found it impossible, from having no landmarks, and from their course being so extremely crooked, to preserve any sort of uniform direction: so it is with Australian savages in thick forests. In North and South America many birds slowly travel northward and southward, urged on by the food they find, as the seasons change; let them continue to do this, till, as in the case of the sheep in Spain, it has become an urgent instinctive desire, and they will gradually accelerate their journey.
They would cross narrow rivers, and if these were converted by subsidence into narrow estuaries, and gradually during centuries to arms of the sea, still we may suppose their restless desire of travelling onwards would impel them to cross such an arm, even if it had become of great width beyond their span of vision. How they are able to preserve a course in any direction, I have said, is a faculty unknown to us. To give another illustration of the means by which I conceive it _possible_ that the direction of migrations have been determined. Elk and reindeer in N. America annually cross, as if they could marvellously smell or see at the distance of a hundred miles, a wide tract of absolute desert, to arrive at certain islands where there is a scanty supply of food; the changes of temperature, which geology proclaims, render it probable that this desert tract formerly supported some vegetation, and thus these quadrupeds might have been annually led on, till they reached the more fertile spots, and so acquired, like the sheep of Spain, their migratory powers.
{288} The distinction between _faculty_ and _instinct_ corresponds in some degree to that between perception of a stimulus and a specific reaction. I imagine that the author would have said that the sensitiveness to light possessed by a plant is _faculty_, while _instinct_ decides whether the plant curves to or from the source of illumination.
{289} <Note in the original in an unknown handwriting.> At the time when corn was pitched in the market instead of sold by sample, the geese in the town fields of Newcastle <Staffordshire?> used to know market day and come in to pick up the corn spilt.
{290} <Note in original.> Macculloch and others.
{291} I can find no reference to the _transandantes_ sheep in Darwin's published work. He was possibly led to doubt the accuracy of the statement on which he relied. For the case of the sheep returning to their birth-place see p. 17, note 4.{Note 91} Fourthly, with respect to the combs of the hive-bee{292}; here again we must look to some faculty or means by which they make their hexagonal cells, without indeed we view these instincts as mere machines. At present such a faculty is quite unknown: Mr Waterhouse supposes that several bees are led by their instinct to excavate a mass of wax to a certain thinness, and that the result of this is that hexagons necessarily remain. Whether this or some other theory be true, some such means they must possess. They abound, however, with true instincts, which are the most wonderful that are known. If we examine the little that is known concerning the habits of other species of bees, we find much simpler instincts: the humble bee merely fills rude balls of wax with honey and aggregates them together with little order in a rough nest of grass. If we knew the instinct of all the bees, which ever had existed, it is not improbable that we should have instincts of every degree of complexity, from actions as simple as a bird making a nest, and rearing her young, to the wonderful architecture and government of the hive-bee; at least such is _possible_, which is all that I am here considering.
Finally, I will briefly consider under the same point of view one other class of instincts, which have often been advanced as truly wonderful, namely parents bringing food to their young which they themselves neither like nor partake of{293};--for instance, the common sparrow, a granivorous bird, feeding its young with caterpillars. We might of course look into the case still earlier, and seek how an instinct in the parent, of feeding its young at all, was first derived; but it is useless to waste time in conjectures on a series of gradations from the young feeding themselves and being slightly and occasionally assisted in their search, to their entire food being brought to them. With respect to the parent bringing a different kind of food from its own kind, we may suppose either that the remote stock, whence the sparrow and other congenerous birds have descended, was insectivorous, and that its own habits and structure have been changed, whilst its ancient instincts with respect to its young have remained unchanged; or we may suppose that the parents have been induced to vary slightly the food of their young, by a slight scarcity of the proper kind (or by the instincts of some individuals not being so truly developed), and in this case those young which were most capable of surviving were necessarily most often preserved, and would themselves in time become parents, and would be similarly compelled to alter their food for their young. In the case of those animals, the young of which feed themselves, changes in their instincts for food, and in their structure, might be selected from slight variations, just as in mature animals. Again, where the food of the young depends on where the mother places her eggs, as in the case of the caterpillars of the cabbage-butterfly, we may suppose that the parent stock of the species deposited her eggs sometimes on one kind and sometimes on another of congenerous plants (as some species now do), and if the cabbage suited the caterpillars better than any other plant, the caterpillars of those butterflies, which had chosen the cabbage, would be most plentifully reared, and would produce butterflies more apt to lay their eggs on the cabbage than on the other congenerous plants.
