On the Generation of Animals

 Table of Contents

 Book I

 1

 2

 3

 4

 5

 6

 7

 8

 9

 10

 11

 12

 13

 14

 15

 16

 17

 18

 19

 20

 21

 22

 23

 Book II

 1

 2

 3

 4

 5

 6

 7

 8

 Book III

 1

 2

 3

 4

 5

 6

 7

 8

 9

 10

 11

 Book IV

 1

 2

 3

 4

 5

 6

 7

 8

 9

 10

 Book V

 1

 2

 3

 4

 5

 6

 7

 8

1

WE have now spoken about the sterility of mules, and about those animals which are viviparous both externally and within themselves. The generation of the oviparous sanguinea is to a certain extent similar to that of the animals that walk, and all may be embraced in the same general statement; but in other respects there are differences in them both as compared with each other and with those that walk. All alike are generated from sexual union, the male emitting semen into the female. But among the ovipara (1) birds produce a perfect hard-shelled egg, unless it be injured by disease, and the eggs of birds are all two-coloured. (2) The cartilaginous fishes, as has been often said already, are oviparous internally but produce the young alive, the egg changing previously from one part of the uterus to another; and their egg is soft-shelled and of one colour. One of this class alone does not produce the young from the egg within itself, the so-called 'frog'; the reason of which must be stated later. (3) All other oviparous fishes produce an egg of one colour, but this is imperfect, for its growth is completed outside the mother's body by the same cause as are those eggs which are perfected within.

Concerning the uterus of these classes of animals, what differences there are among them and for what reasons, has been stated previously. For in some of the viviparous creatures it is high up near the hypozoma, in others low down by the pudenda; the former in the cartilaginous fishes, the latter in animals both internally and externally viviparous, such as man and horse and the rest; in the ovipara it is sometimes low, as in the oviparous fish, and sometimes high, as in birds.

Some embryos are formed in birds spontaneously, which are called wind-eggs and 'zephyria' by some; these occur in birds which are not given to flight nor rapine but which produce many young, for these birds have much residual matter, whereas in the birds of prey all such secretion is diverted to the wings and wing-feathers, while the body is small and dry and hot. (The secretion corresponding in hen-birds to catamenia, and the semen of the cock, are residues.) Since then both the wings and the semen are made from residual matter, nature cannot afford to spend much upon both. And for this same reason the birds of prey are neither given to treading much nor to laying many eggs, as are the heavy birds and those flying birds whose bodies are bulky, as the pigeon and so forth. For such residual matter is secreted largely in the heavy birds not given to flying, such as fowls, partridges, and so on, wherefore their males tread often and their females produce much material. Of such birds some lay many eggs at a time and some lay often; for instance, the fowl, the partridge, and the Libyan ostrich lay many eggs, while the pigeon family do not lay many but lay often. For these are between the birds of prey and the heavy ones; they are flyers like the former, but have bulky bodies like the latter; hence, because they are flyers and the residue is diverted that. way, they lay few eggs, but they lay often because of their having bulky bodies and their stomachs being hot and very active in concoction, and because moreover they can easily procure their food, whereas the birds of prey do so with difficulty.

Small birds also tread often and are very fertile, as are sometimes small plants, for what causes bodily growth in others turn in them to a seminal residuum. Hence the Adrianic fowls lay most eggs, for because of the smallness of their bodies the nutriment is used up in producing young. And other birds are more fertile than game-fowl, for their bodies are more fluid and bulkier, whereas those of game-fowl are leaner and drier, since a passionate spirit is found rather in such bodies as the latter. Moreover the thinness and weakness of the legs contribute to making the former class of birds naturally inclined to tread and to be fertile, as we find also in the human species; for the nourishment which otherwise goes to the legs is turned in such into a seminal secretion, what Nature takes from the one place being added at the other. Birds of prey, on the contrary, have a strong walk and their legs are thick owing to their habits, so that for all these reasons they neither tread nor lay much. The kestrel is the most fertile; for this is nearly the only bird of prey which drinks, and its moisture, both innate and acquired, along with its heat is favourable to generative products. Even this bird does not lay very many eggs, but four at the outside.

The cuckoo, though not a bird of prey, lays few eggs, because it is of a cold nature, as is shown by the cowardice of the bird, whereas a generative animal should be hot and moist. That it is cowardly is plain, for it is pursued by all the birds and lays eggs in the nests of others.

The pigeon family are in the habit of laying two for the most part, for they neither lay one (no bird does except the cuckoo, and even that sometimes lays two) nor yet many, but they frequently produce two, or three at the most generally two, for this number lies between one and many.

It is plain from the facts that with the birds that lay many eggs the nutriment is diverted to the semen. For most trees, if they bear too much fruit, wither away after the crop when nutriment is not reserved for themselves, and this seems to be what happens to annuals, as leguminous plants, corn, and the like. For they consume all their nutriment to make seed, their kind being prolific. And some fowls after laying too much, so as even to lay two eggs in a day, have died after this. For both the birds the plants become exhausted, and this condition is an excess of secretion of residual matter. A similar condition is the cause of the later sterility of the lioness, for at the first birth she produces five or six, then in the next year four, and again three cubs, then the next number down to one, then none at all, showing that the residue is being used up and the generative secretion is failing along with the advance of years.

