WE have now discussed the other parts of animals, both generally and with reference to the peculiarities of each kind, explaining how each part exists on account of such a cause, and I mean by this the final cause.
There are four causes underlying everything: first, the final cause, that for the sake of which a thing exists; secondly, the formal cause, the definition of its essence (and these two we may regard pretty much as one and the same); thirdly, the material; and fourthly, the moving principle or efficient cause.
We have then already discussed the other three causes, for the definition and the final cause are the same, and the material of animals is their parts of the whole animal the non-homogeneous parts, of these again the homogeneous, and of these last the so-called elements of all matter. It remains to speak of those parts which contribute to the generation of animals and of which nothing definite has yet been said, and to explain what is the moving or efficient cause. To inquire into this last and to inquire into the generation of each animal is in a way the same thing; and, therefore, my plan has united them together, arranging the discussion of these parts last, and the beginning of the question of generation next to them.
Now some animals come into being from the union of male and female, i.e. all those kinds of animal which possess the two sexes. This is not the case with all of them; though in the sanguinea with few exceptions the creature, when its growth is complete, is either male or female, and though some bloodless animals have sexes so that they generate offspring of the same kind, yet other bloodless animals generate indeed, but not offspring of the same kind; such are all that come into being not from a union of the sexes, but from decaying earth and excrements. To speak generally, if we take all animals which change their locality, some by swimming, others by flying, others by walking, we find in these the two sexes, not only in the sanguinea but also in some of the bloodless animals; and this applies in the case of the latter sometimes to the whole class, as the cephalopoda and crustacea, but in the class of insects only to the majority. Of these, all which are produced by union of animals of the same kind generate also after their kind, but all which are not produced by animals, but from decaying matter, generate indeed, but produce another kind, and the offspring is neither male nor female; such are some of the insects. This is what might have been expected, for if those animals which are not produced by parents had themselves united and produced others, then their offspring must have been either like or unlike to themselves. If like, then their parents ought to have come into being in the same way; this is only a reasonable postulate to make, for it is plainly the case with other animals. If unlike, and yet able to copulate, then there would have come into being again from them another kind of creature and again another from these, and this would have gone on to infinity. But Nature flies from the infinite, for the infinite is unending or imperfect, and Nature ever seeks an end.
But all those creatures which do not move, as the testacea and animals that live by clinging to something else, inasmuch as their nature resembles that of plants, have no sex any more than plants have, but as applied to them the word is only used in virtue of a similarity and analogy. For there is a slight distinction of this sort, since even in plants we find in the same kind some trees which bear fruit and others which, while bearing none themselves, yet contribute to the ripening of the fruits of those which do, as in the case of the fig-tree and caprifig.
The same holds good also in plants, some coming into being from seed and others, as it were, by the spontaneous action of Nature, arising either from decomposition of the earth or of some parts in other plants, for some are not formed by themselves separately but are produced upon other trees, as the mistletoe. Plants, however, must be investigated separately.
Of the generation of animals we must speak as various questions arise in order in the case of each, and we must connect our account with what has been said. For, as we said above, the male and female principles may be put down first and foremost as origins of generation, the former as containing the efficient cause of generation, the latter the material of it. The most conclusive proof of this is drawn from considering how and whence comes the semen; for there is no doubt that it is out of this that those creatures are formed which are produced in the ordinary course of Nature; but we must observe carefully the way in which this semen actually comes into being from the male and female. For it is just because the semen is secreted from the two sexes, the secretion taking place in them and from them, that they are first principles of generation. For by a male animal we mean that which generates in another, and by a female that which generates in itself; wherefore men apply these terms to the macrocosm also, naming Earth mother as being female, but addressing Heaven and the Sun and other like entities as fathers, as causing generation.
Male and female differ in their essence by each having a separate ability or faculty, and anatomically by certain parts; essentially the male is that which is able to generate in another, as said above; the female is that which is able to generate in itself and out of which comes into being the offspring previously existing in the parent. And since they are differentiated by an ability or faculty and by their function, and since instruments or organs are needed for all functioning, and since the bodily parts are the instruments or organs to serve the faculties, it follows that certain parts must exist for union of parents and production of offspring. And these must differ from each other, so that consequently the male will differ from the female. (For even though we speak of the animal as a whole as male or female, yet really it is not male or female in virtue of the whole of itself, but only in virtue of a certain faculty and a certain part — just as with the part used for sight or locomotion — which part is also plain to sense-perception.)