{293} This is an expansion of an obscure passage in the Essay of 1842, p. 19.
However vague and unphilosophical these conjectures may appear, they serve, I think, to show that one's first impulse utterly to reject any theory whatever, implying a gradual acquirement of these instincts, which for ages have excited man's admiration, may at least be delayed.
Once grant that dispositions, tastes, actions or habits can be slightly modified, either by slight congenital differences (we must suppose in the brain) or by the force of external circumstances, and that such slight modifications can be rendered inheritable,--a proposition which no one can reject,--and it will be difficult to put any limit to the complexity and wonder of the tastes and habits which may _possibly_ be thus acquired.
_Difficulties in the acquirement by Selection of complex corporeal structures._ After the past discussion it will perhaps be convenient here to consider whether any particular corporeal organs, or the entire structure of any animals, are so wonderful as to justify the rejection _primâ facie_ of our theory{294}. In the case of the eye, as with the more complicated instincts, no doubt one's first impulse is to utterly reject every such theory. But if the eye from its most complicated form can be shown to graduate into an exceedingly simple state,--if selection can produce the smallest change, and if such a series exists, then it is clear (for in this work we have nothing to do with the first origin of organs in their simplest forms{295}) that it may _possibly_ have been acquired by gradual selection of slight, but in each case, useful deviations{296}.
Every naturalist, when he meets with any new and singular organ, always expects to find, and looks for, other and simpler modifications of it in other beings. In the case of the eye, we have a multitude of different forms, more or less simple, not graduating into each other, but separated by sudden gaps or intervals; but we must recollect how incomparably greater would the multitude of visual structures be if we had the eyes of every fossil which ever existed. We shall discuss the probable vast proportion of the extinct to the recent in the succeeding Part. Notwithstanding the large series of existing forms, it is most difficult even to conjecture by what intermediate stages very many simple organs could possibly have graduated into complex ones: but it should be here borne in mind, that a part having originally a wholly different function, may on the theory of gradual selection be slowly worked into quite another use; the gradations of forms, from which naturalists believe in the hypothetical metamorphosis of part of the ear into the swimming bladder in fishes{297}, and in insects of legs into jaws, show the manner in which this is possible. As under domestication, modifications of structure take place, without any continued selection, which man finds very useful, or valuable for curiosity (as the hooked calyx of the teazle, or the ruff round some pigeons' necks), so in a state of nature some small modifications, apparently beautifully adapted to certain ends, may perhaps be produced from the accidents of the reproductive system, and be at once propagated without long-continued selection of small deviations towards that structure{298}. In conjecturing by what stages any complicated organ in a species may have arrived at its present state, although we may look to the analogous organs in other existing species, we should do this merely to aid and guide our imaginations; for to know the real stages we must look only through one line of species, to one ancient stock, from which the species in question has descended. In considering the eye of a quadruped, for instance, though we may look at the eye of a molluscous animal or of an insect, as a proof how simple an organ will serve some of the ends of vision; and at the eye of a fish as a nearer guide of the manner of simplification; we must remember that it is a mere chance (assuming for a moment the truth of our theory) if any existing organic being has preserved any one organ, in exactly the same condition, as it existed in the ancient species at remote geological periods.
{294} The difficulties discussed in the _Origin_, Ed. i. p. 171, vi. p. 207, are the rarity of transitional varieties, the origin of the tail of the giraffe; the otter-like polecat (_Mustela vison_); the flying habit of the bat; the penguin and the logger-headed duck; flying fish; the whale-like habit of the bear; the woodpecker; diving petrels; the eye; the swimming bladder; Cirripedes; neuter insects; electric organs.
Of these, the polecat, the bat, the woodpecker, the eye, the swimming bladder are discussed in the present Essay, and in addition some botanical problems.
{295} In the _Origin_, Ed. vi. p. 275, the author replies to especially to that writer's objection "that natural selection is incompetent to account for the incipient stages of useful structures."
{296} <The following sentence seems to have been intended for insertion here> "and that each eye throughout the animal kingdom is not only most useful, but _perfect_ for its possessor."
{298} This is one of the most definite statements in the present Essay of the possible importance of _sports_ or what would now be called _mutations_. As is well known the author afterwards doubted whether species could arise in this way. See _Origin_, Ed. v. p.
