascertained occurrence of a former Glacial period, seem to me to explain in so satisfactory a manner the present distribution of the Alpine and Arctic productions of Europe and America, that when in other regions we find the same species on distant mountain-summits, we may almost conclude, without other evidence, that a colder climate formerly permitted their migration across the intervening lowlands, now become too warm for their existence.

As the arctic forms moved first southward and afterwards backwards to the north, in unison with the changing climate, they will not have been exposed during their long migrations to any great diversity of temperature; and as they all migrated in a body together, their mutual relations will not have been much disturbed. Hence, in accordance with the principles inculcated in this volume, these forms will not have been liable to much modification. But with the Alpine productions, left isolated from the moment of the returning warmth, first at the bases and ultimately on the summits of the mountains, the case will have been somewhat different; for it is not likely that all the same arctic species will have been left on mountain-ranges far distant from each other, and have survived there ever since ; they will also in all probability, have become mingled with ancient Alpine species, which must have existed on the mountains before the commencement of the Glacial epoch, and which during the coldest period will have been temporarily driven down to the plains ; they will, also, have been subsequently exposed to somewhat different climatal influences. Their mutual relations will thus have been in some degree disturbed; consequently they will have been liable to modification; and they have been modified ; for if we compare the present Alpine plants and animals of the several great European mountainranges one with another, though many of the species remain identically the same, some exist as varieties, some as doubtful forms or sub-species, and some as distinct yet closely allied species representing each other on the several ranges.

In the foregoing illustration I have assumed that at the commencement of our imaginary Glacial period, the arctic productions were as uniform round the polar regions as they are at the present day. But it is also necessary to assume that many sub-arctic and some few temperate forms were the same round the world, for some of the species which now exist on the lower mountain-slopes and on the plains of North America and Europe are the same; and it may be asked how I account for this degree of uniformity in the sub-arctic and temperate forms round the world, at the commencement of the real Glacial period. At the present day, the sub-arctic and northern temperate productions of the Old and New Worlds are separated from each other by the whole Atlantic Ocean and by the northern part of the Pacific. During the Glacial period, when the inhabitants of the Old and New Worlds lived farther southwards than they do at present, they must have been still more completely separated from each other by wider spaces of ocean; so that it may well be asked how the same species could then or previously have entered the two continents. The explanation, I believe, lies in the nature of the climate before the commencement of the Glacial period. At this, the newer Pliocene period, the majority of the inhabitants of the world were specifically the same as now, and we have good reason to believe that the climate was warmer than at the present day. Hence we may suppose that the organisms which now live under latitude 60°. lived during the Pliocene period farther north under the Polar Circle, in latitude 66°-6y* ; and that the present arctic productions then lived on the broken land still nearer to the pole. Now, if we look at a terrestrial globe, we see under the Polar Circle that there is almost continuous land from western Europe, through Siberia, to eastern America. And this continuity of the circumpolar land, with the consequent freedom under a more favourable climate for intermigration, will account for the supposed uniformity of the sub-arctic and temperate productions of the Old and New Worlds, at a period anterior to the Glacial epoch.

Believing, from reasons before alluded to, that our continents have long remained in nearly the same relative position, though subjected to great oscillations of level, I am strongly inclined to extend the above view, and to infer that during some still earlier and still warmer period, such as the older Pliocene period, a large number of the same plants and animals inhabited the almost continuous circumpolar land; and that these plants and animals, both in the Old and New Worlds, began slowly to migrate southwards as the climate became less warm, long before the commencement of the Glacial period. We now see, as I believe, their descendants, mostly in a modified condition, in the central parts of Europe and the United States. On this view we can understand the relationship with very little identity, between the productions of North America and Europe, — a relationship which is highly remarkable, considering the distance of the two areas, and their separation by the whole Atlantic Ocean. We can further understand the singular fact remarked on by several observers that the productions of Europe and America during the later tertiary stages were more closely related to each other than they are at the present time; for during these warmer periods the northern parts of the Old and New Worlds will have been almost continuously united by land, serving as a bridge, since rendered impassable by cold, for the intermigration of their inhabitants.

During the slowly decreasing warmth of the Pliocene period, as soon as the species in common, which inhabited the New and Old Worlds, migrated south of the Polar Circle, they will have been completely cut off from each other. This separation, as far as the more temperate productions are concerned, must have taken place long ages ago. As the plants and animals migrated southward, they will have become mingled in the one great region with the native American productions, and would have had to compete with them; and in the other great region, with those of the Old World. Consequently we have here everything favourable for much modification, — for far more modification than with the Alpine productions, left isolated, within a much more recent period, on the several mountain-ranges and on the arctic lands of Europe and N. America. Hence it has come, that when we compare the now living productions of the temperate regions of the New and Old Worlds, we find very few identical species (though Asa Gray has lately shown that more plants are identical than was formerly supposed), but we find in every great class many forms, which some naturalists rank as geographical races, and others as distinct species ; and a host of closely allied or representative forms which are ranked by all naturalists as specifically distinct.

As on the land, so in the waters of the sea, a slow southern migration of a marine fauna, which, during the Pliocene or even a somewhat earlier period, was nearly uniform along the continuous shores of the Polar Circle, will account, on the theory of modification, for many closely allied forms now living in marine areas completely sundered. Thus, I think, we can understand the presence of some closely allied, still existing and extinct tertiary forms, on the eastern and western shores of temperate North America; and the still more striking fact of many closely allied crustaceans (as described in Dana's admirable work), some fish and other marine animals, inhabiting the Mediterranean and the seas of Japan, — these two areas being now completely separated by the breadth of a whole continent and by wide spaces of ocean.

These cases of close relationship in species either now or formerly inhabiting the seas on the eastern and western shores of North America, the Mediterranean and Japan, and the temperate lands of North America and Europe, are inexplicable on the theory of creation. We cannot maintain that such species have been created alike, in correspondence with the nearly similar physical conditions of the areas; for if we compare, for instance, certain parts of South America with parts of South Africa or Australia, we see countries closely similar in all their physical conditions, with their inhabitants utterly dissimilar.

ALTERNATE GLACIAL PERIODS IN THE NORTH AND SOUTH

But we must return to our more immediate subject. I am convinced that Forbes' view may be largely extended. In Europe we meet with the plainest evidence of the Glacial period, from the western shores of Britain to the Oural range, and southward to the Pyrenees. We may infer from the frozen mammals and nature of the mountain vegetation, that Siberia was similarly affected. In the Lebanon, according to Dr. Hooker, perpetual snow formerly covered the central axis, and fed glaciers which rolled 4000 feet down the valleys. The same observer has recently found great moraines at a low level on the Atlas range in N. Africa. Along the Himalaya, at points 900 miles apart, glaciers have left the marks of their former low descent; and in Sikkim. Dr. Hooker saw maize growing on ancient and gigantic moraines. Southward of the Asiatic continent, on the opposite side of the equator, we know, from the excellent researches of Dr. J. Haast and Dr. Hector, that in New Zealand immense glaciers formerly descended to a low level; and the same plants found by Dr. Hooker on widely separated mountains in this island tell the same story of a former cold period. From facts communicated to me by the Rev. W. B. Clarke, it appears also that there are traces of former glacial action on the mountains of the south-eastern corner of Australia.

