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<h2> CHAPTER VII. MISCELLANEOUS OBJECTIONS TO THE THEORY OF NATURAL SELECTION. </h2>
<p>Longevity—Modifications not necessarily simultaneous—Modifications<br/>
apparently of no direct service—Progressive development—Characters of<br/>
small functional importance, the most constant—Supposed incompetence<br/>
of natural selection to account for the incipient stages of useful<br/>
structures—Causes which interfere with the acquisition through natural<br/>
selection of useful structures—Gradations of structure with changed<br/>
functions—Widely different organs in members of the same class,<br/>
developed from one and the same source—Reasons for disbelieving in<br/>
great and abrupt modifications.<br/></p>
<p>I will devote this chapter to the consideration of various miscellaneous
objections which have been advanced against my views, as some of the
previous discussions may thus be made clearer; but it would be useless to
discuss all of them, as many have been made by writers who have not taken
the trouble to understand the subject. Thus a distinguished German
naturalist has asserted that the weakest part of my theory is, that I
consider all organic beings as imperfect: what I have really said is, that
all are not as perfect as they might have been in relation to their
conditions; and this is shown to be the case by so many native forms in
many quarters of the world having yielded their places to intruding
foreigners. Nor can organic beings, even if they were at any one time
perfectly adapted to their conditions of life, have remained so, when
their conditions changed, unless they themselves likewise changed; and no
one will dispute that the physical conditions of each country, as well as
the number and kinds of its inhabitants, have undergone many mutations.</p>
<p>A critic has lately insisted, with some parade of mathematical accuracy,
that longevity is a great advantage to all species, so that he who
believes in natural selection "must arrange his genealogical tree" in such
a manner that all the descendants have longer lives than their
progenitors! Cannot our critics conceive that a biennial plant or one of
the lower animals might range into a cold climate and perish there every
winter; and yet, owing to advantages gained through natural selection,
survive from year to year by means of its seeds or ova? Mr. E. Ray
Lankester has recently discussed this subject, and he concludes, as far as
its extreme complexity allows him to form a judgment, that longevity is
generally related to the standard of each species in the scale of
organisation, as well as to the amount of expenditure in reproduction and
in general activity. And these conditions have, it is probable, been
largely determined through natural selection.</p>
<p>It has been argued that, as none of the animals and plants of Egypt, of
which we know anything, have changed during the last three or four
thousand years, so probably have none in any part of the world. But, as
Mr. G.H. Lewes has remarked, this line of argument proves too much, for
the ancient domestic races figured on the Egyptian monuments, or embalmed,
are closely similar or even identical with those now living; yet all
naturalists admit that such races have been produced through the
modification of their original types. The many animals which have remained
unchanged since the commencement of the glacial period, would have been an
incomparably stronger case, for these have been exposed to great changes
of climate and have migrated over great distances; whereas, in Egypt,
during the last several thousand years, the conditions of life, as far as
we know, have remained absolutely uniform. The fact of little or no
modification having been effected since the glacial period, would have
been of some avail against those who believe in an innate and necessary
law of development, but is powerless against the doctrine of natural
selection or the survival of the fittest, which implies that when
variations or individual differences of a beneficial nature happen to
arise, these will be preserved; but this will be effected only under
certain favourable circumstances.</p>
<p>The celebrated palaeontologist, Bronn, at the close of his German
translation of this work, asks how, on the principle of natural selection,
can a variety live side by side with the parent species? If both have
become fitted for slightly different habits of life or conditions, they
might live together; and if we lay on one side polymorphic species, in
which the variability seems to be of a peculiar nature, and all mere
temporary variations, such as size, albinism, etc., the more permanent
varieties are generally found, as far as I can discover, inhabiting
distinct stations, such as high land or low land, dry or moist districts.
