ANCESTRAL TREE OF THE MAMMALIA.

_'Systematische Phylogenie,' § 386._

_Perissodactyla_ _Homo_ _Carnivora_

| (_Litopterna_) | | _Pinnipedia_

| | | | |

+-------+ _Anthropoidae_ +------+

_Artiodactyla_ | | |

| | | _Carnassia_

+----------+ _Catarhinæ_ |

| | _Chiroptera_ |

_Proboscidea_ | | | _Insectivora_ |

| | _Platyrhinæ_ | | |

(_Amblypoda_) | | | | +-------+

| | | | | | _Rodentia_

+-------+ | _Simiæ_ +-------+ |

| | | | (_Tillodontia_)

+--+ | | |

_Cetacea_ | | | _Trogontia_

| _Sirenia_ | _Lemures_ _*Ictopsales*_ | _Edentata_

| | | | | | |

_Cetomorpha_ | _Hyracoidea_ | | _*Esthonychales*_

| | | | | |

+---_?_---+------+ | | |

| _*Lemuravidæ*_ | |

_*Condylarthrales*_ | +-------+ |

| | | |

+--------Eutheria s. Placentalia------------------+

|

| _Marsupialia polyprotodontia_

_Marsupialia diprotodontia_ | |

| | |

+-------------Metatheria--------------+

|

| _Monotremata_

| | (_Allotheria_)

| | |

| +-----------------+

| |

Prototheria-----+

|

|

_*Hypotheria s.*_ _*Promammalia*_

_Names in brackets indicate extinct groups.

Names *underlined* indicate hypothetical groups or combinations._

22. Stage of _Simiæ_. Orbit completely separated from the temporal

fossa by an inward extension of the frontal and malar bones meeting the

alisphenoid. Placenta consolidated into a disc, and with a maternal

deciduous portion. Mammæ pectoral only. The dental formula is 2.1.3.3.

All the fingers and toes are protected by flat nails. The tail is long.

The American prehensile-tailed monkeys are a lower side-branch.

23. Stage of _Catarrhinæ Cercopithecidæ_. The dental formula is

2.1.2.3, owing to the loss of one pair of premolars in each jaw.

The frontal and alisphenoid bones are in contact, separating the

parietal from the malar bone; this feature is correlated with the

enlarged brain. The internarial septum is narrow, and the nostrils

look forwards and downwards instead of sidewards--hence the term

'Catarrhinæ.' The external auditory meatus is long and bony. The tail

is long, with the exception of _Macacus inuus_. The body is covered

with a thick coat of furry hair. Catarrhine monkeys have existed, we

know with certainty, since the Miocene.

24. Stage of _Catarrhinæ Anthropoidæ_, or _Apes_. Now represented by

the large apes--namely, the Hylobates or gibbon of South-Eastern Asia,

_Simia satyrus_, the orang-utan of Sumatra and Borneo, _Troglodytes

gorilla_, _T. niger_ and _T. calvus_, the gorilla and the chimpanzees

from Western Equatorial Africa. Of fossils are to be mentioned

Pliopithecus and Dryopithecus from European Miocene, and _Troglodytes

sivalensis_ from the Pliocene of the Punjaub. The tail is reduced

to a few caudal vertebræ, which are transformed into a coccyx, not

visible externally; but in the embryos of apes and man the tail is

still a conspicuous feature. The walk is semierect; in adaptation

to the prevailing arboreal life, the arms are longer than the legs.

The hair of the body is considerably more scanty than in the tailed

monkeys. _Troglodytes calvus_, a species or variety of chimpanzee, is

bald-headed. None of the recent genera of apes can lay claim to a place

in the ancestry of mankind.

25. Stage of _Pithecanthropi_. Hitherto the only known representative

is _Pithecanthropus erectus_, from the Upper Pliocene of Java. In

adaptation to a more erect gait, the legs have become stronger and the

hind-hand has been turned into a flat-soled walking 'foot.' The brain

is considerably enlarged. Presumably it is still devoid of so-called

articulate speech; this is indicated by the fact that children have

to learn the language of their parents, and by the circumstance that

comparative philology declares it impossible to reduce the chief human

languages to anything like one common origin.

26. _Man._ Known with certainty to have existed as an implement-using

creature in the last Glacial epoch. His probable origin cannot,

therefore, have been later than the beginning of the Plistocene. The

place of origin was probably somewhere in Southern Asia.

