<p><SPAN name="link2HCH0014" id="link2HCH0014"></SPAN></p>
<h2> CHAPTER XIV. MUTUAL AFFINITIES OF ORGANIC BEINGS: </h2>
<h3> MORPHOLOGY—EMBRYOLOGY—RUDIMENTARY ORGANS. </h3>
<p>Classification, groups subordinate to groups—Natural system—Rules and<br/>
difficulties in classification, explained on the theory of descent<br/>
with modification—Classification of varieties—Descent always used in<br/>
classification—Analogical or adaptive characters—Affinities,<br/>
general, complex and radiating—Extinction separates and defines<br/>
groups—Morphology, between members of the same class, between parts of<br/>
the same individual—Embryology, laws of, explained by variations not<br/>
supervening at an early age, and being inherited at a corresponding<br/>
age—Rudimentary organs; their origin explained—Summary.<br/></p>
<p>CLASSIFICATION.</p>
<p>From the most remote period in the history of the world organic beings
have been found to resemble each other in descending degrees, so that they
can be classed in groups under groups. This classification is not
arbitrary like the grouping of the stars in constellations. The existence
of groups would have been of simple significance, if one group had been
exclusively fitted to inhabit the land, and another the water; one to feed
on flesh, another on vegetable matter, and so on; but the case is widely
different, for it is notorious how commonly members of even the same
subgroup have different habits. In the second and fourth chapters, on
Variation and on Natural Selection, I have attempted to show that within
each country it is the widely ranging, the much diffused and common, that
is the dominant species, belonging to the larger genera in each class,
which vary most. The varieties, or incipient species, thus produced,
ultimately become converted into new and distinct species; and these, on
the principle of inheritance, tend to produce other new and dominant
species. Consequently the groups which are now large, and which generally
include many dominant species, tend to go on increasing in size. I further
attempted to show that from the varying descendants of each species trying
to occupy as many and as different places as possible in the economy of
nature, they constantly tend to diverge in character. This latter
conclusion is supported by observing the great diversity of forms, which,
in any small area, come into the closest competition, and by certain facts
in naturalisation.</p>
<p>I attempted also to show that there is a steady tendency in the forms
which are increasing in number and diverging in character, to supplant and
exterminate the preceding, less divergent and less improved forms. I
request the reader to turn to the diagram illustrating the action, as
formerly explained, of these several principles; and he will see that the
inevitable result is, that the modified descendants proceeding from one
progenitor become broken up into groups subordinate to groups. In the
diagram each letter on the uppermost line may represent a genus including
several species; and the whole of the genera along this upper line form
together one class, for all are descended from one ancient parent, and,
consequently, have inherited something in common. But the three genera on
the left hand have, on this same principle, much in common, and form a
subfamily, distinct from that containing the next two genera on the right
hand, which diverged from a common parent at the fifth stage of descent.
These five genera have also much in common, though less than when grouped
in subfamilies; and they form a family distinct from that containing the
three genera still further to the right hand, which diverged at an earlier
period. And all these genera, descended from (A), form an order distinct
from the genera descended from (I). So that we here have many species
descended from a single progenitor grouped into genera; and the genera
into subfamilies, families and orders, all under one great class. The
grand fact of the natural subordination of organic beings in groups under
groups, which, from its familiarity, does not always sufficiently strike
us, is in my judgment thus explained. No doubt organic beings, like all
other objects, can be classed in many ways, either artificially by single
characters, or more naturally by a number of characters. We know, for
instance, that minerals and the elemental substances can be thus arranged.