Now as a matter of fact such parts are in the female the so-called uterus, in the male the testes and the penis, in all the sanguinea; for some of them have testes and others the corresponding passages. There are corresponding differences of male and female in all the bloodless animals also which have this division into opposite sexes. But if in the sanguinea it is the parts concerned in copulation that differ primarily in their forms, we must observe that a small change in a first principle is often attended by changes in other things depending on it. This is plain in the case of castrated animals, for, though only the generative part is disabled, yet pretty well the whole form of the animal changes in consequence so much that it seems to be female or not far short of it, and thus it is clear than an animal is not male or female in virtue of an isolated part or an isolated faculty. Clearly, then, the distinction of sex is a first principle; at any rate, when that which distinguishes male and female suffers change, many other changes accompany it, as would be the case if a first principle is changed.
The sanguinea are not all alike as regards testes and uterus. Taking the former first, we find that some of them have not testes at all, as the classes of fish and of serpents, but only two spermatic ducts. Others have testes indeed, but internally by the loin in the region of the kidneys, and from each of these a duct, as in the case of those animals which have no testes at all, these ducts unite also as with those animals; this applies (among animals breathing air and having a lung) to all birds and oviparous quadrupeds. For all these have their testes internal near the loin, and two ducts from these in the same way as serpents; I mean the lizards and tortoises and all the scaly reptiles. But all the vivipara have their testes in front; some of them inside at the end of the abdomen, as the dolphin, not with ducts but with a penis projecting externally from them; others outside, either pendent as in man or towards the fundament as in swine. They have been discriminated more accurately in the Enquiries about Animals.
The uterus is always double, just as the testes are always two in the male. It is situated either near the pudendum (as in women, and all those animals which bring forth alive not only externally but also internally, and all fish that lay eggs externally) or up towards the hypozoma (as in all birds and in viviparous fishes). The uterus is also double in the crustacea and the cephalopoda, for the membranes which include their so-called eggs are of the nature of a uterus. It is particularly hard to distinguish in the case of the poulps, so that it seems to be single, but the reason of this is that the bulk of the body is everywhere similar.
It is double also in the larger insects; in the smaller the question is uncertain owing to the small size of the body.
Such is the description of the aforesaid parts of animals.
With regard to the difference of the spermatic organs in males, if we are to investigate the causes of their existence, we must first grasp the final cause of the testes. Now if Nature makes everything either because it is necessary or because it is better so, this part also must be for one of these two reasons. But that it is not necessary for generation is plain; else had it been possessed by all creatures that generate, but as it is neither serpents have testes nor have fish; for they have been seen uniting and with their ducts full of milt. It remains then that it must be because it is somehow better so. Now it is true that the business of most animals is, you may say, nothing else than to produce young, as the business of a plant is to produce seed and fruit. But still as, in the case of nutriment, animals with straight intestines are more violent in their desire for food, so those which have not testes but only ducts, or which have them indeed but internally, are all quicker in accomplishing copulation. But those which are to be more temperate in the one case have not straight intestines, and in the other have their ducts twisted to prevent their desire being too violent and hasty. It is for this that the testes are contrived; for they make the movement of the spermatic secretion steadier, preserving the folding back of the passages in the vivipara, as horses and the like, and in man. (For details see the Enquiries about Animals.) For the testes are no part of the ducts but are only attached to them, as women fasten stones to the loom when weaving; if they are removed the ducts are drawn up internally, so that castrated animals are unable to generate; if they were not drawn up they would be able, and before now a bull mounting immediately after castration has caused conception in the cow because the ducts had not yet been drawn up. In birds and oviparous quadrupeds the testes receive the spermatic secretion, so that its expulsion is slower than in fishes. This is clear in the case of birds, for their testes are much enlarged at the time of copulation, and all those which pair at one season of the year have them so small when this is past that they are almost indiscernible, but during the season they are very large. When the testes are internal the act of copulation is quicker than when they are external, for even in the latter case the semen is not emitted before the testes are drawn up.
Besides, quadrupeds have the organ of copulation, since it is possible for them to have it, but for birds and the footless animals it is not possible, because the former have their legs under the middle of the abdomen and the latter have no legs at all; now the penis depends from that region and is situated there. (Wherefore also the legs are strained in intercourse, both the penis and the legs being sinewy.) So that, since it is not possible for them to have this organ, they must necessarily either have no testes also, or at any rate not have them there, as those animals that have both penis and testes have them in the same situation.