Moreover, in the case of animals which wander much about and cross freely,
their varieties seem to be generally confined to distinct regions.</p>
<p>Bronn also insists that distinct species never differ from each other in
single characters, but in many parts; and he asks, how it always comes
that many parts of the organisation should have been modified at the same
time through variation and natural selection? But there is no necessity
for supposing that all the parts of any being have been simultaneously
modified. The most striking modifications, excellently adapted for some
purpose, might, as was formerly remarked, be acquired by successive
variations, if slight, first in one part and then in another; and as they
would be transmitted all together, they would appear to us as if they had
been simultaneously developed. The best answer, however, to the above
objection is afforded by those domestic races which have been modified,
chiefly through man's power of selection, for some special purpose. Look
at the race and dray-horse, or at the greyhound and mastiff. Their whole
frames, and even their mental characteristics, have been modified; but if
we could trace each step in the history of their transformation—and
the latter steps can be traced—we should not see great and
simultaneous changes, but first one part and then another slightly
modified and improved. Even when selection has been applied by man to some
one character alone—of which our cultivated plants offer the best
instances—it will invariably be found that although this one part,
whether it be the flower, fruit, or leaves, has been greatly changed,
almost all the other parts have been slightly modified. This may be
attributed partly to the principle of correlated growth, and partly to
so-called spontaneous variation.</p>
<p>A much more serious objection has been urged by Bronn, and recently by
Broca, namely, that many characters appear to be of no service whatever to
their possessors, and therefore cannot have been influenced through
natural selection. Bronn adduces the length of the ears and tails in the
different species of hares and mice—the complex folds of enamel in
the teeth of many animals, and a multitude of analogous cases. With
respect to plants, this subject has been discussed by Nageli in an
admirable essay. He admits that natural selection has effected much, but
he insists that the families of plants differ chiefly from each other in
morphological characters, which appear to be quite unimportant for the
welfare of the species. He consequently believes in an innate tendency
towards progressive and more perfect development. He specifies the
arrangement of the cells in the tissues, and of the leaves on the axis, as
cases in which natural selection could not have acted. To these may be
added the numerical divisions in the parts of the flower, the position of
the ovules, the shape of the seed, when not of any use for dissemination,
etc.</p>
<p>There is much force in the above objection. Nevertheless, we ought, in the
first place, to be extremely cautious in pretending to decide what
structures now are, or have formerly been, of use to each species. In the
second place, it should always be borne in mind that when one part is
modified, so will be other parts, through certain dimly seen causes, such
as an increased or diminished flow of nutriment to a part, mutual
pressure, an early developed part affecting one subsequently developed,
and so forth—as well as through other causes which lead to the many
mysterious cases of correlation, which we do not in the least understand.
These agencies may be all grouped together, for the sake of brevity, under
the expression of the laws of growth. In the third place, we have to allow
for the direct and definite action of changed conditions of life, and for
so-called spontaneous variations, in which the nature of the conditions
apparently plays a quite subordinate part. Bud-variations, such as the
appearance of a moss-rose on a common rose, or of a nectarine on a
peach-tree, offer good instances of spontaneous variations; but even in
these cases, if we bear in mind the power of a minute drop of poison in
producing complex galls, we ought not to feel too sure that the above
variations are not the effect of some local change in the nature of the
sap, due to some change in the conditions. There must be some efficient
cause for each slight individual difference, as well as for more strongly
marked variations which occasionally arise; and if the unknown cause were
to act persistently, it is almost certain that all the individuals of the
species would be similarly modified.</p>
<p>In the earlier editions of this work I underrated, as it now seems
probable, the frequency and importance of modifications due to spontaneous
variability. But it is impossible to attribute to this cause the
innumerable structures which are so well adapted to the habits of life of
each species. I can no more believe in this than that the well-adapted
form of a race-horse or greyhound, which before the principle of selection
by man was well understood, excited so much surprise in the minds of the
older naturalists, can thus be explained.</p>
<p>It may be worth while to illustrate some of the foregoing remarks. With
respect to the assumed inutility of various parts and organs, it is hardly
necessary to observe that even in the higher and best-known animals many
structures exist, which are so highly developed that no one doubts that
they are of importance, yet their use has not been, or has only recently
been, ascertained. As Bronn gives the length of the ears and tail in the
several species of mice as instances, though trifling ones, of differences
in structure which can be of no special use, I may mention that, according
to Dr. Schobl, the external ears of the common mouse are supplied in an
extraordinary manner with nerves, so that they no doubt serve as tactile
organs; hence the length of the ears can hardly be quite unimportant. We
shall, also, presently see that the tail is a highly useful prehensile
organ to some of the species; and its use would be much influence by its
length.</p>
<p>With respect to plants, to which on account of Nageli's essay I shall
confine myself in the following remarks, it will be admitted that the
flowers of the orchids present a multitude of curious structures, which a
few years ago would have been considered as mere morphological differences
without any special function; but they are now known to be of the highest
importance for the fertilisation of the species through the aid of
insects, and have probably been gained through natural selection. No one
until lately would have imagined that in dimorphic and trimorphic plants
the different lengths of the stamens and pistils, and their arrangement,
could have been of any service, but now we know this to be the case.</p>
<p>In certain whole groups of plants the ovules stand erect, and in others
they are suspended; and within the same ovarium of some few plants, one
ovule holds the former and a second ovule the latter position. These
positions seem at first purely morphological, or of no physiological
signification; but Dr. Hooker informs me that within the same ovarium the
upper ovules alone in some cases, and in others the lower ones alone are
fertilised; and he suggests that this probably depends on the direction in
which the pollen-tubes enter the ovarium. If so, the position of the
ovules, even when one is erect and the other suspended within the same
ovarium, would follow the selection of any slight deviations in position
which favoured their fertilisation, and the production of seed.</p>
<p>Several plants belonging to distinct orders habitually produce flowers of
two kinds—the one open, of the ordinary structure, the other closed
and imperfect. These two kinds of flowers sometimes differ wonderfully in
structure, yet may be seen to graduate into each other on the same plant.
