"if crosses act by virtue of being a cross, and not by virtue of
removing an hereditary taint, then the greater the difference between
the two animals crossed the more beneficial will that act be." He then
shows that, the wider the difference the less is the benefit, and
concludes that a cross, as such, has no beneficial effect. A parallel
argument would be, that change of air, as from inland to the sea-coast,
or from a low to an elevated site, is not beneficial in itself, because,
if so, a change to the tropics or to the polar regions should be more
beneficial. In both these cases it may well be that no benefit would
accrue to a person in perfect health; but then there is no such thing
as "perfect health" in man, and probably no such thing as absolute
freedom from constitutional taint in animals. The experiments of Mr.
Darwin, showing the great and immediate good effects of a cross between
distinct strains in plants, cannot be explained away; neither can the
innumerable arrangements to secure cross-fertilisation by insects, the
real use and purport of which will be discussed in our eleventh chapter.
On the whole, then, the evidence at our command proves that, whatever
may be its ultimate cause, close interbreeding _does_ usually produce
bad results; and it is only by the most rigid selection, whether natural
or artificial, that the danger can be altogether obviated.
_Fertile Hybrids among Animals._
One or two more cases of fertile hybrids may be given before we pass on
to the corresponding experiments in plants. Professor Alfred Newton
received from a friend a pair of hybrid ducks, bred from a common duck
(Anas boschas), and a pintail (Dafila acuta). From these he obtained
four ducklings, but these latter, when grown up, proved infertile, and
did not breed again. In this case we have the results of close
interbreeding, with too great a difference between the original species,
combining to produce infertility, yet the fact of a hybrid from such a
pair producing healthy offspring is itself noteworthy.
Still more extraordinary is the following statement of Mr. Low: "It has
been long known to shepherds, though questioned by naturalists, that the
progeny of the cross between the sheep and goat is fertile. Breeds of
this mixed race are numerous in the north of Europe."[55] Nothing
appears to be known of such hybrids either in Scandinavia or in Italy;
but Professor Giglioli of Florence has kindly given me some useful
references to works in which they are described. The following extract
from his letter is very interesting: "I need not tell you that there
being such hybrids is now generally accepted as a fact. Buffon
(_Supplements_, tom. iii. p. 7, 1756) obtained one such hybrid in 1751
and eight in 1752. Sanson (_La Culture_, vol. vi. p. 372, 1865) mentions
a case observed in the Vosges, France. Geoff. St. Hilaire (_Hist. Nat.
Gén. des reg. org._, vol. iii. p. 163) was the first to mention, I
believe, that in different parts of South America the ram is more
usually crossed with the she-goat than the sheep with the he-goat. The
well-known 'pellones' of Chile are produced by the second and third
generation of such hybrids (Gay, 'Hist, de Chile,' vol. i. p. 466,
_Agriculture_, 1862). Hybrids bred from goat and sheep are called
'chabin' in French, and 'cabruno' in Spanish. In Chile such hybrids are
called 'carneros lanudos'; their breeding _inter se_ appears to be not
always successful, and often the original cross has to be recommenced to
obtain the proportion of three-eighths of he-goat and five-eighths of
sheep, or of three-eighths of ram and five-eighths of she-goat; such
being the reputed best hybrids."
With these numerous facts recorded by competent observers we can hardly
doubt that races of hybrids between these very distinct species have
been produced, and that such hybrids are fairly fertile _inter se_; and
the analogous facts already given lead us to believe that whatever
amount of infertility may at first exist could be eliminated by careful
selection, if the crossed races were bred in large numbers and over a
considerable area of country. This case is especially valuable, as
showing how careful we should be in assuming the infertility of hybrids
when experiments have been made with the progeny of a single pair, and
have been continued only for one or two generations.
Among insects one case only appears to have been recorded. The hybrids
of two moths (Bombyx cynthia and B. arrindia) were proved in Paris,
according to M. Quatrefages, to be fertile _inter se_ for eight
generations.
_Fertility of Hybrids among Plants._
Among plants the cases of fertile hybrids are more numerous, owing, in
part, to the large scale on which they are grown by gardeners and
nurserymen, and to the greater facility with which experiments can be
made. Darwin tells us that Kölreuter found ten cases in which two plants
considered by botanists to be distinct species were quite fertile
together, and he therefore ranked them all as varieties of each other.
In some cases these were grown for six to ten successive generations,
but after a time the fertility decreased, as we saw to be the case in
animals, and presumably from the same cause, too close interbreeding.
