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双语《物种起源》 第十一章 地理分布

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2022年07月02日

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CHAPTER XI GEOGRAPHICAL DISTRIBUTION

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 co-extensive with the world

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 accounted for by their 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 northern parts where the circumpolar land is almost continuous, 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; the most 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; for it is a most rare case to find a group of organisms confined to any small spot, having conditions peculiar in only a slight degree; for instance, small areas in the Old World could be pointed out hotter than any in the New World, yet these are not inhabited by a peculiar fauna or flora. Notwithstanding this 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 inhabit a considerably different climate, and they will be found 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 difference of 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, and of great deserts, and sometimes even of large rivers, we find different productions; though as mountain-chains, deserts, etc., 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. No two marine faunas are more distinct, with hardly a fish, shell, or crab in common, than those of the eastern and western shores of South and Central America; yet these great faunas are separated only by the narrow, but impassable, isthmus of Panama. Westward of the shores of America, a wide space of open ocean extends, with not an island as a halting-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 here 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 wholly distinct. On the other hand, proceeding still further 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, 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 hardly one shell, crab or fish is common to the above-named three approximate faunas of Eastern and Western America and the eastern Pacific islands, yet many fish 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 statements, is the affinity of the productions of the same continent or sea, though the species themselves are distinct at different 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, yet clearly related, replace each other. He 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 emeu, like those found in 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 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, though they may be all peculiar species, are essentially American. We may look back to past ages, as shown in the last chapter, and we find American types then prevalent on the American continent and in the American seas. We see in these facts some deep organic bond, prevailing throughout space and time, over the same areas of land and water, and independent of their physical conditions. The naturalist must feel little curiosity, who is not led to inquire what this bond is.

This bond, on my theory, is simply inheritance, that cause which alone, as far as we positively know, produces organisms quite like, or, as we see in the case of varieties nearly like each other. The dissimilarity of the inhabitants of different regions may be attributed to modification through natural selection, and in a quite subordinate degree to the direct influence of different physical conditions. The degree of dissimilarity will depend on the migration of the more dominant forms of life from one region into another having been effected with more or less ease, at periods more or less remote;—on the nature and number of the former immigrants;—and on their action and reaction, in their mutual struggles for life;—the relation of organism to organism 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. On 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.

I believe, as was remarked in the last chapter, in no 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 the individual in its complex struggle for life, so the degree of modification in different species will be no uniform quantity. If, for instance, a number of species, which stand in direct competition with each other, migrate in a body into a new and afterwards isolated country, they will be little liable to modification; for neither migration nor isolation in themselves can do 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 modified.

On 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 have descended from the same progenitor. In the case of those species, which have undergone during whole geological periods but little modification, there is not much difficulty in believing that they may have migrated from the same region; for during the vast geographical and climatal changes which will 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 explained in the last chapter, it is incredible that individuals identically the same should ever have been produced through natural selection from parents specifically distinct.

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 very 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 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 be easily passed over by migration, the fact is given as something remarkable and exceptional. The capacity of migrating across the sea is more distinctly limited in terrestrial mammals, than perhaps in any other organic beings; and, accordingly, we find no inexplicable cases of the same mammal inhabiting distant points of the world. No geologist will feel any difficulty in such cases as Great Britain having been formerly united to Europe, and consequently possessing the same quadrupeds. 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 vast and broken interspace. The great and striking influence which barriers of every kind have had on distribution, is intelligible only on the view that the great majority of species have been produced on one side alone, and have not been able to migrate to the other 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 local, or confined to one area. What a strange anomaly it would be, if, when coming one step lower in the series, to the individuals of the same species, a directly opposite rule prevailed; and species were not local, but had been produced in two or more distinct areas!

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 interrupted or 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 such cases. 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 freshwater productions; and thirdly, the occurrence of the same terrestrial species on islands and on the 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 various occasional means of transport, the belief that this has been the universal 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 distinct species of a genus, which on my theory have all descended from a common progenitor, can have migrated (undergoing modification during some part of their migration) from the area inhabited by their progenitor. If it can be shown to be almost invariably the case, that a region, of which most of its inhabitants are closely related to, or belong to the same genera with the species of a second region, has probably received at some former period immigrants from this other region, my theory will be strengthened; for we can clearly understand, on the principle of modification, why the inhabitants of a region should be related to those of another region, whence it has been stocked. 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 plainly related by inheritance to the inhabitants of the continent. Cases of this nature are common, and are, as we shall hereafter more fully see, inexplicable on the theory of independent creation. This view of the relation of species in one region to those in another, does not differ much (by substituting the word variety for species) from that lately advanced in an ingenious paper by Mr. Wallace, in which he concludes, that “every species has come into existence coincident both in space and time with a pre-existing closely allied species.” And I now know from correspondence, that this coincidence he attributes to generation with modification.

The previous remarks on “single and multiple centres of creation” do not directly bear on another allied question,—namely whether all the individuals of the same species have descended from a single pair, or single hermaphrodite, or whether, as some authors suppose, from many individuals simultaneously created. With those organic beings which never intercross (if such exist), the species, on my theory, must have descended from a succession of improved varieties, which will never have blended with other individuals or varieties, but will have supplanted each other; so that, at each successive stage of modification and improvement, all the individuals of each variety will have descended from a single parent. But in the majority of cases, namely, with all organisms which habitually unite for each birth, or which often intercross, I believe that during the slow process of modification the individuals of the species will have been kept nearly uniform by intercrossing; so that many individuals will have gone on simultaneously changing, and the whole amount of modification will not have been due, at each stage, to descent from a single parent. To illustrate what I mean: our English racehorses differ slightly 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 selecting and training many individuals during many generations.

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 when its climate was different may have been a high road for migration, but now be impassable; 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 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 will dispute that great mutations of level have occurred within the period of existing organisms. Edward Forbes insisted that all the islands in the Atlantic must recently have been connected with Europe or Africa, and Europe likewise with America. Other authors have thus hypothetically bridged over every ocean, and have united almost every island to 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 authorized in admitting such enormous geographical changes within the period of existing species. It seems to me that we have abundant evidence of great oscillations of level in our continents; but not of such vast changes in their position and extension, 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 halting places for plants and for many animals during their migration. In the coral-producing oceans such sunken islands are now marked, as I believe, by rings of coral or atolls standing over them. Whenever it is fully admitted, as I believe 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 continents which are now 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,—a certain degree of relation (as we shall hereafter see) between the distribution of mammals and the depth of the sea,—these and other such facts seem to me opposed to the admission of such prodigious geographical revolutions within the recent period, as are necessitated on the view advanced by Forbes and admitted by his many followers. The nature and relative proportions of the inhabitants of oceanic islands likewise seem to me opposed to the belief of their former continuity with continents. Nor does their almost universally volcanic composition favour the admission that they are the wrecks of sunken continents;—if they had originally existed as mountain-ranges on the land, some at least of the islands would have been formed, like other mountain-summits, of granite, metamorphic schists, old fossiliferous or other such 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 might be called occasional means of distribution. I shall here confine myself to plants. In botanical works, this or that plant is stated to be ill adapted for wide dissemination; but for transport across the sea, the greater or less facilities 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 days. 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 be floated across wide spaces of the sea, whether or not they were injured by the salt-water. Afterwards I tried some larger fruits, capsules, etc., 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 might wash down plants or branches, and that these might be dried on the banks, and then by a fresh rise in the stream be washed into the sea. Hence I was led to dry 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 they 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 seeds germinated after an immersion of 28 days; and as plants with ripe fruit (but not all the same species as in the foregoing experiment) floated, after being dried, for above 28 days, as far as we may infer anything from these scanty facts, we may conclude that the seeds 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 to a favourable spot by an inland gale, they 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 the average length of their flotation and of 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 of his seeds 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 could hardly be transported by any other means; and Alph. de Candolle has shown that such plants generally have restricted ranges.

But 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 coral-islands in the Pacific, procure stones for their tools, solely from the roots of drifted trees, these stones being a valuable royal tax. I find on examination, that when irregularly shaped stones are embedded in the roots of trees, small parcels of earth are very frequently enclosed in their interstices and behind them,—so perfectly that not a particle could be washed away in the longest transport: out of one small portion of earth thus completely enclosed by wood in 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 carcasses of birds, when floating on the sea, sometimes escape being immediately devoured; and seeds of many kinds 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 salt-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 could give many facts showing how frequently birds of many kinds are blown by gales to vast distances across the ocean. We may I think safely assume that under such circumstances their rate of flight would often be 35 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 will 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 I tried, germinated. But the following fact is more important: the crops of birds do not secrete gastric juice, and do not in the least injure, as I know by trial, 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 12 or even 18 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. Mr. Brent informs me that a friend of his had to give up flying carrier-pigeons from France to England, as the hawks on the English coast destroyed so many on their arrival. 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. Freshwater 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 their power of germination. Certain seeds, however, were always killed by this process.

Although the beaks and feet of birds are generally quite clean, I can show that earth sometimes adheres to them: in one instance I removed twenty-two grains of dry argillaceous earth from one foot of a partridge, and in this earth there was a pebble quite as large as the seed of a vetch. Thus seeds might occasionally be transported to great distances; for many facts could be given showing that soil almost everywhere is charged with seeds. Reflect for a moment on the millions of quails which annually cross the Mediterranean; and can we doubt that the earth adhering to their feet would sometimes include a few minute seeds? But I shall presently 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, I can hardly doubt that they must occasionally have transported seeds from one part to another of the arctic and antarctic regions, as suggested by Lyell; and during the Glacial period from one part of the now temperate regions to another. In the Azores, from the large number of the species of plants common to Europe, in comparison with the plants of other oceanic islands nearer to the mainland, and (as remarked by Mr. H. C. Watson) from the somewhat northern character of the flora 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 the seeds of northern plants.

