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双语《物种起源》 第十四章 回顾与结论

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2022年07月05日

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CHAPTER XIV RECAPITULATION AND CONCLUSION

Recapitulation of the difficulties on the theory of Natural Selection—Recapitulation of the general and special circumstances in its favour—Causes of the general belief in the immutability of species—How far the theory of natural selection may be extended—Effects of its adoption on the study of Natural history—Concluding remarks

As this whole volume is one long argument, it may be convenient to the reader to have the leading facts and inferences briefly recapitulated.

That many and grave objections may be advanced against the theory of descent with modification through natural selection, I do not deny. I have endeavoured to give to them their full force. Nothing at first can appear more difficult to believe than that the more complex organs and instincts should have been perfected, not by means superior to, though analogous with, human reason, but by the accumulation of innumerable slight variations, each good for the individual possessor. Nevertheless, this difficulty, though appearing to our imagination insuperably great, cannot be considered real if we admit the following propositions, namely,—that gradations in the perfection of any organ or instinct, which we may consider, either do now exist or could have existed, each good of its kind,—that all organs and instincts are, in ever so slight a degree, variable,—and, lastly, that there is a struggle for existence leading to the preservation of each profitable deviation of structure or instinct. The truth of these propositions cannot, I think, be disputed.

It is, no doubt, extremely difficult even to conjecture by what gradations many structures have been perfected, more especially amongst broken and failing groups of organic beings; but we see so many strange gradations in nature, as is proclaimed by the canon, “Natura non facit saltum,” that we ought to be extremely cautious in saying that any organ or instinct, or any whole being, could not have arrived at its present state by many graduated steps. There are, it must be admitted, cases of special difficulty on the theory of natural selection; and one of the most curious of these is the existence of two or three defined castes of workers or sterile females in the same community of ants; but I have attempted to show how this difficulty can be mastered.

With respect to the almost universal sterility of species when first crossed, which forms so remarkable a contrast with the almost universal fertility of varieties when crossed, I must refer the reader to the recapitulation of the facts given at the end of the eighth chapter, which seem to me conclusively to show that this sterility is no more a special endowment than is the incapacity of two trees to be grafted together, but that it is incidental on constitutional differences in the reproductive systems of the intercrossed species. We see the truth of this conclusion in the vast difference in the result, when the same two species are crossed reciprocally; that is, when one species is first used as the father and then as the mother.

The fertility of varieties when intercrossed and of their mongrel offspring cannot be considered as universal; nor is their very general fertility surprising when we remember that it is not likely that either their constitutions or their reproductive systems should have been profoundly modified. Moreover, most of the varieties which have been experimentised on have been produced under domestication; and as domestication apparently tends to eliminate sterility, we ought not to expect it also to produce sterility.

The sterility of hybrids is a very different case from that of first crosses, for their reproductive organs are more or less functionally impotent; whereas in first crosses the organs on both sides are in a perfect condition. As we continually see that organisms of all kinds are rendered in some degree sterile from their constitutions having been disturbed by slightly different and new conditions of life, we need not feel surprise at hybrids being in some degree sterile, for their constitutions can hardly fail to have been disturbed from being compounded of two distinct organisations. This parallelism is supported by another parallel, but directly opposite, class of facts; namely, that the vigour and fertility of all organic beings are increased by slight changes in their conditions of life, and that the offspring of slightly modified forms or varieties acquire from being crossed increased vigour and fertility. So that, on the one hand, considerable changes in the conditions of life and crosses between greatly modified forms, lessen fertility; and on the other hand, lesser changes in the conditions of life and crosses between less modified forms, increase fertility.

Turning to geographical distribution, the difficulties encountered on the theory of descent with modification are grave enough. All the individuals of the same species, and all the species of the same genus, or even higher group, must have descended from common parents; and therefore, in however distant and isolated parts of the world they are now found, they must in the course of successive generations have passed from some one part to the others. We are often wholly unable even to conjecture how this could have been effected. Yet, as we have reason to believe that some species have retained the same specific form for very long periods, enormously long as measured by years, too much stress ought not to be laid on the occasional wide diffusion of the same species; for during very long periods of time there will always be a good chance for wide migration by many means. A broken or interrupted range may often be accounted for by the extinction of the species in the intermediate regions. It cannot be denied that we are as yet very ignorant of the full extent of the various climatal and geographical changes which have affected the earth during modern periods; and such changes will obviously have greatly facilitated migration. As an example, I have attempted to show how potent has been the influence of the Glacial period on the distribution both of the same and of representative species throughout the world. We are as yet profoundly ignorant of the many occasional means of transport. With respect to distinct species of the same genus inhabiting very distant and isolated regions, as the process of modification has necessarily been slow, all the means of migration will have been possible during a very long period; and consequently the difficulty of the wide diffusion of species of the same genus is in some degree lessened.

As on the theory of natural selection an interminable number of intermediate forms must have existed, linking together all the species in each group by gradations as fine as our present varieties, it may be asked, Why do we not see these linking forms all around us? Why are not all organic beings blended together in an inextricable chaos? With respect to existing forms, we should remember that we have no right to expect (excepting in rare cases) to discover directly connecting links between them, but only between each and some extinct and supplanted form. Even on a wide area, which has during a long period remained continuous, and of which the climate and other conditions of life change insensibly in going from a district occupied by one species into another district occupied by a closely allied species, we have no just right to expect often to find intermediate varieties in the intermediate zone. For we have reason to believe that only a few species are undergoing change at any one period; and all changes are slowly effected. I have also shown that the intermediate varieties which will at first probably exist in the intermediate zones, will be liable to be supplanted by the allied forms on either hand; and the latter, from existing in greater numbers, will generally be modified and improved at a quicker rate than the intermediate varieties, which exist in lesser numbers; so that the intermediate varieties will, in the long run, be supplanted and exterminated.

On this doctrine of the extermination of an infinitude of connecting links, between the living and extinct inhabitants of the world, and at each successive period between the extinct and still older species, why is not every geological formation charged with such links? Why does not every collection of fossil remains afford plain evidence of the gradation and mutation of the forms of life? We meet with no such evidence, and this is the most obvious and forcible of the many objections which may be urged against my theory. Why, again, do whole groups of allied species appear, though certainly they often falsely appear, to have come in suddenly on the several geological stages? Why do we not find great piles of strata beneath the Silurian system, stored with the remains of the progenitors of the Silurian groups of fossils? For certainly on my theory such strata must somewhere have been deposited at these ancient and utterly unknown epochs in the world's history.

I can answer these questions and grave objections only on the supposition that the geological record is far more imperfect than most geologists believe. It cannot be objected that there has not been time sufficient for any amount of organic change; for the lapse of time has been so great as to be utterly inappreciable by the human intellect. The number of specimens in all our museums is absolutely as nothing compared with the countless generations of countless species which certainly have existed. We should not be able to recognise a species as the parent of any one or more species if we were to examine them ever so closely, unless we likewise possessed many of the intermediate links between their past or parent and present states; and these many links we could hardly ever expect to discover, owing to the imperfection of the geological record. Numerous existing doubtful forms could be named which are probably varieties; but who will pretend that in future ages so many fossil links will be discovered, that naturalists will be able to decide, on the common view, whether or not these doubtful forms are varieties? As long as most of the links between any two species are unknown, if any one link or intermediate variety be discovered, it will simply be classed as another and distinct species. Only a small portion of the world has been geologically explored. Only organic beings of certain classes can be preserved in a fossil condition, at least in any great number. Widely ranging species vary most, and varieties are often at first local,—both causes rendering the discovery of intermediate links less likely. Local varieties will not spread into other and distant regions until they are considerably modified and improved; and when they do spread, if discovered in a geological formation, they will appear as if suddenly created there, and will be simply classed as new species. Most formations have been intermittent in their accumulation; and their duration, I am inclined to believe, has been shorter than the average duration of specific forms. Successive formations are separated from each other by enormous blank intervals of time; for fossiliferous formations, thick enough to resist future degradation, can be accumulated only where much sediment is deposited on the subsiding bed of the sea. During the alternate periods of elevation and of stationary level the record will be blank. During these latter periods there will probably be more variability in the forms of life; during periods of subsidence, more extinction.

With respect to the absence of fossiliferous formations beneath the lowest Silurian strata, I can only recur to the hypothesis given in the ninth chapter. That the geological record is imperfect all will admit; but that it is imperfect to the degree which I require, few will be inclined to admit. If we look to long enough intervals of time, geology plainly declares that all species have changed; and they have changed in the manner which my theory requires, for they have changed slowly and in a graduated manner. We clearly see this in the fossil remains from consecutive formations invariably being much more closely related to each other, than are the fossils from formations distant from each other in time.

Such is the sum of the several chief objections and difficulties which may justly be urged against my theory; and I have now briefly recapitulated the answers and explanations which can be given to them. I have felt these difficulties far too heavily during many years to doubt their weight. But it deserves especial notice that the more important objections relate to questions on which we are confessedly ignorant; nor do we know how ignorant we are. We do not know all the possible transitional gradations between the simplest and the most perfect organs; it cannot be pretended that we know all the varied means of Distribution during the long lapse of years, or that we know how imperfect the Geological Record is. Grave as these several difficulties are, in my judgment they do not overthrow the theory of descent with modification.

Now let us turn to the other side of the argument. Under domestication we see much variability. This seems to be mainly due to the reproductive system being eminently susceptible to changes in the conditions of life; so that this system, when not rendered impotent, fails to reproduce offspring exactly like the parent-form. Variability is governed by many complex laws,—by correlation of growth, by use and disuse, and by the direct action of the physical conditions of life. There is much difficulty in ascertaining how much modification our domestic productions have undergone; but we may safely infer that the amount has been large, and that modifications can be inherited for long periods. As long as the conditions of life remain the same, we have reason to believe that a modification, which has already been inherited for many generations, may continue to be inherited for an almost infinite number of generations. On the other hand we have evidence that variability, when it has once come into play, does not wholly cease; for new varieties are still occasionally produced by our most anciently domesticated productions.

