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双语《物种起源》 第十二章 地理分布(续)

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2022年07月03日

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CHAPTER XII GEOGRAPHICAL DISTRIBUTION—continued

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 chapters

As lakes and river-systems are separated from each 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 impassable barrier, that they never would have extended to distant countries. But the case is exactly the reverse. Not only have many fresh-water species, belonging to quite different classes, an enormous range, but allied species prevail in a remarkable manner throughout the world. I well remember, when first collecting in the fresh waters of Brazil, feeling much surprise at the similarity of the fresh-water insects, shells, etc., and at the dissimilarity of the surrounding terrestrial beings, compared with those of Britain.

But this power in fresh-water productions of ranging widely, though so unexpected, 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; and liability to wide dispersal would follow from this capacity as an almost necessary consequence. We can here consider only a few cases. In regard to fish, I believe that the same species never occur in the fresh waters of distant continents. But on the same continent the species often range widely and almost capriciously; for two river-systems will have some fish in common and some different. A few facts seem to favour the possibility of their occasional transport by accidental means; like that of the live fish not rarely dropped by whirlwinds in India, and the vitality of their ova when removed from the water. But I am inclined to attribute the dispersal of fresh-water fish mainly to slight changes within the recent period in the level of the land, having caused rivers to flow into each other. Instances, also, could be given of this having occurred during floods, without any change of level. We have evidence in the loess of the Rhine of considerable changes of level in the land within a very recent geological period, and when the surface was peopled by existing land and fresh-water shells. The wide difference of the fish on opposite sides of continuous mountain-ranges, which from an early period must have parted river-systems and completely prevented their inosculation, seems to lead to this same conclusion. With respect to allied fresh-water fish occurring at very distant points of the world, no doubt there are many cases which cannot at present be explained: but 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. In the second place, 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 fishes confined exclusively to fresh water, so that we may imagine that a marine member of a fresh-water group might travel far along the shores of the sea, and subsequently become modified and adapted to the fresh waters of a distant land.

Some species of fresh-water shells have a very wide range, and allied species, which, on my theory, are descended from a common parent and must have proceeded from a single source, prevail throughout the world. Their distribution at first perplexed me much, as their ova are not likely to be transported by birds, and they are immediately killed by sea water, as are the adults. I could not even understand how some naturalised species have rapidly spread throughout the same country. But two facts, which I have observed—and no doubt many others remain to be observed—throw some light on this subject. When a duck suddenly emerges from a pond covered with duck-weed, I have twice seen these little plants adhering to its back; and it has happened to me, in removing a little duck-weed from one aquarium to another, that I have quite unintentionally stocked the one with fresh-water shells from the other. But another agency is perhaps more effectual: I suspended a duck's feet, which might represent those of a bird sleeping in a natural pond, 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 duck's feet, in damp air, from twelve to twenty hours; and in this length of time a duck or heron might fly at least six or seven hundred miles, and would be sure to alight on a pool or rivulet, if blown across sea to an oceanic island or to any other distant point. Sir Charles Lyell also informs me that a Dyticus has been caught with an Ancylus (a fresh-water shell like a limpet) firmly adhering to it; and a water-beetle of the same family, a Colymbetes, once flew on board the “Beagle,” when forty-five miles distant from the nearest land: how much farther it might have flown with 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 shown, as remarked by Alph. de Candolle, in large groups of terrestrial plants, which have only a very few aquatic members; for these latter seem immediately to acquire, as if in consequence, a very wide range. I think favourable means of dispersal explain this fact. I have before mentioned that earth occasionally, though rarely, 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 I can show are the greatest wanderers, and are occasionally found on the most remote and barren islands in the open ocean; they would not be likely to alight on the surface of the sea, so that the dirt would not be washed off their feet; when making 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 dry weighed only 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 vast distances, and if consequently the range of these plants was not very great. 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 in pellets or in excrement, many hours afterwards. When I saw the great size of the seeds of that fine water-lily, the Nelumbium, and remembered Alph. de Candolle's remarks on this plant, I thought that its distribution must remain quite inexplicable; but Audubon states that he found the seeds of the great southern water-lily (probably, according to Dr. Hooker, the Nelumbium luteum) in a heron's stomach; although I do not know the fact, yet analogy makes me believe that a heron flying to another pond and getting a hearty meal of fish, would probably reject from its stomach a pellet containing the seeds of the Nelumbium undigested; or the seeds might be dropped by the bird whilst feeding its young, in the same way as fish are known sometimes to be dropped.

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 individuals of the species, however few, already occupying any pond, yet as the number of kinds is small, compared with those on the land, the competition will probably be less severe between aquatic than between terrestrial species; consequently an intruder from the waters of a foreign country, would have a better chance of seizing on a place, than in the case of terrestrial colonists. We should, also, remember that some, perhaps many, fresh-water productions are low in the scale of nature, and that we have reason to believe that such low beings change or become modified less quickly than the high; and this will give longer time than the average for the migration of the same aquatic species. We should not forget the probability of many species having formerly ranged as continuously as fresh-water productions ever can range, over immense areas, and having subsequently become extinct in intermediate regions. But the wide distribution of fresh-water plants and of the lower animals, whether retaining the same identical form or in some degree modified, I believe mainly depends on the wide dispersal of their seeds and eggs by animals, more especially by fresh-water birds, which have large powers of flight, and naturally travel from one to another and often distant piece of water. Nature, like a careful gardener, thus takes her seeds from a bed of a particular nature, and drops them in another equally well fitted for them.

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, on the view that all the individuals both of the same and of allied species have descended from a single parent; and therefore have all proceeded from a common birthplace, notwithstanding that in the course of time they have come to inhabit distant points of the globe. I have already stated that I cannot honestly admit Forbes's view on continental extensions, which, if legitimately followed out, would lead to the belief that within the recent period all existing islands have been nearly or quite joined to some continent. This view would remove many difficulties, but it would not, I think, explain all the facts in regard to insular productions. In the following remarks I shall not confine myself to the mere question of dispersal; but shall consider some other facts, which bear 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. If we look to the large size and varied stations of New Zealand, extending over 780 miles of latitude, and compare its flowering plants, only 750 in number, with those on an equal area at the Cape of Good Hope or in Australia, we must, I think, admit that something quite independently of any difference in physical conditions has caused 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 under half-a-dozen flowering plants; yet many have become naturalised on it, as they have on 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 have not been created on oceanic islands; for man has unintentionally stocked them from various sources far more fully and perfectly than has nature.

Although in oceanic islands the number of kinds of inhabitants is scanty, the proportion of endemic species (i.e. those found nowhere else in the world) is often extremely large. If we compare, for instance, the number of the endemic land-shells in Madeira, or of the endemic birds in the Galapagos Archipelago, with the number found on any continent, and then compare the area of the islands with that of the continent, we shall see that this is true. This fact might have been expected on my theory, for, as already explained, species occasionally arriving after long intervals in a new and isolated district, and having to compete with new associates, will be eminently liable to modification, and will 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 on the species which do not become modified having immigrated with facility and in a body, so that their mutual relations have not been much disturbed. Thus in the Galapagos Islands nearly every land-bird, but only two out of the eleven marine birds, are peculiar; and it is obvious that marine birds could arrive at these islands more easily than land-birds. 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 one endemic land bird; and we know from Mr. J. M. Jones's admirable account of Bermuda, that very many North American birds, during their great annual migrations, visit either periodically or occasionally this island. Madeira does not possess one peculiar bird, and many European and African birds are almost every year blown there, as I am informed by Mr. E. V. Harcourt. So that these two islands of Bermuda and Madeira have been stocked by birds, which for long ages have struggled together in their former homes, and have become mutually adapted to each other; and when settled in their new homes, each kind will have been kept by the others to their proper places and habits, and will consequently have been little liable to modification. Madeira, again, is inhabited by a wonderful number of peculiar land-shells, whereas not one species of sea-shell is confined 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 far more easily than land-shells, across three or four hundred miles of open sea. The different orders of insects in Madeira apparently present analogous facts.

