The second objection just named appears to suppose a simultaneous march

of all organic beings from form to form--a transmutation _en masse_ of

the whole--so that to any one among them they would all appear

stationary. Such a view is utterly opposed to the greater number of

zoological and palæontological facts, and to all the necessities of the

Darwinian hypothesis. One species, either with little inherent capacity

for variation, or so circumstanced that such variation as may have

occurred in different individuals has never been accumulated by

selection, may remain without alteration for ages, while other species

differently constituted or circumstanced may have undergone vast

transmutations during the same period. In fact, the derivative

hypothesis is not a theory of things long ago; it is not a curious

speculation into the beginnings of the present condition of things. It

may be appealed to every day in the solution of constantly occurring

problems in morphology.

I will give an example from the subject of our present course. There is

in Australia an animal, the koala (_Phascolarctos cinereus_), rather

larger than a cat, but having more the aspect of a small bear (Fig. 1).

It is covered with a soft woolly fur, and lives entirely among the

boughs of trees, on the leaves of which it feeds. Its tail is a mere

rudiment. Its feet are admirably adapted for grasping the branches on

which it climbs. The hind feet especially are remarkably modified for

this end, being very broad, and having a strong prehensile or opposable

inner toe or hallux, like a thumb. The skeleton of that foot is very

singular (see Fig. 2). The hallux is stout, and placed nearly at a right

angle with the other toes. The next two digits are rather slender,

placed close together, and in the living animal are united almost to the

claws in a common integument. The two outer toes are free and much

stouter than the others, the fourth especially so.

Now, a naturalist of the last century would have looked upon this foot

simply as a piece of machinery beautifully

[Illustration: FIG. 1.--The Koala (_Phascolarctos cinereus_). From

_Gould’s Mammals of Australia_.]

adapted for the particular work it had to perform in the animal’s life.

He would have pointed to the broad palm, the

[Illustration: FIG. 2.--Skeleton of the hind foot of the Koala

(_Phascolarctos cinereus_).]

opposable great toe, and would doubtless, if a worthy representative of

his school, have developed some ingenious theory to show that the

smaller size of the second and third toes, and that being wrapped up to

their ends in skin, added to the efficiency of the foot as a climbing

organ, though indeed he might be at a loss to say why the American

opossums, of precisely similar habits, and with similarly opposable

great toes, have all their other four toes free and equal.

[Illustration: FIG. 3.--Skeleton of the hind foot of the Virginian

Opossum (_Didelphys Virginiana_).]

The philosophical naturalist of the second of the types that I have

sketched out, in investigating this structure, will institute a careful

comparison between the foot of the koala and that of other animals

belonging to the same group.

Among the marsupial animals of Australia, few are so well known as the

kangaroo. Like the koala, it is a vegetable feeder, and these two forms

have some dental and other structural characters in common. But the mode

of progression, and the limbs which effect this, offer the greatest

possible contrast.

In the kangaroo the hind legs are disproportionately large. The foot

especially is long and narrow, and at first sight appears composed of a

single large toe. Its motion along the ground consists of a series of

leaps or hops effected entirely by these powerful hind limbs. On looking

more closely at the foot (see Fig. 4), it will be seen that the first

digit or hallux is entirely wanting, but the other four toes are present

with their complete number of phalanges. The fourth is immensely

developed, the fifth moderately so, but the second and third are reduced

to the most slender rudiments, and are so united in life by a common

integument, that they look like a single toe with a double claw.

Now, here are two feet as unlike as possible in their functions--the one

formed for rapidly hopping along over the arid plains, the other for

slowly and securely climbing among the boughs of the forests--yet

presenting a deep-seated resemblance in a character not found in the

feet of any other known mammal except the immediate allies of these two.

We may call this “conformity to type” without getting much nearer to an

explanation of the phenomenon. Perhaps it is safest to rest at this

stage.

[Illustration: FIG. 4.--Skeleton of the hind foot of the kangaroo

(_Macropus major_).]

But is it not powerfully suggestive--I will not say more, for, of

course, by itself it cannot be considered as a proof--of true

relationship, of inheritance from a common ancestor? We can easily see

that in some manner the great preponderance of the one toe in the

kangaroo, and the reduction of the others, would be advantageous in its

mode of progression, reducing the foot to a narrow spring-board as it

were; and we can see that this attenuation of the second and third toes,

after the first had quite disappeared, might be a stage in the direction

of their total disappearance. But while this was taking place, let us

suppose that one branch of the family took to climbing trees (I must not

enter fully into all that might be supposed on this subject, as I am

merely introducing this as an example of the mode in which morphological

problems are illustrated by these general views), and the variations in

a particular direction, tending towards better climbing, were preserved

and accumulated on the Darwinian hypothesis, the hallux (a common part

in all mammals, only in abeyance when not wanted) was redeveloped in a

form best adapted for its actual purposes, the other digits gradually

resuming their normal condition; these two, however, still preserving

strong reminiscences of the ancestral state.[24]