Man does not actually produce variability; he only unintentionally exposes organic beings to new conditions of life, and then nature acts on the organisation, and causes variability. But man can and does select the variations given to him by nature, and thus accumulate them in any desired manner. He thus adapts animals and plants for his own benefit or pleasure. He may do this methodically, or he may do it unconsciously by preserving the individuals most useful to him at the time, without any thought of altering the breed. It is certain that he can largely influence the character of a breed by selecting, in each successive generation, individual differences so slight as to be quite inappreciable by an uneducated eye. This process of selection has been the great agency in the production of the most distinct and useful domestic breeds. That many of the breeds produced by man have to a large extent the character of natural species, is shown by the inextricable doubts whether very many of them are varieties or aboriginal species.

There is no obvious reason why the principles which have acted so efficiently under domestication should not have acted under nature. In the preservation of favoured individuals and races, during the constantly-recurrent Struggle for Existence, we see the most powerful and ever-acting means of selection. The struggle for existence inevitably follows from the high geometrical ratio of increase which is common to all organic beings. This high rate of increase is proved by calculation, by the effects of a succession of peculiar seasons, and by the results of naturalisation, as explained in the third chapter. More individuals are born than can possibly survive. A grain in the balance will determine which individual shall live and which shall die,—which variety or species shall increase in number, and which shall decrease, or finally become extinct. As the individuals of the same species come in all respects into the closest competition with each other, the struggle will generally be most severe between them; it will be almost equally severe between the varieties of the same species, and next in severity between the species of the same genus. But the struggle will often be very severe between beings most remote in the scale of nature. The slightest advantage in one being, at any age or during any season, over those with which it comes into competition, or better adaptation in however slight a degree to the surrounding physical conditions, will turn the balance.

With animals having separated sexes there will in most cases be a struggle between the males for possession of the females. The most vigorous individuals, or those which have most successfully struggled with their conditions of life, will generally leave most progeny. But success will often depend on having special weapons or means of defence, or on the charms of the males; and the slightest advantage will lead to victory.

As geology plainly proclaims that each land has undergone great physical changes, we might have expected that organic beings would have varied under nature, in the same way as they generally have varied under the changed conditions of domestication. And if there be any variability under nature, it would be an unaccountable fact if natural selection had not come into play. It has often been asserted, but the assertion is quite incapable of proof, that the amount of variation under nature is a strictly limited quantity. Man, though acting on external characters alone and often capriciously, can produce within a short period a great result by adding up mere individual differences in his domestic productions; and every one admits that there are at least individual differences in species under nature. But, besides such differences, all naturalists have admitted the existence of varieties, which they think sufficiently distinct to be worthy of record in systematic works. No one can draw any clear distinction between individual differences and slight varieties; or between more plainly marked varieties and sub-species, and species. Let it be observed how naturalists differ in the rank which they assign to the many representative forms in Europe and North America.

If then we have under nature variability and a powerful agent always ready to act and select, why should we doubt that variations in any way useful to beings, under their excessively complex relations of life, would be preserved, accumulated, and inherited? Why, if man can by patience select variations most useful to himself, should nature fail in selecting variations useful, under changing conditions of life, to her living products? What limit can be put to this power, acting during long ages and rigidly scrutinising the whole constitution, structure, and habits of each creature,—favouring the good and rejecting the bad? I can see no limit to this power, in slowly and beautifully adapting each form to the most complex relations of life. The theory of natural selection, even if we looked no further than this, seems to me to be in itself probable. I have already recapitulated, as fairly as I could, the opposed difficulties and objections: now let us turn to the special facts and arguments in favour of the theory.

On the view that species are only strongly marked and permanent varieties, and that each species first existed as a variety, we can see why it is that no line of demarcation can be drawn between species, commonly supposed to have been produced by special acts of creation, and varieties which are acknowledged to have been produced by secondary laws. On this same view we can understand how it is that in each region where many species of a genus have been produced, and where they now flourish, these same species should present many varieties; for where the manufactory of species has been active, we might expect, as a general rule, to find it still in action; and this is the case if varieties be incipient species. Moreover, the species of the larger genera, which afford the greater number of varieties or incipient species, retain to a certain degree the character of varieties; for they differ from each other by a less amount of difference than do the species of smaller genera. The closely allied species also of the larger genera apparently have restricted ranges, and they are clustered in little groups round other species—in which respects they resemble varieties. These are strange relations on the view of each species having been independently created, but are intelligible if all species first existed as varieties.

As each species tends by its geometrical ratio of reproduction to increase inordinately in number; and as the modified descendants of each species will be enabled to increase by so much the more as they become more diversified in habits and structure, so as to be enabled to seize on many and widely different places in the economy of nature, there will be a constant tendency in natural selection to preserve the most divergent offspring of any one species. Hence during a long-continued course of modification, the slight differences, characteristic of varieties of the same species, tend to be augmented into the greater differences characteristic of species of the same genus. New and improved varieties will inevitably supplant and exterminate the older, less improved and intermediate varieties; and thus species are rendered to a large extent defined and distinct objects. Dominant species belonging to the larger groups tend to give birth to new and dominant forms; so that each large group tends to become still larger, and at the same time more divergent in character. But as all groups cannot thus succeed in increasing in size, for the world would not hold them, the more dominant groups beat the less dominant. This tendency in the large groups to go on increasing in size and diverging in character, together with the almost inevitable contingency of much extinction, explains the arrangement of all the forms of life, in groups subordinate to groups, all within a few great classes, which we now see everywhere around us, and which has prevailed throughout all time. This grand fact of the grouping of all organic beings seems to me utterly inexplicable on the theory of creation.

As natural selection acts solely by accumulating slight, successive, favourable variations, it can produce no great or sudden modification; it can act only by very short and slow steps. Hence the canon of “Natura non facit saltum,” which every fresh addition to our knowledge tends to make more strictly correct, is on this theory simply intelligible. We can plainly see why nature is prodigal in variety, though niggard in innovation. But why this should be a law of nature if each species has been independently created, no man can explain.

Many other facts are, as it seems to me, explicable on this theory. How strange it is that a bird, under the form of woodpecker, should have been created to prey on insects on the ground; that upland geese, which never or rarely swim, should have been created with webbed feet; that a thrush should have been created to dive and feed on sub-aquatic insects; and that a petrel should have been created with habits and structure fitting it for the life of an auk or grebe! and so on in endless other cases. But on the view of each species constantly trying to increase in number, with natural selection always ready to adapt the slowly varying descendants of each to any unoccupied or ill-occupied place in nature, these facts cease to be strange, or might even have been anticipated.

We can to a certain extent understand how it is that there is so much beauty throughout nature ; for this may be largely attributed to the agency of selection. That beauty, according to our sense of it, is not universal, must be admitted by every one who will look at some venomous snakes, at some fishes, and at certain hideous bats with a distorted resemblance to the human face. Sexual selection has given the most brilliant colours, elegant patterns, and other ornaments to the males, and sometimes to both sexes of many birds, butterflies, and other animals. With birds it has often rendered the voice of the male musical to the female, as well as to our ears. Flowers and fruit have been rendered conspicuous by brilliant colours in contrast with the green foliage, in order that the flowers may be easily seen, visited, and fertilised by insects, and the seeds disseminated by birds. How it comes that certain colours, sounds, and forms should give pleasure to man and the lower animals,—that is, how the sense of beauty in its simplest form was first acquired,—we do not know any more than how certain odours and flavours were first rendered agreeable.

As natural selection acts by competition, it adapts and improves the inhabitants of each country only in relation to their co-inhabitants; so that we need feel no surprise at the species of any one country, although on the ordinary view supposed to have been created and specially adapted for that country, being beaten and supplanted by the naturalised productions from another land. Nor ought we to marvel if all the contrivances in nature be not, as far as we can judge, absolutely perfect, as in the case even of the human eye; or if some of them be abhorrent to our ideas of fitness. We need not marvel at the sting of the bee, when used against an enemy, causing the bee's own death; at drones being produced in such great numbers for one single act, and being then slaughtered by their sterile sisters; at the astonishing waste of pollen by our fir-trees; at the instinctive hatred of the queen-bee for her own fertile daughters; at ichneumonidae feeding within the living bodies of caterpillars; or at other such cases. The wonder indeed is, on the theory of natural selection, that more cases of the want of absolute perfection have not been detected.

The complex and little known laws governing the production of varieties are the same, as far as we can judge, with the laws which have governed the production of distinct species. In both cases physical conditions seem to have produced some direct and definite effect, but how much we cannot say. Thus, when varieties enter any new station, they occasionally assume some of the characters proper to the species of that station. With both varieties and species, use and disuse seem to have produced a considerable effect; for it is impossible to resist this conclusion when we look, for instance, at the logger-headed duck, which has wings incapable of flight, in nearly the same condition as in the domestic duck; or when we look at the burrowing tucu-tucu, which is occasionally blind, and then at certain moles, which are habitually blind and have their eyes covered with skin; or when we look at the blind animals inhabiting the dark caves of America and Europe. With varieties and species, correlated variation seems to have played an important part, so that when one part has been modified other parts have been necessarily modified. With both varieties and species, reversions to long-lost characters occasionally occur. How inexplicable on the theory of creation is the occasional appearance of stripes on the shoulders and legs of the several species of the horse-genus and of their hybrids! How simply is this fact explained if we believe that these species are all descended from a striped progenitor, in the same manner as the several domestic breeds of the pigeon are descended from the blue and barred rock-pigeon!

On the ordinary view of each species having been independently created, why should specific characters, or those by which the species of the same genus differ from each other, be more variable than generic characters in which they all agree? Why, for instance, should the colour of a flower be more likely to vary in any one species of a genus, if the other species possess differently coloured flowers, than if all possessed the same coloured flowers? If species are only well-marked varieties, of which the characters have become in a high degree permanent, we can understand this fact; for they have already varied since they branched off from a common progenitor in certain characters, and therefore these same characters would be more likely still to be variable than the generic characters which have been inherited without change for an enormous period. It is inexplicable on the theory of creation why a part developed in a very unusual manner in any one species of a genus, and therefore, as we may naturally infer, of great importance to the species, should be eminently liable to variation; but, on my view, this part has undergone, since the several species branched off from a common progenitor, an unusual amount of variability and modification, and therefore we might expect this part generally to be still variable. But a part may be developed in the most unusual manner, like the wing of a bat, and yet not be more variable than any other structure, if the part be common to many subordinate forms, that is, if it has been inherited for a very long period; for in this case it will have been rendered constant by long-continued natural selection.