The ordinary and open flowers can be intercrossed; and the benefits which
certainly are derived from this process are thus secured. The closed and
imperfect flowers are, however, manifestly of high importance, as they
yield with the utmost safety a large stock of seed, with the expenditure
of wonderfully little pollen. The two kinds of flowers often differ much,
as just stated, in structure. The petals in the imperfect flowers almost
always consist of mere rudiments, and the pollen-grains are reduced in
diameter. In Ononis columnae five of the alternate stamens are
rudimentary; and in some species of Viola three stamens are in this state,
two retaining their proper function, but being of very small size. In six
out of thirty of the closed flowers in an Indian violet (name unknown, for
the plants have never produced with me perfect flowers), the sepals are
reduced from the normal number of five to three. In one section of the
Malpighiaceae the closed flowers, according to A. de Jussieu, are still
further modified, for the five stamens which stand opposite to the sepals
are all aborted, a sixth stamen standing opposite to a petal being alone
developed; and this stamen is not present in the ordinary flowers of this
species; the style is aborted; and the ovaria are reduced from three to
two. Now although natural selection may well have had the power to prevent
some of the flowers from expanding, and to reduce the amount of pollen,
when rendered by the closure of the flowers superfluous, yet hardly any of
the above special modifications can have been thus determined, but must
have followed from the laws of growth, including the functional inactivity
of parts, during the progress of the reduction of the pollen and the
closure of the flowers.</p>
<p>It is so necessary to appreciate the important effects of the laws of
growth, that I will give some additional cases of another kind, namely of
differences in the same part or organ, due to differences in relative
position on the same plant. In the Spanish chestnut, and in certain
fir-trees, the angles of divergence of the leaves differ, according to
Schacht, in the nearly horizontal and in the upright branches. In the
common rue and some other plants, one flower, usually the central or
terminal one, opens first, and has five sepals and petals, and five
divisions to the ovarium; while all the other flowers on the plant are
tetramerous. In the British Adoxa the uppermost flower generally has two
calyx-lobes with the other organs tetramerous, while the surrounding
flowers generally have three calyx-lobes with the other organs
pentamerous. In many Compositae and Umbelliferae (and in some other
plants) the circumferential flowers have their corollas much more
developed than those of the centre; and this seems often connected with
the abortion of the reproductive organs. It is a more curious fact,
previously referred to, that the achenes or seeds of the circumference and
centre sometimes differ greatly in form, colour and other characters. In
Carthamus and some other Compositae the central achenes alone are
furnished with a pappus; and in Hyoseris the same head yields achenes of
three different forms. In certain Umbelliferae the exterior seeds,
according to Tausch, are orthospermous, and the central one coelospermous,
and this is a character which was considered by De Candolle to be in other
species of the highest systematic importance. Professor Braun mentions a
Fumariaceous genus, in which the flowers in the lower part of the spike
bear oval, ribbed, one-seeded nutlets; and in the upper part of the spike,
lanceolate, two-valved and two-seeded siliques. In these several cases,
with the exception of that of the well-developed ray-florets, which are of
service in making the flowers conspicuous to insects, natural selection
cannot, as far as we can judge, have come into play, or only in a quite
subordinate manner. All these modifications follow from the relative
position and inter-action of the parts; and it can hardly be doubted that
if all the flowers and leaves on the same plant had been subjected to the
same external and internal condition, as are the flowers and leaves in
certain positions, all would have been modified in the same manner.</p>
<p>In numerous other cases we find modifications of structure, which are
considered by botanists to be generally of a highly important nature,
affecting only some of the flowers on the same plant, or occurring on
distinct plants, which grow close together under the same conditions. As
these variations seem of no special use to the plants, they cannot have
been influenced by natural selection. Of their cause we are quite
ignorant; we cannot even attribute them, as in the last class of cases, to
any proximate agency, such as relative position. I will give only a few
instances. It is so common to observe on the same plant, flowers
indifferently tetramerous, pentamerous, etc., that I need not give
examples; but as numerical variations are comparatively rare when the
parts are few, I may mention that, according to De Candolle, the flowers
of Papaver bracteatum offer either two sepals with four petals (which is
the common type with poppies), or three sepals with six petals. The manner
in which the petals are folded in the bud is in most groups a very
constant morphological character; but Professor Asa Gray states that with
some species of Mimulus, the aestivation is almost as frequently that of
the Rhinanthideae as of the Antirrhinideae, to which latter tribe the
genus belongs. Aug. St. Hilaire gives the following cases: the genus
Zanthoxylon belongs to a division of the Rutaceae with a single ovary, but
in some species flowers may be found on the same plant, and even in the
same panicle, with either one or two ovaries. In Helianthemum the capsule
has been described as unilocular or tri-locular; and in H. mutabile, "Une
lame PLUS OU MOINS LARGE, s'etend entre le pericarpe et le placenta." In
the flowers of Saponaria officinalis Dr. Masters has observed instances of
both marginal and free central placentation. Lastly, St. Hilaire found
towards the southern extreme of the range of Gomphia oleaeformis two forms
which he did not at first doubt were distinct species, but he subsequently
saw them growing on the same bush; and he then adds, "Voila donc dans un
meme individu des loges et un style qui se rattachent tantot a un axe
verticale et tantot a un gynobase."</p>
<p>We thus see that with plants many morphological changes may be attributed
to the laws of growth and the inter-action of parts, independently of
natural selection. But with respect to Nageli's doctrine of an innate
tendency towards perfection or progressive development, can it be said in
the case of these strongly pronounced variations, that the plants have