The nature or condition of certain structures has been thought by some naturalists to be of no use to the possessor{299}, but to have been formed wholly for the good of other species; thus certain fruit and seeds have been thought to have been made nutritious for certain animals--numbers of insects, especially in their larval state, to exist for the same end--certain fish to be bright coloured to aid certain birds of prey in catching them, &c. Now could this be proved (which I am far from admitting) the theory of natural selection would be quite overthrown; for it is evident that selection depending on the advantage over others of one individual with some slight deviation would never produce a structure or quality profitable only to another species. No doubt one being takes advantage of qualities in another, and may even cause its extermination; but this is far from proving that this quality was produced for such an end. It may be advantageous to a plant to have its seeds attractive to animals, if one out of a hundred or a thousand escapes being digested, and thus aids dissemination: the bright colours of a fish may be of some advantage to it, or more probably may result from exposure to certain conditions in favourable haunts for food, _notwithstanding_ it becomes subject to be caught more easily by certain birds.
is discussed for the case of instincts with a proviso that the same argument applies to structure. It is briefly stated in its general If instead of looking, as above, at certain individual organs, in order to speculate on the stages by which their parts have been matured and selected, we consider an individual animal, we meet with the same or greater difficulty, but which, I believe, as in the case of single organs, rests entirely on our ignorance. It may be asked by what intermediate forms could, for instance, a bat possibly have passed; but the same question might have been asked with respect to the seal, if we had not been familiar with the otter and other semi-aquatic carnivorous quadrupeds. But in the case of the bat, who can say what might have been the habits of some parent form with less developed wings, when we now have insectivorous opossums and herbivorous squirrels fitted for merely gliding through the air{300}. One species of bat is at present partly aquatic in its habits{301}. Woodpeckers and tree-frogs are especially adapted, as their names express, for climbing trees; yet we have species of both inhabiting the open plains of La Plata, where a tree does not exist{302}. I might argue from this circumstance that a structure eminently fitted for climbing trees might descend from forms inhabiting a country where a tree did not exist. Notwithstanding these and a multitude of other well-known facts, it has been maintained by several authors that one species, for instance of the carnivorous order, could not pass into another, for instance into an otter, because in its transitional state its habits would not be adapted to any proper conditions of life; but the jaguar{303} is a thoroughly terrestrial quadruped in its structure, yet it takes freely to the water and catches many fish; will it be said that it is _impossible_ that the conditions of its country might become such that the jaguar should be driven to feed more on fish than they now do; and in that case is it impossible, is it not probable, that any the slightest deviation in its instincts, its form of body, in the width of its feet, and in the extension of the skin (which already unites the base of its toes) would give such individuals a better _chance_ of surviving and propagating young with similar, barely perceptible (though thoroughly exercised), deviations{304}? Who will say what could thus be effected in the course of ten thousand generations? Who can answer the same question with respect to instincts? If no one can, the _possibility_ (for we are not in this chapter considering the _probability_) of simple organs or organic beings being modified by natural selection and the effects of external agencies into complicated ones ought not to be absolutely rejected.
{300} <Note in original.> No one will dispute that the gliding is most useful, probably necessary for the species in question.
{301} <Note in original.> Is this the Galeopithecus? I forget.
<_Galeopithecus_ "or the flying Lemur" is mentioned in the corresponding discussion in the _Origin_, Ed. i. p. 181, vi. p. 217, as formerly placed among the bats. I do not know why it is described as partly aquatic in its habits.> {302} In the _Origin_, Ed. vi. p. 221, the author modified the statement that it _never_ climbs trees; he also inserted a sentence quoting Mr Hudson to the effect that in other districts this woodpecker climbs trees and bores holes. See Mr Darwin's paper, {303} Note by the late Alfred Newton. Richardson in _Fauna {304} <Note in original.> See Richardson a far better case of a polecat animal <_Mustela vison_>, which half-year is aquatic.
PART II{305} ON THE EVIDENCE FAVOURABLE AND OPPOSED TO THE VIEW THAT SPECIES ARE NATURALLY FORMED RACES, DESCENDED FROM COMMON STOCKS {305} In the _Origin_ the division of the work into Parts I and II is omitted. In the MS. the chapters of Part II are numbered afresh, the present being Ch. I of Pt. II. I have thought it best to call it Ch. IV and there is evidence that Darwin had some thought of doing the same. It corresponds to Ch. IX of _Origin_, Ed. i., Ch. X in Ed. vi.