Dean Herbert, who carried on experiments with great care and skill for
many years, found numerous cases of hybrids which were perfectly fertile
_inter se_. Crinum capense, fertilised by three other species--C.
pedunculatum, C. canaliculatum, or C. defixum--all very distinct from
it, produced perfectly fertile hybrids; while other species less
different in appearance were quite sterile with the same C. capense.
All the species of the genus Hippeastrum produce hybrid offspring which
are invariably fertile. Lobelia syphylitica and L. fulgens, two very
distinct species, have produced a hybrid which has been named Lobelia
speciosa, and which reproduces itself abundantly. Many of the beautiful
pelargoniums of our greenhouses are hybrids, such as P. ignescens from a
cross between P. citrinodorum and P. fulgidum, which is quite fertile,
and has become the parent of innumerable varieties of beautiful plants.
All the varied species of Calceolaria, however different in appearance,
intermix with the greatest readiness, and the hybrids are all more or
less fertile. But the most remarkable case is that of two species of
Petunia, of which Dean Herbert says: "It is very remarkable that,
although there is a great difference in the form of the flower,
especially of the tube, of P. nyctanigenaeflora and P. phoenicea the
mules between them are not only fertile, but I have found them seed much
more freely with me than either parent.... From a pod of the
above-mentioned mule, to which no pollen but its own had access, I had a
large batch of seedlings in which there was no variability or difference
from itself; and it is evident that the mule planted by itself, in a
congenial climate, would reproduce itself as a species; at least as much
deserving to be so considered as the various Calceolarias of different
districts of South America."[56]
Darwin was informed by Mr. C. Noble that he raises stocks for grafting
from a hybrid between Rhododendron ponticum and R. catawbiense, and that
this hybrid seeds as freely as it is possible to imagine. He adds that
horticulturists raise large beds of the same hybrid, and such alone are
fairly treated; for, by insect agency, the several individuals are
freely crossed with each other, and the injurious influence of close
interbreeding is thus prevented. Had hybrids, when fairly treated,
always gone on decreasing in fertility in each successive generation, as
Gartner believed to be the case, the fact would have been notorious to
nurserymen.[57]
_Cases of Sterility of Mongrels._
The reverse phenomenon to the fertility of hybrids, the sterility of
mongrels or of the crosses between _varieties_ of the same species, is a
comparatively rare one, yet some undoubted cases have occurred. Gartner,
who believed in the absolute distinctness of species and varieties, had
two varieties of maize--one dwarf with yellow seeds, the other taller
with red seeds; yet they never naturally crossed, and, when fertilised
artificially, only a single head produced any seeds, and this one only
five grains. Yet these few seeds were fertile; so that in this case the
first cross was almost sterile, though the hybrid when at length
produced was fertile. In like manner, dissimilarly coloured varieties of
Verbascum or mullein have been found by two distinct observers to be
comparatively infertile. The two pimpernels (Anagallis arvensis and A.
coerulea), classed by most botanists as varieties of one species, have
been found, after repeated trials, to be perfectly sterile when crossed.
No cases of this kind are recorded among animals; but this is not to be
wondered at, when we consider how very few experiments have been made
with natural varieties; while there is good reason for believing that
domestic varieties are exceptionally fertile, partly because one of the
conditions of domestication was fertility under changed conditions, and
also because long continued domestication is believed to have the effect
of increasing fertility and eliminating whatever sterility may exist.
This is shown by the fact that, in many cases, domestic animals are
descended from two or more distinct species. This is almost certainly
the case with the dog, and probably with the hog, the ox, and the sheep;
yet the various breeds are now all perfectly fertile, although we have
every reason to suppose that there would be some degree of infertility
if the several aboriginal species were crossed together for the first
time.
_Parallelism between Crossing and Change of Conditions._
In the whole series of these phenomena, from the beneficial effects of
the crossing of different stocks and the evil effects of close
interbreeding, up to the partial or complete sterility induced by
crosses between species belonging to different genera, we have, as Mr.
Darwin points out, a curious parallelism with the effects produced by
change of physical conditions. It is well known that slight changes in
the conditions of life are beneficial to all living things. Plants, if
constantly grown in one soil and locality from their own seeds, are
greatly benefited by the importation of seed from some other locality.
