CHAPTER XII

THE CROSS-BREEDING OF RACES

We have seen that there is no simple rule as to the "mating" of

individuals of a species with individuals of another closely allied

but distinct species. Such mating very rarely comes about in natural

conditions, but man by his interference sometimes succeeds in procuring

"hybrids" between allied species. Hybrids between species belonging to

groups so different as to be distinguished by zoologists as distinct

"families" or "orders" are quite unknown under any circumstances.

Such remoteness of natural character and structure as is indicated by

the two great divisions of hoofed mammals–the even-toed (including

sheep, cattle, deer, antelopes, giraffes, pigs and camels), and the

odd-toed (including tapirs, rhinoceroses, horses, asses and zebras)

is an absolute bar to inter-breeding. So, too, the carnivora (cats,

dogs, bears and seals, and smaller kinds) are so remote in their nature

from the rabbits, hares and rats–called "the rodents"–that no mating

between members of the one and the other of these groups has ever been

observed, either in nature or under artificial conditions.

Even when individuals of closely allied species mate with one another

it is a very rare occurrence that the hybrids so produced ripen their

ova and sperms so as to be capable of carrying on the hybrid race,

though sometimes they do ripen them and breed. The great naturalist

Alfred Wallace, in his most valuable and readable book called

"Darwinism," expressed the opinion that the apparent failure of hybrid

races to perpetuate themselves by breeding was to a large extent due

to the small number of individuals used in experiments on this matter,

and the in-and-in breeding which was the consequence. One of the great

generalizations established by Darwin is that in-and-in breeding is,

as a rule, resisted in all animals and plants, and leads when it

occurs to a dying-out of the inbred race by resulting feebleness and

infertility. A large part of Darwin's work consisted in demonstrating

the devices existing in the natural structure and qualities of plants

and animals for securing cross-fertilization among individuals of the

same species but of different stock. Both extremes seem to be barred

in nature–namely, the inter-breeding of stocks so diverse in structure

and quality as to be what we call "distinct species," and again the

inter-breeding of individuals of the same immediate parentage or near

cousinship. What seems to be favoured by the natural structure and

qualities of the plant or the animal is that it shall only breed within

a certain group–the species–and shall within that group avoid constant

self-fertilization or fertilization by near cousins. Thus we find

numerous cases in which, though the same flower has both pollen and

ovules, and might fertilize itself, the visits of insects (specially

made use of by mechanisms in the flower) carry the pollen of one flower

to the ovules of another and to flowers on separate plants growing

at a distance. It is necessary to note that there are, nevertheless,

self-fertilizing flowers, and also self-fertilizing lower animals,

the special conditions of which require and have received careful

examination and consideration, upon which I cannot now enter.

In relation to the question of the possibility of establishing hybrids

between various species experimentally, I must (before going on to the

cognate question of "mongrels") tell of an interesting suggestion made

to me by my friend Professor Alphonse Milne-Edwards not long before he

died, and never published by him. He was director of the Jardin des

Plantes in Paris, where there is a menagerie of living beasts as well

as a botanic garden and great museum collections and laboratories.

He held it to be probable, as many physiologists would agree, that

the fertilization of the egg of one species by the sperm of another,

even a remotely related one, is ultimately prevented by a chemical

incompatibility–chemical in the sense that the highly complex molecular

constitution of such bodies as the anti-toxins and serums with which

physiologists are beginning to deal is "chemical"–and that all the

other and secondary obstacles to fertilization can be overcome or

evaded in the course of experiment. He proposed to inject one species

by "serums" extracted from the other, in such a way as seemed most

likely to bring the chemical state of their reproductive elements into

harmony, that is to say, into a condition in which they should not

be actively antagonistic but admit of fusion and union. He proposed,

by the exchange of living or highly organized fluids (by means of

injection or transfusion) between a male and female of separate

species, to assimilate the chemical constitution of one to that of the

other, and thus possibly so to affect their reproductive elements that

the one could tolerate and fertilize the other. The suggestion is not

unreasonable, but would require a long series of experiments in which

the possibility of producing such "assimilation," even to a small

extent and in respect of less complex processes than those ultimately

aimed at, would have to be, first of all, established. My friend did

not live to commence this investigation, but it is possible that some

day we may see the obstacle to the union of ovum and sperm of species,

which are to some extent allied, removed in this way by transfusion or

injection of important fluids from the one into the other.

