CHAPTER IV. DARWINISM IN GENERAL.

Darwinism, which was originally a technical theory of the biological

schools, has long since become a veritable tangle of the most diverse

problems and opinions, and seems to press hardly upon the religious

conception of the world from many different sides. In its theory of blind

“natural selection” and the fortuitous play of the factors in the struggle

for existence, it appears to surrender the whole of this wonderful world

of life to the rough and ready grip of a process without method or plan.

In the general theory of evolution and the doctrine of the descent of even

the highest from the lowest, it seems to take away all special dignity

from the human mind and spirit, all the freedom and all the nobility of

pure reason and free will; it seems to reduce the higher products of

religion, morality, poetry, and the æsthetic sense to the level of an

ignoble tumult of animal impulses, desires and sensations. Purely

speculative questions relative to the evolution theory, psychological and

metaphysical, logical and epistemological, ethical, æsthetic, and finally

even historical and politico-economical questions have been drawn into the

coil, and usually receive from the Darwinians an answer at once robust and

self-assured. A zoological theory seems suddenly to have thrown light and

intelligibility into the most diverse provinces of knowledge.

But in point of fact it can be shown that Darwinism has not really done

this and cannot do it. It leaves unaffected the problem of the mind with

its peculiar and underivable laws, from the logical to the ethical.

Whether it be right or wrong in its physiological theories, its

genealogical trees and fortuitous factors, preoccupation with this theory

is a task of the second order. Nevertheless it is necessary to study it,

because the chief objections to the religious interpretation of the world

have come from it.

The Development of Darwinism.

In studying it we should like to follow a method somewhat different from

that usually observed in apologetic writings. “Darwinism,” even in its

technical, biological form, never was quite, and is to-day not at all a

unified and consistent system. It has been modified in so many ways and

presented in such different colours, that we must either refrain

altogether from attempting to get into close quarters with it, or we must

make ourselves acquainted to some extent with the phases of the theory as

it has gradually developed up to the present day. This is the more

necessary and useful since it is precisely within the circle of technical

experts that revolts from and criticisms of the Darwinian theory have in

recent years arisen; and these are so incisive, so varied, and so

instructive, that through them we can adjust our standpoint in relation to

the theory better than in any other way. And in thus letting the

biologists speak for themselves, we are spared the fatal task of entering

into the discussion of questions belonging to a region outside our own

particular studies.

We cannot, however, give more than a short sketch. But even such a sketch

may do more towards giving us a general knowledge of the question and

showing us a way out of the difficulties it raises than any of the current

“refutations.” To supplement this sketch, and facilitate a thorough

understanding of the problem, we shall give somewhat fuller references

than are usual to the relevant literature. And the same method will be

pursued in the following chapter, which deals with the mechanical theory

of life. This method throws more upon the reader, but it is probably the

most satisfactory one for the serious student.

The reactions from the Darwinism of the schools which we have just

referred to, and to which the second half of this chapter is devoted, are,

of course, of a purely scientific kind. And while we are devoting our

attention to them, we must not be unfaithful to the canon laid down in the

previous chapter, namely that with reference to the question of teleology

in the religious sense no real answer can be looked for from scientific

study, not even if it be anti-Darwinian. In this case, too, it is

impossible to read the convictions and intuitions of the religious

conception of the world out of a scientific study of nature: they precede

it. But here, too, we may find some accessory support and indirect

corroboration more or less strong and secure. This may be illustrated by a

single example. It will be shown that, on closer study, it is not

impossible to subordinate even the apparently confused tangle of

naturalistic factors of evolution which are summed up in the phrase

“struggle for existence” to interpretation from the religious point of

view. But matters will be in quite a different position if the whole

theory collapses, and instead of evolution and its paths being given over

to confusion and chance, it appears that from the very beginning and at

every point there is a predetermination of fixed and inevitable lines

along and up which it must advance. In many other connections

considerations of a like nature will reveal themselves to us in the course

of our study.

Darwinism, as popularly understood, is the theory that “men are descended

from monkeys,” and in general that the higher forms of life are descended

from the lower, and it is regarded as Darwin’s epoch-making work and his

chief merit—or fault according to the point of view—that he established

the Theory of Descent. This is only half correct, and it leaves out the

real point of Darwinism altogether. The Theory of Descent had its way

prepared by the evolutionist ideas and the speculative nature-philosophy

of Goethe, Schelling, Hegel and Oken; by the suggestions and glimmerings

of the nature-mysticism of the romanticists; by the results of comparative

anatomy and physiology; was already hinted at, at least as far as

derivation of species was concerned, in the works of Linné himself; was

worked out in the “zoological philosophies,” by the elder Darwin, by

Lamarck, Etienne Geoffrey St. Hilaire and Buffon; was in the field long

before Charles Darwin’s time; was already in active conflict with the

antagonistic theory of the “constancy of species,” and had its more or

less decided adherents. Yet undoubtedly it was through and after Darwin

that the theory grew so much more powerful and gained general acceptance.

Darwinism and Teleology.

But the essential and most characteristic importance of Darwin and his

work, the reason for which he was called the Newton of biology, and which

makes Darwinism at once interesting and dangerous to the religious

conception of the world, is something quite special and new. It is its

radical opposition to teleology. Du Bois-Reymond, in his witty lecture

“Darwin versus Galiani,”(4) explains the gist of the matter. “Les dés de

la nature sont pipés” (nature’s dice are loaded). Nature is almost always

throwing aces. She brings forth not what is meaningless and purposeless,

but in great preponderance what is full of meaning and purpose. What

“loaded” her dice like this? Even if the theory of descent be true, in

what way does it directly help the purely scientific interpretation of the

world? Would not this evolution from the lowest to the highest simply be a

series of the most astonishing lucky throws of the dice by which in

perplexing “endeavour after an aim,” the increasingly perfect, and

ultimately the most perfect is produced? And, on the other hand, every

individual organism, from the Amœba up to the most complex vertebrate, is,

in its structure, its form, its functions, a stupendous marvel of

adaptation to its end and of co-ordination of the parts to the whole, and

of the whole and its parts to the functions of the organism, the functions

of nutrition, self-maintenance, reproduction, maintenance of the species,

and so on. How account for the adaptiveness, both general and special,

without _causæ finales_, without intention and purposes, without guidance

towards a conscious aim? How can it be explained as the necessary result

solely of _causæ efficientes_, of blindly working causes without a

definite aim? Darwinism attempts to answer this question. And its answer

is: “What appears to us ‘purposeful’ and ‘perfect’ is in truth only the

manifold adaptation of the forms of life to the conditions of their

existence. And this adaptation is brought about solely by means of these

conditions themselves. Without choice, without aim, without conscious

purpose nature offers a wealth of possibilities. The conditions of

existence act as a sieve. What chances to correspond to them maintains

itself, gliding through the meshes of the sieve, what does not perishes.”