Glancing at instincts, marvellous as some are, they offer no greater difficulty than does corporeal structure on the theory of the natural selection of successive, slight, but profitable modifications. We can thus understand why nature moves by graduated steps in endowing different animals of the same class with their several instincts. I have attempted to show how much light the principle of gradation throws on the admirable architectural powers of the hive-bee. Habit no doubt sometimes comes into play in modifying instincts; but it certainly is not indispensable, as we see, in the case of neuter insects, which leave no progeny to inherit the effects of long-continued habit. On the view of all the species of the same genus having descended from a common parent, and having inherited much in common, we can understand how it is that allied species, when placed under considerably different conditions of life, yet should follow nearly the same instincts; why the thrush of South America, for instance, lines her nest with mud like our British species. On the view of instincts having been slowly acquired through natural selection we need not marvel at some instincts being apparently not perfect and liable to mistakes, and at many instincts causing other animals to suffer.

If species be only well-marked and permanent varieties, we can at once see why their crossed offspring should follow the same complex laws in their degrees and kinds of resemblance to their parents,—in being absorbed into each other by successive crosses, and in other such points,—as do the crossed offspring of acknowledged varieties. On the other hand, these would be strange facts if species have been independently created, and varieties have been produced by secondary laws.

If we admit that the geological record is imperfect in an extreme degree, then such facts as the record gives, support the theory of descent with modification. New species have come on the stage slowly and at successive intervals; and the amount of change, after equal intervals of time, is widely different in different groups. The extinction of species and of whole groups of species, which has played so conspicuous a part in the history of the organic world, almost inevitably follows on the principle of natural selection; for old forms will be supplanted by new and improved forms. Neither single species nor groups of species reappear when the chain of ordinary generation has once been broken. The gradual diffusion of dominant forms, with the slow modification of their descendants, causes the forms of life, after long intervals of time, to appear as if they had changed simultaneously throughout the world. The fact of the fossil remains of each formation being in some degree intermediate in character between the fossils in the formations above and below, is simply explained by their intermediate position in the chain of descent. The grand fact that all extinct organic beings belong to the same system with recent beings, falling either into the same or into intermediate groups, follows from the living and the extinct being the offspring of common parents. As the groups which have descended from an ancient progenitor have generally diverged in character, the progenitor with its early descendants will often be intermediate in character in comparison with its later descendants; and thus we can see why the more ancient a fossil is, the oftener it stands in some degree intermediate between existing and allied groups. Recent forms are generally looked at as being, in some vague sense, higher than ancient and extinct forms; and they are in so far higher as the later and more improved forms have conquered the older and less improved organic beings in the struggle for life. Lastly, the law of the long endurance of allied forms on the same continent,—of marsupials in Australia, of edentata in America, and other such cases,—is intelligible, for within a confined country, the recent and the extinct will naturally be allied by descent.

Looking to geographical distribution, if we admit that there has been during the long course of ages much migration from one part of the world to another, owing to former climatal and geographical changes and to the many occasional and unknown means of dispersal, then we can understand, on the theory of descent with modification, most of the great leading facts in Distribution. We can see why there should be so striking a parallelism in the distribution of organic beings throughout space, and in their geological succession throughout time; for in both cases the beings have been connected by the bond of ordinary generation, and the means of modification have been the same. We see the full meaning of the wonderful fact, which must have struck every traveller, namely, that on the same continent, under the most diverse conditions, under heat and cold, on mountain and lowland, on deserts and marshes, most of the inhabitants within each great class are plainly related; for they will generally be descendants of the same progenitors and early colonists. On this same principle of former migration, combined in most cases with modification, we can understand, by the aid of the Glacial period, the identity of some few plants, and the close alliance of many others, on the most distant mountains, under the most different climates; and likewise the close alliance of some of the inhabitants of the sea in the northern and southern temperate zones, though separated by the whole intertropical ocean. Although two areas may present the same physical conditions of life, we need feel no surprise at their inhabitants being widely different, if they have been for a long period completely separated from each other; for as the relation of organism to organism is the most important of all relations, and as the two areas will have received colonists from some third source or from each other, at various periods and in different proportions, the course of modification in the two areas will inevitably be different.

On this view of migration, with subsequent modification, we can see why oceanic islands should be inhabited by few species, but of these, that many should be peculiar. We can clearly see why those animals which cannot cross wide spaces of ocean, as frogs and terrestrial mammals, should not inhabit oceanic islands; and why, on the other hand, new and peculiar species of bats, which can traverse the ocean, should so often be found on islands far distant from any continent. Such facts as the presence of peculiar species of bats, and the absence of all other mammals, on oceanic islands, are utterly inexplicable on the theory of independent acts of creation.

The existence of closely allied or representative species in any two areas, implies, on the theory of descent with modification, that the same parents formerly inhabited both areas; and we almost invariably find that wherever many closely allied species inhabit two areas, some identical species common to both still exist. Wherever many closely allied yet distinct species occur, many doubtful forms and varieties of the same species likewise occur. It is a rule of high generality that the inhabitants of each area are related to the inhabitants of the nearest source whence immigrants might have been derived. We see this in nearly all the plants and animals of the Galapagos archipelago, of Juan Fernandez, and of the other American islands being related in the most striking manner to the plants and animals of the neighbouring American mainland; and those of the Cape de Verde archipelago and other African islands to the African mainland. It must be admitted that these facts receive no explanation on the theory of creation.

The fact, as we have seen, that all past and present organic beings constitute one grand natural system, with group subordinate to group, and with extinct groups often falling in between recent groups, is intelligible on the theory of natural selection with its contingencies of extinction and divergence of character. On these same principles we see how it is, that the mutual affinities of the species and genera within each class are so complex and circuitous. We see why certain characters are far more serviceable than others for classification;—why adaptive characters, though of paramount importance to the being, are of hardly any importance in classification; why characters derived from rudimentary parts, though of no service to the being, are often of high classificatory value; and why embryological characters are the most valuable of all. The real affinities of all organic beings are due to inheritance or community of descent. The natural system is a genealogical arrangement, in which we have to discover the lines of descent by the most permanent characters, however slight their vital importance may be.

The framework of bones being the same in the hand of a man, wing of a bat, fin of the porpoise, and leg of the horse,—the same number of vertebrae forming the neck of the giraffe and of the elephant,—and innumerable other such facts, at once explain themselves on the theory of descent with slow and slight successive modifications. The similarity of pattern in the wing and leg of a bat, though used for such different purpose,—in the jaws and legs of a crab,—in the petals, stamens, and pistils of a flower, is likewise intelligible on the view of the gradual modification of parts or organs, which were alike in the early progenitor of each class. On the principle of successive variations not always supervening at an early age, and being inherited at a corresponding not early period of life, we can clearly see why the embryos of mammals, birds, reptiles, and fishes should be so closely alike, and should be so unlike the adult forms. We may cease marvelling at the embryo of an air-breathing mammal or bird having branchial slits and arteries running in loops, like those in a fish which has to breathe the air dissolved in water, by the aid of well-developed branchiae.

Disuse, aided sometimes by natural selection, will often tend to reduce an organ, when it has become useless by changed habits or under changed conditions of life; and we can clearly understand on this view the meaning of rudimentary organs. But disuse and selection will generally act on each creature, when it has come to maturity and has to play its full part in the struggle for existence, and will thus have little power of acting on an organ during early life; hence the organ will not be much reduced or rendered rudimentary at this early age. The calf, for instance, has inherited teeth, which never cut through the gums of the upper jaw, from an early progenitor having well-developed teeth; and we may believe, that the teeth in the mature animal were reduced, during successive generations, by disuse or by the tongue and palate having been fitted by natural selection to browse without their aid; whereas in the calf, the teeth have been left untouched by selection or disuse, and on the principle of inheritance at corresponding ages have been inherited from a remote period to the present day. On the view of each organic being and each separate organ having been specially created, how utterly inexplicable it is that parts, like the teeth in the embryonic calf or like the shrivelled wings under the soldered wing-covers of some beetles, should thus so frequently bear the plain stamp of inutility! Nature may be said to have taken pains to reveal, by rudimentary organs and by homologous structures, her scheme of modification, which it seems that we wilfully will not understand.

I have now recapitulated the chief facts and considerations which have thoroughly convinced me that species have changed, and are still slowly changing by the preservation and accumulation of successive slight favourable variations. Why, it may be asked, have all the most eminent living naturalists and geologists rejected this view of the mutability of species? It cannot be asserted that organic beings in a state of nature are subject to no variation; it cannot be proved that the amount of variation in the course of long ages is a limited quantity; no clear distinction has been, or can be, drawn between species and well-marked varieties. It cannot be maintained that species when intercrossed are invariably sterile, and varieties invariably fertile; or that sterility is a special endowment and sign of creation. The belief that species were immutable productions was almost unavoidable as long as the history of the world was thought to be of short duration; and now that we have acquired some idea of the lapse of time, we are too apt to assume, without proof, that the geological record is so perfect that it would have afforded us plain evidence of the mutation of species, if they had undergone mutation.

But the chief cause of our natural unwillingness to admit that one species has given birth to other and distinct species, is that we are always slow in admitting any great change of which we do not see the intermediate steps. The difficulty is the same as that felt by so many geologists, when Lyell first insisted that long lines of inland cliffs had been formed, and great valleys excavated, by the slow action of the coast-waves. The mind cannot possibly grasp the full meaning of the term of a hundred million years; it cannot add up and perceive the full effects of many slight variations, accumulated during an almost infinite number of generations.

Although I am fully convinced of the truth of the views given in this volume under the form of an abstract, I by no means expect to convince experienced naturalists whose minds are stocked with a multitude of facts all viewed, during a long course of years, from a point of view directly opposite to mine. It is so easy to hide our ignorance under such expressions as the “plan of creation,” “unity of design,” etc., and to think that we give an explanation when we only restate a fact. Any one whose disposition leads him to attach more weight to unexplained difficulties than to the explanation of a certain number of facts will certainly reject my theory. A few naturalists, endowed with much flexibility of mind, and who have already begun to doubt on the immutability of species, may be influenced by this volume; but I look with confidence to the future, to young and rising naturalists, who will be able to view both sides of the question with impartiality. Whoever is led to believe that species are mutable will do good service by conscientiously expressing his conviction; for only thus can the load of prejudice by which this subject is overwhelmed be removed.

