Page:EB1911 - Volume 02.djvu/303

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288
ARACHNIDA

respiratory lamellae, and of other parts, was for the first time described, and in which the new facts discovered were shown uniformly to support the hypothesis that Limulus is an Arachnid. A list of these memoirs is given at the close of this article (2, 3, 4, 5 and 13). The Eurypterines (Gigantostraca) were included in the identification, although at that time they were supposed to possess only five pairs of anterior or prosomatic appendages. They have now been shown to possess six pairs (fig. 47), as do Limulus and Scorpio.

Fig. 2.—Ventral surface of the entosternum of Limulus polyphemus, Latr. Letters as in fig. 1 with the addition of NF, neural fossa protecting the aggregated ganglia of the central nervous system; PVP, left posterior ventral process; PMP, posterior median process. Natural size.

(From Lankester.)


Fig. 3.—Entosternum of scorpion (Palamnaeus indus, de Geer); dorsal surface.
asp, Paired anterior process of the sub-neural arch.
snp, Sub-neural arch.
ap, Anterior lateral process (same as RAP and LAP in fig. 1).
lmp, Lateral median process (same as ALR and PLR of fig. 1).
pp, Posterior process (same as PLP in fig. 1).
pf, Posterior flap or diaphragm of Newport.
m1 and m2, Perforations of the diaphragm for the passage of muscles.
DR, The paired dorsal ridges.
GC, Gastric canal or foramen.
AC, Arterial canal or foramen.

(After Lankester, loc. cit.)

The various comparisons previously made between the structure of Limulus and the Eurypterines on the one hand, and that of a typical Arachnid, such as Scorpio, on the other, had been vitiated by erroneous notions as to the origin of the nerves supplying the anterior appendages of Limulus (which were finally removed by Alphonse Milne-Edwards in his beautiful memoir (6) on the structure of that animal), and secondly by the erroneous identification of the double sternal plates of Limulus, called “chilaria,” by Owen, with a pair of appendages (7). Once the identity of the chilaria with the pentagonal sternal plate of the scorpion is recognized—an identification first insisted on by Lankester—the whole series of segments and appendages in the two animals, Limulus and Scorpio, are seen to correspond most closely, segment for segment, with one another (see figs. 7 and 8). The structure of the prosomatic appendages or legs is also seen to present many significant points of agreement (see figures), but a curious discrepancy existed in the six-jointed structure of the limb in Limulus, which differed from the seven-jointed limb of Scorpio by the defect of one joint. R. I. Pocock of the British Museum has observed that in Limulus a marking exists on the fourth joint, which apparently indicates a previous division of this segment into two, and thus establishes the agreement of Limulus and Scorpio in this small feature of the number of segments in the legs (see fig. 11).

It is not desirable to occupy the limited space of this article by a full description of the limbs and segments of Limulus and Scorpio. The reader is referred to the complete series of figures here given, with their explanatory legends (figs 12, 13, 14, 15). Certain matters, however, require comment and explanation to render the comparison intelligible. The tergites, or chitinized dorsal halves of the body rings, are fused to form a “prosomatic carapace,” or carapace of the prosoma, in both Limulus and Scorpio (see figs. 7 and 8). This region corresponds in both cases to six somites, as indicated by the presence of six pairs of limbs. On the surface of the carapace there are in both animals a pair of central eyes with simple lens and a pair of lateral eye-tracts, which in Limulus consist of closely-aggregated simple eyes, forming a “compound” eye, whilst in Scorpio they present several separate small eyes. The microscopic structure of the central and the lateral eyes has been shown by Lankester and A. G. Bourne (5) to differ; but the lateral eyes of Scorpio were shown by them to be similar in structure to the lateral eyes of Limulus, and the central eyes of Scorpio to be identical in structure with the central eyes of Limulus (see below).

Fig. 4.—Ventral surface of the same entosternum as that drawn in fig. 3. Letters as in fig. 3 with the addition of NC, neural canal or foramen.

(After Lankester, loc. cit.)

Fig. 5.—Entosternum of one of the mygalomorphous spiders; ventral surface. Ph.N., pharyngeal notch. The posterior median process with its repetition of triangular segments closely resembles the same process in Limulus.

(From Lankester, loc. cit.)

Fig. 6.—Dorsal surface of the same entosternum as that drawn in fig. 5. Ph.N., pharyngeal notch.

(After Lankester, loc. cit.)

Following the prosoma is a region consisting of six segments (figs. 14 and 15), each carrying a pair of plate-like appendages in both Limulus and Scorpio. This region is called the mesosoma. The tergites of this region and those of the following region, the metasoma, are fused to form a second or posterior carapace in Limulus, whilst remaining free in Scorpio. The first pair of foliaceous appendages in each animal is the genital operculum; beneath it are found the openings of the genital ducts. The second pair of mesosomatic appendages in Scorpio are known as the “pectens.” Each consists of an axis, bearing numerous blunt tooth-like processes arranged in a series. This is represented in Limulus by the first gill-bearing appendage. The leaves (some 150 in number) of the gill-book (see figure) correspond to the tooth-like processes of the pectens of Scorpio. The next four pairs of appendages (completing the mesosomatic series of six) consist, in both Scorpio and Limulus, of a base carrying each 130 to 150 blood-holding, leaf-like plates, lying on one another like the leaves of a book. Their minute structure is closely similar in the two cases; the leaf-like plates receive blood from the great sternal sinus, and serve as respiratory organs. The difference between the gill-books of Limulus and the lung-books of Scorpio depends on the fact that the latter are adapted to aerial respiration, while the former serve for aquatic respiration. The appendage carrying the gill-book stands out on the surface of the body in Limulus, and has other portions developed besides the gill-book and its base; it is fused with its fellow of the opposite side. On the other hand, in Scorpio, the gill-book-bearing appendage has sunk below the surface, forming a recess or chamber for itself, which communicates with the exterior by an oval or circular “stigma” (fig. 10, stg). That this in-sinking has taken place, and that the lung-books or in-sunken gill-books of Scorpio really represent appendages (that is to say, limbs or parapodia) is proved by their developmental history (see