Considering that the several above means of transport, and that several other means, which without doubt remain to be discovered, have been in action year after year, for centuries and 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 seawater; 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 in any great degree; but would remain as distinct as we now see them to be. 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 so long an 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 wanderers only by one means, namely, in dirt sticking to their feet, which is in itself a rare accident. Even in this case, how small would the chance be 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. I do not doubt that out of twenty seeds or animals transported to an island, even if far less well-stocked than Britain, scarcely more than one would be so well fitted to its new home, as to become naturalised. But this, as it seems to me, is no valid argument against what would be effected by occasional means of transport, during the long lapse of geological time, whilst an island was being upheaved and formed, 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, would be sure to germinate and survive.

Dispersal during the Glacial period.—The identity of many plants and animals, on mountain-summits, separated from each other by hundreds of miles of lowlands, where the 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 to the other. It is indeed a remarkable fact to see so many of the same plants 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 several 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 rocks scored by drifted icebergs and coast-ice, plainly reveal a former cold period.

The former influence of the glacial climate on the distribution of the inhabitants of Europe, as explained with remarkable clearness by Edward Forbes, is substantially as follows. But we shall follow the changes more readily, by supposing a new glacial period to come slowly on, and then pass away, as formerly occurred. As the cold came on, and as each more southern zone became fitted for arctic beings and ill-fitted for their former more temperate inhabitants, the latter would be supplanted and arctic productions would take their places. The inhabitants of the more temperate regions would at the same time travel 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, we should have a uniform 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. We may suppose that the Glacial period came on a little earlier or later in North America than in Europe, so will the southern migration there have been a little earlier or later; but this will make no difference in the final result.

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 higher and higher, as the warmth increased, whilst their brethren were pursuing their northern journey. Hence, when the warmth had fully returned, the same arctic species, which had lately lived in a body together on the lowlands of the Old and New Worlds, would be left isolated on distant mountain-summits (having been exterminated on all lesser heights) and in the arctic regions of both hemispheres.

Thus we can understand the identity of many plants at points so immensely remote as on the mountains of the United States and 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 migration as the cold came on, and the re-migration on the returning warmth, will 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 permitted their former migration across the low intervening tracts, since become too warm for their existence.

If the climate, since the Glacial period, has ever been in any degree warmer than at present (as some geologists in the United States believe to have been the case, chiefly from the distribution of the fossil Gnathodon), then the arctic and temperate productions will at a very late period have marched a little further north, and subsequently have retreated to their present homes; but I have met with no satisfactory evidence with respect to this intercalated slightly warmer period, since the Glacial period.

The arctic forms, during their long southern migration and re-migration northward, will have been exposed to nearly the same climate, and, as is especially to be noticed, they will have kept in a body together; consequently their mutual relations will not have been much disturbed, and, in accordance with the principles inculcated in this volume, they will not have been liable to much modification. But with our 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 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 its coldest period will have been temporarily driven down to the plains; they will, also, have been 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 this we find has been the case; for if we compare the present Alpine plants and animals of the several great European mountain-ranges, though very many of the species are identically the same, some present varieties, some are ranked as doubtful forms, and some few are distinct yet closely allied or representative species.

In illustrating what, as I believe, actually took place during the Glacial period, I assumed that at its commencement the arctic productions were as uniform round the polar regions as they are at the present day. But the foregoing remarks on distribution apply not only to strictly arctic forms, but also to many sub-arctic and to some few northern temperate forms, for some of these are the same on the lower mountains and on the plains of North America and Europe; and it may be reasonably asked how I account for the necessary degree of uniformity of the sub-arctic and northern temperate forms round the world, at the commencement of the 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 Atlantic Ocean and by the extreme northern part of the Pacific. During the Glacial period, when the inhabitants of the Old and New Worlds lived further southwards than at present, they must have been still more completely separated by wider spaces of ocean. I believe the above difficulty may be surmounted by looking to still earlier changes of climate of an opposite nature. We have good reason to believe that during the newer Pliocene period, before the Glacial epoch, and whilst the majority of the inhabitants of the world were specifically the same as now, the climate was warmer than at the present day. Hence we may suppose that the organisms now living under the climate of latitude 60°, during the Pliocene period lived further north under the Polar Circle, in latitude 66°-67°; and that the strictly arctic productions then lived on the broken land still nearer to the pole. Now if we look at a globe, we shall see that under the Polar Circle there is almost continuous land from western Europe, through Siberia, to eastern America. And to this continuity of the circumpolar land, and to the consequent freedom for intermigration under a more favourable climate, I attribute the necessary amount of uniformity in the sub-arctic and northern 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 large, but partial oscillations of level, I am strongly inclined to extend the above view, and to infer that during some 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 most remarkable, considering the distance of the two areas, and their separation by the 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 inter-migration 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 must have been completely cut off from each other. This separation, as far as the more temperate productions are concerned, took place long ages ago. And as the plants and animals migrated southward, they will have become mingled in the one great region with the native American productions, and 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 the two Worlds. 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 areas completely sundered. Thus, I think, we can understand the presence of many existing and tertiary representative forms on the eastern and western shores of temperate North America; and the still more striking case of many closely allied crustaceans (as described in Dana's admirable work), of some fish and other marine animals, in the Mediterranean and in the seas of Japan,—areas now separated by a continent and by nearly a hemisphere of equatorial ocean.

These cases of relationship, without identity, of the inhabitants of seas now disjoined, and likewise of the past and present inhabitants of the temperate lands of North America and Europe, are inexplicable on the theory of creation. We cannot say that they 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 the southern continents of the Old World, we see countries closely corresponding in all their physical conditions, but with their inhabitants utterly dissimilar.

But we must return to our more immediate subject, the Glacial period. I am convinced that Forbes's view may be largely extended. In Europe we have the plainest evidence of the cold 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. 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 gigantic ancient moraines. South of the equator, we have some direct evidence of former glacial action in New Zealand; and the same plants, found on widely separated mountains in this island, tell the same story. If one account which has been published can be trusted, we have direct evidence of glacial action in 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 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 Equatorial South America, glaciers once extended far below their present level. In central Chile I was astonished at the structure of a vast mound of detritus, about 800 feet in height, crossing a valley of the Andes; and this I now feel convinced was a gigantic moraine, left far below any existing glacier. Further south on both sides of the continent, from lat. 41° to the southernmost extremity, we have the clearest evidence of former glacial action, in huge boulders transported far from their parent source.

We do not know that the Glacial epoch was strictly simultaneous at these several far distant points on opposite sides of the world. But we have good evidence in almost every case, that the epoch was included within the latest geological period. We have, also, excellent evidence, that it endured for an enormous time, as measured by years, at each point. The cold may have come on, or have ceased, earlier at one point of the globe than at another, but seeing that it endured for long at each, and that it was contemporaneous in a geological sense, it seems to me probable that it was, during a part at least of the period, actually simultaneous throughout the world. Without some distinct evidence to the contrary, we may at least admit as probable that the glacial action was simultaneous on the eastern and western sides of North America, in the Cordillera under the equator and under the warmer temperate zones, and on both sides of the southern extremity of the continent. If this be admitted, it is difficult to avoid believing that the temperature of the whole world was at this period simultaneously cooler. But it would suffice for my purpose, if the temperature was at the same time lower along certain broad belts of longitude.

On this view of the whole world, or at least of broad longitudinal belts, having been simultaneously colder from pole to pole, much light can be thrown on the present distribution of identical and allied species. In America, Dr. Hooker has shown that between forty and fifty of the flowering plants of Tierra del Fuego, forming no inconsiderable part of its scanty flora, are common to Europe, enormously remote as these two points are; and there are many closely allied species. On the lofty mountains of equatorial America a host of peculiar species belonging to European genera occur. On the highest mountains of Brazil, some few European genera were found by Gardner, which do not exist in the wide intervening hot countries. So on the Silla of Caraccas the illustrious Humboldt long ago found species belonging to genera characteristic of the Cordillera. On the mountains of Abyssinia, several European forms and some few representatives of the peculiar flora of the Cape of Good Hope occur. At the Cape of Good Hope a very few European species, believed not to have been introduced by man, and on the mountains, some few representative European forms are found, which have not been discovered in the intertropical parts of Africa. 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 collected on the loftier peaks of Java raises a picture of a collection made on a hill in Europe! Still more striking is the fact that southern Australian forms are clearly represented by 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 as far north as Japan.

On the southern mountains of Australia, Dr. F. Müller 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 throughout the world, the plants growing on the more lofty mountains, and on the temperate lowlands of the northern and southern hemispheres, are sometimes identically the same; but they are much oftener specifically distinct, though related to each other in a most remarkable manner.

This brief abstract applies to plants alone: some strictly analogous facts could be given on the distribution of terrestrial animals. In marine productions, similar cases occur; as an example, I may quote a remark by the highest authority, Professor 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, etc., 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.