We must not lose sight of the fact, in the midst of these various

and diverging observations about the fertilization of the ova of one

species by sperms of another species, that there is such a thing as

"parthenogenesis," or virgin-birth. In some of the insects and lower

forms of animals the egg-cell habitually and regularly develops and

gives rise to a new individual without being fertilized at all. And in

other cases by special treatment, such as rubbing with a brush, or in

the case of marine animals by addition of certain salts to the water

in which the eggs are floating–or, again, in the case of the eggs of

the common frog by gently scratching them with a needle–the eggs which

usually and regularly require to be penetrated by and fused with a

spermatozoon or sperm-filament before they will develop, proceed to

develop into complete new individuals without the action upon them

of any spermatozoon. In such marine animals as the sea-urchins or

sea-eggs it has been found that the eggs deposited in pure sea-water,

though they would die and decompose if left there alone, can be made to

develop and proceed on their growth by the addition to the sea-water of

the sperm filaments of a star-fish (the feather star or comatula). The

spermatozoa or sperm-filaments do not, however, in this case fuse with

the egg-cells. They mechanically pierce the egg-coat, but contribute no

substance to the embryo into which the egg develops. They have merely

served, like the scratch of a needle on the frog's egg and the brushing

of insects' eggs, to start the egg on its growth, to "stimulate" it and

set changes going. It appears thus that the fertilizing sperm-filaments

of organisms generally have two separate and very important influences

upon the egg-cells with which they fuse. The one is to stimulate

the egg and start the changes of embryonic growth; the other is

to contribute some living material from the male parent to the new

individual arising from the growth and shaping of the egg-cell. The

first influence can be exercised without the second, as is seen in

the case of the eggs of some sea-urchins stimulated to growth by the

spermatozoa of some star-fishes. It happens that these marine animals

are convenient for study and experiment because their eggs are small

and transparent and that they and the spermatozoa are freely passed

into the sea-water at the breeding season, in which the fertilization

of the eggs takes place.

When these facts are considered we have to admit that in the mating

of two species which will not regularly and naturally breed together,

there may be a limited action of the spermatic element which may

stimulate the egg to development without contributing by fusion in

the regular way to the actual substance of the young so produced,

or only contributing an amount insufficient to produce a full and

normal development of the hybrid young. Such cases not improbably

sometimes occur in higher animals, though they have not been, as yet,

shown to exist except in the experiments with sea-urchins' eggs and

feather-star's sperm.

In all animals and plants, but especially in domesticated and

cultivated stocks or strains, varieties arise which, by natural or

artificial separation, breed apart, and give rise to what are called

"races." Such races in natural conditions may become species. Species

are races or groups of individuals, which, by long estrangement (not

necessarily local isolation) from the parent stock and by adaptation

to special conditions of life, have become more or less "stable"–that

is, permanent and unchanging in the conditions to which they have

become adapted. They acquire by one device or another the habit of

not breeding with the stock from which they originally diverged–a

repugnance which may be overcome by human contrivance or by natural

accident, but is, nevertheless, an effective and real quality.

Distinct forms, which have not arrived at the stability and separation

characteristic of species, are spoken of as "races," or "varieties."

It is very generally the case that the "races" of one species can

inter-breed freely with one another, and with the original stock, when

it still exists. Comparatively little is known as to the behaviour

of wild or naturally-produced "races." Practically all our views on

the subject of "races" and their inter-breeding are derived from our

observation of the immense number and range of "races" and "breeds"

produced by man–as farmer, fancier, and horticulturist. It has been

generally received as a rule, that the various races produced in the

farm or garden by breeding from a species, will inter-breed freely, and

produce offspring which are fertile. A special and important series of

races, in which human purpose and voluntary selection necessarily have

a leading part, are the races of man.

The offspring of parents of two different races is called a mongrel,

whilst the term "hybrid" has been of late limited, for the sake of

convenience, to the offspring of parents of two different species.

Mongrels, it has been generally held, are fertile–often more fertile

than pure-bred individuals whose parents are both of the same race,

whilst "hybrids" are contrasted with them, in being infertile. We have

seen that infertility is not an absolute rule in the case of hybrids,

and it appears that there is also a source of error in the observations

which lead to the notion that "mongrels" are always fertile. The fact

is that observations on this matter have nearly always been made with

domesticated animals and plants which are, of course, selected and

bred by man on account of their fertility, and thus are exceptionally

characterized by fertility, which is transmitted in an exceptional

degree to the races or varieties which are experimentally inter-bred,

and, consequently, may be expected to produce fertile mongrels. Alfred

Russel Wallace insisted upon this fact, and pointed out that in a few

cases colour varieties of a given species of plant have been found to

be incapable of inter-breeding, or only produce very few "mongrels."

