CHAPTER XX

THE CLASSICAL TRADITION IN MODERN MORPHOLOGY

To write a history of contemporary movements from a purely objective

standpoint is well recognised to be an impossible task. It is difficult

for those in the stream to see where the current is carrying them: the

tendencies of the present will only become clear some twenty years in

the future.

I propose, therefore, in this concluding chapter to deal only with

certain characteristics of modern work on the problems of form which

seem to me to be derived directly from the older classical tradition of

Cuvier and von Baer.

The present time is essentially one of transition. Complete uncertainty

reigns as to the main principles of biology. Many of us think that the

materialistic and simplicist method has proved a complete failure, and

that the time has come to strike out on entirely different lines. Just

in what direction the new biology will grow out is hard to see at

present, so many divergent beginnings have been made--the materialistic

vitalism of Driesch, the profound intuitionalism of Bergson, the

psychological biology of Delpino, France, Pauly, A. Wagner and W.

Mackenzie. But if any of these are destined to give the future direction

to biology, they will in a measure only be bringing biology back to its

pre-materialistic tradition, the tradition of Aristotle, Cuvier, von

Baer and J. Mueller. It may well be that the intransigent materialism of

the 19th century is merely an episode, an aberration rather, in the

history of biology--an aberration brought about by the over-rapid

development of a materialistic and luxurious civilisation, in which

man's material means have outrun his mental and moral growth.

Two movements seem significant in the morphology of the last decade or

so of the 19th century--first, the experimental study of form, and

second, the criticism of the concepts or prejudices of evolutionary

morphology.

The period was characterised also by the great interest taken in

cytology, following upon the pioneer work of Hertwig, van Beneden and

others on the behaviour of the nuclei in fertilisation and

maturation.[519] This line of work gained added importance in connection

with contemporary research and speculation on the nature of hereditary

transmission, and it has in quite recent years received an additional

stimulus from the re-discovery of Mendelian inheritance. Its importance,

however, seems to lie rather in its possible relation to the problems of

heredity than in any meaning it may have for the problems of form. More

significant is the revolt against the cell-theory started by Sedgwick[520]

and Whitman,[521] on the ground that the organism is something more than

an aggregation of discrete, self-centred cells.

The experimental work on the causes of the production and restoration of

form infused new life into morphology. It opened men's eyes to the fact

that the developing organism is very much a living, active, responsive

thing, quite capable of relinquishing at need the beaten track of normal

development which its ancestors have followed for countless generations,

in order to meet emergencies with an immediate and purposive reaction.

It was cases of this kind, cases of active regulation in development and

regeneration, that led men like G. Wolff and H. Driesch to cast off the

bonds of dogmatic Darwinism and declare boldly for vitalism and

teleology.

There was the famous case of the regeneration of the lens in Amphibia

from the edge of the iris--an entirely novel mode of origin, not

occurring in ontogeny. The fact seems to have been discovered first by

Colucci in 1891, and independently by G. Wolff in 1895.[522] The

experiment was later repeated and confirmed by Fischel and other

workers. Wolff drew from this and other facts the conclusion that the

organism possesses a faculty of "primary purposiveness" which cannot

have arisen through natural selection.[523] And, as is well known, Driesch

derived one of his most powerful arguments in favour of vitalism from

the extraordinary regenerative processes shown by _Tubularia_ and

_Clavellina_ in the course of which the organism actually demolishes and

rebuilds a part or the whole of its structure. But under the influence

of physiologists like Loeb many workers held fast to materialistic

methods and conceptions.

The great variety of regulative response of which the organism showed

itself capable made it very difficult for the morphologist to uphold the

generalisations which he had drawn from the facts of normal undisturbed

development. The germ-layer theory was found inadequate to the new

facts, and many reverted to the older criterion of homology based on

destiny rather than origin. The trend of opinion was to reject the

ontogenetic criterion of homology, and to refuse any morphological or

phylogenetic value to the germ-layers.[524]

The biogenetic law came more and more into disfavour, as the developing

organism more and more showed itself to be capable of throwing off the

dead-weight of the past, and working out its own salvation upon original

and individual lines.[525] A. Giard in particular called attention to a

remarkable group of facts which went to show that embryos or larvae of

the same or closely allied species might develop in most dissimilar ways

according to the conditions in which they found themselves.[526] His

classical case of "poecilogeny" was that of the shrimp _Palaemonetes

varians_, the fresh-water form of which develops in an entirely

different way from the salt-water form.

Experimental workers indeed were inclined to rule the law out of

account, to disregard completely the historical element in development,

and this was perhaps the chief weakness of the neo-vitalist systems

which took their origin in this experimental work.

From the side also of descriptive morphology the biogenetic law

underwent a critical revision. It was studied as a fact of embryology

and without phylogenetic bias by men like Oppel, Keibel, Mehnert, O.

Hertwig and Vialleton,[527] and they arrived at a critical estimate of it

very similar to that of von Baer.

Theoretical objections to the biogenetic law had been raised from time

to time by many embryologists, but the positive testing of it by the

comparison of embryos in respect of the degree of development of their

different organs starts with Oppel's work of 1891.[528] He studied a large

number of embryos of different species at different stages of their

development, and determined the relative time of appearance of the

principal organs and their relative size. His results are summarised in

tabular form and have reference to all the more important organs. He was

led to ascribe a certain validity to the biogenetic law, but he drew

particular attention to the very considerable anomalies in the time of

appearance which are shown by many organs, anomalies which had been

classed by Haeckel under the name of heterochronies.

Oppel's main conclusions were as follows:--"There are found in the

developmental stages of different Vertebrates 'similar ontogenetic

series,' that is to say, Vertebrates show at definite stages

similarities with one another in the degree of development of the

different organs. Early stages resemble one another, so also do later

stages; equivalent stages of closely allied species resemble one

another, and older stages of lower animals resemble younger stages of

higher animals; young stages are more alike than old stages.... The

differences which these similar series show (for which reason they

cannot be regarded as identical) may be designated as temporal

disturbances in the degree of development of the separate organs or

organ-systems. Some organs show very considerable temporal dislocations,

others a moderate amount, others again an inconsiderable amount. Among

the developmental stages of various higher animals can be found some

which correspond to the ancestral forms and also to the lower types

which resemble these ancestral forms. On the basis of the tabulated data

here given there can be distinguished with certainty in the ontogeny of

Amniotes a pro-fish stage, a fish-stage, a land-animal stage, a

pro-amniote stage, and following on these a fully developed reptile,

bird or mammal stage."[529]

Oppel's methods were employed by Keibel[530] in his investigations on the

development of the pig, which formed the model for the well-known series

of _Normentafeln_ of the ontogeny of Vertebrates which were issued in

later years under Keibel's editorship. Keibel was more critical of the

biogenetic law than Oppel, and he held that the ancestral stages

distinguished by Oppel could not be satisfactorily established. He

suggested an interesting explanation of heterochrony in development,

according to which the premature or retarded appearance of organs in

ontogeny stands in close relation with the time of their entering upon

functional activity. Thus in many mammals the mesodermal part of the

allantois often appears long before the endodermal part, though this is

phylogenetically older. This Keibel ascribes to the fact that the

endodermal part is almost functionless. "One can directly affirm," he

writes, "that the time of appearance of an organ depends in an eminent

degree upon the time when it has to enter upon functional activity. This

moment is naturally dependent upon the external conditions. Among the

highest Vertebrates, the mammals, the traces of phylogeny shown in

ontogeny are to a great extent obliterated through the adaptation of

ontogeny to the external conditions, and through the modifications which

the germs of more highly organised animals necessarily exhibit from the

very beginning as compared with germs which do not reach such a high

level of development" (p. 754, 1897).

Study of individual variation in the time of appearance of the organs in

embryos of the same species was prosecuted with interesting results by

Bonnet,[531] Mehnert,[532] and Fischel.[533] Fischel found that variability

was greatest among the younger embryos, and became progressively less in

later stages. Like von Baer (_supra_, p. 114) he inferred that

regulatory processes were at work during development which brought

divergent organs back to the normal and enabled them to play their part

as correlated members of a functional whole.

Important theoretical views were developed by Mehnert[534] in a series of

publications appearing from 1891 to 1898. Like Keibel, Mehnert

emphasised the importance of function in determining the late or early

appearance of organs, but he conceived the influence of function to be

exerted not only in ontogeny, but also throughout the whole course of

phylogeny, by reason of the transmission to descendants of the effects

of functioning in the individual life.

In his paper of 1897 Mehnert details the results of an extensive

examination of the development of the extremities throughout the Amniote

series. He finds that in all cases a pentadactylate rudiment is formed,

even in those forms in which only a few of the elements of the hand or

foot come to full development. But whereas in forms with a normally

developed hand, _e.g._ the tortoise and man, all the digits develop and

differentiate at about the same rate, in forms which have in the adult

reduced digits, _e.g._ the ostrich and the pig, these vestigial digits

undergo a very slow and incomplete differentiation, while the others

develop rapidly and completely. He draws a general distinction between

organs that are phylogenetically progressive and such as are

phylogenetically regressive, and seeks to prove that progressive organs

show an ontogenetic acceleration and regressive organs a retardation.[535]

The acceleration or retardation affects not only the mass-growth of the

organs, but also their histological differentiation.

Now between progression and functioning and between regression and

functional atrophy there is obviously a close connection. Loss of

function is well known to be one of the chief causes of the degeneration

of organs in the individual life, and on the other hand, as Roux has

pointed out, all post-embryonic development is ruled and guided by

functioning. It is thus in the long run functioning that brings about

phylogenetic progression, absence of functional activity that causes

phylogenetic regression. This comes about through the transmission of

acquired functional characters, a transmission which Mehnert conceives

to be extraordinarily accurate and complete.