Looking to America; in the northern half, ice-borne fragments of rock have been observed on the eastern side of the continent, as far south as lat. 36° -37°, and on the shores of the Pacific, where the climate is now so different, as far south as lat. 46°. Erratic boulders have, also, been noticed on the Rocky Mountains. In the Cordillera of South America, nearly under the equator, glaciers once extended far below their present level. In Central Chile I examined a vast mound of detritus with great boulders, crossing the Portillo valley, which there can hardly be a doubt once formed a huge moraine; and Mr. D. Forbes informs me that he found in various parts of the Cordillera, from lat. 13° to 30° S., at about the height of 12,000 feet, deeply-furrowed rocks, resembling those with which he was familiar in Norway, and likewise great masses of detritus, including grooved pebbles. Along this whole space of the Cordillera true glaciers do not now exist even at much more considerable heights. Farther south on both sides of the continent, from lat. 41° to the southernmost extremity, we have the clearest evidence of former glacial action, in numerous immense boulders transported far from their parent source.

From these several facts, namely from the glacial action having extended all round the northern and southern hemispheres — from the period having been in a geological sense recent in both hemispheres — from its having lasted in both during a great length of time, as may be inferred from the amount of work effected — and lastly from glaciers having recently descended to a low level along the whole line of the Cordillera, it at one time appeared to me that we could not avoid the conclusion that the temperature of the whole world had been simultaneously lowered during the Glacial period. But now Mr. CroU, in a series of admirable memoirs, has attempted to show that a glacial condition of climate is the result of various physical causes, brought into operation by an increase in the eccentricity of the earth's orbit. All these causes tend towards the same end; but the most powerful appears to be the indirect influence of the eccentricity of the orbit upon oceanic currents. According to Mr. Croll, cold periods regularly recur every ten or fifteen thousand years; and these at long intervals are extremely severe, owing to certain contingencies, of which the most important, as Sir C. Lyell has shown, is the relative position of the land and water. Mr. Croll believes that the last great Glacial period occurred about 240,000 years ago, and endured with slight alterations of climate for about 160,000 years. With respect to more ancient Glacial periods, several geologists are convinced from direct evidence that such occurred during the Miocene and Eocene formations, not to mention still more ancient formations. But the most important result for us, arrived at by Mr. Croll, is that whenever the northern hemisphere passes through a cold period the temperature of the southern hemisphere is actually raised, with the winters rendered much milder, chiefly through changes in the direction of the ocean-currents. So conversely it will be with the northern hemisphere, whilst the southern passes through a Glacial period. This conclusion throws so much light on geographical distribution that I am strongly inclined to trust in it; but I will first give the facts, which demand an explanation.

In South America, Dr. Hooker has shown that besides many closely allied species, between forty and fifty of the flowering plants of Tierra del Fuego, forming no inconsiderable part of its scanty flora, are common to North America and Europe, enormously remote as these areas in opposite hemispheres are from each other. On the lofty mountains of equatorial America a host of peculiar species belonging to European genera occur. On the Organ mountains of Brazil, some few temperate European, some Antarctic, and some Andean genera were found by Gardner, which do not exist in the low intervening hot countries. On the Silla of Caraccas, the illustrious Humboldt long ago found species belonging to genera characteristic of the Cordillera.

In Africa, several forms characteristic of Europe and some few representatives of the flora of the Cape of Good Hope occur on the mountains of Abyssinia. At the Cape of Good Hope a very few European species, beHeved not to have been introduced by man, and on the mountains several representative European forms are found, which have not been discovered in the intertropical parts of Africa. Dr. Hooker has also lately shown that several of the plants living on the upper parts of the lofty island of Fernando Po and on the neighbouring Cameroon mountains, in the Gulf of Guinea, are closely related to those on the mountains of Abyssinia, and likewise to those of temperate Europe. It now also appears, as I hear from Dr. Hooker, that some of these same temperate plants have been discovered by the Rev. R. T. Lowe on the mountains of the Cape Verde islands. This extension of the same temperate forms, almost under the equator, across the whole continent of Africa and to the mountains of the Cape Verde archipelago, is one of the most astonishing facts ever recorded in the distribution of plants.

On the Himalaya, and on the isolated mountain-ranges of the peninsula of India, on the heights of Ceylon, and on the volcanic cones of Java, many plants occur, either identically the same or representing each other, and at the same time representing plants of Europe, not found in the intervening hot lowlands. A list of the genera of plants collected on the loftier peaks of Java, raises a picture of a collection made on a hillock in Europe ! Still more striking is the fact that peculiar Australian forms are represented by certain plants growing on the summits of the mountains of Borneo. Some of these Australian forms, as I hear from Dr. Hooker, extend along the heights of the peninsula of Malacca, and are thinly scattered on the one hand over India, and on the other hand as far north as Japan.

On the southern mountains of Australia, Dr. F. Miiller has discovered several European species; other species, not introduced by man, occur on the lowlands ; and a long list can be given, as I am informed by Dr. Hooker, of European genera, found in Australia, but not in the intermediate torrid regions. In the admirable 'Introduction to the Flora of New Zealand/ by Dr. Hooker, analogous and striking facts are given in regard to the plants of that large island. Hence we see that certain plants growing on the more lofty mountains of the tropics in all parts of the world, and on the temperate plains of the north and south, are either the same species or varieties of the same species. It should, however, be observed that these plants are not strictly arctic forms ; for, as Mr. H. C. Watson has remarked, "in receding from polar towards equatorial latitudes, the Alpine or mountain floras really become less and less Arctic." Besides these identical and closely allied forms, many species inhabiting the same widely sundered areas, belong to genera not now found in the intermediate tropical lowlands.

These brief remarks apply to plants alone; but some few analogous facts could be given in regard to terrestrial animals. In marine productions, similar cases likewise occur; as an example, I may quote a statement by the highest authority, Prof. Dana, that "it is certainly a wonderful fact that New Zealand should have a closer resemblance in its Crustacea to Great Britain, its antipode, than to any other part of the world." Sir J. Richardson, also, speaks of the reappearance on the shores of New Zealand, Tasmania, &c., of northern forms of fish. Dr. Hooker informs me that twenty-five species of Algae are common to New Zealand and to Europe, but have not been found in the intermediate tropical seas.

From the foregoing facts, namely, the presence of temperate forms on the highlands across the whole of equatorial Africa, and along the Peninsula of India, to Ceylon and the Malay Archipelago, and in a less well-marked manner across the wide expanse of tropical South America, it appears almost certain that at some former period, no doubt during the most severe part of a Glacial period, the lowlands of these great continents were everywhere tenanted under the equator by a considerable number of temperate forms. At this period the equatorial climate at the level of the sea was probably about the same with that now experienced at the height of from five to six thousand feet under the same latitude, or perhaps even rather cooler. During this, the coldest period, the lowlands under the equator must have been clothed with a mingled tropical and temperate vegetation, like that described by Hooker as growing luxuriantly at the height of from four to five thousand feet on the lower slopes of the Himalayas, but with perhaps a still greater preponderance of temperate forms. So again in the mountainous islands of Fernando Po, in the Gulf of Guinea, Mr. Mann found temperate European forms beginning to appear at the height of about five thousand feet. On the mountains of Panama, at the height of only two thousand feet, Dr. Seemann found the vegetation like that of Mexico, "with forms of the torrid zone harmoniously blended with those of the temperate."