In this case there is of course no relation to genealogical succession,
and no cause can at present be assigned for their falling into groups. But
with organic beings the case is different, and the view above given
accords with their natural arrangement in group under group; and no other
explanation has ever been attempted.</p>
<p>Naturalists, as we have seen, try to arrange the species, genera and
families in each class, on what is called the Natural System. But what is
meant by this system? Some authors look at it merely as a scheme for
arranging together those living objects which are most alike, and for
separating those which are most unlike; or as an artificial method of
enunciating, as briefly as possible, general propositions—that is,
by one sentence to give the characters common, for instance, to all
mammals, by another those common to all carnivora, by another those common
to the dog-genus, and then, by adding a single sentence, a full
description is given of each kind of dog. The ingenuity and utility of
this system are indisputable. But many naturalists think that something
more is meant by the Natural System; they believe that it reveals the plan
of the Creator; but unless it be specified whether order in time or space,
or both, or what else is meant by the plan of the Creator, it seems to me
that nothing is thus added to our knowledge. Expressions such as that
famous one by Linnaeus, which we often meet with in a more or less
concealed form, namely, that the characters do not make the genus, but
that the genus gives the characters, seem to imply that some deeper bond
is included in our classifications than mere resemblance. I believe that
this is the case, and that community of descent—the one known cause
of close similarity in organic beings—is the bond, which, though
observed by various degrees of modification, is partially revealed to us
by our classifications.</p>
<p>Let us now consider the rules followed in classification, and the
difficulties which are encountered on the view that classification either
gives some unknown plan of creation, or is simply a scheme for enunciating
general propositions and of placing together the forms most like each
other. It might have been thought (and was in ancient times thought) that
those parts of the structure which determined the habits of life, and the
general place of each being in the economy of nature, would be of very
high importance in classification. Nothing can be more false. No one
regards the external similarity of a mouse to a shrew, of a dugong to a
whale, of a whale to a fish, as of any importance. These resemblances,
though so intimately connected with the whole life of the being, are
ranked as merely "adaptive or analogical characters;" but to the
consideration of these resemblances we shall recur. It may even be given
as a general rule, that the less any part of the organisation is concerned
with special habits, the more important it becomes for classification. As
an instance: Owen, in speaking of the dugong, says, "The generative
organs, being those which are most remotely related to the habits and food
of an animal, I have always regarded as affording very clear indications
of its true affinities. We are least likely in the modifications of these
organs to mistake a merely adaptive for an essential character." With
plants how remarkable it is that the organs of vegetation, on which their
nutrition and life depend, are of little signification; whereas the organs
of reproduction, with their product the seed and embryo, are of paramount
importance! So again, in formerly discussing certain morphological
characters which are not functionally important, we have seen that they
are often of the highest service in classification. This depends on their
constancy throughout many allied groups; and their constancy chiefly
depends on any slight deviations not having been preserved and accumulated
by natural selection, which acts only on serviceable characters.</p>
<p>That the mere physiological importance of an organ does not determine its
classificatory value, is almost proved by the fact, that in allied groups,
in which the same organ, as we have every reason to suppose, has nearly
the same physiological value, its classificatory value is widely
different. No naturalist can have worked at any group without being struck
with this fact; and it has been fully acknowledged in the writings of
almost every author. It will suffice to quote the highest authority,
Robert Brown, who, in speaking of certain organs in the Proteaceae, says
their generic importance, "like that of all their parts, not only in this,
but, as I apprehend in every natural family, is very unequal, and in some
cases seems to be entirely lost." Again, in another work he says, the
genera of the Connaraceae "differ in having one or more ovaria, in the
existence or absence of albumen, in the imbricate or valvular aestivation.