This has been established in the case of two dissimilarly-coloured

varieties of mullein. Also the red and the blue pimpernel (the poor

man's weather-glass, Anagallis), which are classed by botanists as two

varieties of one species, have been found after repeated trials to

be definitely incapable of inter-breeding. Wallace insists in regard

to crossing, that some degree of difference favours fertility, but a

little more tends to infertility. We must remember that the fertility

of both plants and animals is very easily upset. Changed conditions of

life–such as domestication–may lead (we do not know why) to complete

or nearly complete infertility; and, again, "change of air," or of

locality, has an extraordinary and not-as-yet-explained effect on

fertility.

"Oh, the little more and how much it is!

And the little less, and what worlds away!"

Infertile horses sent from their native home to a different climate

(as, for instance, from Scotland to Newmarket) become fertile. A

judicious crossing of varieties or races threatened with infertility

will often lead to increased vigour and fertility in the new

generation, just as change of locality will produce such a result.

Physiological processes which are not obvious and cannot be exactly

estimated or measured are then, we must conclude, largely connected

with the question of sterility and fertility. Mr. Darwin has collected

facts which go far to prove that colour (as in the case of the black

pigs of Virginia, which I cited in Chapter X.), instead of being

a trifling and unimportant character, as was supposed by the older

naturalists, is really one of great significance, often correlated

with important constitutional differences. It is pointed out by Alfred

Wallace that in all the recorded cases in which a decided infertility

occurs between varieties (or races) of the same species of plants (such

as those just cited), those varieties are distinguished by a difference

of colour. He gives reasons for thinking that the correlation of colour

with infertility which has been detected in several cases in plants may

also extend to animals in a state of nature. The constant preference

of animals–even mere varieties of dog, sheep, horses, and pigeons–for

their like, has been well established by observation. Colour is one of

the readiest appeals to the eye in guiding animals in such selection

and association, and is connected with deep-seated constitutional

qualities. "Birds of a feather flock together" is a popular statement

confirmed by the careful observation of naturalists. Thus we arrive at

some indication of features which may determine the inter-breeding, or

the abstention from inter-breeding, of diverse races sprung from one

original stock. The "colour bar" is not merely the invention of human

prejudice, but already exists in wild plants and animals.

We now come to the questions, the assertions, the beliefs, and the acts

concerning the inter-breeding of human races, to the consideration of

which I have been preparing the way. The dog-fancier has generally a

great contempt for "mongrels." Breeders generally dislike accidental

crosses, because they interfere with the purpose which the breeder

has in view of producing animals or plants of a quality, form, and

character which he has determined on before-hand. This interference

with his purpose seems to be the explanation of beliefs and statements,

to the prejudice of "mongrels." Really, as is well known to great

breeders and horticulturists, a determined and selective crossing of

breeds is the very foundation of the breeder's art, and there is no

reason to suppose that a "mongrel" is necessarily, or even probably,

inferior in vigour or in qualities which are advantageous in the

struggle for life in "natural"–that is to say, "larger"–conditions

of an animal's or plant's life; not those limited conditions for

which the breeder intends his products. Indeed, the very opposite

is the case. In nature, as Mr. Darwin showed, there are innumerable

contrivances to ensure the cross-breeding of allied but distinct

strains. Dog-owners who are not exclusively bent upon possessing a

dog which shows in a perfect way the "points" of a breed favoured by

the fashion of the moment, or fitting it for some special employment,

know very well that a "mongrel" may often exhibit finer qualities

of intelligence, or endurance, than those exhibited by a dog of

pure-bred "race." And the very "races" which are spoken of to-day as

"pure-bred," or "thoroughbred," have (as is well known) been produced

as "mongrels"–that is to say, by crossing or mating individuals of

previously-existing distinct and pure breeds. The history of many such

"mongrel breeds," now spoken of as "thoroughbred," is well known.

The English racehorse was gradually produced by the "mongrelizing,"

or cross-breeding, of several breeds or races–the English warhorse,

the Arab, the Barb. A very fine mongrel stock having at last been

obtained, it was found, or, at any rate, was considered to be

demonstrated, that no further improvement (for the purposes aimed

at, namely, flat-racing) could be effected by introducing the blood

of other stock. The offspring of the "mongrels" Herod, Matchem, and

Eclipse accordingly became established as "the" English racehorse, and

thenceforward was mated only within its own race or stock, and was kept

pure or "thoroughbred." Another well-known mongrel breed which is now

kept pure, or nearly so, is that of the St. Bernard's dog, a blend of

Newfoundland, Bloodhound, and English Mastiff.