It should be observed that the northern species and forms found in the southern parts of the southern hemisphere, and on the mountain-ranges of the intertropical regions, are not arctic, but belong to the northern temperate zones. As Mr. H. C. Watson has recently remarked, “In receding from polar towards equatorial latitudes, the Alpine or mountain floras really become less and less arctic.” Many of the forms living on the mountains of the warmer regions of the earth and in the southern hemisphere are of doubtful value, being ranked by some naturalists as specifically distinct, by others as varieties; but some are certainly identical, and many, though closely related to northern forms, must be ranked as distinct species.

Now let us see what light can be thrown on the foregoing facts, on the belief, supported as it is by a large body of geological evidence, that the whole world, or a large part of it, was during the Glacial period simultaneously much colder than at present. 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 came slowly on, all the tropical plants and other productions will have retreated from both sides towards the equator, followed in the rear by the temperate productions, and these by the arctic; but with the latter we are not now concerned. The tropical plants probably suffered much extinction; how much no one can say; perhaps formerly the tropics supported as many species as we see at the present day crowded together at the Cape of Good Hope, and in parts of temperate Australia. As we know that many tropical plants and animals can withstand a considerable amount of cold, many might have escaped extermination during a moderate fall of temperature, more especially by escaping into the warmest spots. But the great fact to bear in mind is, that all tropical productions will have suffered to a certain extent. On the other hand, the temperate productions, after migrating nearer to the equator, though they will have been placed under somewhat new conditions, will have suffered less. And it is certain that many temperate plants, if protected from the inroads of competitors, can withstand a much warmer climate than their own. Hence, it seems to me possible, bearing in mind that the tropical productions were in a suffering state and could not have presented a firm front against intruders, that a certain number of the more vigorous and dominant temperate forms might have penetrated the native ranks and have reached or even crossed the equator. The invasion would, of course, have been greatly favoured by high land, and perhaps by a dry climate; for Dr. Falconer informs me that it is the damp with the heat of the tropics which is so destructive to perennial plants from a temperate climate. On the other hand, the most humid and hottest districts will have afforded an asylum to the tropical natives. The mountain-ranges north-west of the Himalaya, and the long line of the Cordillera, seem to have afforded two great lines of invasion: and it is a striking fact, lately communicated to me by Dr. Hooker, that all the flowering plants, about forty-six in number, common to Tierra del Fuego and to Europe still exist in North America, which must have lain on the line of march. But I do not doubt that some temperate productions entered and crossed even the lowlands of the tropics at the period when the cold was most intense,—when arctic forms had migrated some twenty-five degrees of latitude from their native country and covered the land at the foot of the Pyrenees. At this period of extreme cold, I believe that the climate under the equator at the level of the sea was about the same with that now felt there at the height of six or seven thousand feet. During this the coldest period, I suppose that large spaces of the tropical lowlands were clothed with a mingled tropical and temperate vegetation, like that now growing with strange luxuriance at the base of the Himalaya, as graphically described by Hooker.

Thus, as I believe, a considerable number of plants, a few terrestrial animals, and some marine productions, migrated during the Glacial period from the northern and southern temperate zones into the intertropical regions, and some even crossed the equator. As the warmth returned, these temperate forms would naturally ascend the higher mountains, being exterminated on the lowlands; those which had not reached the equator, would re-migrate northward or southward towards their former homes; but the forms, chiefly northern, which had crossed the equator, would travel still further from their homes into the more temperate latitudes of the opposite hemisphere. Although we have reason to believe from geological evidence that the whole body of arctic shells underwent scarcely any modification during their long southern migration and re-migration northward, the case may have been wholly different with those intruding forms which settled themselves on the intertropical mountains, and in the southern hemisphere. These being surrounded by strangers will have had to compete with many new forms of life; and it is probable that selected modifications in their structure, habits, and constitutions will have profited them. Thus many of these wanderers, though still plainly related by inheritance to their brethren of the northern or southern hemispheres, now exist in their new homes as well-marked varieties or as distinct species.

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 plants and allied forms have apparently migrated from the north to the south, than in a reversed direction. We see, however, a few southern vegetable forms on the mountains of Borneo and Abyssinia. I suspect that this preponderant migration from north to 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 they became commingled during the Glacial period, the northern forms were enabled to beat the less powerful southern forms. Just in the same manner as we see at the present day, that very many European productions cover the ground in La Plata, and in a lesser degree in Australia, and have to a certain extent beaten the natives; whereas extremely few southern forms have become naturalised in any part of Europe, 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 thirty or forty years from Australia. Something of the same kind must have occurred on the intertropical mountains: no doubt before the Glacial period they were stocked with endemic Alpine forms; but these have almost everywhere largely 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 the naturalised; and if the natives have not been actually exterminated, their numbers have been greatly reduced, and this is the first stage towards extinction. A mountain is an island on the land; and the intertropical mountains before the Glacial period must have been completely isolated; and I believe that the productions of these islands on the land yielded to those produced within the larger areas of the north, just in the same way as the productions of real islands have everywhere lately yielded to continental forms, naturalised by man's agency.

I am far from supposing that all difficulties are removed on the view here given in regard to the range and affinities of the allied species which live in the northern and southern temperate zones and on the mountains of the intertropical regions. Very many difficulties remain to be solved. I do not pretend to indicate the exact lines and means of migration, or the reason why certain species and not others have migrated; why certain species have been modified and have given rise to new groups of forms, and 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 ranges twice or thrice as far, and is twice or thrice as common, as another species within their own homes.

I have said that many difficulties remain to be solved: some of the most remarkable are stated with admirable clearness by Dr. Hooker in his botanical works on the antarctic regions. These cannot be here discussed. I will only say that as far as regards the occurrence of identical species at points so enormously remote as Kerguelen Land, New Zealand, and Fuegia, I believe that towards the close of the Glacial period, icebergs, as suggested by Lyell, have been largely concerned in their dispersal. But the existence of several quite distinct species, belonging to genera exclusively confined to the south, at these and other distant points of the southern hemisphere, is, on my theory of descent with modification, a far more remarkable case of difficulty. For some of these species are so distinct, that we cannot suppose that there has been time since the commencement of the Glacial period for their migration, and for their subsequent modification to the necessary degree. The facts seem to me to indicate that peculiar and very distinct species have migrated in radiating lines from some common centre; 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 Glacial period, when the antarctic lands, now covered with ice, supported a highly peculiar and isolated flora. I suspect that before this flora was exterminated by the Glacial epoch, a few forms were widely dispersed to various points of the southern hemisphere by occasional means of transport, and by the aid, as halting-places, of existing and now sunken islands, and perhaps at the commencement of the Glacial period, by icebergs. By these means, as I believe, the southern shores of America, Australia, New Zealand have become slightly tinted by the same peculiar forms of vegetable life.

Sir C. Lyell in a striking passage has speculated, in language almost identical with mine, on the effects of great alternations of climate on geographical distribution. I believe that the world has recently felt one of his great cycles of change; and that on this view, combined with modification through natural selection, a multitude of facts in the present distribution both of the same and of allied forms of life can be explained. The living waters may be said to have flowed during one short period from the north and from the south, and to have crossed at the equator; but to have flowed with greater force from the north so as to have freely inundated the south. As the tide leaves its drift in horizontal lines, though 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 a great height 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 serve as a record, full of interest to us, of the former inhabitants of the surrounding lowlands.

第十一章 地理分布

今日的分布不能用物理条件的差别来解释——障碍物的重要性——同一大陆上生物的亲缘——创造的中心——由于气候的变化、土地高低的变化及偶然途径的散布方法——冰期中的散布,与世界的分布一样广

考察地球表面的生物分布时,我们注意的第一件大事便是,各地生物的相似或不相似都不能全部用气候等物理条件来解释。近来,几乎每一个研究这个问题的作者都得出了这种结论。仅仅美洲的情形差不多就足以证明这种结论的正确性了;因为,如果排除北极地区几乎是连续的陆地,所有作者都赞同新旧世界之间的区分是地理分布的最基本分界之一;然而,如果在美洲的广袤大陆上旅行,从美国的中部到最南端,将会遇到极多样的物理条件:潮湿不堪的地区、干燥的沙漠、巍巍的高山、草原、森林、沼泽地、湖泊和大河,各种温度都有。旧世界几乎没有一种气候或外界条件不能与新世界相平行——至少接近同一物种的一般需要,因为一群生物局限在具有稍微特殊条件的小区域里的现象,还很少见。例如,旧世界里有些小块地方比新世界的任何地方更热,但这里的动植物群并不奇特啊。尽管旧世界和新世界的条件具有这种平行现象,它们的生物却是何等不同呵!