Any one of these characters singly is frequently of more than generic
importance, though here even, when all taken together, they appear
insufficient to separate Cnestis from Connarus." To give an example among
insects: in one great division of the Hymenoptera, the antennae, as
Westwood has remarked, are most constant in structure; in another division
they differ much, and the differences are of quite subordinate value in
classification; yet no one will say that the antennae in these two
divisions of the same order are of unequal physiological importance. Any
number of instances could be given of the varying importance for
classification of the same important organ within the same group of
beings.</p>
<p>Again, no one will say that rudimentary or atrophied organs are of high
physiological or vital importance; yet, undoubtedly, organs in this
condition are often of much value in classification. No one will dispute
that the rudimentary teeth in the upper jaws of young ruminants, and
certain rudimentary bones of the leg, are highly serviceable in exhibiting
the close affinity between Ruminants and Pachyderms. Robert Brown has
strongly insisted on the fact that the position of the rudimentary florets
is of the highest importance in the classification of the Grasses.</p>
<p>Numerous instances could be given of characters derived from parts which
must be considered of very trifling physiological importance, but which
are universally admitted as highly serviceable in the definition of whole
groups. For instance, whether or not there is an open passage from the
nostrils to the mouth, the only character, according to Owen, which
absolutely distinguishes fishes and reptiles—the inflection of the
angle of the lower jaw in Marsupials—the manner in which the wings
of insects are folded—mere colour in certain Algae—mere
pubescence on parts of the flower in grasses—the nature of the
dermal covering, as hair or feathers, in the Vertebrata. If the
Ornithorhynchus had been covered with feathers instead of hair, this
external and trifling character would have been considered by naturalists
as an important aid in determining the degree of affinity of this strange
creature to birds.</p>
<p>The importance, for classification, of trifling characters, mainly depends
on their being correlated with many other characters of more or less
importance. The value indeed of an aggregate of characters is very evident
in natural history. Hence, as has often been remarked, a species may
depart from its allies in several characters, both of high physiological
importance, and of almost universal prevalence, and yet leave us in no
doubt where it should be ranked. Hence, also, it has been found that a
classification founded on any single character, however important that may
be, has always failed; for no part of the organisation is invariably
constant. The importance of an aggregate of characters, even when none are
important, alone explains the aphorism enunciated by Linnaeus, namely,
that the characters do not give the genus, but the genus gives the
character; for this seems founded on the appreciation of many trifling
points of resemblance, too slight to be defined. Certain plants, belonging
to the Malpighiaceae, bear perfect and degraded flowers; in the latter, as
A. de Jussieu has remarked, "The greater number of the characters proper
to the species, to the genus, to the family, to the class, disappear, and
thus laugh at our classification." When Aspicarpa produced in France,
during several years, only these degraded flowers, departing so
wonderfully in a number of the most important points of structure from the
proper type of the order, yet M. Richard sagaciously saw, as Jussieu
observes, that this genus should still be retained among the
Malpighiaceae. This case well illustrates the spirit of our
classifications.</p>
<p>Practically, when naturalists are at work, they do not trouble themselves
about the physiological value of the characters which they use in defining
a group or in allocating any particular species. If they find a character
nearly uniform, and common to a great number of forms, and not common to
others, they use it as one of high value; if common to some lesser number,
they use it as of subordinate value. This principle has been broadly
confessed by some naturalists to be the true one; and by none more clearly
than by that excellent botanist, Aug. St. Hilaire. If several trifling
characters are always found in combination, though no apparent bond of
connexion can be discovered between them, especial value is set on them.
As in most groups of animals, important organs, such as those for
propelling the blood, or for aerating it, or those for propagating the
race, are found nearly uniform, they are considered as highly serviceable
in classification; but in some groups all these, the most important vital
organs, are found to offer characters of quite subordinate value. Thus, as
Fritz Muller has lately remarked, in the same group of crustaceans,
Cypridina is furnished with a heart, while in two closely allied genera,
namely Cypris and Cytherea, there is no such organ; one species of
Cypridina has well-developed branchiae, while another species is destitute
of them.</p>
<p>We can see why characters derived from the embryo should be of equal
importance with those derived from the adult, for a natural classification
of course includes all ages. But it is by no means obvious, on the
ordinary view, why the structure of the embryo should be more important
for this purpose than that of the adult, which alone plays its full part
in the economy of nature. Yet it has been strongly urged by those great
naturalists, Milne Edwards and Agassiz, that embryological characters are
the most important of all; and this doctrine has very generally been
admitted as true. Nevertheless, their importance has sometimes been
exaggerated, owing to the adaptive characters of larvae not having been
excluded; in order to show this, Fritz Muller arranged, by the aid of such
characters alone, the great class of crustaceans, and the arrangement did
not prove a natural one. But there can be no doubt that embryonic,
excluding larval characters, are of the highest value for classification,
not only with animals but with plants. Thus the main divisions of
flowering plants are founded on differences in the embryo—on the
number and position of the cotyledons, and on the mode of development of
the plumule and radicle. We shall immediately see why these characters
possess so high a value in classification, namely, from the natural system
being genealogical in its arrangement.</p>
<p>Our classifications are often plainly influenced by chains of affinities.
