Page:EB1911 - Volume 03.djvu/254

 group with Great Britain as creditor nations, while Canada, Australasia and the South American countries fall into a group with the United States as undeveloped and indebted countries, So also of other countries, each belongs naturally to one group or another. (10) The excess of imports or exports may vary indefinitely at different times according as a creditor country is receiving or lending at the time, or according as a debtor country is borrowing or paying off its debts at the time, but the permanent characteristics are always to be considered. BALANOGLOSSUS, the general name given to certain peculiar, opaque, worm-like animals which live an obscure life under stones, and burrow in the sand from between tide-marks down to the abyssal regions of the sea. Their colour is usually some tone of yellow with dashes of red, brown and green, and they frequently emit a pungent odour. The name has reference to the tongue-shaped muscular proboscis by which the animal works its way through the sand. The proboscis is not the only organ of locomotion, being assisted by the succeeding segment of the body, the buccal segment or collar. By the waves of contraction executed by the proboscis accompanied by inflation of the collar, progression is effected, sometimes with marvellous rapidity. The third body region or trunk may attain a great length, one or two feet, or even more, and is also muscular, but the truncal muscles are of subordinate importance in locomotion, serving principally to promote the peristaltic contractions of the body by which the food is carried through the gut. The function of alimentation is closely associated with that of locomotion, somewhat as in the burrowing earthworm; in the excavation of its burrows the sand is passed through the body, and any nutrient matter that may adhere to it is extracted during its passage through the intestine, the exhausted sand being finally ejected through the vent at the orifice of the burrow and appearing at low tide as a worm casting. In accordance with this manner of feeding, the mouth is kept permanently open and prevented from collapsing by a pair of skeletal cornua belonging to a sustentacular apparatus (the nuchal skeleton), the body of which lies within the narrow neck of the proboscis; the latter is inserted into the collar and surrounded by the anterior free flap of this segment of the body.

When first discovered by J. F. Eschscholtz at the Marshall Islands in 1825, Balanoglossus was described as a worm-like animal belonging to the Echinoderm order of Holothurians or sea-cucumbers. In 1865 Kowalevsky discovered that the organs of respiration consist of numerous pairs of gill-slits leading from the digestive canal through the thickness of the body-wall to the exterior. On this account the animal was subsequently placed by Gegenbaur in a special class of Vermes, the Enteropneusta. In 1883–1886 Bateson showed by his embryological researches that the Enteropneusta exhibit chordate (vertebrate) affinities in respect of the coelomic, skeletal and nervous systems as well as in regard to the respiratory system, and, further, that the gill-slits are formed upon a plan similar to that of the gill-slits of Amphioxus, being subdivided by tongue-bars which depend from the dorsal borders of the slits.

Coelom and Pore-canals.—In correspondence with the tri-regional differentiation of the body in its external configuration, the coelom (body-cavity, perivisceral cavity) is divided into three portions completely separated from one another by septa:—(1) proboscis-coelom, or first body-cavity; (2) the collar-coelom, or second body-cavity; (3) truncal coelom, or third body-cavity. Of these divisions of the coelom the first two communicate with the exterior by means of a pair of ciliated pore-canals placed at the posterior end of their respective segments. The proboscis-pores are highly variable, and frequently only one is present, that on the left side; sometimes the pore-canals of the proboscis unite to open by a common median orifice, and sometimes their communication with the proboscis-coelom appears to be occluded, and finally the pore-canals may be quite vestigial. The collar-pores are remarkable for their constancy; this is probably owing co the fact that they have become adapted to a special function, the inhalation of water to render the collar turgid during progression. There are reasons for supposing that the truncal coelom was at one time provided with pore-canals, but supposed vestiges of these structures have only been described for one genus, Spengelia, in which they lie near the anterior end of the truncal coelom.