在南半球,如果我们把南纬二十五度到三十五度之间的澳洲、南非洲和南美洲西部的广袤陆地加以比较,将会看出一些地方在一切条件上都是极端相似的,然而不可能指出更加决然不同的三种动植物群了。我们再把南美洲的南纬三十五度以南、二十五度以北的生物加以比较,因而气候条件相当不同;然而两者的相互关系,比它们和气候相近的澳洲、非洲的生物之间的关系,更加无比地密切。关于海栖生物也可举出类似的事实。

在一般观察里,我们注意的第二件大事是,阻碍自由迁徙的任何种类的障碍物,都与各地区生物的差异有密切而重要的关系。我们从新旧两世界几乎所有陆栖生物的重大差异中,可以看到这一点,不过北部地方是个例外,那里的陆地几乎连接,气候差异也微小,北温带地方的类型大概可以自由迁徙的,就像严格的北极生物目前所进行的那样。我们在同纬度下的澳洲、非洲和南美洲生物之间的重大差异中,也可看到同样的事实:因为这些地方的相互隔离几乎登峰造极。在各个大陆上,我们也看到同样的事实;巍峨而连续的山脉、大沙漠,甚至大河的两边,可以看到不同的生物;虽然,由于山脉、沙漠等等并不像隔离大陆的海洋那样无法逾越,也不像海洋持续得那样长久,所以同一大陆上生物的差异比起不同大陆程度要低得多。

关于海洋,我们可以看到同样的法则。没有比中、南美洲东西海岸的海栖动物差别更大了,没有一种鱼类、贝类、蟹类是相同的;但两个大动物群仅仅为巴拿马地峡所分割,狭小但无法逾越。美洲海岸的西方展开了广阔无边的海洋,没有迁徙者可以停脚的岛屿;在这里看到另一种障碍物,一越过这里,我们就在太平洋东部诸岛那里遇到别种完全不同的动物群。所以三种海栖动物群在相同的气候下,形成彼此相距不远的平行线,而分布到遥远的北方和南方;但是,由于被不可逾越的陆地或大海这样障碍物所隔开,是完全不同的。另一方面,从太平洋热带地方的东部诸岛再向西行,就不再遇到不可逾越的障碍物,那里有可以作为停脚处所的无数岛屿,经过半个地球的旅程后,便到达非洲海岸;在这广阔的空间,我们不会遇到断然不同的海栖动物群。虽然在上述美洲东部、美洲西部和太平洋东部诸岛的三种相近动物群中,没有一个贝类、蟹类、鱼类是共同的,但是还有许多鱼类从太平洋分布到印度洋,而且在几乎完全相反的子午线上的太平洋东部诸岛和非洲东部海岸,还有许多共同的贝类。

第三件大事,一部分已包括在上述的叙述里,是同一大陆、海洋里的生物都具有亲缘关系,虽然物种本身在不同地点和场所是不相同的。这是一个具有最广泛普遍性的法则,每一个大陆都有了无数的事例。然而学者旅行时,譬如说从北到南,总是惊异于亲缘密切而物种不同的连续生物群逐次更替,会听到密切近似而种类不同的鸟唱着近似的调子,会看到它们的巢构造相似却不同,卵的颜色几乎同样。麦哲伦海峡附近的平原上,栖息着美洲鸵鸟(Rhea)的一个物种,而在以北的拉普拉塔平原栖息着同属的另一物种;但没有像同纬度上非洲和澳洲那样的真正鸵鸟或鸸鹋(emu)。在同一拉普拉塔平原上可看到刺鼠(agouti)和绒鼠(bizcacha),和欧洲野兔和家兔的习性大同小异,而且都属于啮齿类的同一个目,但是构造上显然呈现美洲的模式。登上巍峨的科迪勒拉峰,可看到绒鼠的一个高山种;注视河流,看不到海狸(beaver)或麝香鼠(musk-rat),但可看到海狸鼠(coypu)和水豚(capybara),都是南美洲模式的啮齿类。不胜枚举啊。如果我们观察一下美洲海岸的岛屿,不管地质构造多么不同,但其生物本质上都是美洲模式,哪怕全是特殊的物种。如同前章所说的,我们可以回顾一下过去的时代,会看到美洲模式的生物当时在美洲大陆上和海洋里都是占优势的。在这等事实里我们看到某种深入的有机联系透过时空、遍及水陆的同一地域且与物理条件无关。学者如果不想深究这种联系是什么,一定是缺乏好奇心。

按照我的理论,这种联系就是传承,据我们确切知道的来说,单单这个原因就会使生物彼此十分相像,或者如在变种里所看到那样,使它们彼此近乎相像。不同地区生物的不相像,可以归因于通过自然选择的变异,其次大概要归因于不同的物理条件的直接影响。不相像的程度,取决于占优势的生物类型在或短或长的遥远时期内,从一处到另一处地方的迁徙多少受到了有效的阻碍;——取决于先前移来的生物的性质和数量,——取决于生活斗争中生物之间的相互作用反作用;——如我前面常提起的,生物和生物的联系是重中之重的关系。这样,障碍物由于制约迁徙,便发挥出高度的重要性,正如时间对于通过自然选择的缓慢变异过程所发挥的作用一样。分布广、个体多而且已经在它们广布的家乡里战胜了许多竞争者的物种,当扩张到新地方的时候,有取得新地位的最佳机会。在新家乡,它们会遇到新条件,而且会常常进一步变异和改进,这样,就得到进一步的胜利,并且产生成群的变异后代。依据这种变异传承原理,我们就能理解为什么属的一部分,全属,甚至一科会如此普遍和显著地局限在一个地方。

如前章所述,我不相信有必然发展的法则存在。各物种的变异性都有其独立性质,并且只有在复杂的生活斗争中有利于个体的时候,才能被自然选择所利用,所以不同物种的变异量不是整齐划一的。如果有若干物种经过直接的互相竞争后,集体地移进一个新的后来成为孤立的地方时,就很少发生变异;因为移动和孤立本身并不起任何作用。只有使生物相互间发生新的关系,并且以较小的程度与周围的物理条件发生新的联系时,这些原则才起作用。如前章所述,有些生物类型从极遥远的地质时代起就保持了差不多相同的性状,所以某些物种曾在广大的空间内迁徙,但未发生大变异。

按照这种观点,同属的若干物种虽然栖息在世界上相距极远的地方,但因都是从同一个祖先传下来的,原先一定是在同一个原产地发生的。至于那些在整个地质时期里很少变化的物种,不难相信都是从同一地移来的;因为自古以来,在地理上和气候上的巨变期间,几乎任何大量的迁徙都是可能的。但是在许多其他情形里,有理由相信同一属的诸物种是在比较近代的时期内产生的,对这方面的解说就极难。同样显然地,同种的个体虽然现今栖息在相距很远而孤立的地方,但一定来自双亲最初产生的地点,因为,前章已经说明,从不同物种的双亲通过自然选择产生一模一样的个体是不可信的。

我们现在看学者们宽泛讨论过的问题,即物种系在地球表面上一处,还是在多处创造出来的呢。至于同一物种如何从一处地方迁徙到今日所看到的那样相距很远而孤立的若干地方,无疑是极难理解的。然而,每一物种最初产生在一处地方的这种简单观点使人神往,排斥这种观点的人,也就排斥了普通的发生以及其后迁徙的真实原因,并且会把神迹的作用招引进来。普遍承认在大多数情形下,一个物种的栖息地总是连续的;如果一种动物栖息在相距很远的两处地方,或者具有迁徙时不易通过的中间地带的两处地方时,那么这种事情就被认为是值得注意的例外。迁徙时跨越大海的能力,显然仅限于陆栖哺乳动物,非任何其他生物所能及,因此同一哺乳动物栖息在相距很远的地方并不难解。大不列颠具有和欧洲其他大陆相同的四足兽类,没有一个地质学者觉得有什么难解,因为两地一度是相连的。但是,如果同一物种能在隔开的两地产生,那么为什么看不见一种欧洲和澳洲或南美洲共有的哺乳动物呢?生活条件是近乎相同的,所以许多欧洲的动植物已在美洲和澳洲归化了;而且在南北半球的这等相距很远的地方也有若干完全相同的土著植物。我认为,回答是某些植物由于有各种散布方法,曾经移徙过了广阔而断开的中间地带,但哺乳动物无法迁徙。各种障碍物对于分布有重大而显著的影响,只有大多数的物种产生在障碍物的一边,而不能迁徙到另一边的这种观点,才能解释。少数科,许多亚科,很多属,更多数目的属的分部,只局限在单一地方;若干学者曾经观察到,最自然的属,即其物种的相互联系最密切的那些属,一般都局限在同一地。我们更下去一步,即下到同种的个体,如果有正相反的法则,物种并不局限于一地,而产生于两个以上地方,这将是何等奇怪的反常啊!