Several eminent naturalists have of late published their belief that a multitude of reputed species in each genus are not real species; but that other species are real, that is, have been independently created. This seems to me a strange conclusion to arrive at. They admit that a multitude of forms, which till lately they themselves thought were special creations, and which are still thus looked at by the majority of naturalists, and which consequently have every external characteristic feature of true species,—they admit that these have been produced by variation, but they refuse to extend the same view to other and very slightly different forms. Nevertheless they do not pretend that they can define, or even conjecture, which are the created forms of life, and which are those produced by secondary laws. They admit variation as a vera causa in one case, they arbitrarily reject it in another, without assigning any distinction in the two cases. The day will come when this will be given as a curious illustration of the blindness of preconceived opinion. These authors seem no more startled at a miraculous act of creation than at an ordinary birth. But do they really believe that at innumerable periods in the earth's history certain elemental atoms have been commanded suddenly to flash into living tissues? Do they believe that at each supposed act of creation one individual or many were produced? Were all the infinitely numerous kinds of animals and plants created as eggs or seed, or as full grown? and in the case of mammals, were they created bearing the false marks of nourishment from the mother's womb? Although naturalists very properly demand a full explanation of every difficulty from those who believe in the mutability of species, on their own side they ignore the whole subject of the first appearance of species in what they consider reverent silence.

It may be asked how far I extend the doctrine of the modification of species. The question is difficult to answer, because the more distinct the forms are which we may consider, by so much the arguments fall away in force. But some arguments of the greatest weight extend very far. All the members of whole classes can be connected together by chains of affinities, and all can be classified on the same principle, in groups subordinate to groups. Fossil remains sometimes tend to fill up very wide intervals between existing orders. Organs in a rudimentary condition plainly show that an early progenitor had the organ in a fully developed state; and this in some instances necessarily implies an enormous amount of modification in the descendants. Throughout whole classes various structures are formed on the same pattern, and at an embryonic age the species closely resemble each other. Therefore I cannot doubt that the theory of descent with modification embraces all the members of the same class. I believe that animals have descended from at most only four or five progenitors, and plants from an equal or lesser number.

Analogy would lead me one step further, namely, to the belief that all animals and plants have descended from some one prototype. But analogy may be a deceitful guide. Nevertheless all living things have much in common, in their chemical composition, their germinal vesicles, their cellular structure, and their laws of growth and reproduction. We see this even in so trifling a circumstance as that the same poison often similarly affects plants and animals; or that the poison secreted by the gall-fly produces monstrous growths on the wild rose or oak-tree. Therefore I should infer from analogy that probably all the organic beings which have ever lived on this earth have descended from some one primordial form, into which life was first breathed.

When the views entertained in this volume on the origin of species, or when analogous views are generally admitted, we can dimly foresee that there will be a considerable revolution in natural history. Systematists will be able to pursue their labours as at present; but they will not be incessantly haunted by the shadowy doubt whether this or that form be in essence a species. This I feel sure, and I speak after experience, will be no slight relief. The endless disputes whether or not some fifty species of British brambles are true species will cease. Systematists will have only to decide (not that this will be easy) whether any form be sufficiently constant and distinct from other forms, to be capable of definition; and if definable, whether the differences be sufficiently important to deserve a specific name. This latter point will become a far more essential consideration than it is at present; for differences, however slight, between any two forms, if not blended by intermediate gradations, are looked at by most naturalists as sufficient to raise both forms to the rank of species. Hereafter we shall be compelled to acknowledge that the only distinction between species and well-marked varieties is, that the latter are known, or believed, to be connected at the present day by intermediate gradations, whereas species were formerly thus connected. Hence, without quite rejecting the consideration of the present existence of intermediate gradations between any two forms, we shall be led to weigh more carefully and to value higher the actual amount of difference between them. It is quite possible that forms now generally acknowledged to be merely varieties may hereafter be thought worthy of specific names, as with the primrose and cowslip; and in this case scientific and common language will come into accordance. In short, we shall have to treat species in the same manner as those naturalists treat genera, who admit that genera are merely artificial combinations made for convenience. This may not be a cheering prospect; but we shall at least be freed from the vain search for the undiscovered and undiscoverable essence of the term species.

The other and more general departments of natural history will rise greatly in interest. The terms used by naturalists of affinity, relationship, community of type, paternity, morphology, adaptive characters, rudimentary and aborted organs, etc., will cease to be metaphorical, and will have a plain signification. When we no longer look at an organic being as a savage looks at a ship, as at something wholly beyond his comprehension; when we regard every production of nature as one which has had a history; when we contemplate every complex structure and instinct as the summing up of many contrivances, each useful to the possessor, nearly in the same way as when we look at any great mechanical invention as the summing up of the labour, the experience, the reason, and even the blunders of numerous workmen; when we thus view each organic being, how far more interesting, I speak from experience, will the study of natural history become!

A grand and almost untrodden field of inquiry will be opened, on the causes and laws of variation, on correlation of growth, on the effects of use and disuse, on the direct action of external conditions, and so forth. The study of domestic productions will rise immensely in value. A new variety raised by man will be a far more important and interesting subject for study than one more species added to the infinitude of already recorded species. Our classifications will come to be, as far as they can be so made, genealogies; and will then truly give what may be called the plan of creation. The rules for classifying will no doubt become simpler when we have a definite object in view. We possess no pedigrees or armorial bearings; and we have to discover and trace the many diverging lines of descent in our natural genealogies, by characters of any kind which have long been inherited. Rudimentary organs will speak infallibly with respect to the nature of long-lost structures. Species and groups of species, which are called aberrant, and which may fancifully be called living fossils, will aid us in forming a picture of the ancient forms of life. Embryology will reveal to us the structure, in some degree obscured, of the prototypes of each great class.

When we can feel assured that all the individuals of the same species, and all the closely allied species of most genera, have within a not very remote period descended from one parent, and have migrated from some one birthplace; and when we better know the many means of migration, then, by the light which geology now throws, and will continue to throw, on former changes of climate and of the level of the land, we shall surely be enabled to trace in an admirable manner the former migrations of the inhabitants of the whole world. Even at present, by comparing the differences of the inhabitants of the sea on the opposite sides of a continent, and the nature of the various inhabitants of that continent in relation to their apparent means of immigration, some light can be thrown on ancient geography.

The noble science of Geology loses glory from the extreme imperfection of the record. The crust of the earth with its embedded remains must not be looked at as a well-filled museum, but as a poor collection made at hazard and at rare intervals. The accumulation of each great fossiliferous formation will be recognised as having depended on an unusual concurrence of circumstances, and the blank intervals between the successive stages as having been of vast duration. But we shall be able to gauge with some security the duration of these intervals by a comparison of the preceding and succeeding organic forms. We must be cautious in attempting to correlate as strictly contemporaneous two formations, which include few identical species, by the general succession of their forms of life. As species are produced and exterminated by slowly acting and still existing causes, and not by miraculous acts of creation and by catastrophes; and as the most important of all causes of organic change is one which is almost independent of altered and perhaps suddenly altered physical conditions, namely, the mutual relation of organism to organism,—the improvement of one being entailing the improvement or the extermination of others; it follows, that the amount of organic change in the fossils of consecutive formations probably serves as a fair measure of the lapse of actual time. A number of species, however, keeping in a body might remain for a long period unchanged, whilst within this same period, several of these species, by migrating into new countries and coming into competition with foreign associates, might become modified; so that we must not overrate the accuracy of organic change as a measure of time. During early periods of the earth's history, when the forms of life were probably fewer and simpler, the rate of change was probably slower; and at the first dawn of life, when very few forms of the simplest structure existed, the rate of change may have been slow in an extreme degree. The whole history of the world, as at present known, although of a length quite incomprehensible by us, will hereafter be recognised as a mere fragment of time, compared with the ages which have elapsed since the first creature, the progenitor of innumerable extinct and living descendants, was created.

In the distant future I see open fields for far more important researches. Psychology will be based on a new foundation, that of the necessary acquirement of each mental power and capacity by gradation. Light will be thrown on the origin of man and his history.

Authors of the highest eminence seem to be fully satisfied with the view that each species has been independently created. To my mind it accords better with what we know of the laws impressed on matter by the Creator, that the production and extinction of the past and present inhabitants of the world should have been due to secondary causes, like those determining the birth and death of the individual. When I view all beings not as special creations, but as the lineal descendants of some few beings which lived long before the first bed of the Silurian system was deposited, they seem to me to become ennobled. Judging from the past, we may safely infer that not one living species will transmit its unaltered likeness to a distant futurity. And of the species now living very few will transmit progeny of any kind to a far distant futurity; for the manner in which all organic beings are grouped, shows that the greater number of species of each genus, and all the species of many genera, have left no descendants, but have become utterly extinct. We can so far take a prophetic glance into futurity as to foretel that it will be the common and widely-spread species, belonging to the larger and dominant groups, which will ultimately prevail and procreate new and dominant species. As all the living forms of life are the lineal descendants of those which lived long before the Silurian epoch, we may feel certain that the ordinary succession by generation has never once been broken, and that no cataclysm has desolated the whole world. Hence we may look with some confidence to a secure future of equally inappreciable length. And as natural selection works solely by and for the good of each being, all corporeal and mental endowments will tend to progress towards perfection.

It is interesting to contemplate an entangled bank, clothed with many plants of many kinds, with birds singing on the bushes, with various insects flitting about, and with worms crawling through the damp earth, and to reflect that these elaborately constructed forms, so different from each other, and dependent on each other in so complex a manner, have all been produced by laws acting around us. These laws, taken in the largest sense, being Growth with Reproduction; Inheritance which is almost implied by reproduction; Variability from the indirect and direct action of the external conditions of life, and from use and disuse; a Ratio of Increase so high as to lead to a Struggle for Life, and as a consequence to Natural Selection, entailing Divergence of Character and the Extinction of less-improved forms. Thus, from the war of nature, from famine and death, the most exalted object which we are capable of conceiving, namely, the production of the higher animals, directly follows. There is grandeur in this view of life, with its several powers, having been originally breathed into a few forms or into one; and that, whilst this planet has gone cycling on according to the fixed law of gravity, from so simple a beginning endless forms most beautiful and most wonderful have been, and are being, evolved.