been caught in the act of progressing towards a higher state of
development? On the contrary, I should infer from the mere fact of the
parts in question differing or varying greatly on the same plant, that
such modifications were of extremely small importance to the plants
themselves, of whatever importance they may generally be to us for our
classifications. The acquisition of a useless part can hardly be said to
raise an organism in the natural scale; and in the case of the imperfect,
closed flowers, above described, if any new principle has to be invoked,
it must be one of retrogression rather than of progression; and so it must
be with many parasitic and degraded animals. We are ignorant of the
exciting cause of the above specified modifications; but if the unknown
cause were to act almost uniformly for a length of time, we may infer that
the result would be almost uniform; and in this case all the individuals
of the species would be modified in the same manner.</p>
<p>From the fact of the above characters being unimportant for the welfare of
the species, any slight variations which occurred in them would not have
been accumulated and augmented through natural selection. A structure
which has been developed through long-continued selection, when it ceases
to be of service to a species, generally becomes variable, as we see with
rudimentary organs; for it will no longer be regulated by this same power
of selection. But when, from the nature of the organism and of the
conditions, modifications have been induced which are unimportant for the
welfare of the species, they may be, and apparently often have been,
transmitted in nearly the same state to numerous, otherwise modified,
descendants. It cannot have been of much importance to the greater number
of mammals, birds, or reptiles, whether they were clothed with hair,
feathers or scales; yet hair has been transmitted to almost all mammals,
feathers to all birds, and scales to all true reptiles. A structure,
whatever it may be, which is common to many allied forms, is ranked by us
as of high systematic importance, and consequently is often assumed to be
of high vital importance to the species. Thus, as I am inclined to
believe, morphological differences, which we consider as important—such
as the arrangement of the leaves, the divisions of the flower or of the
ovarium, the position of the ovules, etc., first appeared in many cases as
fluctuating variations, which sooner or later became constant through the
nature of the organism and of the surrounding conditions, as well as
through the intercrossing of distinct individuals, but not through natural
selection; for as these morphological characters do not affect the welfare
of the species, any slight deviations in them could not have been governed
or accumulated through this latter agency. It is a strange result which we
thus arrive at, namely, that characters of slight vital importance to the
species, are the most important to the systematist; but, as we shall
hereafter see when we treat of the genetic principle of classification,
this is by no means so paradoxical as it may at first appear.</p>
<p>Although we have no good evidence of the existence in organic beings of an
innate tendency towards progressive development, yet this necessarily
follows, as I have attempted to show in the fourth chapter, through the
continued action of natural selection. For the best definition which has
ever been given of a high standard of organisation, is the degree to which
the parts have been specialised or differentiated; and natural selection
tends towards this end, inasmuch as the parts are thus enabled to perform
their functions more efficiently.</p>
<p>A distinguished zoologist, Mr. St. George Mivart, has recently collected
all the objections which have ever been advanced by myself and others
against the theory of natural selection, as propounded by Mr. Wallace and
myself, and has illustrated them with admirable art and force. When thus
marshalled, they make a formidable array; and as it forms no part of Mr.
Mivart's plan to give the various facts and considerations opposed to his
conclusions, no slight effort of reason and memory is left to the reader,
who may wish to weigh the evidence on both sides. When discussing special
cases, Mr. Mivart passes over the effects of the increased use and disuse
of parts, which I have always maintained to be highly important, and have
treated in my "Variation under Domestication" at greater length than, as I
believe, any other writer. He likewise often assumes that I attribute
nothing to variation, independently of natural selection, whereas in the
work just referred to I have collected a greater number of
well-established cases than can be found in any other work known to me. My
judgment may not be trustworthy, but after reading with care Mr. Mivart's
book, and comparing each section with what I have said on the same head, I
never before felt so strongly convinced of the general truth of the
conclusions here arrived at, subject, of course, in so intricate a
subject, to much partial error.</p>
<p>All Mr. Mivart's objections will be, or have been, considered in the
present volume. The one new point which appears to have struck many
readers is, "That natural selection is incompetent to account for the
incipient stages of useful structures." This subject is intimately
connected with that of the gradation of the characters, often accompanied
by a change of function, for instance, the conversion of a swim-bladder
into lungs, points which were discussed in the last chapter under two
headings. Nevertheless, I will here consider in some detail several of the
cases advanced by Mr. Mivart, selecting those which are the most
illustrative, as want of space prevents me from considering all.</p>
<p>The giraffe, by its lofty stature, much elongated neck, fore legs, head
and tongue, has its whole frame beautifully adapted for browsing on the
higher branches of trees. It can thus obtain food beyond the reach of the
other Ungulata or hoofed animals inhabiting the same country; and this
must be a great advantage to it during dearths. The Niata cattle in South
America show us how small a difference in structure may make, during such
periods, a great difference in preserving an animal's life. These cattle
can browse as well as others on grass, but from the projection of the
lower jaw they cannot, during the often recurrent droughts, browse on the
twigs of trees, reeds, etc., to which food the common cattle and horses
are then driven; so that at these times the Niatas perish, if not fed by
their owners. Before coming to Mr. Mivart's objections, it may be well to
explain once again how natural selection will act in all ordinary cases.