Further, with those animals at any rate that have external testes, the semen is collected together before emission, and emission is due to the penis being heated by its movement; it is not ready for emission at immediate contact as in fishes.
All the vivipira have their testes in front, internally or externally, except the hedgehog; he alone has them near the loin. This is for the same reason as with birds, because their union must be quick, for the hedgehog does not, like the other quadrupeds, mount upon the back of the female, but they conjugate standing upright because of their spines.
So much for the reasons why those animals have testes which have them, and why they are sometimes external and sometimes internal.
All those animals which have no testes are deficient in this part, as has been said, not because it is better to be so but simply because of necessity, and secondly because it is necessary that their copulation should be speedy. Such is the nature of fish and serpents. Fish copulate throwing themselves alongside of the females and separating again quickly. For as men and all such creatures must hold their breath before emitting the semen, so fish at such times must cease taking in the sea-water, and then they perish easily. Therefore they must not mature the semen during copulation, as viviparous land-animals do, but they have it all matured together before the time, so as not to be maturing it while in contact but to emit it ready matured. So they have no testes, and the ducts are straight and simple. There is a small part similar to this connected with the testes in the system of quadrupeds, for part of the reflected duct is sanguineous and part is not; the fluid is already semen when it is received by and passes through this latter part, so that once it has arrived there it is soon emitted in these quadrupeds also. Now in fishes the whole passage resembles the last section of the reflected part of the duct in man and similar animals.
Serpents copulate twining round one another, and, as said above, have neither testes nor penis, the latter because they have no legs, the former because of their length, but they have ducts like for on account of their extreme length the seminal fluid would take too long in its passage and be cooled if it were further delayed by testes. (This happens also if the penis is large; such men are less fertile than when it is smaller because the semen, if cold, is not generative, and that which is carried too far is cooled.) So much for the reason why some animals have testes and others not. Serpents intertwine because of their inaptitude to cast themselves alongside of one another. For they are too long to unite closely with so small a part and have no organs of attachment, so they make use of the suppleness of their bodies, intertwining. Wherefore also they seem to be slower in copulation than fish, not only on account of the length of the ducts but also of this elaborate arrangement in uniting.
It is not easy to state the facts about the uterus in female animals, for there are many points of difference. The vivipara are not alike in this part; women and all the vivipara with feet have the uterus low down by the pudendum, but the cartilaginous viviparous fish have it higher up near the hypozoma. In the ovipara, again, it is low in fish (as in women and the viviparous quadrupeds), high in birds and all oviparous quadrupeds. Yet even these differences are on a principle. To begin with the ovipara, they differ in the manner of laying their eggs, for some produce them imperfect, as fishes whose eggs increase and are finally developed outside of them. The reason is that they produce many young, and this is their function as it is with plants. If then they perfected the egg in themselves they must needs be few in number, but as it is, they have so many that each uterus seems to be an egg, at any rate in the small fishes. For these are the most productive, just as with the other animals and plants whose nature is analogous to theirs, for the increase of size turns with them to seed.
But the eggs of birds and the quadrupedal ovipara are perfect when produced. In order that these may be preserved they must have a hard covering (for their envelope is soft so long as they are increasing in size), and the shell is made by heat squeezing out the moisture for the earthy material; consequently the place must be hot in which this is to happen. But the part about the hypozoma is hot, as is shown by that being the part which concocts the food. If then the eggs must be within the uterus, then the uterus must be near the hypozoma in those creatures which produce their eggs in a perfect form. Similarly it must be low down in those which produce them imperfect, for it is profitable that it should be so. And it is more natural for the uterus to be low down than high up, when Nature has no other business in hand to hinder it; for its end is low down, and where is the end, there is the function, and the uterus itself is naturally where the function is.
We find differences in the vivipara also as compared with one another. Some produce their young alive, not only externally, but also internally, as men, horses, dogs, and all those which have hair, and among aquatic animals, dolphins, whales, and such cetacea.
But the cartilaginous fish and the vipers produce their young alive externally, but first produce eggs internally. The egg is perfect, for so only can an animal be generated from an egg, and nothing comes from an imperfect one. It is because they are of a cold nature, not hot as some assert, that they do not lay their eggs externally.