Oceanic islands are sometimes deficient in certain classes, and their places are apparently occupied by the other inhabitants; in the Galapagos Islands reptiles, and in New Zealand gigantic wingless birds, take the place of mammals. In the plants of the Galapagos Islands, Dr. Hooker has shown that the proportional numbers of the different orders are very different from what they are elsewhere. Such cases are generally accounted for by the physical conditions of the islands; but this explanation seems to me not a little doubtful. Facility of immigration, I believe, has been at least as important as the nature of the conditions.

Many remarkable little facts could be given with respect to the inhabitants of remote islands. For instance, in certain islands not tenanted by mammals, some of the endemic plants have beautifully hooked seeds; yet few relations are more striking than the adaptation of hooked seeds for transportal by the wool and fur of quadrupeds. This case presents no difficulty on my view, for a hooked seed might be transported to an island by some other means; and the plant then becoming slightly modified, but still retaining its hooked seeds, would form an endemic species, having as useless an appendage as any rudimentary organ,—for instance, as the shrivelled wings under the soldered elytra 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, though it would have no chance of successfully competing in stature with a fully developed tree, when established on an island and having to compete with herbaceous plants alone, might readily gain an advantage by growing taller and taller and overtopping the other plants. If so, natural selection would often tend to add to the stature of herbaceous plants when growing on an island, to whatever order they belonged, and thus convert them first into bushes and ultimately into trees.

With respect to the absence of whole orders on oceanic islands, Bory St. Vincent long ago remarked that Batrachians (frogs, toads, newts) have never been found on any of the many islands with which the great oceans are studded. I have taken pains to verify this assertion, and I have found it strictly true. I have, however, been assured that a frog exists on the mountains of the great island of New Zealand; but I suspect that this exception (if the information be correct) may be explained through glacial agency. This general absence of frogs, toads, and newts on so many oceanic islands cannot be accounted for by their physical conditions; indeed it seems that islands are peculiarly well 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 spawn are known to be immediately killed by sea-water, on my view we can see that there would be great difficulty in their transportal across the sea, and therefore why they do not exist on any oceanic island. 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, but have not finished my search; as yet I 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 connected with the mainland; moreover, icebergs formerly brought boulders to its western shores, and they may have formerly transported foxes, as so frequently now happens in the arctic regions. Yet it cannot be said that small islands will not support small mammals, for they occur in many parts of the world on very small islands, if 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 volcanic 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 thought that mammals appear and disappear at a quicker rate than other and lower animals. Though terrestrial mammals do not occur on oceanic islands, a.rial 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 of the same species have enormous ranges, and are found on continents and on far distant islands. Hence we have only to suppose that such wandering species have been modified through natural selection in their new homes in relation to their new position, and we can understand the presence of endemic bats on islands, with the absence of all terrestrial mammals.

Besides the absence of terrestrial mammals in relation to the remoteness of islands from continents, there is also a relation, to a certain extent independent of distance, between the depth of the sea separating an island from the neighbouring mainland, and the presence in both of the same mammiferous species or of allied species in a more or less modified condition. Mr. Windsor Earl has made some striking observations on this head in regard to the great Malay Archipelago, which is traversed near Celebes by a space of deep ocean; and this space separates two widely distinct mammalian faunas. On either side the islands are situated on moderately deep submarine banks, and they are inhabited by closely allied or identical quadrupeds. No doubt some few anomalies occur in this great archipelago, and there is much difficulty in forming a judgment in some cases owing to the probable naturalisation of certain mammals through man's agency; but we shall soon have much light thrown on the natural history of this archipelago by the admirable zeal and researches of Mr. Wallace. I have not as yet had time to follow up this subject in all other quarters of the world; but as far as I have gone, the relation generally holds good. We see Britain separated by a shallow channel from Europe, and the mammals are the same on both sides; we meet with analogous facts on many islands separated by similar channels from Australia. The West Indian Islands stand on a deeply submerged bank, nearly 1000 fathoms in depth, and here we find American forms, but the species and even the genera are distinct. As the amount of modification in all cases depends to a certain degree on the lapse of time, and as during changes of level it is obvious that islands separated by shallow channels are more likely to have been continuously united within a recent period to the mainland than islands separated by deeper channels, we can understand the frequent relation between the depth of the sea and the degree of affinity of the mammalian inhabitants of islands with those of a neighbouring continent,—an inexplicable relation on the view of independent acts of creation.

All the foregoing remarks on the inhabitants of oceanic islands,—namely, the scarcity of kinds—the richness in endemic forms in particular classes or sections of classes,—the absence of whole groups, as of batrachians, and of terrestrial mammals notwithstanding the presence of a.rial bats,—the singular proportions of certain orders of plants,—herbaceous forms having been developed into trees, etc.,—seem to me to accord better with the view of occasional means of transport having been largely efficient in the long course of time, than with the view of all our oceanic islands having been formerly connected by continuous land with the nearest continent; for on this latter view the migration would probably have been more complete; and if modification be admitted, all the forms of life would have been more equally modified, in accordance with the paramount importance of the relation of organism to organism.

I do not deny that there are many and grave difficulties in understanding how several of the inhabitants of the more remote islands, whether still retaining the same specific form or modified since their arrival, could have reached their present homes. But the probability of many islands having existed as halting-places, of which not a wreck now remains, must not be overlooked. I will here give a single instance of one of the cases of difficulty. 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. Dr. Aug. A. Gould has given several interesting cases in regard to the land-shells of the islands of the Pacific. Now it is notorious that land-shells are very easily killed by salt; their eggs, at least such as I have tried, sink in sea-water and are killed by it. Yet there must be, on my view, some unknown, but highly efficient means for their transportal. Would the just-hatched young occasionally crawl on and 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 found that several species did in this state withstand uninjured an immersion in sea-water during seven days: one of these shells was the Helix pomatia, and after it had again hybernated I put it in sea-water for twenty days, and it perfectly recovered. As this species has a thick calcareous operculum, I removed it, and when it had formed a new membranous one, I immersed it for fourteen days in sea-water, and it recovered and crawled away: but more experiments are wanted on this head.

The most striking and important fact for us in regard to the inhabitants of islands, is their affinity to those of the nearest mainland, without being actually the same species. Numerous instances could be given of this fact. I will give only one, that of the Galapagos Archipelago, situated under the equator, between 500 and 600 miles from the shores of South America. Here almost every product of the land and water bears the unmistakeable stamp of the American continent. There are twenty-six land birds, and twenty-five of these are ranked by Mr. Gould as distinct species, supposed to have been created here; yet the close affinity of most of these birds to American species in every character, in their habits, gestures, and tones of voice, was manifest. So it is with the other animals, and with nearly all the plants, as shown by Dr. Hooker in his admirable memoir on the Flora of this archipelago. The naturalist, looking at the inhabitants of these volcanic islands in the Pacific, distant several hundred miles from the continent, yet 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 plain a 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 resembles closely 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 climate, height, and size of the islands, between the Galapagos and Cape de Verde Archipelagos: but what an entire and absolute difference in their inhabitants! The inhabitants of the Cape de Verde Islands are related to those of Africa, like those of the Galapagos to America. I believe this grand fact can receive 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, whether by occasional means of transport or by formerly continuous land, from America; and the Cape de Verde Islands from Africa; and that 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 are related to those of the nearest continent, or of other near islands. The exceptions are few, and most of them can be explained. Thus the plants of Kerguelen Land, though standing nearer to Africa than to America, 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 plants 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 almost disappears on the view that both New Zealand, South America, and other southern lands were long ago partially stocked from a nearly intermediate though distant point, namely from the antarctic islands, when they were clothed with vegetation, before the commencement of the 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, and is at present inexplicable: but this affinity is confined to the plants, and will, I do not doubt, be some day explained.