Often the word "mongrel" is limited in its use to signify an

undesired or undesirable result of the cross-breeding of individuals

of established races. But this is not quite fair to mongrels in

general, since, as we have seen, the name really refers only to the

fact they are crosses between two breeds. When they happen to suit

some artificial and arbitrary requirement they are favoured, and made

the starting-point of a new breed, and kept pure in their own line;

but when they do not fit some capricious demand of the breeder they

are sneered at and condemned, although they may be fine and capable

animals. No doubt some mongrels between races differing greatly from

one another, or having some peculiar mixture of incompatible qualities

the exact nature of which we have not ascertained, are wanting in

vigour, and cannot be readily established as a new breed. In nature

the success of the mongrel depends on whether or not its mixture of

qualities makes it fitter than others to the actual conditions of its

life, and able to survive in the competition for food and place. In

man's breeding operations with varieties of domesticated animals and

"cultivated" plants, the survival of the mongrel depends upon its

fitting some arbitrary standard applied by man, who destroys those

which do not suit his fancy, and selects for survival and continued

breeding those which do.

What is called "miscegenation," or the inter-breeding of human races,

must be looked at from both these points of view. We require to know

how far, if at all, the mixed or mongrel offspring of a human race A

with a human race B is really inferior to either of the original stocks

A and B, judged by general capacity and life-preserving qualities in

the varied conditions of the great area of the habitable globe. And

how far an arbitrary or fanciful standard is set up by human races,

similar to that set up by the "fancier" or cultivator of breeds of

domestic animals. The matter is complicated by the fact that what we

loosely speak of as "races" of man are of very various degrees of

consanguinity or nearness to one another in blood, that is, in stock or

in ultimate ancestry. It is also complicated by the fact that we cannot

place any reliance upon the antipathies or preferences shown by the

general sentiment of a race in this (or other matters) as necessarily

indicating what is beneficial for humanity in general or for the

immediate future of any section of it. Nor have we any assurance that

what is called "sexual selection"–the preference or taste in the matter

of choosing a mate–is among human beings necessarily anything of

greater importance–so far as the prosperity of a race or of humanity in

general is concerned–than a mere caprice or a meaningless persistence

of the human mind in favouring a choice which is habitual and

traditional. I have referred to this point again in the last paragraph

of this chapter.

In regard to marriage between individuals of different European

nationalities, a certain amount of unwillingness exists on the part of

both men and women which cannot be ascribed to any deep-seated inborn

antipathy, but is due to a mistrust of the unknown "foreigner," which

very readily disappears on acquaintance, or may arise from dislike

of the laws and customs of a foreign people. English, French, Dutch,

Scandinavians, Germans, Russians, Greeks, Italians and Spaniards have

no deep-rooted prejudices on the subject, and readily intermarry when

circumstances bring them into association. Though the Jews by their

present traditional practice are opposed to marriage with those not

of their faith, there is no effective aversion of a racial kind to

such unions, and in early times they have been very frequent. During

the "captivity" in Babylon and again after the "dispersal" by the

Romans, the original Jewish race was practically swamped by mixture

with cognate Oriental races who adopted the Jewish faith. So far from

there being inborn prejudice against intermarriage of the peoples above

cited, it is very generally admitted that such "miscegenation" leads

frequently to the foundation of families of fine quality. The blend is

successful, as may be seen in the number of prominent Englishmen who

have Huguenot, German, Dutch, or Jewish blood in their veins.

But when we come to the intermarriage of members of the white race of

Europe with members of either the negroid (black) race or of the yellow

and red mongoloid race, a much greater and more deeply-rooted aversion

is found, and this is extended even to members of the Caucasian race

who, possibly by prehistoric mixture with negro-like races, are very

dark-skinned, as is the case with the Aryan population in India and

Polynesia. It is a very difficult matter; in fact, it seems to me not

possible in our present knowledge of the facts, to decide whether

there is a natural inborn or congenital disinclination to the marriage

of the white race, especially of the Anglo-Saxon branch of it, with

"coloured" people, or whether the whole attitude (as I am inclined to

think) is one of "pride of race," an attitude which can be defended

on the highest grounds, though it may lead to erroneous beliefs as to

the immediate evil results of such unions, and to an unreasonable and

cruel treatment both of the individuals so intermarrying and of their

offspring. There is little or no evidence of objection to mixed unions

on the part of the coloured people with whites, no evidence of physical

dislike to the white man or white woman, but, on the contrary, ready

acquiescence.