It is an old idea of the naturalistic philosophies, dating from

Empedocles, which Darwin worked up into the theory of “natural selection”

through “the survival of the fittest” “in the struggle for existence.” Of

course the assumption necessary to his idea is that the forms of life are

capable of variation, and of continually offering in ceaseless flux new

properties and characters to the sieve of selection, and of being raised

thereby from the originally homogeneous to the heterogeneous, from the

simple to the complex, from the lower to the higher. This is the theory of

descent, and it is, of course, an essential part and the very foundation

of Darwin’s theory. But it is _the doctrine of descent based upon natural

selection_ that is Darwinism itself.

The Characteristic Features of Darwinism.

We do not propose to expound the Darwinian theory for the hundredth time;

a knowledge of it must be taken for granted. We need only briefly call to

mind the characteristic features and catchwords of the theory as Darwin

founded it, which have also been the starting points of subsequent

modifications and controversies.

All living creatures are bound together in genetic solidarity. Everything

has evolved through endless deviations, gradations, and differentiations,

but at the same time by a perfectly continuous process. Variation

continually produced a crop of heterogeneous novelties. The struggle for

existence sifted these out. Heredity fixed and established them. Without

method or plan variations continue to occur (indefinite variations). They

manifest themselves in all manner of minute changes (“fluctuating”

variations). Every part, every function of an organism may be subject

individually to variation and selection. The world is strictly governed by

what is useful. The whole organisation as well as the individual organs

and functions bear the stamp of utility, at least, they must bear it if

the theory is correct. In the general continuity the transitions are

always easy; there are no fundamentally distinct “types,” architectural

plans, or groups of forms. Where gaps yawn the intermediate links have

gone amissing. There is no fundamental difference between _genus_,

_species_, and _variety_. Even the most complicated organ such as the eye,

the most puzzling function such as the instinct of the bee, may be

explained as the outcome of many more primitive stages.

The chief evidences of the theory of descent are to be found in

homologies, in the correspondences of organs and functions, as revealed by

comparative anatomy and physiology, in the recapitulation revealed by

embryology, in the structure of parasites, in rudimentary organs and

reversions to earlier stages, in the distribution of animals and plants,

and in the possibility of still transforming, at least to a slight extent,

one species into another, by experimental breeding.

Transformation and differentiation go on in nature as a vast, ceaseless,

but blind process of selection. In artificial selection evolution is

secured by choosing the most fit for breeding purposes; so it is secured

in natural selection by the favouring and survival of those forms which

are the most fit among the many unfit or less fit, which happened to be

exposed to the struggle for existence, that is, to the competition for the

means of subsistence, to the struggle with enemies, to hostile

environment, and to dangers of every kind. The adaptation thus brought

about is of a purely “passive” kind. The variations arise fortuitously out

of the organism, and present themselves for selection in the struggle for

existence; they are not actively acquired by means of the struggle. The

secondary factors of evolution recognised are: correlation in the growth

and in the development of parts, the origin of new characters through use,

their disappearance through disuse (Lamarck), the transmission of

characters thus acquired, the influence of environment and sexual

selection.(5)

The Darwinian theory, the interpretation of the teleological in the

animate world by means of the theory of descent based upon natural

selection, entered like a ferment into the scientific thought-movement,

and in a space of forty years it has itself passed through a series of

stages, differentiations, and transformations which have in part resulted

in the present state of the theory, and have in part anticipated it. These

are represented by the names of workers belonging to a generation which

has for the most part already passed away: Darwin’s collaborateurs, such

as Alfred Russel Wallace, who independently and simultaneously expounded

the theory of natural selection, Haeckel and Fritz Müller, Nägeli and

Askenasy, von Kölliker, Mivart, Romanes and others. The differentiation

and elaboration of Darwin’s theories has gone ever farther and farther;

the grades and shades of doctrine held by his disciples are now almost

beyond reckoning.

Various Forms of Darwinism.

The great majority of these express what may be called popular Darwinism

[“Darwinismus vulgaris”], theoretically worthless, but practically

possessed of great powers of attraction and propagandism. It expresses in

the main a conviction, usually left unexplained, that everything “happens

naturally,” that man is really descended from monkeys, and that life has

“evolved from lower stages” of itself, that dualism is wrong, and that

monism is the truth. It is exactly the standpoint of the popular

naturalism we have already described, which here mingles unsuspectingly

and without scruple Lamarckian and other principles with the Darwinian,

which is enthusiastic on the one hand over the “purely mechanical”

interpretation of nature, and on the other drags in directly psychical

motives, unconscious consciousness, impulses, spontaneous

self-differentiation of organisms, which nevertheless adheres to “monism”

and possibly even professes to share Goethe’s conception of nature!

Above this stratum we come to that of the real experts, the only one which

concerns us in the least. Here too we find an ever-growing distance

between divergent views, the most manifold differences amounting sometimes

to mutual exclusion. These differences occur even with reference to the

fundamental doctrine generally adhered to, the doctrine of descent. To one

party it is a proved fact, to another a probable, scientific working

hypothesis, to a third a “rescuing plank.” One party is always finding

fresh corroborations, another new difficulties. And within the same group

we find the contrasts of believers in monophyletic and believers in

polyphyletic evolution, the mechanists and the half-confessed or

thoroughgoing vitalists, the preformationists and the believers in

epigenesis. Opinions differ even more widely in regard to the _rôle_ of

the “struggle for existence” in the production of species. On the one hand

we have the Darwinism of Darwin freed from inconsequent additions and

formulated as orthodox “neo-Darwinism”; on the other hand we have

heterodox Lamarckism. The “all-sufficiency” of natural selection is

proclaimed by some, its impotence by others. Indefinite variation is

opposed by orthogenesis, fluctuating variation by saltatory mutation

(Halmatogenesis in “Greek”), passive adaptation by the spontaneous

activity and self-regulation of the living organism. The struggle for

existence is variously regarded as the chief factor, or as a co-operating

factor, or as an indifferent, or even an inimical factor in the

origination of new species.

