The Evolution of Man, vol 2 - Ernst Haeckel (sight word books .TXT) 📗

of same (rudiment of uterus), g genital cord, h testicle, (h apostrophe, lower and h double apostrophe, upper testicular ligament), o ovary, o apostrophe lower ovarian ligament, i inguinal ligament of primitive kidney, d diaphragmatic ligament of primitive kidney, nn accessory kidneys, n permanent kidneys, under them the S-shaped ureters, between these the rectum, v bladder, a umbilical artery. (From Kolliker.))

The primitive or primordial kidneys of the amniote embryo were formerly called the “Wolffian bodies,” and sometimes “Oken’s bodies.” They act for a time as kidneys, absorbing unusable juices from the embryonic body and conducting them to the cloaca—afterwards to the allantois. There the primitive urine accumulates, and thus the allantois acts as bladder or urinary sac in the embryos of man and the other Amniotes. It has, however, no genetic connection with the primitive kidneys, but is a pouch-like growth from the anterior wall of the rectum (Figure 1.147 u). Thus it is a product of the visceral layer, whereas the primitive kidneys are a product of the middle layer. Phylogenetically we must suppose that the allantois originated as a pouch-like growth from the cloaca-wall in consequence of the expansion caused by the urine accumulated in it and excreted by the kidneys. It is originally a blind sac of the rectum. The real bladder of the vertebrate certainly made its first appearance among the Dipneusts (in Lepidosiren), and has been transmitted from them to the Amphibia, and from these to the Amniotes. In the embryo of the latter it protrudes far out of the not yet closed ventral wall. It is true that many of the fishes also have a “bladder.” But this is merely a local enlargement of the lower section of the nephroducts, and so totally different in origin and composition from the real bladder. The two structures can be compared from the physiological point of view, and so are ANALOGOUS, as they have the same function; but not from the morphological point of view, and are therefore not HOMOLOGOUS. The false bladder of the fishes is a mesodermic product of the nephroducts; the true bladder of the Dipneusts, Amphibia, and Amniotes is an entodermic blind sac of the rectum.

In all the Anamnia (the lower amnionless Craniotes, Cyclostomes, Fishes, Dipneusts, and Amphibia) the urinary organs remain at a lower stage of development to this extent, that the primitive kidneys (protonephri) act permanently as urinary glands. This is only so as a passing phase of the early embryonic life in the three higher classes of Vertebrates, the Amniotes. In these the permanent or after or secondary (really tertiary) kidneys (renes or metanephri) that are distinctive of these three classes soon make their appearance. They represent the third and last generation of the vertebrate kidneys. The permanent kidneys do not arise (as was long supposed) as independent glands from the alimentary tube, but from the last section of the primitive kidneys and the nephroduct. Here a simple tube, the secondary renal duct, develops, near the point of its entry into the cloaca; and this tube grows considerably forward. With its blind upper or anterior end is connected a glandular renal growth, that owes its origin to a differentiation of the last part of the primitive kidneys. This rudiment of the permanent kidneys consists of coiled urinary canals with Malpighian capsules and vascular coils (without ciliated funnels), of the same structure as the segmental mesonephridia of the primitive kidneys. The further growth of these metanephridia gives rise to the compact permanent kidneys, which have the familiar bean-shape in man and most of the higher mammals, but consist of a number of separate folds in the lower mammals, birds, and reptiles. As the permanent kidneys grow rapidly and advance forward, their passage, the ureter, detaches altogether from its birth-place, the posterior end of the nephroduct; it passes to the posterior surface of the allantois. At first in the oldest Amniotes this ureter opens into the cloaca together with the last section of the nephroduct, but afterwards separately from this, and finally into the permanent bladder apart from the rectum altogether. The bladder originates from the hindmost and lowest part of the allantoic pedicle (urachus), which enlarges in spindle shape before the entry into the cloaca. The anterior or upper part of the pedicle, which runs to the navel in the ventral wall of the embryo, atrophies subsequently, and only a useless string-like relic of it is left as a rudimentary organ; that is the single vesico-umbilical ligament. To the right and left of it in the adult male are a couple of other rudimentary organs, the lateral vesico-umbilical ligaments. These are the degenerate string-like relics of the earlier umbilical arteries.

Though in man and all the other Amniotes the primitive kidneys are thus early replaced by the permanent kidneys, and these alone then act as urinary organs, all the parts of the former are by no means lost. The nephroducts become very important physiologically by being converted into the passages of the sexual glands. In all the Gnathostomes—or all the Vertebrates from the fishes up to man—a second similar canal develops beside the nephroduct at an early stage of embryonic evolution. The latter is usually called the Mullerian duct, after its discoverer, Johannes Muller, while the former is called the Wolffian duct. The origin of the Mullerian duct is still obscure; comparative anatomy and ontogeny seem to indicate that it originates by differentiation from the Wolffian duct. Perhaps it would be best to say: “The original primary nephroduct divides by differentiation (or longitudinal cleavage) into two secondary nephroducts, the Wolffian and the Mullerian ducts.” The latter (Figure 2.387 m) lies just on the inner side of the former (Figure 2.387 w). Both open behind into the cloaca.

However uncertain the origin of the nephroduct and its two products, the Mullerian and the Wolffian ducts, may be, its later development is clear enough. In all the Gnathostomes the Wolffian duct is converted into the spermaduct, and the Mullerian duct into the oviduct. Only one of them is retained in each sex; the other either disappears altogether, or only leaves relics in the shape of rudimentary organs. In the male sex, in which the two Wolffian ducts become the spermaducts, we often find traces of the Mullerian ducts, which I have called “Rathke’s canals” (Figure 2.394 c). In the female sex, in which the two Mullerian ducts form the oviducts, there are relics of the Wolffian ducts, which are called “the ducts of Gaertner.”