At least they certainly produce their eggs in a soft envelope, the reason being that they have but little heat and so their nature does not complete the process of drying the egg-shell. Because, then, they are cold they produce soft-shelled eggs, and because the eggs are soft they do not produce them externally; for that would have caused their destruction.
The process is for the most part the same as in birds, for the egg descends and the young is hatched from it near the vagina, where the young is produced in those animals which are viviparous from the beginning. Therefore in such animals the uterus is dissimilar to that of both the vivipara and ovipara, because they participate in both classes; for it is at once near the hypozoma and also stretching along downwards in all the cartilaginous fishes. But the facts about this and the other kinds of uterus must be gathered from inspection of the drawings of dissections and from the Enquiries. Thus, because they are oviparous, laying perfect eggs, they have the uterus placed high, but, as being viviparous, low, participating in both classes.
Animals that are viviparous from the beginning all have it low, Nature here having no other business to interfere with her, and their production having no double character. Besides this, it is impossible for animals to be produced alive near the hypozoma, for the foetus must needs be heavy and move, and that region in the mother is vital and would not be able to bear the weight and the movement. Thirdly, parturition would be difficult because of the length of the passage to be traversed; even as it is there is difficulty with women if they draw up the uterus in parturition by yawning or anything of the kind, and even when empty it causes a feeling of suffocation if moved upwards. For if a uterus is to hold a living animal it must be stronger than in ovipara, and therefore in all the vivipara it is fleshy, whereas when the uterus is near the hypozoma it is membranous. And this is clear also in the case of the animals which produce young by the mixed method, for their eggs are high up and sideways, but the living young are produced in the lower part of the uterus.
So much for the reason why differences are found in the uterus of various animals, and generally why it is low in some and high in others near the hypozoma.
Why is the uterus always internal, but the testes sometimes internal, sometimes external? The reason for the uterus always being internal is that in this is contained the egg or foetus, which needs guarding, shelter, and maturation by concoction, while the outer surface of the body is easily injured and cold. The testes vary in position because they also need shelter and a covering to preserve them and to mature the semen; for it would be impossible for them, if chilled and stiffened, to be drawn up and discharge it. Therefore, whenever the testes are visible, they have a cuticular covering known as the scrotum. If the nature of the skin is opposed to this, being too hard to be adapted for enclosing them or for being soft like a true ‘skin’, as with the scaly integument of fish and reptiles, then the testes must needs be internal. Therefore they are so in dolphins and all the cetacea which have them, and in the oviparous quadrupeds among the scaly animals. The skin of birds also is hard so that it will not conform to the size of anything and enclose it neatly. (This is another reason with all these animals for their testes being internal besides those previously mentioned as arising necessarily from the details of copulation.) For the same reason they are internal in the elephant and hedgehog, for the skin of these, too, is not well suited to keep the protective part separate.
[The position of the uterus differs in animals viviparous within themselves and those externally oviparous, and in the latter class again it differs in those which have the uterus low and those which have it near the hypozoma, as in fishes compared with birds and oviparous quadrupeds. And it is different again in those which produce young in both ways, being oviparous internally and viviparous externally. For those which are viviparous both internally and externally have the uterus placed on the abdomen, as men, cattle, dogs, and the like, since it is expedient for the safety and growth of the foetus that no weight should be upon the uterus.]
The passages also are different through which the solid and liquid excreta pass out in all the vivipara. Wherefore both males and females in this class all have a part whereby the urine is voided, and this serves also for the issue of the semen in males, of the offspring in females. This passage is situated above and in front of the passage of the solid excreta. The passage is the same as that of the solid nutriment in all those animals that have no penis, in all the ovipara, even those of them that have a bladder, as the tortoises. For it is for the sake of generation, not for the evacuation of the urine, that the passages are double; but because the semen is naturally liquid, the liquid excretion also shares the same passage. This is clear from the fact that all animals produce semen, but all do not void liquid excrement. Now the spermatic passages of the male must be fixed and must not wander, and the same applies to the uterus of the female, and this fixing must take place at either the front or the back of the body. To take the uterus first, it is in the front of the body in vivipara because of the foetus, but at the loin and the back in ovipara. All animals which are internally oviparous and externally viviparous are in an intermediate condition because they participate in both classes, being at once oviparous and viviparous. For the upper part of the uterus, where the eggs are produced, is under the hypozoma by the loin and the back, but as it advances is low at the abdomen; for it is in that part that the animal is viviparous. In these also the passage for solid excrement and for copulation is the same, for none of these, as has been said already, has a separate pudendum.