In general Mehnert adopts the functional standpoint of Cuvier, von Baer,

and Roux. His considered judgment as to the phylogenetic value of the

biogenetic law closely resembles that formed by von Baer, for he admits

recapitulation only as regards the single organs, not as regards the

organism as a whole. He has, however, much more sympathy with the law

than either Keibel or Oppel, though he agrees that it cannot be used for

the construction of ancestral trees. But he ascribes to it as a fact of

development considerable importance. The following passage gives a good

summary of his view as to the scope and validity of the law. "The

biogenetic law has not been shaken by the attacks of its opponents. The

assertion is still true that individual organogenesis is exclusively

dependent on phylogeny. But we must not expect to find that all the

stages in the development of the separate organs, which coexisted in any

member of the phylogenetic series, appear _at the same time_ in the

individual ontogeny of the descendants, because each organ possesses its

own specific rate of development. In this way it comes about naturally

that organs which become differentiated rapidly, as, for example, the

medullary tube, as a rule dominate earlier periods of ontogeny than do

the organs of locomotion. For the same reason the cerebral hemispheres

of man are almost as large in youth as in maturity. The picture which an

embryo gives is not a repetition in detail of one and the same

phylogenetic stage; it consists rather of an assemblage of organs, some

of which are at a phyletically early stage of development, while others

are at a phyletically older stage."[536]

A different line of attack was that adopted by O. Hertwig in a series of

papers, which contain also what is perhaps the best critical estimate of

the present position and value of descriptive morphology.[537]

It had not escaped the notice of many previous observers that quite

early embryos not infrequently show specific characters even before the

characters proper to their class, order and genus are developed--in

direct contradiction of the law of von Baer. Thus L. Agassiz[538] had

remarked in 1859 that specific characteristics were often developed

precociously. "The Snapping Turtle, for instance, exhibits its small

crosslike sternum, its long tail, its ferocious habits, even before it

leaves the egg, before it breathes through lungs, before its derm is

ossified to form a bony shield, etc.; nay, it snaps with its gaping jaws

at anything brought near, when it is still surrounded by its amnion and

allantois, and its yolk still exceeds in bulk its whole body" (p. 269).

Wilhelm His,[539] in the course of an acute and damaging criticism of the

biogenetic law as enunciated by Haeckel, showed clearly that by careful

examination the very earliest embryos of a whole series of Vertebrates

could be distinguished with certainty from one another. "An identity in

external form of different animal embryos, despite the common

affirmation to the contrary, does not exist. Even at early stages in

their development embryos possess the characters of their class and

order, nay, we can hardly doubt, of their species and sex, and even

their individual characteristics" (201).

This specificity of embryos was affirmed with even greater confidence by

Sedgwick in a paper critical of von Baer's law.[540] He wrote:--"If v.

Baer's law has any meaning at all, surely it must imply that animals so

closely allied as the fowl and duck would be indistinguishable in the

early stages of development; and that in two species so closely similar

that I was long in doubt whether they were distinct species, viz.,

_Peripatus capensis_ and _Balfouri_, it would be useless to look for

embryonic differences; yet I can distinguish a fowl and a duck embryo on

the second day by the inspection of a single transverse section through

the trunk, and it was the embryonic differences between the Peripatuses

which led me to establish without hesitation the two separate

species.... I need only say ... that a species is distinct and

distinguishable from its allies from the very earliest stages all

through the development, although these embryonic differences do not

necessarily implicate the same organs as do the adult differences" (p.

39).

Hertwig interprets this fact of the specific distinctness of closely

allied embryos in the light of the preformistic conception of heredity.

According to this view the whole adult organisation is represented in

the structure of the germ-plasm contained in the fertilised ovum, from

which it follows that the ova of two different species, and also their

embryos at every stage of development, must be as distinct from one

another as are the adults themselves, even though the differences may

not be so obvious. If this be the case there can be no real

recapitulation in ontogeny of the phylogeny of the race, for the

egg-cell represents not the first term in phylogeny, but the last. The

egg-cell _is_ the organism in an undeveloped state; it has a vastly more

complicated structure than was possessed by the primordial cell from

which its race has sprung, and it can in no way be considered the

equivalent of this ancestral cell.

Hertwig puts this vividly when he says that "the hen's egg is no more

the equivalent of the first link in the phylogenetic chain than is the

hen itself" (p. 160, 1906, b).

If ontogeny is not a recapitulation of phylogeny, how is it that the

early embryonic stages are so alike, even in animals of widely different

organisation? Hertwig's answer to this is very interesting. He takes the

view that many of the processes characterising early embryonic

development are the means necessarily adopted for attaining certain

ends. Such are the processes of segmentation, the formation of a

blastula, of cell-layers, of medullary folds where the nervous system is

a closed tube, the formation of the notochord as a necessary condition

of the development of the vertebral column, and so on. "Looked at from

this standpoint it cannot surprise us that in all animal phyla the

earliest embryonic processes take place in similar fashion, so that we

observe the occurrence both in Vertebrates and Invertebrates of a

segmentation-process, a morula-stage, a blastula and a gastrula. If now

these developmental processes do not depend on chance, but, on the

contrary, are rooted in the nature of the animal cell itself, we have no

reason for inferring from the recurrence of a similar

segmentation-process, morula, blastula, and gastrula in all classes of

the animal kingdom the common descent of all animals from one

blastula-like or gastrula-like ancestral form. We recognise rather in

the successive early stages of animal development only the manifestation

of special laws, by which the shaping of animal forms (as distinct from

plant forms) is brought about" (p. 178, 1906, b).

"The principal reason why certain stages recur in ontogeny with such

constancy and always in essentially the same manner is that they provide

under all circumstances the necessary pre-conditions through which alone

the later and higher stages of ontogeny can be realised. The unicellular

organism can by its very nature transform itself into a multicellular

organism only by the method of cell-division. Hence, in all Metazoa,

ontogeny must start with a segmentation-process, and a similar statement

could be made with regard to all the later stages" (p. 57, 1906, a).

Similarities in early development are therefore no evidence of common

descent, and in the same way the resemblances of adult animals, subsumed

under the concepts of homology and the unity of plan, are not

necessarily due to community of descent, but may also be brought about

by the similarity or identity of the laws which govern the evolution of

these animals. In the absence, therefore, of positive evidence as to the

actual lines of descent (to be obtained only from palaeontology),

homological resemblance cannot be taken as proof of blood relationship,

for homology is a wider concept than homogeny. The only valid definition

of homology is that adopted in pre-evolutionary days, when those organs

were considered homologous "which agree up to a certain point in

structure and composition, in position, arrangement, and relation to the

neighbouring organs, and accordingly possess identical functions and

uses in the organism" (p. 151, 1906, b).

The concept of homology has thus a value quite independent of any

evolutionary interpretation which may be superadded to it. "Homology is

a mental concept obtained by comparison, which under all circumstances

retains its validity, whether the homology finds its explanation in

common descent or in the common laws that rule organic development" (p.

151, 1906, b). As A. Braun long ago pointed out, "It is not descent

which decides in matters of morphology, but, on the contrary, morphology

which has to decide as to the possibility of descent."[541]

Hertwig, in a word, reverts to the pre-evolutionary conception of

homology. "We see in homology," he writes, "only the expression of

regularities (_Gesetzmaessigkeiten_) in the organisation of the animals

showing it, and we regard the question, how far this homology can be

explained by common descent and how far by other principles, as for the

present an open one, requiring for its solution investigations specially

directed towards its elucidation" (p. 179, 1906, b).

Holding, as he does, that no definite conclusions can be drawn from the

facts of comparative anatomy and embryology as to the probable lines of

descent of the animal kingdom, Hertwig accords very little value to

phylogenetic speculation. It is, he admits, quite probable that the

archetype of a class represents in a general sort of way the ancestral

form, but this does not, in his opinion, justify us in assuming that

such generalised types ever existed and gave origin to the present-day

forms. "It is not legitimate to picture to ourselves the ancestral forms

of the more highly organised animals in the guise of the lower animals

of the present day--and that is just what we do when we speak of

Proselachia, Proamphibia and Proreptilia" (p. 155, 1906, b).

He rejects on the same general grounds the evolutionary dogma of

monophyletic or almost monophyletic descent, and admits with Koelliker,

von Baer, Wigand, Naegeli and others that evolution may quite well have

started many times and from many different primordial cells.

There is indeed a great similarity between the views developed by O.

Hertwig and those held by the older critics of Darwinism--von Baer,

Koelliker, Wigand, E. von Hartmann and others. It is true the

philosophical standpoint is on the whole different, for while many of

that older generation were vitalists Hertwig belongs to the mechanistic

school.

But both Hertwig and the older school agree in pointing out the _petitio

principii_ involved in the assumption that the archetype represents the

ancestral form; both reject the simplicist conception of a monophyletic

evolution (which may be likened to the "one animal" idea of the

transcendentalists); both admit the possibility that evolution has taken

place along many separate and parallel lines, and explain the

correspondences shown by these separate lines by the similarity of the

intrinsic laws of evolution; finally, both emphasise the fact that we

know nothing of the actual course of evolution save the few indications

that are furnished by palaeontology, and both insist upon the unique

importance of the palaeontological evidence.[542]

It was a curious but very typical characteristic of evolutionary

morphology that its devotees paid very little attention to the positive

evidence accumulated by the palaeontologists,[543] but shut themselves up

in their tower of ivory and went on with their work of constructing

ideal genealogies. It was perhaps fortunate for their peace of mind that

they knew little of the advances made by palaeontology, for the evidence

acquired through the study of fossil remains was distinctly unfavourable

to the pretty schemes they evolved.

As Neumayr, Zittel, Deperet, Steinmann and others have pointed out, the

palaeontological record gives remarkably little support to the ideal

genealogies worked out by morphologists. There is, for instance, a

striking absence of transition forms between the great classificatory

groups. A few types are known which go a little way towards bridging

over the gaps--the famous _Archaeopteryx_, for example--but these do not

always represent the actual phylogenetic links. There is an almost

complete absence of the archetypal ancestral forms which are postulated

by evolutionary morphology. Amphibia do not demonstrably evolve from an

archetypal Proamphibian, nor do mammals derive from a single generalised

Promammalian type. Few of the hypothetical ancestral types imagined by

Haeckel have ever been found as fossils. The great classificatory groups

are almost as distinct in early fossiliferous strata as they are at the

present day. As Deperet says in his admirable book,[544] in the course of

a presentation of the matured views of the great Karl von Zittel, "We

cannot forget that there exist a vast number of organisms which are not

connected by any intermediate links, and that the relations between the

great divisions of the animal and vegetable kingdoms are much less close

than the theory [of evolution] demands. Even the Archaeopteryx, the

discovery of which made so much stir and appeared to establish a genetic

relation between classes so distinct as Birds and Reptiles, fills up the

gap only imperfectly, and does not indicate the point of bifurcation of

these two classes. Intermediate links are lacking between Amphibia and

Reptiles. Mammals, too, occupy an isolated position, and no zoologist

can deny that they are clearly demarcated from other Vertebrates;

indeed, no fossil mammal is certainly known which comes nearer to the

lower Vertebrates than does Ornithorhynchus at the present day" (p.

115).

To take a parallel from the Invertebrata, B. B. Woodward,[545] after

discussing the phylogeny of the Mollusca as worked out by the

morphologists and comparing it with the probable actual course of the

evolution of the group, as evidenced by fossil shells, sums up as

follows:--"The lacunae in our knowledge of the interrelationships of the

members of the various families and orders of Mollusca are slight

however, compared with the blank caused by the total absence from

palaeontological history of any hint of passage forms between the classes

themselves, or between the Mollusca and their nearest allies. Nor is

this hiatus confined to the Molluscan phylum; it is the same for all

branches of the animal kingdom. There is circumstantial evidence that

transitional forms must have existed, but of actual proof none whatever.