Man has modified some of his animals, without necessarily having attended
to special points of structure, by simply preserving and breeding from the
fleetest individuals, as with the race-horse and greyhound, or as with the
game-cock, by breeding from the victorious birds. So under nature with the
nascent giraffe, the individuals which were the highest browsers and were
able during dearths to reach even an inch or two above the others, will
often have been preserved; for they will have roamed over the whole
country in search of food. That the individuals of the same species often
differ slightly in the relative lengths of all their parts may be seen in
many works of natural history, in which careful measurements are given.
These slight proportional differences, due to the laws of growth and
variation, are not of the slightest use or importance to most species. But
it will have been otherwise with the nascent giraffe, considering its
probable habits of life; for those individuals which had some one part or
several parts of their bodies rather more elongated than usual, would
generally have survived. These will have intercrossed and left offspring,
either inheriting the same bodily peculiarities, or with a tendency to
vary again in the same manner; while the individuals less favoured in the
same respects will have been the most liable to perish.</p>
<p>We here see that there is no need to separate single pairs, as man does,
when he methodically improves a breed: natural selection will preserve and
thus separate all the superior individuals, allowing them freely to
intercross, and will destroy all the inferior individuals. By this process
long-continued, which exactly corresponds with what I have called
unconscious selection by man, combined, no doubt, in a most important
manner with the inherited effects of the increased use of parts, it seems
to me almost certain that an ordinary hoofed quadruped might be converted
into a giraffe.</p>
<p>To this conclusion Mr. Mivart brings forward two objections. One is that
the increased size of the body would obviously require an increased supply
of food, and he considers it as "very problematical whether the
disadvantages thence arising would not, in times of scarcity, more than
counterbalance the advantages." But as the giraffe does actually exist in
large numbers in Africa, and as some of the largest antelopes in the
world, taller than an ox, abound there, why should we doubt that, as far
as size is concerned, intermediate gradations could formerly have existed
there, subjected as now to severe dearths. Assuredly the being able to
reach, at each stage of increased size, to a supply of food, left
untouched by the other hoofed quadrupeds of the country, would have been
of some advantage to the nascent giraffe. Nor must we overlook the fact,
that increased bulk would act as a protection against almost all beasts of
prey excepting the lion; and against this animal, its tall neck—and
the taller the better—would, as Mr. Chauncey Wright has remarked,
serve as a watch-tower. It is from this cause, as Sir S. Baker remarks,
that no animal is more difficult to stalk than the giraffe. This animal
also uses its long neck as a means of offence or defence, by violently
swinging its head armed with stump-like horns. The preservation of each
species can rarely be determined by any one advantage, but by the union of
all, great and small.</p>
<p>Mr. Mivart then asks (and this is his second objection), if natural
selection be so potent, and if high browsing be so great an advantage, why
has not any other hoofed quadruped acquired a long neck and lofty stature,
besides the giraffe, and, in a lesser degree, the camel, guanaco and
macrauchenia? Or, again, why has not any member of the group acquired a
long proboscis? With respect to South Africa, which was formerly inhabited
by numerous herds of the giraffe, the answer is not difficult, and can
best be given by an illustration. In every meadow in England, in which
trees grow, we see the lower branches trimmed or planed to an exact level
by the browsing of the horses or cattle; and what advantage would it be,
for instance, to sheep, if kept there, to acquire slightly longer necks?