Nothing can be easier than to define a number of characters common to all
birds; but with crustaceans, any such definition has hitherto been found
impossible. There are crustaceans at the opposite ends of the series,
which have hardly a character in common; yet the species at both ends,
from being plainly allied to others, and these to others, and so onwards,
can be recognised as unequivocally belonging to this, and to no other
class of the Articulata.</p>
<p>Geographical distribution has often been used, though perhaps not quite
logically, in classification, more especially in very large groups of
closely allied forms. Temminck insists on the utility or even necessity of
this practice in certain groups of birds; and it has been followed by
several entomologists and botanists.</p>
<p>Finally, with respect to the comparative value of the various groups of
species, such as orders, suborders, families, subfamilies, and genera,
they seem to be, at least at present, almost arbitrary. Several of the
best botanists, such as Mr. Bentham and others, have strongly insisted on
their arbitrary value. Instances could be given among plants and insects,
of a group first ranked by practised naturalists as only a genus, and then
raised to the rank of a subfamily or family; and this has been done, not
because further research has detected important structural differences, at
first overlooked, but because numerous allied species, with slightly
different grades of difference, have been subsequently discovered.</p>
<p>All the foregoing rules and aids and difficulties in classification may be
explained, if I do not greatly deceive myself, on the view that the
natural system is founded on descent with modification—that the
characters which naturalists consider as showing true affinity between any
two or more species, are those which have been inherited from a common
parent, all true classification being genealogical—that community of
descent is the hidden bond which naturalists have been unconsciously
seeking, and not some unknown plan of creation, or the enunciation of
general propositions, and the mere putting together and separating objects
more or less alike.</p>
<p>But I must explain my meaning more fully. I believe that the ARRANGEMENT
of the groups within each class, in due subordination and relation to each
other, must be strictly genealogical in order to be natural; but that the
AMOUNT of difference in the several branches or groups, though allied in
the same degree in blood to their common progenitor, may differ greatly,
being due to the different degrees of modification which they have
undergone; and this is expressed by the forms being ranked under different
genera, families, sections or orders. The reader will best understand what
is meant, if he will take the trouble to refer to the diagram in the
fourth chapter. We will suppose the letters A to L to represent allied
genera existing during the Silurian epoch, and descended from some still
earlier form. In three of these genera (A, F, and I) a species has
transmitted modified descendants to the present day, represented by the
fifteen genera (a14 to z14) on the uppermost horizontal line. Now, all
these modified descendants from a single species are related in blood or
descent in the same degree. They may metaphorically be called cousins to
the same millionth degree, yet they differ widely and in different degrees
from each other. The forms descended from A, now broken up into two or
three families, constitute a distinct order from those descended from I,
also broken up into two families. Nor can the existing species descended
from A be ranked in the same genus with the parent A, or those from I with
parent I. But the existing genus F14 may be supposed to have been but
slightly modified, and it will then rank with the parent genus F; just as
some few still living organisms belong to Silurian genera. So that the
comparative value of the differences between these organic beings, which
are all related to each other in the same degree in blood, has come to be
widely different. Nevertheless, their genealogical ARRANGEMENT remains
strictly true, not only at the present time, but at each successive period
of descent. All the modified descendants from A will have inherited
something in common from their common parent, as will all the descendants
from I; so will it be with each subordinate branch of descendants at each
successive stage. If, however, we suppose any descendant of A or of I to
have become so much modified as to have lost all traces of its parentage
in this case, its place in the natural system will be lost, as seems to
have occurred with some few existing organisms. All the descendants of the
genus F, along its whole line of descent, are supposed to have been but
little modified, and they form a single genus. But this genus, though much
isolated, will still occupy its proper intermediate position. The
representation of the groups as here given in the diagram on a flat
surface, is much too simple. The branches ought to have diverged in all
directions. If the names of the groups had been simply written down in a
linear series the representation would have been still less natural; and
it is notoriously not possible to represent in a series, on a flat
surface, the affinities which we discover in nature among the beings of
the same group. Thus, the natural system is genealogical in its