All the classes of Mollusca appear fully fledged, as it were. No form

has as yet been discovered of which it could be said that it in any way

approached the hypothecated prorhipidoglossate mollusc, still less one

linking all the classes" (p. 79).

Pointing in the same direction as the absence of transitional forms is

the undeniable fact that all the great groups of animals appear with all

their typical characters at a very early geological epoch. Thus, in the

Silurian age a very rich fauna has already developed, and

representatives are found of all the main Invertebrate groups--sponges,

corals, hydroid colonies, five types of Echinoderms, Bryozoa,

Brachiopods, Worms, many types of Mollusca and Arthropoda. Of

Vertebrates, at least two types of fish are present--Ganoids and

Elasmobranchs. In the very earliest fossiliferous rocks of all, the

Precambrian formation, there are remains of Molluscs, Trilobites and

Gigantostraca, similar to those which flourished in Cambrian and

Silurian times.

The contributions of palaeontology to the solution of the problems of

descent posed by morphology are, however, not all of this negative

character. The law of recapitulation is in some well-controlled cases

triumphantly vindicated by palaeontology. Thus Hyatt and others found

that in Ammonites the first formed coils of the shell often reproduce

the characters belonging to types known to be ancestral, and what is

more they have demonstrated the actual occurrence of the phenomenon

known as acceleration or tachygenesis, often postulated by speculative

morphologists.[546] This is the tendency universally shown by embryos to

reproduce the characters of their ancestors at earlier and earlier

stages in their development.

The most valuable contribution made by palaeontologists to morphology and

to the theory of evolution arose out of the careful and methodical study

of the actual succession of fossil forms as exemplified in limited but

richly represented groups. Classical examples were the researches of

Hilgendorf[547] on the evolution of _Planorbis multiformis_ in the

lacustrine deposits of Steinheim, those of Waagen[548] on the phylogeny of

_Ammonites subradiatus_, and the work of Neumayr and Paul[549] on

_Paludina_ (_Vivipara_).

These investigations demonstrated that it was possible to follow out

step by step in superjacent strata the actual evolution of fossil

species and to establish the actual "phyletic series."

To take an example from among the Vertebrates, Deperet has shown (_loc.

cit._, pp. 184-9), that the European Proboscidea, belonging to the three

different types of the Elephants, Mastodons and Dinotheria, have evolved

since the Oligocene epoch along five distinct but continuous lines. The

Dinotherian stock is represented at the beginning of the Miocene by the

relatively small form _D. cuvieri_; this changes progressively

throughout Miocene times into _D. laevius_, _D. giganteum_, and _D.

gigantissimum_. Among the Mastodons two quite distinct phyletic series

can be distinguished, the first commencing with _Palaeomastodon

beadnelli_ of the Oligocene, and evolving between the Miocene and

Pliocene into _Mastodon arvernensis_, after traversing the forms _M.

angustidens_ and _M. longirostris_, the second starting with the _M.

turicensis_ of the Lower Miocene and evolving through _M. borsoni_ into

the _M. americanus_ of the Quaternary. The phyletic series of the true

elephants in Europe are relatively short, and go back only to the

Quaternary, _Elephas antiquus_ giving origin to the Indian elephant, _E.

priscus_ to the African.

The careful study of phyletic series brought to light the significant

fact that these lines of filiation tend to run for long stretches of

time parallel to, and distinct from one another, without connecting

forms. This is clearly exemplified in the case of the Proboscidea, and

many other examples could be quoted. Almost all rich genera are

polyphyletic in the sense that their component species evolve along

separate and parallel lines of descent.[550] "Such great genera as the

genus _Hoplites_ among the Ammonites, the genus _Cerithium_ among the

Gastropoda, the genus _Pecten_ or the genus _Trigonia_ among the

Lamellibranchs, each comprise perhaps more than twenty independent

phyletic series" (Deperet, p. 200).

Variation along the phyletic lines is gradual[551] and determinate, and

appears to obey definite laws. The earliest members of a phyletic series

are usually small in size and undifferentiated in structure, while the

later members show a progressive increase in size and complexity. Rapid

extinction often supervenes soon after the line has reached the maximum

of its differentiation.

The general picture which palaeontology gives us of the evolution of the

animal kingdom is accordingly that of an immense number of phyletic

lines which evolve parallel to one another, and without coalescing,

throughout longer or shorter periods of geological times. "Each of these

lines culminates sooner or later in mutations of great size and highly

specialised characters, which become extinct and leave no descendants.

When one line disappears by extinction it hands the torch, so to speak,

to another line which has hitherto evolved more slowly, and this line in

its turn traverses the phases of maturity and old age which lead it

inevitably to its doom. The species and genera of the present day belong

to lines that have not reached the senile phase; but it may be surmised

that some of them, _e.g._ elephants, whales, and ostriches, are

approaching this final phase of their existence" (Deperet, p. 249).

It is one of the paradoxes of biological history that the

palaeontologists have always laid more stress upon the functional side of

living things than the morphologists, and have, as a consequence, shown

much more sympathy for the Lamarckian theory of evolution. The American

palaeontologists in particular--Cope, Hyatt, Ryder, Dall, Packard,

Osborn--have worked out a complete neo-Lamarckian theory based upon the

fossil record.

The functional point of view was well to the fore in the works of those

great palaeontologists, L. Ruetimeyer (1825-1895) and V. O. Kowalevsky

(1842-83), who seem to have carried on the splendid tradition of Cuvier.

Speaking of Kowalevsky's classical memoir, _Versuch einer natuerlichen

Classification der fossilen Hufthiere_, Osborn[552] writes:--"This work is

a model union of the detailed study of form and function with theory and

the working hypothesis. It regards the fossil not as a petrified

skeleton, but as having belonged to a moving and feeding animal; every

joint and facet has a meaning, each cusp a certain significance. Rising

to the philosophy of the matter, it brings the mechanical perfection and

adaptiveness of different types into relation with environment, with

changes of herbage, with the introduction of grass. In this survey of

competition it speculates upon the causes of the rise, spread, and

extinction of each animal group. In other words, the fossil quadrupeds

are treated _biologically_--so far as is possible in the obscurity of

the past" (p. 8). The same high praise might with justice be accorded to

the work of Cope on the functional evolution of the various types of

limb-skeleton in Vertebrates, and on the evolution of the teeth as well

as to the work of other American palaeontologists, including Osborn

himself.

Osborn's law of "adaptive radiation," which links on to Darwin's law of

divergence,[553] constitutes a brilliant vindication of the functional

point of view. "According to this law each isolated region, if large and

sufficiently varied in its topography, soil, climate, and vegetation,

will give rise to a diversified mammalian fauna. From primitive central

types branches will spring off in all directions, with teeth and

prehensile organs modified to take advantage of every possible

opportunity of securing food, and in adaptation of the body, limbs and

feet to habitats of every kind, as shown in the diagram [on p. 363]. The

larger the region and the more diverse the conditions, the greater the

variety of mammals which will result.

"The most primitive mammals were probably small insectivorous or

omnivorous forms, therefore with simple, short-crowned teeth, of

slow-moving, ambulatory, terrestrial, or arboreal habit, and with short

feet provided with claws. In seeking food and avoiding enemies in

different habitats the limbs and feet radiate in four diverse

directions; they either become _fossorial_ or adapted to digging habits,

_natatorial_ or adapted to _amphibious_ and finally to _aquatic_

habits, _cursorial_ or adapted to swift-moving, terrestrial progression,

_arboreal_ or adapted to tree life. Tree life leads, as its final stage,

into

LIMBS AND FEET.

Volant.

/

Fossorial. Arboreal.

\ /

Short-limbed, plantigrade, } Ambulatory

pentadactyl, unguiculate } or

Stem. } Terrestrial.

/ \

Natatorial. Cursorial

Amphibious. Digitigrade.

/ \

Aquatic Unguligrade.

TEETH.

Omnivorous.

{ Grass.

{ Fish. | { Herb.

Carnivorous { Flesh. | Herbivorous { Shrub.

\ { Carrion. | / { Fruit.

\ | / { Root.

\ | /

\ | / Myrmecophagous.

\ | / / Dentition reduced.

\ | / /

\ | / /

\ | / /

\ |/ /

Stem: Insectivorous.

the parachute types of the flying squirrels and phalangers, or into the

true flying types of the bats.... Similarly in the case of the teeth,

insectivorous and omnivorous types appear to be more central and ancient

than either the exclusively carnivorous or herbivorous types. Thus the

extremes of carnivorous adaptation, as in the case of the cats, of

omnivorous adaptation, as in the case of the bears, of herbivorous

adaptation, as in the case of the horses, or myrmecophagous adaptation,

as in the case of the anteaters, are all secondary" (_loc. cit._, pp.

23-4).

We have now reached the end of our historical survey of the problems of

form. What the future course of morphology will be no one can say. But

one may hazard the opinion that the present century will see a return to

a simpler and more humble attitude towards the great and unsolved

problems of animal form. Dogmatic materialism and dogmatic theories of

evolution have in the past tended to blind us to the complexity and

mysteriousness of vital phenomena. We need to look at living things with

new eyes and a truer sympathy. We shall then see them as active, living,

passionate beings like ourselves, and we shall seek in our morphology to

interpret as far as may be their form in terms of their activity.

This is what Aristotle tried to do, and a succession of master-minds

after him. We shall do well to get all the help from them we can.

[519] See E. B. Wilson's masterly book, _The Cell in

Development and Inheritance_, New York and London, 1900.

[520] _Q.J.M.S._, xxvi. 1886.

[521] _Wood's Holl Biological Lectures_ for 1893.

[522] _Arch. f. Ent.-Mech._, i., pp. 380-90, 1895.

[523] _Beitraege zur Kritik der Darwinschen Lehre_,

Leipzig, 1898.

[524] See E. B. Wilson, "The Embryological Criterion of

Homology," _Wood's Holl Biological Lectures_, Boston,

pp. 101-24, 1895; Braem, _Biol. Centrblt._, xv., 1895;

T. H. Morgan, _Arch. f. Ent.-Mech._, xviii.; J. W.

Jenkinson, _Mem. Manchester Lit. Phil. Soc._, 1906, and

_Vertebrate Embryology_, Oxford, 1913; A. Sedgwick,

article "Embryology" in _Ency. Brit._, p. 318, vol. xi.,

11th Ed. (1910).

[525] For a detailed treatment of this important point see

the remarkable volume of E. Schulz (Petrograd),

_Prinzipien der rationellen vergleichenden Embryologie_,

Leipzig, 1910.