In every district some one kind of animal will almost certainly be able to
browse higher than the others; and it is almost equally certain that this
one kind alone could have its neck elongated for this purpose, through
natural selection and the effects of increased use. In South Africa the
competition for browsing on the higher branches of the acacias and other
trees must be between giraffe and giraffe, and not with the other ungulate
animals.</p>
<p>Why, in other quarters of the world, various animals belonging to this
same order have not acquired either an elongated neck or a proboscis,
cannot be distinctly answered; but it is as unreasonable to expect a
distinct answer to such a question as why some event in the history of
mankind did not occur in one country while it did in another. We are
ignorant with respect to the conditions which determine the numbers and
range of each species, and we cannot even conjecture what changes of
structure would be favourable to its increase in some new country. We can,
however, see in a general manner that various causes might have interfered
with the development of a long neck or proboscis. To reach the foliage at
a considerable height (without climbing, for which hoofed animals are
singularly ill-constructed) implies greatly increased bulk of body; and we
know that some areas support singularly few large quadrupeds, for instance
South America, though it is so luxuriant, while South Africa abounds with
them to an unparalleled degree. Why this should be so we do not know; nor
why the later tertiary periods should have been much more favourable for
their existence than the present time. Whatever the causes may have been,
we can see that certain districts and times would have been much more
favourable than others for the development of so large a quadruped as the
giraffe.</p>
<p>In order that an animal should acquire some structure specially and
largely developed, it is almost indispensable that several other parts
should be modified and coadapted. Although every part of the body varies
slightly, it does not follow that the necessary parts should always vary
in the right direction and to the right degree. With the different species
of our domesticated animals we know that the parts vary in a different
manner and degree, and that some species are much more variable than
others. Even if the fitting variations did arise, it does not follow that
natural selection would be able to act on them and produce a structure
which apparently would be beneficial to the species. For instance, if the
number of individuals existing in a country is determined chiefly through
destruction by beasts of prey—by external or internal parasites,
etc.—as seems often to be the case, then natural selection will be
able to do little, or will be greatly retarded, in modifying any
particular structure for obtaining food. Lastly, natural selection is a
slow process, and the same favourable conditions must long endure in order
that any marked effect should thus be produced. Except by assigning such
general and vague reasons, we cannot explain why, in many quarters of the
world, hoofed quadrupeds have not acquired much elongated necks or other
means for browsing on the higher branches of trees.</p>
<p>Objections of the same nature as the foregoing have been advanced by many
writers. In each case various causes, besides the general ones just
indicated, have probably interfered with the acquisition through natural
selection of structures, which it is thought would be beneficial to
certain species. One writer asks, why has not the ostrich acquired the
power of flight? But a moment's reflection will show what an enormous
supply of food would be necessary to give to this bird of the desert force
to move its huge body through the air. Oceanic islands are inhabited by
bats and seals, but by no terrestrial mammals; yet as some of these bats
are peculiar species, they must have long inhabited their present homes.
Therefore Sir C. Lyell asks, and assigns certain reasons in answer, why
have not seals and bats given birth on such islands to forms fitted to
live on the land? But seals would necessarily be first converted into
terrestrial carnivorous animals of considerable size, and bats into
terrestrial insectivorous animals; for the former there would be no prey;
for the bats ground-insects would serve as food, but these would already
be largely preyed on by the reptiles or birds, which first colonise and
abound on most oceanic islands. Gradations of structure, with each stage
beneficial to a changing species, will be favoured only under certain
peculiar conditions. A strictly terrestrial animal, by occasionally
hunting for food in shallow water, then in streams or lakes, might at last
be converted into an animal so thoroughly aquatic as to brave the open
ocean. But seals would not find on oceanic islands the conditions
favourable to their gradual reconversion into a terrestrial form. Bats, as
formerly shown, probably acquired their wings by at first gliding through
the air from tree to tree, like the so-called flying squirrels, for the
sake of escaping from their enemies, or for avoiding falls; but when the
power of true flight had once been acquired, it would never be reconverted
back, at least for the above purposes, into the less efficient power of
gliding through the air. Bats, might, indeed, like many birds, have had
their wings greatly reduced in size, or completely lost, through disuse;
but in this case it would be necessary that they should first have
acquired the power of running quickly on the ground, by the aid of their
hind legs alone, so as to compete with birds or other ground animals; and
for such a change a bat seems singularly ill-fitted. These conjectural
remarks have been made merely to show that a transition of structure, with
each step beneficial, is a highly complex affair; and that there is
nothing strange in a transition not having occurred in any particular
case.</p>
<p>Lastly, more than one writer has asked why have some animals had their
mental powers more highly developed than others, as such development would
be advantageous to all? Why have not apes acquired the intellectual powers
of man? Various causes could be assigned; but as they are conjectural, and
their relative probability cannot be weighed, it would be useless to give
them. A definite answer to the latter question ought not to be expected,
seeing that no one can solve the simpler problem, why, of two races of
savages, one has risen higher in the scale of civilisation than the other;
and this apparently implies increased brain power.</p>
<p>We will return to Mr. Mivart's other objections. Insects often resemble
for the sake of protection various objects, such as green or decayed
leaves, dead twigs, bits of lichen, flowers, spines, excrement of birds,
and living insects; but to this latter point I shall hereafter recur. The
resemblance is often wonderfully close, and is not confined to colour, but
extends to form, and even to the manner in which the insects hold
themselves. The caterpillars which project motionless like dead twigs from
the bushes on which they feed, offer an excellent instance of a
