Page:EB1911 - Volume 07.djvu/578

Rh larval forms (nauplius), and appear only late in the course of development, after many of the trunk-limbs are fully formed. In the development of the Phyllopod Branchipus, the eyes are at first sessile, and the lateral lobes of the head on which they are set grow out and become movably articulated, forming the peduncles. The most important evidence in favour of their appendicular nature is afforded by the phenomena of regeneration. When the eye-stalk is removed from a living lobster or prawn, it is found that under certain conditions a many-jointed appendage like the flagellum of an antennule or antenna may grow in its place. It is open to question, however, how far the evidence from such “heteromorphic regeneration” can be regarded as conclusive on the points of homology. The fact that in certain rare cases among insects a leg may apparently be replaced by a wing tends to show that under exceptional conditions similar forms may be assumed by non-homologous parts.

The antennules (or first antennae) are almost universally regarded as true appendages, though they differ from all the other appendages in the fact that they are always innervated from the “brain” (or preoral ganglia), and that they are uniramous in the nauplius larva and in all the Entomostracan orders. As regards their innervation an apparent exception is found in the case of Apus, where the nerves to the antennules arise, behind the brain, from the oesophageal commissures, but this is, no doubt, a secondary condition, and the nerve-fibres have been traced forwards to centres within the brain. In the Malacostraca, the antennules are often biramous, but there is considerable doubt as to whether the two branches represent the endopodite and exopodite of the other limbs, and three branches are found in the Stomatopoda and in some Caridea. In the great majority of Crustacea the antennules are purely sensory in function and carry numerous “olfactory” hairs. They may, however, be natatory as in many Ostracoda and Copepoda, or prehensile, as in some Copepoda. The most peculiar modification, perhaps, is that found in the Cirripedia (Thyrostraca), in the larvae of which the antennules develop into organs of attachment, bearing the openings of the cement-glands, and becoming, in the adult, involved in the attachment of the animal to its support.

The antennae (second antennae) are of special interest on account of the clear evidence that, although preoral in position in all adult Crustacea, they were originally postoral appendages. In the nauplius larva they lie rather at the sides than in front of the mouth, and their basal portion carries a hook-like masticatory process which assists the similar processes of the mandibles in seizing food. In the primitive Phyllopoda, and less distinctly in some other orders, the nerves supplying the antennae arise, not from the brain, but from the circum-oesophageal commissures, and even in those cases where the nerves and the ganglia in which they are rooted have been moved forwards to the brain, the transverse commissure of the ganglia can still be traced, running behind the oesophagus.

The functions of the antennae are more varied than is the case with the antennules. In many Entomostraca (Phyllopoda, Cladocera, Ostracoda, Copepoda) they are important, and sometimes the only, organs of locomotion. In some male Phyllopoda they form complex “claspers” for holding the female. They are frequently organs of attachment in parasitic Copepoda, and they may be completely pediform in the Ostracoda. In the Malacostraca they are chiefly sensory, the endopodite forming a long flagellum, while the exopodite may form a lamellar “scale,” probably useful as a balancer in swimming, or may disappear altogether. A very curious function sometimes discharged by the antennules or antennae of Decapods is that of forming a respiratory siphon in sand-burrowing species.

The mandibles, like the antennae, have, in the nauplius, the form of biramous swimming limbs, with a masticatory process originating from the proximal part of the protopodite. This form is retained, with little alteration in some adult Copepoda, where the biramous “palp” still aids in locomotion. A somewhat similar structure is found also in some Ostracoda. In most cases, however, the palp loses its exopodite and it often disappears altogether, while the coxal segment forms the body of the mandible, with a masticatory edge variously armed with teeth and spines. In a few Ostracoda, by a rare exception, the masticatory process is reduced or suppressed, and the palp alone remains, forming a pediform appendage used in locomotion as well as in the prehension of food. In parasitic blood-sucking forms the mandibles often have the shape of piercing stylets, and are enclosed in a tubular proboscis formed by the union of the upper lip (labrum) with the lower lip (hypostome or paragnatha).

The maxillulae and maxillae (or, as they are often termed, first and second maxillae) are nearly always flattened leaf-like appendages, having gnathobasic lobes or endites borne by the segments of the protopodite. The endopodite, when present, is unsegmented or composed of few segments and forms the “palp,” and outwardly-directed lobes representing the exopodite and epipodites may also be present. These limbs undergo great modification in the different groups. The maxillulae are sometimes closely connected with the “paragnatha” or lobes of the lower lip, when these are present, and it has been suggested that the paragnatha are really the basal endites which have become partly separated from the rest of the appendage.