[526] "La Poecilogonie," _Bull. Sci. France et Belgique_,

xxxix., pp. 153-87, 1905.

[527] _Un probleme de l'evolution. La loi biogenetique

fondamentale_, Paris and Montpellier, 1908.

[528] _Vergleichung des Entwickelungsgrades der Organe zu

verschiedenen Entwickelungszeiten bei Wirbeltieren_,

Jena, 1891.

[529] Quoted by Keibel, _Ergebn. Anat. Entwick._, vii., p.

741.

[530] "Studien zur Entwickelungsgeschichte des Schweines,"

Schwalbe's _Morphol. Arbeiten_, iii., 1893, and v.,

1895.

_Normentafeln zur Entwickelungsgeschichte des

Schweines_, Jena, 1897.

"Das biogenetische Grundgesetz und die Cenogenese,"

_Ergebn. Anat. Entw._, vii., pp. 722-92, 1897.

"U. d. Entwickelungsgrad der Organe," _Handb. vergl.

exper. Entwick. der Wirbelthiere_, iii., 3, pp. 131-48,

1906.

[531] "Beitraege zur Embryologie der Wiederkaeuer," _Arch.

Anat. Entw._, 1889.

[532] "Die individ. Variation d. Wirbeltierembryo,"

_Morph. Arbeit._, v., 1895.

[533] "U. Variabilitaet u. Wachstum d. embryonalen

Koerpers," _Morph. Jahrb._, xxiv., 1896.

[534] "Gastrulation u. Keimblaetterbildung der _Emys

lutaria taurica_," _Morph. Arbeit._, i., 1891.

"Kainogenese," _Morph. Arbeit._, vii., pp. 1-156, 1897,

and also separately. _Biomechanik, erschlossen aus dem

Prinzipe der Organogenese_, Jena, 1898.

[535] This law was foreshadowed by Reichert in 1837, when he

wrote:--"We notice in our investigation of embryos of different

animal forms that it is those organs, those systems, which in the

fully developed individual are peculiarly perfect, that in their

earliest rudiments and also throughout the whole course of their

development appear with the most striking distinctness" (Mueller's

_Archiv_, p. 135, 1837). See also his _Entwick. Kopf. nackt.

Amphib._, p. 198, 1838. So, too, Rathke notes how the elongated

shape of the snake appears even in very early embryonic stages

(_Entwick. Natter._, p. 111, 1839).

[536] Quoted by Keibel (p. 790, 1897) from the

_Biomechanik_.

[537] _Die Zelle und die Gewebe_, Jena, 1898, and the

subsequent editions of this text-book, published under

the title of _Allgemeine Biologie. Die Entwickelung der

Biologie im neunzehnten Jahrhundert_, Jena, 1900, 2nd

ed., 1908. "Ueber die Stellung der vergl.

Entwickelungslehre zur vergl. Anatomie, zur Systematik

und Descendenztheorie," _Handb. vergl. exper.

Entwickelungslehre der Wirbeltiere_, iii., 3, pp.

149-80, Jena, 1906. (1906, b). Also in Pt. I. of Vol. I.

(1906, a).

[538] _An Essay on Classification_, London, 1859.

[539] _Unsere Koerperform_, Leipzig, 1874.

[540] _Q.J.M.S._, xxxvi., pp. 35-52, 1894.

[541] Quoted by Hertwig. See also K. Goebel, "Die

Grundprobleme der heutigen Pflanzenmorphologie," _Biol.

Centrbl._, xxv., pp. 65-83, 1905.

[542] This is also emphasised by Fleischmann in his critical study of

evolutionary morphology entitled _Die Descendenztheorie_, Leipzig,

1901.

[543] The same remark applies to the bulk of speculation as to the

factors of evolution, with the exception of the contributions made

to evolution theory by the palaeontologists by profession, such as

Cope.

[544] _Les Transformations du Monde animal_, Paris, 1907.

[545] "Malacology _versus_ Palaeoconchology," _Proc.

Malacological Soc._, viii., pp. 66-83, 1908.

[546] Particularly by E. Perrier, "La Tachygenese," _Ann.

Sci. nat._ (_Zool._) (8), xvi., 1903.

[547] _Monatsber. k. Akad. Wiss._, Berlin, pp. 474-504,

1866.

[548] _Geognost. u. Palaeont. Beitraege_, ii., Heft 2, pp.

181-256, 1869.

[549] _Abhand. k.k. Geol. Reichsanstalt_, vii., Wien,

1875.

[550] The case for polyphyletism is very strongly put by

G. Steinmann in his book, _Die geologischen Grundlagen

der Abstammungslehre_, Leipzig, 1908.

[551] The steps in this chronological variation were

termed by Waagen "mutations."

[552] _The Age of Mammals in Europe, Asia, and North

America_, New York, 1910.

[553] _Origin of Species_, 6th ed., Chap. IV.

INDEX

ACTINOZOAN THEORY of Vertebrate Descent, 299-300

Adaptation as Conservative Principle--

Cuvier, 39, 76

Adaptation, Ecological--

Von Baer, 123

H. Milne-Edwards, 199

Lamarck, 221, 222, 223, 224, 227

Treviranus, 225 f.n.

C. Darwin, 231-2, 235, 239

Haeckel, 248, 263

Gegenbaur, 263

V. O. Kowalevsky, 362

Osborn, 362-4

Adaptation, Ecological, and Classification--

Bronn, 203

Adaptation of Parts. _See_ "Correlation, Functional," and "Conditions of

Existence"

Adaptive Radiation (Osborn), 362-4

Agassiz, A., 288 f.n., 295

On Coelom, 296

Agassiz, L.--

Criticism of Vertebral Theory of Skull, 157

Membrane and Cartilage Bones, 164

Transcendentalism, 203

Classification, 203 f.n.

Three-fold Parallelism, 230, 255

Influence on Darwin, 238

Specific Distinctness of Embryos, 353

Albertus Magnus, 17

Alcmaeon, 1

Aldrovandus, 18

Allman, 209

Analogy. _See also_ Homology.

Aristotle, 8-10

Owen, 108

Haeckel, 251

Gegenbaur, 266

Lankester, 267

Anaxagoras, 14

Anaximander, 14

Anaximenes, 1

Animal and Vegetative Lives--

Aristotle, 16, 32

Buffon, 26-7

Bergson, 26 f.n.

Cuvier, 26, 32

Bichat, 27-9

Oken, 94

K. G. Carus, 94

Von Baer, 116, 123, 131

Remak (Sensory and trophic layers), 210

Gegenbaur, 263

Annelid Theory of Vertebrate Descent, 274-85, 301

Archetype, Anatomical, 246, 302-3

E. Geoffroy, 54, 67

Owen, 104-7, 110

J. V. Carus, Huxley, 204

C. Darwin, 238 f.n.

Archetype, Anatomical, as Ancestral--

C. Darwin, 235, 247

Haeckel, 251

Gegenbaur, 265

Sedgwick, 300

Criticism of this idea--

O. Hertwig, 355-7

Archetype, Embryological, 168, 246, 302-3

Von Baer, 126, 132

Reichert, 139, 147, 149

Rathke, 151, 153

Huxley, 159-61

Archetype, Embryological, as Ancestral--

C. Darwin, 233, 236-7

Haeckel, 254, 289-91

Gegenbaur, 266

O. and R. Hertwig, 298

Sedgwick, 300

A. Kowalevsky, 300

Arendt, 162

Aristotle, 2-16, 17, 345, 364

_Historia Animalium_, 2

_De Partibus Animalium_, 2, 9

Knowledge of Animals, 3, 4

Comparative Embryology, 4

Classification of Animals, 4-6

Unity of Plan, 6-7, 10

Homology and Analogy, 7-10

Teleology and Correlation, 10-12

Law of Compensation, 11

Division of Labour, 12

Degrees of Composition--homogeneous and heterogeneous parts, 12-14, 169

Law of Development (Von Baer), 14

Scale of Beings, 14-16

Functional attitude, 15-16, 197

Animal and Vegetative Lives, 16, 32

Ascidian Theory of Vertebrate Descent, 269-73, 304

Atomists, 16

Atomists, "Biological," 192-4

Audouin, V.--

Unity of plan in Arthropods, 85-6

Law of Compensation, 86

Marine Zoology, 195

Autenrieth, 90, 96

Avicenna, 17

BABAK, E., 333

Baer, K. E. von, 113-32, 133, 251, 304, 345, 356

Founder of Embryology, 113

_Entwickelungsgeschichte der Thiere_, 114

Regulation of Development, 114, 350

Development as Differentiation, 115, 128

Germ-Layer Theory, 115-6, 118-119, 208-9, 296

Morphological Differentiation, 116-7

Histological Differentiation, 117-8

Tissues and Germ-Layers, 118

Double symmetrical Development, 118, 279

Criticism of Meckel-Serres Law, 120-3, 304

Theory of Types, 123-4, 289, 291

Law of Development, 124-6

Embryological Criterion, 126-8, 132, 138

Embryological Archetype, 126, 132

Types of Development, 127-8

Von Baer and Cuvier, 128-30

Functional attitude, 129

Relation to Transcendentalists, 129, 131

Criticism of Scale of Beings, 130

Vertebral Theory of Skull, 131, 142

Serial Homology, 131-2

Gill-slits, Gill-arches and Aortic arches, 135-6, 146

Membrane and Cartilage Bones, 162-3

Degrees of Composition, 172

Ova of Mammals, 175-6

Segmentation of Ovum, 186

Criticism of Evolution Theory, 229, 242

Influence on Darwin, 236, 238

Criticism of Darwinism, 242

Teleology and Correlation, 242

On Ascidians, 271

Baer's Law. _See_ "Development, Von Baer's Law"

Bagge, 187

_Balanoglossus_ Theory of Vertebrate Descent, 285-7

Balbiani, 330

Balfour, F. M., 247, 299

Annelid Theory, 282-4

Gastrulation and Gastraea Theory, 295

Mesoderm, 296 f.n.

Coelom, 297

Barfurth, D., 330

Barry, M., 186, 188

Bateson, W.--

Metamerism, Vegetative Repetition, 286

_Balanoglossus_ Theory, 286-7

On Phylogenetic Speculation, 302

Beard, J., 285

Belon, 18

Beneden van, and Julin, 271, 285, 346

Bensley, A. B., 311 f.n.

Bergmann, 187

Bergson, H., 26 f.n., 341, 345

Bernard, Claude, 195, 314

Bert, P., 315

Bichat, X., 27-30, 118, 132, 169, 178, 263

Animal and Vegetative Lives, 27-9

"General Anatomy," 29-30

_Vie propre_ of Tissues, 30

Biogenetic Law. _See_"Development, Haeckel's Law"

Bischoff, 138

Segmentation, 186, 188

Blainville, de, 96, 128, 141, 199 f.n.

