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|OriginOfSpecies - 475 Rows|
|01 - Variations Under Domestication||01-08 - Breeds of the Domestic Pigeons, their Differences and Origin||40||
Great as are the differences between the breeds of the pigeon, I am fully convinced that the common opinion of naturalists is correct, namely, that all are descended from the rock-pigeon (Columba livia), including under this term several geographical races or sub-species, which differ from each other in the most trifling respects.
As several of the reasons which have led me to this belief are in some degree applicable in other cases, I will here briefly give them. If the several breeds are not varieties, and have not proceeded from the rock-pigeon, they must have descended from at least seven or eight aboriginal stocks; for it is impossible to make the present domestic breeds by the crossing of any lesser number: how, for instance, could a pouter be produced by crossing two breeds unless one of the parent-stocks possessed the characteristic enormous crop?
The supposed aboriginal stocks must all have been rock-pigeons, that is, they did not breed or willingly perch on trees.
But besides C. livia, with its geographical sub-species, only two or three other species of rock-pigeons are known; and these have not any of the characters of the domestic breeds.
Hence the supposed aboriginal stocks must either still exist in the countries where they were originally domesticated, and yet be unknown to ornithologists; and this, considering their size, habits, and remarkable characters, seems improbable; or they must have become extinct in the wild state.
But birds breeding on precipices, and good fliers, are unlikely to be exterminated; and the common rock-pigeon, which has the same habits with the domestic breeds, has not been exterminated even on several of the smaller British islets, or on the shores of the Mediterranean.
Hence the supposed extermination of so many species having similar habits with the rock-pigeon seems a very rash assumption.
Moreover, the several above-named domesticated breeds have been transported to all parts of the world, and, therefore, some of them must have been carried back again into their native country; but not one has become wild or feral, though the dovecot-pigeon, which is the rock-pigeon in very slightly altered state, has become feral in several places.
Again, all recent experience shows that it is difficult to get wild animals to breed freely under domestication, yet on the hypothesis of the multiple origin of our pigeons, it must be assumed that at least seven or eight species were so thoroughly domesticated in ancient times by half-civilised man, as to be quite prolific under confinement.
An argument of great weight, and applicable in several other cases, is, that the above-specified breeds, though agreeing generally with the wild rock-pigeon in constitution, habits, voice, colouring, and in most parts of their structure, yet are certainly highly abnormal in other parts; we may look in vain through the whole great family of Columbidae for a beak like that of the English carrier, or that of the short-faced tumbler, or barb; for reversed feathers like those of the Jacobin; for a crop like that of the pouter; for tail-feathers like those of the fantail.
Hence it must be assumed not only that half-civilised man succeeded in thoroughly domesticating several species, but that he intentionally or by chance picked out extraordinarily abnormal species; and further, that these very species have since all become extinct or unknown.
So many strange contingencies are improbable in the highest degree.
|10 - On The Geological Succession of Organic Beings||10-04 - Groups of species follow the same general rules in their appearance and disappearance as do single species||10||
Groups of species, that is, genera and families, follow the same general rules in their appearance and disappearance as do single species, changing more or less quickly, and in a greater or lesser degree.
A group does not reappear after it has once disappeared; or its existence, as long as it lasts, is continuous.
I am aware that there are some apparent exceptions to this rule, but the exceptions are surprisingly few, so few, that E. Forbes, Pictet, and Woodward (though all strongly opposed to such views as I maintain) admit its truth; and the rule strictly accords with my theory.
For as all the species of the same group have descended from some one species, it is clear that as long as any species of the group have appeared in the long succession of ages, so long must its members have continuously existed, in order to have generated either new and modified or the same old and unmodified forms.
Species of the genus Lingula, for instance, must have continuously existed by an unbroken succession of generations, from the lowest Silurian stratum to the present day.
We have seen in the last chapter that the species of a group sometimes falsely appear to have come in abruptly; and I have attempted to give an explanation of this fact, which if true would have been fatal to my views.
But such cases are certainly exceptional; the general rule being a gradual increase in number, till the group reaches its maximum, and then, sooner or later, it gradually decreases.
If the number of the species of a genus, or the number of the genera of a family, be represented by a vertical line of varying thickness, crossing the successive geological formations in which the species are found, the line will sometimes falsely appear to begin at its lower end, not in a sharp point, but abruptly; it then gradually thickens upwards, sometimes keeping for a space of equal thickness, and ultimately thins out in the upper beds, marking the decrease and final extinction of the species.
This gradual increase in number of the species of a group is strictly conformable with my theory; as the species of the same genus, and the genera of the same family, can increase only slowly and progressively; for the process of modification and the production of a number of allied forms must be slow and gradual, one species giving rise first to two or three varieties, these being slowly converted into species, which in their turn produce by equally slow steps other species, and so on, like the branching of a great tree from a single stem, till the group becomes large.
|02 - Variations Under Nature||02-04 - Wide-ranging, much diffused, and common Species vary most||10||
Guided by theoretical consideration, I thought that some interesting results might be obtained in regard to the nature and relations of the species which vary most, by tabulating all the varieties in several well-worked floras.
At first this seemed a simple task; but Mr. H. C. Watson, to whom I am much indebted for valuable advice and assistance on this subject, soon convinced me that there were many difficulties, as did subsequently Dr. Hooker, even in stronger terms.
I shall reserve for a future work the discussion of these difficulties, and the tables of the proportional numbers of the varying species.
Dr. Hooker permits me to add that after having carefully read my manuscript, and examined the tables, he thinks that the following statements are fairly well established.
The whole subject, however, treated as it necessarily here is with much brevity, is rather perplexing, and allusions cannot be avoided to the "struggle for existence," "divergence of character," and other questions, hereafter to be discussed.
|05 - Laws of Variation||05-03 - Acclimatisation||10||
Habit is hereditary with plants, as in the period of flowering, in the time of sleep, in the amount of rain requisite for seeds to germinate, &c., and this leads me to say a few words on acclimatisation.
As it is extremely common for distinct species belonging to the same genus to inhabit hot and cold countries, if it be true that all the species of the same genus are descended from a single parent-form, acclimatisation must be readily effected during a long course of descent.
It is notorious that each species is adapted to the climate of its own home: species from an arctic or even from a temperate region cannot endure a tropical climate, or conversely.
So again, many succulent plants cannot endure a damp climate.
But the degree of adaptation of species to the climates under which they live is often overrated.
We may infer this from our frequent inability to predict whether or not an imported plant will endure our climate, and from the number of plants and animals brought from different countries which are here perfectly healthy.
We have reason to believe that species in a state of nature are closely limited in their ranges by the competition of other organic beings quite as much as, or more than, by adaptation to particular climates.
But whether or not this adaptation is in most cases very close, we have evidence with some few plants, of their becoming, to a certain extent, naturally habituated to different temperatures; that is, they become acclimatised: thus the pines and rhododendrons, raised from seed collected by Dr. Hooker from the same species growing at different heights on the Himalaya, were found to possess in this country different constitutional powers of resisting cold.
Mr. Thwaites informs me that he has observed similar facts in Ceylon; analogous observations have been made by Mr. H. C. Watson on European species of plants brought from the Azores to England; and I could give other cases.
In regard to animals, several authentic instances could be adduced of species having largely extended, within historical times, their range from warmer to cooler latitudes, and conversely; but we do not positively know that these animals were strictly adapted to their native climate, though in all ordinary cases we assume such to be the case; nor do we know that they have subsequently become specially acclimatised to their new homes, so as to be better fitted for them than they were at first.