The law which causes the inhabitants of an archipelago, though specifically distinct, to be closely allied to those of the nearest continent, we sometimes see displayed on a small scale, yet in a most interesting manner, within the limits of the same archipelago. Thus the several islands of the Galapagos Archipelago are tenanted, as I have elsewhere shown, in a quite marvellous manner, by very closely related species; so that the inhabitants of each separate island, though mostly distinct, are related in an incomparably closer degree to each other than to the inhabitants of any other part of the world. And this is just what might have been expected on my view, for the islands are situated so near each other that they would almost certainly receive immigrants from the same original source, or from each other. But this dissimilarity between the endemic inhabitants of the islands may be used as an argument against my views; for it may be asked, how has it happened in the several islands situated within sight of each other, having the same geological nature, the same height, climate, etc., that many of the immigrants should have been differently modified, though only in a small degree. This long appeared 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 for its inhabitants; whereas it cannot, I think, be disputed that the nature of the other inhabitants, 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 those inhabitants of the Galapagos Archipelago which are found in other parts of the world (laying on one side for the moment the endemic species, which cannot be here fairly included, as we are considering how they have come to be modified since their arrival), we find a considerable amount of difference in the several islands. This difference might indeed have been expected on the view of the islands having 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. Hence when in former times an immigrant settled on any one or more of the islands, or when it subsequently spread from one island to another, it would undoubtedly be exposed to different conditions of life in the different islands, for it would have to compete with different sets of organisms: a plant, for instance, would find the best-fitted ground more perfectly occupied by distinct plants in one island than in another, and it 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 on continents some species spreading widely and remaining the same.

The really surprising fact in this case of the Galapagos Archipelago, and in a lesser degree in some analogous instances, is that the new species formed in the separate islands have not quickly spread 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 across the archipelago, and gales of wind are extraordinarily rare; so that the islands are far more effectually separated from each other than they appear to be on a map. Nevertheless a good many species, both those found in other parts of the world and those confined to the archipelago, are common to the several islands, and we may infer from certain facts that these have probably spread from some one island to the others. But we often take, I think, an erroneous view of the probability of closely allied species invading each other's territory, when put into free intercommunication. Undoubtedly if one species has any advantage whatever 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 in nature, both probably will hold their own places and keep separate 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 new countries, we are apt to infer that most species would thus spread; but we should remember that the forms which become naturalised in new countries are not generally closely allied to the aboriginal inhabitants, but are very distinct species, 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, are distinct on each; 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 there 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 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 some 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 and representative species, which inhabit the several islands of the Galapagos Archipelago, not having universally spread from island to island. In many other instances, as in the several districts of the same continent, pre-occupation has probably played an important part in checking the commingling of species under the same conditions of life. 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.

The principle which determines the general character of the fauna and flora of oceanic islands, namely, that the inhabitants, when not identically the same, yet are plainly related to the inhabitants of that region whence colonists could most readily have been derived,—the colonists having been subsequently modified and better fitted to their new homes,—is of the widest application throughout nature. We see this on every mountain, in every lake and marsh. For Alpine species, excepting in so far as the same forms, chiefly of plants, have spread widely throughout the world during the recent Glacial epoch, are related to those of the surrounding lowlands;—thus we have in South America, Alpine humming-birds, Alpine rodents, Alpine plants, etc., all of strictly American forms, and it is obvious that a mountain, as it became slowly upheaved, would naturally 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 given the same general forms to the whole world. We see this same principle in the blind animals inhabiting the caves of America and of Europe. Other analogous facts could be given. And it will, I believe, be universally found to be 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, showing, in accordance with the foregoing view, that at some former period there has been intercommunication or migration between the two regions. And wherever many closely-allied species occur, there will be found many forms which some naturalists rank as distinct species, and some as varieties; these doubtful forms showing us the steps in the process of modification.

This relation between the power and extent of migration of a species, either at the present time or at some former period under different physical conditions, and the existence at remote points of the world of other species allied to it, 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 it would be difficult to prove it. Amongst mammals, we see it strikingly displayed in Bats, and in a lesser degree in the Felidae and Canidae. We see it, if we compare the distribution of butterflies and beetles. So it is with most fresh-water productions, in which so many genera range over the world, and many individual species have enormous ranges. It is not meant that in world-ranging genera all the species have a wide range, or even that they have on an average a wide range; but only that some of the species range very widely; for the facility with which widely-ranging species vary and give rise to new forms will largely determine their average range. For instance, two varieties of the same species inhabit America and Europe, and the species thus has an immense range; but, if the variation had been a little greater, the two varieties would have been ranked as distinct species, and the common range would have been greatly reduced. Still less is it meant, that a species which apparently has 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 on the view of all the species of a genus having descended from a single parent, though now distributed to the most remote points of the world, we ought to find, and I believe as a general rule we do find, that some at least of the species range very widely; for it is necessary that the unmodified parent should range widely, undergoing modification during its diffusion, and should place itself under diverse conditions favourable for the conversion of its offspring, firstly into new varieties and ultimately into new species.

In considering the wide distribution of certain genera, we should bear in mind that some are extremely ancient, and must have branched off from a common parent at a remote epoch; so that in such cases there will have been ample time for great climatal and geographical changes and for accidents of transport; and consequently for the migration of some of the species into all quarters of the world, where they may have become slightly modified in relation to their new conditions. There is, also, some reason to believe from geological evidence that organisms low in the scale within each great class, generally change at a slower rate than the higher forms; and consequently the lower forms will have had a better chance of ranging widely and of still retaining the same specific character. This fact, together with the seeds and eggs of many low forms being very minute and better fitted for distant transportation, probably accounts for a law which has long been observed, and which has lately been admirably discussed by Alph. de Candolle in regard to plants, namely, that the lower any group of organisms is, the more widely it is apt to range.

The relations just discussed,—namely, low and slowly-changing organisms ranging more widely than the high,—some of the species of widely-ranging genera themselves ranging widely,—such facts, as alpine, lacustrine, and marsh productions being related (with the exceptions before specified) to those on the surrounding low lands and dry lands, though these stations are so different—the very close relation of the distinct species which inhabit the islets of the same archipelago,—and especially the striking relation of the inhabitants of each whole archipelago or island to those of the nearest mainland,—are, I think, utterly inexplicable on the ordinary view of the independent creation of each species, but are explicable on the view of colonisation from the nearest and readiest source, together with the subsequent modification and better adaptation of the colonists to their new homes.

Summary of 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 all the changes of climate and of the level of the land, which have certainly occurred within the recent period, and of other similar changes which may have occurred within the same period; if we remember how profoundly ignorant we are with respect to the many and curious means of occasional transport,—a subject which has hardly ever been properly experimentised on; if we bear in mind how often a species may have ranged continuously over a wide area, and then have become extinct in the intermediate tracts, I think the difficulties in believing that all the individuals of the same species, wherever located, have descended from the same parents, are not insuperable. And we are led to this conclusion, which has been arrived at by many naturalists under the designation of single centres of creation, by some general considerations, more especially from the importance of barriers and from the analogical distribution of sub-genera, genera, and families.

With respect to the distinct species of the same genus, which on my theory must have spread from one parent-source; if we make the same allowances as before for our ignorance, and remember that some forms of life change most slowly, enormous periods of time being thus granted for their migration, I do not think that the difficulties are insuperable; though they often are in this case, and in that of the individuals of the same species, extremely grave.

As exemplifying the effects of climatal changes on distribution, I have attempted to show how important has been the influence of the modern Glacial period, which I am fully convinced simultaneously affected the whole world, or at least great meridional belts. As showing how diversified are the means of occasional transport, I have discussed at some little length the means of dispersal of fresh-water productions.