Bojanus, 96, 97

Bonnet, C.--

Scale of Beings, 22-3, 220, 227

Evolution, 215

Regeneration, 315

Bonnet, R., 350

Bonnier, G., on Albertus Magnus, 17

Born, G., 330

Boveri, T., 270 f.n., 333

Braem, 347 f.n.

Braun, A., 355

Breschet, 138, 173

Bronn, H. G., 200-3, 248

_Naturphilosophie_, 201

Functional attitude, 201-3

Geometry of Organism, 201, 249

Theory of Types, 202

Principle of Connections, 202

Intrinsic Laws of Evolution, 202

Division of Labour, 202

Ecological Adaptation and Classification, 203

Brown, R., 171

Bruch, C., 203 f.n.

Buechner, 194, 248

Buffon, 24-7, 336

Scale of Beings, 24, 215

Unity of Plan, 24

Evolution, 24-5, 214

Classification, 25-6

Animal and Vegetative Lives, 26-7

Homology and Analogy, 27

Burckhardt, R., 3 f.n., 268 f.n.

Burdin, 96

Burmeister, 249 f.n.

Butler, S., 226 f.n., 313, 335-42

Relation to Lamarck, 335-7

Psychological Vitalism, 336-41

Heredity and Memory, 337-41

The Two Stages of Development, 337-9

Consciousness and Habit, 337-9

Recapitulation Theory, 339-40

Teleology, 341

CABANIS, 215

Camper, P., 45, 46

Carter, 293 f.n.

Carus, J. V.--

Criticism of Embryological Criterion, 167

Morphology and Physiology, 194

Vertebral Theory of Skull, 203

On Archetype, 204

Evolution, 230

Carus, K.G.--

Law of Parallelism, 94, 249

Vertebral Theory, 96

Geometry of Skeleton, 98-100

Splanchnoskeleton, 98, 140

Causal Morphology, 312-3, 315-34

Cell-Theory--

Schwann, 169, 173-86, 188

C. F. Wolff, 170

Schleiden, 170-2

Criticism of Schwann-Schleiden Theory, 185-8

Virchow, Leydig, 188

Cell-Theory and Germ-Layer Theory--

Remak, 209-12

Cell-Theory as Disintegrative--

Schwann, 180-5, 248

Vogt, 190-1

Virchow, 191

Haeckel, 248

Criticism of this idea--

Reichert, 192-3, 194

J. V. Carus, 194

Sedgwick, Whitman, 346

Cell-Theory, Influence on Morphology, 190

Cenogenesis, 258-9, 323

Chabry, 331

Child, C. M., 333

Chun, C, 317, 332

Classification of Animals--

Aristotle, 4-6

Rondeletius, Aldrovandus, Gesner, 18

Linnaeus, 22

Buffon, 25-6

Cuvier, 39-41

E. Geoffroy, 60

L. Agassiz, 203 f.n.

Lamarck, 216-7, 227, 228

Classification and Ecological Adaptation (Bronn), 203

Classification as Genealogical--

Buffon, 24-5

Lamarck, 218, 228

C. Darwin, 233, 234, 247

Haeckel, 250-1, 254

Criticism of this idea, 303, 304,

O. Hertwig, 356

Classification, Phylogenetic--

Haeckel's, 289-94

Claus, 259

Co-adaptation, 326 f.n.

Coelom--

Remak, 211

A. Kowalevsky, 270, 295, 297

Haeckel, 291, 295, 296

Lankester, 291, 297

Coelom, Theory of, 295-301

Cohen, 189

Coiter, 18

Colucci, 346

Compensation, Law of--

Aristotle, 11

Goethe, 49

E. Geoffroy, 72-3

Audouin, 86.

German Transcendentalists, 100

Condillac, 215

Conditions of Existence, Principle of--

Cuvier, 34, 75-6, 239

Gegenbaur, 263-4

Roux, 324, 326

Spencer, Weismann, 326 f.n.

Disregard for--

Lamarck, 226

C. Darwin, 232, 238-41

Haeckel, 248, 264

Conklin, 333

Connections, Principle of--

Goethe, 47

E. Geoffroy, 53-4, 62-3, 71, 74, 261

Audouin, 85

Connections, Principle of--_contd._

German Transcendentalists, 100

J. F. Meckel, 101

Owen, 107-8

Bronn, 202

C. Darwin, 234-5

Gegenbaur, 261

Semper, 279

In Embryology, 168

Main Principle of Morphology, 246, 302

Convergence--

Milne-Edwards, 199

I. Geoffroy St Hilaire, 199 f.n., 206

C. Darwin, 236

Friedmann, Willey, Vialleton, 306 f.n.

Convergence, Rejected by Evolutionary Morphologists, 305, 312

Hubrecht, 305-6

Cope, E. D., 342, 357 f.n., 361, 362

Correlation, Functional--

Aristotle, 10-12

Cuvier, 35-8, 239, 241

E. Geoffroy, 77

Von Hartmann, 240-1

Radl, 240 f.n., 241

Von Baer, 242

Gegenbaur, 264

Disregarded by--

C. Darwin, 235, 238-41

Haeckel, 248, 264

Coste, 134, 138, 176, 187

Crampton, 332

Cunningham, J. T., 284

Cuvier, 26, 31-44, 89, 196, 197, 199 f.n., 278, 345, 361

Functional attitude, 31-6, 65, 75-8, 200, 305

Animal and Vegetative Lives, 32

Degrees of Composition, 32-3

Teleology, 33-5

Functional Adaptedness, 33-5, 324

Principle of Conditions of Existence, 34, 75-6, 239

Correlation, 35-8, 239, 241

Metabolism, 38

Adaptation as Conservative Principle, 39, 76

Classification, 39-41

Principle of Subordination of Characters, 40

Criticism of Scale of Beings, 39-40, 130

Type Theory, 41, 124, 289, 291

Criticism of Evolution-Theory, 41-4, 129, 304

Variation, Limits of, 42

Palaeontological Succession, 43

Polemic with Geoffroy, 64-5, 74-8

Criticism of Vertebral Theory of Skull, 97-8

Influence on J. F. Meckel, 101

Criticism of Meckel-Serres Law, 129-30, 304

As Embryologist, 130

Criticism of Lamarck, 228

Cytology, 346

Cytoplasm of Egg, Organ-forming Stuffs, 332-3

DALL, 361

D'Alton, 113

Dareste, C., 315

Darwin, Charles, 78, 230-41, 271, 304, 307, 336, 362

Systematist and Field Naturalist, 230, 231

Palaeontological Succession, 231

Ecological Adaptation, 231-2, 235, 239

Species Problem, 231

Functional Adaptation, Disregard for, 232, 238-41

Classification as genealogical, 233, 234, 247

Unity of Plan due to Community of Descent, 233, 234-5, 239, 247

Embryological Archetype as ancestral, 233, 236-7

Rejects Meckel-Serres Law, 233, 236

Interpretation of Vestigial Organs, 233, 237

Organism as Historical Being, 233, 308

Rejects Scale of Beings, 234

Homology, 234-5, 247

Principle of Connections, 234-5

Anatomical Archetype as ancestral, 235, 247

Von Baer's Law interpreted phylogenetically, 236-7

Modifications inherited at corresponding age, 237

Monophyletism and Polyphyletism, 238

Causes of Success, 238, 241

Darwin, Erasmus, 214, 226 f.n., 229, 336

Darwin, Sir Francis, 344

Daubenton, 26

Degrees of Composition--

Aristotle, 12-14, 169

Glisson, 19

Malpighi, 20

Bichat, 29-30

Cuvier, 32-3,

Dujardin, 169, 188

Von Baer, 172

Effect of Invention of Microscope, 20

Relation to Cell-Theory, 169

Delage, 333

Delage and Herouard, 273 f.n.

Delpino, 345

Demaillet, 44

Democritus, 16

Deperet, C, 357

On Cuvier, 43

Absence of intermediary forms in Palaeontology, 358

Phyletic series and Polyphyletism, 360-1

Development, Von Baer's Law--

Aristotle, 14

Von Baer, 124-6

Prevost and Dumas, 125 f.n.

Reichert, 149-50, 351 f.n.

Milne-Edwards, 205-8

Lereboullet, 206-8

Criticised by--

Agassiz, 352-3

His, 353

Sedgwick, 353

O. Hertwig, 354

Phylogenetic Interpretation of--

Darwin, 236-7

Gegenbaur, 266

Relation to Haeckel's Law, 254, 256, 257

Development, Biogenetic Law (Haeckel)--

Haeckel, 251, 253-9, 291-4

F. Mueller, 252-3, 254, 257

Gegenbaur, 262

Roux, 319

Butler, 339-40

Orr, 342

Criticism of--

Vialleton, 348

Oppel, 348-9

Keibel, 349-50

Mehnert, 350-2

O. Hertwig, 352, 354-5

His, 353

Relation to Laws of Meckel-Serres and Von Baer, 254, 256, 257, 303, 309

Relation to Heredity and Development, 312-3

Influence of Causal Morphology, 347-8

Palaeontological Evidence for, 359

Development, Meckel-Serres Law--

Harvey, 18

Hunter, 22

E. Geoffroy, 69-70, 72

Serres, 80-3, 94, 203-4, 205-6

Kielmeyer, Autenrieth, Oken, 90

Development, Meckel-Serres Law-_contd._

Tiedemann, 91

J. F. Meckel, 91-3

K. G. Carus, 94

Criticism of--

Von Baer, 120-3, 304

Cuvier, 129-30, 304

Milne-Edwards, 205

Lereboullet, 206-8

C. Darwin, 233, 236

Analogy with Biogenetic Law, 254-7, 262, 303, 304, 309

Development, Meckel-Serres Law, Theory of Three-fold Parallelism--

L. Agassiz, 230, 255

Tiedemann, Vogt, 255 f.n.

Haeckel, 254-5

Development, The two periods of--

Roux, 320-4, 325, 327, 335

Butler, 337-9

Diogenes of Apollonia, 1

Disintegration. _See_ "Cell-Theory," and "Materialistic Attitude"

Division of Labour, Principle of--

Aristotle, 12

Milne-Edwards, 197-8

Bronn, 202

Gegenbaur, 264

Dohrn, A., 269, 274-8

Annelid Theory of Vertebrate Descent, 274-7, 303

Principle of Function-Change, 276-8, 307

Functional Attitude, 277-8, 307

Formal Attitude, 306

Doellinger, I., 113, 157

Dollo, 311

Donne, 173

D'Orbigny, 43

Driesch, H., 242, 331, 332, 333, 334, 345, 346-7

Duges, A., 86-8, 100, 134, 142, 146

Unity of Plan, 87

Polyzoic conception of Organism, 87-8

Membrane and Cartilage Bones, 163

Dujardin, 169, 188

Dumas. _See_ Prevost and Dumas

Dumeril, 96

Dumortier, 173

Dutrochet, 99 f.n., 130, 134

Duverney, 19

EAR-OSSICLES, Homology of--

E. Geoffroy, 56

Spix, 100

Rathke, 141, 150

Reichert, 144-7

_Echelle des etres. See_ "Scale of Beings."

