Earthworms and Their Allies. Beddard Frank Evers

The mouth leads into a buccal cavity which later becomes the pharynx, a portion of the tube which is much thickened by muscular walls dorsally. Then follows a very short section of the oesophagus and in the fifth segment this becomes the gizzard, a very characteristic organ with thick muscular walls quite smooth and with a very thick lining of structureless membrane. After this is a narrower tube, the rest of the oesophagus. Into this open in each of segments VII, VIII, IX a pair of calciferous glands; these are diverticula of the gut with much folded walls, the cells of which secrete carbonate of lime. In the XIIth segment or so, the oesophagus suddenly widens out to form the intestine which runs as such to the end of the body. This wider tube has a ridge running along its dorsal side, the typhlosole. Along the dorsal surface of the intestine and the oesophagus is seen a red tube, contractile during the life of the worm, which is the dorsal blood vessel and whose contained blood is coloured red, as is the blood of vertebrated animals, by haemoglobin. But in the earthworm the colouring matter is not situated in corpuscles as in the vertebrate. The dorsal vessel is connected by a few pairs of equally contractile transverse trunks with a ventral vessel which is not contractile. There are other branches of these main longitudinal trunks and some minor longitudinal trunks which we shall not stop to describe further. The nervous system of the worm consists of a pair of ganglia which lie above the gut in the third segment; they are connected by a commissure running round the gut with a chain of closely fused pairs of ganglia, one for each segment to the very end of the body. In each of the segments, except the first two or three, there are a pair of excretory organs known as nephridia; these are essentially coiled glandular tubes opening on to the exterior by the regularly placed pores already referred to in considering the external characters. The tube ends in a funnel-shaped, and therefore dilated, mouth, which opens into the segment in front of that which contains the rest of the organ; a nephridium therefore lies in two segments. The only other important organs which are left for consideration are those devoted to the reproduction of the species. The essential organs are the spermaries and the ovaries. Of the former there are two pairs of minute whitish bodies which lie in segments X and XI on either side of the nerve cord attached to the anterior septal wall of their segments. The ovaries are not in the following, but in the XIIIth, segment, and occupy an identical position in that segment. A short tube with a funnel or trumpet-shaped and wide orifice opens into the cavity of the XIIIth segment opposite to each, and, perforating the septum, opens on to the exterior on the XIVth segment. A similar but larger and more folded pair of trumpet-shaped funnels opens in the same way opposite to each spermary. But in this case the two tubes of the sperm ducts run backwards for some way and those of each side after joining open on to the XVIIIth segment by the pores already mentioned. On the XVIIth and XIXth segments open two glands which are long and tubular in form and much coiled. These are the spermiducal glands and each opens in common with a muscular sac containing the long and ornamented seta referred to in describing the various external orifices. It will be noticed that the sperm duct has no direct connection with these glands but only indirectly through the external gutter which connects the three male orifices of each side of the body. Segments IX-XII inclusive contain certain sacs which depend from, and are formed as outgrowths of, the septa of those segments. These are the sperm sacs in which the male germ cells undergo their development. A corresponding body (but very much smaller) is sometimes found in relation to the ovary but has not been actually described in the particular species dealt with here. Finally, in segments VIII and IX are a pair (that is four altogether) of roundish sacs, with two or three minute diverticula, known as the spermathecae. In the diverticula of these sacs are stored the sperm derived from another individual.

      This completes the general sketch of the structure of Notiodrilus tamajusi which we have selected as a type. In this same genus are a large number of species which differ from that selected in various small structural points. Thus in N. annectens (Beddard), a species from New Zealand, the spermaries and ovaries are attached to the posterior, instead of to the anterior, wall of their segments, and there are neither calciferous glands nor modified setae upon segments XVII and XIX. In all essentials however the two types agree and are thus to be looked upon as referable to the same genus. Starting from the structure of these types we may now sketch in quite a brief way the main divergencies of structure shown in the group of Oligochaeta.

      We shall naturally begin with the family Megascolecidae of which a type has just been described.

      Within the limits of the same sub-family as that which contains Notiodrilus, i. e. the Acanthodrilinae, the changes of structure affect all the principal organs of the body except the nervous system, but are not very large and vary from genus to genus. They are mainly perhaps in the direction of reduction and simplification. Thus in Chilota, Maheina and Yagansia the spermaries are reduced to one pair in either the Xth or XIth segment, while in Yagansia one pair of spermathecae and of spermiducal glands have also disappeared. In Microscolex the spermaries remain normal, but one pair of spermathecae and of spermiducal glands have disappeared, the remaining organs of these series being in the IXth and XVIIth segments respectively. In Microscolex, Chilota and Yagansia, moreover, there is a further degeneration in the disappearance of the calciferous glands. These glands are often absent and sometimes less developed in the New Zealand Maoridrilus, which is otherwise not a degenerate form and differs characteristically from Notiodrilus by the fact that the paired nephridia alternate in position in successive segments, being now in front of the dorsal, and in other segments in front of the ventral, pairs of setae. While these genera are somewhat degenerate, the New Zealand Plagiochaeta has undergone specialisation in an upward direction. For the setae of each segment are increased to a large number much exceeding eight.

      It is not a long step to the sub-families Diplocardiinae and Trigastrinae. In the first of these, an American race confined to the northern and central parts of that continent, the male pore shows a tendency to move backwards, being situated on any of segments XVIII-XXI. The two spermiducal glands follow it, but are always placed one pair in front and one behind, as in Notiodrilus. In this group we get a new feature of specialisation in the duplication or triplication of the gizzard.

      So too with the Trigastrinae where there are either two or three gizzards; but in this sub-family another modification has become apparent. The paired nephridia have disappeared and their place is taken by several, often quite numerous, pairs of much smaller nephridia called on that account 'micronephridia' instead of 'meganephridia.' To this sub-family belong the especially African but also American and Malayan Dichogaster, whose name is derived from the important fact that it possesses two gizzards.

      Not far off is to be placed another sub-family, that of the Octochaetinae, which is New Zealand and Indian in range, the intermediate countries being, strange to say, not populated by this race of Oligochaeta. The group contains several genera of which Octochaetus, Eutyphoeus, and Dinodrilus are the best known. All these worms agree in the main features of their anatomy with Notiodrilus; but they have diverged in different directions. Thus in Octochaetus the typical two pairs of gonads and glands belonging to the generative system have been retained, while the nephridial system consists of micronephridia; in Eutyphoeus, one pair of spermiducal glands has disappeared, and as a general rule the species of this genus have only one pair of spermaries and the corresponding pair of sperm ducts. They are close to Octochaetus. The third genus mentioned, Dinodrilus, is a New Zealand form specialised in possessing 12 setae in each segment. Otherwise it is not far removed from Octochaetus.

      A fifth sub-family is also easily referable to the type whose structure has been dealt with as a preliminary to the present survey. That sub-family is the Ocnerodrilinae which is American and African in range. These worms are somewhat degenerate in comparison with their allies. Thus the calciferous glands are reduced to a single pair or to a single gland in the IXth segment, the nephridia though regular and paired have no covering plexus of blood vessels, and the worms themselves are slender and delicate, being indeed often aquatic in habit. The spermiducal glands, which are as in the former sub-families independent of the sperm ducts though sometimes opening in common with them into a short pocket-like ingrowth of the skin, are reduced in their minute structure and much simpler than in the other types.

      The genus Kerria is the least reduced perhaps. It has the male pores on segment XVIII with a pair of spermiducal glands on the segments preceding and