于是,就像许多其他学者一样,我认为各个物种仅在一地产生,以后在过去和现在的条件下按其迁徙和生存力量所允许,再从该地迁徙出去,这种观点可能最有道理。无疑在许多情况下,无法解释同一物种怎么能从一地移到另一地,但是在最近地质时代肯定发生过地理气候变化,想必会打破许多物种从前的连续分布,弄得不连续了。所以我们不得不考虑到,分布连续性的例外是否够多,是否性质严重,致使我们放弃从一般考察看来是可能的那一观点——各个物种都是在一个地区内产生,并且尽可能远地从那里迁徙出去。如把现在生活在相距很远的隔离地点的同一物种的所有例外情况都加以讨论,实在是不胜厌烦,我也从来不妄言能给许多事例提出任何解释。但是,几句引言以后,我要对少数最显著的事实提出讨论;即,相距很远的山顶上以及北极、南极相距很远的地点生存同一物种;其次,淡水生物的广阔分布(见下章);第三,同一陆栖物种出现在数百英里大海隔开的岛屿及其大陆上。同一物种生存在地球表面上相距很远而孤立的地点,这件事如果能在许多事例中根据各个物种从一个单一的产地迁徙去的这种观点加以解释,那么,考虑到我们对于从前气候地理的变化以及各种一时的输送方法一无所知,我看单一产地是普遍法则的观点,是无比稳妥的。

讨论这个问题,就能够同时考察对于我们同等重要的一件事,即同属若干物种(依我的理论必然都是从一个共同祖先传下来)是否从祖先栖息的地区进行迁徙,而且在迁徙的某段时间发生变异。栖息一地的大多数物种与另一地的物种密切近似或者同属,如果可以表明一地大概在以往的某一时代接受过另一地的生物,是几乎不变的事实,那我的理论就更加巩固了;因为依据变异原理,可以清楚地理解,为什么一地的生物与另一地相关,相互往来。例如,距离大陆几百英里之处隆起,形成的火山岛,随着时间的推移,大概会从大陆接受少数的生物,而它们的后代虽已变异,但因遗传仍会和大陆的生物明显有关系。这种性质的个案是普遍的,并且如以后还要进一步看到的,用独立创造的理论无解。一地的物种和另一地有联系的这种观点,与华莱斯先生最近雄文所主张的大同小异(用变种一词代替物种),他断言,“各物种的产生,和以前存在的密切近似的物种在空间时间上都是一致的”。通过通信,我现在已明白,他把这种一致归因于伴随着变异的传承。

前面“创造的中心单一还是多个”的话题,和另一个近似的问题并没有直接关系——即同种的所有个体是否从一对配偶传下来的,是否从一个雌雄同体个体传下来的,或者如某些作者所设想的那样,是从许多同时创造出来的个体传下来的。关于从不杂交的生物(如果存在),依我看,各个物种一定是从连续改进的变种传下来的,变种曾经互相淘汰,但决不和其他个体或变种相混合;所以,在变异改进的每一连续阶段,同一变体的一切个体都是从单一亲体传下来的。但在大多数情形下,即每次生育时习惯上须行交配和经常进行杂交的一切生物,我认为同种的个体在缓慢的变异过程中,会因互相杂交而差不多保持一致;许多个体会同时进行变化,并且在每一阶段上变异的全量不会是只从单一亲体传下来的。举一个实例来说明我的意思:英国的赛马和每一个其他马品种都略不相同,但是它们的异点和优越性并不是单从任何一对亲体传下来的,而是归功于每一世代中对于许多个体继续进行了仔细的选择和训练。

我在上面选出了三类事实,作为“创造的单一中心”学说的最大困难问题,在讨论它们之前,必须稍微说一说散布的方法。

散布的方法。——赖尔爵士等作者已经精干地讨论了这个问题。我在这里只能举出重要事实的最简单的摘要。气候变化对于迁徙一定有过强有力的影响。一地在从前气候不同的时候,大概曾经是迁徙的大路,今日却不能通过,下面对于这方面的问题不得不细论。陆地水平的变化一定也曾有过重要的影响:狭窄的地峡现在把两种海栖动物群隔开;如果地峡在水中沉没,或者曾经沉没过,两种动物群就会混合在一起,或者从前混合过了。今日的海洋所在之处,在以前的时代或有陆地把岛屿,甚至可能诸大陆连接在一起,陆栖生物就可以从这地跑到别地去。陆地水平的巨大变化,曾经发生在现今生物的存在期间,没有地质学者争论过这一点。福布斯主张,大西洋的一切岛屿,在最近的过去一定曾与欧洲或非洲相连,并且欧洲也与美洲相连。其他的作者们就这样假想各海洋都有过陆路可通,而且几乎把每一个岛屿与某大陆连接在一起。如果福布斯的论点果然可信的话,那么必须承认,几乎没有一个岛屿在最近的过去是不和大陆相连的。这一观点便可快刀斩乱麻似的解决同一物种分布到相距极远的地点的问题,而且消除了许多难点;但据我所能判断,我们无权承认现今物种存在的期间有过这样巨大的地理变化。在我看来,关于陆地水平的巨大变动固然有丰富的证据,但是并没有证据证明其位置和范围有过重大的变化,以致在近代彼此相连,且和各个中间海岛相连。我直率承认,先前有过许多岛屿现在沉海了,而从前可能作为动植物迁徙时的歇脚地点。在产生珊瑚的海里就有这种沉下的岛屿,现今上面有珊瑚环,即环礁(atolls)做标志。总有一天会承认各个物种曾是从单一的产地产生的,充分承认这一点,并且随着时间的推移,在我们知道了关于分布方法的确实情形时,就能稳妥地推测从前陆地的范围了。但我不相信将来能够证明今日天各一方的许多大陆在近代曾连续地,或者差不多连续地连在一起,并且和许多现存的海岛连在一起。若干关于分布的事实,——例如在几乎每个大陆两边,海栖动物群存在巨大差异,——若干陆地甚至海洋的第三纪生物和该处现存生物有密切关系——哺乳动物和海洋深度有某种关系(以后还要讲到)——依我看这类事实都和近代曾发生过极大的地理变化的说法正相反,而这种变化对于福布斯所提出并被其追随者所承认的观点必不可少。依我看,海岛生物的性质及其相对的比例,也与海岛从前曾与大陆相连这一观点正相反。况且岛屿几乎普遍都有火山的成分,这也不能支持都是大陆沉没后残遗物的说法;——如果原来作为大陆的山脉而存在的话,那么,至少有些岛会像其他山峰那样是由花岗岩、变质片岩、古代化石岩等岩石所构成,而不单是由火山物质叠积而成。

现在我必须对所谓意外的分布法说几句话,其实叫偶然的分布法更为适当些。这里单说植物。植物学著作常常说这种或那种植物不适于广泛传播;但是,关于跨海输送难易可以说几乎一无所知。伯克利先生帮助我做几种试验前,甚至连种子对海水损害作用有多大的抵抗力也不知道。我惊奇地发现,87种种子中有64种浸泡28日后还能出芽,并且有少数浸泡137日后还能成活。为了便利,我主要试验了没有蒴或果肉的小种子;这些种子几天之后都沉下去了,所以无论是否会受海水的损害,都不能漂浮过广阔的海面。后来我试验了一些较大的果实和蒴等等,其中有些能漂浮很长时间。众所周知,新鲜木材和干燥木材的浮力大不同;而且我发现洪水往往把植物或枝条冲下来,在海岸上晒干,然后溪水泛滥再把它们带入海里。于是,我把94种植物带有成熟果实的茎和枝加以干燥,然后放到海水里去。大多数很快沉下去了,但是有些在新鲜时只能漂浮短时间,干燥后却能漂浮很长的时间。例如,成熟的榛子即刻便会沉下,但干燥后却能漂浮90日,而且种子以后还能发芽;带有成熟浆果的石刁柏(asparagus)能漂浮23日,干燥后却能漂浮85日,而且种子以后还能发芽;苦爹莱(Helosciadium)的成熟种子两日便沉下,干燥后大约能漂浮90日,而且以后还会发芽。总计起来,这94种干植物中,有18种能漂浮28日以上,其中有些还能漂浮更久。这就是说,八十九分之六十四的种子浸水28日后还能发芽;并且九十四分之十八带有成熟果实的植物(与上述试验的物种并不完全相同)干燥后能漂浮28日;所以,如果从这些贫乏的事实能够做出任何推论的话,我们便可断言,任何地方百分之十四种植物种子大概能漂流28日,而且还会保持发芽力。约翰斯顿(Johnston)的“地文图”上表明,若干大西洋流的平均流速一昼夜为33英里(有些海流速一昼夜为60英里);按照这种平均速度,一地可能有百分之十四种植物的种子漂过924英里的海面而达到另一地,而且搁浅之后如果有向陆风将其吹到适宜的地点,大概还会发芽。

我试验以后,马滕斯(M.Martens)也进行了相似试验,不过方法更好,把种子放盒子里,漂浮在海上,所以种子有时浸湿有时暴露在空气中,就像真的漂浮植物一般。他试验了98个种子,大多数和我的不同,但是所选用的是许多大果实和海边植物的种子,可以延长平均漂浮时间并加强对海水损害作用的抵抗力。另一方面,他没有事先使带有果实的植物或枝条干燥;如我们说过的,干燥可使某些植物漂浮得长久些。结果是,九十八分之十八种植物的种子漂浮了42日,而且以后还能发芽。但是我并不怀疑暴露在波浪中的植物,比起我们的试验中不受剧烈波动影响的植物,漂浮时间要短些。所以,大概可以更稳妥地假定,一个植物区系的百分之十种植物的种子,干燥之后大概可以漂过900英里宽的海面,而且还能发芽。大果实常比小果实漂浮得更长久,这是有趣的,因为具有大种子、大果实的植物很难由其他任何方法来输送;德康多尔阐明,这种植物在分布范围上一般是有限的。

种子有时候可由另一种方法来输送。漂流木常被冲到很多岛上,甚至位于最广阔的大洋中央的岛上去;太平洋珊瑚岛上的土人专从漂流木的根间搜求做工具用的石子,这种石子竟作为贵重的税品。我细观后发现形状不规则的石子嵌在树根中间时,间隙里和石子后面常常藏着小块泥土——完全严密地包藏在里边,极长久的运输期间也不会有一点冲洗出去;一株约50年生橡树的根间,有一小块泥土严密地藏在那里,小泥土上有三株双子叶植物发芽了:我肯定这个观察是准确的。我还可以指出,鸟的尸体漂浮在海上,有时不致即刻葬身鱼腹,这种漂流鸟的嗉囊里有许多种类的种子,很久还保持活力,例如豌豆和大巢菜浸在海水里只要几天便死去;但是在人造海水中漂浮过30日的鸽子的嗉囊内,种子几乎全能发芽,这使我惊奇。