If the difficulties be not insuperable in admitting that in the long course of time the individuals of the same species, and likewise of allied species, have proceeded from some one source; then I think all the grand leading facts of geographical distribution are explicable on the theory of migration (generally of the more dominant forms of life), together with subsequent modification and the multiplication of new forms. We can thus understand the high importance of barriers, whether of land or water, which separate our several zoological and botanical provinces. We can thus understand the localisation of sub-genera, genera, and families; 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 in so mysterious a manner linked together by affinity, and are likewise linked to the extinct beings which formerly inhabited the same continent. Bearing in mind that the mutual relations of organism to organism are 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 new inhabitants entered one region; 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 in 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 different 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, as we do find, some groups of beings greatly, and some only slightly modified,—some developed in great force, some existing in scanty numbers—in the different 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 of these a great number should be endemic or peculiar; and why, in relation to the means of migration, one group of beings, even within the same class, should have all its species endemic, and another group should have all its species common to other quarters 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 possess their own peculiar species of a.rial mammals or bats. We can see why there should be some relation between the presence of mammals, in a more or less modified condition, and the depth of the sea between an island 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 likewise be related, but less closely, to those of the nearest continent or other source whence immigrants were probably derived. We can see why in two areas, however distant from each other, there should be a correlation, in the presence of identical species, of varieties, of doubtful species, and of distinct but representative species.

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 exceptions to the rule are so few, that they may fairly be attributed to our not having as yet discovered in an intermediate deposit the forms which are therein absent, but which occur 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 migration at some former period under different conditions or by occasional means of transport, and 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, belonging either to a certain period of time, or to a certain area, are often characterised by trifling characters in common, as of sculpture or colour. In looking to the long succession of ages, as in now looking to distant provinces throughout the world, we find that some organisms differ little, whilst others belonging to a different class, or to a different order, or even only to a different family of the same order, differ greatly. In both time and space the lower members of each class generally change less than the higher; but there are in both cases marked exceptions to the rule. On my theory these several relations throughout time and space are intelligible; for whether we look to the forms of life which have changed during successive ages within the same quarter of the world, or to those which have changed after having migrated into distant quarters, in both cases the forms within each class have been connected by the same bond of ordinary generation; and the more nearly any two forms are related in blood, the nearer they will generally stand to each other in time and space; in both cases the laws of variation have been the same, and modifications have been accumulated by the same power of natural selection.

第十二章 地理分布(续)

淡水生物的分布——论海洋岛上的生物——两栖类和陆栖哺乳类不存在——岛屿生物与最近大陆上生物的关系——从最近原产地移来的生物及其以后的变化——前章和本章的提要

湖泊和河流系统被陆地障碍物所隔开,可想而知,淡水生物在同一地区里不会分布很广,又因海是更加难以克服的障碍物,所以不会扩张到遥远的地区。但是情形恰恰相反。不但属于不同纲的许多淡水物种有广大的分布,而且亲缘物种也令人瞩目地遍布于世界。第一次在巴西淡水中采集生物时,我记得十分清楚,对于那里的淡水昆虫、贝类等与不列颠很相似而周围陆栖生物与不列颠很不相似,我感到非常惊奇。

但是,关于淡水生物广为分布的能力,尽管出乎意料,我想在大多数情形里可以做这样的解释:它们以一种对自己极有用的方式变得适合于在本乡本土里从一池塘到另一池塘,从一河流到另一河流经常进行短途迁徙;从这种能力发展为广远散布是近乎必然的结果。这里只能考虑少数几个例子。关于鱼类,我想同一个淡水物种绝没有在两个相距遥远的大陆上存在。但在同一大陆上,物种常常分布很广,而且变化莫测;因为在两个河流系统里物种有同有异。少数事实似乎有利于淡水鱼类由于意外方法而偶然地被输送出去的可能性。例如,活鱼被旋风卷起落在印度,并不是很稀有的事,鱼卵离开水以后保持生活力。但我倾向于将淡水鱼的散布主要归因于在最近时期里陆地水平的变化而使河流相互流通。还有,河流相互流通的事也发生在洪水期,这里没有陆地水平的变化。我们有莱茵河黄土地的证据,在新近地质时期内出现过陆地水平的大变,地面上曾经栖居着现有陆栖淡水贝类。连续的山脉自古以来就是分水岭,彻底防止了河流系统合并,两侧鱼类大不相同,也导致了相同的结论。至于亲缘淡水鱼出现在世界上相隔遥远的地点,无疑有许多个案现在无法解释:但有些淡水鱼属于很古的类型,在这等情形下,巨大的地理变化就有充分的时间,因而也有充分的时间和方法进行大量的迁徙。再者,咸水鱼类被给予小心处理,就能慢慢地习惯于淡水生活;按照法伦西奈(Valenciennes)的意见,几乎没有一类鱼族群只在淡水里生活,所以可以想象,属于淡水群的海栖物种可以沿着海岸游得很远,并且变异适应远地的淡水。

淡水贝类的某些物种分布很广,并且亲缘物种也遍布全世界,根据我们的学说,从共同祖先传下的近似物种,一定是来自单一源头。它们的分布情况起初使我大惑不解,它们的卵不像是能由鸟类输送的;并且卵与成体一样,都会立刻被海水杀死。我甚而不能理解某些归化的物种怎么能够在同一地区里很快地分散。但是我所观察的两个事实——无疑其他事实还有待观察——对于这一问题有一定的启发。当鸭子从盖满浮萍(duckweed)的池塘突然冒出时,我曾两次看到这些小植物附着在鸭背上;并且发生过这样的事情:把一些浮萍从一个水族培养器移到另一个时,我曾无意中把一个水族培养器里的贝类移入到另一个。不过还有一种媒介物或者更有效力:我把鸭爪挂在一个水族培养器里,其中有许多淡水贝类的卵正在孵化,鸭爪代表睡在天然池塘中的鸟爪;我找到许多极端细小的、刚刚孵化的贝类爬在它的脚上,并且极牢固地附着在那里,脚离开水时并不脱落,但再长大一些就会自己落下。这些刚刚孵出的软体动物虽然本性上是水栖的,但在鸭爪上,在潮湿的空气中,能活到12至20小时;在这样一段时间里,鸭或苍鹭(heron)至少可以飞行六七百英里;如果被风吹过海面到达海岛或其他遥远的地点,必然会降落在池塘或小河里。赖尔爵士告诉我,曾捉到一只龙虱(Dytiscus),有盾螺(Ancylus,一种像帽贝[limpet]的淡水贝)牢固地附着在上面;并且同科的水甲虫细纹龙虱(Colymbetes),有一次飞到贝格尔号船上,当时此船距离最近的陆地是四十五英里:没有人能说清它可以被顺风吹到多远。

关于植物,早就知道很多淡水甚至沼泽物种分布得非常之远,在大陆上、最遥远的海洋岛上,都是如此。德康多尔说过,含有极少数水栖成员的陆栖植物的大群显著表现了这一点;似乎由于水栖,便立刻获得了广大的分布范围。我想,这一点可以由有利的散布方法加以说明。我以前说过,少量泥土偶然会附着在鸟脚和喙上。涉禽类徘徊池塘淤泥边缘受惊飞起时,脚上极可能带着泥土。可以表明,这一目的鸟漫游极广;有时来到最遥远的不毛海岛上,不大会降落在海面,脚上泥土不致洗掉;到达陆地之后,必然会飞到天然的淡水栖息地。我不相信植物学者能体会到塘泥里含有何等多的种子;我做过几个小试验,这里只能举出最惊人的例子:我在二月里从小池塘边的水下三个不同地点取出三调羹污泥,干燥以后只有六又四分之三盎司重;我把它盖起来,在书房里放了六个月,当每一植株长出来时,把它拔出并加以计算;这些植物属于很多种类,共计有537株;而那块黏软的淤泥早餐杯就可以盛下!考虑到这一点,我想,水鸟不把淡水植物的种子输送到遥远地点,这些植物的分布范围不广,倒是不能解释的事情了。这同样的媒介对于某些小型淡水动物的卵大概也会有作用。

