Читать книгу A Text-book of Entomology - A. S. Packard - Страница 14

The segments are merely thickenings of the skin connected by folds or duplications of the integument, and not actually separate or individual rings or segments. This is shown by longitudinal (sagittal) sections through the body, and also by soaking or boiling the entire insect in caustic potash, when it is seen that the integument is continuous and not actually subdivided into separate somites or arthromeres, since they are seen to be connected by a thin intersegmental membrane (Fig. 16). But this segmentation or metamerism of the integument is, however, the external indication of the segmentation of the arthropodan body most probably inherited from the worms, being a disposition of the soft parts which is characteristic of the vermian type. This segmentation of the integument is correlated with the serial repetition of the ganglia of the nervous system, of the ostia of the dorsal vessel, the primitive disposition of the segmental and reproductive organs, of the soft, muscular dissepiments which correspond to the suture between the segments, and with the metameric arrangement of the muscles controlling the movements of the segments on each other, and which internal segmentation or metamerism is indicated very early in embryonic life by the mesoblastic somites.

Fig. 16.—Diagram of the anterior part of an insect, showing the membranous intersegmental folds, g.—After Graber.

In the unjointed worms, as Graber states, the body forms a single but flexible lever. In the earthworm the muscular tube or body-wall is enclosed by a stiffer cuticle, divided into segments; hence the worm can move in all required directions, but only by sections, as seen in Fig. 16, which represents the thickened integument divided into segments, and folded inward between each segment, this thin portion of the skin being the intersegmental fold. Each segment corresponds to a special zone of the subdivided muscular tube (m), the fascia extending longitudinally. The figure shows the mode of attachment of the fascia of the muscle-tube to the segment. The anterior edge is inserted on the stiff, unyielding, inner surface of each segment: the hinder edge of the muscle is attached to the thin, flexible, intersegmental fold, which thus acts as a tendon on which the muscle can exert its force. (Graber.)

Fig. 17.—Diagram of the integument and arrangement of the segmental muscles: A, relaxed; m, muscle; g, membranous articulation; r, chitinous ring. B, the same contracted on both sides. C, on one side.—After Graber.

“Fig. 17 makes this still clearer. The muscles (m) extend between two segments immediately succeeding each other. Supposing the anterior one (A) to be stationary, what do we then see when the muscle contracts? Does it also become shorter? The intersegmental fold is drawn forwards, and hence the entire hinder segment moves forward and is shoved into the front one, and so on with the others, as at B. Afterwards, if the strain of the muscle is relieved by the diminishing action of the tensely stretched, intersegmental membrane, it again returns to a state of rest.” (Graber.)

Fig. 18.—Diagrams to demonstrate the mechanism of the motion of the segmented body in the Arthropoda: One larger segment (cf) and 4 smaller. The exoskeleton is indicated by black lines, the interarticular membranes by dotted lines. The hinges between consecutive segments are marked at, tergal (dorsal) skeleton; s, sternal (ventral) skeleton; d, dorsal longitudinal muscles = extensors (and flexors in an upward direction); v, ventral longitudinal muscles = flexors. In B, the row of segments is stretched; in A, by the contraction of the muscles (d) bent upward; in C, downward; tg, tergal; sg, sternal interarticular membranes.—After Lang.

While we look upon the dermal tube of worms as a single but flexible lever, the body of the arthropods, as Graber states, is a linear system of stiff levers. We have here a series of stiff, solid rings, or hooks, united by the intersegmental membrane into a whole. When the muscles, extending from one ring to the next behind contract, and so on through the entire series, the rings approximate each other.

The ectoskeletal segments bend to one side by the contraction of the muscles on one side, the point of the outer segmental fold opposite the fixed point becoming converted into the turning-point (C).

The usual result of the arrangement of the locomotive system is the simple curving of the body (C), and then the alternate bending of the body to right and left, which produces the serpentine movements characteristic of the earthworms, the centipede, and many insect larvæ. The most striking example of the wonderful variety of movements which can be made by an insect are those of the Syrphus larva. When feeding amid a herd of aphides, it is seen to now raise the front part of the body erect and stiff, then to bend it down, or rapidly turn it to either side, or move it in a complete circle. (Graber, pp. 23–26.)