活鸟运输种子,不失为高度有效的媒体。我能够举出许多事实来表明,许多种类的鸟常常被大风吹过很远的海面。我看可以稳妥地假定,在这种情形下,飞行时速常常是35英里;有些作者做过更高的估计。我从未见过养分丰富的种子能通过鸟肠的事例;但是坚果种子甚至能通过火鸡的消化器官而不损坏。在两个月的期间,我在花园里从小鸟的粪便里检出了12种种子,看上去都是完好的,试验了一些,还能发芽。但是下述的事实更加重要:鸟的嗉囊并不分泌胃液,而且根据我的试验,一点也不会损害种子的发芽力;鸟看到大批的食物饱餐后,可以肯定地断言,谷粒在12,甚至18小时内,不会全部进入沙囊里。鸟在这一段时间里会轻易被风吹到500英里以外,而且我们知道,鹰是找寻疲态鸟的,被撕裂的嗉囊含有物很容易就此散布出去。布伦特先生告诉我,他朋友曾经不得不放弃信鸽从法国到英国的放飞,因为英国海岸有鹰将刚到的信鸽大批杀死。有些鹰和猫头鹰把捕获物囫囵吞下,经过12到20小时的时间,吐出的食物团块中,我根据动物园所做的试验知道,还有能发芽的种子。有些燕麦、小麦、粟、加那利草(canary)、大麻、三叶草和甜菜的种子,在不同食肉鸟的胃里经过12到21小时之后还能发芽;两粒甜菜的种子经过二日又十四小时后,还能生长。我发现淡水鱼类吃多种陆、水生植物的种子,鱼常常被鸟吃掉,这样,种子就可能从一地输送到另一地。我曾把许多种类的种子塞进死鱼的胃里,随后拿给鱼鹰、鹳和鹈鹕去吃,隔了许多小时之后,鸟把种子集在小团块里吐出来了,或者跟着粪便排出去;排出的种子中若干还保持了发芽力。然而,有些种子经过这种过程之后总是死掉的。

鸟喙和鸟爪一般是清洁的,但我可以证明有时候也沾有泥土:有一次我曾从一只鹧鸪的脚上取出22英厘干黏土,泥土中有一块大巢菜种子大小的小石子。所以有时候种子能输送很远,有大量事实证明,泥土几乎都带有种子的。想想每年几百万鹌鹑飞过地中海,我们还能怀疑附着在鸟爪上的泥土有时候含有几颗小种子吗?这个问题下文再讨论。

我们知道冰山有时负载着土石,甚至挟带着树枝、骨头和陆栖鸟巢,所以不必怀疑,如赖尔所提出的,有时想必在北极区和南极区把种子从一地输送到另一地;而且在冰期,从现在的温带的一地把种子输送到另一地。相对于靠近大陆的大西洋其他岛屿上的物种来比较,亚速尔群岛有大量的植物物种和欧洲共通,相对于纬度,植物多少带有北方的性状(如沃森先生所说),我由此推测,这些岛屿上的部分种子是在冰期由冰带去的。我曾请求赖尔爵士写信给哈通(Hartung)先生,问他那些岛上是否见过漂石,他回答,看到过花岗岩和其他岩石的巨大碎块,而这些岩石不是该群岛原来就有的。因此我们可以稳妥地推论,冰山曾把拖来的岩石卸在这海中群岛的岸上,岩石至少有可能带来了少数北方植物的种子。

考虑到这几种输送方法,以及今后无疑有待发现的其他输送方法,几多万年以来,年复一年地起着作用,我想,许多植物如果没有这样被广泛输送出去,简直是奇哉怪也。这种输送方法有时被称为意外的,但这说法不完全正确;海流不是意外的,盛行风的风向也不是意外的。这里应当注意,任何输送方法很少能把种子运到很远的距离,种子如受海水作用太久,就不能再保持活力,也不能在鸟类的嗉囊或肠子里长久携带。然而,这种方法却足以通过几百英里宽的海面,或者从这岛到那岛、从大陆到邻近的岛进行偶然的输送,但不能从一个相距很远的大陆输送到另一个大陆。相距很远的大陆上植物区系不会因这种方法而大事混淆起来,而仍然像今日看到的一样,保持着区分。海流由于走向,不会把种子从北美洲带到不列颠,但大概会而且实际把种子从西印度带到我国的西海岸,在那里,哪怕没有因长久的海水浸泡而死去,也不会忍耐我国的气候的。差不多每年总有一两只陆鸟被风吹过整个大西洋,从北美洲来到爱尔兰和英格兰的西海岸;但是这稀有的漂泊者只有一种方法可以输送种子,即附着在鸟爪的泥土里,而这本身却是罕见的意外。甚至在这种情形下,一粒种子落在适宜的土壤上而达到成熟,其机会是何等之少啊!但是,因为像大不列颠那样生物繁多的岛,根据现在所能知道的,在最近的几世纪内没有通过偶然的输送方法从欧洲或者任何其他大陆接纳过迁徙者(很难证明这一点),就主张生物贫乏的岛,离大陆更远,便不会用相似的方法接纳迁徙者,那就大错特错了。如果有二十种种子或动物输入一个岛,纵使其生物远不如不列颠那样繁多,能很好适应新家乡而归化的,无疑不会多于一个种类。但在悠久的地质时期内,当那个岛正在隆起并且没有繁多的生物栖息以前,对于偶然的输送方法的效果,我看并不能做出有效的反对议论。在一个几乎不毛的岛上,只有少数或者没有破坏性的昆虫或鸟类生存在那里,差不多每一粒偶然来到的种子,如果气候适宜,都会发芽成活的。

冰期中的散布。——在数百英里低地隔开的山顶上有许多相同的动植物,而高山种不能在低地成活,这是既知的关于同一物种生活在相距很远的地点而彼此间显然没有可能从一地迁徙到另一地的最显著事例之一。在阿尔卑斯或比利牛斯的积雪区和欧洲极北部分,有何等多的同种植物存在,这的确是值得注意的事实;但美国怀特山(White Mountains)上的植物和加拿大拉布拉多(Labrador)的植物完全相同,阿萨·格雷说,它们和欧洲最高山上的植物也几乎完全相同,这是更值得注意的。早在1747年,这样的事实就使葛美伦(Gmelin)断言同一物种一定是在若干不同的地点独立创造的;要不是阿加西斯等人唤起了对于冰期的注意,我们也许要停留在这种观点里的。冰期,如以后就要讲到的,可对此做简单的解释。几乎有各种各样的有机无机的证据来证明,在很近的地质时期内,欧洲中部和北美都是处于北极的气候之下的。苏格兰和威尔士的山岳用山腰的划痕、表面的磨光和翘起的漂石,表明那里的山谷以前曾经充满了冰川,这比火灾劫后的房屋废墟更清楚地说明以往的情形。欧洲气候的变化如此之大,以致意大利北部古代冰川所留下的巨大冰碛上,现在已经长满了葡萄和玉米。美国的大部分地方所看到的漂石和有冰川近岸冰划痕的岩石,明白地显示出从前那里有寒冰时期。

从前冰期气候对于欧洲生物分布的影响,如福布斯所清楚解释的,大致如下。但如果假定新冰期是慢慢而来的,随后就像从前的情形那样又慢慢过去,会更易追踪这变化。当寒冷到来,各南方地带适于北极生物,不适合以前的温带生物,后者遭淘汰,北方生物乘虚而入。同时温带生物南移,否则会被障碍所阻挡而死亡。山上雪冰遮盖,从前的高山生物降到平地来。寒冷达到极点时,清一色的北极动植物群会布满欧洲中部各地,向南直达阿尔卑斯和比利牛斯,甚至可以伸延到西班牙。现在美国的温带地区同样也布满北极动植物,而且和欧洲的动植物大致相同;因为我们假定曾向南方各地迁徙的现在北极圈的生物,在全世界都是显著一致的。我们可以假定北美的冰期来得比欧洲略早或略晚,所以朝南迁徙也略早或略晚,但对于最后的结果无关宏旨。

回暖,北极生物北退,后面紧紧跟着的是温带地区生物。当山脚下冰雪消融,北极生物遂占据融解清空的地方,温暖渐渐增加,渐渐向上迁移,这时候一部分兄弟则启程北去。因此,充分回暖时,曾经共同生活在欧洲和北美洲低地的同种生物,又再次见于新旧世界的寒冷地区,孤立于相距很远的山顶上了,低地上的北极生物则全部灭绝。

这样,我们就能理解在远隔万里的各地,如北美和欧洲的高山,为什么许多植物是相同的。这样,我们还能理解为什么各个山脉的高山植物与其正北方或近乎正北方的北极类型更是特别有关系:寒冷到来时的第一次迁徙以及温暖回还时的再迁徙,一般是向着正南和正北的。例如,苏格兰的高山植物,如沃森先生所说的,以及比利牛斯的高山植物,如雷蒙德(Ramond)所说的,和斯堪的纳维亚北部的植物特别相似;美国的和拉布拉多相似;西伯利亚山上的和俄国北极区相似。这观点是以从前确有冰期为根据的,所以在我看来,它能极其满意地解释欧洲和美洲的高山植物以及北极植物现在的分布状况。因此,当我们在其他地区发现同一物种生活在相距很远的山顶上,纵使没有其他证据,几乎也可以断定,寒冷的气候曾经允许它们通过中间低地进行迁徙,而现在中间低地已变得太暖和,不适于生存了。