第十四章 回顾与结论

对自然选择学说难点的复述——支持自然选择学说的一般和特殊情况的复述——一般相信物种不变的原因——自然选择学说可以引申到什么程度——自然选择学说的采用对于博物学研究的影响——结束语

因为全书是一篇绵长的争论,所以把主要的事实和推论简略复述一遍,可能给予读者一些方便。

我不否认,有许多严重的异议可以提出来反对通过自然选择的变异传承学说。我努力全盘接受异议。比较复杂的器官和本能的完善并不依靠优于、等于人类理性的方法,而是依靠对于个体所有者有利的无数轻微变异的积累,初看没有比这更难以置信的了。然而,虽然在我们想象中这好像是不可克服的大难点,可是如果承认下述命题,这就不是真实的难点:任何器官或本能的级进完善,不管是现在存在的还是可能存在的,可以认为对于它的种类都是有利的,——全部器官和本能都有极轻微程度的变异——最后,生存斗争导致构造、本能上有利偏差的保存。这些命题的正确性,我想是无可争辩的。

毫无疑问,甚至猜想一下许多构造是通过什么样的中间级进而完善的,也有极端困难,特别对于已经不连续的、衰败的生物群来说,更加如此;但是我们看到自然界里有那么多奇异的级进,这一点“自然界里没有飞跃”的准则已经宣布了,所以应该慎言任何器官或本能,或者整个生物不可能通过许多级进的步骤而达到现在的状态。必须承认,有特别困难的事例来反对自然选择学说,其中最奇妙的一个就是同一蚁群中有两三种工蚁即不育雌蚁的明确等级;但是,我已经试图阐明这些难点是可以克服的。

物种在第一次杂交时普遍的不育性,与变种在杂交时普遍的能育性形成极其明显的对比,就此提请读者参阅第八章末所提出的事实复述。依我看来,事实决定性地表明这种不育性不是特殊的禀赋,有如两棵树木不能嫁接在一起一样;而只是基于杂交物种生殖系统的体质差异的偶然事件。使同样两个物种进行互交,即一个物种先用做父本,后用做母本,结果出现的大量差异里,可看到上述结论的正确性。

变种杂交的能育性及其混种后代的能育性不能看作是千篇一律的。只要记住,其体质或者生殖系统不可能得到深刻改变,普遍的能育性也就不足为奇了。而且,试验过的变种大多数是在家养状况下产生的;由于家养状况显然倾向于消除不育性,就不该希望又产生不育性。

杂种后代的不育性与物种第一次杂交的不育性大不相同,因为其生殖器的机能或多或少不灵了,而第一次杂交时两方面的器官都是完美无缺的。我们连续地看到,各种各样的生物都由于新的生活条件的轻微变化而扰乱了体质,从而变成某种程度的不育,所以看到杂种有某种程度的不育是不足为奇的,因为其体质由于两种体制的结合简直不可能不被扰乱。这种平行现象得到另一批平行而截然相反的事实的支持;即一切生物的活力和能育性由于生活条件的轻微变化而增加,而轻微变异类型或者变种的后代通过杂交会增加活力和能育性。所以,一方面生活条件的大变和大事变异的类型之间杂交,减少了能育性;另一方面,生活条件的小变和小变异的类型之间杂交,增加了能育性。

就地理分布而言,变异传承学说所遭遇的难点颇为严重。同一物种的一切个体、同一属或甚至更高级的群的一切物种都是从共同的祖先传下来的;因此,现在不管在地球上怎样遥远和隔离的地点发现,它们一定是在连续世代的过程中从某一地点迁徙到一切其他地点的。这是怎样发生的,往往连猜测也完全不可能。然而,既然有理由相信,某些物种曾经在极长的时间保持同一物种的类型(如以年代来计算是极其长久的),就不应过分强调同一物种的偶然的广泛散布;因为在很长久的时期里总有良好的机会通过许多方法来进行广泛迁徙的。不连续或中断的分布常常可以由物种在中间地带的灭绝来解释。不能否认,我们对于在现代时期内曾经影响地球的各种气候变化和地理变化的全部范围还是很无知的;而这些变化则往往有利于迁徙。作为一个例证,我曾经企图示明冰期对于同一物种和代表性物种在地球上的分布的影响曾是如何有效。我们对于许多偶然的输送方法还是极无知的。至于生活在遥远而隔离地区的同属不同物种,因为变异的过程必然是缓慢的,所以迁徙的一切方法在很长的时期里便成为可能;结果同属物种广泛散布的难点就在一定程度上减小了。

按照自然选择学说,一定有无数的中间类型曾经存在过,以微细的级进把每一群中的一切物种联结在一起,就像现存变种那样,因此可以问:为什么周围没有看到这些联结类型呢?为什么所有生物并没有混杂成不能分解的混沌状态呢?关于现存的类型,应该记住我们没有权利去希望(极少的例子除外)在它们之间发现直接联结的环节,只能在各个现存类型和某一灭绝、淘汰掉的类型之间发现这种环节。如果一个广阔的地区在长久时期内保持了连续的状态,并且其气候等生活条件从某一物种所占有的区域不知不觉地变化到为一个密切近似物种所占有的区域,即使如此,也没有正当的权利去希望中间地带常常找到中间变种。因为有理由相信,任何时期每一属中只有少数物种发生变化;而且一切变异都是逐渐完成的。我还阐明,起初也许在中间地带存在的中间变种,容易被任何方面的近似类型所淘汰;因为后者由于生存的数目较大,比起数目少的中间变种一般能以较快的速率发生变化和改进;结果中间变种长远看就要被淘汰和消灭掉。

世界上现存生物和灭绝生物之间以及各个连续时期内灭绝物种和更加古老物种之间,都有无数联结的环节已经灭绝。按照这一学说来看,为什么在每一地质层中没有填满这等环节呢?为什么化石遗物的每一次采集没有为生物类型的级进和变化提供明证呢?但是并没有这种证据啊,而这是反对我的理论的许多异议中最明显有力的异议。还有,为什么整群的近似物种好像是突然出现在地质诸阶段之中呢?(虽然这常常是一种假象。)为什么志留纪之下没有发现巨大的地层含有志留纪化石群的祖先遗骸呢?因为,按照我的理论,这样的地层一定在世界历史这古老而完全蒙昧的时代里已经沉积于某处了。

我只能根据地质记录比大多数地质学家所认为的更不完全这一假设来回答上述问题和严重异议。毋庸置疑,进行任何数量的生物变化,记录在案的时间是不够的;亘古以来的时间之长,绝非人类智力所能把握。全部博物馆内的标本数目与肯定生存过的无数物种的无数世代比较起来,是完全不足道的。即使研究生物是周密进行的,除非同样得到过去祖先和现在状态之间的许多中间环节,否则无法辨识一个物种是否是一个或多个物种的祖先;而由于地质记录不完全,我们也无希望找到这么许多环节。可以举出无数现存的可疑类型,也许是变种呢;但是谁敢说将来会发现众多的化石环节,让学者能够按照通行的观点决定这些可疑类型是否应该叫作变种?只要任何两个物种间的大部分环节未知,若发现任何一个环节或中间变种,就会干脆被列为另一个物种的。只有世界的一小部分曾经过地质勘探。只有某些纲的生物才能在化石状态中至少以任何大量的数目保存下来。分布广的物种最常变异,变种起初又常是地方性的——由于这两个原因,要发现中间环节就更不可能。地方变种不等到相当的变异改进之后,是不会分布到遥远地区的;等散布开了,并且在一个地层中被发现的时候,就好像是在那里被突然创造出来似的,于是就干脆列为新物种。大多数地层在沉积中是断断续续的,我相信,延续的时间大概比物种类型的平均延续时间更短。连续的地质层都被长久的空白间隔时间所分开;因为含有化石的地质层,其厚度足以抵抗未来的陵蚀作用,只能在海底下降而有大量沉积物沉积的地方,才能得到堆积。在水平面上升和静止的交替时期,地质记录是空白的。在后面这样的时期中,生物类型大概会有更多的变异性;在下降的时期,大概有更多的灭绝。

关于志留纪地质层以下缺乏富含化石的地层一点,我只能回到第九章提出的假说。地质记录不完整,大家都承认;但不完整到我要求的程度,很少人会承认。如果我们观察到足够悠长的间隔时间,地质学说就明白地宣告一切物种都变化了,而且是以我的理论所要求的方式发生变化,因为都是缓慢且以渐进方式变化的。我们在连续地质层里的化石遗骸中清楚地看到这种情形,它们的彼此关系一定远比时间相隔很远的地质层中的化石更加密切。

以上就是可以正当提出来反对我的理论的几种主要异议和难点的概要;我现在简要地复述了针对性的回答和解释。多年来我一直感到这些难点沉甸甸的,不怀疑它们的分量。但值得特别注意的是,更加重要的异议与我们坦白无知的那些问题有关;而且我们还不知道自己无知到什么程度。我们还不知道在最简单和最完善器官之间一切可能的过渡级进;也不能假装已经知道,悠久岁月里各种各样的分布方法,或者地质记录是怎样的不完全。尽管这几种难点是严重的,但在我的判断中,决不足以推翻变异传承学说。

现在让我们谈谈争论的另一面。在家养状况下可看到大量变异性。似乎主要是由于生殖系统尤其易于受生活条件变化的影响;所以这个生殖系统在没有变成无能的时候,不能繁殖跟亲类型一模一样的后代。变异性受许多复杂的法则支配——被相关生长、使用不使用,以及周围条件的直接作用所支配。要确定家养生物曾经发生过多少变异,难度很大;但是可以稳妥地推论,变异量是大的,而且变异能够长久地遗传下去。只要生活条件保持不变,就有理由相信,曾经遗传过许多世代的变异可以继续遗传几乎无限的世代。另一方面,有证据说,变异性一旦发生作用,就不会全部停止;即使最古老的家养生物也会偶尔产生新变种。

变异性实际上不是由人引起的;人只是无意识地把生物放在新的生活条件下,于是自然就对生物的体制发生作用,而引起变异。但是人能够并且确实选择了自然给予的变异,从而把变异按照任何需要的方式累积起来。这样,人可以使动植物适应自己的利益或爱好。可以有计划地或者无意识地这样做,就是保存当时对自己最有用的个体,但没有改变品种的任何企图。人肯定能借着在每一连续世代中选择那些非有训练的眼睛就不能辨识出来的极其微细的个体差异,来大大影响品种的性状。这种选择过程在形成最显著最有用的家养品种中起过重大作用。人所产生的许多品种在很大程度上具有自然物种的性状,这已由许多品种究竟是变种还是本土物种这一难解的疑问所示明了。

