Variability—Individual differences—Doubtful species—Wide ranging, much diffused, and common species vary most—Species of the larger genera in any country vary more than the species of the smaller genera—Many of the species of the larger genera resemble varieties in being very closely, but unequally, related to each other, and in having restricted ranges
Before applying the principles arrived at in the last chapter to organic beings in a state of nature, we must briefly discuss whether these latter are subject to any variation. To treat this subject at all properly, a long catalogue of dry facts should be given; but these I shall reserve for my future work. Nor shall I here discuss the various definitions which have been given of the term species. No one definition has as yet satisfied all naturalists; yet every naturalist knows vaguely what he means when he speaks of a species. Generally the term includes the unknown element of a distinct act of creation. The term “variety” is almost equally difficult to define; but here community of descent is almost universally implied, though it can rarely be proved. We have also what are called monstrosities; but they graduate into varieties. By a monstrosity I presume is meant some considerable deviation of structure in one part, either injurious to or not useful to the species, and not generally propagated. Some authors use the term “variation” in a technical sense, as implying a modification directly due to the physical conditions of life; and “variations” in this sense are supposed not to be inherited: but who can say that the dwarfed condition of shells in the brackish waters of the Baltic, or dwarfed plants on Alpine summits, or the thicker fur of an animal from far northwards, would not in some cases be inherited for at least some few generations? and in this case I presume that the form would be called a variety.
Again, we have many slight differences which may be called individual differences, such as are known frequently to appear in the offspring from the same parents, or which may be presumed to have thus arisen, from being frequently observed in the individuals of the same species inhabiting the same confined locality. No one supposes that all the individuals of the same species are cast in the very same mould. These individual differences are highly important for us, as they afford materials for natural selection to accumulate, in the same manner as man can accumulate in any given direction individual differences in his domesticated productions. These individual differences generally affect what naturalists consider unimportant parts; but I could show by a long catalogue of facts, that parts which must be called important, whether viewed under a physiological or classificatory point of view, sometimes vary in the individuals of the same species. I am convinced that the most experienced naturalist would be surprised at the number of the cases of variability, even in important parts of structure, which he could collect on good authority, as I have collected, during a course of years. It should be remembered that systematists are far from pleased at finding variability in important characters, and that there are not many men who will laboriously examine internal and important organs, and compare them in many specimens of the same species. I should never have expected that the branching of the main nerves close to the great central ganglion of an insect would have been variable in the same species; I should have expected that changes of this nature could have been effected only by slow degrees: yet quite recently Mr. Lubbock has shown a degree of variability in these main nerves in Coccus, which may almost be compared to the irregular branching of the stem of a tree. This philosophical naturalist, I may add, has also quite recently shown that the muscles in the larvae of certain insects are very far from uniform. Authors sometimes argue in a circle when they state that important organs never vary; for these same authors practically rank that character as important (as some few naturalists have honestly confessed) which does not vary; and, under this point of view, no instance of an important part varying will ever be found: but under any other point of view many instances assuredly can be given.
There is one point connected with individual differences, which seems to me extremely perplexing: I refer to those genera which have sometimes been called “protean” or “polymorphic,” in which the species present an inordinate amount of variation; and hardly two naturalists can agree which forms to rank as species and which as varieties. We may instance Rubus, Rosa, and Hieracium amongst plants, several genera of insects, and several genera of Brachiopod shells. In most polymorphic genera some of the species have fixed and definite characters. Genera which are polymorphic in one country seem to be, with some few exceptions, polymorphic in other countries, and likewise, judging from Brachiopod shells, at former periods of time. These facts seem to be very perplexing, for they seem to show that this kind of variability is independent of the conditions of life. I am inclined to suspect that we see in these polymorphic genera variations in points of structure which are of no service or disservice to the species, and which consequently have not been seized on and rendered definite by natural selection, as hereafter will be explained.
Those forms which possess in some considerable degree the character of species, but which are so closely similar to some other forms, or are so closely linked to them by intermediate gradations, that naturalists do not like to rank them as distinct species, are in several respects the most important for us. We have every reason to believe that many of these doubtful and closely-allied forms have permanently retained their characters in their own country for a long time; for as long, as far as we know, as have good and true species. Practically, when a naturalist can unite two forms together by others having intermediate characters, he treats the one as a variety of the other, ranking the most common, but sometimes the one first described, as the species, and the other as the variety. But cases of great difficulty, which I will not here enumerate, sometimes occur in deciding whether or not to rank one form as a variety of another, even when they are closely connected by intermediate links; nor will the commonly-assumed hybrid nature of the intermediate links always remove the difficulty. In very many cases, however, one form is ranked as a variety of another, not because the intermediate links have actually been found, but because analogy leads the observer to suppose either that they do now somewhere exist, or may formerly have existed; and here a wide door for the entry of doubt and conjecture is opened.
Hence, in determining whether a form should be ranked as a species or a variety, the opinion of naturalists having sound judgment and wide experience seems the only guide to follow. We must, however, in many cases, decide by a majority of naturalists, for few well-marked and well-known varieties can be named which have not been ranked as species by at least some competent judges.