CHAPTER IV ON THE NUMBER OF INTERMEDIATE FORMS REQUIRED ON THE THEORY OF COMMON DESCENT; AND ON THEIR ABSENCE IN A FOSSIL STATE I must here premise that, according to the view ordinarily received, the myriads of organisms, which have during past and present times peopled this world, have been created by so many distinct acts of creation. It is impossible to reason concerning the will of the Creator, and therefore, according to this view, we can see no cause why or why not the individual organism should have been created on any fixed scheme.
That all the organisms of this world have been produced on a scheme is certain from their general affinities; and if this scheme can be shown to be the same with that which would result from allied organic beings descending from common stocks, it becomes highly improbable that they have been separately created by individual acts of the will of a Creator. For as well might it be said that, although the planets move in courses conformably to the law of gravity, yet we ought to attribute the course of each planet to the individual act of the will of the Creator{306}. It is in every case more conformable with what we know of the government of this earth, that the Creator should have imposed only general laws. As long as no method was known by which races could become exquisitely adapted to various ends, whilst the existence of species was thought to be proved by the sterility{307} of their offspring, it was allowable to attribute each organism to an individual act of creation.
But in the two former chapters it has (I think) been shown that the production, under existing conditions, of exquisitely adapted species, is at least _possible_. Is there then any direct evidence in favour <of> or against this view? I believe that the geographical distribution of organic beings in past and present times, the kind of affinity linking them together, their so-called "metamorphic" and "abortive" organs, appear in favour of this view. On the other hand, the imperfect evidence of the continuousness of the organic series, which, we shall immediately see, is required on our theory, is against it; and is the most weighty objection{308}. The evidence, however, even on this point, as far as it goes, is favourable; and considering the imperfection of our knowledge, especially with respect to past ages, it would be surprising if evidence drawn from such sources were not also imperfect.
{306} In the Essay of 1842 the author uses astronomy in the same manner as an illustration. In the _Origin_ this does not occur; the reference to the action of secondary causes is more general, _e.g._ {307} It is interesting to find the argument from sterility given so prominent a place. In a corresponding passage in the _Origin_, Ed. i. p. 480, vi. p. 659, it is more summarily treated. The author gives, as the chief bar to the acceptance of evolution, the fact that "we are always slow in admitting any great change of which we do not see the intermediate steps"; and goes on to quote Lyell on geological action. It will be remembered that the question of sterility remained a difficulty for Huxley.
{308} Similar statements occur in the Essay of 1842, p. 24, note 1, and in the _Origin_, Ed. i. p. 299.
As I suppose that species have been formed in an analogous manner with the varieties of the domesticated animals and plants, so must there have existed intermediate forms between all the species of the same group, not differing more than recognised varieties differ. It must not be supposed necessary that there should have existed forms exactly intermediate in character between any two species of a genus, or even between any two varieties of a species; but it is necessary that there should have existed every intermediate form between the one species or variety of the common parent, and likewise between the second species or variety, and this same common parent. Thus it does not necessarily follow that there ever has existed <a> series of intermediate sub-varieties (differing no more than the occasional seedlings from the same seed-capsule,) between broccoli and common red cabbage; but it is certain that there has existed, between broccoli and the wild parent cabbage, a series of such intermediate seedlings, and again between red cabbage and the wild parent cabbage: so that the broccoli and red cabbage are linked together, but not _necessarily_ by directly intermediate forms{309}. It is of course possible that there _may_ have been directly intermediate forms, for the broccoli may have long since descended from a common red cabbage, and this from the wild cabbage. So on my theory, it must have been with species of the same genus. Still more must the supposition be avoided that there has necessarily ever existed (though one _may_ have descended from <the> other) directly intermediate forms between any two genera or families--for instance between the genus _Sus_ and the Tapir{310}; although it is necessary that intermediate forms (not differing more than the varieties of our domestic animals) should have existed between Sus and some unknown parent form, and Tapir with this same parent form. The latter may have differed more from Sus and Tapir than these two genera now differ from each other. In this sense, according to our theory, there has been a gradual passage (the steps not being wider apart than our domestic varieties) between the species of the same genus, between genera of the same family, and between families of the same order, and so on, as far as facts, hereafter to be given, lead us; and the number of forms which must have at former periods existed, thus to make good this passage between different species, genera, and families, must have been almost infinitely great.