没有明显理由表明,家养状况下曾经如此有效地发生了作用的原理,为什么不能在自然状况下起作用。在不断反复的“生存斗争”中,受惠的个体或族得到生存,从中我们可以看到最强有力和经常发生作用的选择手段。一切生物都依照几何级数高速率增加,必然会引起生存斗争。这种高增加率可用计算来证明,连续的特殊季节,以及在新区归化都会产生这种效果,详见第三章。产生出来的个体比可能生存的多。天平上的些微之差便可决定个体的生死存亡,——哪些变种或物种将增量,哪些将减量或最后灭绝。同一物种的个体彼此在各方面进行最密切的竞争,因此之间的斗争一般最为剧烈;同一物种的变种之间,斗争几乎也是同样剧烈,其次就是同属的物种之间;另一方面,在自然系统上相距很远的生物之间,斗争也常常是剧烈的。某些个体在任何年龄或任何季节比与其相竞争的个体只要占有最轻微的优势,或者对周围物理条件具有任何轻微程度的较好适应,结果就会改变平衡。

对于雌雄异体的动物,在大多数情形下雄者之间为了占有雌者,就会发生斗争。最强有力的雄者,或与生活条件斗争最成功的雄者,一般会留下最多的后代。但是成功往往取决于雄者具有特别武器,或者防御手段,或者魅力;轻微的优势就会导致胜利。

地质学清楚地表明,各个陆地都曾发生过巨大的物理变化,因此,可以预料生物在自然状况下曾经变异,有如在家养状况下普遍发生变异那样。如果在自然状况下有任何变异性的话,那么要说自然选择不曾发生作用,那就是无法解释的事实了。常常有人主张,变异量在自然状况下是有严格限制的量,但是这个主张是无法证实的。虽然只是作用于外部性状而且往往心血来潮,人类却能够在短暂的时期内由累积家养生物的个体差异而产生巨大的结果;并且人人都承认自然物种至少呈现个体差异。但是,除了个体差异外,所有学者都承认有自然变种存在,认为有足够的区别而值得分类学著作加以记载。没有人可以在个体差异和轻微变种之间,在特征明确的变种和亚种、物种之间划出明显的区别。请注意,学者给予欧洲、北美许多代表性类型的分级是有不同意见的。

倘若自然界存在变异性,而且有强有力的动因随时准备进行选择,我们为什么要怀疑,变异在任何方面有利于生物的,会在极其复杂的生活关系下得到保存、累积和遗传呢?人既能耐心选择对他有用的变异,为什么在变化着的生活条件下有利于自然生物的变异,自然不会加以选择呢?对于这种在悠久年代中发生作用并严格检查每一生物的整个体制、构造和习性——助长好的并排除坏的——的力量能够加以限制吗?对于这种缓慢而美妙地使每一类型适应于最复杂的生活关系的力量,我看是漫无边际的。哪怕我们不看得更远,自然选择学说本身依我看也是可信的。我已经尽可能公正地复述了对方提出的难点和异议,现在转而谈一谈支持这个学说的特殊事实和论点。

物种只是特征强烈显著的、稳定的变种,而且每一物种首先作为变种而存在,根据这一观点,便能理解,在一般假定由特殊创造行为产生出来的物种和公认为由次要法则产生出来的变种之间,为什么没有一条界线可定。根据这同一观点,还能理解在一个属的许多物种曾经产生出来且现今仍为繁盛的地区,为什么同样的物种要呈现许多变种;因为在物种工厂很活跃的地方,一般来说,可以预料还在活跃;如果变种是初始物种,情形就确是这样。还有,大属的物种提供较大数量的变种即初始物种,那么在某种程度上就会保持变种的性状;因为它们之间的差异量比小属物种的差异量为小。大属的密切近似物种显然在分布上要受到限制,并且围绕着其他物种聚成小群——这两方面都和变种相似。根据每一物种都是独立创造的观点,这些关系就是奇特的,但是如果所有物种都是首先作为变种而存在的话,那么这些关系便是可以理解的了。

各个物种都倾向于按几何级数繁殖而过量增加;而且其变异后代由于习性和构造上更加多样化而相应增量,便能在自然组成中攫取许多决然不同的场所,自然选择就不断倾向于保存任一物种分歧最大的后代。所以在长久连续的变异过程中,同一物种的诸变种所特有的轻微差异便趋于增大而成为同一属物种所特有的较大差异。改进了的新变种不可避免地要淘汰消灭掉改进较少的和中间的旧变种;这样,物种在很大程度上就成为确定的、界限分明的了。属于较大群的优势物种倾向于诞生优势的新类型;结果每一大群便倾向于变得更大,同时在性状上更加分歧。但是所有的群不能都这样继续增大,世界容纳不下它们,所以占优势的群体就要打倒较不占优势的群体。这种大群继续增大以及性状继续分歧的倾向,加上几乎不可避免的大量灭绝的可能,说明了一切生物类型都是按照群下有群来排列的,所有这些群都包括在我们周围到处可见、自始至终占有优势的少数大纲之内。把一切生物都归群的这一伟大事实,根据特创说,依我看是完全不能解释的。

自然选择仅能借着轻微的、连续的、有利的、变异的积累而起作用,所以不能产生巨变或突变;只能取短小缓慢的步骤。“自然界里没有飞跃”这一格言已被每次新增加的知识所进一步证实,因此,根据我这个学说,格言就简单明了了。我们能够理解,为什么自然界在多样性上是浪费的,但在创新上是吝啬的。但是如果每一物种都是独立创造,那么,为什么这应当是自然界的法则,就没有人能解了。

依我看,根据我这个学说,还有许多其他事实可以得到解释。这是多么奇怪的创造啊:啄木鸟形态的鸟会在地面上捕食昆虫;少游泳或不游泳的高地鹅具有蹼脚;鸫鸟潜水并吃水中的昆虫;海燕具有适于海雀或生活的习性和构造!如此等等不一而足。但是根据各个物种都不断力求增量,而自然选择总是在使每一物种的缓慢变异着的后代适应于自然界中未被占据或占据得不好的地方的观点,上述事实就不足为奇,甚至是可以预测的了。

自然选择由竞争而起作用,使各地生物得到适应,只是相对于同住者的完善程度而言;所以任何一地的物种,虽然按通常的观点假定是为了那个地区创造出来而特别适应该地的,却被外地移来的归化生物所打倒淘汰,对此我们不必惊奇。如果自然界里的一切设计,就我们所能判断的来说,并不是绝对完善的;如果其中有些与我们的合适观念相反,对此也不必惊奇。蜜蜂的刺,会引起蜜蜂自己的死亡;雄蜂为了一次交配而被产生出那么多,交配之后便被不育的姊妹们杀死;冷杉花粉的惊人浪费;蜂后对于能育的女儿们所具有的本能仇恨;姬蜂在毛虫的活体内求食;诸如此类的例子,也不足为奇。从自然选择学说看来,奇怪的事情实际上倒是未发现更多缺乏绝对完善的例子。

支配产生变种的复杂而未知的法则,就我们所能判断的来说,与支配产生明确物种的法则是相同的。在这两种场合里,物理条件似乎只产生了一点点直接的效果;可当变种进入任何新地点以后,有时便取得该地物种所固有的某些性状。对于变种和物种,使用和不使用似乎产生了一些效果;若看到以下情形,就难以反驳这一结论。例如,翅膀不能飞翔的大头鸭所处的条件几乎与家鸭相同;穴居的栉鼠有时是盲目的,某些鼹鼠通常是盲目的,而且眼睛上被皮肤遮盖着;栖息在美洲和欧洲暗洞里的动物是盲目的。对于变种和物种,相关生长似乎发挥了重要作用。因此,某一部分发生变异时,其他部分也必然要发生。长久亡失的性状有时会在变种和物种中复现。马属的若干物种及其杂种偶尔会在肩上和腿上出现条纹,根据特创说,这一事实将无法解释!如果相信这些物种都是从具有条纹的祖先传下的,就像鸽的若干家养品种都是从具有条纹的蓝色岩鸽传下来的那样,那么上述事实的解释将是何等的简单!

按照每一物种都是独立创造的通常观点,为什么物种的性状,即同属的诸物种彼此相区别的性状比所共有的属的性状更多变异呢?比方说,一个属的任何一种花的颜色,为什么当所谓独立创造的其他物种具有不同颜色的花时,要比一切物种的花都同色时更易发生变异呢?如果说物种只是特征很显著的变种,其性状已经高度稳定了,那这种事实就能理解;因为这些物种从一个共同祖先分支出来以后在某些性状上已经发生变异了,这就是彼此赖以区别的性状;所以这些性状比长期未变遗传下来的属的性状就更易变异。特创说就不能解释在一属的单独一个物种里,以很异常方式发育起来因而可以自然地推想对于该物种有巨大重要性的部分,为什么显著易于变异;但根据我的观点,自从若干物种由一个共同祖先分支出来以后,这部分已经有大量的变异变化,可以预料一般还要发生变异。但如蝙蝠的翅膀,部分可能以最异常的方式发育起来,如果是许多附属类型所共有的,也就是说,如果已经遗传很长时间,就不会比其他构造更容易发生变异;因为在这种情形下,长久连续的自然选择就会使它恒定了。

看一看本能,某些本能虽然很神奇,可是按照连续的、轻微而有益的变异之自然选择学说,它们并不比肉体构造提供更大的难点。这样,便能理解为什么自然在赋予同纲的不同动物以各种本能时,是以级进的步骤进行的。我试图阐明过,级进原理对于蜜蜂美妙的建筑能力提供了多大的启示。在本能的改变中,习性无疑往往起作用;但肯定不是不可缺少的,就像在中性昆虫的情形中所看到的那样,并不留下后代去继承长久连续的习性的效果。根据同属的一切物种都是从共同祖先传下来、遗传了许多共同性状这一观点,便能了解近似物种处在极不相同的条件之下时,怎么还具有几乎同样的本能;为什么南美洲热带和温带的鸫像我英国的物种那样用泥土涂抹巢的内侧。根据本能是通过自然选择缓慢获得的观点,我们对某些本能并不完全、容易犯错,而且许多本能会使其他动物蒙受损失,就不必大惊小怪了。