That varieties of this doubtful nature are far from uncommon cannot be disputed. Compare the several floras of Great Britain, of France or of the United States, drawn up by different botanists, and see what a surprising number of forms have been ranked by one botanist as good species, and by another as mere varieties. Mr. H. C. Watson, to whom I lie under deep obligation for assistance of all kinds, has marked for me 182 British plants, which are generally considered as varieties, but which have all been ranked by botanists as species; and in making this list he has omitted many trifling varieties, but which nevertheless have been ranked by some botanists as species, and he has entirely omitted several highly polymorphic genera. Under genera, including the most polymorphic forms, Mr. Babington gives 251 species, whereas Mr. Bentham gives only 112,—a difference of 139 doubtful forms! Amongst animals which unite for each birth, and which are highly locomotive, doubtful forms, ranked by one zoologist as a species and by another as a variety, can rarely be found within the same country, but are common in separated areas. How many of those birds and insects in North America and Europe, which differ very slightly from each other, have been ranked by one eminent naturalist as undoubted species, and by another as varieties, or, as they are often called, as geographical races! Many years ago, when comparing, and seeing others compare, the birds from the separate islands of the Galapagos Archipelago, both one with another, and with those from the American mainland, I was much struck how entirely vague and arbitrary is the distinction between species and varieties. On the islets of the little Madeira group there are many insects which are characterized as varieties in Mr. Wollaston's admirable work, but which it cannot be doubted would be ranked as distinct species by many entomologists. Even Ireland has a few animals, now generally regarded as varieties, but which have been ranked as species by some zoologists. Several most experienced ornithologists consider our British red grouse as only a strongly-marked race of a Norwegian species, whereas the greater number rank it as an undoubted species peculiar to Great Britain. A wide distance between the homes of two doubtful forms leads many naturalists to rank both as distinct species; but what distance, it has been well asked, will suffice? if that between America and Europe is ample, will that between the Continent and the Azores, or Madeira, or the Canaries, or Ireland, be sufficient? It must be admitted that many forms, considered by highly-competent judges as varieties, have so perfectly the character of species that they are ranked by other highly-competent judges as good and true species. But to discuss whether they are rightly called species or varieties, before any definition of these terms has been generally accepted, is vainly to beat the air.
Many of the cases of strongly-marked varieties or doubtful species well deserve consideration; for several interesting lines of argument, from geographical distribution, analogical variation, hybridism, etc., have been brought to bear on the attempt to determine their rank. I will here give only a single instance,—the well-known one of the primrose and cowslip, or Primula veris and elatior. These plants differ considerably in appearance; they have a different flavour and emit a different odour; they flower at slightly different periods; they grow in somewhat different stations; they ascend mountains to different heights; they have different geographical ranges; and lastly, according to very numerous experiments made during several years by that most careful observer G?rtner, they can be crossed only with much difficulty. We could hardly wish for better evidence of the two forms being specifically distinct. On the other hand, they are united by many intermediate links, and it is very doubtful whether these links are hybrids; and there is, as it seems to me, an overwhelming amount of experimental evidence, showing that they descend from common parents, and consequently must be ranked as varieties.
Close investigation, in most cases, will bring naturalists to an agreement how to rank doubtful forms. Yet it must be confessed, that it is in the best-known countries that we find the greatest number of forms of doubtful value. I have been struck with the fact, that if any animal or plant in a state of nature be highly useful to man, or from any cause closely attract his attention, varieties of it will almost universally be found recorded. These varieties, moreover, will be often ranked by some authors as species. Look at the common oak, how closely it has been studied; yet a German author makes more than a dozen species out of forms, which are very generally considered as varieties; and in this country the highest botanical authorities and practical men can be quoted to show that the sessile and pedunculated oaks are either good and distinct species or mere varieties.
When a young naturalist commences the study of a group of organisms quite unknown to him, he is at first much perplexed to determine what differences to consider as specific, and what as varieties; for he knows nothing of the amount and kind of variation to which the group is subject; and this shows, at least, how very generally there is some variation. But if he confine his attention to one class within one country, he will soon make up his mind how to rank most of the doubtful forms. His general tendency will be to make many species, for he will become impressed, just like the pigeon or poultry-fancier before alluded to, with the amount of difference in the forms which he is continually studying; and he has little general knowledge of analogical variation in other groups and in other countries, by which to correct his first impressions. As he extends the range of his observations, he will meet with more cases of difficulty; for he will encounter a greater number of closely-allied forms. But if his observations be widely extended, he will in the end generally be enabled to make up his own mind which to call varieties and which species; but he will succeed in this at the expense of admitting much variation,—and the truth of this admission will often be disputed by other naturalists. When, moreover, he comes to study allied forms brought from countries not now continuous, in which case he can hardly hope to find the intermediate links between his doubtful forms, he will have to trust almost entirely to analogy, and his difficulties will rise to a climax.
Certainly no clear line of demarcation has as yet been drawn between species and sub-species—that is, the forms which in the opinion of some naturalists come very near to, but do not quite arrive at the rank of species; or, again, between sub-species and well-marked varieties, or between lesser varieties and individual differences. These differences blend into each other in an insensible series; and a series impresses the mind with the idea of an actual passage.
Hence I look at individual differences, though of small interest to the systematist, as of high importance for us, as being the first step towards such slight varieties as are barely thought worth recording in works on natural history. And I look at varieties which are in any degree more distinct and permanent, as steps leading to more strongly marked and more permanent varieties; and at these latter, as leading to sub-species, and to species. The passage from one stage of difference to another and higher stage may be, in some cases, due merely to the long-continued action of different physical conditions in two different regions; but I have not much faith in this view; and I attribute the passage of a variety, from a state in which it differs very slightly from its parent to one in which it differs more, to the action of natural selection in accumulating (as will hereafter be more fully explained) differences of structure in certain definite directions. Hence I believe a well-marked variety may be justly called an incipient species; but whether this belief be justifiable must be judged of by the general weight of the several facts and views given throughout this work.
It need not be supposed that all varieties or incipient species necessarily attain the rank of species. They may whilst in this incipient state become extinct, or they may endure as varieties for very long periods, as has been shown to be the case by Mr. Wollaston with the varieties of certain fossil land-shells in Madeira. If a variety were to flourish so as to exceed in numbers the parent species, it would then rank as the species, and the species as the variety; or it might come to supplant and exterminate the parent species; or both might co-exist, and both rank as independent species. But we shall hereafter have to return to this subject.
From these remarks it will be seen that I look at the term species, as one arbitrarily given for the sake of convenience to a set of individuals closely resembling each other, and that it does not essentially differ from the term variety, which is given to less distinct and more fluctuating forms. The term variety, again, in comparison with mere individual differences, is also applied arbitrarily, and for mere convenience sake.