Now let us see whether Mr. Croll's conclusion that when the northern hemisphere suffered from the extreme cold of the great Glacial period, the southern hemisphere was actually warmer, throws any clear light on the present apparently inexplicable distribution of various organisms in the temperate parts of both hemispheres, and on the mountains of the tropics. The Glacial period, as measured by years, must have been very long; and when we remember over what vast spaces some naturalised plants and animals have spread within a few centuries, this period will have been ample for any amount of migration. As the cold became more and more intense, we know that Arctic forms invaded the temperate regions; and, from the facts just given, there can hardly be a doubt that some of the more vigorous, dominant and widest-spreading temperate forms invaded the equatorial lowlands. The inhabitants of these hot lowlands would at the same time have migrated to the tropical and subtropical regions of the south, for the southern hemisphere was at this period warmer. On the decline of the Glacial period, as both hemispheres gradually recovered their former temperatures, the northern temperate forms living on the lowlands under the equator, would have been driven to their former homes or have been destroyed, being replaced by the equatorial forms returning from the south. Some, however, of the northern temperate forms would almost certainly have ascended any adjoining high land, where, if sufficiently lofty, they would have long survived like the Arctic forms on the mountains of Europe. They might have survived, even if the climate was not perfectly fitted for them, for the change of temperature must have been very slow, and plants undoubtedly possess a certain capacity for acclimatisation, as shown by their transmitting to their offspring different constitutional powers of resisting heat and cold.

In the regular course of events the southern hemisphere would in its turn be subjected to a severe Glacial period, with the northern hemisphere rendered warmer; and then the southern temperate forms would invade the equatorial lowlands. The northern forms which had before been left on the mountains would now descend and mingle with the southern forms. These latter, when the warmth returned, would return to their former homes, leaving some few species on the mountains, and carrying southward with them some of the northern temperate forms which had descended from their mountain fastnesses. Thus, we should have some few species identically the same in the northern and southern temperate zones and on the mountains of the intermediate tropical regions. But the species left during a long time on these mountains, or in opposite hemispheres, would have to compete with many new forms and would be exposed to somewhat different physical conditions; hence they would be eminently liable to modification, and would generally now exist as varieties or as representative species; and this is the case. We must, also, bear in mind the occurrence in both hemispheres of former Glacial periods; for these will account, in accordance with the same principles, for the many quite distinct species inhabiting the same widely separated areas, and belonging to genera not now found in the intermediate torrid zones.

It is a remarkable fact strongly insisted on by Hooker in regard to America, and by Alph. de Candolle in regard to Australia, that many more identical or slightly modified species have migrated from the north to the south, than in a reversed direction. We see, however, a few southern forms on the mountains of Borneo and Abyssinia. I suspect that this preponderant migration from the north to the south is due to the greater extent of land in the north, and to the northern forms having existed in their own homes in greater numbers, and having consequently been advanced through natural selection and competition to a higher stage of perfection, or dominating power, than the southern forms. And thus, when the two sets became commingled in the equatorial regions, during the alternations of the Glacial periods, the northern forms were the more powerful and were able to hold their places on the mountains, and afterwards to migrate southward with the southern forms ; but not so the southern in regard to the northern forms. In the same manner at the present day, we see that very many European productions cover the ground in La Plata, New Zealand, and to a lesser degree in Australia, and have beaten the natives; whereas extremely few southern forms have become naturalised in any part of the northern hemisphere, though hides, wool, and other objects likely to carry seeds have been largely imported into Europe during the last two or three centuries from La Plata and during the last forty or fifty years from Australia. The Neilgherrie mountains in India, however, offer a partial exception ; for here, as I hear from Dr. Hooker, Australian forms are rapidly sowing themselves and becoming naturalised. Before the last great Glacial period, no doubt the intertropical mountains were stocked with endemic Alpine forms; but these have almost everywhere yielded to the more dominant forms generated in the larger areas and more efficient workshops of the north. In many islands the native productions are nearly equalled, or even outnumbered, by those which have become naturalised; and this is the first stage towards their extinction. Mountains are islands on the land, and their inhabitants have yielded to those produced within the larger areas of the north, just in the same way as the inhabitants of real islands have everywhere yielded and are still yielding to continental forms naturalised through man's agency.

The same principles apply to the distribution of terrestrial animals and of marine productions, in the northern and southern temperate zones, and on the intertropical mountains. When, during the height of the Glacial period, the oceancurrents were widely different to what they now are, some of the inhabitants of the temperate seas might have reached the equator ; of these a few would perhaps at once be able to migrate southward, by keeping to the cooler currents, whilst others might remain and survive in the colder depths until the southern hemisphere was in its turn subjected to a glacial climate and permitted their further progress; in nearly the same manner as, according to Forbes, isolated spaces inhabited by Arctic productions exist to the present day in the deeper parts of the northern temperate seas.

I am far from supposing that all the difficulties in regard to the distribution and affinities of the identical and allied species, which now live so widely separated in the north and south, and sometimes on the intermediate mountain-ranges, are removed on the views above given. The exact lines of migration cannot be indicated. We cannot say why certain species and not others have migrated ; why certain species have been modified and have given rise to new forms, whilst others have remained unaltered. We cannot hope to explain such facts, until we can say why one species and not another becomes naturalised by man's agency in a foreign land ; why one species ranges twice or thrice as far, and is twice or thrice as common, as another species within their own homes.

Various special difficulties also remain to be solved ; for instance, the occurrence, as shown by Dr. Hooker, of the same plants at points so enormously remote as Kerguelen Land, New Zealand, and Fuegia; but icebergs, as suggested by Lyell, may have been concerned in their dispersal. The existence at these and other distant points of the southern hemisphere, of species, which, though distinct, belong to genera exclusively confined to the south, is a more remarkable case. Some of these species are so distinct, that we cannot suppose that there has been time since the commencement of the last Glacial period for their migration and subsequent modification to the necessary degree. The facts seem to indicate that distinct species belonging to the same genera have migrated in radiating lines from a common genera; and I am inclined to look in the southern, as in the northern hemisphere, to a former and warmer period, before the commencement of the last Glacial period, when the .Vntarctic lands, now covered with ice, supported a highly ^ peculiar and isolated flora. It may be suspected that before this flora was exterminated during the last Glacial epoch, a few forms had been already widely dispersed to various points of the southern hemisphere by occasional means of transport, and by the aid as halting-places, of now sunken islands. Thus the southern shores of America, Australia, and New Zealand may have become slightly tinted by the same peculiar forms of life.

Sir C. Lyell in a striking passage has speculated, in language almost identical with mine, on the effects of great alterations of climate throughout the world on geographical distribution. And we have now seen that Mr. Croll's conclusion that successive Glacial periods in the one hemisphere coincide with warmer periods in the opposite hemisphere, together with the admission of the slow modification of species, explains a multitude of facts in the distribution of the same and of the allied forms of life in all parts of the globe. The living waters have flowed during one period from the north and during another from the south, and in both cases have reached the equator; but the stream of life has flowed with greater force from the north than in the opposite direction, and has consequently more freely inundated the south. As the tide leaves its drift in horizontal lines, rising higher on the shores where the tide rises highest, so have the living waters left their living drift on our mountain summits, in a line gently rising from the Arctic lowlands to great altitude under the equator. The various beings thus left stranded may be compared with savage races of man, driven up and surviving in the mountain fastnesses of almost every land, which serves as a record, full of interest to us, of the former inhabitants of the surrounding lowlands.




Distribution of fresh-water productions — On the inhabitants of oceanic islands — Absence of Batrachians and of terrestrial Mammals — On the relation of the inhabitants of islands to those of the nearest mainland — On colonisation from the nearest source with subsequent modification — Summary of the last and present chapter.

FRESH-WATER PRODUCTIONS

AS lakes and river-systems are separated from each l\ Other by barriers of land, it might have been thought -*- -^ that fresh-water productions would not have ranged widely within the same country, and as the sea is apparently a still more formidable barrier, that they would never have extended to distant countries. But the case is exactly the reverse. Not only have many fresh-water species, belonging to different classes, an enormous range, but allied species prevail in a remarkable manner throughout the world. When first collecting in the fresh waters of Brazil, I well remember feeling much surprise at the similarity of the fresh-water insects, shells, &c., and at the dissimilarity of the surroimding terrestrial beings, compared with those of Britain.