如果物种只是特征很显著的、稳定的变种,便能立刻看出为什么杂交后代在类似亲体的程度和性质上——连续杂交而相互吸收等等方面——就像公认的变种杂交后代那样遵循同样的复杂法则。如果物种是独立创造的,并且变种是通过次要法则产生出来的,这种类似就成为怪事了。

承认地质记录不完全到极端的程度,地质记录所提供的事实就强有力地支持了变异传承学说。新物种缓慢地在连续的间隔时间内出现;而不同的群经过相等的间隔时间之后的变化量是大不相同的。物种和整个物种群的灭绝,在有机世界的历史中作用非常显著,几乎不可避免地是自然选择原理的结果;因为旧的类型要被改进了的新类型淘汰。单独一个物种也好,整群的物种也罢,普通世代的链条一旦断绝,就不再出现了。优势类型逐渐散布,其后代缓慢变异,使得生物类型经过长久的间隔时间以后,看来好像是在全世界范围内同时发生变化似的。各个地质层的化石遗骸的性状在某种程度上是介于上、下地质层之间的,这一事实可以简单地由它们在传承链中处于中间地位来解释。一切灭绝生物都能与一切现存生物分类在一起,要么同群,要么属于中间群,这一伟大事实是现存生物和灭绝生物都作为共同祖先后代的自然结果。由于物种群从早期祖先传承下来时一般已在性状上发生了分歧,祖先及其早期后代往往在性状上比后期后代处于中间的位置;所以便能理解为什么化石越古,往往就越处于现存的类似群某种程度上的中间。现代类型一般被模糊地看作比古代灭绝类型为高;因为后来的、改进了的类型在生活斗争中战胜了较老的改进较少的生物。最后,同一大陆的近似类型——如澳洲的有袋类、美洲的贫齿类和其他这类例子——长久延续的法则也是可以理解的,因为在同一局促地区里,现存生物和灭绝生物由于传承自然是近似的。

看一看地理分布,如果承认由于以前的气候和地理变化以及许多偶然和未知的散布方法,在悠长的岁月中曾经有过从世界的某一部分到另一部分的大量迁徙,那么根据变异传承学说,便能理解有关分布的大多数主要事实。为什么生物在整个空间内的分布和在整个时间内的地质演替会有这么动人的平行现象;因为在这两种情形里,生物通常都由世代的纽带所联结,而且变异的方法也是一样的。我们体会了想必曾经引起每一个旅行家注意的奇异事实的全部意义,即同一大陆上,在最不相同的条件下,炎热和寒冷下,高山和低地上,在沙漠和沼泽里,每一大纲里的生物大部分是显然相关联的;都是同一祖先和早期移住者的后代嘛。根据以前迁徙的同一原理,在大多数情形里它与变异相结合,借冰期之助,便能理解最遥远的高山上的、最不相同的气候下少数植物的同一性,以及许多其他生物的密切近似性;同样地还能理解虽被整个热带海洋隔开的北温带和南温带海里的某些生物的密切相似性。虽然两个地区呈现同样的生活条件,如果长久时期内是彼此分开的,那么对于其生物的大不相同就不必大惊小怪;因为,由于生物和生物之间的关系是一切关系中最重要的,且这两个地区在不同时期内会从第三个地区或者彼此相互接受不同比例的移住者,地区的生物变异过程就必然是不同的。

依据这个迁徙,外加以后变异的观点,便能理解为什么只有少数物种栖息在海洋岛上,而其中许多物种是特殊类型。我们清楚知道那些不能横渡广阔海面的动物群的物种,如蛙类和陆栖哺乳类为什么不栖息在海洋岛上;另一方面,还可理解,像蝙蝠这些能够横渡海洋的动物,其特殊的新物种为什么往往见于远离大陆的岛上。海洋岛上有蝙蝠的特殊物种存在,却没有所有其他陆栖哺乳类,根据独立创造的学说,这情形就完全无法解释了。

任何两个地区有密切近似的或代表性物种存在,从变异传承学说的观点看,意味着同一亲类型曾经在这两个地区栖息过;并且,无论何地,如果有许多密切近似物种栖息在两个地区,必然还会在那里发现两地共有的某些同一物种。无论何地,如果有许多密切近似的而区别分明的物种发生,那么同一物种的许多可疑类型和变种也会同样在那里发生。各地的生物必与移入者最近根源地的生物有关联,这是具有高度一般性的法则。从加拉帕戈斯群岛、胡安·斐尔南德斯群岛(Juan Fernandez)等美洲岛屿上,几乎所有的动植物与邻近的美洲大陆都有触目惊心的关系,在佛得角群岛等非洲岛屿上,生物与非洲大陆也有关系,就可以看到这一点。必须承认,根据特创说,这些事实是得不到解释的。

我们已经看到,一切过去的和现代的生物构成一个自然大系统,都可群下分群,而且灭绝的群往往介于现代群之间,这一点根据自然选择及其所引起的灭绝和性状分歧的学说,是可以理解的。根据这些同样的原理便能理解,每一纲里的物种和属的相互亲缘关系为何如此复杂和曲折。还能理解,为什么某些性状比其他性状在分类学上更有用;——为什么适应的性状虽对于生物具有高度重要性,在分类学上却几乎无足轻重;为什么从残迹器官而来的性状虽对于生物没用,却往往在分类学上具有高度的价值;还有,胚胎的性状为什么往往是最有价值的。一切生物的真实亲缘关系,可以归因于遗传或传承的共同性。自然系统是一种依照谱系的排列,必须依最恒定的性状去发现传承路线,不管其在生活上多么不重要。

人的手、蝙蝠的翅膀、海豚的鳍和马的腿都由相似的骨骼构成,——长颈鹿颈和象颈的脊椎数目相同,——不计其数的这类事实,依据伴随着缓慢、微小而连续的变异的生物传承学说,立刻可以得到解释。蝙蝠的翅膀和腿,——螃蟹的颚和腿,——花的花瓣、雄蕊和雌蕊,虽然用于极不同的目的,但结构样式都相似。这些器官或部分在各个纲的早期祖先中原来是相似的,但以后逐渐发生了变异。根据这观点,上述的相似性同样可以解释。连续变异不总是在早期年龄中发生,并且它的遗传是在相应的而不是在更早的龄期;依据这一原理可清楚地理解,为什么哺乳类、鸟类、爬行类和鱼类的胚胎会如此密切相似,而在成体类型中又如此不相似。对于呼吸空气的哺乳类或鸟类的胚胎就像必须依靠发达的鳃来呼吸水中溶解空气的鱼类那样具有鳃裂和弧状动脉,不用大惊小怪。

不使用,有时借自然选择之助,往往倾向于使器官在生活习性或生活条件改变时废弃而缩小;根据这一观点便能理解残迹器官的意义。但是不使用和选择一般是在每一生物到达成熟期并且必须在生存斗争中发挥充分作用的时期,才能对每一生物发生作用,所以对于早龄期的器官没有什么影响力;因此器官在这早期不会大幅度缩小或成为残迹。比方说,小牛从具有发达牙齿的早期祖先遗传了牙齿,却从来不穿出上颚牙床;可以相信,由于舌和颚通过自然选择变得非常适于吃草,而无须牙齿的帮助,所以成年动物的牙齿在连续的世代中由于不使用而缩小了;可是在小牛中,牙齿却没有受到选择或不使用的影响,并且依据遗传在相应年龄的原理,从远古期一直遗传至今。带着毫无用处的鲜明印记的部分,例如小牛胚胎的牙齿或许多甲虫的联合鞘翅下的萎缩翅,竟会如此经常发生,根据每一生物以及它的一切不同部分都是特创的观点,这是多么不可理解!可以说自然曾经煞费苦心地利用残迹器官以及同源的构造来泄露其变异计划,只是我们固执不愿意理解而已。

上述事实和论据使我完全相信,物种曾经发生变化,而且仍然在缓慢变化,保存和积累连续的轻微有利变异。对此我已做了复述。试问,为什么所有在世的最卓越博物学者和地质学者都拒绝物种的可变性观点呢?不能主张生物在自然状况下不发生变异;不能证明变异量在悠久年代的过程中是一种有限的量;在物种和特征显著的变种之间未曾有,也不能有清楚的界限。不能主张物种杂交必然是不育的,而变种杂交必然是能育的;不能主张不育性是创造的一种特殊禀赋和标志。只要把地球的历史想成是短暂的,几乎不可避免地就要相信物种是不变的产物;既然对于时间的推移已经有某种概念,就不会无根无据地去假定地质记录已经完美无缺,认为物种若有过变异,地质记录就会向我们提供有关物种变异的明证。

但是,我们天然地不愿意承认一个物种会产生其他不同物种,主要原因在于我们总是迟缓地承认自己不知道中间步骤的任何巨变。这就像那么多地质学者所感到的难点一样,如赖尔最初主张长排内陆岩壁的形成和巨大山谷的凹下都是由海岸波浪的缓慢作用所致。人脑不可能把握亿年之计的全部意义;而经过几乎无限世代累积的许多轻微变异,其全部效果如何更是不能累加领会的了。

虽然我坚信本书在提要形式下提出来的观点是正确的,但并不期望说服富有经验的博物学者,他们的思想装满了大量事实,而对于这些事实,长久以来其观点却与我正好相反。在“创造计划”“统一设计”之类的说法下,我们的无知多么容易被隐藏起来,而且还会拿只复述事实充当解释。无论何人,只要性情偏重尚未解释的难点,而不重视许多事实的解释,就必然要反对我的理论。思维灵活并且已经开始怀疑物种不变性的少数学者,可以受到本书的影响;但是我满怀信心地看着将来,后起之秀的博物学者,将会不偏不倚地看待问题的两个方面。凡是已被引导到相信物种可变的人,如果认认真真表达自己的确信,就做了好事;只有这样,才能把这一问题上铺天盖地的偏见重负移去。