The arrangement and mode of working of the muscles, says Lang, is illustrated by Fig. 18, which shows us five segments, one larger (ct) and four smaller, in vertical projection. The thicker portion of the integument is marked by strong outlines, the delicate and flexible interarticular membranes (tg, sg) in dotted lines. The hinges between two consecutive segments are marked a. A dorsal muscle (d) is attached to the larger segment (ct), and runs through the smaller segments, being inserted in the dorsal portion of the crust (t) of each by means of a bundle of fibres. A ventral muscle (v) does the same on the sternal side (s).

“The skeletal segments,” adds Lang, “may be compared to a double-armed lever, whose fulcrum lies in the hinges. If the dorsal muscle contracts, it draws the dorsal arm of the lever (the tergal portion of the skeleton) in the direction of the pull towards the larger segments; the tergal interarticular membranes become folded, the ventral stretched, and the four segments bend upward (Fig. 18, A). If the ventral muscle contracts, while at the same time the dorsal slackens, the row of segments will be bent downwards (Fig. 18, C).”

L. B. Sharp suggests, that in the Crustacea the rings formed by “the regularity and stress of muscular action” would be hardened by the deposition of lime at the most prominent portion, i.e. between what we have called the intersegmental folds. (American Naturalist, 1893, p. 89.) Cope also states that “with the beginning of induration of the integument, segmentation would immediately appear, for the movements of the body and limbs would interrupt the deposit at such points as would experience the greatest flexure. The muscular system would initiate the process, since flexure depends on its contractions, and its presence in animals prior to the induration of the integuments in the order of phylogeny, furnishes the conditions required.” (The Primary Factors of Organic Evolution, p. 268, 1895.)

It is apparent that the jointed or metameric structure of the bodies of insects and other arthropods is an inheritance from the segmented worms. In the worms the body is a continuous dermo-muscular tube, while in arthropods this tube is divided into regions, and the cuticle is thicker and more resistant. To go back to the incipient stages in the process of segmentation of the body, we conceive that the worms probably arose from a creeping gastrula-like form, the gastræa. The act of creeping gradually induced an elongated shape of the body. The movement of such an organism in a forward direction would gradually evolve a fore and aft, dorsal and ventral, and bilateral symmetry. As soon as this was attained, as the effect of creeping over rough irregular surfaces there would result mechanical lateral strains intermittently acting during the serpentine movements of the worm. The integument would, we can readily suppose, tend to bend or yield, or become permanently wrinkled, at more or less regular intervals. The arrangement of the muscles would gradually conform to this habit of creeping, and finally the nervous system and other organs more directly connected with the creeping movements of the organism would tend to be correlated in their arrangement with that of the segments. In this way the homonomous segments of the annelid body probably became developed, and their relations and shapes were eventually fixed by inheritance. After this stage was reached, and limbs began to appear, the segments would tend to become heteronomous, and to be grouped into regions.

Fig. 19.—Dujardinia rotifera, with jointed tentacles and caudal appendages.—With some changes, after Quatrefages.

The origin of the joints or segments in the limbs of arthropods was probably due to the mechanical strains to which what were at first soft fleshy outgrowths along the sides of the body became subjected. Indeed, certain annelid worms of the family Syllidæ have segmented tentacles and parapodia, as in Dujardinia (Fig. 19). We do not know enough about the habits of these worms to understand how this metamerism may have arisen, but it is possibly due to the act of pushing or repeated efforts to support the body while creeping over the bottom among broken shells, over coarse gravel, or among seaweeds.

It is obvious, however, that the jointed structure of the limbs of arthropods, if we are to attempt any explanation at all of the origin of such structure, was primarily due mainly to lateral strains and impacts resulting from the primitive endeavors of the ancestral arthropods to raise and to support the body while thus raised, and then to push or drag it forward by means of the soft, partially jointed, lateral limbs which were armed with bristles, hooks, or finally claws.

On the other hand, by adaptation, or as the result of parasitism and consequent lack of active motion, the original number of segments may by disuse be diminished. Thus in adult wasps and bees, the last three or four abdominal segments may be nearly lost, though the larval number is ten. During metamorphosis the body is made over, and the number, shape, and structure of the segments greatly modified. In the female of the Stylopidæ the thorax loses all traces of segments, and is fused with the head, and the abdominal segments are faintly marked, losing their chitin.

While the maxillæ have several joints, the mandibles are 1–jointed, but there are traces of two joints in Campodea, certain beetles, etc. In the antenna there is a great elasticity in respect to the number of joints, which vary from one or two to a hundred or more. It is likewise so in the thoracic legs, where the number of tarsal joints varies from one to five; also in the cercopoda, the number of joints varying from one or two to twelve or more.