The same thing happens with animals; and the benefit we ourselves
experience from "change of air" is an illustration of the same
phenomenon. But the amount of the change which is beneficial has its
limits, and then a greater amount is injurious. A change to a climate a
few degrees warmer or colder may be good, while a change to the tropics
or to the arctic regions might be injurious.
Thus we see that, both slight changes of conditions and a slight amount
of crossing, are beneficial; while extreme changes, and crosses between
individuals too far removed in structure or constitution, are injurious.
And there is not only a parallelism but an actual connection between the
two classes of facts, for, as we have already shown, many species of
animals and plants are rendered infertile, or altogether sterile, by the
change from their natural conditions which occurs in confinement or in
cultivation; while, on the other hand, the increased vigour or fertility
which is invariably produced by a judicious cross may be also effected
by a judicious change of climate and surroundings. We shall see in a
subsequent chapter, that this interchangeability of the beneficial
effects of crossing and of new conditions, serves to explain some very
puzzling phenomena in the forms and economy of flowers.
_Remarks on the Facts of Hybridity._
The facts that have now been adduced, though not very numerous, are
sufficiently conclusive to prove that the old belief, of the universal
sterility of hybrids and fertility of mongrels, is incorrect. The
doctrine that such a universal law existed was never more than a
plausible generalisation, founded on a few inconclusive facts derived
from domesticated animals and cultivated plants. The facts were, and
still are, inconclusive for several reasons. They are founded,
primarily, on what occurs among animals in domestication; and it has
been shown that domestication both tends to increase fertility, and was
itself rendered possible by the fertility of those particular species
being little affected by changed conditions. The exceptional fertility
of all the varieties of domesticated animals does not prove that a
similar fertility exists among natural varieties. In the next place, the
generalisation is founded on too remote crosses, as in the case of the
horse and the ass, the two most distinct and widely separated species of
the genus Equus, so distinct indeed that they have been held by some
naturalists to form distinct genera. Crosses between the two species of
zebra, or even between the zebra and the quagga, or the quagga and the
ass, might have led to a very different result. Again, in pre-Darwinian
times it was so universally the practice to argue in a circle, and
declare that the fertility of the offspring of a cross proved the
identity of species of the parents, that experiments in hybridity were
usually made between very remote species and even between species of
different genera, to avoid the possibility of the reply: "They are both
really the same species;" and the sterility of the hybrid offspring of
such remote crosses of course served to strengthen the popular belief.
Now that we have arrived at a different standpoint, and look upon a
species, not as a distinct entity due to special creation, but as an
assemblage of individuals which have become somewhat modified in
structure, form, and constitution so as to adapt them to slightly
different conditions of life; which can be differentiated from other
allied assemblages; which reproduce their like, and which usually breed
together--we require a fresh set of experiments calculated to determine
the matter of fact,--whether such species crossed with their near allies
do always produce offspring which are more or less sterile _inter se_.
Ample materials for such experiments exist, in the numerous
"representative species" inhabiting distinct areas on a continent or
different islands of a group; or even in those found in the same area
but frequenting somewhat different stations.
To carry out these experiments with any satisfactory result, it will be
necessary to avoid the evil effects of confinement and of too close
interbreeding. If birds are experimented with, they should be allowed as
much liberty as possible, a plot of ground with trees and bushes being
enclosed with wire netting overhead so as to form a large open aviary.
The species experimented with should be obtained in considerable
numbers, and by two separate persons, each making the opposite
reciprocal cross, as explained at p. 155. In the second generation these
two stocks might be themselves crossed to prevent the evil effects of
too close interbreeding. By such experiments, carefully carried out with
different groups of animals and plants, we should obtain a body of facts
of a character now sadly wanting, and without which it is hopeless to
expect to arrive at a complete solution of this difficult problem. There
are, however, some other aspects of the question that need to be
considered, and some theoretical views which require to be carefully
examined, having done which we shall be in a condition to state the
general conclusions to which the facts and reasonings at our command
seem to point.
_Sterility due to changed Conditions and usually correlated with other
Characters, especially with Colour._
The evidence already adduced as to the extreme susceptibility of the
reproductive system, and the curious irregularity with which infertility
or sterility appears in the crosses between some varieties or species
while quite absent in those between others, seem to indicate that
sterility is a characteristic which has a constant tendency to appear,
either by itself or in correlation with other characters. It is known to
be especially liable to occur under changed conditions of life; and, as
such change is usually the starting-point and cause of the development
of new species, we have already found a reason why it should so often
appear when species become fully differentiated.
