  THE INSECT WORLD: BEING A Popular Account of the Orders of Insects; TOGETHER WITH A DESCRIPTION OF THE HABITS AND ECONOMY OF BY A New Edition, REVISED AND CORRECTED BY P. MARTIN DUNCAN, F.R.S. ————— D. APPLETON AND CO., NEW YORK. This popular French book on Insects has been placed in my hands in order that the scientific portions of it should be examined and, if necessary, corrected. This task has been a light one, for the book had already passed through the able editorship of Mr. Jansen. But I have added a short notice of the Thysanoptera, which did not appear in M. Figuier's original work, and also the necessary information respecting the evolution of Stylops. P. MARTIN DUNCAN.
It is not intended to investigate the anatomy of insects in this work thoroughly; but, as we are about to treat of the habits and economy of certain created beings, it is necessary first to explain the principal parts of their structure, and the stages which every perfect insect or imago has undergone before arriving at that state. We, therefore, proceed to explain, as simply as possible, the anatomy of an insect, and the functions of its organs. If we take an insect, and turn it over, and examine it carefully, the first thing that strikes us is that it is divided into three parts: the head; the thorax, or chest; and the abdomen, or stomach. The head (Fig. 1) is a kind of box, formed of a single piece, having here and there joints more or less strongly marked, sometimes scarcely visible. It is furnished in front with an opening—often very small—which is the mouth; and with some for the eyes, and with others for the insertion of the antennÆ or horns. The integuments of the head are generally harder than the other parts of the body. It is necessary that this should be so. Insects often live and die in the midst of substances which offer some resistance. It is necessary, therefore, that the head should be strong enough to overcome such resistance. The head contains the masticatory organs, which, frequently having to attack hard substances, must be strongly supported. The exception to this rule is among insects which live by suction. It would be out of place here to mention the numerous modifi cations of the head which are presented in the immense class of insects. The eyes of insects are of two kinds. There are compound eyes, or eyes composed of many lenses, united by their margins and forming hexagonal facettes; and there are also simple eyes, or ocelli. The exterior of the eye is called the cornea (Fig. 2), each facette being a cornea; and the facettes, which vary in size even in the same eye, unite and form a common cornea, which is represented by the entire figure. In order to show the immense number of the facettes possessed by many insects, we give the following list:—
The facettes appear to be most numerous in insects of the genus ScarabÆus (a genus of beetles). They are so minute, that they can only be detected with a magnifying glass. Looked at in front, a compound eye may be considered an agglomeration of simple eyes; but internally this is hardly correct. On the under side of each facette we find a body of a gelatinous appearance, transparent, and usually conical; the base of this occupies the centre of the facette in such a manner as to leave around it a ring to receive some colouring matter. This body diminishes in thickness towards its other extremity, and terminates in a point where it joins a nervous filament proceeding from the optic nerve. These cones, agreeing in number with the facettes, play the part of the crystalline lens in the eyes of animals. They are straight and parallel with each other. A pigment fills all the spaces between the cones, and between the nervous filaments, and covers the under side of each cornea, except at the centre. This pigment varies much in colour. There are almost always two layers, of which the exterior one is the more brilliant. In fact, these eyes often sparkle with fire, like precious stones. M. Lacordaire, in his "Introduction À l'Entomologie," from which we borrow the greater part of this information, has summed up as follows, the manner in which, according to M. MÜller, the visual organs of insects operate:— "Each facette, with its lens and nervous filament, separated from those surrounding them by the pigment in which they are enclosed, form an isolated apparatus, impenetrable to all rays of light, except those which fall perpendicularly on the centre of the facette, which alone is devoid of pigment. All rays falling obliquely are absorbed by that pigment which surrounds the gelatinous cone. It results partly from this, and partly from the immobility of the eye, that the field of vision of each facette is very limited, and that there are as many objects reflected on the optic filaments as there are corneÆ. The extent, then, of the field of vision will be determined, not by the diameter of these last, but by the diameter of the entire eye, and will be in proportion to its size and convexity. But whatever may be the size of the eyes, like their fields of vision, they are independent of each other; there is always a space, greater or less, between them; and the insect cannot see objects in front of this space without turning its head. What a peculiar sensation must result from the multiplicity of images on the optic filaments! This is not more easily explained than that which happens with animals which, having two eyes, see only one image; and probably the same is the case with insects. But these eyes usually look in opposite directions, and should see two images, as in the chameleon, whose eyes move independently of each other. The clearness and length of vision will depend, continues M. MÜller, on the diameter of the sphere of which the entire eye forms a segment, on the number and size of the facettes, and the length of the cones or lenses. The larger each facette, taken separately, and the more brilliant