{309} In the _Origin_, Ed. i. p. 280, vi. p. 414 he uses his newly-acquired knowledge of pigeons to illustrate this point.
What evidence{311} is there of a number of intermediate forms having existed, making a passage in the above sense, between the species of the same groups? Some naturalists have supposed that if every fossil which now lies entombed, together with all existing species, were collected together, a perfect series in every great class would be formed.
Considering the enormous number of species requisite to effect this, especially in the above sense of the forms not being _directly_ intermediate between the existing species and genera, but only intermediate by being linked through a common but often widely different ancestor, I think this supposition highly improbable. I am however far from underrating the probable number of fossilised species: no one who has attended to the wonderful progress of palæontology during the last few years will doubt that we as yet have found only an exceedingly small fraction of the species buried in the crust of the earth. Although the almost infinitely numerous intermediate forms in no one class may have been preserved, it does not follow that they have not existed. The fossils which have been discovered, it is important to remark, do tend, the little way they go, to make good the series; for as observed by Buckland they all fall into or between existing groups{312}. Moreover, those that fall between our existing groups, fall in, according to the manner required by our theory, for they do not directly connect two existing species of different groups, but they connect the groups themselves: thus the Pachydermata and Ruminantia are now separated by several characters, <for instance> the Pachydermata{313} have both a tibia and fibula, whilst Ruminantia have only a tibia; now the fossil Macrauchenia has a leg bone exactly intermediate in this respect, and likewise has some other intermediate characters. But the Macrauchenia does not connect any one species of Pachydermata with some one other of Ruminantia but it shows that these two groups have at one time been less widely divided. So have fish and reptiles been at one time more closely connected in some points than they now are. Generally in those groups in which there has been most change, the more ancient the fossil, if not identical with recent, the more often it falls between existing groups, or into small existing groups which now lie between other large existing groups. Cases like the foregoing, of which there are many, form steps, though few and far between, in a series of the kind required by my theory.
{313} The structure of the Pachyderm leg was a favourite with the author. It is discussed in the Essay of 1842, p. 48. In the present Essay the following sentence in the margin appears to refer to Pachyderms and Ruminants: "There can be no doubt, if we banish all fossils, existing groups stand more separate." The following occurs between the lines "The earliest forms would be such as others could radiate from."
As I have admitted the high improbability, that if every fossil were disinterred, they would compose in each of the Divisions of Nature a perfect series of the kind required; consequently I freely admit, that if those geologists are in the right who consider the lowest known formation as contemporaneous with the first appearances of life{314}; or the several formations as at all closely consecutive; or any one formation as containing a nearly perfect record of the organisms which existed during the whole period of its deposition in that quarter of the globe;--if such propositions are to be accepted, my theory must be abandoned.
If the Palæozoic system is really contemporaneous with the first appearance of life, my theory must be abandoned, both inasmuch as it limits _from shortness of time_ the total number of forms which can have existed on this world, and because the organisms, as fish, mollusca{315} and star-fish found in its lower beds, cannot be considered as the parent forms of all the successive species in these classes. But no one has yet overturned the arguments of Hutton and Lyell, that the lowest formations known to us are only those which have escaped being metamorphosed <illegible>; if we argued from some considerable districts, we might have supposed that even the Cretaceous system was that in which life first appeared. From the number of distant points, however, in which the Silurian system has been found to be the lowest, and not always metamorphosed, there are some objections to Hutton's and Lyell's view; but we must not forget that the now existing land forms only 1/5 part of the superficies of the globe, and that this fraction is only imperfectly known. With respect to the fewness of the organisms found in the Silurian and other Palæozoic formations, there is less difficulty, inasmuch as (besides their gradual obliteration) we can expect formations of this vast antiquity to escape entire denudation, only when they have been accumulated over a wide area, and have been subsequently protected by vast superimposed deposits: now this could generally only hold good with deposits accumulating in a wide and deep ocean, and therefore unfavourable to the presence of many living things. A mere narrow and not very thick strip of matter, deposited along a coast where organisms most abound, would have no chance of escaping denudation and being preserved to the present time from such immensely distant ages{316}.