如果冰期以来的气候比现在略温暖(某些美国地质学家认为这样,主要根据条鳍鱼纲化石[Gnathodon]的分布),那么北极生物和温带生物会在晚近时期进一步向北方略进,然后后退到目前栖息位置;但我没有看到满意的证据,证明冰期以来有这种稍暖时期插入。

北极类型随着气候的变化,起初向南,后来再退北,长途迁徙时,遇到的气候不相上下;必须特别注意,是集体迁徙,所以相互关系不会受到很大的扰乱。因此,按照本书反复强调的原理,它们将不会发生很大的变异。但高山生物在温暖回还的时候就被隔离了,起初在山脚下,最终在山顶上,其情形就有些不同了;因为所有相同的北极物种都留在彼此相距很远的山脉中,而且能在那里生存是不可能的事情;它们还很可能和古代高山物种相混合,这些古代高山物种在冰期开始前想必已经生长在山上,并且在最冷的时期一定会暂时被驱逐到平地上来,还会受到多少不同气候的影响。它们的相互关系在某种程度上会因此受扰乱,结果容易发生变异;而且我们发现事实确是如此;如果我们拿欧洲几大山脉上现在的高山动植物来互相比较,虽然许多物种还是相同的,有些却成为变种,有些成为可疑的类型,更有少数成为代表各个山脉的密切近似但不相同的物种了。

在上述例证里,我描述了冰期的想象情景,假定冰期开始时,环绕北极地方的北极生物就像今日那样一致。但是上述关于生物分布的议论,不仅仅适用于严格的北极类型,而且适用于许多亚北极和某些北温带的类型,因为其中某些类型在今日北美洲和欧洲的平原以及低坡上是相同的;可以合理质问:我怎样解释冰期开始时全世界的亚北极和北温带类型必要的一致程度。目前,新旧世界的亚极带以及北温带的生物被整个大西洋和北太平洋隔开了。冰期中,新旧世界的生物居住在比现在更南的位置,想必更加完全地被更广阔的海洋隔开了。我认为,只要考察更早时期相反性质的气候变化,就可以克服上述的难点。我们有可靠的理由相信,在新上新世时期,冰期之前,世界上大多数生物在种别上和今日是相同的,并且当时的气候要比今日暖和。因此,我们可以假定,今日生活在纬度六十度气候之下的生物,在上新世却生活在纬度六十六度至六十七度之间北极圈下的更北方;而严格的北极生物当时则生活在更接近北极的中断陆地上。现在看一看地球仪,就可知道在北极圈下,有差不多连续的陆地从西欧通过西伯利亚一直连到美洲东部。这种环极陆地的连续性,使生物在较适宜的气候下可以自由迁徙,于是新旧世界的亚北极生物和北温带生物在冰期以前的必要一致性,便可得到解释。

根据上述各种理由,可以相信我们的大陆虽然经过地面水平的巨大局部变动,但长久保持了几乎相同的相对位置,我极愿意扩大上述观点,并做出推论,即在更早和最热的时期,例如旧上新世的时期,大量同样的动植物都栖息在几乎连续的环极陆地上;而且,无论新旧世界的动植物,在冰期没有开始之前很久,随着气候的逐渐变冷,开始慢慢南移。我认为,欧洲中部和美国看到的它们的后代大多数已发生了变化。根据这种观点,我们就能理解为什么北美洲和欧洲的生物之间的关系很少是相同的,——如果考虑到两个大陆的距离以及它们被整个大西洋所隔开,就可以知道这是一个高度值得注意的关系。我们还能进一步理解某些观察者所提出的一件奇异事实:第三纪末期欧洲和美洲的生物之间的相互关系比起今日更为密切;因为在这温暖的时期,新旧世界的北部差不多被陆地连接在一起,可以作为桥梁供两处生物迁徙,后来由于寒冷,桥梁就不通了。

上新世慢慢降温的期间,栖息在新旧世界的共同物种一向北极圈以南迁徙,相互之间就要完全隔绝。就温带生物来说,在很久的时期以前就发生了这种隔离。当动植物向南迁移,就会在一处大地区与美洲土著生物相混合,而且势必发生竞争;在另一处大地区则和旧世界的生物发生竞争。于是,各种事情都有利于发生大量变异——远比高山植物发生的变异为大,因为后者仅在极其近代的期间内被隔离在两个世界的若干山脉和北极陆地上。因此,比较新旧世界温带地区的现存生物时,我们只找到很少数相同的物种(虽然阿萨·格雷最近指出两地植物相同的情况比从前料想的为多),但我们在每一个大纲里可以找到许多类型,某些学者列为地理族,另外一些学者则列为不同的物种;还有大量密切近似的或代表的类型被所有学者列为不同的物种。

陆地上如此,海水里也是这样,海栖动物群在上新世,甚至在更早的期间沿着北极圈的连续岸边几乎一致地缓慢向南迁徙,根据变异的学说,便可解释今日完全隔离的海洋里生活的类型何以密切近似。这样,我想便能理解北美洲温带东西两岸有许多至今仍然生存的第三纪代表类型;还有更值得注意的个案,即许多密切近似甲壳类(如代那的大作所描述的)、栖息在地中海和日本海的某些鱼类以及其他海栖动物——地中海和日本海今日已被整个的大陆和半个地球的赤道海洋的所隔开了。

现在栖息在分隔海中,以及北美洲和欧洲的温带陆地的过去和现在不同物种之间的密切关系,用创造学说是无解的。我们不能说,该地的物理条件相似,因而创造的物种也是相似的;因为,比方我们把南美洲的某些部分和南非洲或澳洲加以比较,便知道这些地方的一切物理条件都是密切相似的,但其生物却完全不相似。

我们必须回到更直接的冰期主题。我相信福布斯的观点大可扩展。在欧洲,从不列颠西海岸到乌拉尔山脉,并且南到比利牛斯山,我们看到冰期最明显的证据。根据冰冻的哺乳动物和山岳植被的性质,可以推论西伯利亚也曾受过相似影响。沿着喜马拉雅山,在距离900英里的各地,冰川留下了从前下泻的痕迹;胡克博士在锡金看到过玉蜀黍生长在古代的巨大冰碛上。赤道以南,我们拥有新西兰有过冰川作用的直接证据;该岛上距离很远的山上发现有同样的植物,也说明了同样的情况。如果发表的单例可信,那么我们便拥有了澳洲东南角有冰川活动的直接证据。

再看美洲;北美大陆的东侧,南至北纬三十六度至三十七度处,曾发现冰川带来的岩石碎片,在气候已经大变的太平洋沿岸,南至北纬46度的地方也有,落基山脉也看到过漂石。在近赤道的南美科迪勒拉山,冰川一度远远扩张到今日的高度以下。我在智利的中部吃惊地看到一个巨大岩屑堆结构,高度800英尺左右,横跨安第斯山脉的山谷,我现在确信这是巨大的冰碛,遗迹比任何现有冰川都低得多。这个大陆两边的更南方,从南纬四十一度到最南端,有巨大漂石是从遥远的原产地运来的,这里有从前冰川活动的最明显证据。

我们不知道冰期在世界反面的这几个遥远地点是严格同时的,但我们在几乎每一个个案中都有充分证据,冰期属于最后的地质年代之内。我们还有很好的证据,在每个地点,用年度量,冰期持续了很久的时间。在不同地点,冰期出现、结束有早有晚,但考虑到在每个地点冰期持续很久,而且按照地质学的意义来说都是属于近代的,依我看,冰期至少在部分时期,全世界实际上是同时的。没有明确的相反证据,我们至少可以承认,北美的东西两面,在赤道和暖和的温带科迪勒拉山,以及美洲最南端的两面,冰川作用是同时的。如果承认这一点,不可避免地要认为,全世界的温度,在冰期曾经同时降低。但是,如果沿着某些经线宽条带同时降低温度,就足够满足我的目的了。

根据整个世界从北极到南极同时降温的这个观点,至少是经线宽条带同时降温,就可以大大有助于说明相同和亲缘物种的现今分布情况。在南美洲,胡克博士曾阐明,火地岛的显花植物(在该地贫乏的植物群中构成了不小的部分)有四五十种和欧洲植物相同,而且存在许多密切近似的物种,尽管两地相距遥远。在赤道下的美洲高山上,生有大群属于欧洲属的特殊物种。在巴西的最高山上,加德纳(Gardner)看到几个欧洲的属,它们却不生长于中间广袤的热带地方。在加拉加斯(Caraccas)的西拉(Silla),著名的洪堡很久以前就发现了属于科迪勒拉山的特有属的物种。在非洲阿比西尼亚的山上,有若干欧洲的类型以及好望角的特有植物群的少数代表。在好望角,有极少数的欧洲物种可以相信不是人为引进的,并且山上有不见于非洲热带地方的若干欧洲代表类型。在喜马拉雅山,印度半岛与外界隔离的山脉上,锡兰的高地上,以及爪哇的火山顶上,生长有完全相同或彼此代表,并且同时代表欧洲,但不见于中间炎热低地的许多植物。爪哇的高峰上所采集的各属植物目录,竟是欧洲小丘上采集物的百草图!还有更动人的事实,生在婆罗洲山顶上的某些植物竟明确代表南澳洲类型。某些澳洲类型,我听胡克博士说,沿着马六甲半岛高地扩张出去,一面稀疏地散布在印度,一面向北去,直达日本。