The same applies to the passages in the male, whether they have testes or no, as to the uterus of the ovipara. For in all of them, not only in the ovipara, the ducts adhere to the back and the region of the spine. For they must not wander but be settled, and that is the character of the region of the back, which gives continuity and stability. Now in those which have internal testes, the ducts are fixed from the first, and they are fixed in like manner if the testes are external; then they meet together towards the region of the penis.
The like applies to the ducts in the dolphins, but they have their testes hidden under the abdominal cavity.
We have now discussed the situation of the parts contributing to generation, and the causes thereof.
The bloodless animals do not agree either with the sanguinea or with each other in the fashion of the parts contributing to generation. There are four classes still left to deal with, first the crustacea, secondly the cephalopoda, thirdly the insects, and fourthly the testacea. We cannot be certain about all of them, but that most of them copulate is plain; in what manner they unite must be stated later.
The crustacea copulate like the retromingent quadrupeds, fitting their tails to one another, the one supine and the other prone. For the flaps attached to the sides of the tail being long prevent them from uniting with the belly against the back. The males have fine spermatic ducts, the females a membranous uterus alongside the intestine, cloven on each side, in which the egg is produced.
The cephalopoda entwine together at the mouth, pushing against one another and enfolding their arms. This attitude is necessary, because Nature has bent backwards the end of the intestine and brought it round near the mouth, as has been said before in the treatise on the parts of animals. The female has a part corresponding to the uterus, plainly to be seen in each of these animals, for it contains an egg which is at first indivisible to the eye but afterwards splits up into many; each of these eggs is imperfect when deposited, as with the oviparous fishes. In the cephalopoda (as also in the crustacea) the same passage serves to void the excrement and leads to the part like a uterus, for the male discharges the seminal fluid through this passage. And it is on the lower surface of the body, where the mantle is open and the sea-water enters the cavity. Hence the union of the male with the female takes place at this point, for it is necessary, if the male discharges either semen or a part of himself or any other force, that he should unite with her at the uterine passage. But the insertion, in the case of the poulps, of the arm of the male into the funnel of the female, by which arm the fishermen say the male copulates with her, is only for the sake of attachment, and it is not an organ useful for generation, for it is outside the passage in the male and indeed outside the body of the male altogether.
Sometimes also cephalopoda unite by the male mounting on the back of the female, but whether for generation or some other cause has not yet been observed.
Some insects copulate and the offspring are produced from animals of the same name, just as with the sanguinea; such are the locusts, cicadae, spiders, wasps, and ants. Others unite indeed and generate; but the result is not a creature of the same kind, but only a scolex, and these insects do not come into being from animals but from putrefying matter, liquid or solid; such are fleas, flies, and cantharides. Others again are neither produced from animals nor unite with each other; such are gnats, ‘conopes’, and many similar kinds. In most of those which unite the female is larger than the male. The males do not appear to have spermatic passages. In most cases the male does not insert any part into the female, but the female from below upwards into the male; this has been observed in many cases (as also that the male mounts the female), the opposite in few cases; but observations are not yet comprehensive enough to enable us to make a distinction of classes. And generally it is the rule with most of the oviparous fish and oviparous quadrupeds that the female is larger than the because this is expedient in view of the increase of bulk in conception by reason of the eggs. In the female the part analogous to the uterus is cleft and extends along the intestine, as with the other animals; in this are produced the results of conception. This is clear in locusts and all other large insects whose nature it is to unite; most insects are too small to be observed in this respect.
Such is the character of the generative organs in animals which were not spoken of before. It remains now to speak of the homogeneous parts concerned, the seminal fluid and milk. We will take the former first, and treat of milk afterwards.
Some animals manifestly emit semen, as all the sanguinea, but whether the insects and cephalopoda do so is uncertain. Therefore this is a question to be considered, whether all males do so, or not all; and if not all, why some do and some not; and whether the female also contributes any semen or not; and, if not semen, whether she does not contribute anything else either, or whether she contributes something else which is not semen. We must also inquire what those animals which emit semen contribute by means of it to generation, and generally what is the nature of semen, and of the so-called catamenia in all animals which discharge this liquid.