the pigment placed between the lenses, the more distinct will be the image of objects at a distance, and the less distinct that of objects near. With the latter the luminous rays diverge considerably; while those from the former are more parallel. In the first case, in traversing the pigment, they impinge obliquely on the crystalline, and consequently confuse the vision; in the second, they fall more perpendicularly on each facette. "Objects do not appear of the same size to each optic filament, unless the eye is a perfect section of a sphere, and its convexity concentric with that of the optic nerve. Whenever it is otherwise, the image corresponds more or less imperfectly with the size of the object, and is more or less incorrect. Hence it follows, that elliptical or conical eyes, which one generally finds among insects, are less perfect than those referred to above. "The differences which exist in the organisation of the eye among insects are explicable, to a certain point, on the theory which we are about to explain in a few words. Those species which live in the same substances on which they feed, and those which are parasitical, have small and flattened eyes; those, on the contrary, which have to seek their food, and which need to see objects at a distance, have large or very convex eyes. For the same reason the males, which have to seek their females, have larger eyes than the latter. The position of the eyes depends also on their size and shape; those which are flat, and have consequently a short field of vision, are placed close together, and rather in front than at the sides of the head, and often adjoining. Spherical and convex eyes, on the contrary, are placed on the sides, and their axes are opposite. But the greater field of vision which they are able to take in makes up for this position." Almost all insects are provided with a pair of compound eyes, which are placed on the sides of the head. The size and form of these organs are very variable, as we shall presently see. They are generally placed behind the antennÆ. Although simple eyes (ocelli or stemmata) are common, they do not exist in all the orders of insects. They are generally round, and more or less convex and black, and there are three in the majority of cases. When there is this number they are most frequently placed in a triangle behind, and at a greater or less distance from the antennÆ. Under the cornea, which varies in convexity, is found a transparent, rather hard, and nearly globular body, which is the true crystalline resting on a mass, which represents the vitreous body. This vitreous body is enclosed in an expansion of the optic nerve. Besides these, there is a pigment, most frequently red-brown, sometimes black, or blood-red. The organisation of these eyes is analogous to the eyes of fishes, and their refractive power is very great. With these eyes insects can only see such objects as are at a short distance. Of what use then can stemmata be to insects also provided with compound eyes? It has been remarked that most insects having this arrangement of eyes feed on the pollen of plants, and it has been surmised that the stemmata enable them to distinguish the parts of the flowers. The antennÆ, commonly called horns, are two flexible appendages, of very variable form, which are joined to different parts of the head, and are always two in number. The joints of which they are made up have the power of motion, which enables the insect to move them in any direction. The antennÆ consist of three parts: the basal joint, commonly distinguished by its form, length, and colour; the club, formed by a gradual or sudden thickening of the terminal joints, of which the number, form, and size present great variations; lastly, the stalk, formed by all the joints of the antennÆ, except the basal, when no club exists, and in case of the existence of a club, of all those between it and the basal one. We give as examples the antennÆ of two beetles, one of the genus Asida, the other of the genus Zygia (Figs. 3 and 4).
Insects, for the most part, while in repose, place their antennÆ on their backs, or along the sides of the head, or even on the thorax. Others are provided with cavities in which the antennÆ repose either wholly or in part. During their different movements, insects move their antennÆ more or less, sometimes slowly and with regularity, at other times in all directions. Some insects impart to their antennÆ a perpetual vibration. During flight they are directed in front, perpendicular to the axis of the body, or else they repose on the back. What is the use of the antennÆ, resembling as they do, feathers, saws, clubs, &c.? Everything indicates that these organs play a very important part in the life of insects, but their functions are imperfectly understood. Experience has shown that they only play a subordinate part as feelers, and have nothing to do with the senses of taste or smell. There is no other function for them to fulfil, except that of hearing. On this hypothesis the antennÆ will be the principal instruments for the transmission of sound-waves. The membrane at their base represents a trace of the tympanum which exists among the higher animals. This membrane then will have some connection with an auditory nerve. The mouth of insects is formed after two general types, which correspond to two kinds of requirements. It is suited in the one case to break solid substances, in the other to imbibe liquids. At first sight there seems no similarity between the mouth of a biting insect and of one living by suction. But on examination it is found that the parts of the mouth in the one are exactly analogous to the same parts in the other, and that they have only modifications suiting them to the different purposes which they have to fulfil. The mouth of a biting insect is composed of an upper lip, a pair of mandibles, a pair of jaws, and a lower lip (Fig. 5).