And among the representatives of these different standpoints there are

most interesting personal differences: in some, like Weismann, we find a

great loyalty to, and persistence in the position once arrived at, in

others the most surprising transitions and changes of opinion. Thus

Fleischmann, a pupil of Selenka’s, after illustrating during many years of

personal research the orthodox Darwinian standpoint, finally developed

into an outspoken opponent not only of the theory of selection but of the

doctrine of descent. So also Friedmann.(6) Driesch started from the

mechanical theory of life and advanced through the connected series of his

own biological essays to vitalism. Romanes, a prominent disciple of

Darwin, ended in Christian theism, and Wallace, the discoverer of “the

struggle for existence,” landed in spiritualism.

Nothing like an exhaustive view of the present state of Darwinism and its

many champions can here be attempted. But it will be necessary to get to

know what we may call its possibilities by a study of typical and leading

examples. In the course of our study many of the problems to which the

theory gives rise will reveal themselves, and their orientation will be

possible.

This task falls naturally into two subdivisions: (1) the present state of

the theory of Evolution and Descent, and how far the religious conception

of the world is or is not affected by it; (2) the truth as to the

originative and directive factors of Evolution, especially as to “natural

selection in the struggle for existence,” whether they are tenable and

sufficient, and what attitude religion must take towards them. These two

problems must be kept distinct throughout, and must be discussed in order.

For the validity of what is characteristically _Darwinism_ is in no way

decided by proving descent and evolution, although it appears so in most

popular expositions.(7)

The Theory of Descent.

Again and again we hear and read, even in scientific circles and journals,

that Darwinism breaks down at many points, that it is insufficient, and

even that it has quite collapsed. Even the assurances of its most

convinced champions are rather forced, and are somewhat suggestive of

bills payable in the future.(8) But here again it is obvious that we must

distinguish clearly between the Theory of Descent and Darwinism. Of the

Theory of Descent it is by no means true that it has “broken down.” With a

slight exaggeration, but on the whole with justice, Weismann has asserted

that the Theory of Descent is to-day a “generally accepted truth.” Even

Weismann’s most pronounced opponents, such as Eimer, Wolff, Reinke, and

others, are at one with him in this, that there has been evolution in some

form; that there has been a progressive transformation of species; that

there is real (not merely ideal) relationship or affiliation connecting

our modern forms of life, up to and including man, with the lower and

lowest forms of bygone æons.

The evidences are the same as those adduced by Darwin and before his time,

but they have been multiplied and more sharply defined:—namely, that the

forms of life can be arranged in an ascending scale of evolution, both in

their morphological and their physiological aspects, both as regards the

general type and the differentiation of individual organs and particular

characters, bodily and mental. All the rubrics used by Darwin in this

connection, from comparative anatomy, from the palæontological record

itself, and so on, have been filled out with ever-increasing detail.

Palæontology, in particular, is continually furnishing new illustrations

of descent and new evidence of its probability, more telling perhaps in

respect of general features and particular groups than in regard to the

historical process in detail. For certain species and genera palæontology

discloses the primitive forms, discovers “synthetic types” which were the

starting-point for diverging branches of evolution, bridges over or

narrows the yawning gulfs in evolution by the discovery of “intermediate

forms”; and, in the case of certain species, furnishes complete

genealogical trees. The same holds true of the facts of comparative

anatomy, embryology, and so on. In all detailed investigations into an

animal type, in the study of the structure, functions, or the instincts of

an ant, or of a whale or of a tape-worm, the standpoint of the theory of

descent is assumed, and it proves a useful clue for further investigation.

In regard to man—so we are assured—the theory finds confirmation through

the discovery of the Neanderthal, Spy, Schipka, La Naulette skulls and

bones—the remains of a prehistoric human race, with “pithecoid” (ape-like)

characters. And the theory reaches its climax in Dubois’ discovery of the

remains of “Pithecanthropus,” the upright ape-man, in Java, 1891-92, the

long sought-for Missing Link between animals and man;(9) and in the still

more recent proofs of “affinity of blood” between man and ape, furnished

by experiments in transfusion. Friedenthal has revived the older

experiments of transfusing the blood of one animal into another, the blood

of an animal of one species into that of another, of related species into

related species, more remote into more remote, and finally even from

animals into man. The further apart the two species are, the more

different are the physiological characters of the blood, and the more

difficult does a mingling of the two become. Blood of a too distantly

related form does not unite with that of the animal into which it is

transfused, but the red corpuscles of the former are destroyed by the

serum of the latter, break up and are eliminated. In nearly related

species or races, however, the two kinds of blood unite, as in the case of

horse and ass, or of hare and rabbit. Human blood serum behaves in a

hostile fashion to the blood of eel, pigeon, horse, dog, cat, and even to

that of Lemuroids, or that of the more remotely related “non-anthropoid”

monkey; human blood transfused from a negro into a white unites readily,

as does also that of orang-utan transfused into a gibbon. But human blood

also unites without any breaking-up or disturbance with the blood of a

chimpanzee; from which the inference is that man is not to be placed in a

separate sub-order beside the other sub-orders of the Primates, the

platyrrhine and catarrhine monkeys, not even in a distinct sub order

beside the catarrhines; but is to be included with them in one zoological

sub-order. This classification was previously suggested by Selenka on

other grounds, namely, because of the points in common in the embryonic

development of the catarrhine monkeys and of man, and their common

distinctiveness as contrasted with the platyrrhines.(10)

Haeckel’s Evolutionist Position.