Ehlers, 284

Eisig, H., 284, 285

Embryology, Comparative, Early Workers--

Aristotle, 4, 113

Fabricius, Harvey, 18, 113

Malpighi, 20, 113

Oken and Kieser, 90, 113

Haller, C. F. Wolff, J. F. Meckel, Tiedemann, 113

Embryology, Experimental, 317, 318, 330-3

Embryological Archetype. _See_ "Archetype, Embryological"

Embryological Criterion of Homology, 133-168, 347

Goethe, 49

E. Geoffroy, 72, 110

Cuvier, 75, 110, 130

Owen, 110-1

Von Baer, 126-8, 132, 138

Rathke, 138, 140-1

J. Mueller, 138

Reichert, 138-9, 144-7, 163

Vogt, 156-7

Huxley, 158-9, 166

Koelliker, 165-6

Criticised by--

Owen, J. V. Carus, 167

Empedocles, 1, 15

Engramm (Semon), 343

_Entwicklungsgesetz._ _See_ "Evolution, Intrinsic Laws of"

_Entwicklungsmechanik_, 315

Erasistratus, 17

Evolution Theory--

Lucretius, 16

Buffon, 24-5, 214

Cuvier's criticism, 41-4, 129, 304

E. Geoffroy, 66-9, 73, 228

J. F. Meckel, 92-3, 215, 228

Leibniz, 213

Kant, 213-4

Erasmus Darwin, 214, 229

C. Bonnet, Oken, Robinet, Treviranus, 215

Tiedemann, 215, 255 f.n.

Lamarck, 215-29

Von Baer, 229, 242

I. Geoffroy St Hilaire, J. V. Carus, 230

Charles Darwin, 230-41

Von Hartmann, 240-1, 244, 356

Koelliker, 243

Owen, 244

Milne-Edwards, 244-5

Haeckel, 250-9

Gegenbaur, 265

The Organism as an Historical Being, 308-13

C. Darwin, 233, 308

Haeckel, 252, 257

Sedgwick, 308

Roux, 313, 322-4

Butler, 313, 336-41

Evolution-Theory, Influence on Morphology, 302-13

Evolution, Intrinsic Laws of, 241

J. F. Meckel, 93

Bronn, 202

Von Baer, 229, 242, 356

Koelliker, Naegeei, 243, 356

Owen, 244

Von Hartmann, 244, 356

Milne-Edwards, 244-5

O. Hertwig, 354-5, 356-7

Wigand, 356

Deperet, 361

FABRICIUS, 18, 113

Fallopius, 18

Fischel, 346, 350

Fischer, 328

Fleischmann, 357 f.n.

Flourens, 46, 315

Fontana, 172

Forbes, E., 196

Formal Attitude, 246, 305

Goethe, 49

E. Geoffroy, 62-3, 71, 75-8, 305

Haeckel, 249, 257, 260

Gegenbaur, 261, 263

Semper, 279

Adopted by Evolutionary Morphologists, 302-8, 311-2, 314

Hubrecht, 305-6

Dohrn, 306

France, R., 345

Friedmann, 306 f.n.

Fuld, 333

Functional Adaptation, 316-7, 318, 320-9, 333, 344, 351

Functional Attitude--

Aristotle, 15-6, 197

Bichat, 27-9

Cuvier, 31-6, 65, 75-8, 200, 305

Goethe, 49-50

J. F. Meckel, 101

Owen, 109, 110, 111

Von Baer, 129

Milne-Edwards, 195, 197-200

J. Mueller, Reichert, 200

Bronn, 201-3

Lamarck, 222-6, 307, 335

Gegenbaur, 260, 263-4

Dohrn, 277-8, 307

Roux, 320-9, 335

Houssay, 333

Butler, 336-41

G. Wolff, 346

Driesch, 346-7

Giard, 347

E. Schulz, 347 f.n.

Keibel, 349-50

Mehnert, 350-1

American Palaeontologists, 361, 362

Ruetimeyer, 361

V. O. Kowalevsky, 361-2

Osborn, 362-4

Function-Change, Principle of--

Dohrn, 276-8, 306, 307

Eisig, 284

Fuerbringer, M., 282 f.n., 284, 323 f.n.

GALEN, 17

Gastraea Theory, 269, 288-95, 298, 299-3O1, 303

Gastrula, Discovery of, 288

Gaupp, E., 310 f.n.

Gegenbaur, C, 247, 260-7, 271, 285, 286, 288 f.n.

Division of Egg-nucleus, 188

Functional Attitude, 260, 263-4

Formal Attitude, 261, 263

Principle of Connections, 261

Embryology and Comparative Anatomy, 261-2, 263

Biogenetic and Meckel-Serres Laws, 262

Homology, 261, 263, 265, 266-7

Adaptation and Correlation, 263-4

Archetype as ancestral, 263 f.n, 265

On Phylogenetic Speculation, 265-6

Embryological Archetype, 266

Membrane and Cartilage Bones, 309, 310

Gemmill, J. F., 285 f.n., 312 f.n.

Geoffroy, Etienne, St Hilaire, 40, 52-78, 141

Unity of Plan, 52-65, 70 ff., as conservative, 75, 78

Principle of Connections, 53-4, 62-3, 71, 74, 261

Unity of Composition, 54, 70-1, 75-6, 200, 305

Archetype, 54, 67

Metastasis, 55-6, 59, 74

Opercular Bones, 56

Unity of Composition of Sternum, 57-60

Classification, 60

Vertebrates and Articulates, 60-4, 274, 278-9, 303

Formal Attitude, 62-3, 65, 71, 75-8, 305

Cephalopods and Vertebrates, 64-5

Scale of Beings, 64

Polemic with Cuvier, 64-5, 74-8

Evolution, 66-9, 73, 228

Biogenetic Law, 69

Teratology, 69, 315

Meckel-Serres Law, 70, 72

Criteria of Homology, 71, 72, 110

Law of Compensation, 72-3

Criticism of his Principles, 74

Relation to German Transcendentalists, 89, 100-1

Vertebral Theory of Skull, 96, 97

Influence on Darwin, 234-5, 238

Geoffroy, Isidore, St Hilaire, 65 f.n., 199 f.n., 230

Geometry of the Organism, 33

K. G. Carus, 98-100, 249

Bronn, 201, 249

Haeckel, J. Mueller, Burmeister, G. Jaeger, 249

Germinal Vesicle (Egg-nucleus), 175-7, 188, 291 f.n.

Germ-Layer Theory--

Von Baer, 115-6, 118-9, 208-9, 296

Pander, 119-20, 209

C. F. Wolff, 119-20

Rathke, 136, 208

Lereboullet, Bischoff, 208

Huxley, 208, 289

Remak, 209-12, 296

Germ-Layers and Gastraea Theory--

Haeckel, 289-95

Lankester, Balfour, 295

Germ-Layer Theory, Influence of Causal Morphology on, 347

Gesner, 18

Giard, A.--

On Ascidian Theory, 271-3

Adaptive Homology, 273

Poecilogeny, 347-8

Glisson, F., 19

Gluge, 173

Goebel, K., 356 f.n.

Goethe, 45-51, 65, 89, 250

Unity of Plan, 45-7, 51

Homology, 47

Principle of Connections, 47

Formal and Functional Attitudes, 48-50

Teleology, 48

Metamorphosis of Plants, 48

Repetition of parts, 48-9

Vertebral Theory of Skull, 49, 96, 97

Law of Compensation, 49

Embryological Criterion, 49

Organisms as Nature's Works of Art, 50

Goette, 259

Graaf, von, 175

Grew, N., 169

Gruber, 330

HAECKEL, Ernst, 247-60, 271, 314, 342, 353, 357

His sources, 248-50

Materialism, 248, 250

On Teleology, Heredity and Adaptation, 248, 263

Correlation, Disregard for, 248, 264

Geometry of the Organism (Promorphology), 249

Repetition of Parts (Tectology), 249-50

Classification as Genealogical, 250-1, 254

Archetype as ancestral, 251

Homology and Analogy, 251

Biogenetic Law, 251, 253-9, 291-4

Three-fold parallelism, 254-5

Scale of Beings, 255, 256-7

Organism as an Historical Being, 257

Prussianism, 257

Palingenesis, 258

Cenogenesis, 258-9

Heterotopy, Heterochrony, 259

Gastraea Theory, 269, 288-95

Phylogenetic Classification, 289-94

Criticism of Theory of Types, Monophyletism, 289, 291

Gastraea Theory and Biogenetic Law, 291-4

Primary stages of Ontogeny and Phylogeny, 291-3

Coelom, 291, 295, 296

Experimental Embryology, 317

Haller, 113

Harting, 284 f.n.

Hartmann, E. von--

On Darwin's conception of correlation, 240-1

Evolution, 244, 356

Hartog, M., 344

Harvey, 18, 113

Hatschek, 270 f.n., 299

Helmholtz, H. von, 195

Henle, 172

Hensen, V., 209 f.n.

Herbst, C., 333

Herder, 46

Heredity and Memory, 336-44

Hering, E., 341-2

"Heritage" Characters, 309, 322

Herlitzka, 332

Herophilus, 17

Hertwig, O., 163, 330, 331, 346

On C. F. Wolff, 119

Fertilisation, 291 f.n.

Membrane and Cartilage Bones, 309-10

Biogenetic Law, 352, 354-5

Von Baer's Law, 354

Intrinsic Laws of Evolution, 354-5, 356-7

Homology not necessarily Homogeny, 355-7

Unity of Plan not necessarily due to Community of Descent, 355-7

On Phylogenetic Speculation, 356

Hertwig, O. and R.--

Coelom Theory, 297-8

Nervous System of Coelentera, 299

Heterochrony, 259, 348, 349-52

Heterogeneous Generation (Koelliker), 243

Heterotopy, 259

Hilgendorf, 359

Hill, 311

Hippocratic Treatises, 2

His, W., 206 f.n., 209 f.n.

