M Database Inspector (cheetah)
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|01 - Variations Under Domestication||01-13 - Summary||10||
To sum up on the origin of our domestic races of animals and plants.
Changed conditions of life are of the highest importance in causing variability, both by acting directly on the organisation, and indirectly by affecting the reproductive system.
It is not probable that variability is an inherent and necessary contingent, under all circumstances.
The greater or less force of inheritance and reversion, determine whether variations shall endure.
Variability is governed by many unknown laws, of which correlated growth is probably the most important.
Something, but how much we do not know, may be attributed to the definite action of the conditions of life. Some, perhaps a great, effect may be attributed to the increased use or disuse of parts.
The final result is thus rendered infinitely complex.
In some cases the intercrossing of aboriginally distinct species appears to have played an important part in the origin of our breeds.
When several breeds have once been formed in any country, their occasional intercrossing, with the aid of selection, has, no doubt, largely aided in the formation of new sub-breeds; but the importance of crossing has been much exaggerated, both in regard to animals and to those plants which are propagated by seed.
|05 - Laws of Variation||05-13 - Summary||10||
Our ignorance of the laws of variation is profound.
Not in one case out of a hundred can we pretend to assign any reason why this or that part has varied.
But whenever we have the means of instituting a comparison, the same laws appear to have acted in producing the lesser differences between varieties of the same species, and the greater differences between species of the same genus.
Changed conditions generally induce mere fluctuating variability, but sometimes they cause direct and definite effects; and these may become strongly marked in the course of time, though we have not sufficient evidence on this head.
Habit in producing constitutional peculiarities and use in strengthening and disuse in weakening and diminishing organs, appear in many cases to have been potent in their effects.
Homologous parts tend to vary in the same manner, and homologous parts tend to cohere.
Modifications in hard parts and in external parts sometimes affect softer and internal parts.
When one part is largely developed, perhaps it tends to draw nourishment from the adjoining parts; and every part of the structure which can be saved without detriment will be saved.
Changes of structure at an early age may affect parts subsequently developed; and many cases of correlated variation, the nature of which we are unable to understand, undoubtedly occur.
Multiple parts are variable in number and in structure, perhaps arising from such parts not having been closely specialised for any particular function, so that their modifications have not been closely cheeked by natural selection.
It follows probably from this same cause, that organic beings low in the scale are more variable than those standing higher in the scale, and which have their whole organisation more specialised.
Rudimentary organs, from being useless, are not regulated by natural selection, and hence are variable.
Specific characters- that is, the characters which have, come to differ since the several species of the same genus branched off from a common parent- are more variable than generic characters, or those which have long been inherited, and have not differed from this same period.
|07 - Instinct||07-11 - Summary||10||
I have endeavoured briefly in this chapter to show that the mental qualities of our domestic animals vary, and that the variations are inherited.
Still more briefly I have attempted to show that instincts vary slightly in a state of nature.
No one will dispute that instincts are of the highest importance to each animal.
Therefore I can see no difficulty, under changing conditions of life, in natural selection accumulating slight modifications of instinct to any extent, in any useful direction. In some cases habit or use and disuse have probably come into play.
I do not pretend that the facts given in this chapter strengthen in any great degree my theory; but none of the cases of difficulty, to the best of my judgment, annihilate it.
On the other hand, the fact that instincts are not always absolutely perfect and are liable to mistakes; that no instinct has been produced for the exclusive good of other animals, but that each animal takes advantage of the instincts of others; that the canon in natural history, of 'natura non facit saltum' is applicable to instincts as well as to corporeal structure, and is plainly explicable on the foregoing views, but is otherwise inexplicable, all tend to corroborate the theory of natural selection.
This theory is, also, strengthened by some few other facts in regard to instincts; as by that common case of closely allied, but certainly distinct, species, when inhabiting distant parts of the world and living under considerably different conditions of life, yet often retaining nearly the same instincts.
For instance, we can understand on the principle of inheritance, how it is that the thrush of South America lines its nest with mud, in the same peculiar manner as does our British thrush: how it is that the male wrens (Troglodytes) of North America, build 'cock-nests,' to roost in, like the males of our distinct Kitty-wrens, a habit wholly unlike that of any other known bird.
Finally, it may not be a logical deduction, but to my imagination it is far more satisfactory to look at such instincts as the young cuckoo ejecting its foster-brothers, ants making slaves, -- the larvae of ichneumonidae feeding within the live bodies of caterpillars, not as specially endowed or created instincts, but as small consequences of one general law, leading to the advancement of all organic beings, namely, multiply, vary, let the strongest live and the weakest die.
|08 - Hybridism||08-09 - Summary||10||
Summary of Chapter.
First crosses between forms sufficiently distinct to be ranked as species, and their hybrids, are very generally, but not universally, sterile.
The sterility is of all degrees, and is often so slight that the two most careful experimentalists who have ever lived, have come to diametrically opposite conclusions in ranking forms by this test.
The sterility is innately variable in individuals of the same species, and is eminently susceptible of favourable and unfavourable conditions.
The degree of sterility does not strictly follow systematic affinity, but is governed by several curious and complex laws.
It is generally different, and sometimes widely different, in reciprocal crosses between the same two species.
It is not always equal in degree in a first cross and in the hybrid produced from this cross.
In the same manner as in grafting trees, the capacity of one species or variety to take on another, is incidental on generally unknown differences in their vegetative systems, so in crossing, the greater or less facility of one species to unite with another, is incidental on unknown differences in their reproductive systems.
There is no more reason to think that species have been specially endowed with various degrees of sterility to prevent them crossing and blending in nature, than to think that trees have been specially endowed with various and somewhat analogous degrees of difficulty in being grafted together in order to prevent them becoming inarched in our forests.
The sterility of first crosses between pure species, which have their reproductive systems perfect, seems to depend on several circumstances; in some cases largely on the early death of the embryo.
The sterility of hybrids, which have their reproductive systems imperfect, and which have had this system and their whole organisation disturbed by being compounded of two distinct species, seems closely allied to that sterility which so frequently affects pure species, when their natural conditions of life have been disturbed.
This view is supported by a parallelism of another kind; namely, that the crossing of forms only slightly different is favourable to the vigour and fertility of their offspring; and that slight changes in the conditions of life are apparently favourable to the vigour and fertility of all organic beings.
It is not surprising that the degree of difficulty in uniting two species, and the degree of sterility of their hybrid-offspring should generally correspond, though due to distinct causes; for both depend on the amount of difference of some kind between the species which are crossed.
Nor is it surprising that the facility of effecting a first cross, the fertility of the hybrids produced, and the capacity of being grafted together though this latter capacity evidently depends on widely different circumstances should all run, to a certain extent, parallel with the systematic affinity of the forms which are subjected to experiment; for systematic affinity attempts to express all kinds of resemblance between all species.
First crosses between forms known to be varieties, or sufficiently alike to be considered as varieties, and their mongrel offspring, are very generally, but not quite universally, fertile.
Nor is this nearly general and perfect fertility surprising, when we remember how liable we are to argue in a circle with respect to varieties in a state of nature; and when we remember that the greater number of varieties have been produced under domestication by the selection of mere external differences, and not of differences in the reproductive system.
In all other respects, excluding fertility, there is a close general resemblance between hybrids and mongrels.
Finally, then, the facts briefly given in this chapter do not seem to me opposed to, but even rather to support the view, that there is no fundamental distinction between species and varieties.