The average type of the Theory of Descent of the older or orthodox school,

which still lingers in the background with its Darwinism unshaken, is that

set forth by Haeckel, scientifically in his “Generelle Morphologie der

Organismen” (1866), and “Systematische Phylogenie” (1896), and popularly

in his “Natural History of Creation” and “Riddles of the Universe,” with

their many editions. We may assume that it is well known, and need only

briefly recall its chief characteristics. The “inestimable value,” the

“incomparable significance,” the “immeasurable importance” of the Theory

of Descent lies, according to Haeckel, in the fact that by means of it we

can explain the origin of the forms of life “in a mechanical manner.” The

theory, especially in regard to the descent of man from the apes, is to

him not a working hypothesis or tentative mode of representation; it is a

result comparable to Newton’s law of gravitation or the Kant-Laplace

cosmogony. It is “a certain historical fact.” The proofs of it are those

already mentioned.

What is especially Haeckelian is the “fundamental biogenetic law,”

“ontogeny resembles phylogeny,” that is to say, in development, especially

in embryonic development, the individual recapitulates the history of the

race. Through “palingenesis,” man, for instance, recapitulates his

ancestral stages (protist, gastræad, vermine, piscine, and simian). This

recapitulation is condensed, disarranged, or obscured in detail by

“cenogenesis” or “cænogenesis.” The groups and types of organisms exhibit

the closest genetic solidarity. The genealogical tree of man in particular

runs directly through a whole series. From the realm of the protists it

leads to that of the gastræadæ (nowadays represented by the Cœlentera),

thence into the domain of the worms, touches the hypothetical “primitive

chordates” (for the necessary existence of which “certain proofs” can be

given), the class of tunicates, ascends through the fishes, amphibians and

reptiles to forms parallel to the modern monotremes, then directly through

the marsupials to the placentals, through lemuroids and baboons to the

anthropoid apes, from them to the “famous Pithecanthropus” discovered in

Java, out of which _homo sapiens_ arose. (The easy transition from one

group of forms to another is to be noted. For it is against this point

that most of the opposition has been directed, whether from “grumbling”

critics, or thoroughgoing opponents of the Theory of Descent.)

Haeckel’s facile method of constructing genealogical trees, which ignores

difficulties and discrepant facts, has met with much criticism and

ridicule even among Darwinians. The “orator of Berlin,” Du Bois-Reymond,

declared that if he must read romances he would prefer to read them in

some other form than that of genealogical trees. But they have at least

the merit that they give a vivid impression of what is most plausible and

attractive in the idea of descent, and moreover they have helped towards

orientation in the discussion. Nor can we ignore the very marked taxonomic

and architectonic talent which their construction displays.

Weismann’s Evolutionist Position.

The most characteristic representative, however, of the modern school of

unified and purified Darwinism is not Haeckel, but the Freiburg zoologist,

Weismann. Through a long series of writings he has carried on the conflict

against heterodox, and especially Lamarckian theories of evolution, and

has developed his theories of heredity and the causes of variation, of the

non-transmissibility of acquired characters, and the all-sufficiency of

natural selection. In his latest great work, in two volumes, “Lectures on

the Theory of Descent,”(11) he has definitely summed up and systematised

his views. These will interest us when we come to inquire into the problem

of the factors operative in evolution. For the moment we are only

concerned with his attitude to the Theory of Descent as such. It is

precisely the same as Haeckel’s, although he is opposed to Haeckel in

regard to the strictly Darwinian standpoint. The Theory of Descent has

conquered, and it may be said with assurance, for ever. That is the firm

conviction on which the whole work is based, and it is really rather

treated as a self-evident axiom than as a statement to be proved. Weismann

takes little trouble to prove it. All the well-known, usually very clear

proofs from palæontology, comparative anatomy, &c., which we are

accustomed to meet with in evolutionist books are wanting here, the

genealogical trees of the Equidæ, with the gradually diminishing number of

toes and the varying teeth, of _Planorbis multiformis_, of the ammonites,

the graduated series of stages exhibited by individual organs, for

instance, from the ganglion merely sensitive to light up to the intricate

eye, or from the rayed skeleton of the paired fins in fishes up to the

five-fingered hands and feet of the higher vertebrates, &c. These are only

briefly touched upon in the terse “Introduction,” and the whole of the

comprehensive work is then directed to showing what factors can have been

operative, and to proving that they must have been “Darwinian” (selection

in the struggle for existence), and not Lamarckian or any other. This is

shown in regard to the coloration of animals, the phenomena of mimicry,

the protective arrangements of plants, the development of instinct in

animals, and the origin of flowers.

In reality Weismann only adduces _one_ strict proof, and even that is only

laying special stress on what is well known in comparative embryology;

namely, the possibility of “predicting” on the basis of the theory of

descent, as Leverrier “predicted” Neptune. For instance, in the lower

vertebrates from amphibians upwards there is an _os centrale_ in the

skeleton of wrist, but there is none in man. Now if man be descended from

lower vertebrates, and if the fundamental biogenetic law be true (that

every form of life recapitulates in its own development, especially in its

embryonic development, the evolution of its race, though with

abbreviations and condensations), it may be predicted that the _os

centrale_ is to be found in the early embryonic stages of man. And

Rosenberg found it. In the same way the “gill-clefts” of the fish-like

ancestors have long since been discovered in the embryo of the higher

vertebrates and of man. Weismann himself “predicted” that the markings of

the youngest stage of the caterpillars of the Sphingidæ (hawk-moths) would

be found to be not oblique but longitudinal stripes, and ten years later a

fortunate observation verified the prediction. Because of the abundance of

evidential facts Weismann does not go into any detailed proof of

evolution. “One can hardly take up any work, large or small, on the finer

or more general structural relations, or on the development of any animal,

without finding in it proofs for the evolution theory.”

But assured as the doctrine of descent appears,(12) and certain as it is

that it has not only maintained its hold since Darwin’s day, but has

strengthened it and has gained adherents, this foundation of Darwinism is

nevertheless not the unanimous and inevitable conclusion of all scientific

men in the sense and to the extent that the utterances of Weismann and

others would lead us to suppose. Apart from all apologetic attempts either

in religious, ethical, or æsthetic interests, apart, too, from the

superior standpoint of the philosophers, who have not, so to speak, taken

the theory very seriously, but regard it as a provisional theory, as a

more or less necessary and useful method of grouping our ideas in regard

to the organic world, there are even among the biologists themselves some

who, indifferent towards religious or philosophical or naturalistic dogma,

hold strictly to fact, and renounce with nonchalance any pretensions at

completeness of knowledge if the data do not admit of it, and on these

grounds hold themselves aloof from evolutionist generalisation. From among

these come the counsels of “caution,” admissions that the theory is a

scientific hypothesis and a guide to research, but not knowledge, and

confessions that the Theory of Descent as a whole is verifiable rather as

a general impression than in detail.