We have now stated in which birds wind-eggs are found, and also what sort of birds lay many eggs or few, and for what reasons. And wind-eggs, as said before, come into being because while it is the material for generation that exists in the female of all animals, birds have no discharge of catamenia like viviparous sanguinea (for they occur in all these latter, more in some, less in others, and in some only enough in quantity just to mark the class). The same applies to fish as to birds, and so in them as in birds is found an embryonic formation without impregnation, but it is less obvious because their nature is colder. The secretion corresponding to the catamenia of vivipara is formed in birds at the appropriate season for the discharge of superfluous matter, and, because the region near the hypozoma is hot, it is perfected so far as size is concerned, but in birds and fishes alike it is imperfect for generation without the seminal fluid of the male; the cause of this has been previously given. Wind-eggs are not formed in the flying birds, for the same reason as prevents their laying many eggs; for the residual matter in birds of prey is small, and they need the male to give an impulse for the discharge of it. The wind-eggs are produced in greater numbers than the impregnated but smaller in size for one and the same reason; they are smaller in size because they are imperfect, and because they are smaller in size they are more in number. They are less pleasant for food because they are less concocted, for in all foods the concocted is more agreeable. It has been sufficiently observed, then, that neither birds' nor fishes' eggs are perfected for generation without the males. As for embryos being formed in fish also (though in a less degree) without the males, the fact has been observed especially in river fish, for some are seen to have eggs from the first, as has been written in the Enquiries concerning them. And generally speaking in the case of birds even the impregnated eggs are not wont for the most part to attain their full growth unless the hen be trodden continually. The reason of this is that just as with women intercourse with men draws down the secretion of the catamenia (for the uterus being heated attracts the moisture and the passages are opened), so this happens also with birds; the residual matter corresponding to the catamenia advances a little at a time, and is not discharged externally, because its amount is small and the uterus is high up by the hypozoma, but trickles together into the uterus itself. For as the embryo of the vivipara grows by means of the umbilical cord, so the egg grows through this matter flowing to it through the uterus. For when once the hens have been trodden, they all continue to have eggs almost without intermission, though very small ones. Hence some are wont to speak of wind-eggs as not coming into being independently but as mere relics from a previous impregnation. But this is a false view, for sufficient observations have been made of their arising without impregnation in chickens and goslings. Also the female partridges which are taken out to act as decoys, whether they have ever been impregnated or not, immediately on smelling the male and hearing his call, become filled with eggs in the latter case and lay them in the former. The reason why this happens is the same as in men and quadrupeds, for if their bodies chance to be in rut they emit semen at the mere sight of the female or at a slight touch. And such birds are of a lascivious and fertile nature, so that the impulse they need is but small when they are in this excited condition, and the secreting activity takes place quickly in them, wind-eggs forming in the unimpregnated and the eggs in those which have been impregnated growing and reaching perfection swiftly.

Among creatures that lay eggs externally birds produce their egg perfect, fish imperfect, but the eggs of the latter complete their growth outside as has been said before. The reason is that the fish kind is very fertile; now it is impossible for many eggs to reach completion within the mother and therefore they lay them outside. They are quickly discharged, for the uterus of externally oviparous fishes is near the generative passage. While the eggs of birds are two-coloured, those of all fish are one-coloured. The cause of the double colour may be seen from considering the power of each of the two parts, the white and the yolk. For the matter of the egg is secreted from the blood [No bloodless animal lays eggs,] and that the blood is the material of the body has been often said already. The one part, then, of the egg is nearer the form of the animal coming into being, that is the hot part; the more earthy part gives the substance of the body and is further removed. Hence in all two-coloured eggs the animal receives the first principle of generation from the white (for the vital principle is in that which is hot), but the nutriment from the yolk. Now in animals of a hotter nature the part from which the first principle arises is separated off from the part from which comes the nutriment, the one being white and the other yellow, and the white and pure is always more than the yellow and earthy; but in the moister and less hot the yolk is more in quantity and more fluid. This is what we find in lake birds, for they are of a moister nature and are colder than the land birds, so that the so-called 'lecithus' or yolk in the eggs of such birds is large and less yellow because the white is less separated off from it. But when we come to the ovipara which are both of a cold nature and also moister (such is the fish kind) we find the white not separated at all because of the small size of the eggs and the quantity of the cold and earthy matter; therefore all fish eggs are of one colour, and white compared with yellow, yellow compared with white. Even the wind-eggs of birds have this distinction of colour, for they contain that out of which will come each of the two parts, alike that whence arises the principle of life and that whence comes the nutriment; only both these are imperfect and need the influence of the male in addition; for wind-eggs become fertile if impregnated by the male within a certain period. The difference in colour, however, is not due to any difference of sex, as if the white came from the male, the yolk from the female; both on the contrary come from the female, but the one is cold, the other hot. In all cases then where the hot part is considerable it is separated off, but where it is little it cannot be so; hence the eggs of such animals, as has been said, are of one colour. The semen of the male only puts them into form; and therefore at first the egg in birds appears white and small, but as it advances it is all yellow as more of the sanguineous material is continually mixed with it; finally as the hot part is separated the white takes up a position all round it and equally distributed on all sides, as when a liquid boils; for the white is naturally liquid and contains in itself the vital heat; therefore it is separated off all round, but the yellow and earthy part is inside. And if we enclose many eggs together in a bladder or something of the kind and boil them over a fire so as not to make the movement of the heat quicker than the separation of the white and yolk in the eggs, then the same process takes place in the whole mass of the eggs as in a single egg, all the yellow part coming into the middle and the white surrounding it.

We have thus stated why some eggs are of one colour and others of two.