Whilst we have to admit that there are great defects in the older

(invertebrate) portion of our pedigree, we have all the more reason to

be satisfied with the positive results of our investigation of the more

recent (vertebrate) part of it. All modern researches have confirmed

the views of Lamarck, Darwin, and Huxley, and they allow of no doubt

that the nearest vertebrate ancestors of mankind were a series of

Tertiary Primates.

Particularly valuable are the admirable attempts of the two zoologists,

Paul and Fritz Sarasin,[22] to throw light upon the human phylogeny by

painstaking comparison of all the skeletal parts of man with those of

the anthropoid apes. They have shown that among the lower races of man

the primitive Veddahs of Ceylon approach the apes most nearly, and that

among the latter the chimpanzee stands nearest to man.

[22] 'Ergebnisse naturwissenschaftlicher Forschungen auf Ceylon,' vols.

4 and 5. (With an atlas of 84 plates; 1893.)

The direct descent of man from some extinct ape-like form is now beyond

doubt, and admits of being traced much more clearly than the origin

of many another mammalian order. The pedigrees of the Elephants, the

Sirenia, the Cetacea, and, above all, of the Edentata, for example,

are much more obscure and difficult to explain. In many parts of their

organization--for example, in the number and structure of his five

digits and toes--man and monkeys have remained much more primitive than

most of the Ungulata.

The immense significance of this positive knowledge of the origin of

man from some Primate does not require to be enforced. Its bearing

upon the highest questions of philosophy cannot be exaggerated. Among

modern philosophers no one has perceived this more deeply than Herbert

Spencer.[23] He is one of those older thinkers who before Darwin were

convinced that the theory of development is the only way to solve

the 'enigma of the world.' Spencer is also the champion of those

evolutionists who lay the greatest weight upon _progressive heredity_,

or the much combated _heredity of acquired characters_. From the first

he has severely attacked and criticised the theories of Weismann, who

denies this most important factor of phylogeny, and would explain

the whole of transformism by the 'all-sufficiency of selection.' In

England the theories of Weismann were received with enthusiastic

acclamation, much more so than on the Continent, and they were called

'Neo-Darwinism,' in opposition to the older conception of Evolution,

or 'Neo-Lamarckism.' Neither of those expressions is correct. Darwin

himself was convinced of the fundamental importance of progressive

heredity quite as much as his great predecessor Lamarck; as were also

Huxley and Spencer.

[23] 'Principles of Biology': 'The Factors of Organic Evolution'; 'The

Inadequacy of Natural Selection.'

Three times I had the good fortune to visit Darwin at Down, and on each

occasion we discussed this fundamental question in complete harmony.

I agree with Spencer in the conviction that progressive heredity is

an indispensable factor in every true monistic theory of Evolution,

and that it is one of its most important elements. If one denies with

Weismann the heredity of acquired characters, then it becomes necessary

to have recourse to purely mystical qualities of germ-plasm. I am of

the opinion of Spencer, that in that case it would be better to accept

a mysterious creation of all the various species as described in the

Mosaic account.

If we look at the results of modern anthropogeny from the highest point

of view, and compare all its empirical arguments, we are justified in

affirming that _the descent of man from an extinct Tertiary series of

Primates is not a vague hypothesis, but an historical fact_.

Of course, this fact cannot be proved _exactly_. We cannot explain all

the innumerable physical and chemical processes, all the physiological

mutations, which have led during untold millions of years from the

simplest Monera and from the unicellular Protista upwards to the

chimpanzee and to man. But the same consideration applies to all

historical facts. We all believe that Aristotle, Cæsar, and King Alfred

did live; but it is impossible to give a proof within the meaning of

modern exact science. We believe firmly in the former existence of

these and other great heroes of thought, because we know well the works

they have left behind them, and we see their effects in the history

of human culture. These indirect arguments do not furnish stronger

evidence than those of our history as vertebrates. We know of many

Jurassic mammals only a single bone, the under jaw. We all believe that

these mammals possessed also an upper jaw, a skull, and other bones.

But the so-called 'exact school,' which regards the transformation of

species as a hypothesis not proven, must suppose that the mandibula was

the only bone in the body of these curious animals.

Looking forward to the twentieth century, I am convinced that it will

universally accept our theory of descent, and that future science

will regard it as the greatest advance made in our time. I have no

doubt that the influence of the study of anthropogeny upon all other

branches of science will be fruitful and auspicious. The work done in

the present century by Lamarck and Darwin will in all future times be

considered one of the greatest conquests made by thinking man.

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