Virchow’s Position.

Warnings of this kind have come occasionally from Du Bois-Reymond, but the

true type of this group, and its mode of thought, is Virchow. It will

repay us and suffice us to make acquaintance with it through him. His

opposition to Darwinism and the theory of descent was directed at its most

salient point: the descent of man from the apes. In lectures and

treatises, at zoological and anthropological congresses, especially at the

meetings of his own Anthropological-Ethnological Society in Berlin, from

his “Vorträge über Menschen-und Affen-Schädel” (Lectures on the Skulls of

Man and Apes, 1869), to the disputes over Dubois’ _Pithecanthropus

erectus_ in the middle of the nineties, he threw the whole weight of his

immense learning—ethnological and anthropological, osteological, and above

all “craniological”—into the scale against the Theory of Descent and its

supporters. Virchow has therefore been reckoned often enough among the

anti-Darwinians, and has been quoted by apologists and others as against

Darwinism, and he has given reason for this, since he has often taken the

field against “the Darwinists” or has scoffed at their “longing for a

pro-anthropos.”(13) Sometimes even it has been suggested that he was

actuated by religious motives, as when he occasionally championed not only

freedom for science, but, incidentally, the right of existence for “the

churches,” leaving, for instance, in his theory of psychical life, gaps in

knowledge which faith might occupy in moderation and modesty. But this

last proves nothing. With Virchow’s altogether unemotional nature it is

unlikely that religious or spiritual motives had any rôle in the

establishment of his convictions, and in Haeckel’s naïve blustering at

religion, there is, so to speak, more religion than in the cold-blooded

connivance with which Virchow leaves a few openings in otherwise frozen

ponds for the ducks of faith to swim in! And he has nothing of the pathos

of Du Bois-Reymond’s “ignorabimus.” He is the neutral, prosaic scientist,

who will let nothing “tempt him to a transcendental consideration,”(14)

either theological or naturalistic, who holds tenaciously to matters of

fact, who, without absolutely rejecting a general theory, will not concern

himself about it, except to point out every difficulty in the way of it;

in short, he is the representative of a mood that is the ideal of every

investigator and the despair of every theoriser.

His lecture of 1869 already indicates his subsequent attitude. “Considered

logically and speculatively” the Theory of Descent seems to him

“excellent,”(15) indeed a logical moral(!) hypothesis, but unproved in

itself, and erroneous in many of its particular propositions. As far back

as 1858, before the publication of Darwin’s great work, he stated at the

Naturalists’ Congress in Carlsruhe, that the origin of one species out of

another appeared to him a necessary scientific inference, but——And

throughout the whole lecture he alternates between favourable recognition

of the theory in general, and emphasis of the difficulties which confront

it in detail. The skull, which, according to Goethe’s theory, has evolved

from three modified vertebræ, is fundamentally different in man and

monkeys, both in regard to its externals, crests, ridges and shape, and

especially in regard to the nature of the cavity which it forms for the

brain. Specifically distinctive differences in the development and

structure of the rest of the body must also be taken into account. The

so-called ape-like structures in the skull and the rest of the body, which

occasionally occur in man (idiots, microcephaloids, &c.) cannot be

regarded as atavisms and therefore as proofs of the Theory of Descent;

they are of a pathological nature, entirely facts _sui generis_, and “not

to be placed in a series with the normal results of evolution.” A man

modified by disease “is still thoroughly a man, not a monkey.”

Virchow continued to maintain this attitude and persisted in this kind of

argument. He energetically rejected all attempts to find “pithecoid”

characters in the prehistoric remains of man. He declared the narrow and

less arched forehead, the elliptical form, and the unusually large frontal

cavities of the “Neanderthal skull” found in the Wupperthal in 1856, to be

simply pathological features, which occur as such in certain examples of

_homo sapiens_.(16) He explained the abnormal appearance of the jaw from

the Moravian cave of Schipka as a result of the retention of teeth,(17)

accompanied by directly “antipithecoid” characters.

The proceedings at the meetings of the Ethnological Society in 1895, at

which Dubois was present, had an almost dramatic character.(18) In the

diverse opinions of Dubois, Virchow, Nehring, Kollmann, Krause and others,

we have almost an epitome of the present state of the Darwinian question.

Virchow doubted whether the parts put together by Dubois (the head of a

femur, two molar teeth, and the top of a skull) belonged to the same

individual at all, disputed the calculations as to the large capacity of

the skull, placed against Dubois’ very striking and clever drawing of the

curves of the skull-outline, which illustrated, with the help of the

Pithecanthropus, the gradual transition from the skull of a monkey to that

of man, his own drawing, according to which the Pithecanthropus curve

simply coincides with that of a gibbon (_Hylobates_), and asserted that

the remains discovered were those of a species of gibbon, refusing even to

admit that they represented a new genus of monkeys. He held fast to his

_ceterum censeo_: “As yet no diluvial discovery has been made which can be

referred to a man of a pithecoid type.” Indeed, his polemic or “caution”

in regard to the Theory of Descent went even further. He not only refused

to admit the proof of the descent of man from monkey, he would not even

allow that the descent of one race from another has been demonstrated.(19)

In spite of all the plausible hypotheses it remains “so far only a _pium

desiderium_.” The race obstinately maintains its specific distinctness,

and resists variation, or gradual transformation into another. The negro

remains a negro in America, and the European colonist of Australia remains

a European.

Yet all Virchow’s opposition may be summed up in the characteristic words,

which might almost be called his motto, “I warn you of the need for

caution,” and it is not a seriously-meant rejection of the Theory of

Descent. In reality he holds the evolution-idea as an axiom, and in the

last-named treatise he shows distinctly how he conceives of the process.