(FIGURE 2.399. Female sexual organs of a Monotreme (Ornithorhynchus, Figure 2.269). o ovaries, t oviducts, u womb, sug urogenital sinus; at u apostrophe is the outlet of the two wombs, and between them the bladder (vu). cl cloaca. (From Gegenbaur.)

FIGURES 2.400 AND 2.401. Original position of the sexual glands in the ventral cavity of the human embryo (three months old).

FIGURE 2.400 male (natural size). h testicles, gh conducting ligament of the testicles, wg spermaduct, h bladder, uh inferior vena cava, nn accessory kidneys, n kidneys.

FIGURE 2.401 female, slightly magnified. r round maternal ligament (underneath it the bladder, over it the ovaries). r apostrophe kidneys, s accessory kidneys, c caecum, o small reticle, om large reticle (stomach between the two), l spleen. (From Kolliker.))

We obtain the most interesting information with regard to this remarkable evolution of the nephroducts and their association with the sexual glands from the Amphibia (Figures 2.390 to 2.395). The first structure of the nephroduct and its differentiation into Mullerian and Wolffian ducts are just the same in both sexes in the Amphibia, as in the mammal embryos (Figures 2.392 and 2.396). In the female Amphibia the Mullerian duct develops on either side into a large oviduct (Figure 2.393 od), while the Wolffian duct acts permanently as ureter (u). In the male Amphibia the Mullerian duct only remains as a rudimentary organ without any functional significance, as Rathke’s canal (Figure 2.394 c); the Wolffian duct serves also as ureter, but at the same time as spermaduct, the sperm-canals (ve) that proceed from the testicles (t) entering the fore part of the primitive kidneys and combining there with the urinary canals.

In the mammals these permanent amphibian features are only seen as brief phases of the earlier period of embryonic development (Figure 2.392). Here the primitive kidneys, which act as excretory organs of urine throughout life in the amnionless Vertebrates, are replaced in the mammals by the permanent kidneys. The real primitive kidneys disappear for the most part at an early stage of development, and only small relics of them remain. In the male mammal the epididymis develops from the uppermost part of the primitive kidney; in the female a useless rudimentary organ, the epovarium, is formed from the same part. The atrophied relic of the former is known as the paradidymis, that of the latter as the parovarium.

(FIGURE 2.402. Urogenital system of a human embryo of three inches in length, double natural size. h testicles, wg spermaducts, gh conducting ligament, p processus vaginalis, b bladder, au umbilical arteries, m mesorchium, d intestine, u ureter, n kidney, nn accessory kidney. (From Kollman.))

The Mullerian ducts undergo very important changes in the female mammal. The oviducts proper are developed only from their upper part; the lower part dilates into a spindle-shaped tube with thick muscular wall, in which the impregnated ovum develops into the embryo. This is the womb (uterus). At first the two wombs (Figure 2.399 u) are completely separate, and open into the cloaca on either side of the bladder (vu), as is still the case in the lowest living mammals, the Monotremes. But in the Marsupials a communication is opened between the two Mullerian ducts, and in the Placentals they combine below with the rudimentary Wolffian ducts to form a single “genital cord.” The original independence of the two wombs and the vaginal canals formed from their lower ends are retained in many of the lower Placentals, but in the higher they gradually blend and form a single organ. The conjunction proceeds from below (or behind) upwards (or forwards). In many of the Rodents (such as the rabbit and squirrel) two separate wombs still open into the simple and single vaginal canal; but in others, and in the Carnivora, Cetacea, and Ungulates, the lower halves of the wombs have already fused into a single piece, though the upper halves (or “horns”) are still separate (“two-horned” womb, uteris bicornis). In the bats and lemurs the “horns” are very short, and the lower common part is longer. Finally, in the apes and in man the blending of the two halves is complete, and there is only the one simple, pear-shaped uterine pouch, into which the oviducts open on each side. This simple uterus is a late evolutionary product, and is found ONLY in the ape and man.

(FIGURES 2.403 TO 2.406. Origin of human ova in the female ovary.

FIGURE 2.403. Vertical section of the ovary of a new-born female infant, a ovarian epithelium, b rudimentary string of ova, c young ova in the epithelium, d long string of ova with follicle-formation (Pfluger’s tube), e group of young follicles, f isolated young follicle, g blood-vessels in connective tissue (stroma) of the ovary. In the strings the young ova are distinguished by their considerable size from the surrounding follicle-cells. (From Waldeyer.)

FIGURE 2.404. Two young Graafian follicles, isolated. In 1 the follicle-cells still form a simple, and in 2 a double, stratum round the young ovum; in 2 they are beginning to form the ovolemma or the zona pellucida (a).

FIGURES 2.405 AND 2.406. Two older Graafian follicles, in which fluid is beginning to accumulate inside the eccentrically thickened epithelial mass of the follicle-cells (Figure 2.405 with little, 2.406 with much, follicle-water). ei the young ovum, with embryonic vesicle and spot, zp ovolemma or zona pellucida, dp discus proligerus, formed of an accumulation of follicle-cells, which surround the ovum, ff follicle-liquid (liquor folliculi), gathered inside the stratified follicle-epithelium (fe), fk connective-tissue fibrous