It is certainly significant that all the Australian vegetable-feeding

climbing opossums have feet constructed on this type, one that is

similar to that of the kangaroos of the same country, while the American

opossums, further removed geographically, and therefore, in all

probability, in actual relationship, with feet functionally the same,

show no trace of this deep-seated structural peculiarity--a peculiarity

most important for the consideration of the philosophical anatomist, as

it evidently depends on some more far-reaching cause than mere

adaptation to purpose.

* * * * *

In considering a little more fully the application of such views to the

study of morphology, I must say a few words on _classification_. It was

felt at the very outset of the study of natural history that without

some system of classification the subject was little more than a

hopeless chaotic confusion. The first instinct of a zoologist is to

arrange in some sort of order the multitudinous objects with which he

has to deal. In the beginning of science, with little sound knowledge,

such classifications were often mere arbitrary arrangements, founded on

some easily accessible peculiarities, and forming nothing more than a

means by which the distinction between certain objects and certain other

objects could be grasped by the mind of the founder and communicated to

others. Classifications based on such characters became so general, and

were often so carelessly and ignorantly put together, that they

threatened to bring the whole system into disrepute; whereas I have

little hesitation in saying that, in reality, _classification_ is one of

the, if not the, most important aims and ends of the study of

morphology. It is the best contribution which we can make towards the

solution of the great biological problem, for a true classification,

viewed by the light of the derivative hypothesis, is nothing more or

less than an expression of the actual amount of affinity between

different objects. An order, a family, or a genus is no longer a group

of animals linked together by some arbitrarily selected characters, but

a group supposed to have been descended from a common ancestor, and to

have become, by whatever process, gradually differentiated from other

groups of animals.[25]

As in such groups, when once established, there can be no crossing with

other groups (as in human families, to which they are sometimes

compared), all the resemblances which are found between members of

different groups must either be characters inherited from the common

ancestor, perhaps lost through many generations and reappearing at a

subsequent period by the process of “reversion,” or they must be

characters having merely _analogical_ resemblances--_i.e._ characters

developed by variation, but which, owing to similarity of conditions of

existence or other causes, have become similar to each other.

To discriminate between these two classes of characters,--namely, those

that are essential and fundamental, or, in the language of one school,

are dependent on conformity to type, or, according to the derivative

hypothesis, are inherited from remote ancestors, and those that are

modifications to suit the conditions of existence to which the animal

is exposed, or, in other words, adaptive characters,--is a constantly

recurring problem to the systematic morphologist; and the difficulties

that encompass the solution of this problem are the main causes of the

little progress hitherto made towards a general agreement as to

classification otherwise than in the main groups. Let me illustrate this

point by a single and, as it happens, by no means difficult example.

[Illustration: FIG. 5.--The Thylacine (_Thylacinus cynocephalus_). From

Wolf’s _Zoological Sketches_.]

You have before you the skeletons of two animals very similar in their

general or superficial characters--one is the common dog, the other the

carnivorous marsupial, the thylacine, sometimes called “Tasmanian wolf.”

These animals, when wild, have very similar habits. You will see that,

in the general characters of the skeleton, the structure of the limbs,

and the arrangement of the teeth, a remarkable similarity prevails. You

might easily conclude that these animals were related. They were,

indeed, formerly placed near together by systematists.

Now, if I place by the dog another well-known animal, a sheep, you will

see that in many characters of its bones, its feet, its teeth, etc., it

differs far more from the dog than the latter does from the thylacine.

Yet zoologists affirm, without the slightest hesitation, that the sheep

and the dog are far more nearly related to each other than either is to

the thylacine. This assertion is founded on a discrimination of the

essential from the adaptive characters. The dog and the sheep belong to

one great branch of the mammalian class, although they represent

different stocks of that branch. The thylacine belongs to another

primary branch, but in that branch it has taken the place, functionally,

of the dog in the other; its organs have become adapted to perform the

same work.[26]

It has been asserted, in a recent very able pamphlet by an anonymous

writer, “On the Difficulties of the Theory of Natural Selection,”[27]