Guided by theoretical considerations, I thought that some interesting results might be obtained in regard to the nature and relations of the species which vary most, by tabulating all the varieties in several well-worked floras. At first this seemed a simple task; but Mr. H. C. Watson, to whom I am much indebted for valuable advice and assistance on this subject, soon convinced me that there were many difficulties, as did subsequently Dr. Hooker, even in stronger terms. I shall reserve for my future work the discussion of these difficulties, and the tables themselves of the proportional numbers of the varying species. Dr. Hooker permits me to add, that after having carefully read my manuscript, and examined the tables, he thinks that the following statements are fairly well established. The whole subject, however, treated as it necessarily here is with much brevity, is rather perplexing, and allusions cannot be avoided to the “struggle for existence,” “divergence of character,” and other questions, hereafter to be discussed.
Alph. De Candolle and others have shown that plants which have very wide ranges generally present varieties; and this might have been expected, as they become exposed to diverse physical conditions, and as they come into competition (which, as we shall hereafter see, is a far more important circumstance) with different sets of organic beings. But my tables further show that, in any limited country, the species which are most common, that is abound most in individuals, and the species which are most widely diffused within their own country (and this is a different consideration from wide range, and to a certain extent from commonness), often give rise to varieties sufficiently well-marked to have been recorded in botanical works. Hence it is the most flourishing, or, as they may be called, the dominant species,— those which range widely over the world, are the most diffused in their own country, and are the most numerous in individuals,—which oftenest produce well-marked varieties, or, as I consider them, incipient species. And this, perhaps, might have been anticipated; for, as varieties, in order to become in any degree permanent, necessarily have to struggle with the other inhabitants of the country, the species which are already dominant will be the most likely to yield offspring which, though in some slight degree modified, will still inherit those advantages that enabled their parents to become dominant over their compatriots.
If the plants inhabiting a country and described in any Flora be divided into two equal masses, all those in the larger genera being placed on one side, and all those in the smaller genera on the other side, a somewhat larger number of the very common and much diffused or dominant species will be found on the side of the larger genera. This, again, might have been anticipated; for the mere fact of many species of the same genus inhabiting any country, shows that there is something in the organic or inorganic conditions of that country favourable to the genus; and, consequently, we might have expected to have found in the larger genera, or those including many species, a large proportional number of dominant species. But so many causes tend to obscure this result, that I am surprised that my tables show even a small majority on the side of the larger genera. I will here allude to only two causes of obscurity. Fresh-water and salt-loving plants have generally very wide ranges and are much diffused, but this seems to be connected with the nature of the stations inhabited by them, and has little or no relation to the size of the genera to which the species belong. Again, plants low in the scale of organisation are generally much more widely diffused than plants higher in the scale; and here again there is no close relation to the size of the genera. The cause of lowly-organised plants ranging widely will be discussed in our chapter on geographical distribution.
From looking at species as only strongly-marked and well-defined varieties, I was led to anticipate that the species of the larger genera in each country would oftener present varieties, than the species of the smaller genera; for wherever many closely related species (i.e. species of the same genus) have been formed, many varieties or incipient species ought, as a general rule, to be now forming. Where many large trees grow, we expect to find saplings. Where many species of a genus have been formed through variation, circumstances have been favourable for variation; and hence we might expect that the circumstances would generally be still favourable to variation. On the other hand, if we look at each species as a special act of creation, there is no apparent reason why more varieties should occur in a group having many species, than in one having few.
To test the truth of this anticipation I have arranged the plants of twelve countries, and the coleopterous insects of two districts, into two nearly equal masses, the species of the larger genera on one side, and those of the smaller genera on the other side, and it has invariably proved to be the case that a larger proportion of the species on the side of the larger genera present varieties, than on the side of the smaller genera. Moreover, the species of the large genera which present any varieties, invariably present a larger average number of varieties than do the species of the small genera. Both these results follow when another division is made, and when all the smallest genera, with from only one to four species, are absolutely excluded from the tables. These facts are of plain signification on the view that species are only strongly marked and permanent varieties; for wherever many species of the same genus have been formed, or where, if we may use the expression, the manufactory of species has been active, we ought generally to find the manufactory still in action, more especially as we have every reason to believe the process of manufacturing new species to be a slow one. And this certainly is the case, if varieties be looked at as incipient species; for my tables clearly show as a general rule that, wherever many species of a genus have been formed, the species of that genus present a number of varieties, that is of incipient species, beyond the average. It is not that all large genera are now varying much, and are thus increasing in the number of their species, or that no small genera are now varying and increasing; for if this had been so, it would have been fatal to my theory; inasmuch as geology plainly tells us that small genera have in the lapse of time often increased greatly in size; and that large genera have often come to their maxima, declined, and disappeared. All that we want to show is, that where many species of a genus have been formed, on an average many are still forming; and this holds good.
There are other relations between the species of large genera and their recorded varieties which deserve notice. We have seen that there is no infallible criterion by which to distinguish species and well-marked varieties; and in those cases in which intermediate links have not been found between doubtful forms, naturalists are compelled to come to a determination by the amount of difference between them, judging by analogy whether or not the amount suffices to raise one or both to the rank of species. Hence the amount of difference is one very important criterion in settling whether two forms should be ranked as species or varieties. Now Fries has remarked in regard to plants, and Westwood in regard to insects, that in large genera the amount of difference between the species is often exceedingly small. I have endeavoured to test this numerically by averages, and, as far as my imperfect results go, they always confirm the view. I have also consulted some sagacious and most experienced observers, and, after deliberation, they concur in this view. In this respect, therefore, the species of the larger genera resemble varieties, more than do the species of the smaller genera. Or the case may be put in another way, and it may be said, that in the larger genera, in which a number of varieties or incipient species greater than the average are now manufacturing, many of the species already manufactured still to a certain extent resemble varieties, for they differ from each other by a less than usual amount of difference.
Moreover, the species of the large genera are related to each other, in the same manner as the varieties of any one species are related to each other. No naturalist pretends that all the species of a genus are equally distinct from each other; they may generally be divided into sub-genera, or sections, or lesser groups. As Fries has well remarked, little groups of species are generally clustered like satellites around certain other species. And what are varieties but groups of forms, unequally related to each other, and clustered round certain forms—that is, round their parent-species? Undoubtedly there is one most important point of difference between varieties and species; namely, that the amount of difference between varieties, when compared with each other or with their parent-species, is much less than that between the species of the same genus. But when we come to discuss the principle, as I call it, of Divergence of Character, we shall see how this may be explained, and how the lesser differences between varieties will tend to increase into the greater differences between species.