{315} <Pencil insertion by the author.> The parent-forms of Mollusca would probably differ greatly from all recent,--it is not directly that any one division of Mollusca would descend from first time unaltered, whilst others had become metamorphosed from it.
If the several known formations are at all nearly consecutive in time, and preserve a fair record of the organisms which have existed, my theory must be abandoned. But when we consider the great changes in mineralogical nature and texture between successive formations, what vast and entire changes in the geography of the surrounding countries must generally have been effected, thus wholly to have changed the nature of the deposits on the same area. What time such changes must have required! Moreover how often has it not been found, that between two conformable and apparently immediately successive deposits a vast pile of water-worn matter is interpolated in an adjoining district. We have no means of conjecturing in many cases how long a period{317} has elapsed between successive formations, for the species are often wholly different: as remarked by Lyell, in some cases probably as long a period has elapsed between two formations as the whole Tertiary system, itself broken by wide gaps.
{317} <Note in original.> Reflect on coming in of the Chalk, extending from Iceland to the Crimea.
Consult the writings of any one who has particularly attended to any one stage in the Tertiary system (and indeed of every system) and see how deeply impressed he is with the time required for its accumulation{318}.
Reflect on the years elapsed in many cases, since the latest beds containing only living species have been formed;--see what Jordan Smith says of the 20,000 years since the last bed, which is above the boulder formation in Scotland, has been upraised; or of the far longer period since the recent beds of Sweden have been upraised 400 feet, what an enormous period the boulder formation must have required, and yet how insignificant are the records (although there has been plenty of elevation to bring up submarine deposits) of the shells, which we know existed at that time. Think, then, over the entire length of the Tertiary epoch, and think over the probable length of the intervals, separating the Secondary deposits. Of these deposits, moreover, those consisting of sand and pebbles have seldom been favourable, either to the embedment or to the preservation of fossils{319}.
Nor can it be admitted as probable that any one Secondary formation contains a fair record even of those organisms which are most easily preserved, namely hard marine bodies. In how many cases have we not certain evidence that between the deposition of apparently closely consecutive beds, the lower one existed for an unknown time as land, covered with trees. Some of the Secondary formations which contain most marine remains appear to have been formed in a wide and not deep sea, and therefore only those marine animals which live in such situations would be preserved{320}. In all cases, on indented rocky coasts, or any other coast, where sediment is not accumulating, although often highly favourable to marine animals, none can be embedded: where pure sand and pebbles are accumulating few or none will be preserved. I may here instance the great western line of the S. American coast{321}, tenanted by many peculiar animals, of which none probably will be preserved to a distant epoch. From these causes, and especially from such deposits as are formed along a line of coast, steep above and below water, being necessarily of little width, and therefore more likely to be subsequently denuded and worn away, we can see why it is improbable that our Secondary deposits contain a fair record of the Marine Fauna of any one period. The East Indian Archipelago offers an area, as large as most of our Secondary deposits, in which there are wide and shallow seas, teeming with marine animals, and in which sediment is accumulating; now supposing that all the hard marine animals, or rather those having hard parts to preserve, were preserved to a future age, excepting those which lived on rocky shores where no sediment or only sand and gravel were accumulating, and excepting those embedded along the steeper coasts, where only a narrow fringe of sediment was accumulating, supposing all this, how poor a notion would a person at a future age have of the Marine Fauna of the present day. Lyell{322} has compared the geological series to a work of which only the few latter but not consecutive chapters have been preserved; and out of which, it may be added, very many leaves have been torn, the remaining ones only illustrating a scanty portion of the Fauna of each period. On this view, the records of anteceding ages confirm my theory; on any other they destroy it.
{320} <Note in original.> Neither highest or lowest fish (_i.e._ Myxina <?> or Lepidosiren) could be preserved in intelligible condition in fossils.
I am indebted to Prof. Judd for pointing out that Darwin's version of the metaphor is founded on the first edition of Lyell's _Principles_, vol. I. and vol. III.; see the Essay of 1842, p. 27.
Finally, if we narrow the question into, why do we not find in some instances every intermediate form between any two species? the answer may well be that the average duration of each specific form (as we have good reason to believe) is immense in years, and that the transition could, according to my theory, be effected only by numberless small gradations; and therefore that we should require for this end a most perfect record, which the foregoing reasoning teaches us not to expect.
It might be thought that in a vertical section of great thickness in the