But the wide ranging power of fresh-water productions can, I think, in most cases be explained by their having become fitted, in a manner highly useful to them, for short and frequent migrations from pond to pond, or from stream to stream, within their own countries; and liability to wide dispersal would follow from this capacity as an almost necessary consequence. We can here consider only a few cases; of these, some of the most difficult to explain are presented by fish. It was formerly believed that the same fresh-water species never existed on two continents distant from each other. But Dr. Giinther has lately shown that the Galaxias attenuatus inhabits Tasmania, New Zealand, the Falkland Islands, and the mainland of South America. This is a wonderful case, and probably indicates dispersal from an Antarctic centre during a former warm period. This case, however, is rendered in some degree less surprising by the species of this genus having the power of crossing by some unknown means considerable spaces of open ocean: thus there is one species common to New Zealand and to the Auckland Islands, though separated by a distance of about 230 miles. On the same continent fresh-water fish often range widely, and as if capriciously; for in two adjoining river-systems some of the species may be the same, and some wholly different.

It is probable that they are occasionally transported by what may be called accidental means. Thus fishes still alive are not very rarely dropped at distant points by whirlwinds; and it is known that the ova retain their vitality for a considerable time after removal from the water. Their dispersal may, however, be mainly attributed to changes in the level of the land within the recent period, causing rivers to flow into each other. Instances, also, could be given of this having occurred during floods, without any change of level. The wide difference of the fish on the opposite sides of most mountain-ranges, which are continuous, and which consequently must from an early period have completely prevented the inosculation of the river-system on the two sides, leads to the same conclusion. Some fresh-water fish belong to very ancient forms, and in such cases there will have been ample time for great geographical changes, and consequently time and means for much migration. Moreover Dr. Giinther has recently been led by several considerations to infer that with fishes the same forms have a long endurance. Salt-water fish can with care be slowly accustomed to live in fresh water; and, according to Valenciennes, there is hardly a single group of which all the members are confined to fresh water, so that a marine species belonging to a fresh-water group might travel far along the shores of the sea, and could, it is probable, become adapted without much difficulty to the fresh waters of a distant land.

Some species of fresh-water shells have very wide ranges, and allied species which, on our theory, are descended from a common parent, and must have proceeded from a single source, prevail throughout the world. Their distribution at first perplexed mc much, as their ova are not likely to be transported by birds; and the ova, as well as the adults, are immediately killed by sea-water. I could not even understand how some naturalised species have spread rapidly throughout the same country. But two facts, which I have observed — and many others no doubt will be discovered — throw some light on this subject. When ducks suddenly emerge from a pond covered with duck-weed, I have twice seen these little plants adhering to their backs; and it has happened to me, in removing a little duck-weed from one aquarium to another, that I have unintentionally stocked the one with fresh-water shells from the other. But another agency is perhaps more effectual : I suspended the feet of a duck in an aquarium, where many ova of fresh-water shells were hatching; and I found that numbers of the extremely minute and just-hatched shells crawled on the feet, and clung to them so firmly that when taken out of the water they could not be jarred off, though at a somewhat more advanced age they would voluntarily drop off. These just-hatched molluscs, though aquatic in their nature, survived on the (luck's feet, in damp air, from twelve to twenty hours ; and ill this length of time a duck or heron might fly at least six or seven hundred miles, and if blown across the sea to an oceanic island, or to any other distant point, would be sure to alight on a pool or rivulet. Sir Charles Lyell informs me that a Dytiscus has been caught with an Ancylus (a freshwater shell like a limpet) firmly adhering to it; and a water beetle of the same family, a Colymbetes, once dew on board the 'Beagle,' when forty-five miles distant from the nearest land : how much farther it might have been blown by a favouring gale no one can tell.

With respect to plants, it has long been known what enormous ranges many fresh-water, and even marsh species, have, both over continents and to the most remote oceanic islands. This is strikingly illustrated, according to Alph. de Candolle, in those large groups of terrestrial plants, which have very few aquatic members; for the latter seem immediately to acquire, as if in consequence, a wide range. I think favourable means of dispersal explain this fact. I have before mentioned that earth occasionally adheres in some quantity to the feet and beaks of birds. Wading birds, which frequent the muddy edges of ponds, if suddenly flushed, would be the most likely to have muddy feet. Birds of this order wander more than those of any other; and they are occasionally found on the most remote and barren islands of the open ocean; they would not be likely to alight on the surface of the sea, so that any dirt on their feet would not be washed off; and when gaining the land, they would be sure to fly to their natural fresh-water haunts. I do not believe that botanists are aware how charged the mud of ponds is with seeds; I have tried several little experiments, but will here give only the most striking case: I took in February three table-spoonfuls of mud from three different points, beneath water, on the edge of a little pond: this mud when dried weighed only 6}i ounces; I kept it covered up in my study for six months, pulling up and counting each plant as it grew; the plants were of many kinds, and were altogether 537 in number; and yet the viscid mud was all contained in a breakfast cup ! Considering these facts, I think it would be an inexplicable circumstance if water-birds did not transport the seeds of fresh-water plants to unstocked ponds and streams, situated at very distant points. The same agency may have come into play with the eggs of some of the smaller fresh-water animals.

Other and unknown agencies probably have also played a part. I have stated that fresh-water fish eat some kinds of seeds, though they reject many other kinds after having swallowed them; even small fish swallow seeds of moderate size, as of the yellow water-lily and Potamogeton. Herons and other birds, century after century, have gone on daily devouring fish; they then take flight and go to other waters, or are blown across the sea; and we have seen that seeds retain their power of germination, when rejected many hours afterwards in pellets or in the excrement. When I saw the great size of the seeds of that fine water-lily, the Nelumbium, and remembered Alph. de Candolle's remarks on the distribution of this plant, I though that the means of its dispersal must remain inexplicable; but Audubon states that he found the seeds of the great southern water-lily (probably, according to Dr. Hooker, the Nelunibium luteum) in a heron's stomach. Now this bird must often have flown with its stomach thus well stocked to distant ponds, and then getting a hearty meal of fish, analogy makes me believe that it would have rejected the seeds in a pellet in a fit state for germination.

In considering these several means of distribution, it should be remembered that when a pond or stream is first formed, for instance, on a rising islet, it will be unoccupied; and a single seed or egg will have a good chance of succeeding. Although there will always be a struggle for life between the inhabitants of the same pond, however few in kind, yet as the number even in a well-stocked pond is small in comparison with the number of species inhabiting an equal area of land, the competition between them will probably be less severe than between terrestrial species; consequently an intruder from the waters of a foreign country would have a better chance of seizing on a new place, than in the case of terrestrial colonists. We should also remember that many fresh-water productions are low in the scale of nature, and we have reason to believe that such beings become modified more slowly than the high ; and this will give time for the migration of aquatic species. We should not forget the probability of many fresh-water forms having formerly ranged continuously over immense areas, and then having become extinct at intermediate points. But the wide distribution of fresh-water plants and of the lower animals, whether retaining the same identical form or in some degree modified, apparently depends in main part on the wide dispersal of their seeds and eggs by animals, more especially by fresh-water birds, which have great powers of flight, and naturally travel from one piece of water to another.