There is one other point which seems to me worth notice. Varieties generally have much restricted ranges: this statement is indeed scarcely more than a truism, for if a variety were found to have a wider range than that of its supposed parent-species, their denominations ought to be reversed. But there is also reason to believe, that those species which are very closely allied to other species, and in so far resemble varieties, often have much restricted ranges. For instance, Mr. H. C. Watson has marked for me in the well-sifted London Catalogue of plants (4th edition) 63 plants which are therein ranked as species, but which he considers as so closely allied to other species as to be of doubtful value: these 63 reputed species range on an average over 6.9 of the provinces into which Mr. Watson has divided Great Britain. Now, in this same catalogue, 53 acknowledged varieties are recorded, and these range over 7.7 provinces; whereas, the species to which these varieties belong range over 14.3 provinces. So that the acknowledged varieties have very nearly the same restricted average range, as have those very closely allied forms, marked for me by Mr. Watson as doubtful species, but which are almost universally ranked by British botanists as good and true species.
Finally, then, varieties have the same general characters as species, for they cannot be distinguished from species,—except, firstly, by the discovery of intermediate linking forms, and the occurrence of such links cannot affect the actual characters of the forms which they connect; and except, secondly, by a certain amount of difference, for two forms, if differing very little, are generally ranked as varieties, notwithstanding that intermediate linking forms have not been discovered; but the amount of difference considered necessary to give to two forms the rank of species is quite indefinite. In genera having more than the average number of species in any country, the species of these genera have more than the average number of varieties. In large genera the species are apt to be closely, but unequally, allied together, forming little clusters round certain species. Species very closely allied to other species apparently have restricted ranges. In all these several respects the species of large genera present a strong analogy with varieties. And we can clearly understand these analogies, if species have once existed as varieties, and have thus originated: whereas, these analogies are utterly inexplicable if each species has been independently created.