其他未知的媒介大概也发生过作用。我曾经说过,淡水鱼类吃某些种类的种子,但吞下许多别种的种子后再吐出来;甚至小的鱼也会吞下中等大的种子,如黄睡莲和眼子菜属(Potamogeton)的种子。苍鹭和别的鸟,一个世纪又一个世纪地天天在吃鱼;吃鱼后便飞起,并走到别的水中,或者被风吹过海面;我们知道,许多小时以后吐出、随粪便排出的种子,还保持着发芽的能力。以前看到那精致的莲花(Nelumbium)的大型种子,又记得德康多尔关于这种植物分布的意见时,我想它的分布方法一定是不能理解的;但是奥杜旁说,他在苍鹭的胃里找到过南方莲(按照胡克博士的意见,大概是大型北美黄莲花[Nelumbium luteum])的种子。尽管我没有事实证明,但类推的方法使我相信,这种鸟飞到远方的池塘,然后饱吃一顿鱼,会把含有未消化的种子从胃里吐出,或者在给小鸟喂食时掉下,就像大家知道的,有时候将小鱼掉下。

考察这几种分布方法时,应该记住,池塘、河流在例如隆起的小岛上最初形成时,其中是没有生物的;于是单个的种子或卵会获得良好的成活机会。同一池塘的生物之间,不管个体怎么少,总有生存斗争,不过物种数目与陆地相比总是少的,水栖物种的竞争比起陆栖物种就不大剧烈;结果外来的水生生物侵入者在取得新的位置上比陆上的移居者有较好的机会。我们还应记住,许多淡水生物在自然系统上是低级的,有理由相信,这样的生物比高等生物变异慢些;这就使相同水栖物种的迁徙有了较长的时间。我们不应忘记,许多淡水类型从前大概连续分布在广大面积上,然后在中间地点灭绝了。但是淡水植物和低等动物,不论是否保持同一类型或好歹变异了,我想其广泛分布显然主要依靠动物,特别是飞翔力强的且自然地从这一片水飞到另一片遥远的水的淡水鸟类会把种子和卵广泛散布开去。大自然就像细心的园丁,将种子从某性质的花坛取出,丢到同样适合生长的另一个花坛里去。

论海洋岛上的生物。——同一物种和亲缘物种的一切个体都是由一个祖先传承而来,因而全部是自共同的诞生地迁徙出来的,尽管随着时间推移渐渐栖息于天涯海角。根据这一观点,我曾选出有关分布的最大困难的三类事实,现在对其中最后一类加以讨论。我已经说过不能苟同福布斯关于大陆扩张的观点,它如果加以合法光大,就会推论出以下论点:在最近的期间内,所有现存岛屿都曾几乎连接于某个大陆。这个观点可消除许多难点,但我想也无法解释关于岛屿隔绝生物的所有事实。下面,我将不限于讨论散布的问题,同时也要讨论与独立创造学说和变异传承学说之对错有关的某些其他事实。

栖息在海洋岛上的各物种在数量上与同样大小的大陆面积相比是稀少的:德康多尔在植物方面,沃拉斯顿在昆虫方面,都承认了这个事实。看看幅员辽阔、有多种多样生境的南北达780英里的新西兰,一共也不过有750种显花植物;如果把这与繁生在澳洲或好望角同等面积上的物种相比较,我想我们必须承认有某种与不同物理条件无关的原因造成了物种数的如此悬殊差异。甚至条件一致的剑桥郡还具有847种植物,盎格尔西小岛具有764种,但是有若干蕨类植物和引进植物也包括在这些数目里,而且从其他方面讲,这个比较也不十分恰当。有证据证明,阿森松这个不毛岛屿只有不到六种原产地显花植物;可是现在有许多物种已在那里归化了,就像新西兰和每一其他可以举出的海洋岛的情形一样。在圣赫勒拿,有理由相信归化的动植物几乎消灭了许多本地的生物。谁承认每一物种单独创造的学说,就必须承认有足够大量数目的最适应的动植物并不是为海洋岛创造的;因为人类曾经无意地到处引进,使那些岛充满了生物,在这方面远比自然做得更加充分,更加完善。

虽然海洋岛物种数稀少,但是特有种类(即世界其他地方找不到的种类)的比例往往是极大的。例如,如果把马德拉岛特有陆栖贝类,或加拉帕戈斯群岛特有鸟类的数目与任何大陆加以比较,然后把岛屿的面积与大陆加以比较,会看到这是千真万确的。这种事实在我的理论上是可以料想到的,因为,上文说明,物种经过长久的间隔期间以后偶然到达新的隔离地区,势必与新的同住者进行竞争,极容易发生变异,并常常产生成群的变异后代。可是决不能因为一个岛上某一纲物种几乎是特有的,就认为其他纲或同纲其他部分的物种也必然是特有的;这种不同似乎取决于没有变化的物种曾经轻易地集体性移入,所以彼此的相互关系没有受到多大扰乱。例如,加拉帕戈斯群岛上几乎所有陆栖鸟是特有的,而在11种海鸟里只有两种是特有的;显然,海鸟比陆栖鸟更易到达这些岛上。另一方面,百慕大和北美洲的距离,几乎同加拉帕戈斯群岛和南美洲的距离一样,而且百慕大有一种很特殊的土壤,却并没有一种特有的陆栖鸟;从琼斯(J.M.Jones)先生有关百慕大的报告中知道,有很多北美洲的鸟类在年年大迁徙中定期或者偶然来到这个岛上。马德拉岛没有一种特有鸟类,哈考特(E.V.Harcourt)先生告诉我,几乎年年都有很多欧洲和非洲的鸟类被风吹到马德拉。所以,百慕大和马德拉诸岛充满了鸟类,长久以来在那里进行斗争,并且变得相互适应了。因此,定居新家乡以后,每一种类将被其他种类维持在适宜地点上和习性中,结果就不容易发生变化。再者,马德拉栖息着数量惊人的特有陆栖贝类,但没有一种海栖贝类是仅限于这里的海岸的:虽然不知道海栖贝类是怎么散布的,可是能知道它们的卵或幼虫,附着在海藻或漂浮木或涉禽类的脚上,就能输送过三四百英里的海洋,要比陆栖贝类容易得多。栖息在马德拉的不同目的昆虫表现了差不多平行的情形。

海洋岛有时缺少某些纲的动物,其位置显然被其他生物所占据;这样,爬行类在加拉帕戈斯群岛,巨大的无翼鸟在新西兰便代替了哺乳类。讲到加拉帕戈斯群岛的植物,胡克博士阐明,不同目的比例数与其他地方很不相同。这种个案一般都是用岛上物理条件来解释的,但是这种解释很值得怀疑。我认为,移入的便利与否似乎与条件的性质有同等的重要性。

关于遥远岛屿的生物,还有许多可注意的小事情。例如,在没有哺乳动物栖息的某些岛上,有些本地特有植物具有美妙的带钩种子;可是,钩的用途在于让种子适合四足兽的毛或毛皮带走,没有比这种关系更加明显的了。这个个案依我看就不是难点,带钩的种子大概可以由其他方法带到岛上去;于是,那种植物经过轻微变异,就成为本地的特有物种了,它仍然保持它的钩,痕迹器官成为一种无用的附属物,就像许多岛上的甲虫,在愈合的翅鞘下仍有枯缩的翅。再者,岛上经常生有乔木或灌木,它们所属的目在其他地方只包括草本物种;而依照德康多尔所阐明的,乔木不管原因怎样,一般分布的范围是有限的。因此,乔木极少可能到达遥远的海洋岛;而草本植物本来没有机会与充分发育的乔木竞争获胜,一旦定居在岛上,只有草本植物来竞争,就会由于生长得越来越高,高出其他植物,迅速占有优势。在这种情形下,不管草本植物属于哪一目,自然选择就有增加其高度的倾向,这样先变成灌木,然后变成乔木。

关于海洋岛上没有整目的动物,圣樊尚(Bory St.Vincent)很久以前就说过,大洋上点缀着许多岛屿,但从未发现两栖类(蛙、蟾蜍、蝾螈)。我曾煞费苦心地证实这种说法,并且发现它千真万确。但是我确信,新西兰大岛的高山上有蛙。但我怀疑这个例外(如果信息属实)可以用冰川作用来解释。那么多的海洋岛一般都没有蛙、蟾蜍和蝾螈,是不能用海洋岛的物理条件来解释的;其实,岛屿似乎特别适于这类动物:因为蛙已经被带进马德拉、亚速尔和毛里求斯,大量繁生,以致成为可厌之物。由于大家知道这类动物及其卵遇到海水就立刻死亡,依我看很难输送过海,可知为什么不存在于海洋岛上。但是,它们为什么不在那里被创造出来,按照特创论就很难解释了。