ON THE INHABITANTS OF OCEANIC ISLANDS

We now come to the last of the three classes of facts, which I have selected as presenting the greatest amount of difficulty with respect to distribution, on the view that not only all the individuals of the same species have migrated from some one area, but that allied species, although now inhabiting the most distant points, have proceeded from a single area, — the birthplace of their early progenitors. I have already given my reason for disbelieving in continental extensions within the period of existing species, on so enormous a scale that all the many islands of the several oceans were thus stocked with their present terrestrial inhabitants. This view removes many difficulties, but it does not accord with all the facts in regard to the productions of islands. In the following remarks I shall not confine myself to the mere question of dispersal, but shall consider some other cases bearing on the truth of the two theories of independent creation and of descent with modification.

The species of all kinds which inhabit oceanic islands are few in number compared with those on equal continental areas: Alph. de Candolle admits this for plants, and Wollaston for insects. New Zealand, for instance, with its lofty mountains and diversified stations, extending over 780 miles of latitude, together with the outlying islands of Auckland, Campbell and Chatham, contain altogether only 960 kinds of flowering plants ; if we compare this moderate number with the species which swarm over equal areas in South-Western Australia or at the Cape of Good Hope, we must admit that some cause, independently of different physical conditions, has given rise to so great a difference in number. Even the uniform county of Cambridge has 847 plants, and the little island of Anglesea 764, but a few ferns and a few introduced plants are included in these numbers, and the comparison in some other respects is not quite fair. We have evidence that the barren island of Ascension aboriginally possessed less than half-a-dozen flowering plants; yet many species have now become naturalised on it, as they have in New Zealand and on every other oceanic island which can be named.

In St. Helena there is reason to believe that the naturalised plants and animals have nearly or quite exterminated many native productions. He who admits the doctrine of the creation of each separate species, will have to admit that a sufficient number of the best adapted plants and animals were not created for oceanic islands; for man has unintentionally stocked them far more fully and perfectly than did nature.

Although in oceanic islands the species are few in number, the proportion of endemic kinds (i.e. those found nowhere else in the world) is often extremely large. If we compare, for instance, the number of endemic land-shells in Madeira, or of endemic birds in the Galapagos Archipelago, with the number found on any continent, and then compare the area of the island with that of the continent, we shall see that this is true. This fact might have been theoretically expected, for, as already explained, species occasionally arriving after long intervals of time in the new and isolated district, and having to compete with new associates, would be eminently liable to modification, and would often produce groups of modified descendants. But it by no means follows that, because in an island nearly all the species of one class are peculiar, those of another class, or of another section of the same class, are peculiar ; and this difference seems to depend partly on the species which are not modified having immigrated in a body, so that their mutual relations have not been much disturbed ; and partly on the frequent arrival of unmodified immigrants from the mother-country, with which the insular forms have intercrossed. It should be borne in mind that the offspring of such crosses would certainly gain in vigour ; so that even an occasional cross would produce more effect than might have been anticipated. I will give a few illustrations of the foregoing remarks : in the Galapagos Islands there arc 26 land-birds; of these 21 for perhaps 23) are peculiar, whereas of the 11 marine birds only 2 are peculiar ; and it is obvious that marine birds could arrive at these islands much more easily and frequently than landbirds. Bermuda, on the other hand, which lies at about the same distance from North America as the Galapagos Islands do from South America, and which has a very peculiar soil, does not possess a single endemic land-bird : and wo know from Mr. J. M. Jones' admirable account of Bermuda, that very many North American birds occasionally or even frequently visit this island. Almost every year, as I am Informed by Mr. E. V. Harcourt. many European and .African birds are blown to Madeira; this island is inhabited by gcf kinds, of which one alone is peculiar, though very closely related to a European form ; and three or four other species are confined to this island and to the Canaries. So that the Islands of Bermuda and Madeira have been stocked from the neighbouring continents with birds, which for long ages have there struggled together, and have become mutually co-adapted. Hence when settled in their new homes, each kind will have been kept by the others to its proper place and habits, and will consequently have been but little liable to modification. Any tendency to modification will also have been checked by intercrossing with the unmodified immigrants, often arriving from the mother-country. Madeira again is inhabited by a wonderful number of peculiar landshells, whereas not one species of sea-shell is peculiar to its shores; now, though we do not know how sea-shells are dispersed, yet we can see that their eggs or larvae, perhaps attached to seaweed or floating timber, or to the feet of wading birds, might be transported across three or four hundred miles of open sea far more easily than land-shells. The different orders of insects inhabiting Madeira present nearly parallel cases.

Oceanic islands are sometimes deficient in animals of certain whole classes, and their places are occupied by other classes; thus in the Galapagos Islands reptiles, and in New Zealand gigantic wingless birds, take, or recently took, the place of mammals. Although New Zealand is here spoken of as an oceanic island, it is in some degree doubtful whether it should be so ranked; it is of large size, and is not separated from Australia by a profoundly deep sea; from its geological character and the direction of its mountain-ranges, the Rev. W. B. Clarke has lately maintained that this island, as well as New Caledonia, should be considered as appurtenances of Australia. Turning to plants. Dr. Hooker has shown that in the Galapagos Islands the proportional numbers of the different orders are very different from what they are elsewhere. All such differences in number, and the absence of certain whole groups of animals and plants, are generally accounted for by supposed differences in the physical conditions of the islands; but this explanation is not a little doubtful. Facility of immigration seems to have been fully as important as the nature of the conditions.

Many remarkable little facts could be given with respect to the inhabitants of oceanic islands. For instance, in certain islands not tenanted by a single mammal, some of the endemic plants have beautifully hooked seeds; yet few relations are more manifest than that hooks serve for the transportal of seeds in the wool or fur of quadrupeds. But a hooked seed might be carried to an island by other means; and the plant then becoming modified would form an endemic species, still retaining its hooks, which would form a useless appendage like the shrivelled wings under the soldered wingcovers of many insular beetles. Again, islands often possess trees or bushes belonging to orders which elsewhere include only herbaceous species ; now trees, as Alph. de Candolle has shown, generally have, whatever the cause may be, confined ranges. Hence trees would be little likely to reach distant oceanic islands ; and an herbaceous plant, which had no chance of successfully competing with the many fully developed trees growing on a continent, might, when established on an island, gain an advantage over other herbaceous plants by growing taller and taller and overtopping them. In this case, natural selection would tend to add to the stature of the plant, to whatever order it belonged, and thus first convert it into a bush and then into a tree.

ABSENCE OF BATRACHIANS AND TERRESTRIAL MAMMALS ON OCEANIC ISLANDS.

With respect to the absence of whole orders of animals on oceanic islands, Bory St. Vincent long ago remarked that Batrachians (frogs, toads, newts) are never found on any of the many islands with which the great oceans are studded. I have taken pains to verify this assertion, and have found it true, with the exception of New Zealand, New Caledonia, the Andaman Islands, and perhaps the Salomon Islands and the Seychelles. But I have already remarked that it is doubtful whether New Zealand and New Caledonia ought to be classed as oceanic islands; and this is still more doubtful with respect to the Andaman and Salomon groups and the Seychelles. This general absence of frogs, toads, and newts on so many true oceanic islands cannot be accounted for by their physical conditions : indeed it seems that islands are peculiarly fitted for these animals ; for frogs have been introduced into Madeira, the Azores, and Mauritius, and have multiplied so as to become a nuisance. But as these animals and their spavin are immediately killed (with the exception, as far as known, of one Indian species) by sea-water, there would be great difficulty in their transportal across the sea, and therefore we can see why they do not exist on strictly oceanic islands. But why, on the theory of creation, they should not have been created there, it would be very difficult to explain.