He starts with variation (presumably “kaleidoscopic”), which comes about

as a “pathological” phenomenon, that is to say, not spontaneously, but as

the result of environmental stimulus, as the organism’s reaction to

climatic and other conditions of life. The result is an alteration of

previous characteristics, and a new stable race is established by an

“acquired anomaly.”(20)

Other Instances of Dissatisfaction with the Theory of Descent.

What was with Virchow only a suggestion of the need for caution, or

controversial matter to be subsequently allowed for or contradicted, had

more serious consequences to others, and led to still greater hesitancy as

regards evolutionist generalisations and speculations, and sometimes to

sharp antagonism to them.

One of the best known of the earlier examples of this mood is Kerner von

Marilaun’s large and beautiful work on “Plant Life.”(21) He does, indeed,

admit that our species are variations of antecedent forms, but only in a

very limited sense. Within the stocks or grades of organisation which have

always existed, variations have come about, through “hybridisation,”

through the crossing of similar, but relatively different forms; these

variations alter the configuration and appearance in detail, but neither

affect the general character nor cause any transition from “lower” to

“higher.”

Kerner disposes of the chief argument in favour of the theory of descent,

the homology of individual organs, by explaining that the homology is due

to the similarity of function in the different organisms. A similar

argument is used in regard to “ontogeny recapitulating phylogeny.”

Palæontology does not disclose in the plant-world any “synthetic types,”

which might have been the common primitive stock from which many now

divergent branches have sprung, nor does it disclose any “transition

links” really intermediate, for instance, between cryptogams and

gymnosperms, or between gymnosperms and angiosperms. That the higher races

are apparently absent from the earlier strata is not a proof that they

have never existed. The peat-bog flora must have involved the existence of

a large companion-flora, without which the peat could not have been

formed, but all trace of this is absent in the still persistent vestiges

of these times.(22) Life, with energy and matter, has existed as a

phenomenon of the universe from all eternity, and thus its chief forms and

manifestations have not “arisen,” but have always been. If facts such as

these contradict the Kant-Laplace theory of the universe, then the latter

must be corrected in the light of them, not conversely. The extreme

isolation of Kerner and his theory is probably due especially to this

corollary of his views.

Among the most recent examples of antagonism to the Evolution-Theory, the

most interesting is a book by Fleischmann, professor of zoology in

Erlangen, published in 1901, and entitled, “The Theory of Descent.” It

consists of “popular lectures on the rise and decline of a scientific

hypothesis” (namely, the Theory of Descent), and it is a complete

recantation by a quondam Darwinian of the doctrine of his school, even of

its fundamental proposition, the concept of evolution itself. For

Fleischmann is not guilty, like Weismann, of the inaccuracy of using

“Theory of Descent” as equivalent to Darwinism; he is absolutely

indifferent to the theory of natural selection. His book keeps strictly to

matters of fact, and rejects as speculation everything in the least beyond

these; it does not express even an opinion on the question of the origin

of species, but merely criticises and analyses.

It does not bring forward any new and overwhelming arguments in refutation

of the Theory of Descent, but strongly emphasises difficulties that have

always beset it, and discusses these in detail. The old dispute which

interested Goethe, Geoffroy St. Hilaire, and Cuvier, as to the unity or

the fundamental heterogeneity of the “architectural plan” in nature is

revived. Modern zoology recognises not merely the four types of Cuvier,

but seventeen different styles, “phyla,” or groups of forms, to derive one

of which from another is hopeless. And what is true of the whole is true

also of the subdivisions within each phylum; _e.g._, within the vertebrate

phylum with its fishes, amphibians, reptiles, birds and mammals. No bridge

leads from one to the other. This is proved particularly by the very

instance which is the favourite illustration in support of the Theory of

Descent—the fin of fishes and its relation to the five-fingered hand of

vertebrates. The so-called transition forms (Archæopteryx, monotremes,

&c.) are discredited. So with the “stalking-horse” of evolutionists—the

genealogical tree of the Equidæ, which is said to be traceable

palæontologically right back, without a break, from the one-toed horses of

the present day to the normal five-toed ancestry; and so with another

favourite instance of evolution, the history of the pond-snails

(_Planorbis multiformis_), the numerous varieties of which occur with

transitions between them in actual contiguity in the Steinheim beds, and

thus seem to afford an obvious example of the transformation of species.

Against these cases, and against using the palæontological archives as a

basis for the construction of genealogical trees in general, the weighty

and apparently decisive objection is urged, that nowhere are the soft

parts of the earlier forms of life preserved, and that it is impossible to

establish relationships with any certainty on the basis of hard parts

only, such as bones, teeth and shells. Even Haeckel admits that snails of

very different bodily structure may form very similar and even hardly

distinguishable shells.

Fleischmann further asserts that Haeckel’s “fundamental biogenetic law”

has utterly collapsed. “Recapitulation” does not occur. Selenka’s figures

of ovum-segmentation show that there are specific differences in the

individual groups. The origin and development of the blastoderm or

germinal disc has nothing to do with recapitulation of the phylogeny. It

is not the case that the embryos of higher vertebrates are

indistinguishable from one another. Even the egg-cell has a specific

character, and is totally different from any unicellular organism at the

Protistan level. The much-cited “gill-clefts” of higher vertebrates in the

embryonic stage are not persistent reminiscences of earlier lower stages;

they are rudiments or primordia shared by all vertebrates, and developing

differently at the different levels; (thus in fishes they become breathing

organs, and in the higher vertebrates they become in part associated with

the organs of hearing, or in part disappear again).