arrangement, like a pedigree. But the amount of modification which the
different groups have undergone has to be expressed by ranking them under
different so-called genera, subfamilies, families, sections, orders, and
classes.</p>
<p>It may be worth while to illustrate this view of classification, by taking
the case of languages. If we possessed a perfect pedigree of mankind, a
genealogical arrangement of the races of man would afford the best
classification of the various languages now spoken throughout the world;
and if all extinct languages, and all intermediate and slowly changing
dialects, were to be included, such an arrangement would be the only
possible one. Yet it might be that some ancient languages had altered very
little and had given rise to few new languages, whilst others had altered
much owing to the spreading, isolation and state of civilisation of the
several co-descended races, and had thus given rise to many new dialects
and languages. The various degrees of difference between the languages of
the same stock would have to be expressed by groups subordinate to groups;
but the proper or even the only possible arrangement would still be
genealogical; and this would be strictly natural, as it would connect
together all languages, extinct and recent, by the closest affinities, and
would give the filiation and origin of each tongue.</p>
<p>In confirmation of this view, let us glance at the classification of
varieties, which are known or believed to be descended from a single
species. These are grouped under the species, with the subvarieties under
the varieties; and in some cases, as with the domestic pigeon, with
several other grades of difference. Nearly the same rules are followed as
in classifying species. Authors have insisted on the necessity of
arranging varieties on a natural instead of an artificial system; we are
cautioned, for instance, not to class two varieties of the pine-apple
together, merely because their fruit, though the most important part,
happens to be nearly identical; no one puts the Swedish and common turnip
together, though the esculent and thickened stems are so similar. Whatever
part is found to be most constant, is used in classing varieties: thus the
great agriculturist Marshall says the horns are very useful for this
purpose with cattle, because they are less variable than the shape or
colour of the body, etc.; whereas with sheep the horns are much less
serviceable, because less constant. In classing varieties, I apprehend
that if we had a real pedigree, a genealogical classification would be
universally preferred; and it has been attempted in some cases. For we
might feel sure, whether there had been more or less modification, that
the principle of inheritance would keep the forms together which were
allied in the greatest number of points. In tumbler pigeons, though some
of the subvarieties differ in the important character of the length of the
beak, yet all are kept together from having the common habit of tumbling;
but the short-faced breed has nearly or quite lost this habit;
nevertheless, without any thought on the subject, these tumblers are kept
in the same group, because allied in blood and alike in some other
respects.</p>
<p>With species in a state of nature, every naturalist has in fact brought
descent into his classification; for he includes in his lowest grade, that
of species, the two sexes; and how enormously these sometimes differ in
the most important characters is known to every naturalist: scarcely a
single fact can be predicated in common of the adult males and
hermaphrodites of certain cirripedes, and yet no one dreams of separating
them. As soon as the three Orchidean forms, Monachanthus, Myanthus, and
Catasetum, which had previously been ranked as three distinct genera, were
known to be sometimes produced on the same plant, they were immediately
considered as varieties; and now I have been able to show that they are
the male, female, and hermaphrodite forms of the same species. The
naturalist includes as one species the various larval stages of the same
individual, however much they may differ from each other and from the
adult; as well as the so-called alternate generations of Steenstrup, which
can only in a technical sense be considered as the same individual. He
includes monsters and varieties, not from their partial resemblance to the
parent-form, but because they are descended from it.</p>
<p>As descent has universally been used in classing together the individuals
of the same species, though the males and females and larvae are sometimes
extremely different; and as it has been used in classing varieties which
have undergone a certain, and sometimes a considerable amount of
modification, may not this same element of descent have been unconsciously
used in grouping species under genera, and genera under higher groups, all
under the so-called natural system? I believe it has been unconsciously
used; and thus only can I understand the several rules and guides which
have been followed by our best systematists. As we have no written
pedigrees, we are forced to trace community of descent by resemblances of
any kind. Therefore, we choose those characters which are the least likely
to have been modified, in relation to the conditions of life to which each
species has been recently exposed. Rudimentary structures on this view are
as good as, or even sometimes better than other parts of the organisation.