“that on the theory of ‘natural selection’ it is all but impossible,

such are the probabilities against it, that identical structures should

have arisen independently. Yet many structures undeniably exist which,

to all appearance, must have so arisen.” And the “remarkable identity of

structure between certain of the teeth of the large predatory marsupial,

the thylacine, or Tasmanian wolf, and those of the common dog,” is cited

as a case in point. Now, though I am fully willing to admit difficulties

in the theory, quite inexplicable with our present knowledge, as many

almost as the author quoted, I cannot see this one in the same light. It

appears to me that the probabilities, instead of being against the

independent origin of such similar structures (erroneously called

_identical_) as those just mentioned, are exceedingly in their favour. I

cannot in the least see why a marsupial animal should not be carnivorous

and predaceous as well as a placental animal, and if so, why its teeth

should not have come to possess the general attributes essential to

animals of such habits--namely, large, pointed, recurved fangs at each

of the anterior angles of the jaw; the teeth between them much reduced,

so as not to interfere with the piercing and holding action of the

canines; the molars more or less scissor-shaped. These are plainly

adaptive characters, and whatever process has produced them in the one

case is just as likely to have produced them in the other--I might

almost say, must have produced them in the other. So far, however, are

the teeth of the thylacine and the dog from being essentially

“identical,” that in numerous non-adaptive and non-functional

characters, as the number of the incisors, premolars, and molars, the

mode of succession, and the minute structure (all which will be spoken

of at a later period of the course), they widely differ, the dog

conforming in all these points with the ordinary placental mammals, the

thylacine with the remaining marsupials. Such characters, underlying, in

large groups of animals, the various modifications in relation to use,

cannot be too diligently sought out as the true landmarks to guide our

steps through the intricacies that beset our path in tracing affinities.

[Illustration: FIG. 6.--Skull of Thylacine.]

[Illustration: FIG. 7.--Skull of Shepherd’s Dog.]

Another valuable guiding principle in morphological studies is this. It

is a remark of Gegenbaur’s, in his valuable work “On the Structure of

the _Carpus_ and _Tarsus_,” but it must have occurred to any one who has

given much thought to these problems. When we wish to discover the

distinguishing characters between different organisms, it is necessary

to examine them in their most fully developed condition. If, on the

other hand, our object is to trace their resemblance, their intimate

relationships, we must study them in their early embryonic stages. By

these methods we can do much to separate what is secondary or superadded

from what is fundamental or essential in the character of an animal. The

farther back we can carry our researches, the more prominent do the

characters, common to the whole group to which the animal belongs,

become. The more completely mature the specimen, the more do the special

characters of the species or even of the individual predominate.

* * * * *

It is not my province in these lectures to indulge much in speculations.

Indeed, as students of morphology, we are as yet little in a position to

do so. I shall not say much more even on the general views to which I

have lately referred, for I feel that the acquisition of a sound basis

of fact to work with is what is, at present, most needed in comparative

anatomy. The difficulties which beset the beginner, and indeed the more

advanced student, in this subject are very great. As regards the branch

to which I propose more particularly to direct your attention, the

anatomy of the class Mammalia, which, we might suppose, was better

worked out than any other, the information to be found in books is

scattered, fragmentary, unequal, and often untrustworthy; even good

elementary treatises are wanting, much more anything like an exhaustive

work. Moreover, our museum--superior as I believe it to be to any other

of the kind--is, as yet, far from adequate to supply the knowledge

frequently sought for in it.

In considering the special subject for these lectures, I have often

thought that the greatest permanent benefit would be conferred on our

science by collecting together in a systematic form all the available

information upon limited groups of the animal kingdom, supplementing, as

far as possible, the deficiencies of knowledge by fresh observations,

and illustrating the subject by a complete series of preparations. At

the present day it is only by working out a definite branch of limited

extent monographically, that any solid advances in detailed knowledge

can be attained. Courses of lectures on this principle, especially if

they were published so as to reach a wider circle of students than this

theatre is apt to contain, may do much to _advance_ knowledge; but, on

the other hand, they might do less than more elementary lectures, giving

a general outline of a larger variety of topics, to _diffuse_ knowledge,

for it is probable that they would be attractive to only a limited

number of auditors or of readers.

I think it therefore advisable, in the first course I have the honour of

addressing to you, to confine my subject to a survey of the structure of

the animals of the highest class of organised beings; and I think that

this will prove of the greater importance and interest to the audience

assembled here, because it may be presumed that all have already either

commenced or completed the acquisition of a knowledge of the structural

anatomy of one, the most elevated member, of that class. I propose,

therefore, to take human anatomy as a point of departure, and, presuming

on your acquaintance with its details, shall refer only to some of its

general outlines, and shall point out the deviations from and

resemblance to the mammalian structure as we know it in man, in

descending throughout the series of animals composing the class.

