Since Weldon's paper, a large amount of literature on the origin of the adrenals has appeared, a summary of which, up to 1891, is given by Hans Rabl in his paper, and a further summary by Aichel in his paper published in 1900. The result of the investigations up to this latter paper may be summed up by saying that the adrenals, using this term to include all these organs of whatever kind, are in all cases, partly at all events, derived from some part of the walls of either the mesonephric or pronephric excretory organs, but that in addition a separate origin from the sympathetic nervous system must be ascribed to the medullary part of the organ and to the separate paired organs in the Elasmobranchs, which are equivalent to the medullary part in other cases.

The evidence, then, of the transformation of the known vertebrate excretory organs—the pronephros and the mesonephros—leads to the conclusion that in our search for the missing coxal glands of the meso- and pro-somatic regions, we must look for either lymphatic glands, or ductless glands of distinct importance to the body. I have already considered the question in the prosomatic region, and have given my reasons why the pituitary gland must be looked upon as the descendant of the arthropod coxal gland. In this case also the resulting ductless gland is still of functional importance, for disease of it is associated with acromegaly. If, as is possible, it is homologous with the Ascidian hypophysial gland, then it is confirmatory evidence that this latter is said by Julin to be an altered nephridial organ.

Finally, I come to the mesosomatic or branchial region; and here, strikingly enough, we find a perfectly segmental glandular organ of mysterious origin—the thymus gland—segmental with the branchiæ, not necessarily with the myotomes, belonging, therefore, to the appendicular system; and since the branchiæ represent, according to my theory, the basal part of the appendage, such segmental glands would be in the position of coxal glands. Here, then, in the thymus may be the missing mesosomatic coxal glands.

What, then, is the thymus?

The answer to this question has been given recently by Beard, who strongly confirms Kölliker's original view that the thymus is a gland for the manufacture of leucocytes, and that such leucocytes are directly derived from the epithelial cells of the thymus. Kölliker also further pointed out that the blood of the embryo is for a certain period destitute of leucocytes. Beard confirms this last statement, and says that up to a certain stage (varying from 10 to 16 mm. in length of the embryo) the embryos of Raja batis have no leucocytes in the blood or elsewhere. Up to this period the thymus-placode is well formed, and the first leucocytes can be seen to be formed in it from its epithelial cells; then such formation takes place with great rapidity, and soon an enormous discharge of leucocytes occurs from the thymus into the tissue-spaces and blood. He therefore concludes that all lymphoid tissues in the body arise originally from the thymus gland, i.e. from leucocytes discharged from the thymus.

The segmental branchial glands, known by the name of thymus, are, according to this view, the original lymphatic glands of the vertebrate; and it is to be noted that, in fishes and in Amphibia, lymphatic glands, such as we know them in the higher mammals, do not exist; they are characteristic of the higher stages of vertebrate evolution. In the lower vertebrates, the only glandular masses apart from the cell-lining of the body-cavity itself, which give rise to leucocyte-forming tissue, are these segmental branchial glands, or possibly also the modified post-branchial segmental glands, known as the head-kidney in Teleostea, etc.

The importance ascribed by Beard to the thymus in the formation of leucocytes in the lowest vertebrates would be considerably reduced in value if the branchial region of Ammocœtes possessed neither thymus glands nor anything equivalent to them. Such, however, is not the case. Schaffer has shown that in the young Ammocœtes masses of lymphatic glandular tissue are found segmentally arranged in the neighbourhood of each gill-slit—tissue which soon becomes converted into a swarming mass of leucocytes, and shows by its staining, etc., how different it is from a blood-space. The presence of this thymus leucocyte-forming tissue, as described by Schaffer, is confirmed by Beard, and I myself have seen the same thing in my youngest specimen of Ammocœtes.

Further, the very methods by which Kowalewsky has brought to light the segmental lymph-glands of the branchial region of the Crustacea, etc., are the same as those by which Weiss discovered the branchial nephric glands in Amphioxus—excretory organs which Boveri considers to represent the pronephros of the Craniota. In this supposition Boveri is right, in so far that both pronephros and the tubules in Amphioxus belong to the same system of excretory organs; but I entirely agree with van Wijhe that the region in Amphioxus is wrong. The tubules in Amphioxus ought to be represented in the branchial region of the Craniota, not in the post-branchial region; van Wijhe therefore suggests that further researches may homologize them with the thymus gland in the Craniota, not with the pronephros. This suggestion of van Wijhe appears to me a remarkably good one, especially in view of the position of the thymus glands in Ammocœtes and the nephric branchial glands in Amphioxus. If, as I have pointed out, the atrial cavity of Amphioxus has been closed in Ammocœtes by the apposition of the pleural fold with the branchial body-surface, then the remains of the position of the atrial chamber must exist in Ammocœtes as that extraordinary space between the somatic muscles and the branchial basket-work filled with blood-spaces and modified muco-cartilage. It is in this very space, close against the gill-slits, that the thymus glands of Ammocœtes are found, in the very place where the nephric tubules of Amphioxus would be found if its atrial cavity were closed completely. Instead, therefore, of considering with Boveri that the branchial nephric tubules of Amphioxus still exist in the Craniota as the pronephros, and that the atrial chamber has narrowed down to the pronephric duct, I would agree with van Wijhe that the pronephros is post-branchial, and suggest that by the complete closure of the atrial space in the branchial region the branchial nephric tubules have lost all external opening, and consequently, as in all other cases, have changed into lymphatic tissue and become the segmental thymus glands.

As van Wijhe himself remarks, the time is hardly ripe for making any positive statement about the relationship between the thymus gland and branchial excretory organs. There is at present not sufficient consensus of opinion to enable us to speak with any certainty on the subject, yet there is so much suggestiveness in the various statements of different authors as to make it worth while to consider the question briefly.

On the one hand, thymus, tonsils, parathyroids, epithelial cell-nests, and parathymus, are all stated to be derivatives of the epithelium lining the gill-slits, and Maurer would draw a distinction between the organs derived from the dorsal side of the gill-cleft and those derived from the ventral side—the former being thymus, the latter forming the epithelial cell-nests, i.e. parathyroids. The thymus in Ammocœtes, according to Schaffer, lies both ventral and dorsal to the gill-cleft; Maurer thinks that only the dorsal part corresponds to the thymus, the ventral part corresponding to the parathyroids, etc. Structurally, the thymus, parathyroids, and the epithelial cell-nests are remarkably similar, so that the evidence appears to point to the conclusion that, in the neighbourhood of the gill-slits, segmentally arranged organs of a lymphatic character are situated, which give origin to the thymus, parathyroids, tonsils, etc. Now, among these organs, i.e. among those ventrally situated, Maurer places the carotid gland, so that, if he is right, the origin of the carotid gland might be expected to help in the elucidation of the origin of the thymus.