We have, also, seen that it is the most flourishing and dominant species of the larger genera which on an average vary most; and varieties, as we shall hereafter see, tend to become converted into new and distinct species. The larger genera thus tend to become larger; and throughout nature the forms of life which are now dominant tend to become still more dominant by leaving many modified and dominant descendants. But by steps hereafter to be explained, the larger genera also tend to break up into smaller genera. And thus, the forms of life throughout the universe become divided into groups subordinate to groups.
變異性——個(gè)體差異——存疑的物種——分布廣、分散大和普通的物種變異最多——各地大屬的物種比小屬的物種變異更頻繁——大屬里許多物種就像變種,有很密切的、但不均等的相互關(guān)系,并且分布區(qū)域有限
把前一章所得到的各項(xiàng)原則應(yīng)用到自然狀況下的生物之前,必須簡單地討論一下,后者是否容易發(fā)生變異。要充分討論這一問題,必須舉出一長列枯燥無味的事實(shí);不過這些我準(zhǔn)備留到將來的著作里。這里也不討論物種這個(gè)術(shù)語的各種定義。至今沒有一項(xiàng)定義能使全體學(xué)者都滿意;然而談到物種的時(shí)候,他們都模糊地知道是什么意思。這術(shù)語一般含有創(chuàng)世作用這一未知要素?!白兎N”這個(gè)術(shù)語幾乎也是同樣地難下定義;但是幾乎普遍地蘊(yùn)含世系群落的意義,雖然很少能夠得到證明。還有所謂畸形也難以解釋,但它們逐漸變成變種。我認(rèn)為畸形是指構(gòu)造上某部分顯著偏差而言,對(duì)于物種要么是有害的,要么是無用的,一般不加以傳播。有些作者是在專門意義上來使用“變異”術(shù)語的,它的含義是直接由物理的生活條件所引起的一種變化;這種意義的“變異體”假定為不能遺傳的;但是波羅的海半咸水里貝類的矮化狀態(tài)、阿爾卑斯山頂?shù)陌参?、極北地區(qū)動(dòng)物的增厚毛皮,誰能說在某些情形下至少不遺傳數(shù)代呢?我認(rèn)為這種情況下,該類型是可以稱為變種的。
此外,還有許多微小差異,都可叫作個(gè)體差異。比如我們熟悉的經(jīng)常在同父母的后代中所出現(xiàn)的,或者在同一局限區(qū)域內(nèi)棲息的同種個(gè)體中所經(jīng)常觀察到的而且可以設(shè)想也是這樣發(fā)生的差異。沒有人會(huì)假設(shè),同種的一切個(gè)體都是在相同的模型里鑄造出來的。這種個(gè)體差異對(duì)于我們十分重要,因?yàn)檫@為自然選擇提供了材料,可以積累,就像人類在家養(yǎng)生物里朝著一定方向積累個(gè)體差異那樣。這種個(gè)體差異,一般作用于學(xué)者們認(rèn)為不重要的那些部分;但是我可以用一連串事實(shí)闡明,無論從生理學(xué)或分類學(xué)的觀點(diǎn)來看,都必須稱為重要的那些部分,有時(shí)在同種個(gè)體中也會(huì)發(fā)生變異。我相信,哪怕經(jīng)驗(yàn)最豐富的學(xué)者也會(huì)對(duì)變異性個(gè)案之多感到驚奇,即使是構(gòu)造的重要部分也不例外;只需花上若干年,就可以同我一樣搜集到這種權(quán)威的材料。應(yīng)該記住,分類學(xué)家很不樂意在重要性狀中發(fā)現(xiàn)變異性,而且很少有人愿意費(fèi)神去檢查重要的內(nèi)部器官,并在同種的許多標(biāo)本間加以比較。我從來不會(huì)料到,昆蟲的靠近大中央神經(jīng)節(jié)的主干神經(jīng)分枝,在同一個(gè)物種里會(huì)發(fā)生變異;本來還認(rèn)為這種性質(zhì)的變異只能緩慢地進(jìn)行;然而最近盧伯克(Lubbock)爵士闡明,胭脂蟲(Coccus)的主干神經(jīng)具有一定程度的變異,幾乎可以與樹干的不規(guī)則分枝相提并論。我補(bǔ)充一句,這位富有哲理的學(xué)者最近還闡明,某些昆蟲幼蟲的肌肉絕非千篇一律。有人說重要器官?zèng)Q不變異,這往往是循環(huán)論證,因?yàn)檎沁@些人實(shí)際上把不變異的性狀當(dāng)作重要的(少數(shù)學(xué)者老實(shí)坦白過)。在這種觀點(diǎn)下,自然就找不到重要器官發(fā)生變異的例子了;但在任何其他觀點(diǎn)下,卻可以確鑿地舉出許多例子來。
同個(gè)體差異相關(guān)的,有一點(diǎn)使我非常困惑:我是指有人稱為“變形的”(protean)或“多形的”(polymorphic)那些屬,其中的物種表現(xiàn)了無節(jié)制的變異量。關(guān)于這些類型應(yīng)列為物種還是變種,幾乎沒有兩個(gè)學(xué)者意見一致??梢耘e植物里的懸鉤子屬(Rubus)、薔薇屬(Rosa)、山柳菊屬(Hieracium)以及昆蟲類和腕足類(Brachiopod shells)的幾屬為例。在大多數(shù)多形的屬里,有些物種具有穩(wěn)定的和一定的性狀。除了少數(shù)例外,在一個(gè)地方為多形的屬,似乎在別處也是多形的,并且從腕足類來判斷,在早先的時(shí)代也是這樣的。這些事實(shí)很使人困惑,因?yàn)樗鼈兯坪蹶U明這種變異是獨(dú)立于生活條件之外的。我猜想,在某些多形的屬里所看到的變異,處于對(duì)物種是無用的或無害的構(gòu)造點(diǎn),因此,自然選擇對(duì)于它們就不起作用,從而不能固定下來,詳見后文的說明。
