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capsule of the Graafian follicle (theca folliculi).)

In the male mammals there is the same fusion of the Mullerian and Wolffian ducts at their lower ends. Here again they form a single genital cord (Figure 2.397 g), and this opens similarly into the original urogenital sinus, which develops from the lowest section of the bladder (v). But while in the male mammal the Wolffian ducts develop into the permanent spermaducts, there are only rudimentary relics left of the Mullerian ducts. The most notable of these is the “male womb” (uterus masculinus), which originates from the lowest fused part of the ducts, and corresponds to the female uterus. It is a small, flask-shaped vesicle without any physiological significance, which opens into the ureter between the two spermaducts and the prostate folds (vesicula prostatica).

(FIGURE 2.407. A ripe human Graafian follicle. a the mature ovum, b the surrounding follicle-cells, c the epithelial cells of the follicle, d the fibrous membrane of the follicle, e its outer surface.)

The internal sexual organs of the mammals undergo very distinctive changes of position. At first the germinal glands of both sexes lie deep inside the ventral cavity, at the inner edge of the primitive kidneys (Figures 2.386 g and 2.392 k), attached to the vertebral column by a short mesentery (mesorchium in the male, mesovarium in the female). But this primary arrangement is retained permanently only in the Monotremes (and the lower Vertebrates). In all other mammals (both Marsupials and Placentals) they leave their original cradle and travel more or less far down (or behind), following the direction of a ligament that goes from the primitive kidneys to the inguinal region of the ventral wall. This is the inguinal ligament of the primitive kidneys, known in the male as the Hunterian ligament (Figure 2.400 gh), and in the female as the “round maternal ligament” (Figure 2.401 r). In woman the ovaries travel more or less towards the small pelvis, or enter into it altogether. In the male the testicles pass out of the ventral cavity, and penetrate by the inguinal canal into a sac-shaped fold of the outer skin. When the right and left folds (“sexual swellings”) join together they form the scrotum. The various mammals bring before us the successive stages of this displacement. In the elephant and the whale the testicles descend very little, and remain underneath the kidneys. In many of the rodents and carnassia they enter the inguinal canal. In most of the higher mammals they pass through this into the scrotum. As a rule, the inguinal canal closes up. When it remains open the testicles may periodically pass into the scrotum, and withdraw into the ventral cavity again in time of rut (as in many of the marsupials, rodents, bats, etc.).

The structure of the external sexual organs, the copulative organs that convey the fecundating sperm from the male to the female organism in the act of copulation, is also peculiar to the mammals. There are no organs of this character in most of the other Vertebrates. In those that live in water (such as the Acrania and Cyclostomes, and most of the fishes) the ova and sperm-cells are simply ejected into the water, where their conjunction and fertilisation are left to chance. But in many of the fishes and amphibia, which are viviparous, there is a direct conveyance of the male sperm into the female body; and this is the case with all the Amniotes (reptiles, birds, and mammals). In these the urinary and sexual organs always open originally into the last section of the rectum, which thus forms a cloaca (Chapter 2.22). Among the mammals this arrangement is permanent only in the Monotremes, which take their name from it (Figure 2.399 cl). In all the other mammals a frontal partition is developed in the cloaca (in the human embryo about the beginning of the third month), and this divides it into two cavities. The anterior cavity receives the urogenital canal, and is the sole outlet of the urine and the sexual products; the hind or anus-cavity passes the excrements only.

Even before this partition has been formed in the Marsupials and Placentals, we see the first trace of the external sexual organs. First a conical protuberance rises at the anterior border of the cloaca-outlet—the sexual prominence (phallus, Figure 2.402 A, e, B, e). At the tip it is swollen in the shape of a club (“acorn” glans). On its under side there is a furrow, the sexual groove (sulcus genitalis, f), and on each side of this a fold of skin, the “sexual pad” (torus genitalis, h l). The sexual protuberance or phallus is the chief organ of the sexual sense (Chapter 2.25); the sexual nerves spread on it, and these are the principal organs of the specific sexual sensation. As erectile bodies (corpora cavernosa) are developed in the male phallus by peculiar modifications of the blood-vessels, it becomes capable of erecting periodically on a strong accession of blood, becoming stiff, so as to penetrate into the female vagina and thus effect copulation. In the male the phallus becomes the penis; in the female it becomes the much smaller clitoris; this is only found to be very large in certain apes (Ateles). A prepuce (“foreskin”) is developed in both sexes as a protecting fold on the anterior surface of the phallus.

(FIGURE 408. The human ovum after issuing from the Graafian follicle, surrounded by the clinging cells of the discus proligerus (in two radiating crowns). z ovolemma (zona pellucida, with radial porous canals), p cytosoma (protoplasm of the cell-body, darker within, lighter without), k nucleus of the ovum (embryonic vesicle). (From Nagel, magnified 250 times.) (Cf. Figures 1.1 and 1.14.)