I trust that some further interest may be given thereby to the daily

work of the student of our profession. Human anatomy is too often

learned as a mere collection of hard names applied to a complicated

network of structures, the form, position, and relation of which have to

be got up, probably to be forgotten soon afterwards. It might, however,

be made a far more attractive and useful subject if taught by the light

of a wider morphology. But I am afraid that very little of our

anatomical teaching, either by books or lectures, is of this class at

present. If any comparative anatomy is introduced, instead of

enlightening and illustrating the subject, it often only adds another

load to the already over-burdened memory--for instance, after the usual

dry, detailed and technical description of the part treated of, a

disquisition is added on what is called its “transcendental” anatomy,

extremely incomprehensible to most minds, and consisting chiefly in the

imposition of a new set of names to parts of which the student has just

succeeded in mastering the old ones.

All this ought to be reversed; the essential nature of the part in

question, as deduced from comparative anatomy, should be first announced

with a glance at its principal modifications; then its special

characters as seen in man will be a subject of intelligent interest. I

know from experience that after studying and teaching human anatomy for

many years on the ordinary methods, there were many parts the meaning

and nature of which I never understood until I began to dissect animals;

and increase of knowledge in this direction constantly throws light on

apparently unmeaning or incomprehensible parts of human structure.

One word more by way of introduction. I began with the mention of my

immediate predecessor in this chair. To him I must once again return.

The subject matter of the present course will embrace many points

treated of by him, more or less fully, in some of his lectures delivered

in this theatre, and many on which I have had the advantage of his

conversation and counsel. His teaching has entered so deeply into, and

mingled so closely with, observations and reflections that may have

suggested themselves in the course of my work in the museum, that in

many cases it would be difficult to trace the sources of information

that I may have to impart, and I may, perhaps, appear guilty of

appropriating what should belong to another. Let me acknowledge then,

once for all, how deeply I am indebted to Professor Huxley, not only for

the information conveyed in the public manner of lectures and books, but

also for the generous way in which, on all occasions, his time, his

knowledge, his thoughts, have been freely given to me. And I say this

the more willingly, because I know that I am but one of many whose

labours have been lightened, whose efforts have been stimulated, whose

difficulties have been smoothed, by his encouragement and support, by

his candid and judicious criticism, and by the example of his often

self-sacrificing devotion to the advancement of scientific truth.

I also desire, in conclusion, Mr. President, to take this opportunity of

publicly expressing the obligations which I, as well as numbers of

others, feel towards you and your predecessors in that chair, as well as

to the former and present members of the Council of the College,

individually and collectively, for the immense aid that you have given

to the progress of philosophical biology in this country, and I may say,

in the whole world, by the maintenance and augmentation of John Hunter’s

Museum. An epoch of revolution appears to be at hand in our profession,

which may lead to a material alteration in the respective positions and

opportunities of the various corporate bodies. Whatever changes may take

place, the College of Surgeons will always look back with satisfaction

to the fact that, for the first seventy years of the century, when these

studies were less appreciated than they are now, or will be hereafter,

it has, with scanty aid from the national resources, cherished the

growth of a truly national institution, the benefits of which are not

confined to any one class or profession, but are freely open to the

whole community. I can say, moreover, with perfect assurance, speaking

both from my own experience and from knowledge of the history of the

museum, as recorded in its archives, that any deficiencies which exist

in the condition of the collection, any needs which it does not supply,

must be due to other causes than want of encouragement to the officers

of the establishment, or want of liberality in supplying the requisite

funds, on the part of the Council of the College.

IX

RECENT ADVANCES IN NATURAL SCIENCE IN RELATION TO THE CHRISTIAN

FAITH[28]

I have been requested by the Subjects Committee of the Congress to place

before you a brief statement of some of the advances which have recently

been made in natural science, with a view to open a discussion upon

their relations, real or supposed, to religious belief. The particular

advances which, as I am given to understand, were especially in the

minds of the Committee in proposing this question, are those which have

resulted in the more or less general adoption by scientific men of the

view of the sequence of events which have taken place and are still

taking place in the universe, to which the term “evolution” is now

commonly applied.

All that is embraced by this term, the various realms of nature in which

its manifestations are traced, the various shades of meaning attached to

it by different persons, would constitute far too large and complex a

subject to be treated of in the time to which addresses to this meeting

are wisely restricted. I will therefore select for special consideration

the only point in the application of the theory upon which I can speak

with any practical knowledge--one which is, however, in the eyes of many

of very vital interest. It is the one, at all events, which at the

present moment attracts most attention; the new ideas upon it being

received with enthusiasm by some, and with distrust, if not with

abhorrence, by others.

The doctrine of continuity, or of direct relation of event to some

preceding event according to a natural and orderly sequence is now

generally recognised in the inorganic world; and although the modern

expansion of this doctrine as applied to the living inhabitants of the

earth appears to many so startling, and has met with so much opposition,

it is, in a more restricted application, a very old and widespread

article of scientific as well as of popular faith.

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