有些類型,在相當(dāng)程度上具有物種的性狀,但同其他類型密切相似,或者由中間級(jí)進(jìn)同其他類型密切相關(guān),學(xué)者們不愿列為不同的物種;其實(shí)它們?cè)谌舾煞矫鎸?duì)我們是極其重要的。我們很有理由相信,這些密切親緣的存疑類型有許多曾在本地長久持續(xù)保存它們的性狀,據(jù)我們所知,和良好的真種一樣天長地久。實(shí)際上,學(xué)者們能夠用具有中間性狀的其他類型把兩個(gè)類型連接在一起,就是把一個(gè)類型當(dāng)作另一個(gè)的變種;他把最普通的一個(gè),但常常是最初記載的類型作為物種,而把另一個(gè)作為變種??墒窃跊Q定是否把一個(gè)類型作為另一類型的變種時(shí),哪怕兩者被中間連鎖緊密地連接在一起,也是有嚴(yán)重困難的,我并不準(zhǔn)備在這里把這些困難列舉出來;即使中間連鎖具有一般所假定的雜種性質(zhì),也常常不能解決這種困難。然而在很多情形下,一個(gè)類型之所以列為另一個(gè)的變種,并非因?yàn)榇_已找到了中間連鎖,而是因?yàn)橛^察者采用了類推的方法,便假設(shè)中間連鎖現(xiàn)在確在某些地方生存著,或者它們從前可能生存過;這樣,就為疑惑、臆測打開了大門。
因此,當(dāng)決定一個(gè)類型應(yīng)列為物種還是變種的時(shí)候,有健全判斷力、豐富經(jīng)驗(yàn)的學(xué)者的意見,似乎是應(yīng)當(dāng)遵循的唯一指針。然而在許多情況下,我們必須依據(jù)大多數(shù)學(xué)者的意見來決定,因?yàn)楹苌儆袠?biāo)記顯著而熟知的變種不曾被至少幾位能干的鑒定者列為物種的。
具有這種存疑性質(zhì)的變種所在皆是,無可爭辯。把不同學(xué)者所著的幾部英、法、美植物志比較一下,就可看出有何等驚人數(shù)目的類型,往往先后被列為真物種和區(qū)區(qū)變種。多方幫助我而使我感激萬分的沃森(H. C. Watson)先生告訴我說,現(xiàn)在有182種英國植物一般被當(dāng)作變種,但是過去統(tǒng)統(tǒng)都被列為物種;開列這張名單時(shí),省略了許多細(xì)小的變種,然而它們也曾被列為物種,此外把若干高度多形的屬完全省略了。在包含著最多形的類型的屬之下,巴賓頓(Babington)先生列舉了251個(gè)物種,而本瑟姆(Bentham)先生只列舉了112個(gè)物種——就是說差額有139個(gè)存疑類型!在每次生育必須交配、具有高度移動(dòng)性的動(dòng)物里,分別被學(xué)者列為物種和變種的存疑類型,在同一地區(qū)很少看到,但在分隔的地區(qū)卻很普通。在北美洲和歐洲,有多少鳥和昆蟲,彼此差異很微,卻分別被大學(xué)者或列為無可懷疑的物種,或列為變種,或常把它們稱為地理族!多年前,我曾比較過、看別人比較過加拉帕戈斯群島上鳥類的相互異同,以及這些鳥與美洲大陸的鳥的異同,深深感到物種和變種之間的區(qū)別是何等的含糊和任意。小馬德拉群島的小島上有許多昆蟲,沃拉斯頓(Wollaston)先生的力作把它們看作變種,但許多昆蟲學(xué)者毫無疑問會(huì)將它們列為物種。甚至愛爾蘭也有少數(shù)動(dòng)物,曾被學(xué)者看作物種,但現(xiàn)在一般卻被看作變種。若干經(jīng)驗(yàn)豐富的鳥類學(xué)家認(rèn)為英國的紅松雞只是挪威種的一個(gè)特性顯著的族,然而大多數(shù)人則把它列為英國特有的非存疑物種。兩個(gè)存疑類型的原產(chǎn)地如果相距遙遠(yuǎn),許多學(xué)者就會(huì)把雙方都列為物種;但是,有人問得好,多少距離是足夠遙遠(yuǎn)的呢?如果美洲和歐洲距離足夠的話,那么歐洲到亞速爾群島、馬德拉群島、加那利群島、愛爾蘭之間的距離是否足夠呢?必須承認(rèn),有許多被鑒定家認(rèn)為是變種的類型,擁有著完美的物種性狀,也就被另外一些鑒定家列為貨真價(jià)實(shí)的物種了。但在這些術(shù)語的定義還沒有得到普遍接受之前,就來討論什么應(yīng)該稱為物種,什么應(yīng)該稱為變種,乃是無的放矢啊。
許多關(guān)于特征顯著的變種或存疑物種的個(gè)案,很值得考慮;因?yàn)樵谠噲D決定它們的級(jí)位上,從地理分布、相似變異、雜交等方面已經(jīng)展開了若干有趣的論據(jù)路線。我在這里只提出一個(gè)實(shí)例——眾所周知的報(bào)春花屬(primrose)和櫻草(cowslip)或黃花九輪草(Primula veris)和高報(bào)春(elatior)。這些植物外表大不相同,味道不同,氣味不同,開花期略微不同,生境有點(diǎn)不同,上山高度不同,地理分布區(qū)不同,最后是仔細(xì)的觀察者蓋特納(G?rtner)多年來所做的大量實(shí)驗(yàn)表明,它們雜交非常困難。簡直無法指望有更好的證據(jù)來證明兩個(gè)類型是不同物種了。另一方面,它們由許多中間連鎖聯(lián)合起來,而這些連鎖是否雜種是存疑的。依我看,鋪天蓋地的實(shí)驗(yàn)證據(jù)表明,它們從共同的親種傳下來,因此必須列為變種。
在大多數(shù)情形下,過細(xì)的調(diào)查可以使學(xué)者們對(duì)存疑類型的分級(jí)取得一致的意見。然而必須坦言,在研究得最透徹的地區(qū),所見到的存疑類型的數(shù)目也最多。我驚異地發(fā)現(xiàn),如果自然狀況下的任何動(dòng)植物對(duì)人極有用,或?yàn)榱巳魏卧蚰芤鹑藗兊拿芮凶⒁?,那么它的變種就幾乎普遍地記載下來了。而且這些變種往往被某些作者列為物種??纯雌胀ǖ臋禈洌╫ak),研究得何等精細(xì)呀;然而,一位德國作者竟從其他學(xué)者普遍認(rèn)為是變種的類型中確定了十二個(gè)以上的物種;在英國,可以舉出一些植物學(xué)的最高權(quán)威和實(shí)際工作者,有的認(rèn)為無梗的和有梗的櫟樹是物種,有的僅僅認(rèn)為它們是變種。
青年學(xué)者開始研究陌生的生物類群時(shí),倍感困惑的首先就是決定什么是物種的差異,什么是變種的差異。他對(duì)這個(gè)生物類群所發(fā)生的變異量和變異種類一無所知;這至少可以表明,生物發(fā)生某種變異是多么普遍。但是,如果把注意力集中于一個(gè)地區(qū)里的某一類生物,就會(huì)很快決定如何去分級(jí)大部分的存疑類型。他一般傾向于定出許多物種,就像前文講過的養(yǎng)鴿和養(yǎng)雞愛好者那樣,他所不斷研究著的那些類型的差異量將會(huì)給他深刻的印象;而在其他地區(qū)和其他生物類群的相似變異方面他缺少一般知識(shí),無法用來校正他的最初印象。等到他擴(kuò)大了觀察范圍,就會(huì)遇到更多困難;他將遇到數(shù)目更多的密切近似類型。但是,如果進(jìn)一步擴(kuò)大他的觀察范圍,最后將能夠有所決定何謂變種,何謂物種;不過他要在這方面獲得成功,代價(jià)是承認(rèn)大量變異,然而這樣承認(rèn)是否正確,往往會(huì)引起其他學(xué)者的爭議。何況,如果從現(xiàn)今已不連續(xù)的地區(qū)找來親緣類型加以研究,他就沒有希望找到存疑類型的中間連鎖,于是不得不幾乎完全依賴類推的方法,這就會(huì)使他的困難登峰造極。