We care not how trifling a character may be—let it be the mere
inflection of the angle of the jaw, the manner in which an insect's wing
is folded, whether the skin be covered by hair or feathers—if it
prevail throughout many and different species, especially those having
very different habits of life, it assumes high value; for we can account
for its presence in so many forms with such different habits, only by
inheritance from a common parent. We may err in this respect in regard to
single points of structure, but when several characters, let them be ever
so trifling, concur throughout a large group of beings having different
habits, we may feel almost sure, on the theory of descent, that these
characters have been inherited from a common ancestor; and we know that
such aggregated characters have especial value in classification.</p>
<p>We can understand why a species or a group of species may depart from its
allies, in several of its most important characteristics, and yet be
safely classed with them. This may be safely done, and is often done, as
long as a sufficient number of characters, let them be ever so
unimportant, betrays the hidden bond of community of descent. Let two
forms have not a single character in common, yet, if these extreme forms
are connected together by a chain of intermediate groups, we may at once
infer their community of descent, and we put them all into the same class.
As we find organs of high physiological importance—those which serve
to preserve life under the most diverse conditions of existence—are
generally the most constant, we attach especial value to them; but if
these same organs, in another group or section of a group, are found to
differ much, we at once value them less in our classification. We shall
presently see why embryological characters are of such high classificatory
importance. Geographical distribution may sometimes be brought usefully
into play in classing large genera, because all the species of the same
genus, inhabiting any distinct and isolated region, are in all probability
descended from the same parents.</p>
<p>ANALOGICAL RESEMBLANCES.</p>
<p>We can understand, on the above views, the very important distinction
between real affinities and analogical or adaptive resemblances. Lamarck
first called attention to this subject, and he has been ably followed by
Macleay and others. The resemblance in the shape of the body and in the
fin-like anterior limbs between dugongs and whales, and between these two
orders of mammals and fishes, are analogical. So is the resemblance
between a mouse and a shrew-mouse (Sorex), which belong to different
orders; and the still closer resemblance, insisted on by Mr. Mivart,
between the mouse and a small marsupial animal (Antechinus) of Australia.
These latter resemblances may be accounted for, as it seems to me, by
adaptation for similarly active movements through thickets and herbage,
together with concealment from enemies.</p>
<p>Among insects there are innumerable instances; thus Linnaeus, misled by
external appearances, actually classed an homopterous insect as a moth. We
see something of the same kind even with our domestic varieties, as in the
strikingly similar shape of the body in the improved breeds of the Chinese
and common pig, which are descended from distinct species; and in the
similarly thickened stems of the common and specifically distinct Swedish
turnip. The resemblance between the greyhound and race-horse is hardly
more fanciful than the analogies which have been drawn by some authors
between widely different animals.</p>
<p>On the view of characters being of real importance for classification,
only in so far as they reveal descent, we can clearly understand why
analogical or adaptive characters, although of the utmost importance to
the welfare of the being, are almost valueless to the systematist. For
animals, belonging to two most distinct lines of descent, may have become
adapted to similar conditions, and thus have assumed a close external
resemblance; but such resemblances will not reveal—will rather tend
to conceal their blood-relationship. We can thus also understand the
apparent paradox, that the very same characters are analogical when one
group is compared with another, but give true affinities when the members
of the same group are compared together: thus the shape of the body and
fin-like limbs are only analogical when whales are compared with fishes,
being adaptations in both classes for swimming through the water; but
between the the several members of the whale family, the shape of the body
and the fin-like limbs offer characters exhibiting true affinity; for as
these parts are so nearly similar throughout the whole family, we cannot
doubt that they have been inherited from a common ancestor. So it is with
fishes.</p>
<p>Numerous cases could be given of striking resemblances in quite distinct
beings between single parts or organs, which have been adapted for the
same functions. A good instance is afforded by the close resemblance of
the jaws of the dog and Tasmanian wolf or Thylacinus—animals which
are widely sundered in the natural system. But this resemblance is
confined to general appearance, as in the prominence of the canines, and
in the cutting shape of the molar teeth. For the teeth really differ much:
thus the dog has on each side of the upper jaw four pre-molars and only
two molars; while the Thylacinus has three pre-molars and four molars. The
molars also differ much in the two animals in relative size and structure.