A curious aversion to marriages with whites on the part both of North

American Indians and of negroes is, however, recorded from time to

time in the official reports of the United States Government.

Two beliefs about such unions are more or less prevalent among white

men in the regions where they not infrequently occur. Neither of these

beliefs is supported by anything like conclusive evidence. The one

is that such unions lead to the production of relatively infertile

offspring; the mixed breed or stock is said to die out after a few

(some seven or eight) generations. It is, however, the fact that the

circumstances under which this occurs suggest that it is not due to

a natural and necessary infertility. The other assertion is that the

offspring of parents–one of white race and the other of black, yellow

or brown–tend by some strange fatality to inherit the bad qualities of

both races and the good qualities of neither. This is a case to which

must be applied the saying, "Give a dog a bad name and hang him."

The white man in North America, in India, and in New Zealand desires

the increase and prosperity of his own race. Like the fancier set on

the production of certain breeds of domesticated animals, he has no

toleration for a "mongrel." In so far as it is true that miscegenation

(marriage of white and coloured race) produces a stock which rapidly

dies out–this is due to the adverse conditions, the opposition and

hostility to which the mixed race is exposed by the attitude of the

dominant white race. To the same cause is due the development of

ignoble and possibly dangerous characteristics in the unfortunate

offspring of these marriages more frequently than in those who find

their natural place and healthy up-bringing either in the white or

the coloured sections of the community. The "half-breed" is in some

countries inexorably rejected by the race of his or her white parent

and forced to take up an equivocal association with the coloured race.

That some, at any rate, of the evils attributed to "miscegenation" are

due to the baneful influence of "pride of race" is evident from the

fact that the Portuguese (with the exception of a small aristocratic

class) have not since the early days of the fourteenth century,

perhaps in consequence of established association with the Moorish

and other North African races, shown that pride of race and aversion

to mixture with dark-skinned races which is so strong a feature in

the Anglo-Saxons, their successors and rivals as colonists. The

long-standing admixture of black blood in the Portuguese population

before the colonization of South America, has led to a toleration on

the part of the Portuguese colonists of "miscegenation," both with

Indians and the liberated descendants of imported negro slaves. The

consequence is that in Brazil there is no condemnation of black blood;

children of mixed parentage and of coloured race attend the same

schools as those of European blood, and freely associate with them.

There is no notion that that portion of the population which is of

mixed negro, Indian, and white blood is less vigorous or fertile than

the unmixed, nor that vice and feebleness are the characteristics of

the former, whilst virtue and capacity belong to the latter.

The determined hostility of the Anglo-Saxon race in North America and

in British India to "miscegenation" is in the case of the United States

to be explained by the peculiar relation of a large slave population

in the Southern States to a pure white slave-owning race: whilst in

India we have a handful of white men temporarily stationed as rulers

of millions of "natives," but never accepting India as their home. The

attitude of the Anglo-Saxon race to the North American Indians, and

also to the Maoris of New Zealand, has never been so extreme in the

matter of miscegenation as it has been to negroid people and to the

very different though dark-skinned people of the East. In support of

that opinion may be cited the fact that some of "the first families of

Virginia" are proud of their descent from Pocahontes, the Algonkian

"Princess" who married the Englishman Rolfe. In New Zealand there are

many families of mixed Anglo-Saxon and Maori blood. Though they are not

ostracized, as are the half-breeds of negro blood in the United States,

there is a firm tendency to relegate the half-breeds in New Zealand

to the Maori section of the population, which it must be remembered

includes some of the richest and most prosperous landowners in the

colony.

It may be questioned whether there is in this matter a greater "pride

of race" among Anglo-Saxons than among other Northern European peoples.

Neither the French nor the Germans have established great colonies

like the English, nor undertaken the administration of a huge Eastern

Empire, and have, therefore, not shown what attitude they would adopt

under such circumstances. The tolerance and easy-going humanitarianism

of the French in relation to "miscegenation" in their dependencies in

past times has never had the significance or practical importance which

it would have possessed in the English Colonies and in the great Indian

Empire.