Causal Morphology, 316

Cytoplasm of Egg, Organ-forming Stuffs, 333

Specific Distinctness of Embryos, 353

Histological Differentiation (von Baer), 117-8

Histology. _See also_ "Cell-Theory"

Malpighi, 20

Stensen, 21

Bichat, 29-30, 169, 178

Von Baer, 117-8

Schwann, 178

Remak, 209-12

Hofer, B., 330

Hofmeister, 185

Homogeny, 267, 303, 355

Homology, 168, 303, 355-7. _See also_ "Connections, Principle of," and

"Embryological Criterion"

Aristotle, 7-10

Belon, 18

Buffon, 27

Goethe, 47

E. Geoffroy, 53, 71

Serres, 80

Owen, 107-9

Lamarck, 227

C. Darwin, 234-5, 247

Haeckel, 251

Gegenbaur, 261, 263, 265, 266-7

Giard, 273

Semper, 279

O. Hertwig, 355-7

Braun, 355

Homology, Genetic Definition of--

Gegenbaur, 266

Lankester, 267

O. Hertwig's criticism, 355-7

Homoplasy, 267

Hooke, R., 20, 169

Houssay, F., 19 f.n., 333

Hubrecht, A. A. W., 284, 295 f.n., 301, 305-6

Hunter, J., 22, 315

Huschke, 134-5, 136, 141, 146

Huxley, T. H., 157, 238, 247

On Rathke, 154 f.n.

Embryological Criterion, 158-9, 166

Embryological Archetype, 159-61

Criticism of Vertebral Theory of Skull, 161-2

Membrane and Cartilage Bones, 166-7

On Archetype, 204

Germ-Layer Theory, 208, 289

Criticism of Three-fold Parallelism, 230 f.n.

Coelom, 297

Ancestry of Marsupials, 311

Hyatt, A., 359, 361

INSTINCT and Morphogenesis, Analogy of, vi., 307, 312

Lamarck, 220, 226

JACOBSON , 164

Jaeger, G., 249 f.n.

_Jardin des Plantes_, Paris, 19

Jenkinson, J. W., 347 f.n.

On His, 316

Jones, Wharton, 138, 176

Julin, C., 271, 285

Jussieu, de, 40

KANT, I.--

Teleology, 35, 213, 242

Unity of Plan, 46, 213-4

Evolution, 213-4

Keibel, F., 348, 349-50

Kerkring, 131

Kielmeyer, 89, 90, 96

Kieser, 90

Kleinenberg, N., 277

Kohlbrugge, J., 44 f.n., 65 f.n.

Koelliker, A.--

On C. F. Wolff, 119

Vertebral Theory of Skull, 157

Membrane and Cartilage Bones, 164-6, 310

Embryological Criterion, 165-6

Cell-division, 187

Intrinsic Laws of Evolution, 243, 356

Saltatory Variation, 243

Kowalevsky, A., 269-71, 284, 285, 299, 300

Development of Amphioxus, 270

Ascidians, 270-1

Coelom, 270, 295, 297

Gastrula, 288

Kowalevsky, V. O., 361-2

Krause, 176

Kupffer, 271

LACAZE-DUTHIERS, H. de, 203 f.n., 315-6

On Ascidians, 271, 273

Lamarck, 44, 66, 78, 215-29

Relation to Buffon, 215

Scale of Beings, 215-8, 220-1, 227-8

As Evolutionary, 218, 220

Classification, 216-7, 227, 228

Species Problem, 216, 227

Materialism, 218-9, 222-3, 225-6

Psychological Vitalism, 219, 220-6, 307, 335

_Sentiment interieur_, 219-20, 222-3, 225

Ecological Adaptation, 221, 222, 223, 224, 227

Laws of Evolution, 221-5

Transmission of Acquired Characters, 221-2, 224

Subtle Fluids, 222

Use and Disuse, 223-4

Independence of Current Thought, 226-7

Homology and Analogy, 227

Reception of his Theory, 228-9

Lamarck and Butler, 335-7

Lang, A., 301

Lankester, Sir E. Ray, 247

Homology, Homogeny, Homoplasy, and Analogy, 267

_Balanoglossus_ Theory of Vertebrate Descent, 287

Germ-Layer Theory and Phylogenetic Classification, 291

Planula Theory, 295

On Coelom Theory, 296-7, 299 f.n.

Latreille, 86, 100

Laurencet, 64

Lavocat, 203 f.n.

Leeuenhoek, 20, 21, 169

Leibniz, 23, 213, 343

Lereboullet--

Von Baer's Law, 206-8

Germ-layer Theory, 208

Gastrula, 288 f.n.

Leucippus, 16

Leuckart, 193 f.n., 194, 297

Levy, O., 333

Leydig, 187, 188, 275 f.n., 285

Linnaeus, 22

Loeb, J., 333, 347

_Loi de Balancement_. _See_ "Compensation, Law of"

Loven, 186, 196

Lucretius, 16

On the Soul, 222 f.n.

Ludwig, 193, 194, 314

Lyell, Sir C., 228 f.n.

Lyonnet, 22

MACBRIDE, E. W., 287 f.n.

M'Kendrick, J.--

On Fontana, 172

Mackenzie, W., 345

Malpighi, M., 20-1, 113, 169

Marine Zoology, Rise of, 195-6

Materialistic Attitude, 246-7, 345, 364

Schwann, 180-5

Vogt, 190-1

Virchow, 191

Ludwig, 193

Materialistic Physiology, 193-4, 314-5, 347

Lamarck, 218-9, 222-3, 225-6

The Darwinians, 241, 308

Haeckel, 248, 250

Roux, 315, 317, 318-9, 329

Semon, 343

Rignano, 344

Loeb, 347

Criticism of this attitude--

Reichert, 192-3

Meckel, D. A., 95

Meckel, J. F., 113

Meckel-Serres Law, 91-3

Evolution, 92-3, 215, 228

Teratology, 93-4

Repetition of Parts, 95

Vertebral Theory of Skull, 96

Eclecticism, 101

Meckel's Cartilage, 141, 145

Meckel-Serres Law. _See_ "Development, Meckel-Serres Law"

Mehnert, E., 348, 350-2

Membrane and Cartilage Bones, 162-7, 309-10

Memory and Heredity, 336-44

Mendelism, 346

Mesenchyme, 298

Mesoderm, 209-11, 296, 297, 298

Metabolism--

Cuvier, 38

Schwann, 182-5

Roux, 324, 329

Metamerism, 94, 95, 100, 109, 131-2, 266-7, 274-5, 279, 282, 286, 299, 301

Metamorphosis of Plants, 48, 235

Metastasis, Principle of--

E. Geoffroy, 55-6, 59, 74

Owen, 106

Metschnikoff, E., 278 f.n., 285, 288

Criticism of Ascidian Theory, 271

Coelom, 295, 296, 297

Meyen, 170, 185

Meyer, E., 284

Meyranx, 64

Microscope, Invention of, 19

Milne-Edwards, H., 12, 86, 238

Marine Zoology, 195

Functional Attitude, 195, 197-200

Unity of Plan, 197

Division of Labour, 197-8

Ecological Adaptation, Convergence, 199

Von Baer's Law, Polemic with Serres, 204-8

Evolution, 244-5

Mirbel, 170, 171

Mivart, St G., 277

Mohl, von, 170, 185

Moldenhawer, 170

Moleschott, 194

Moquin-Tandon, A., 87

Morgan, T. H., 317 f.n., 332, 333, 347 f.n.

Mosaic Theory of Development, 330-3

Mueller, F., Biogenetic Law, 252-3, 254, 257

Mueller, H., 166

Mueller, J., 136, 209 f.n., 260, 285, 309, 345

Embryological Criterion, 138

Vertebral Theory of Skull, 142-4, 154, 157

On Reichert, 150

Cell Theory, 172-3

Division of Egg-nucleus, 188

Vitalism, 192

Marine Zoology, 196

Functional Attitude, 200

Mutations (Waagen), 361 f.n.

NAEGELI, 185, 243 f.n., 356

_Naturphilosophie._ _See_ "Philosophy of Nature"

Nesbitt, R., 162

Neumayr, 357, 360

Nussbaum, M., 330

OKEN, L., 89, 113, 131, 134, 149

Meckel-Serres Law, 90-1

Teratology, 91

Repetition of Parts, 94-5

Serial Homology, 95-6, 100

Vertebral Theory, 96, 97, 98

On Geoffroy, 100

Influence on Serres, 205

Evolution, 215

Ollier, 315

Oppel, A., 318 f.n., 324 f.n., 327, 348-9

Orr, H. F., 342

Osborn, H. F., 214 f.n., 361

On V. O. Kowalevsky, 362

Functional Attitude, 362-4

Law of Adaptive Radiation, 362-4

Owen, R., 97, 102-12, 204

Eclecticism, 102

Vertebral Theory of Skeleton, 103-7

Archetype of Vertebrate Skeleton, 104-7, 110

Vertebral Theory of Skull, 104-6

Metastasis, 106

Principle of Connections, 107-8

Anatomy and Embryology, 108

Homology and Analogy, 108

Classes of Homology, 108-9, 266

Functional Attitude, 109, 110, 111

Embryological Criterion, 110, 167

Homological and Teleological Compoundedness, 110-1

Vegetative Repetition of Parts, 111, 286

Unity of Plan as Conservative Principle, 112

Influence on Darwin, 234, 235, 238

Evolution, 244

PACKARD, 361

Palaeontological Record, 357-61

Absence of connecting forms, 357-9

Biogenetic Law, 359

Phyletic Series, 359-61

Palaeontological Succession--

Cuvier, 43

E. Geoffroy, 67

L. Agassiz, 230, 255

C. Darwin, 231

Milne-Edwards, 245

Tiedemann, 255 f.n.

Paley, W., 341

Palingenesis (Haeckel), 258, 323

Pander, 113, 119-20, 133, 208, 209

Parallelism, Theory of. _See_ "Development, Meckel-Serres Law"

Three-fold. _See_ "Development, Meckel-Serres Law"

Paris Museum of Natural History, 19, 89, 101

Paul, 360

Pauly, A., 345

Perrault, C., 19

Perrier, E., 88, 359 f.n.

Pflueger, E., 317, 330

Philipeaux, 315

"Philosophy of Nature," 89, 94, 98, 203, 248

Phyletic Series, 359-61

Physiology, Separation from Morphology, 194, 247, 260, 314

Physiology of Development, 315

Planula Theory (Lankester), 295

Plato, 15

Pockels, 138

Poecilogeny (Giard), 347-8

Poli, 175

Polyphyletism--

Darwin, 238

Von Baer, 242, 356

Koelliker, Wigand, Naegeli, 356

Deperet, 360-1

Steinmann, 360 f.n.