Though Fleischmann’s vigorous protest against over-hastiness in

construction and over-confidence on the part of the adherents of the

doctrine of descent is very interesting, and may often be justified in

detail, it is difficult to resist the impression that the wheat has been

rejected with the chaff.(23)

Even a layman may raise the following objections: Admitting that the great

groups of forms cannot be traced back to one another, the palæontological

record still proves, though it may be only in general outline, that within

each phylum there has been a gradual succession and ascent of forms. How

is the origin of what is new to be accounted for? Without doing violence

to our thinking, without a sort of intellectual autonomy, we cannot rest

content with the mere fact that new elements occur. So, in spite of all

“difficulties,” the assumption of _an actual descent_ quietly forces

itself upon us as the only satisfactory clue. And the fact, which

Fleischmann does not discuss, that even at present we may observe the

establishment of what are at least new breeds, impels us to accept an

analogous origin of new species. Even if the biogenetic law really “finds

its chief confirmation in its exceptions,” even if we cannot speak of a

strict recapitulation of earlier stages of evolution, there are

indisputable facts which are most readily interpreted as reminiscences, as

due to affiliation (ideal or hereditary), with ancestral forms. (Note, for

instance, Weismann’s “prediction,” &c.(24)) Even if Archæopteryx and other

intermediate forms cannot be regarded as connecting links in the strict

sense, _i.e._, as being stages in the actual pedigree, yet the occurrence

of reptilian and avian peculiarities side by side in one organism, goes

far to prove the close relationship of the two classes.

Fleischmann’s book strengthens the impression gained elsewhere, that a

general survey of the domain of life as a whole gives force and

convincingness to the Theory of Descent, while a study of details often

results in breaking the threads and bringing the difficulties into

prominence. But the same holds true of many other theoretical

constructions, and yet we do not seriously doubt their validity. (Take,

for instance, the Kant-Laplace theory, and theories of ethnology, of the

history of religion, of the history of language, and so on.) And it is

quite commonly to be observed that those who have an expert and specialist

knowledge, who are aware of the refractoriness of detailed facts, often

take up a sceptical attitude towards every comprehensive theory, though

the ultimate use of detailed investigation is to make the construction of

general theories possible. Fleischmann does exactly what, say, an

anthropologist would do if, under the impression of the constancy and

distinctiveness of the human races, which would become stronger the more

deeply he penetrated, he should resignedly renounce all possibility of

affiliating them, and should rest content with the facts as he found them.

Similarly, those who are most intimately acquainted with the races of

domesticated animals often resist most strenuously all attempts, although

these seem to others a matter of course, to derive our “tame” forms from

“wild” species living in freedom.

But to return. Even where the Theory of Descent is recognised, whether

fully or only half-heartedly, the recognition does not always mean the

same thing. Even the adherents of the general, but in itself quite vague

view that a transformation from lower forms to higher, and from similar to

different forms, has taken place, may present so many points of

disagreement, and may even stand in such antagonism to one another, that

onlookers are apt to receive the impression that they occupy quite

different standpoints, and are no longer at one even in the fundamentals

of their hypotheses.

The most diverse questions and answers crop up; whether evolution has been

brought about “monophyletically” or “polyphyletically,” _i.e._, through

one or many genealogical trees; whether it has taken place in a continuous

easy transition from one type to another, or by leaps and bounds; whether

through a gradual transformation of all organs, each varying individually,

or through correlated “kaleidoscopic” variations of many kinds throughout

the whole system; whether it is essentially asymptotic, or whether

organisms pass from “labile” phases of vital equilibrium by various

halting-places to stable states, which are definitive, and are, so to

speak, the blind alleys and terminal points of evolutionary possibilities,

_e.g._, the extinct gigantic saurians, and perhaps also man. And to these

problems must be added the various answers to the question, What precedes,

or may have preceded, the earliest stages of life of which we know? Whence

came the first cell? Whence the first living protoplasm? and How did the

living arise from the inorganic? These deeper questions will occupy us in

our chapter on the theory of life. Some of the former, in certain of their

aspects, will be considered in the sixth chapter, which deals with factors

in evolution.

The Theory of Descent itself and the differences that obtain even among

its adherents can best be studied by considering for a little the works of

Reinke and of Hamann.

Reinke, Professor of Botany in Kiel, has set forth his views in his book,

“Die Welt als Tat,”(25) and more recently in his “Einleitung in die

theoretische Biologie” (1901). Both books are addressed to a wide circle

of readers. Reinke and Hamann both revive some of the arguments and

opinions set forth in the early days of Darwinism by Wigand,(26) an author

whose works are gradually gaining increased appreciation.

It is Reinke’s “unalterable conviction” that organisms have evolved, and

that they have done so after the manner of fan-shaped genealogical trees.

The Theory of Descent is to him an axiom of modern biology, though as a

matter of fact the circumstantial evidence in favour of it is extremely

fragmentary. The main arguments in favour of it appear to him to be the

general ones; the homologies and analogies revealed by comparative

morphology and physiology, the ascending series in the palæontological

record, vestigial organs, parasitic degeneration, the origin of those

vital associations which we call consortism and symbiosis. These he

illustrates mainly by examples from his own special domain and personal

observation.

The simplest unicellular forms of life are to be thought of as at the

beginning of evolution; and, since mechanical causes cannot explain their

ascent, it must be assumed that they have an inherent “phylogenetic

potential of development,” which, working epigenetically, results in

ascending evolution. He leaves us to choose between monophyletic and

polyphyletic evolution, but himself inclines towards the latter,

associating with it a rehabilitation of Wigand’s theory of the primitive

cells. If, in the beginning, primitive forms of life arose (probably as

unicellulars) from the not-living, it is not obvious why we need think of

only one so arising, and, if many did so, why they should not have

inherent differences which would at once result in typically different

evolutionary series and groups of forms. But evolution does not go on _ad

libitum_ or _ad infinitum_, for the capacity for differentiation and

transformation gradually diminishes. The organisation passes from a labile

state of equilibrium to an increasingly stable state, and at many points

it may reach a terminus where it comes to a standstill. Man, the dog, the

horse, the cereals, and fruit trees appear to Reinke to have reached their

goal. The preliminary stages he calls “Phylembryos,” because they bear to

the possible outcome of their evolution the same relation that the embryo

does to the perfect individual. Thus, _Phenacodus_ may be regarded as the

Phylembryo of the modern horse. It is quite conceivable that each of our

modern species may have had an independent series of Phylembryos reaching

back to the primitive cells. But the palæontological record, and

especially its synthetic types, lead Reinke rather to assume that instead

of innumerable series, there have been branching genealogical trees, not

one, however, but several.

These views, together or separately, which are characterised chiefly by

the catch-words “polyphyletic descent,” “labile and stable equilibrium,”

and so on, crop up together or separately in the writings of various

evolutionists belonging to the opposition wing. They are usually

associated with a denial of the theory of natural selection, and with

theories of “Orthogenesis,” “Heterogenesis,” and “Epigenesis.”