The limbs of the post-cephalic series show little differentiation among themselves in many Entomostraca. In the Phyllopoda they are for the most part all alike, though one or two of the anterior pairs may be specialized as sensory (Apus) or grasping (Estheriidae) organs. In the Cirripedia (Thyrostraca) the six pairs of biramous cirriform limbs differ only slightly from each other, and in many Copepoda this is also the case. In other Entomostraca considerable differentiation may take place, but the series is never divided into definite “tagmata” or groups of similarly modified appendages. It is highly characteristic of the Malacostraca, however, that the trunk-limbs are divided into two sharply defined tagmata corresponding to the thoracic and abdominal regions respectively, the limit between the two being marked by the position of the male genital openings. The thoracic limbs have the endopodites converted, as a rule, into more or less efficient walking-legs, and the exopodites are often lost, while the abdominal limbs more generally preserve the biramous form and are, in the more primitive types, natatory. These tagmata may again be subdivided into groups preserving a more or less marked individuality. For example, in the Amphipoda (fig. 4) the abdominal appendages are constantly divided into an anterior group of three natatory “swimmerets” and a posterior group of three limbs used chiefly in jumping or in burrowing. In nearly all Malacostraca the last pair of abdominal appendages (uropods) differ from the others, and in the more primitive groups they form, with the telson, a lamellar “tail-fan” (fig. 3, T), used in springing backwards through the water. In the thoracic series it is usual for one or more of the anterior pairs to be pressed into the service of the mouth, forming “foot-jaws” or maxillipeds. In the Decapoda three pairs are thus modified, and in the Tanaidacea, Isopoda and Amphipoda only one. In the Schizopoda and Cumacea the line of division is less sharp, and the varying number of so-called maxillipeds recognized by different authors gives rise to some confusion of terminology in systematic literature.

Gills.—In many of the smaller Entomostraca (Copepoda and most Ostracoda) no special gills are present, and respiration is carried on by the general surface of the body and limbs. When present, the branchiae are generally differentiations of parts of the appendages, most often the epipodites, as in the Phyllopoda. In the Cirripedia, however, they are vascular processes from the inner surface of the mantle or shell-fold, and in some Ostracoda they are outgrowths from the sides of the body. In the primitive Malacostraca the gills were probably, as in the Phyllopoda and in Nebalia, the modified epipodites of the thoracic limbs, and this is the condition found in some Schizopoda. In the Cumacea and Tanaidacea only the first thoracic limb has a branchial epipodite. In the Amphipoda, the gills though arising from the inner side of the bases of the thoracic legs are probably also epipodial in nature. In the Isopoda the respiratory function has been taken over by the abdominal appendages, both rami or only the inner becoming thin or flattened. In the Decapoda the branchial system is more complex. The gills are inserted at the base of the thoracic limbs, and lie within a pair of branchial chambers covered by the carapace. Three series are distinguished, podobranchiae, attached to the proximal segments of the appendages, pleurobranchiae, springing from the body-wall, and an intermediate series, arthrobranchiae, inserted on the articular membrane of the joint between the limb and the body. The podobranchiae are clearly epipodites, or, more correctly, parts of the epipodites, and it is probable that the arthro- and pleurobranchiae are also epipodial in origin and have migrated from the proximal segment of the limbs on to the adjacent body-wall.

Adaptations for aërial respiration are found in some of the land-crabs, where the lining membrane of the gill-chamber is beset with vascular papillae and acts as a lung. In some of the terrestrial Isopoda or woodlice (Oniscoidea) the abdominal appendages have ramified tubular invaginations of the integument, filled with air and resembling the tracheae of insects.

Internal Structure: Alimentary System.—In almost all Crustacea the food-canal runs straight through the body, except at its anterior end, where it curves downwards to the ventrally-placed mouth. In a few cases its course is slightly sinuous or twisted, but the only cases in which it is actually coiled upon itself are found in the Cladocera of the family Lynceidae (Alonidae) and in a single recently-discovered genus of Cumacea (Sympoda). As in all Arthropoda, it is composed of three divisions, a fore-gut or stomodaeum, ectodermal in origin and lined by an inturning of the chitinous cuticle, a mid-gut formed by endoderm and without a cuticular lining, and a hind-gut or proctodaeum, which, like the fore-gut, is ectodermal and is lined by cuticle. The relative proportions of these three divisions vary considerably, and the extreme abbreviation of the mid-gut found in the common crayfish (Astacus) is by no means typical of the class. Even in the closely-related lobster (Homarus) the mid-gut may be 2 or 3 in. long.

In a few Entomostraca (some Phyllopoda and Ostracoda) the chitinous lining of the fore-gut develops spines and hairs which help to triturate and strain the food, and among the Ostracods there is occasionally (Bairdia) a more elaborate armature of toothed plates moved by muscles. It is among the Malacostraca, however, and especially in the Decapoda, that the “gastric mill” reaches its greatest perfection. In most Decapods the “stomach” or dilated portion of the fore-gut is divided into two chambers, a large anterior “cardiac” and a smaller posterior “pyloric.” In the narrow