The adult dentition is preceded by a widely different milk dentition. Any
one may, of course, deny that the teeth in either case have been adapted
for tearing flesh, through the natural selection of successive variations;
but if this be admitted in the one case, it is unintelligible to me that
it should be denied in the other. I am glad to find that so high an
authority as Professor Flower has come to this same conclusion.</p>
<p>The extraordinary cases given in a former chapter, of widely different
fishes possessing electric organs—of widely different insects
possessing luminous organs—and of orchids and asclepiads having
pollen-masses with viscid discs, come under this same head of analogical
resemblances. But these cases are so wonderful that they were introduced
as difficulties or objections to our theory. In all such cases some
fundamental difference in the growth or development of the parts, and
generally in their matured structure, can be detected. The end gained is
the same, but the means, though appearing superficially to be the same,
are essentially different. The principle formerly alluded to under the
term of ANALOGICAL VARIATION has probably in these cases often come into
play; that is, the members of the same class, although only distantly
allied, have inherited so much in common in their constitution, that they
are apt to vary under similar exciting causes in a similar manner; and
this would obviously aid in the acquirement through natural selection of
parts or organs, strikingly like each other, independently of their direct
inheritance from a common progenitor.</p>
<p>As species belonging to distinct classes have often been adapted by
successive slight modifications to live under nearly similar circumstances—to
inhabit, for instance, the three elements of land, air and water—we
can perhaps understand how it is that a numerical parallelism has
sometimes been observed between the subgroups of distinct classes. A
naturalist, struck with a parallelism of this nature, by arbitrarily
raising or sinking the value of the groups in several classes (and all our
experience shows that their valuation is as yet arbitrary), could easily
extend the parallelism over a wide range; and thus the septenary, quinary,
quaternary and ternary classifications have probably arisen.</p>
<p>There is another and curious class of cases in which close external
resemblance does not depend on adaptation to similar habits of life, but
has been gained for the sake of protection. I allude to the wonderful
manner in which certain butterflies imitate, as first described by Mr.
Bates, other and quite distinct species. This excellent observer has shown
that in some districts of South America, where, for instance, an Ithomia
abounds in gaudy swarms, another butterfly, namely, a Leptalis, is often
found mingled in the same flock; and the latter so closely resembles the
Ithomia in every shade and stripe of colour, and even in the shape of its
wings, that Mr. Bates, with his eyes sharpened by collecting during eleven
years, was, though always on his guard, continually deceived. When the
mockers and the mocked are caught and compared, they are found to be very
different in essential structure, and to belong not only to distinct
genera, but often to distinct families. Had this mimicry occurred in only
one or two instances, it might have been passed over as a strange
coincidence. But, if we proceed from a district where one Leptalis
imitates an Ithomia, another mocking and mocked species, belonging to the
same two genera, equally close in their resemblance, may be found.