在物種和亞種之間,當(dāng)然還沒有劃出過明確的界限——亞種就是類型里面有些學(xué)者認(rèn)為已很接近物種,但還沒有完全達(dá)到物種那一級(jí);還有,在亞種和顯著的變種之間,在較不顯著的變種和個(gè)體差異之間也是一筆糊涂賬。這些差異被一個(gè)不易察覺的系列彼此混合,而該系列令人產(chǎn)生存在實(shí)際過渡的印象。
因此,我認(rèn)為,個(gè)體差異雖對(duì)分類學(xué)家無足輕重,但對(duì)我們卻很重要,這是分辨輕度變種的第一步,而博物學(xué)著作認(rèn)為不值得記載那些變種。我認(rèn)為,任何程度上比較顯著、比較永久的變種都是走向更顯著、更永久變種的步驟;而后者是走向亞種,走向物種的步驟。從一個(gè)階段的差異到另一個(gè)高級(jí)階段的過渡,在某種情況下,可能僅僅是由于長久連續(xù)居于兩個(gè)不同地區(qū)不同物理?xiàng)l件之下的結(jié)果;但這種觀點(diǎn)使我信心不足。我把一個(gè)變種從略不同于親種的狀態(tài)到更加不同的狀態(tài)的過渡,歸因于自然選擇的累積(容以后詳論)作用,在某個(gè)確定的方向積累構(gòu)造的差異。所以我認(rèn)為顯著的變種可以理直氣壯地叫作初始物種;但是這種觀點(diǎn)是否合理,必須根據(jù)本書所舉出的各種事實(shí)和論點(diǎn),通盤權(quán)衡,加以判斷。
不必設(shè)想一切變種或初始物種都能達(dá)到物種的一級(jí)。它們也許會(huì)在初始狀態(tài)中絕滅,或者長時(shí)期地停留在變種的階段,如沃拉斯頓先生所指出的馬德拉地方某些化石陸地貝類的變種便是這樣。如果一個(gè)變種很繁盛,而超過了親種的數(shù)目,那就會(huì)列為物種,而親種就當(dāng)作變種了;或者它會(huì)淘汰消滅親種;或者兩者并存,都排列為獨(dú)立的物種。我們以后還要回來討論這一問題。
從上述可以看出,我認(rèn)為物種這個(gè)術(shù)語是為了便利而任意加于一群互相密切類似的個(gè)體的,它和變種這個(gè)術(shù)語在本質(zhì)上并沒有區(qū)別,變種是指區(qū)別較少而波動(dòng)較多的類型。還有,變種這個(gè)名詞和個(gè)體差異比較,也是為了便利而任意取用的。
在理論的指導(dǎo)下,我曾經(jīng)想,將若干編著完備的植物志中的所有變種排列成表,對(duì)于變化最多的物種的性質(zhì)和關(guān)系,也許能獲得一些有趣的結(jié)果。乍看,這似乎是一件簡單的工作;但是,不久沃森先生使我相信其中難點(diǎn)重重,我深深感謝他在這個(gè)問題上的寶貴忠告和幫助,以后胡克博士也這么說,甚至語氣更重。這些難點(diǎn)和各變異物種的比例數(shù)目表,將留在將來的著作里再予討論。胡克博士細(xì)讀了我的原稿,檢查了表格之后,他允許我補(bǔ)充說明,他認(rèn)為下面的論述可以成立。然而,這里雖然講得很簡單,但整個(gè)問題是相當(dāng)令人困惑的,并且不能不涉及“生存斗爭”“性狀的分歧”等問題,容以后討論。
德康多爾等人闡明,分布很廣的植物一般會(huì)出現(xiàn)變種;這在意料之中,因?yàn)楸┞对诓煌奈锢項(xiàng)l件之下,還要和各類不同的生物進(jìn)行競爭(以后將看到,這一點(diǎn)是更重要的條件)。但是我的表格進(jìn)一步闡明,在任何有限制的地區(qū)里,越是普通的物種,即個(gè)體越多的物種,以及在自己的區(qū)域內(nèi)分散越廣的物種(這和分布廣的意義不同,和普通也略有不同),往往發(fā)生特征足夠顯著的變種,記載在植物學(xué)著作中。因此,越是繁盛的物種,或者稱為優(yōu)勢物種——它們分布最廣,在本區(qū)域內(nèi)分散最廣,個(gè)體最多——就越產(chǎn)生顯著的變種,或我所稱的初始物種。這也許在預(yù)料之中,因?yàn)樽鳛樽兎N,要在任何程度上變成永久,必定要和該區(qū)域內(nèi)的其他居住者進(jìn)行斗爭;已經(jīng)占優(yōu)勢的物種,最有可能產(chǎn)生特定后代,雖然有輕微變異,還是繼承了使親種戰(zhàn)勝同地生物的那些優(yōu)點(diǎn)。
如果把任何植物志上記載的某地方生長的植物分作相等的兩個(gè)群,把所有大屬的植物放在一邊,所有小屬的植物放在另一邊,則可發(fā)現(xiàn)大屬那邊很普通的、極分散的物種或優(yōu)勢物種略多。這也在預(yù)料之中,僅僅因?yàn)樵谌魏蔚赜騼?nèi)棲息著同屬的許多物種,就表明該地有機(jī)、無機(jī)的條件里存在有利于該屬的東西;結(jié)果,在大屬里,即含有許多物種的屬里,可望發(fā)現(xiàn)比例數(shù)目較多的優(yōu)勢物種。但是,可使這種結(jié)果曖昧不明的原因?qū)嵲诙啵嫫婀治业谋砀裆踔帘砻鞔髮龠@一邊略占多數(shù)。我在這里只提出兩個(gè)曖昧的原因。淡水產(chǎn)喜鹽的植物一般分布很廣,且極分散,但這一點(diǎn)似乎和它們居住地方的性質(zhì)有關(guān),而和該物種所歸的屬之大小關(guān)系很少或沒有關(guān)系。還有,體制低級(jí)的植物一般比高級(jí)的植物分散得更加廣闊;而且這和屬的大小也沒有密切關(guān)聯(lián)。體制低級(jí)的植物分布廣的原因,將在“地理分布”一章討論。
由于我把物種看作只是特性顯著、定義明確的變種,所以預(yù)料各地大屬的物種應(yīng)比小屬的物種更常出現(xiàn)變種;因?yàn)?,無論哪里有許多密切近似物種(即同屬的物種)形成,一般應(yīng)有許多變種即初始物種正在形成。哪里有許多大樹生長,哪里可望找到幼苗。哪里有屬的許多物種因變異而形成,哪里的條件必有利于變異;因此,可望這些條件一般還會(huì)繼續(xù)有利于變異。相反,我們?nèi)绻迅鱾€(gè)物種看作是特別創(chuàng)造出來的,就沒有明顯的理由來說明,為什么含有多數(shù)物種的類群比含有少數(shù)物種的類群會(huì)發(fā)生更多的變種。