The external sexual member (phallus) is found at various stages of development within the mammal class, both in regard to size and shape, and the differentiation and structure of its various parts; this applies especially to the terminal part of the phallus, the glans, both the larger glans penis of the male and the smaller glans clitoridis of the female. The part of the cloaca from the upper wall of which it forms belongs to the proctodaeum, the ectodermic invagination of the rectum (Chapter 2.27); hence its epithelial covering can develop the same horny growths as the corneous layer of the epidermis. Thus the glans, which is quite smooth in man and the higher apes, is covered with spines in many of the lower apes and in the cat, and in many of the rodents with hairs (marmot) or scales (guinea-pig) or solid horny warts (beaver). Many of the Ungulates have a free conical projection on the glans, and in many of the Ruminants this “phallus-tentacle” grows into a long cone, bent hook-wise at the base (as in the goat, antelope, gazelle, etc.). The different forms of the phallus are connected with variations in the structure and distribution of the sensory corpuscles—i.e. the real organs of the sexual sense, which develop in certain papillae of the corium of the phallus, and have been evolved from ordinary tactile corpuscles of the corium by erotic adaptation (Chapter 2.25).

The formation of the corpora cavernosa, which cause the stiffness of the phallus and its capability of penetrating the vagina, by certain special structures of their spongy vascular spaces, also shows a good deal of variety within the vertebrate stem. This stiffness is increased in many orders of mammals (especially the carnassia and rodents) by the ossification of a part of the fibrous body (corpus fibrosum). This penis-bone (os priapi) is very large in the badger and dog, and bent like a hook in the marten; it is also very large in some of the lower apes, and protrudes far out into the glans. It is wanting in most of the anthropoid apes; it seems to have been lost in their case (and in man) by atrophy.

The sexual groove on the under side of the phallus receives in the male the mouth of the urogenital canal, and is changed into a continuation of this, becoming a closed canal by the juncture of its parallel edges, the male urethra. In the female this only takes place in a few cases (some of the lemurs, rodents, and moles); as a rule, the groove remains open, and the borders of this “vestibule of the vagina” develop into the smaller labia (nymphae). The large labia of the female develop from the sexual pads (tori genitales), the two parallel folds of the skin that are found on each side of the genital groove. They join together in the male, and form the closed scrotum. These striking differences between the two sexes cannot yet be detected in the human embryo of the ninth week. We begin to trace them in the tenth week of development, and they are accentuated in proportion as the difference of the sexes develops.

Sometimes the normal juncture of the two sexual pads in the male fails to take place, and the sexual groove may also remain open (hypospadia). In these cases the external male genitals resemble the female, and they are often wrongly regarded as cases of hermaphrodism. Other malformations of various kinds are not infrequently found in the human external sexual organs, and some of them have a great morphological interest. The reverse of hypospadia, in which the penis is split open below, is seen in epispadia, in which the urethra is open above. In this case the urogenital canal opens above at the dorsal root of the penis; in the former case down below. These and similar obstructions interfere with a man’s generative power, and thus prejudicially affect his whole development. They clearly prove that our history is not guided by a “kind Providence,” but left to the play of blind chance.

We must carefully distinguish the rarer cases of real hermaphrodism from the preceding. This is only found when the essential organs of reproduction, the genital glands of both kinds, are united in one individual. In these cases either an ovary is developed on the right and a testicle on the left (or vice versa); or else there are testicles and ovaries on both sides, some more and others less developed. As hermaphrodism was probably the original arrangement in all the Vertebrates, and the division of the sexes only followed by later differentiation of this, these curious cases offer no theoretical difficulty. But they are rarely found in man and the higher mammals. On the other hand, we constantly find the original hermaphrodism in some of the lower Vertebrates, such as the Myxinoides, many fishes of the perch-type (serranus), and some of the Amphibia (ringed snake, toad). In these cases the male often has a rudimentary ovary at the fore end of the testicle; and the female sometimes has a rudimentary, inactive testicle. In the carp also and some other fishes this is found occasionally. We have already seen how traces of the earlier hemaphrodism can be traced in the passages of the Amphibia.

Man has faithfully preserved the main features of his stem-history in the ontogeny of his urinary and sexual organs. We can follow their development step by step in the human embryo in the same advancing gradation that is presented to us by the comparison of the urogenital organs in the Acrania, Cyclostomes; Fishes, Amphibia, Reptiles, and then (within the mammal series) in the Monotremes, Marsupials, and the various Placentals. All the peculiarities of urogenital structure that distinguish the mammals from the rest of the Vertebrates are found in man; and in all special structural features he resembles the apes, particularly the anthropoid apes. In proof of the fact that the special features of the mammals have been inherited by man, I will, in conclusion, point out the identical way in which the ova are formed in the ovary. In all the mammals the mature ova are contained in special capsules, which are known as the Graafian follicles, after their discoverer, Roger de Graaf (1677). They

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