In almost all the cases of infertility or sterility between varieties or
species, we have some external differences with which it is correlated;
and though these differences are sometimes slight, and the amount of the
infertility is not always, or even usually, proportionate to the
external difference between the two forms crossed, we must believe that
there is some connection between the two classes of facts. This is
especially the case as regards colour; and Mr. Darwin has collected a
body of facts which go far to prove that colour, instead of being an
altogether trifling and unimportant character, as was supposed by the
older naturalists, is really one of great significance, since it is
undoubtedly often correlated with important constitutional differences.
Now colour is one of the characters that most usually distinguishes
closely allied species; and when we hear that the most closely allied
species of plants are infertile together, while those more remote are
fertile, the meaning usually is that the former differ chiefly in the
_colour_ of their flowers, while the latter differ in the form of the
flowers or foliage, in habit, or in other structural characters.
It is therefore a most curious and suggestive fact, that in all the
recorded cases, in which a decided infertility occurs between varieties
of the same species, those varieties are distinguished by a difference
of colour. The infertile varieties of Verbascum were white and yellow
flowered respectively; the infertile varieties of maize were red and
yellow seeded; while the infertile pimpernels were the red and the blue
flowered varieties. So, the differently coloured varieties of
hollyhocks, though grown close together, each reproduce their own colour
from seed, showing that they are not capable of freely intercrossing.
Yet Mr. Darwin assures us that the agency of bees is necessary to carry
the pollen from one plant to another, because in each flower the pollen
is shed before the stigma is ready to receive it. We have here,
therefore, either almost complete sterility between varieties of
different colours, or a prepotent effect of pollen from a flower of the
same colour, bringing about the same result.
Similar phenomena have not been recorded among animals; but this is not
to be wondered at when we consider that most of our pure and valued
domestic breeds are characterised by definite colours which constitute
one of their distinctive marks, and they are, therefore, seldom crossed
with these of another colour; and even when they are so crossed, no
notice would be taken of any slight diminution of fertility, since this
is liable to occur from many causes. We have also reason to believe that
fertility has been increased by long domestication, in addition to the
fact of the original stocks being exceptionally fertile; and no
experiments have been made on the differently coloured varieties of wild
animals. There are, however, a number of very curious facts showing that
colour in animals, as in plants, is often correlated with constitutional
differences of a remarkable kind, and as these have a close relation to
the subject we are discussing, a brief summary of them will be here
given.
_Correlation of Colour with Constitutional Peculiarities._
The correlation of a white colour and blue eyes in male cats with
deafness, and of the tortoise-shell marking with the female sex of the
same animal, are two well-known but most extraordinary cases. Equally
remarkable is the fact, communicated to Darwin by Mr. Tegetmeier, that
white, yellow, pale blue, or dun pigeons, of all breeds, have the young
birds born naked, while in all other colours they are well covered with
down. Here we have a case in which colour seems of more physiological
importance than all the varied structural differences between the
varieties and breeds of pigeons. In Virginia there is a plant called the
paint-root (Lachnanthes tinctoria), which, when eaten by pigs, colours
their bones pink, and causes the hoofs of all but the black varieties to
drop off; so that black pigs only can be kept in the district.[58]
Buckwheat in flower is also said to be injurious to white pigs but not
to black. In the Tarentino, black sheep are not injured by eating the
Hypericum crispum--a species of St. John's-wort--which kills white
sheep. White terriers suffer most from distemper; white chickens from
the gapes. White-haired horses or cattle are subject to cutaneous
diseases from which the dark coloured are free; while, both in Thuringia
and the West Indies, it has been noticed that white or pale coloured
cattle are much more troubled by flies than are those which are brown or
black. The same law even extends to insects, for it is found that
silkworms which produce white cocoons resist the fungus disease much
better than do those which produce yellow cocoons.[59] Among plants, we
have in North America green and yellow-fruited plums not affected by a
disease that attacked the purple-fruited varieties. Yellow-fleshed
peaches suffer more from disease than white-fleshed kinds. In Mauritius,
white sugar-canes were attacked by a disease from which the red canes
were free. White onions and verbenas are most liable to mildew; and
red-flowered hyacinths were more injured by the cold during a severe
winter in Holland than any other kinds.[60]
These curious and inexplicable correlations of colour with
constitutional peculiarities, both in animals and plants, render it
probable 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; and if so, the fact is of the highest importance as
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