There is, on account of the sporadic and exceptional occurrence of

modern instances, no information of any value as to the results of

mixture of other races of man. In early times and among more primitive

or less civilized peoples there appears to have been, when immigration

or conquest gave the opportunity, no obstacle to a free intermixture of

an incoming race with the natives of an invaded territory. The "pride

of race" has, nevertheless, throughout historic time been a frequent

factor in the adjustment of populations of diverse races, and though

"colour" has been a frequent "test" or symbol of the superior and

exclusive race, it has not been the only characteristic exalted to such

importance. Such "pride of race" has frequently excluded the members of

a closely allied but conquered racial group from intermarriage with the

conquerors, and has only disappeared after centuries of persistence.

The term "blue blood" is interesting in this connection. It is the

"saing d'azure" of the Gothic invaders, the conquerors of the Iberian

and Moorish people of Spain. It refers not to any "blueness" of the

blood itself, such as distinguishes veinous from arterial blood, but

to the blue colour of the veins as seen through the colourless skin of

a northern race (the Goths), as compared with the invisibility of the

veins when the skin is rendered more or less opaque by a brown pigment,

as in the Moors and the swarthy Iberians.

Among the people of Western Europe marriage has assumed more and more

a character which is almost unknown in the rest of the world. Whatever

the future may be in regard to this matter, there is no doubt possible

that the place given to women in Western Europe by the ideals of

chivalry and the practice of the northern race (which has so largely

displaced the traditions of the Roman Empire) has established a

relation of the sexes in which marriage and consequent parentage have

ceased to be regarded as a mere regularization of animal desire and

appetite. The accepted, but not always consciously recognized, view

of marriage in Western Europe is that the union so sanctioned and the

families thereby produced should be the result not of the mere physical

necessity of irresponsible victims of an impulse common to all animals,

but the outcome of the deliberate choice of man and woman attracted to

one another by sympathy, understanding and reciprocal admiration, based

upon knowledge of character, mental gifts and aspirations, as well as

upon bodily charm. A rarely-expressed but none the less deeply-seated

conviction exists that from such unions children of the finest nature,

nurtured in circumstances most likely to make them worthy members of

the community, will be born and reared. It is this conviction which

leads to, or at any rate endorses, the exclusiveness which is described

as "pride of race." The Anglo-Saxon man and equally the Anglo-Saxon

woman (as well as the allied races of neighbouring nationalities)

recognize a responsibility, a race duty, resulting from accumulated

tradition, the heirloom of long ages of family life, which causes the

man to be ashamed of, and the woman to shrink with instinctive horror

from, union with an individual of a remote race with whom there can be

no real sympathy, no intimate understanding. That seems to me to be the

explanation and the justification of the "colour bar."

In relation to the probable effectiveness of sexual selection among

uncivilized peoples in favouring and maintaining a particular type or

form of features, hair, etc., characteristic of the race, independently

of the life-preserving value of such qualities, I may mention, before

quitting this difficult but strangely fascinating subject, a fact

observed by a traveller in Africa, and related to me by him. Other

similar facts are on record. Among the negroes employed as "porters"

by my friend, some thirty in number, was one who had a narrow aquiline

nose and thin lips. He was as black and as woolly-haired as any of

them, but would if of fair complexion have been regarded by Europeans

as a very handsome, fine-featured man. Such cases are not uncommon

in parts of Africa, where probably an unrecognized mixture with Arab

or Hamite blood has occurred. My friend expected this man to be a

favourite, on account of what to him appeared to be "good looks," with

the girls of the villages at which he camped during a three months'

journey. At every such village, as they journeyed on, the travellers

were received with joy and good nature. The negro porters were fêted

and made much of by the young women. But one alone was unpopular and

regarded with ridicule and dislike. This was the handsome negro with

the fine, well-modelled nose and beautiful European lips. The black

beauties turned their backs on him, in spite of his amiable character

and kindly overtures. They invariably and by open confession preferred

the men with the thickest lips, the broadest noses, and the most

thoroughly (as we should say) degraded prognathous appearance and

disgusting expression. Hence no doubt the young negresses were likely

to perpetuate in their offspring the features which are characteristic

of their race, and hence it is probable that mere capricious sexual

selection of individuals most completely conforming to a preferred

type–irrespective of the value of the features preferred–may have great

effect in both the selection and the maintenance of the peculiarities

of the type. Dark skin may thus have been selected, until it became

actually black; a slight curling of the hair, until it became woolly;

thickish lips and broadish nose, until they became excessive in

thickness and breadth.

Secrets of Earth and Sea · 第 12 / 22 章