Altogether no less than ten genera are enumerated, which include species
that imitate other butterflies. The mockers and mocked always inhabit the
same region; we never find an imitator living remote from the form which
it imitates. The mockers are almost invariably rare insects; the mocked in
almost every case abounds in swarms. In the same district in which a
species of Leptalis closely imitates an Ithomia, there are sometimes other
Lepidoptera mimicking the same Ithomia: so that in the same place, species
of three genera of butterflies and even a moth are found all closely
resembling a butterfly belonging to a fourth genus. It deserves especial
notice that many of the mimicking forms of the Leptalis, as well as of the
mimicked forms, can be shown by a graduated series to be merely varieties
of the same species; while others are undoubtedly distinct species. But
why, it may be asked, are certain forms treated as the mimicked and others
as the mimickers? Mr. Bates satisfactorily answers this question by
showing that the form which is imitated keeps the usual dress of the group
to which it belongs, while the counterfeiters have changed their dress and
do not resemble their nearest allies.</p>
<p>We are next led to enquire what reason can be assigned for certain
butterflies and moths so often assuming the dress of another and quite
distinct form; why, to the perplexity of naturalists, has nature
condescended to the tricks of the stage? Mr. Bates has, no doubt, hit on
the true explanation. The mocked forms, which always abound in numbers,
must habitually escape destruction to a large extent, otherwise they could
not exist in such swarms; and a large amount of evidence has now been
collected, showing that they are distasteful to birds and other
insect-devouring animals. The mocking forms, on the other hand, that
inhabit the same district, are comparatively rare, and belong to rare
groups; hence, they must suffer habitually from some danger, for
otherwise, from the number of eggs laid by all butterflies, they would in
three or four generations swarm over the whole country. Now if a member of
one of these persecuted and rare groups were to assume a dress so like
that of a well-protected species that it continually deceived the
practised eyes of an entomologist, it would often deceive predaceous birds
and insects, and thus often escape destruction. Mr. Bates may almost be
said to have actually witnessed the process by which the mimickers have
come so closely to resemble the mimicked; for he found that some of the
forms of Leptalis which mimic so many other butterflies, varied in an
extreme degree. In one district several varieties occurred, and of these
one alone resembled, to a certain extent, the common Ithomia of the same
district. In another district there were two or three varieties, one of
which was much commoner than the others, and this closely mocked another
form of Ithomia. From facts of this nature, Mr. Bates concludes that the
Leptalis first varies; and when a variety happens to resemble in some
degree any common butterfly inhabiting the same district, this variety,
from its resemblance to a flourishing and little persecuted kind, has a
better chance of escaping destruction from predaceous birds and insects,
and is consequently oftener preserved; "the less perfect degrees of
resemblance being generation after generation eliminated, and only the
others left to propagate their kind." So that here we have an excellent
illustration of natural selection.</p>
<p>Messrs. Wallace and Trimen have likewise described several equally
striking cases of imitation in the Lepidoptera of the Malay Archipelago
and Africa, and with some other insects. Mr. Wallace has also detected one
such case with birds, but we have none with the larger quadrupeds. The
much greater frequency of imitation with insects than with other animals,
is probably the consequence of their small size; insects cannot defend
themselves, excepting indeed the kinds furnished with a sting, and I have
never heard of an instance of such kinds mocking other insects, though
they are mocked; insects cannot easily escape by flight from the larger
animals which prey on them; therefore, speaking metaphorically, they are
reduced, like most weak creatures, to trickery and dissimulation.</p>
<p>It should be observed that the process of imitation probably never
commenced between forms widely dissimilar in colour. But, starting with
species already somewhat like each other, the closest resemblance, if
beneficial, could readily be gained by the above means, and if the
imitated form was subsequently and gradually modified through any agency,
the imitating form would be led along the same track, and thus be altered
to almost any extent, so that it might ultimately assume an appearance or
colouring wholly unlike that of the other members of the family to which
it belonged. There is, however, some difficulty on this head, for it is
necessary to suppose in some cases that ancient members belonging to
several distinct groups, before they had diverged to their present extent,
accidentally resembled a member of another and protected group in a
sufficient degree to afford some slight protection, this having given the
basis for the subsequent acquisition of the most perfect resemblance.</p>
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