We shall discuss them later when we are considering the factors in

evolution. But we must first take notice of a work in which the theories

opposed to Darwinian orthodoxy have been most decisively and aggressively

set forth. As far back as 1892 O. Hamann, then a lecturer on zoology in

Göttingen, gathered these together and brought them into the field,

against Haeckel in particular, in his book “Entwicklungslehre und

Darwinismus.”(27)

Hamann’s main theme is that Darwinism overlooks the fact that “there

cannot have been an origin of higher types from types already finished.”

For this “unfortunate and unsupported assumption” there are no proofs in

embryology, palæontology, or anatomy. He adopts and expands the arguments

and anti-Haeckelian deliverances of His in embryology, of Snell and Heer

in palæontology, of Kölliker and von Baer in their special interpretation

of evolution, of Snell particularly as regards the descent of man. It is

impossible to derive Metazoa from Protozoa in their present finished state

of evolution; even the Amoeba is so exactly adapted in organisation and

functional activity to the conditions of its existence that it is a

“finished” type. It is only by a stretch of fancy that fishes can be

derived from worms, or higher vertebrates from fishes. One of his

favourite arguments—and it is a weighty one, though neglected by the

orthodox Darwinians—is that living substance is capable, under similar

stimuli, of developing spontaneously and afresh, at quite different points

and in different groups, similar organs, such as spots sensitive to light,

accumulations of pigment, eye-spots, lenses, complete eyes, and similarly

with the notochord, the excretory organs, and the like. Therefore homology

of organs is no proof of their hereditary affiliation.(28) They rather

illustrate “iterative evolution.”

Another favourite argument is the fact of “Pædogenesis.” Certain animals,

such as _Amphioxus lanceolatus_, _Peripatus_, and certain Medusæ, are very

frequently brought forward as examples of persistent primitive stages and

“transitional connecting links.” But considered from the point of view of

Pædogenesis, they all assume quite a different aspect, and seem rather to

represent very highly evolved species, and to be, not primitive forms, but

conservative and regressive forms. Pædogenesis is the phenomenon exhibited

by a number of species, which may stop short at one of the stages of their

embryonic or larval development, become sexually mature, and produce

offspring without having attained their own fully developed form.

Another argument is the old, suggestive, and really important one urged by

Kölliker, that “inorganic nature shows a natural system among minerals

(crystals) just as much as animals and plants do, yet in the former there

can be no question of any genetic connection in the production of forms.”

Yet another argument is found in the occurrence of “inversions” and

anomalies in the palæontological succession of forms, which to some extent

upsets the Darwinian-Haeckelian genealogical trees. (Thus there are forms

in the Cambrian whose alleged ancestors do not appear till the Silurian.

Foraminifera and other Protozoa do not appear till the Silurian.)

From embryology in particular, as elsewhere in general, we read the

“fundamental biogenetic law,” that evolution is from the general to the

special, from the imperfect to the more perfect, from what is still

indefinite and exuberant to the well-defined and precise, but never from

the special to the special. According to Hamann’s hypothesis we must think

of evolution as going on, so to speak, not about the top but about the

bottom. The phyla or groups of forms are great trunks bearing many

branches and twigs, but not giving rise to one another. Still less do the

little side branches of one trunk bear the whole great trunk of another

animal or plant phylum. But they all grow from the same roots among the

primitive forms of life. Unicellulars these must have been, but not like

our “Protists.” They should be thought of as primitive forms having within

themselves the potentialities of the most diverse and widely separate

evolution-series to which they gave rise, as it were, along diverging

fan-like rays.

It would be instructive to follow some naturalist into his own particular

domain, for instance a palæontologist into the detailed facts of

palæontology, or an embryologist into those of embryology, in order to

learn whether these corroborate the assumptions of the Theory of Descent

or not. It is just in relation to these detailed facts that criticisms or

even denials of the theory have been most frequent. Koken, otherwise a

convinced supporter of the theory, inquires in his “Vorwelt,” _apropos_ of

the tortoises, what has become of the genealogical trees that were

scattered abroad in the world as proved facts in the early days of

Darwinism. He asserts, in regard to _Archæopteryx_, the instance which is

always put forward as the intermediate link in the evolution of birds,

that it does not show in any of its characters a fundamental difference

from any of the birds of to-day, and further, that, through convergent

development under similar influences, similar organs and structural

relations result, iterative arrangements which come about quite

independently of descent. He maintains, too, that the principle of the

struggle for existence is rather disproved than corroborated by the

palæontological record.

In embryology, so competent an authority as O. Hertwig—himself a former

pupil of Haeckel’s—has reacted from the “fundamental biogenetic law.” His

theory of the matter is very much that of Hamann which we have already

discussed; development is not so much a recapitulation of finished

ancestral types as the laying down of foundations after the pattern of

generalised simple forms, not yet specialised; and from these foundations

the special organs rise to different levels and grades of differentiation

according to the type.(29) But we must not lose ourselves in details.

Looking back over the whole field once more, we feel that we are justified

in maintaining with some confidence that the different pronouncements in

regard to the detailed application and particular features of the Theory

of Descent, and the different standpoints that are occupied even by

evolutionists, are at least sufficient to make it obvious that, even if

evolution and descent have actually taken place, they have not run so

simple and smooth a course as the over-confident would have us believe;

that the Theory of Descent rather emphasises than clears away the riddles

and difficulties of the case, and that with the mere corroboration of the

theory we shall have gained only something relatively external, a clue to

creation, which does not so much solve its problems as restate them. The

whole criticism of the “right wing,” from captious objections to actual

denials, proves this indisputably. And it seems likely that in the course

of time a sharpening of the critical insight and temper will give rise to

further reactions from the academic theory as we have come to know it.(30)

On the other hand, it may be assumed with even greater certainty that the

general evolutionist point of view and the great arguments for descent in

some form or other will ultimately be victorious if they are not so

already, and that, sooner or later, we shall take the Theory of Descent in

its most general form as a matter of course, just as we now do the

Kant-Laplace theory.

Naturalism and Religion · 第 4 / 12 章