澳洲南方的山上,米勒博士曾发现过若干欧洲的物种;不是人为引进的其他物种则生长在低地;胡克博士告诉我,见于澳洲但不见于中间炎热地方的欧洲植物属可以列成一个长目录。胡克博士的力作《新西兰植物区系概论》里,关于该大岛的某些植物也举出了类似和动人的事实。因此,我们知道某些生长在世界各地热带的较高的高山上的植物,以及生长在南北温带平原上的植物,有时候一模一样,但大部分不是同一物种,却显而易见相互有亲缘。

这简单的叙述只适用于植物;但在陆栖动物分布方面,也可举出一些严格类似的事实。海栖动物中也有同样的情形;我愿援引最高权威代拿教授的一段叙述为例:“新西兰和大不列颠处在地球上的对趾点,但是两地甲壳类的密切相似,超过其他任何部分,这的确妙不可言。”理查森爵士也说,在新西兰,塔斯马尼亚(Tasmania)等海岸,有北方的鱼重现。胡克博士告诉我说,新西兰和欧洲有二十五个藻类的物种是共通的,但它们不见于中间的热带海中。

应该注意,南半球的南部、热带区域的山脉上发现的北方物种和类型,不属于北极,而属于北温带。沃森先生最近说:“高山植物系从北极向赤道退却时,其实变得越来越不属于北极了。”许多生长在温暖区域山上以及南半球的类型,其价值是可疑的,被某些学者列为不同物种,而被另一些学者列为变种;但有一些肯定与北方类型相同,而许多与北方类型密切相关的,则必须列为物种。

下面看看若接受大批地质学证据支持的观点会得到什么启发,让我们同意,在冰期整个世界,或者世界大部分,比现在同时寒冷得多。冰期,如用年代来计算,必然是极长久的;我们如果记得某些归化的动植物在数百年内曾经分布到何等广大的空间,那么,这一时期对于任何数量的迁徙将是绰绰有余的。当寒冷渐渐增强,所有热带动植物从两边退向赤道,后面跟着温带生物,再后面是北极生物,但后者我们现在不考虑。热带植物可能大量灭绝,数量说不清。也许以前的热带所支持的物种与现在所见拥挤在好望角和澳洲温带部分地方的一样多。我们知道,许多热带动植物可以承受相当程度的寒冷,在降温温和的时候逃过灭绝厄运,特别是躲藏到最热的地点。但必须记住的要点是,所有热带生物都或多或少受到灾祸。另一方面,温带生物迁入赤道地带,尽管会处于比较新的环境,受灾却不大。可以肯定,许多温带植物如果受庇护免遭竞争者的侵入,都可以承受比原产地炎热得多的气候。因此,依我看,考虑到热带生物处于受灾状态,无法与入侵者抗衡,一定数量的生机勃勃的主流温带类型有可能渗透土著队伍,达到甚至跨越赤道。当然,入侵遇到高地,也许是干燥气候,则一切顺利。福尔克纳博士告诉我,对于亚热带气候过来的多年生植物,最具破坏性的是热带的高温加上潮湿。另一方面,最最潮湿高温的地区会庇护热带土著生物。西北走向的喜马拉雅山脉,长条的科迪勒拉山,似乎提供了两条大的入侵路线。最近胡克博士告诉我一个惊人事实,火地岛和欧洲共有的所有显花植物总计46种,在北美依然存在,这想必处于生物挺进路线上。但我不怀疑,某些温带生物在冰期鼎盛时进入乃至跨越了热带低地,北极类型从原产地迁徙大约二十五纬度,覆盖了比利牛斯山脚的土地。在这个酷寒时期,我认为,海平面上的赤道地带气候大概和现在的六七千英尺高处的感觉差不多相同。在这最冷的时期,我想赤道区域的大片低地一定覆盖着混生的热带植被和温带植被,就像胡克所描述的现在繁生在喜马拉雅山低坡上的植物一样。

我认为,冰期有大量的植物,若干陆生动物和一些海生生物从南北温带迁徙入热带地区,一些甚至跨越了赤道。回暖时,这些温带类型自然要爬升到高山上去,在低地上则灭绝了;没有抵达赤道的类型,要朝北或者朝南回迁,回到老家;但主要是北方的类型,跨越赤道后继续前进,远离故乡,来到南半球的温带纬度。尽管根据地质证据有理由认为,北极贝类在长途南迁北归中整体上很少变异,但对于赤道地带上山定居还有进入南半球的入侵类型来说,情况可能截然不同吧。它们受到陌生生物围困,不得不与许多新生物进行竞争,也许其构造、习性、体质的有选择变异会使它们获益。所以,这些漂泊者中,有不少在新家成为特征显著的变种或者不同的物种,尽管它们仍然因遗传因素与北半球或者南半球的兄弟们明显相关。

关于美洲,胡克坚决主张,关于澳洲,德康多尔坚决主张,相同的植物、相关类型从北向南的迁徙,多于从南向北的迁徙,这是值得注意的事实。然而,我们在婆罗洲和阿比西尼亚的山上还看到少量南方的植物类型。我猜想这种偏重于从北向南的迁徙,是由于北方陆地范围大,且北方类型在故乡生存的数量多,结果,通过自然选择和竞争,便较南方类型达到完善阶段高,即占有优势的力量。这样,在冰期两群生物相混合时,北方类型就有力量,能够战胜不强的南方类型。今日还有这种情形,我们看到很多的欧洲生物布满拉普拉塔,并且小程度地占据澳洲,一定程度上打败了那里的土著生物;然而,近两三世纪从拉普拉塔,近三四十年从澳洲,虽然有容易附着种子的兽皮、羊毛等媒介物大批输入,但是在欧洲任何地方归化的南方类型却为数极少。热带高山上想必出现过同样的事情:冰期前无疑充满了特有的高山类型,但是这些几乎到处都屈服于北方的较大地区和高效生物车间中产生出来的占优势类型了。在许多岛屿上,土著生物和外来的归化生物差不多数目相等,甚至已属少数;哪怕没有被消灭,数目也大幅减少,而这是灭绝的第一步。山是陆地上的岛;冰期前赤道地区的高山想必是彻底孤立的。我认为,这些陆地岛屿上的生物已屈服于北方大地域内产生出来的生物,就像真正的岛上生物最近到处屈服于由人力而归化的大陆生物一样。

今日生活在南北温带、热带山脉上的近似物种的亲缘及其分布的所有难点,我远非设想都可用上述观点来消除。许多难点悬而未决。我并不声称要指出迁徙的精确路线和方式,为什么某些物种迁徙了,而其他物种没有迁徙;为什么某些物种变异且产生了新类型群,而其他物种却依然保持不变。除非我们能说明,为什么某一物种能够借人力在异乡归化,而其他物种不能如此;为什么某一物种比另一物种在家乡分布得远两三倍,多两三倍,否则就不能指望解释上述事实。

我说过有各种难点留待解决:例如,胡克博士在讨论北极区的植物学著作中清清楚楚地阐明了其中一些最引人注目的难点,在此无法赘述。我只能说一说,在凯尔盖朗岛(Kerguelen Land)、新西兰和富其亚(Fuegia)这样辽远的地点,生长着同样的物种;我认为,冰期快结束时,按照赖尔的意见,冰山大概对于它们的散布有关系。在南半球的这等地方以及其他远隔地方生存若干不同的物种,但完全属于南方的属,根据我的变异传承理论,这是一个更值得注意的难点。有些物种非常不同,我们不能设想,自从冰期开始以来,有足够的时间可供它们迁徙,然后进行必要程度的变异。这种事实似乎指明了同属的不同物种是从一个共同的中心点向四面八方迁徙的;并且我以为南半球和北半球一样,在冰期开始以前,曾有较温暖的时期,那时候,现在覆盖着冰的南极地方,支持了一个高度特殊而孤立的植物群。可以设想,在冰期消灭这个植物群之前,少数类型由于偶然的输送方法以及由于现今已沉没了的岛屿作为歇脚点的帮助,也许发生在冰期开始前,就已经在南半球的各处地方广阔地散布开了。这样,我认为,美洲、澳洲、新西兰的南岸,大概会稍微沾染上这种植物的特殊类型。

赖尔爵士在一篇雄文里,用和我几乎一样的说法来推论全世界气候大转变对于地理分布的影响。我认为,世界最近感觉到了一个大变化周期,根据这个观点,外加通过自然选择进行变异的观点,可以解释相同或亲缘生物类型分布在地球各处的许多事实。生命之水在一个短暂时期,可以说从北向南流,也从南向北流,在赤道交叉了。但是水流自北向南流者,其力量较大,结果它就能自由地在南方泛滥。正如潮水沿着水平线把漂流物留下,但在潮水最高的岸边上升更高,所以生命之水流沿着从北极低地到赤道高地这一条徐徐上升的线把漂流的生物留在我们的山顶上。这样搁浅留下来的生物可以和人类的未开化种族相比拟,被驱逐到并且生存在差不多各处的山间险要之处,这些地方就有我们感兴趣的一种记录,表明周围低地的既往居住者。

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