resemblance of this kind. The cases of the imitation of such objects as
the excrement of birds, are rare and exceptional. On this head, Mr. Mivart
remarks, "As, according to Mr. Darwin's theory, there is a constant
tendency to indefinite variation, and as the minute incipient variations
will be in ALL DIRECTIONS, they must tend to neutralize each other, and at
first to form such unstable modifications that it is difficult, if not
impossible, to see how such indefinite oscillations of infinitesimal
beginnings can ever build up a sufficiently appreciable resemblance to a
leaf, bamboo, or other object, for natural selection to seize upon and
perpetuate."</p>
<p>But in all the foregoing cases the insects in their original state no
doubt presented some rude and accidental resemblance to an object commonly
found in the stations frequented by them. Nor is this at all improbable,
considering the almost infinite number of surrounding objects and the
diversity in form and colour of the hosts of insects which exist. As some
rude resemblance is necessary for the first start, we can understand how
it is that the larger and higher animals do not (with the exception, as
far as I know, of one fish) resemble for the sake of protection special
objects, but only the surface which commonly surrounds them, and this
chiefly in colour. Assuming that an insect originally happened to resemble
in some degree a dead twig or a decayed leaf, and that it varied slightly
in many ways, then all the variations which rendered the insect at all
more like any such object, and thus favoured its escape, would be
preserved, while other variations would be neglected and ultimately lost;
or, if they rendered the insect at all less like the imitated object, they
would be eliminated. There would indeed be force in Mr. Mivart's
objection, if we were to attempt to account for the above resemblances,
independently of natural selection, through mere fluctuating variability;
but as the case stands there is none.</p>
<p>Nor can I see any force in Mr. Mivart's difficulty with respect to "the
last touches of perfection in the mimicry;" as in the case given by Mr.
Wallace, of a walking-stick insect (Ceroxylus laceratus), which resembles
"a stick grown over by a creeping moss or jungermannia." So close was this
resemblance, that a native Dyak maintained that the foliaceous
excrescences were really moss. Insects are preyed on by birds and other
enemies whose sight is probably sharper than ours, and every grade in
resemblance which aided an insect to escape notice or detection, would
tend towards its preservation; and the more perfect the resemblance so
much the better for the insect. Considering the nature of the differences
between the species in the group which includes the above Ceroxylus, there
is nothing improbable in this insect having varied in the irregularities
on its surface, and in these having become more or less green-coloured;
for in every group the characters which differ in the several species are
the most apt to vary, while the generic characters, or those common to all
the species, are the most constant.</p>
<p>The Greenland whale is one of the most wonderful animals in the world, and
the baleen, or whalebone, one of its greatest peculiarities. The baleen
consists of a row, on each side of the upper jaw, of about 300 plates or
laminae, which stand close together transversely to the longer axis of the
mouth. Within the main row there are some subsidiary rows. The extremities
and inner margins of all the plates are frayed into stiff bristles, which
clothe the whole gigantic palate, and serve to strain or sift the water,
and thus to secure the minute prey on which these great animals subsist.
The middle and longest lamina in the Greenland whale is ten, twelve, or
even fifteen feet in length; but in the different species of Cetaceans
there are gradations in length; the middle lamina being in one species,
according to Scoresby, four feet, in another three, in another eighteen
inches, and in the Balaenoptera rostrata only about nine inches in length.
The quality of the whalebone also differs in the different species.</p>
<p>With respect to the baleen, Mr. Mivart remarks that if it "had once
attained such a size and development as to be at all useful, then its
preservation and augmentation within serviceable limits would be promoted
by natural selection alone. But how to obtain the beginning of such useful
development?" In answer, it may be asked, why should not the early
progenitors of the whales with baleen have possessed a mouth constructed
something like the lamellated beak of a duck? Ducks, like whales, subsist
by sifting the mud and water; and the family has sometimes been called
Criblatores, or sifters. I hope that I may not be misconstrued into saying
that the progenitors of whales did actually possess mouths lamellated like
the beak of a duck. I wish only to show that this is not incredible, and
that the immense plates of baleen in the Greenland whale might have been
developed from such lamellae by finely graduated steps, each of service to
its possessor.</p>
<p>The beak of a shoveller-duck (Spatula clypeata) is a more beautiful and
complex structure than the mouth of a whale. The upper mandible is
furnished on each side (in the specimen examined by me) with a row or comb
formed of 188 thin, elastic lamellae, obliquely bevelled so as to be
pointed, and placed transversely to the longer axis of the mouth. They
arise from the palate, and are attached by flexible membrane to the sides
of the mandible. Those standing towards the middle are the longest, being
about one-third of an inch in length, and they project fourteen
one-hundredths of an inch beneath the edge. At their bases there is a
short subsidiary row of obliquely transverse lamellae. In these several
respects they resemble the plates of baleen in the mouth of a whale. But
towards the extremity of the beak they differ much, as they project
inward, instead of straight downward. The entire head of the shoveller,
though incomparably less bulky, is about one-eighteenth of the length of
the head of a moderately large Balaenoptera rostrata, in which species the
baleen is only nine inches long; so that if we were to make the head of
the shoveller as long as that of the Balaenoptera, the lamellae would be
six inches in length, that is, two-thirds of the length of the baleen in
this species of whale. The lower mandible of the shoveller-duck is
furnished with lamellae of equal length with these above, but finer; and
in being thus furnished it differs conspicuously from the lower jaw of a
whale, which is destitute of baleen. On the other hand, the extremities of
these lower lamellae are frayed into fine bristly points, so that they
thus curiously resemble the plates of baleen. In the genus Prion, a member
of the distinct family of the Petrels, the upper mandible alone is
furnished with lamellae, which are well developed and project beneath the
margin; so that the beak of this bird resembles in this respect the mouth
of a whale.</p>
<p>From the highly developed structure of the shoveller's beak we may proceed
(as I have learned from information and specimens sent to me by Mr.