Mammals offer another and similar case. I have carefully searched the oldest voyages, and have not found a single instance, free from doubt, of a terrestrial mammal (excluding domesticated animals kept by the natives) inhabiting an island situated above 300 miles from a continent or great continental island; and many islands situated at a much less distance are equally barren. The Falkland Islands, which are inhabited by a wolf-like fox, come nearest to an exception ; but this group cannot be considered as oceanic, as it lies on a bank in connection with the mainland at the distance of about 280 miles ; moreover, icebergs formerly brought boulders to its western shores, and they may have formerly transported foxes, as now frequently happens in the arctic regions. Yet it cannot be said that small islands will not support at least small mammals, for they occur in many parts of the world on very small islands, when lying close to a continent ; and hardly an island can be named on which our smaller quadrupeds have not become naturalised and greatly multiplied. It cannot be said, on the ordinary view of creation, that there has not been time for the creation of mammals ; many vol- |

canic islands are sufficiently ancient, as shown by the stupendous degradation which they have suffered, and by their tertiary strata : there has also been time for the production of endemic species belonging to other classes ; and on continents it is known that new species of mammals appear and disappear at a quicker rate than other and lower animals. Although terrestrial mammals do not occur on oceanic islands, aerial mammals do occur on almost every island. New Zealand possesses two bats found nowhere else in the world: Norfolk Island, the Viti Archipelago, the Bonin Islands, the Caroline and Marianne Archipelagoes, and Mauritius, all possess their peculiar bats. Why, it may be asked, has the supposed creative force produced bats and no other mammals on remote islands? On my view this question can easily be answered ; for no terrestrial mammal can be transported across a wide space of sea, but bats can fly across. Bats have been seen wandering by day far over the Atlantic Ocean ; and two North American species either regularly or occasionally visit Bermuda, at the distance of 600 miles from the mainland. I hear from Mr. Tomes, who has specially studied this family, that many species have enormous ranges, and are found on continents and en far distant islands. Hence we have only to suppose that such wandering species have been modified in their new homes in relation to their new position, and we can understand the presence of endemic bats on oceanic islands, with the absence of all other terrestrial mammals.

Another interesting relation exists, namely between the depth of the sea separating islands from each other or from the nearest continent, and the degree of affinity of their mammalian inhabitants. Mr. Windsor Earl has made some striking observations on this head, since greatly extended by Mr. Wallace's admirable researches, in regard to the great Malay Archipelago, which is traversed near Celebes by a space of deep ocean, and this separates two widely distinct mammalian faunas. On either side the islands stand on a moderately shallow submarine bank, and these islands are inhabited by the same or by closely allied quadrupeds. I have not as yet had time to follow up this subject in all quarters of the world ; but as far as I have gone, the relation holds good. For instance, Britain is separated by a shallow channel from Europe, and the mammals are the same on both sides ; and so it is with all the islands near the shores of Australia. The West Indian Islands, on the other hand, stand on a deeply submerged bank, nearly 1000 fathoms in depth, and here wc find American forms, but the species and even the genera are quite distinct. As the amount of modification which animals of all kinds undergo partly depends on the lapse of time, and as the islands which are separated from each other or from the mainland by shallow channels, are more likely to have been continuously united within a recent period than the islands sepiarated by deeper channels, we can understand how it is that a relation exists between the depth of the sea separating two mammalian faunas, and the degree of their affinity, — a relation which is quite inexplicable on the theory of independent acts of creation.

The foregoing statements in regard to the inhabitants of oceanic islands, — namely, the fewness of the species, with a large proportion consisting of endemic forms — the members of certain groups, but not those of other groups in the same class, having been modified — the absence of certain whole orders, as of batrachians and of terrestrial mammals, notwithstanding the presence of aerial bats, — the singular proportions of certain orders of plants, — herbaceous forms having been developed into trees, &c., — seem to me to accord better with the belief in the efficiency of occasional means of transport, carried on during a long course of time, than with the belief in the former connection of all oceanic islands with the nearest continent; for on this latter view it is probable that the various classes would have immigrated more uniformly, and from the species having entered in a body their mutual relations would not have been much disturbed, and consequently they would either have not been modified, or all the species in a more equable manner.

I do not deny that there are many and serious difficulties in understanding how many of the inhabitants of the more remote islands, whether still retaining the same specific form or subsequently modified, have reached their present homes. But the probability of other islands having once existed as halting-places, of which not a wreck now remains, must not be overlooked. I will specify one difficult case. Almost all oceanic islands, even the most isolated and smallest, are inhabited by land-shells, generally by endemic species, but sometimes by species found elsewhere, — striking instances of which have been given by Dr. A. A. Gould in relation to the Pacific. Now it is notorious that land-shells are easily killed by sea-water ; their eggs, at least such as I have tried, sink in it and are killed. Yet there must be some unknown, but occasionally efficient means for their transportal. Would the just-hatched young sometimes adhere to the feet of birds roosting on the ground, and thus get transported? It occurred to me that land-shells, when hybernating and having a membranous diaphragm over the mouth of the shell, might be floated in chinks of drifted timber across moderately wide arms of the sea. And I find that several species in this state withstand uninjured an immersion in sea- water during seven days : one shell, the Helix pomatia, after having been thus treated and again hybernating was put into sea-water for twenty days, and perfectly recovered. During this length of time the shell might have been carried by a marine current of average swiftness, to a distance of 660 geographical miles. As this Helix has a thick calcareous operculum. I removed it, and when it had formed a new membranous one, I again immersed it for fourteen days in sea-water, and again it recovered and crawled away. Baron Aucapitaine has since tried similar experiments ; he placed 100 land-shells, belonging to ten species, in a box pierced with holes, and immersed it for a fortnight in the sea. Out of the hundred shells, twenty-seven recovered. The presence of an operculum seems to have been of importance, as out of twelve specimens of Cyclostoma elegans, which is thus furnished, eleven revived. It is remarkable, seeing how well the Helix pomatia resisted with me the salt-water, that not one of fifty-four specimens belonging to four other species of Helix tried by Aucapitaine, recovered. It is, however, not at all probable that land-shells have often been thus transported ; the feet of birds offer a more probable method.

ON THE RELATIONS OF THE INHABITANTS OF ISLANDS TO THOSE OF THE NEAREST MAINLAND

The most striking and important fact for us is the affinity of the species which inhabit islands to those of the nearest mainland, without being actually the same. Numerous instances could be given. The Galapagos Archipelago, situated under the equator, lies at the distance of between 500 and 600 miles from the shores of South America. Here almost every product of the land and of the water bears the unmistakeable stamp of the American continent. There are twenty-six land-birds; of these, twenty-one, or perhaps twenty-three, are ranked as distinct species, and would commonly be assumed to have been here created : yet the close affinity of most of these birds to American species is manifest in every character, in their habits, gestures, and tones of voice. So it is with the other animals, and with a large proportion of the plants, as shown by Dr. Hooker in his admirable Flora of this archipelago. The naturalist, looking at the inhabitants of these volcanic islands in the Pacific, distant several hundred miles from the continent, feels that he is standing on American land. Why should this be so? why should the species which are supposed to have been created in the Galapagos Archipelago, and nowhere else, bear so plainly the stamp of affinity to those created in America? There is nothing in the conditions of life, in the geological nature of the islands, in their height or climate, or in the proportions in which the several classes are associated together, which closely resembles the conditions of the South American coast: in fact, there is a considerable dissimilarity in all these respects. On the other hand, there is a considerable degree of resemblance in the volcanic nature of the soil, in the climate, height and size of the islands, between the Galapagos and Cape Verde Archipelagoes: but what an entire and absolute difference in their inhabitants ! The inhabitants of the Cape Verde Islands are related to those of Africa, like those of the Galapagos to America. Facts such as these, admit of no sort of explanation on the ordinary view of independent creation : whereas on the view here maintained, it is obvious that the Galapagos Islands would be likely to receive colonists from America, whether by occasional means of transport or (though I do not believe in this doctrine) by formerly continuous land, and the Cape Verde Islands from Africa; such colonists would be liable to modification, — the principle of inheritance still betraying their original birthplace.