Now it is thought that all animals are generated out of semen, and that the semen comes from the parents. Wherefore it is part of the same inquiry to ask whether both male and female produce it or only one of them, and to ask whether it comes from the whole of the body or not from the whole; for if the latter is true it is reasonable to suppose that it does not come from both parents either. Accordingly, since some say that it comes from the whole of the body, we must investigate this question first.
The proofs from which it can be argued that the semen comes from each and every part of the body may be reduced to four. First, the intensity of the pleasure of coition; for the same state of feeling is more pleasant if multiplied, and that which affects all the parts is multiplied as compared with that which affects only one or a few. Secondly, the alleged fact that mutilations are inherited, for they argue that since the parent is deficient in this part the semen does not come from thence, and the result is that the corresponding part is not formed in the offspring. Thirdly, the resemblances to the parents, for the young are born like them part for part as well as in the whole body; if then the coming of the semen from the whole body is cause of the resemblance of the whole, so the parts would be like because it comes from each of the parts. Fourthly, it would seem to be reasonable to say that as there is some first thing from which the whole arises, so it is also with each of the parts, and therefore if semen or seed is cause of the whole so each of the parts would have a seed peculiar to itself. And these opinions are plausibly supported by such evidence as that children are born with a likeness to their parents, not in congenital but also in acquired characteristics; for before now, when the parents have had scars, the children have been born with a mark in the form of the scar in the same place, and there was a case at Chalcedon where the father had a brand on his arm and the letter was marked on the child, only confused and not clearly articulated. That is pretty much the evidence on which some believe that the semen comes from all the body.
On examining the question, however, the opposite appears more likely, for it is not hard to refute the above arguments and the view involves impossibilities. First, then, the resemblance of children to parents is no proof that the semen comes from the whole body, because the resemblance is found also in voice, nails, hair, and way of moving, from which nothing comes. And men generate before they yet have certain characters, such as a beard or grey hair. Further, children are like their more remote ancestors from whom nothing has come, for the resemblances recur at an interval of many generations, as in the case of the woman in Elis who had intercourse with the Aethiop; her daughter was not an Aethiop but the son of that daughter was. The same thing applies also to plants, for it is clear that if this theory were true the seed would come from all parts of plants also; but often a plant does not possess one part, and another part may be removed, and a third grows afterwards. Besides, the seed does not come from the pericarp, and yet this also comes into being with the same form as in the parent plant.
We may also ask whether the semen comes from each of the homogeneous parts only, such as flesh and bone and sinew, or also from the heterogeneous, such as face and hands. For if from the former only, we object that resemblance exists rather in the heterogeneous parts, such as face and hands and feet; if then it is not because of the semen coming from all parts that children resemble their parents in these, what is there to stop the homogeneous parts also from being like for some other reason than this? If the semen comes from the heterogeneous alone, then it does not come from all parts; but it is more fitting that it should come from the homogeneous parts, for they are prior to the heterogeneous which are composed of them; and as children are born like their parents in face and hands, so they are, necessarily, in flesh and nails. If the semen comes from both, what would be the manner of generation? For the heteroeneous parts are composed of the homogneous, so that to come from the former would be to come from the latter and from their composition. To make this clearer by an illustration, take a written name; if anything came from the whole of it, it would be from each of the syllables, and if from these, from the letters and their composition. So that if really flesh and bones are composed of fire and the like elements, the semen would come rather from the elements than anything else, for how can it come from their composition? Yet without this composition there would be no resemblance. If again something creates this composition later, it would be this that would be the cause of the resemblance, not the coming of the semen from every part of the body.
Further, if the parts of the future animal are separated in the semen, how do they live? and if they are connected, they would form a small animal.
And what about the generative parts? For that which comes from the male is not similar to what comes from the female.
Again, if the semen comes from all parts of both parents alike, the result is two animals, for the offspring will have all the parts of both. Wherefore Empedocles seems to say what agrees pretty well with this view (if we are to adopt it), to a certain extent at any rate, but to be wrong if we think otherwise. What he says agrees with it when he declares that there is a sort of tally in the male and female, and that the whole offspring does not come from either, ‘but sundered is the fashion of limbs, some in man’s...’ For why does not the female generate from herself if the semen comes from all parts alike and she has a receptacle ready in the uterus? But, it seems, either it does not come from all the parts, or if it does it is in the way Empedocles says, not the same parts coming from each parent, which is why they need intercourse with each other.