哺乳类提供了另一相似个案。我仔细地搜索了最古老的航海记录,还没有结束搜索,并没有找到过一个确定无疑的事例可以证明陆栖哺乳类(土人饲养的家畜除外)栖息在离开大陆或大的陆岛300英里以外的岛屿上;在许多离开大陆更近的岛屿上也同样找不到。福克兰群岛有一种似狼的狐狸,极像是例外;但是这群岛屿不能看作海洋岛,位于与大陆相连的沙洲上;而且冰山曾把漂石带到它的西海岸,也可能把狐狸带过去,如今这在北极地区是常有的事。可是我们不能说小岛养不活小的哺乳类,因为在世界上许多地方它们生活在靠近大陆的小岛上;几乎不能举出一个岛,小型四足兽不能在那里归化并大事繁生。按照特创论的一般观点,不能说那里没有足够的时间来创造哺乳类;许多火山岛是十分古老的,从遭受过的巨大陵蚀作用以及第三纪的地层可以看出:那里还有时间来产生本地所特有的、属于其他纲的物种;我们知道,哺乳动物的新物种在大陆上比其他低于它们的动物以较快的速率产生和消灭。虽然陆栖哺乳类不见于海洋岛,空中哺乳类却几乎每一岛上都有。新西兰有两种世界其他地方找不到的蝙蝠:诺福克岛、维提群岛(Viti)、小笠原群岛、加罗林和马利亚纳群岛、毛里求斯,都有特产蝙蝠。试问,为什么那假定的创造力在遥远的岛上产生出蝙蝠而不产生其他哺乳类呢?根据我的观点,这个问题容易解答;因为没有陆栖动物能够渡过海洋的广阔空间,但蝙蝠却能飞过去。人们曾经看到蝙蝠在白天远远地在大西洋上空飞翔;并且有两种北美蝙蝠或经常或偶然地飞到离大陆600英里的百慕大。我从专门研究这一科动物的汤姆斯(Tomes)先生那里听到,许多同类物种具有广大的分布范围,并且可以在大陆上和遥远的岛上找到。因此,只要设想这类漫游的物种在新家乡由于新位置而发生自然选择变异就可以了,并且由此就能理解,为什么海洋岛虽有本地的特有蝙蝠,却没有一切陆栖哺乳类。

除了海岛与大陆的遥远度与陆栖哺乳类的关系外,还有一种关系,一定程度上与距离无关,就是把岛屿与邻近大陆分开的海水深度和两地好歹有变异的相同或亲缘哺乳类物种存在的关系。埃尔(Windsor Earl)先生对这个问题做过一些发人深省的观察,涉及大马来群岛,以一条深海的空间在西里伯斯(Celebes)附近隔开,分隔出两个十分不同的哺乳类世界。这些岛两边的海都是相当浅的大陆架,岛上有相同的或密切近似的四足兽栖息。这个大群岛无疑出现了少数异常情形,对于某些个案很难形成判断,某些哺乳类通过人类的作用有可能归化。但是华莱士先生满腔热情的研究很快让群岛的博物史大白于天下。我还来不及跟进这个问题在世界各地的情形;但是据我研究所及,这种关系一般是正确的。例如,不列颠和欧洲被一条浅海峡隔开,两边的哺乳类是相同的;澳洲海岸浅海峡对岸的许多岛屿也是这样。另一方面,西印度诸岛位于下沉很深的沙洲上,深度几达1000英寻,那里找到了美洲的类型,但是物种甚至属却不同。由于所有个案的变化量一定程度上取决于时间的长短,而且在水平变化时由浅海峡隔离的岛屿显然比由深海峡隔离的更有可能在近代与大陆持续连成一片,所以能够理解,海水深度和海岛哺乳类与邻近大陆哺乳类的亲缘程度之间往往存在着关系——这种关系根据独立创造的学说是讲不通的。

以上是关于海洋岛生物的叙述——即,物种数稀少——某些纲或者纲的部分中本地的特有类型很丰富——整个群,如两栖类和陆栖哺乳类,全部缺如,但能飞的蝙蝠是存在的——某些植物目表现特别的比例——草本类型发展成乔木,等等——在我看来,似乎更符合在悠久过程中偶然输送的方法普遍有效的观点,而不是一切海洋岛以前曾和最近大陆由连续陆地连在一起的观点。因为按照后一观点,移入也许会更彻底,同时根据生物间关系头等重要的因素,如果允许,一切生物类型会发生相等的变异。

要理解较遥远岛屿上的若干生物(不管仍保持同一物种的类型还是抵达以后发生变化)究竟如何到达现在的家乡,我不否认是存在许多严重难点的。但是,决不能忽视,许多岛屿曾经作为歇脚点,而现在没有留下一点遗迹。我愿详细说明一个困难的例子。几乎一切海洋岛,哪怕是最孤立、最小的海洋岛,都有陆栖贝类栖息着,一般是本地特有的物种,但有时是其他地方也有的物种。古尔德博士曾举出若干太平洋岛屿陆栖贝类的有趣例子。众所周知,陆栖贝类容易被海水杀死;贝卵,至少是我试验过的卵,在海水里下沉并且被杀死了。可是我认为一定还有某些未知但非常有效的方法来输送它们。刚孵化的幼体有时会不会附着于栖息在地上的鸟的脚上而输送过去呢?我想起休眠时期贝壳口上具有薄膜的陆栖贝类,在漂流木的隙缝中可以浮过相当阔的海湾。并且我发现有几个物种在这种状态下沉没在海水里七天而不受损害:一种是罗马蜗牛(Helix pomatia)经过这样处理以后,在休眠中再放人海水中二十天,能够完全复活。这种蜗牛具有一片厚的石灰质厣(operculum),我把厣除去,等到新的膜厣形成以后,再把它浸入海水里十四天,它还是会复活,并且爬走了。这方面需要做更多的试验。

关于岛上物种对我们来说最触目惊心最重要的事实是,与最近大陆的并不实际相同的物种有亲缘关系。这一点能够举出无数的例子来。这里举一例,位于赤道的加拉帕戈斯群岛距离南美洲的海岸有500—600英里之远。那里几乎每一陆上和水里的生物都带着明确无误的美洲大陆的印记。有二十六种陆栖鸟,其中二十五种被古尔德先生列为不同的物种,而且被假定是在那里创造出来的;可是这些鸟的大多数与美洲物种的密切亲缘关系,表现在每一性状上,习性、姿势和鸣声上。其他动物也是如此。胡克博士在所著该群岛的植物志大作中说,大部分植物也是这样。学者们在离开大陆几百英里远的太平洋火山岛上观察生物时,会感到自己是站在美洲大陆上。为什么会这样呢?为什么假定加拉帕戈斯群岛而不是其他地方创造出来的物种这样清楚地和美洲创造出来的物种有亲缘关系印记呢?在生活条件、岛上的地质、岛的高度或气候方面,在共同居住的几个纲的比例方面,没有一件是与南美沿岸的条件密切相似的:事实上,在所有这些方面都是区别相当大的。另一方面,加拉帕戈斯群岛和佛得角群岛,在土壤的火山性质、气候、高度和岛的大小方面,则有相当程度的类似:但是它们的生物却是何等完全和绝对地不同呀!佛得角群岛的生物与非洲相关联,就像加拉帕戈斯群岛的生物与美洲相关联一样。我认为,对于这伟大的事实,根据独立创造的一般观点是得不到任何解释的;相反的,根据本书所主张的观点,显然,加拉帕戈斯群岛很可能接受从美洲来的移住者,不管这是由于偶然的输送方法,还是以前是连续的陆地。而且佛得角群岛也接受从非洲来的移住者;这样的移住者虽然容易发生变异——而传承的原理依然泄露了其原产地在何处。