Many analogous facts could be given: indeed it is an almost universal rule that the endemic productions of islands t are related to those of the nearest continent, or of the nearest large island. The exceptions are few, and most of them can be explained. Thus although Kerguelen Land stands nearer to Africa than to America, the plants are related, and that very closely, as we know from Dr. Hooker's account, to those of America: but on the view that this island has been mainly stocked by seeds brought with earth and stones on icebergs, drifted by the prevailing currents, this anomaly disappears. New Zealand in its endemic pianos is much more closely related to Australia, the nearest mainland, than to any other region: and this is what might have been expected ; but it is also plainly related to South America, which, although the next nearest continent, is so enormously remote, that the fact becomes an anomaly. But this difficulty partially disappears on the view that New Zealand. South America, and the other southern lands have been stocked in part from a nearly intermediate though distant point, namely from the antarctic islands, when they were clothed with vegetation, during a warmer tertiary period, before the commencement of the last Glacial period. The affinity, which though feeble, I am assured by Dr. Hooker is real, between the flora of the south-western corner of Australia and of the Cape of Good Hope, is a far more remarkable case : but this affinity is confined to the plants, and will, no doubt, some day be explained.

The same law which has determined the relationship between the inhabitants of islands and the nearest mainland, is sometimes displayed on a small scale, but in a most interesting manner, within the limits of the same archipelago. Thus each separate island of the Galapagos Archipelago is tenanted, and the fact is a marvellous one, by many distinct species ; but these species are related to each other in a very much closer manner than to the inhabitants of the .American continent, or of any other quarter of the world. This is what might have been expected, for islands situated so near to each other would almost necessarily receive immigrants from the same original source, and from each other. But how is it that many of the immigrants have been differently modified, though only in a small degree, in islands situated within sight of each other, having the same geological nature, the same height, climate, &c. ? This long aiiiK'arcd to me a great difficulty: but it arises in chief part from the deeply-seated error of considering the physical conditions of a country as the most important: whereas it cannot be disputed that the nature of the other species with which each has to compete, is at least as important, and generally a far more important element of success. Now if we look to the species which inhabit the Galapagos Archipelago, and are likewise found in other parts of the world, we find that they differ considerably in the several islands. This difference might indeed have been expected if the islands have been stocked by occasional means of transport — a seed, for instance, of one plant having been brought to one island, and that of another plant to another island, though all proceeding from the same general source. Hence, when in former times an immigrant first settled on one of the islands, or when it subsequently spread from one to another, it would undoubtedly be exposed to different conditions in the different islands, for it would have to compete with a different set of organisms; a plant, for instance, would find the ground best fitted for it occupied by somewhat different species in the different islands, and would be exposed to the attacks of somewhat different enemies. If then it varied, natural selection would probably favour different varieties in the different islands. Some species, however, might spread and yet retain the same character throughout the group, just as we see some species spreading widely throughout a continent and remaining the same.

The really surprising fact in this case of the Galapagos Archipelago, and in a lesser degree in some analogous cases, is that each new species after being formed in any one island, did not spread quickly to the other islands. But the islands, though in sight of each other, are separated by deep arms of the sea, in most cases wider than the British Channel, and there is no reason to suppose that they have at any former period been continuously united. The currents of the sea are rapid and sweep between the islands, and gales of wind are extraordinarily rare ; so that the islands are far more effectually separated from each other than they appear on a map. Nevertheless some of the species, both of those found in other parts of the world and of those confined to the archipelago, are common to the several islands; and we may infer from their present manner of distribution, that they have spread from one island to the others. But we often take, I think, an erroneous view of tlie probability of closely-allied species invading each other's territory, when put into free intercommunication. Undoubtedly, if one species has any advantat^^e over another, it will in a very brief time wholly or in part supplant it; but if both are equally well fitted for their own places, both will prob"bly hold their separate places for almost any length of time. Being familiar with the fact that many species, naturalised through man's agency, have spread with astonishing rapidity over wide areas, we are apt to infer that most species would thus spread; but we should remember that the species which become naturalised in new countries are not generally closely allied to the aboriginal inhabitants, but are very distinct forms, belonging in a large proportion of cases, as shown by Alph. de Candolle, to distinct genera. In the Galapagos Archipelago, many even of the birds, though so well adapted for flying from island to island, differ on the different islands; thus there are three closely-allied species of mocking-thrush, each confined to its own island. Now let us suppose the mocking-thrush of Chatham Island to be blown to Charles Island, which has its own mocking-thrush ; why should it succeed in establishing itself there? We may safely infer that Charles Island is well stocked with its own species, for annually more eggs are laid and young birds hatched, than can possibly be reared; and we may infer that the mocking-thrush peculiar to Charles Island is at least as well fitted for its home as is the species peculiar to Chatham Island. Sir C. Lyell and Mr. Wollaston have communicated to me a remarkable fact bearing on this subject; namely, that Madeira and the adjoining islet of Porto Santo possess many distinct but representative species of land-shells, some of which live in crevices of stone; and although large quantities of stone are annually transported from Porto Santo to Madeira, yet this latter island has not become colonised by the Porto Santo species; nevertheless both islands have been colonised by European land-shells, which no doubt had some advantage over the indigenous species. From these considerations I think we need not greatly marvel at the endemic species which inhabit the several islands of the Galapagos Archipelago, not having all spread from island to island. On the same continent, also, preoccupation has probably played an important part in checking the commingling of the species which inhabit different districts with nearly the same physical conditions. Thus, the south-east and south-west corners of Australia have nearly the same physical conditions and are united by continuous land, yet they are inhabited by a vast number of distinct mammals, birds, and plants; so it is, according to Mr. Bates, with the butterflies and other anim^als inhabiting the great, open, and continuous valley of the Amazons.

The same principle which governs the general character of the inhabitants of oceanic islands, namely, the relation to the source whence colonists could have been most easily derived, together with their subsequent modification, is of the widest application throughout nature. We see this on every mountain-summit, in every lake and marsh. For Alpine species, excepting in as far as the same species have become widely spread during the Glacial epoch, are related to those of the surrounding lowlands; thus we have in South America, Alpine humming-birds, Alpine rodents, Alpine plants, all strictly belonging to American forms ; and it is obvious that a mountain, as it became slowly upheaved, would be colonised from the surrounding lowlands. So it is with the inhabitants of lakes and marshes, excepting in so far as great facility of transport has allowed the same forms to prevail throughout large portions of the world. We see this same principle in the character of most of the blind animals inhabiting the caves of America and of Europe. Other analogous facts could be given. It will, I believe, be found universally true, that wherever in two regions, let them be ever so distant, many closely allied or representative species occur, there will likewise be found some identical species ; and wherever many closely-allied species occur, there will be found many forms which some naturalists rank as distinct species, and others as mere varieties ; these doubtful forms showing us the steps in the progress of modification.

