M Database Inspector (cheetah)
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|OriginOfSpecies - 475 Rows|
|06 - Difficutiles in Theory||06-04 - Transitions in Habits of Life||20||
Here, as on other occasions, I lie under a heavy disadvantage, for, out of the many striking cases which I have collected, I can only give one or two instances of transitional habits and structures in allied species; and of diversified habits, either constant or occasional, in the same species.
And it seems to me that nothing less than a long list of such cases is sufficient to lessen the difficulty in any particular case like that of the bat.
|06 - Difficutiles in Theory||06-07 - Organs of extreme Perfection||20||
In searching for the gradations through which an orgain in any species has been perfected, we ought to look exclusively to its lineal progenitors; but this is scarcely ever possible, and we are forced to look to other species and genera of the same group, that is to the collateral descendants from the same parent-form, in order to see what gradations are possible, and for the chance of some gradations having been transmitted in an unaltered or little altered condition.
But the state of the same organ in distinct classes may incidentally throw light on the steps by which it has been perfected.
The simplest organ which can be called an eye consists of an optic nerve, surrounded by pigment-cells, and covered by translucent skin, but without any lens or other refractive body.
We may, however, according to M. Jourdain, descend even a step lower and find aggregates of pigment-cells, apparently serving as organs of vision, without any nerves, and resting merely on sarcodic tissue.
Eyes of the above simple nature are not capable of distinct vision, and serve only to distinguish light from darkness.
In certain star-fishes, small depressions in the layer of pigment which surrounds the nerve are filled, as described by the author just quoted, with transparent gelatinous matter, projecting with a convex surface, like the cornea in the higher animals.
He suggests that this serves not to form an image, but only to concentrate the luminous rays and render their perception more easy.
In this concentration of the rays we gain the first and by far the most important step towards the formation of a true, picture-forming eye; for we have only to place the naked extremity of the optic nerve, which in some of the lower animals lies deeply buried in the body, and in some near the surface, at the right distance from the concentrating apparatus, and an image will be formed on it.
|06 - Difficutiles in Theory||06-08 - Means of Transition||20||
We should be extremely cautious in concluding that an organ could not have been formed by transitional gradations of some kind.
Numerous cases could be given amongst the lower animals of the same organ performing at the same time wholly distinct functions; thus in the larva of the dragon-fly and in the fish Cobitis the alimentary canal respires, digests, and excretes.
In the Hydra, the animal may be turned inside out, and the exterior surface will then digest and the stomach respire.
In such cases natural selection might specialise, if any advantage were thus gained, the whole or part of an organ, which had previously performed two functions, for one function alone, and thus by insensible steps greatly change its nature.
Many plants are known which regularly produce at the same time differently constructed flowers; and if such plants were to produce one kind alone, a great change would be effected with comparative suddenness in the character of the species.
It is, however, probable that the two sorts of flowers borne by the same plant were originally differentiated by finely graduated steps, which may still be followed in some few cases.
Again, two distinct organs, or the same organ under two very different forms, may simultaneously perform in the same individual the same function, and this is an extremely important means of transition: to give one instance,- there are fish with gills or branchiae that breathe the air dissolved in the water, at the same time that they breathe free air in their swimbladders, this latter organ being divided by highly vascular partitions and having a ductus pneumaticus for the supply of air.
To give another instance from the vegetable kingdom: plants climb by three distinct means, by spirally twining, by clasping a support with their sensitive tendrils, and by the emission of aerial rootlets; these three means are usually found in distinct groups, but some few species exhibit two of the means, or even all three, combined in the same individual. In all such cases one of the two organs might readily be modified and perfected so as to perform all the work, being aided during the progress of modification by the other organ; and then this other organ might be modified for some other and quite distinct purpose, or be wholly obliterated.
|06 - Difficutiles in Theory||06-09 - Cases of Difficulty||20||
These organs appear at first to offer another and far more serious difficulty; for they occur in about a dozen kinds of fish, of which several are widely remote in their affinities.
When the same organ is found in several members of the same class, especially if in members having very different habits of life, we may generally attribute its presence to inheritance from a common ancestor; and its absence in some of the members to loss through disuse or natural selection.
So that, if the electric organs had been inherited from some one ancient progenitor, we might have expected that all electric fishes would have been specially related to each other; but this is far from the case.
Nor does geology at all lead to the belief that most fishes formerly possessed electric organs, which their modified descendants have now lost.
But when we look at the subject more closely, we find in the several fishes provided with electric organs, that these are situated in different parts of the body,- that they differ in construction, as in the arrangement of the plates, and, according to Pacini, in the process or means by which the electricity is excited- and lastly, in being supplied with nerves proceeding from different sources, and this is perhaps the most important of all the differences.
Hence in the several fishes furnished with electric organs, these cannot be considered as homologous, but only as analogous in function.
Consequently there is no reason to suppose that they have been inherited from a common progenitor; for had this been the case they would have closely resembled each other in all respects.
Thus the difficulty of an organ, apparently the same, arising in several remotely allied species, disappears, leaving only the lesser yet still great difficulty; namely, by what graduated steps these organs have been developed in each separate group of fishes.
The luminous organs which occur in a few insects, belonging to widely different families, and which are situated in different parts of the body, offer, under our present state of ignorance, a difficulty almost exactly parallel with that of the electric organs.
Other similar cases could be given; for instance in plants, the very curious contrivance of a mass of pollen-grains, borne on a foot-stalk with an adhesive gland, is apparently the same in Orchis and Asclepias,- genera almost as remote as is possible amongst flowering plants; but here again the parts are not homologous.
In all cases of beings, far removed from each other in the scale of organisation, which are furnished with similar and peculiar organs, it will be found that although the general appearance and function of the organs may be the same, yet fundamental differences between them can always be detected.
For instance, the eyes of cephalopods or cuttle-fish and of vertebrate animals appear wonderfully alike; and in such widely sundered groups no part of this resemblance can be due to inheritance from a common progenitor.
Mr. Mivart has advanced this case as one of special difficulty, but I am unable to see the force of his argument.
An organ for vision must be formed of transparent tissue, and must include some sort of lens for throwing an image at the back of a darkened chamber.
Beyond this superficial resemblance, there is hardly any real similarity between the eyes of cuttle-fish and vertebrates, as may be seen by consulting Hensen's admirable memoir on these organs in the Cephalopoda.
It is impossible for me here to enter on details, but I may specify a few of the points of difference.
The crystalline lens in the higher cuttle-fish consists of two parts, placed one behind the other like two lenses, both having a very different structure and disposition to what occurs in the vertebrata.
The retina is wholly different, with an actual inversion of the elemental parts, and with a large nervous ganglion included within the membranes of the eye.
The relations of the muscles are as different as it is possible to conceive, and so in other points. Hence it is not a little difficult to decide how far even the same terms ought to be employed in describing the eyes of the Cephalopoda and Vertebrata.
It is, of course, open to any one to deny that the eye in either case could have been developed through the natural selection of successive slight variations; but if this be admitted in the one case, it is clearly possible in the other; and fundamental differences of structure in the visual organs of two groups might have been anticipated, in accordance with this view of their manner of formation.
As two men have sometimes independently hit on the same invention, so in the several foregoing cases it appears that natural selection, working for the good of each being, and taking advantage of all favourable variations, has produced similar organs, as far as function is concerned, in distinct organic beings, which owe none of their structure in common to inheritance from a common progenitor.