能够举出许多类似的事实:岛上的特有生物与最近大陆、最近大岛上的生物相关联,实在是一个近乎普遍的规律。例外是少数,并且大部分的例外是可以解释的。例如,虽然凯尔盖朗岛距离非洲比美洲近,但是从胡克博士的报告里可以知道,植物却与美洲相关联,并且关联得很密切。但是根据岛上植物主要是借顺风海流漂来的冰山把种子连着泥土石块带来的观点看来,异常就消失了。新西兰在本地特有植物上与最近的大陆澳洲之间的关联比其他地区更密切。这是可想而知的,但是它又清楚地与南美洲相关联,南美洲虽说是第二个最近的大陆,可离得那么遥远,所以就成为异常了。但是根据下述观点看来,这个难点就部分地消失了:新西兰、南美洲和其他南方陆地的一部分生物是从一个近乎中间的虽然遥远的地点即南极诸岛而来的,那是冰期开始前南极诸岛长满了植物的时候。澳洲西南角和好望角的植物群的亲缘关系虽然薄弱,但是胡克博士使我确信这种关系是真实的,这是更值得注意的个案,目前无法解释;但是这种亲缘关系只限于植物,并且无疑将来会得到解释。

导致异物种的群岛生物和最近大陆生物之间有亲缘关系的法则,有时可以小规模但极有趣地在同一群岛的范围内表现出来。例如,如前所述,加拉帕戈斯群岛各离岛上都奇特地有亲缘物种栖息着;这些离岛物种彼此不同种,但之间的关联比与世界其他地区无疑更加密切。按我的观点,这是可想而知的,因为这样接近的岛屿几乎必然地会从同一根源接受移住者,也彼此接受移住者。但是离岛特有生物之间的不同可能被用来反对我的观点:试问,许多移住者在彼此相望的,具有同一地质性质,同一高度、气候等的诸岛上怎么会发生不同的(虽然差别不大)变异呢?长久以来这对我是个难点,但这主要是出于认为一地区的物理条件头等重要这一根深蒂固的错误观点;然而我认为无可辩驳的是,各物种必须进行竞争,因而其他物种的性质至少也是同等重要的,并且一般是更加重要的成功要素。现在,如果观察栖息在加拉帕戈斯群岛同时也见于世界各地的物种(暂时撇下特有物种,这里无法公平讨论,因为当前是考虑物种到达后如何渐渐变异的),就可以发现各岛上有相当大的差异。如果认为岛屿生物曾由偶然的输送方法而来——比方说,一种植物的种子被带到一个岛上,另一种植物的种子被带到另一个岛上,那么上述的差异的确是可以预料到的。因此,一种移住者在以前时期内在诸岛中的一个或多个岛上定居下来时,或者以后在诸岛间散布时,无疑会遭遇到不同岛上的不同条件,因为势必要与一批不同的生物进行竞争。比方说,一种植物在各岛上会遇到最适合的土地已被不同的物种所完美地或者欠完美地占据,还会受到多少不同的敌人的打击。如果这物种就此变异了,自然选择就会在不同岛上有利于不同变种的产生。尽管如此,有些物种还会散布开去,并且在整个群中保持同一性状,正如我们看到一个大陆上广泛散布的物种保持着同一性状一样。

加拉帕戈斯群岛这一个案以及在程度较差的某些类似的例子里,真正奇异的事实是,每一新物种在各岛上一旦形成,并不迅速散布到其他岛上。但是,这些岛虽然隔海相望,却有很深的海湾分开,大多比不列颠海峡还要宽,并且没有理由去设想以前是连续地联结在一起的。诸岛之间海流湍急,大风异常稀少;所以诸岛彼此的分离远比地图上所表现的更加明显。虽然如此,世界各地可以找到的和只见于这群岛的许多物种,是各岛共有的;根据某些事实可以推想,它们是从一个岛散布到众岛去的。但是,我想,往往对于密切近似物种自由往来时,便有侵占对方领土的可能性,采取了错误的观点。毫无疑问,如果一个物种比其他物种占有任何优势,就会在很短的时间内全部或部分淘汰对方;但是如果两者能同样好地适应在自然界的位置,那么大概都会坚守阵地,并且分开至几乎任何长的时间。我们熟悉经过人的媒介而归化的许多物种曾经以惊人的速度在新地区里进行散布,就会容易推想大多数物种也是这样散布的;但应该记住,在新地区归化的物种与土著生物一般并不是密切近似的,而是很不相同的物种,如德康多尔所阐明的,在大多数情形下不是同属的。在加拉帕戈斯群岛,甚至许多鸟类,虽然那么适于从一个岛飞到另一个岛,但在不同的岛上还是不同种的。例如,效舌鸫(mocking-thrush)有三个密切近似的物种,每一个物种只局限于自己的岛上。现在,让我们设想查塔姆岛的效舌鸫被风吹到查尔斯岛(Charles),而后者已有另一种效舌鸫:为什么它该成功地定居在那里呢?可以稳妥地推论,查尔斯岛已经繁生着自己的物种,每年产生的蛋多得根本养育不活;还可以推论,查尔斯岛所特有的效舌鸫对于自己家乡的良好适应,至少不比查塔姆岛的特有物种差。赖尔爵士和沃拉斯顿先生曾经写信告诉我一个与本问题有关的重要事实;即马德拉和附近的圣港(Porto Santo)小岛具有许多不同而表现为代表物种的陆栖贝类,其中有些生活在石缝里;虽然有大量石块每年从圣港输送到马德拉,可是马德拉并没有圣港的物种移住进来;相反,两岛上都有欧洲的陆栖贝类栖息着,无疑比本地物种占有某些优势。根据这些观察,我想,对于加拉帕戈斯群岛诸岛特有的代表物种并没有普遍散布,就不必大惊小怪了。再者,同一大陆上,先入为主对于阻止相同物理条件下栖息的不同地区的物种混入,大概有重要的作用。例如,澳洲的东南部和西南部物理条件几乎相同,并且由连续的陆地连着,可是有巨大数量的不同哺乳类、鸟类和植物栖息着。

决定海岛动植物通性的这一原理,在整个自然界有着最广泛的应用,即移住者尽管不同种,却与它们最容易迁出的原产地关系明显,以后移住者变异,更好地适应新家。在每一山顶、湖泊和沼泽里都可看到这个原理,因为高山物种都与周围低地的物种相关联,除非同一类型,主要是植物,在冰期已经全世界广泛散布。例如,南美洲的高山蜂鸟、高山啮齿类、高山植物等,一切都严格属于美洲的类型;而且显然,一座山缓慢隆起时,生物自然会从周围的低地移来。湖泊沼泽的生物也是这样,除非极方便的输送允许同一普遍类型散布到全世界。从美洲和欧洲穴居的盲目动物,也可看到这同一原理。还能举出其他类似的事实。我相信,以下情形将被认为是普遍正确的,即两个地区不管距离多远,凡有许多密切近似或代表的物种存在,在那里便一定也有某些相同的物种。根据上述观点,它们会表明以前两个地区曾经有相互交流或迁徙。不管在什么地方,凡有许多密切近似的物种,那里也会有被某些学者列为不同物种而被其他学者列为变种的许多类型;可疑类型向我们示明了变异过程中的步骤。