The relation between the power and extent of migration in certain species, either at the present or at some former period, and the existence at remote points of the world of closely-allied species, is shown in another and more general way. Mr. Gould remarked to me long ago, that in those genera of birds which range over the world, many of the species have very wide ranges. I can hardly doubt that this rule is generally true, though difficult of proof. Amongst mammals, we see it strikingly displayed in Bats, and In a lesser degree in the Felidae and Canidae. We see the same rule in the distribution of butterflies and beetles. So it is with most of the inhabitants of fresh water, for many of the genera in the most distinct classes range over the world, and many of the species have enormous ranges. It is not meant that all, but that some of the species have very wide ranges in the genera which range very widely. Nor is it meant that the species in such genera have on an average a very wide range ; for this will largely depend on how far the process of modification has gone; for instance, two varieties of the same species inhabit America and Europe, and thus the species has an immense range; but, if variation were to be carried a little further, the two varieties would be ranked as distinct species, and their range would be greatly reduced. Still less is it meant, that species which have the capacity of crossing barriers and ranging widely, as in the case of certain powerfully-winged birds, will necessarily range widely ; for we should never forget that to range widely implies not only the power of crossing barriers, but the more important power of being victorious in distant lands in the struggle for life with foreign associates. But according to the view that all the species of a genus, though distributed to the most remote points of the world, are descended from a single progenitor, we ought to find, and I believe as a general rule we do find, that some at least of the species range very widely. We should bear in mind that many genera in all classes are of ancient origin, and the species in this case will have had ample time for dispersal and subsequent modification. There is also reason to believe from geological evidence that within each great class the lower organisms change at a slower rate than the higher; consequently they will have had a better chance of ranging widely and of still retaining the same specific character. This fact, together with that of the seeds and eggs of most lowly organised forms being very minute and better fitted for distant transportal, probably accounts for a law which has long been observed, and which has lately been discussed by Alph. de Candolle in regard to plants, namely, that the lower any group of organisms stands the more widely it ranges.

The relations just discussed, — namely, lower organisms ranging more widely than the higher, — some of the species of widely-ranging genera themselves ranging widely, — such facts, as alpine, lacustrine, and marsh productions being generally related to those which live on the surrounding low lands and dry lands, — the striking relationship between the inhabitants of islands and those of the nearest mainland — the still closer relationship of the distinct inhabitants of the islands in the same archipelago — are inexplicable on the ordinary view of the independent creation of each species, but are explicable if we admit colonisation from the nearest or readiest source, together with the subsequent adaptation of the colonists to their new homes.

SUMMARY OF THE LAST AND PRESENT CHAPTERS

In these chapters I have endeavoured to show, that if we make due allowance for our ignorance of the full effects of changes of climate and of the level of the land, which have certainly occurred within the recent period, and of other changes which have probably occurred, — if we remember how ignorant we are with respect to the many curious means of occasional transport, — if we bear in mind, and this is a very important consideration, how often a species may have ranged continuously over a wide area, and then have become extinct in the intermediate tracts, — the difficulty is not insuperable in believing that all the individuals of the same species, wherever found, are descended from common parents. And we are led to this conclusion, which has been arrivedatbymany naturalists underthe designation of single centres of creation, by various general considerations, more especially from the importance of barriers of all kinds, and from the analogical distribution of sub-genera, genera, and families.

With respect to distinct species belonging to the same genus, which on our theory have spread from one parentsource ; if we make the same allowances as before for our ignorance, and remember that some forms of life have changed very slowly, enormous periods of time having been thus granted for their migration, the difficulties are far from insuperable; though in this case, as in that of the individuals of the same species, they are often great.

As exemplifying the effects of climatal changes on distribution. I have attempted to show how important a part the last Glacial period has played, which affected even the equatorial regions, and which, during the alternations of the cold in the north and south, allowed the productions of opposite hemispheres to mingle, and left some of them stranded on the mountain-summits in all parts of the world. As showing how diversified are the means of occasional transport, I have discussed at some little length the means of dispersal of freshwater productions.

If the difficulties be not insuperable in admitting that in the long course of time all the individuals of the same species, and likewise of the several species belonging to the same genus, have proceeded from some one source ; then all the grand leading facts of geographical distribution are explicable on the theory of migration, together with subsequent modification and the multiplication of new forms. We can thus understand the high importance of barriers, whether of land or water, in not only separating, but in apparently forming the several zoological and botanical provinces. We can thus understand the concentration of related species within the same areas; and how it is that under different latitudes, for instance in South America, the inhabitants of the plains and mountains, of the forests, marshes, and deserts, are linked together in so mysterious a manner, and are likewise linked to the extinct beings which formerly inhabited the same continent. Bearing in mind that the mutual relation of organism to organism is of the highest importance, we can see why two areas having nearly the same physical conditions should often be inhabited by very different forms of life; for according to the length of time which has elapsed since the colonists entered one of the regions, or both; according to the nature of the communication which allowed certain forms and not others to enter, either in greater or lesser numbers; according or not, as those which entered happened to come into more or less direct competition with each other and with the aborigines : and according as the immigrants were capable of varying more or less rapidly, there would ensue in the two or more regions, independently of their physical conditions, infinitely diversified conditions of life, — there would be an almost endless amount of organic action and reaction, — and we should find some groups of beings greatly, and some only slightly modified, — some developed in great force, some existing in scanty numbers — and this we do find in the several great geographical provinces of the world.

On these same principles we can understand, as I have endeavoured to show, why oceanic islands should have few inhabitants, but that of these, a large proportion should be endemic or peculiar; and why, in relation to the means of migration, one group of beings should have all its species peculiar, and another group, even within the same class, should have all its species the same with those in an adjoining quarter of the world. We can see why whole groups of organisms, as batrachians and terrestrial mammals, should be absent from oceanic islands, whilst the most isolated islands should possess their own peculiar species of aerial mammals or bats. We can see why, in islands, there should be some relation between the presence of mammals, in a more or less modified condition, and the depth of the sea between such islands and the mainland. We can clearly see why all the inhabitants of an archipelago, though specifically distinct on the several islets, should be closely related to each other; and should likewise be related, but less closely, to those of the nearest continent, or other source whence immigrants might have been derived. We can see why, if there exist very closely allied or representative species in two^ areas, however distant from each other, some identical species will almost always there be found.

As the late Edward Forbes often insisted, there is a striking parallelism in the laws of life throughout time and space; the laws governing the succession of forms in past times being nearly the same with those governing at the present time the differences in different areas. We see this in many facts. The endurance of each species and group of species is continuous in time ; for the apparent exceptions to the rule are so few, that they may fairly be attributed to our not having as yet discovered in an intermediate deposit certain forms which are absent in it, but which occur both above and below : so in space, it certainly is the general rule that the area inhabited by a single species, or by a group of species, is continuous, and the exceptions, which are not rare, may, as I have attempted to show, be accounted for by former migrations under different circumstances, or through occasional means of transport, or by the species having become extinct in the intermediate tracts. Both in time and space species and groups of species have their points of maximum development. Groups of species, living during the same period of time, or living within the same area, are often characterised by trifling features in common, as of sculpture or colour. In looking to the long succession of past ages, as in looking to distant provinces throughout the world, we find that species in certain classes differ little from each other, whilst those in another class, or only in a different section of the same order, differ greatly from each other. In both time and space the lowly organised members of each class generally change less than the highly organised; but there are in both cases marked exceptions to the rule. According to our theory, these several relations throughout time and space are intelligible ; for whether we look to the allied forms of life which have changed during successive ages, or to those which have changed after having migrated into distant quarters, in both cases they are connected by the same bond of ordinary generation; in both cases the laws of variation have been the same, and modifications have been accumulated by the same means of natural selection.