Polyzoic Conception of Organism--

Duges, 87

Perrier, 88

Prevost and Dumas, 125 f.n., 134, 175, 186

Promorphology (Haeckel), 249

Protoplasm, 169, 188-9

Purkinje, 172, 173, 175, 176, 189

QUATREFAGES, A. de, 172, 195-6

RADL, E., on Goethe, 48

Correlation, 240 f.n., 241

On Darwin's Critics, 242 f.n.

On Cuvier's Critics, 278 f.n.

Rathke, H., 133, 136-7, 174, 194, 269, 351 f.n.

Discovery of Gill-slits in Pig and Chick, 134

Discovery of Gill-slits in Man, 135

Germ-Layer Theory, 136, 208

Embryological Criterion, 138, 140-1

Homologies of Gill-arches, 139-41, 146, 150

Development of Skull, 141, 150-4

Vertebral Theory of Skull, 141, 154-6

Embryological Archetype, 151, 153

Membrane and Cartilage Bones, 163, 166

Rauber, A., 330

Reaumur, 22, 315

Recapitulation Theory. _See_ "Development, Biogenetic Law"

Regeneration, 315, 318, 333, 346

Regulatory Processes in Development, 114, 319, 333, 346-7, 350

Reichert, C. B., Embryological Criterion, 138-9, 144-7, 163

Archetype, 139, 147, 149

Homologies of Gill-arches and Ear-ossicles, 144-7

Vertebral Theory of Skull, 147-9, 157

Von Baer's Law, 149-50, 351 f.n.

Membrane and Cartilage Bones, 163, 165, 166, 310

Criticism of "Biological Atomists," 192-3, 194

Functional Attitude, 193, 200

Remak, R., 118, 288 f.n.

On Vertebrae, 157

Cell Theory, 173, 187-8, 209

Microscopical Technique, 209 f.n.

Germ-Layer Theory, 209-12, 296

Cells, Tissues and Germ-Layers, 209-12

Mesoderm, 209-11

Coelom, 211, 296

Repetition of Parts within the Organism, Theory of. _See also_

"Vertebral Theory of Skull"

Goethe, 48-9

Duges, 87-8

Oken, 94-5

J. F. Meckel, D. A. Meckel, 95

Haeckel (Tectology), 249-50

Reymond, E. du Bois, 194, 314

Rignano, E., 343-4

Robinet, 23, 215

Rondeletius, 18

Rosenhof, Roesel von, 22

Roux, W., 313, 315-29, 344, 351

_Entwicklungsmechanik_, 315, 317-8

Materialistic Attitude, 315, 317, 318-9, 329

Functional Adaptation, 316-7, 318, 320-9, 333

Experimental Embryology, 317, 318, 330-1

Simple and Complex Components, 318-20

Functional Definition of Life, 320

Functional Attitude, 320-9, 335

The Two Periods of Development, 320-4, 325, 327, 335

Mosaic Theory of Development, 323, 330-1

Metabolism, 324, 329

Structure, Functional and Non-functional, 324-6

Functional Unity of Organism, 326

Functional Adaptation of Blood-vessels, 326-9

Form as manifestation of Activity, 329

Ruini, C., 18

Rusconi, 133-4, 186

Ruetimeyer, L., 361

Ryder, 361

SACHS, J. von, 170

St Ange, M., 146

Salensky, 259

Saltatory Variation--

E. Geoffroy, 78

Von Baer, 242

Koelliker, 243

Owen, 244

Sarcode, 169

Sars, M., 186, 196

Savigny, J. C., 83-5, 100, 137, 271

Scale of Beings, 89, 206, 214-5

Aristotle, 14-6

Anaximander, Anaxagoras, 14

Empedocles, Plato, 15

Albertus Magnus, 17

C. Bonnet, 22-3

Robinet, 23

Buffon, 24

E. Geoffroy, 64

Lamarck, 215-8, 220-1, 227-8

As Evolutionary, 218, 220

Haeckel, 256-7

Criticism of this idea--

Cuvier, 39-40, 130

Von Baer, 130

Milne-Edwards, 205

Lereboullet, 207

Darwin, 234

Haeckel, 255

Relation to Evolution-Theory, 214-5

Schepelmann, 333

Schleiden, 170-2

Schmieden, 328

Schults, C. H., 173

Schultze, Max, 189

Schultze, O., 331

Schulz, E., 347 f.n.

Schwann, Theodor, 169, 173-86, 248

Physiological Standpoint, 173, 179, 180, 182

Development of Cells, 174-5, 179-80

Cellular Nature of Ovum, 175-7

Development of Tissues from Cells, 177-8

Histology, 178

Materialism and Teleology, 180-3, 185

Cell-metabolism, 182-5

Cells as organic Crystals, 184-5

Sedgwick, A., 347 f.n.

Actinozoan Theory of Vertebrate Descent, 299-300

Metamerism, 299

Embryological Archetype, 300

Organism as Historical Being, 308

Cell-Theory, 346

Von Baer's Law, 353

Segmentation of Ovum, 186-8

Seiler, 138

Selection, Natural and Artificial, 307 f.n.

Self-Differentiation (Roux), 319, 320-1, 322, 323, 324, 327

Self-Regulation (Roux), 319

Semon, R., 342-3

Semper, C., 259, 269, 278-82, 284, 286

Annelid Theory, 274, 278-82

Metamerism, 274, 279, 282

Follower of Geoffroy, 278

Unity of Plan and Composition, 279, 303

Principle of Connections, 279

Formal Attitude, 279

_Sentiment interieur_ (Lamarck), 219-20, 222-3, 225

Serial Homology. _See_ "Metamerism"

Serres, E., 79-83, 91, 100, 205-6, 257 f.n.

Criteria of Homology, 80

Law of parallelism, 80-3, 94, 203-4, 205-6

Law of Multiple Formation, 80-1

Unity of Plan, 83, 205, 206

Teratology, 83

Meckel's Cartilage, 145 f.n.

Transcendentalism, 205-6

Concrescence Theory, 206 f.n.

Severino, 18

Sharpey, 162, 176

Siebold, von, 186

Skull, Development of, 139-62.

_See also_ "Vertebral Theory"

Spallanzani, 315

Species-Problem--

Cuvier, 42

Lamarck, 216, 227

Darwin, 231

Spencer, H., 326 f.n.

Spengel, 285, 287

Spinoza, 343

Spix, 96, 97, 100, 141

Stannius, 165

Steenstrup, 309

Steinmann, G., 357, 360 f.n.

Stensen (Steno), 21

Swammerdam, 20, 21-2

TACHYGENESIS, 359

Technique, Microscopical, 209 f.n., 268

Tectology (Haeckel), 249

Teleology--

Aristotle, 10

Cuvier, 33-5

Kant, 35, 213, 242

Von Baer, 242

Owen, Von Hartmann, 244

Butler, 341

G. Wolff, Driesch, 346

Criticism of--

Goethe, 48

Schwann, 180-2

The Darwinians, 241

Haeckel, 248

Evolutionary Morphologists, 308

Teratology, 69, 83, 91, 93, 315

Thienemann, 23 f.n.

Thompson, D'Arcy W., 2 f.n.

Thomson, A., 176

Thomson, J. Arthur, 215 f.n.

Tiedemann, 91, 113, 215, 255 f.n.

Tissues and Germ-Layers, 118, 209-12

Transcendental Anatomy, Relation to Evolutionary Morphology, 302-8, 312

Transcendentalism, French and German Schools, 89, 100

Trembley, 22, 315

Treviranus, 141, 170, 215, 225 f.n.

Turpin, 173

Types, Theory of (Cuvier and Von Baer)--

Cuvier, 41, 124, 289, 291

Von Baer, 123-4, 289, 291

Bronn, 202

Lereboullet, 207

Types, Theory of (Cuvier and Von Baer)--_contd._

Criticised by--

E. Geoffroy, 60

Haeckel, 289, 291

Lankester, 291

Type-Theory and Evolution, 304

UNGER, 185

Unity of Composition, Principle of, Geoffroy, 54, 70-2, 75-6, 200, 305

Unity of Plan, 88, 241, 278-9, 303, 312. _See also_ "Archetype"

Aristotle, 6-7, 10

Belon, Severino, 18

Perrault, 19

Robinet, 23

Buffon, 24

Cuvier, 41

Goethe, 45-7, 51

Vicq D'Azyr, 45

Camper, 45, 46

Herder, 46

Kant, 46, 213-4

E. Geoffroy, 52-65, 70 ff.

Serres, 83, 205, 206

Savigny, 83

Audouin, 85-6

Latreille, 86

Duges, 86-7

J. F. Meckel, 101

Milne-Edwards, 197

Semper, 279

Haeckel, 289, 291

Lankester, 291

Unity of Plan as due to Community of Descent--

Darwin, 233, 234-5, 239, 247

Haeckel, 250-1

Gegenbaur, 263 f.n., 265

Criticism of this idea--

O. Hertwig, 355-7

Unity of Plan as Conservative Principle--

E. Geoffroy, 75, 78

Owen, 112

Gegenbaur, 263-4

Evolutionary Morphologists, 307

VALENTIN, 138, 173, 176

Variation, Limits of, Cuvier, 42

Vegetative Repetition of Parts--

Owen, 111, 286

Bateson, 286

Velpeau, 138

Vertebral Theory of Skull, 49, 96-9, 104-6, 131, 141-4, 147-9, 154-7,

161-2, 165, 203, 235, 310 f.n.

Vertebrate Descent, 269-87, 299-301, 304

Verworn, M., 330

Vesalius, 18

Vestigial Organs, 233, 237, 309, 312

Vialleton, L., 306 f.n., 348

Vicq d'Azyr, 45, 95

Virchow, R., 188, 191

Vitalism, Psychological--

Lamarck, 219, 220-6, 307, 335

Butler, 336-41

Orr, Cope, 342

Ward, 343

Delpino, France, Pauly, A. Wagner, Mackenzie, 345

Vogt, C.--

Criticism of Vertebral Theory, 156-7

Capillaries, 179

Segmentation, 186

Materialistic Attitude, 190-1

Threefold Parallelism, 255 f.n.

WAAGEN, 359, 361 f.n.

Wagner, A., 345

Wagner, R., 176

Ward, J., 343

Weber, 138

Weismann, A., 240, 323, 326 f.n., 330-1, 343

Werneck, 173

Whitman, C. O., 346

Wigand, A., 242 f.n., 356

Willey, A., 273 f.n., 306 f.n.

Williamson, 309

Willis, 19

Wilson, E. B., 331, 332-3, 346 f.n., 347 f.n.

Wolff, C. F., 113

Germ-layer Theory, 119-20

Cells, 170

Wolff, G., 346-7

Woodward, B. B., 358

Wotton, E., 17

ZELENY, 333

Zittel, K. von, 357, 358

Zoja, 331

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Form and Function: A Contribution to the History of Animal Morphology · 第 20 / 20 章