几位卓越的博物学者最近发表己见,认为每一属中都有许多公认的物种并非真实物种;而其他物种才是真实的,就是说,被独立创造出来的。依我看来,这是奇谈怪论。他们承认,许多类型直到最近还自认为是特创的且大多数学者也是这样看,因而具有真实物种的一切外部特征,——他们承认这些类型是由变异产生的,却拒绝把同一观点引申到其他稍微不同的类型。然而,他们并不声称自己能够确定,甚至猜测,哪些是被创造出来的生物类型,哪些是由次要法则产生出来的。他们在某一种情形下承认变异是真实原因,而在另一种情形下却又武断否认,又不指明这两种情形有何区别。总有一天,这会被当作怪例来说明先入之见的盲目性。这些作者对奇迹创造行为并不比对通常的生殖感到更大的惊奇。但是他们是否真的相信,在地球历史的无数时期中,某些元素的原子会突然被命令骤变成活的组织呢?他们相信在每次假定的创造行为中都有一个或多个个体产生出来吗?所有无限多种类的动植物在被创造出来时,究竟是卵或种子,还是充分长成的成体?在哺乳类的情形下,是带着营养的虚假印记从母体子宫内被创造出来的吗?尽管可以正当地要求那些相信物种可变性的人对每一个难点都做出全面解释,但学者们自己方面却忽视物种初次出现的整个问题,所谓敬而远之的沉默。

可以问,我要把物种变异的学说扩展到多远。这个问题是难于回答的,因为所讨论的类型愈是不同,论点的力量就愈小。但是最有力的论点可以扩展到很远。整个纲的一切成员可以由亲缘链联结在一起,都能够按群下分群的同一原理来分类。化石遗骸有时倾向于把现存诸目之间的巨大空隙填充起来。残迹状态下的器官清楚地表明,早期祖先的这种器官是充分发达的;在某些情形里这必然意味着后代已发生过大量变异。在整个纲里,各种构造都是在同一样式下形成的,而且胚胎期的物种彼此密切相似。所以我不能怀疑变异传承学说笼络了同一大纲的一切成员。我相信动物至多是从四五种祖先传下来的,植物是从少于等于四五个的祖先传下来的。

类比法引导我更进一步,认为一切动植物都是从某一种原型传下来的。但类比法可能误导。然而,一切生物在化学成分、生发泡、细胞构造、生长和生殖法则上都有许多共同点。甚至在以下那样不重要的事实里也能看到这一点,即同一毒质常常同样地影响各种动植物;瘿蜂分泌的毒质能引起野蔷薇或橡树产生畸形。我因此以类比法推论,曾经在地球上生活过的一切生物,也许都是从某一原始类型传下来的,它才最初获得了生命。

本书有关物种起源的观点,或者类似的观点,一旦普遍接受,我们就能够隐约地预见到博物学将会发生重大革命。分类学者能和现在一样劳动,但不会再遭这个或那个类型本质上是否为真实物种这一朦胧疑问的不断骚扰。我有把握,这是如释重负;我是经验之谈。近五十个物种的英国树莓类(bramble)是否为真实物种这一无休止的争论将结束。分类学者只消决定(这点并不容易)任何类型是否充分恒定,能否与其他类型有区别,就能下定义了;如果能够下定义,只消决定那些差异是否充分重要,值得给以物种名。后述一点比现在的待遇远为重要;因为任何两个类型的差异不管如何轻微,如果不被中间级进混合在一起,大多数学者会认为这两个类型都足以提升物种的地位。从此以后,将不得不承认物种和特征显著的变种之间的唯一区别是:变种现在由公认或据信被中间级进联结起来,而物种却是以前被这样联结起来的。因此,在不拒绝考虑任何两个类型之间目前存在着中间级进的情况下,我们将被引导着更加仔细地去权衡,更加高度地去评价它们之间的实际差异量。十分可能,现在一般被认为只是变种的类型,今后可能会被认为值得给以物种名,比如报春花属和樱草;在这种情形下,科学语言和百姓语言就一致了。总而言之,必须用学者对待属那样的态度来对待物种,承认属只不过是图方便而做的人为组合。这或者不是令人振奋的展望;但是,对于物种这一术语没有发现的、不可能发现的本质,我们至少不必再做徒劳的探索。

博物学的其他更一般的部门将会大大地引起兴趣。学者所用的术语如亲缘关系、关系、模式的同一性、父性、形态学、适应的性状、残迹和萎缩器官等等,将不再是比喻,而会有明确的意义。当我们不再像未开化人把船看作是完全不可理解的东西那样地来看生物的时候;当我们把自然界的每一产品看成是都具有悠久历史的时候;当我们把每一种复杂的构造和本能看成是各个对于所有者都有用处的设计的综合,就像任何伟大的机械发明是无数工人的劳动、经验、理性甚至错误的综合的时候;当我们这样观察每一生物的时候,博物学的研究将变得——我根据经验来说——有趣得多!

在变异的原因和法则、相关法则、使用和不使用的效果、外界条件的直接作用等等方面,将会开辟一片广大的、几乎未经前人踏过的研究领域。家养生物的研究价值将大大提高。人类培育出来一个新变种,比起在有记载的无数物种中增添一个物种,会成为远远更重要、更有趣的研究课题。分类学将尽可能按谱系进行;那时才能真的显示出所谓创造的计划。当我们看到确定目标时,分类学规则无疑会变得更加简单。我们不拥有谱系或族徽;必须依据各种长久遗传下来的性状去发现和追踪自然谱系中的许多分歧的传承线。残迹器官将会确凿无误地表明长久亡失的构造的性质。称作畸变,又可以富于幻想地称作活化石的物种和物种群,将帮助我们构成一张古代生物类型的图画。胚胎学则会揭露出每一大纲内原始类型的构造,不过多少有点模糊而已。

如果我们能够确定同一物种的所有个体以及大多数属的所有密切近似物种,曾经在不很遥远的时期内从一个祖先传下来,并且从某一诞生地迁移出来;如果更好地知道迁移的许多方法,而且依据地质学现在对于以前的气候变化和地平面变化所提出的见解以及今后继续提出的解释,那么我们就确能以令人赞叹的方式追踪出全世界生物过去的迁移情况。甚至在现在,如果把大陆相对两边海栖生物的差异加以比较,而且把该大陆上各种生物的性质与其看上去的迁移方法加以比较,那么我们就能对古地理状况多少提出一些阐述。

地质学这门高尚的科学,由于地质记录的极端不完全而黯然失色。埋藏着生物遗骸的地壳不能看作充实的博物馆,收藏的只是偶然的、片段的、贫乏的物品而已。每一含有化石的巨大地质层的堆积将被看作可遇不可求,而连续阶段之间的空白间隔是极长久的。但是通过以前和以后的生物类型的比较,就能多少可靠地测出这些间隔的持续时间。我们必须慎用生物类型的一般演替,把两个含有极少相同物种的地质层关联成严格属于同一时期。因为物种的产生和灭绝是由于缓慢发生作用的、现今依然存在的原因,而不是由于创造的奇迹行为和灾变;因为生物变化的一切原因中最重要的是一种几乎与变化的或者突变的物理条件无关的原因,即生物和生物之间的相互关系,——一种生物的改进会引起其他生物的改进或灭绝;所以,连续地质层化石中的生物变化量大概可以作为一种合理尺度来测定实际的时间过程。可是,许多物种在集体中可能长时期保持不变,然而在同一时期里,其中若干物种,由于迁徙到新的地区并与外地的同住者进行竞争,可能发生变异;所以对于把生物变化作为时间尺度的准确性,不得有过高的评价。在地球历史的早期,也许生命类型比较少而简单,变化速度可能比较缓慢;在生命曙光初照时,极少的最简单构造的类型存在,变化速度可能极度缓慢。现在知道的整个世界历史,尽管悠久得无法理解,但与最早的生物创造出来,即不计其数的灭绝和现存后代的祖先以来的世代相比,以后将看作区区的时间片段。

我看到了遥远将来重要得多的广阔研究领域。心理学将建筑在新的基础上,即每一智力和智能都是由级进而必然获得的。人类的起源及其历史也将由此得到说明。

最卓越的作者们对于每一物种曾被独立创造的观点似乎心满意足。依我看来,世界上过去的和现在的生物之产生和灭绝就像决定个体生死的原因一样,是由于次要原因,这与我们所知道的造物主在物质上打下印记的法则更相符合。当我把一切生物不看作是特别的创造物,而看作是远在志留纪第一层沉积很久以前就生活着的某些少数生物的直系后代,依我看来,它们变得尊贵了。以古推今,可以稳妥地设想,没有一个现存物种会把原封不动的外貌传递到遥远的未来。并且现今生活的物种将很少把任何种类的后代传到极遥远的未来;因为依据一切生物分类的方式看来,每一属的大多数物种以及许多属的一切物种都没有留下后代,而是完全灭绝了。展望未来,可以预言,最后胜利并且产生占有优势的新物种,将是较大优势群的普通的、广泛分布的物种。既然一切现存生物类型都是远在志留纪以前生存过的生物的直系后代,便可肯定,通常的世代演替从来没有中断过,而且从来没有任何灾变曾使全世界变成荒芜。因此我们可以多少安心地去眺望一个长久得同样无法把握的、稳定的未来。因为自然选择只是根据并且为了每一生物的利益而工作,所以一切肉体的和精神的禀赋都倾向于走向完善化。

凝视树木交错的河岸,许多种类的无数植物覆盖其上,群鸟鸣于灌木丛中,各种昆虫飞来飞去,蠕虫在湿土里爬动,并且默想一下,这些构造精巧的类型,彼此这样相异,并以这样复杂的方式相互依存,而它们都是由于在我们周围发生作用的法则产生出来的,这岂非有趣之事。这些法则就其最广泛的意义来说,就是伴随着“生殖”的“生长”;几乎包含在生殖以内的“遗传”;由于生活条件的间接、直接作用以及由于使用不使用所引起的“变异性”:“生殖率”如此之高以致引起“生存斗争”,因而导致“自然选择”,并引起“性状分歧”和较少改进类型的“灭绝”。这样,从自然界的战争里,从饥饿和死亡里,便能体会到最可赞美的目的,即高级动物的产生,直接随之而至。认为生命及其若干能力原来是由“造物主”注入少数类型或一个类型中去的,而且随着地球按照引力的既定法则持续运行,最美丽最奇异的类型从如此简单的始端,过去、曾经而且现今还在进化着,无穷无尽;这种生命观点是极其壮丽的。

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