為了測試這種預(yù)料的正確性,我把十二個(gè)地區(qū)的植物及兩個(gè)地區(qū)的鞘翅類昆蟲排列為差不多相等的兩群,大屬的物種排一邊,小屬的物種排另一邊;結(jié)果毫無例外地證明了,大屬一邊比小屬一邊產(chǎn)生變種的物種比例更高。另外,產(chǎn)生任何變種的大屬物種,一律比小屬的物種所產(chǎn)生的變種平均更多。如果采用另一種分群方法,徹底排除表內(nèi)只有一個(gè)到四個(gè)物種的最小屬,這兩個(gè)結(jié)果也一樣。這些事實(shí)清楚地表明,物種僅是顯著標(biāo)記而永久的變種而已;無論哪里同屬的物種大量形成,或者不妨說,哪里物種制造廠活動(dòng)過,一般應(yīng)該發(fā)現(xiàn)這些工廠仍在活動(dòng),特別是我們可以有充分的理由相信,新種的制造是一個(gè)緩慢的過程。如果把變種看作初始物種,上述這一點(diǎn)肯定屬實(shí);因?yàn)槲业谋砀褚话闱宄乇砻鳎瑹o論哪里屬的物種大量形成,這個(gè)屬的物種產(chǎn)生的變種(即初始物種)就會(huì)在平均數(shù)以上。倒不是說所有大屬現(xiàn)在變異都很大,因而都在增加物種數(shù)量,也不是說小屬現(xiàn)在都不變異,不增加物種;否則我的學(xué)說就要受到滅頂之災(zāi)。地質(zhì)學(xué)明白地告訴我們,小屬隨著時(shí)間的推移常常會(huì)大事增大;而大屬常常已經(jīng)達(dá)到頂點(diǎn),而衰落消失。我們所要闡明的僅僅是,哪里有屬的物種大量形成,一般說來就有許多物種還在形成;這可謂言之有理。
大屬的物種和其中有記載的變種之間,有值得注意的其他關(guān)系。我們已經(jīng)看到,辨別物種和顯著變種并沒有顛撲不破的標(biāo)準(zhǔn);在存疑類型之間沒有找到中間連鎖的時(shí)候,學(xué)者就不得不依據(jù)它們之間的差異量來決定,用類推的方法來判斷其差異量是否足夠把一方或雙方升到物種的等級(jí)。因此,差異量就成為解決兩個(gè)類型究竟應(yīng)該列為物種還是變種的極其重要的標(biāo)準(zhǔn)。弗里斯(Fries)曾就植物,韋斯特伍德(Westwood)曾就昆蟲說明,大屬里物種之間的差異量往往極小。我曾努力以平均數(shù)來測試這種情形,所得到的粗淺結(jié)果總是證實(shí)這種觀點(diǎn)。我還詢問過幾位睿智的、經(jīng)驗(yàn)豐富的觀察者,他們?nèi)贾笠操澩@種意見。所以,在這方面,大屬的物種比小屬的物種更像變種。這種情形可換一種說法,也就是說,在大屬里,超過平均數(shù)的變種即初始物種現(xiàn)在還在制造中,許多已經(jīng)制造成的物種在某種程度上還是和變種相似,因?yàn)檫@些物種彼此的差異不及普通的差異量大。
而且,大屬內(nèi)物種的相互關(guān)系,同任何一個(gè)物種的變種是相似的。沒有一位學(xué)者宣稱,屬內(nèi)的全部物種在彼此區(qū)別上是相等的;一般地可以把它們區(qū)分為亞屬、組(sections)或更小的類群。弗里斯說得好,小群物種一般就像衛(wèi)星環(huán)繞在其他物種的周圍。因此,所謂變種,還不是一群類型,它們的彼此關(guān)系不均等,環(huán)繞在某些類型——即環(huán)繞在其親種的周圍?變種和物種之間無疑存在著一個(gè)極重要的不同點(diǎn),即變種彼此之間的差異量,或與其親種的差異量,比起同屬的物種之間要小得多。但是,當(dāng)我們討論到我稱為“性狀的分歧”的原則時(shí),將會(huì)看到如何解釋這一點(diǎn),變種之間的小差異將傾向于增大為物種之間的大差異。
我看還有一點(diǎn)值得注意。變種的分布范圍一般都十分有限;這話確是不講自明的,如果發(fā)現(xiàn)一個(gè)變種比它的假定親種有更廣闊的分布范圍,那就應(yīng)該把名稱倒轉(zhuǎn)過來了。但是也有理由相信,同其他物種密切相似的并且類似變種的物種,常常有極有限的分布范圍。例如,沃森先生曾把精選的《倫敦植物名錄》(第四版)列為物種的63種植物指給我看,但他認(rèn)為它們同其他物種太相似,所以價(jià)值存疑。根據(jù)沃森先生所做的英國區(qū)劃,這63個(gè)所謂物種的分布范圍平均為6.9區(qū)。在同一《名錄》里,記載著53個(gè)公認(rèn)的變種,分布范圍為7.7區(qū);而這些變種所屬的物種的分布范圍為14.3區(qū)。所以公認(rèn)的變種和密切相似的類型具有幾乎一樣的有限平均分布范圍,后者就是沃森先生指出的所謂存疑物種,但它們幾乎普遍地被英國學(xué)者們列為貨真價(jià)實(shí)的物種了。
最后,變種具有與物種相同的一般性狀,無法和物種區(qū)別——除非,第一,發(fā)現(xiàn)了中間的連鎖類型,而這種連鎖的出現(xiàn)不能影響其所連接的類型的實(shí)際性狀;第二,兩者之間具有一定的差異量,因?yàn)閮蓚€(gè)類型如果差異很小,一般列為變種,雖然并沒有發(fā)現(xiàn)中間的連鎖類型,但是給予兩個(gè)類型物種地位所需要的差異量,卻是不確定的。在任何地方,含有超過平均數(shù)的物種的屬,其中的物種也有超過平均數(shù)的變種。在大屬里,物種易于密切但不均等地相互近似,環(huán)繞某些物種形成小群。與其他物種密切近似的物種顯然具有有限的分布范圍。在上述這些方面,大屬的物種極類似于變種。如果物種曾經(jīng)作為變種而生存過,并且是由變種產(chǎn)生的,我們便可以明白這種類似性;然而,如果各物種是獨(dú)立創(chuàng)造的,這種類似性就完全不能解釋了。
我們還看到,大屬中越是繁盛的優(yōu)勢物種,平均變種越多;而我們以后將看到,變種傾向于變成新物種。因此大屬傾向于變得更大;自然界中,現(xiàn)在占優(yōu)勢的生物類型由于留下了許多變異了的優(yōu)勢后代,傾向于更加占有優(yōu)勢。但是經(jīng)過以后要說明的步驟,大屬也有分裂為小屬的傾向。這樣,全世界的生物類型就在類群之下又分為類群了。
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