Fig. 3.—Echidna hystrix. A, Lower surface of brooding female; B; dissection showing a dorsal view of the pouch and mammary glands; ††, the two tufts of hair in the lateral folds of the mammary pouch from which the secretion flows, b.m, Pouch; cl, cloaca; g.m, groups of mammary glands. (From Wiedersheim's Comparative Anatomy, after W. Haacke.)

In the Marsupials the pouch shelters the young, which are born in an exceedingly imperfect state, minute, nude, and blind, with a "larval" mouth fitted only to grasp in a permanent fashion the teat, upon which they are carefully fixed by the parent. But even later the pouch is made use of as a temporary harbour of refuge: from the pouch of female Kangaroos at the Zoological Gardens may frequently be observed to protrude the tail and hind-legs of a young Kangaroo as big as a Cat, and perfectly well able to take care of itself.

In the Monotremata (in Echidna) there is a deep fold of the skin which lodges the unhatched egg, and into which the mammary glands open, one on either side. This structure is only periodically developed, and arises from two rudiments, one corresponding to each mammary area; but in the female with eggs or young there is but a single deep depression, which occupies the same region of the body as the marsupial pouch of the

Marsupials.[[7]] It is usually held that this structure is not of precisely the same morphological value as the pouch of the Marsupial; and the difference is expressed by terming the one (that of Echidna) the mammary pouch, and the other the marsupium. At first sight it may appear to be an unnecessary refinement to separate two structures which have so many and such obvious likenesses. It is not quite certain, however, that the difference is not even more profound than later opinions seem to indicate. The Monotremata not only have no teats, as has already been pointed out, but the mammary glands themselves are of a perfectly different nature to those of the higher mammals, including the Marsupials. There is therefore no a priori objection to the view that the accessory parts developed in connexion with the mammary glands should also be different. The teat of the higher Mammalia grows up round the area upon which the ducts of the mammary glands open; it is a fold of skin which eventually assumes the cylindrical form of the adult teat, and which includes the ducts of the milk glands. It has been suggested that the two folds of skin which form the mammary pouch of Echidna are to be looked upon as the equivalent of the commencing teat of the higher mammal.[[8]] In this case it is clear that the marsupial folds of the Marsupial cannot correspond accurately with the apparently similar folds of Echidna, because there are teats as well. It is the teats which correspond to the marsupial folds of Echidna. This view is in apparent contradiction to an interesting discovery in a specimen of a Phalanger by Dr. Klaatsch.[[9]] This Marsupial, like most others, has a well-developed marsupial pouch, in which the young are lodged at birth; but round two of the teats is another distinct fold on either side, the outer wall of which forms the general wall of the pouch. Dr. Klaatsch thinks that these smaller and included pouches are the equivalents of the mammary pouches of Echidna. They contain teats, but this comparison does not do away with the validity of Gegenbaur's suggestion already referred to, because the teats are (see above)

secondary. If this fact be fairly to be interpreted in the sense which Dr. Klaatsch attaches to it, we have an interesting case of the growth of a new organ out of and partly replacing an old organ. In the Monotremes there is a pouch which facilitates or performs both nutritive and protective functions; in the Phalanger these two functions are carried on in separate pouches; finally, in other Marsupials, there is a return to the undifferentiated state of affairs found in the Monotremata, but with the help of a new organ not found in them.

Fig. 4.—Diagram of the development of the nipple (in vertical section). A, Indifferent stage, glandular area flat; B, elevation of the glandular area with the nipple; C, elevation of the periphery of the glandular area into the false teat, a, Periphery of the glandular area; b, glandular area; gl, glands. (From Gegenbaur.)

Though so characteristic of Marsupials, the marsupial pouch is not always developed in them. It is present in all the Kangaroos, Wallabies, and Wombats, in fact in the Diprotodonts. It is also present in a number of the carnivorous Polyprotodont Marsupials; but in Phascologale it is only present in rudiment, and in Myrmecobius it is entirely obsolete. In the American Opossums the state of the pouch is variable. "Generally absent, sometimes merely composed of two lateral folds of skin separate at each end, rarely complete," is Mr. Thomas' summary in his definition of the family Didelphyidae.[[10]] Another curious feature of the pouch in the Marsupials is the variability in the position of the mouth of the pouch: in all the Diprotodonts it looks forward; but in many Polyprotodonts it looks backward. This, however, has some connexion with the habitual attitude of the possessor: in the Kangaroo, leaping along on its hind-legs, it is requisite that the pouch should open forwards; but in the dog-like Thylacine, going on all fours, the fact that the pouch

opens backwards is less disadvantageous to the contained young.

The male Thylacine has a pouch which is quite or very nearly as well formed as in the female. There are also rudiments of a pouch in the male foetuses of many Marsupials, especially of those belonging to the Polyprotodont section of the order, though these rudiments are by no means confined to that subdivision. Up to so late a period as the age of four months (length 19.8 cm.) the male Dasyurus ursinus has a pouch.