某物种在现在或古代不同环境下的迁徙能力和迁徙范围,与亲缘物种在世界遥远地点的存在有关系,这以另一普通的方式表示出来。古尔德先生很久以前告诉我,在世界各处散布的那些鸟属中,许多物种分布范围是广阔的。我不能怀疑这条规律是普遍正确的,虽然其很难被证明。在哺乳类中,我们看见这条规律显著地表现在蝙蝠中,并以较小的程度表现在猫科和狗科里。比较蝴蝶和甲虫的分布,可看到同样的规律。淡水生物大多数也是这样,有许多属分布在世界各处,而且许多物种具有广大的分布范围。这并不是说,在分布全世界的属里一切物种都广泛分布,也不是说平均起来属于广泛分布,而是说其中某些物种有很广阔的分布范围,因为平均分布范围大部分取决于广泛分布的物种变异产生新类型的难易程度。比方说,同一物种的两个变种栖息在美洲和欧洲,因此这个物种就有很广的分布范围;但是,如果变异进行得更厉害,两个变种就会被列为不同的物种,共同的分布范围就大大缩小了。这更不是说,表面上能越过障碍物而分布广远的物种,如某些善飞的鸟类,就必然分布得很广。永远不要忘记,分布广远不仅意味着具有越过障碍物的能力,而且意味着具有在遥远地区与异地同住者进行生存斗争并获胜这种更加重要的能力。但是按照一属的一切物种,虽然分布到世界最遥远的地点,都是从单一祖先传下来的观点,就应该找到,并且我相信我们一般确能找到,至少某些物种是分布得很广远的。因为未变异祖先一定要广泛分布,在分散过程中进行变异,一定要使自己处于各种环境中,有利于将后代先变成新变种,最终变成新物种。

考察某些属的广泛分布时,应该记住,许多属的起源都是很古的,共同的祖先在遥远的古代必定出现分叉;在这种情形下,物种将有大量的时间经历气候和地理大变迁,以及偶然的输送,结果某些物种迁徙到了世界各地,在散布地根据新环境可能略微变异。从地质的证据看来,也有理由相信,在每一个大的纲里比较低等的生物的变化速率,比起高等类型一般更加缓慢,结果就会分布广远而仍然有保持同一物种性状的较好机会。这个事实,外加许多低级类型的种子和卵都很细小,适于远地输送,也许说明了一个早经观察到的法则,即任何群的生物越低级,分布得越广远;最近又有德康多尔在植物方面讨论过这一点。

刚刚讨论过的关系——即变化缓慢的低等生物比高等生物分布更加广远,——分布广远的属,其某些物种的分布也广远,——高山、湖泊和沼泽的生物与周围低地和干地的生物有关联(例外情况前面已经明确),尽管环境十分不同,诸如此类——同一群岛中诸岛上的不同物种有密切的亲缘关系,——特别是整个群岛或岛屿上的生物和最近大陆的生物之间有显著关系,——我想,根据各物种独立创造的普通观点,这些事实都是完全得不到解释的,但是如果承认从最近的或最便利的原产地的移居以及移居者以后对于新家乡的变异适应,这就可以得到解释。

前章和本章提要。——这两章竭力阐明,如果充分承认我们自己对于近代必然发生过的气候、陆地水平变化以及可能发生过的其他变化所产生的全部影响是无知的;如果记得我们自己对于许多奇妙的偶然输送方法是何等无知——这个题目还没有得到适当的实验验证;如果记得,一个物种在广大面积上连续地分布,而后在中间地带灭绝了,是何等频繁发生的事情——那么,我认为要相信同一物种的一切个体,不管是在哪里发现的,都传自共同的祖先,就没有不可克服的困难了。我们根据各种一般的论点,特别是根据各种障碍物的重要性,并且根据亚属、属和科的相类似的分布,得出上述结论,许多学者在单一创造中心的名称下也得出这一结论。

至于同一属的不同物种,按照我的理论,必定是从一个原产地散布出去的;如果我们像前面那样承认自己的无知,记得某些生物类型变化得很缓慢,因而有大量时间可供它们迁徙,那么难点决不是不能克服的;虽然在这种情形下,就像在同一物种的个体的情形下一样,难点往往是很大的。

为了说明气候变化对于分布的影响,我试图阐明最近的一次冰期发生过多么重要的作用,我坚信它同时影响了全世界,至少触及大径向带。为了说明偶然的输送方法是何等丰富多彩,我略为详细地讨论了淡水生物的散布方法。

如果承认同一物种以及关联物种的个体在时间的悠久过程中曾经从同一原产地出发,并没有不可克服的难点;那么地理分布的一切主要事实,我想都可以依据迁徙(一般指优势生物类型)的理论,以及此后新类型的变异和繁生,得到解释。这样,我们便能理解,水陆障碍物在分开各个动植物区域上有至关重要的作用。这样,我们还能理解亚属、属、科的定位,在不同的纬度下,比方说在南美洲,平原和山上的生物,森林、沼泽和沙漠的生物,如何以神秘的方式因亲缘关联起来,并且同样的与过去栖息在同一大陆上的灭绝生物相关联。如果记住生物之间的相互关系是至关重要的,我们就能明白为什么具有几乎相同物理条件的两个地区常常栖息着很不相同的生物类型;因为根据移住者进入一个地区以来所经过的时间长度;根据交流性质容许某些类型而不是其他类型以或多或少的数量迁入;根据那些移入的生物是否碰巧相互以及与土著生物进行或多或少的直接竞争;并且根据移入的生物发生变异的快慢,所以在不同的地区里就会发生与物理条件无关的无限多样性的生活条件,——那里就会有几乎无限量的有机的作用和反作用,——并且我们就会发现某些群的生物大大地变异了,某些群的生物只是轻微地变异了,——某些群的生物大量发展了,某些群的生物仅以微小的数量存在着——的确可以在世界上几个大的地理区里看到这种情形。

依据这些同样的原理,如我曾经竭力阐明的,我们便能理解,为什么海洋岛只有少数生物,而其中有一大部分又是本地所特有的;由于与迁徙方法的关系,为什么一群生物的一切物种,甚至同纲生物的一切物种都是本地特有的,而另一群的一切生物都与世界各地共有。我们能明白为什么整个群的生物,如两栖类和陆栖哺乳类,不存在于海洋岛上,同时最孤立的岛也有自己特有的空中哺乳类即蝙蝠的物种。我们还能明白,为什么在岛上存在的或多或少经过变异的哺乳类和这些岛与大陆之间的海洋深度有某种关系。我们能清楚地知道,为什么一个群岛的一切生物,虽然在若干小岛上具有不同的物种,然而彼此有密切的关系;并且和最近大陆或移住者发源的其他可能原产地的生物同样有关系,不过关系较不密切。我们更能知道,两个地区不论相距多么远,为什么总可以找到关联的物种,表现为相同物种、变种、可疑物种、不同但代表物种的存在。

正如已故的福布斯所经常主张的,生命法则在整个时间空间中有惊人的平行现象:支配生物类型在过去时期内演替的法则与支配生物类型在今日不同地区内的差异的法则,几乎是相同的。在许多事实中可以看到这种情形。在时间上每一物种和每一群物种的存在都是连续的;因为对这一规律的例外少之又少,其例外可以正当地归因于我们还没有在中间的沉积层里发现某些类型,这些类型不见于其中,却见于它的上部和下部:在空间内也是这样,一般规律肯定是,一个物种或一群物种所栖息的地区是连续的,而例外的情形虽然不少,如我曾经想阐明的,都可以根据以前在不同情况下的迁徙,或者根据偶然的输送方法,或者根据物种在中间地带的灭绝而得到解释。在时间、空间里,物种以及物种群都有其发展的极大点。生存在某一时期、某一地区的物种群,常常有共同的微细特征,如刻纹或颜色。当我们观察过去悠久的连续时代时,正如现在观察整个世界的遥远地区,发现某些物种彼此之间的差异很小,而不同纲、不同目、同目不同科的物种彼此之间的差异却很大。在时间、空间里,每一纲的低级体制的成员比高级体制一般变化较少;但是在这两种情形里,这条规律都有显著的例外。按照我的理论,贯穿时间空间的这些关系是可以理解的;因为不论观察同一地区连续时代中发生变化的生物类型,还是观察迁入遥远地方以后曾经发生变化的生物类型,同一纲内的类型都被普通世代的同一个纽带联结起来;任何两个类型的血缘越近,则在时空中彼此一般靠得越近。在这两种情形里,变异法则都是一样的,而且变异都是由同一个自然选择的力量累积起来的。

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