Enteron.—Not only is the coelom thus subdivided, but the enteron (gut, alimentary canal, digestive tube) itself shows indications of three main subsections in continuity with one another:—(1) proboscis-gut (Eicheldarm, stomochord, vide infra); (2) collar-gut (buccal cavity, throat); (3) truncal gut extending from the collar to the vent.

Stomochord.—The proboscis-gut occurs as an outgrowth from the anterior dorsal wall of the collar-gut, and extends forward into the basal (posterior) region of the proboscis, through the neck into the proboscis-coelom, ending blindly in front. Although an integral portion of the gut, it has ceased to assist in alimentation, its epithelium undergoes vacuolar differentiation and hypertrophy, and its lumen becomes more or less vestigial. It has, in fact, become metamorphosed into a resistant supporting structure resembling in some respects the notochord of the true Chordata, but probably not directly comparable with the latter structure, being related to it solely by way of substitution. On account of the presence and mode of origin (from the gut-wall) of this organ Bateson introduced the term hemichorda as a phyletic name for the class Enteropneusta. As the proboscis-gut appears to have undoubtedly skeletal properties, and as it also has topographical relations with the mouth, it has been designated in English by the non-committal term stomochord. It is not a simple diverticulum of the collar-gut, but a complex structure possessing paired lateral pouches and a ventral convexity (ventral caecum) which rests in a concavity at the front end of the body of the nuchal skeleton (fig. 3). In some species (Spengelidae) there is a long capillary vermiform extension of the stomochord in front. The nuchal skeleton is a non-cellular laminated thickening of basement-membrane underlying that portion of the stomochord which lies between the above-mentioned pouches and the orifice into the throat. At the point where the stomochord opens into the buccal cavity the nuchal skeleton bifurcates, and the two cornua thus produced pass obliquely backwards and downwards embedded in the wall of the throat, often giving rise to projecting ridges that bound a dorsal groove of the collar-gut which is in continuity with the wall of the stomochord (fig. 3).

Nervous System.—At the base of the epidermis (which is in general ciliated) there is over the entire surface of the body a layer of nerve-fibres, occurring immediately outside the basement-membrane which separates the epidermis from the subjacent musculature. The nervous system is thus essentially epidermal in position and diffuse in distribution; but an interesting concentration of nerve-cells and fibres has taken place in the collar-region, where a medullary tube, closed in from the outside, opens in front and behind by anterior and posterior neuropores. This is the collar nerve-tube. Sometimes the central canal is wide and uninterrupted between the two neuropores; in other cases it becomes broken up into a large number of small closed medullary cavities, and in others again it is obsolete. In one family, the Ptychoderidae, the medullary tube of the collar is connected at intermediate points with the epidermis by means of a variable number of unpaired outgrowths from its dorsal wall, generally containing an axial lumen derived from and in continuity with the central canal. These hollow roots terminate blindly in the dorsal epidermis of the collar, and place the nervous layer of the latter in direct connexion with the fibres of the nerve-tube. The exact significance of these roots is a matter for speculation, but it seems possible that they are epiphysial structures remotely comparable with the epiphysial (pineal) complex of the craniate vertebrates. In accordance with this view there would be also some probability in favour of regarding the collar nerve-tube of the Enteropneusta as the equivalent of the cerebral vesicle only of Amphioxus and the Ascidian tadpole, and also of the primary fore-brain of vertebrates.

Special thickenings of the diffuse nervous layer of the epidermis occur in certain regions and along certain lines. In the neck of the proboscis the fibrous layer is greatly thickened, and other intensifications of this layer occur in the dorsal and ventral middle lines of the trunk extending to the posterior end of the body. The dorsal epidermal nerve-tract is continued in front into the ventral wall of the collar nerve-tube, and at the point of junction there is a circular commissural thickening following the posterior rim of the collar and affording a special connexion between the dorsal and ventral nerve-tracts. From the ventral surface of the collar nerve-tube numerous motor fibres may be seen passing to the subjacent musculature. These fibres are not aggregated into roots.