Salvin), without any great break, as far as fitness for sifting is
concerned, through the beak of the Merganetta armata, and in some respects
through that of the Aix sponsa, to the beak of the common duck. In this
latter species the lamellae are much coarser than in the shoveller, and
are firmly attached to the sides of the mandible; they are only about
fifty in number on each side, and do not project at all beneath the
margin. They are square-topped, and are edged with translucent, hardish
tissue, as if for crushing food. The edges of the lower mandible are
crossed by numerous fine ridges, which project very little. Although the
beak is thus very inferior as a sifter to that of a shoveller, yet this
bird, as every one knows, constantly uses it for this purpose. There are
other species, as I hear from Mr. Salvin, in which the lamellae are
considerably less developed than in the common duck; but I do not know
whether they use their beaks for sifting the water.</p>
<p>Turning to another group of the same family. In the Egyptian goose
(Chenalopex) the beak closely resembles that of the common duck; but the
lamellae are not so numerous, nor so distinct from each other, nor do they
project so much inward; yet this goose, as I am informed by Mr. E.
Bartlett, "uses its bill like a duck by throwing the water out at the
corners." Its chief food, however, is grass, which it crops like the
common goose. In this latter bird the lamellae of the upper mandible are
much coarser than in the common duck, almost confluent, about twenty-seven
in number on each side, and terminating upward in teeth-like knobs. The
palate is also covered with hard rounded knobs. The edges of the lower
mandible are serrated with teeth much more prominent, coarser and sharper
than in the duck. The common goose does not sift the water, but uses its
beak exclusively for tearing or cutting herbage, for which purpose it is
so well fitted that it can crop grass closer than almost any other animal.
There are other species of geese, as I hear from Mr. Bartlett, in which
the lamellae are less developed than in the common goose.</p>
<p>We thus see that a member of the duck family, with a beak constructed like
that of a common goose and adapted solely for grazing, or even a member
with a beak having less well-developed lamellae, might be converted by
small changes into a species like the Egyptian goose—this into one
like the common duck—and, lastly, into one like the shoveller,
provided with a beak almost exclusively adapted for sifting the water; for
this bird could hardly use any part of its beak, except the hooked tip,
for seizing or tearing solid food. The beak of a goose, as I may add,
might also be converted by small changes into one provided with prominent,
recurved teeth, like those of the Merganser (a member of the same family),
serving for the widely different purpose of securing live fish.</p>
<p>Returning to the whales. The Hyperoodon bidens is destitute of true teeth
in an efficient condition, but its palate is roughened, according to
Lacepede, with small unequal, hard points of horn. There is, therefore,
nothing improbable in supposing that some early Cetacean form was provided
with similar points of horn on the palate, but rather more regularly
placed, and which, like the knobs on the beak of the goose, aided it in
seizing or tearing its food. If so, it will hardly be denied that the
points might have been converted through variation and natural selection
into lamellae as well-developed as those of the Egyptian goose, in which
case they would have been used both for seizing objects and for sifting
the water; then into lamellae like those of the domestic duck; and so
onward, until they became as well constructed as those of the shoveller,
in which case they would have served exclusively as a sifting apparatus.
From this stage, in which the lamellae would be two-thirds of the length
of the plates of baleen in the Balaenoptera rostrata, gradations, which
may be observed in still-existing Cetaceans, lead us onward to the
enormous plates of baleen in the Greenland whale. Nor is there the least
reason to doubt that each step in this scale might have been as
serviceable to certain ancient Cetaceans, with the functions of the parts
slowly changing during the progress of development, as are the gradations
in the beaks of the different existing members of the duck-family. We
should bear in mind that each species of duck is subjected to a severe
struggle for existence, and that the structure of every part of its frame
must be well adapted to its conditions of life.</p>
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