The lower lip and the jaws carry on the outside certain appendages or filaments which have received the name of palpi. When speaking of sucking insects, and in general of the various orders of insects, we shall speak more in detail of the various parts of the mouth. The thorax (Fig. 6), the second primary division of the body of insects, plays almost as important a part as the head. It consists of three segments or rings, which are in general joined together—the prothorax, the mesothorax, and the metathorax, each of which bears a pair of legs. The wings are attached to the two posterior segments. All insects have six true legs. There is no exception whatever to this rule, though some may not be developed. From the segments to which they are attached, the legs are called anterior, posterior, and intermediate. The legs are composed of four parts: the trochanter, a short joint which unites the thigh to the body; the thigh or femur; the tibia, answering to the shank in animals; and the tarsus, or foot, composed of a variable number of pieces placed end to end, and called the phalanges. We take as examples the hind leg of a Heterocerus (Fig. 7), and the front leg of a Zophosis (Fig. 8) (genera of beetles). We shall not dwell on the different parts, as they perform functions which will occupy us later, when speaking of the various species of the great class of insects.
The functions which the legs of insects have to perform consist in walking, swimming, or jumping. In walking, says M. Lacordaire, insects move their legs in different ways. Some move their six legs successively, or only two or three at a time without distinction, but never both legs of the same pair together, consequently one step is not the same as another. The walk of insects is sometimes very irregular, especially when the legs are long; and they often hop rather than walk. Others have one kind of step, and walk very regularly. They commence by moving the posterior and anterior legs on the same side and the intermediate ones on the opposite side. The first step made, these legs are put down, and the others raised in their turn to make a second. Running does not change the order of the movements, it only makes them quicker—very rapid in some species, and surpassing in proportion that of all other animals; but in others the pace is slow. Some insects rather crawl than walk. In swimming, the posterior legs play the principal part. The other legs striking the water upwards or downwards, produce an upward or downward motion. The animal changes its course at will by using the legs on one side only, in the same way as one turns a rowing boat with one oar without the aid of a rudder. Swimming differs essentially from walking, for the foot being surrounded by a resisting medium, the legs on both sides are moved at the same time. The act of jumping is principally performed by the hind legs. Insects which jump have these legs very largely developed, as in Fig. 9. When about to jump they bring the tibia into contact with the thigh, which is often furnished with a groove to receive it, having on each side a row of spines. The leg then suddenly straightens like a spring, and the foot being placed firmly on the ground, sends the insect into the air, and at the same time propels forward. The jump is greater in proportion as the leg is longer. To treat here in a general manner of the wings of insects would be useless. We shall refer to them at length in their proper place, when treating of the various types of winged insects. In the perfect insect the abdomen does not carry either the wings or the legs. It is formed of nine segments, which are without appendages, with the exception of the posterior ones, which often carry small organs differing much in form and function. These are saws, probes, forceps, stings, augers, &c. We shall consider these different organs in their proper places. With vertebrate animals, which have an interior skeleton suited to furnish points of resistance for their various movements, the skin is a more or less soft covering, uniformly diffused over the exterior of the body, and intended only to protect it against external injury. In insects the points of resistance are changed from the interior to the exterior. The skin is altered by Nature to fit it to this purpose. It is hard, and presents between the segments only membranous intervals, which allow the hard parts to move in all directions. We are examining a perfect insect; we have glanced at its skeleton, and the different appendages which spring from it. The principal organs which are contained in the body remain to be examined. We will first study the digestive apparatus. This apparatus consists of a lengthened tubular organ, swollen at certain points, forming more or less numerous convolutions, and provided with two distinct orifices. This alimentary canal is always situated in the median line of the body, traverses its whole length, and is at first surrounded by, and then passes above, the nervous ganglia. [1] In its most complicated form the alimentary canal is composed of an oesophagus, or gullet, of a crop, of a gizzard, of a chylific ventricle or stomach, a small intestine, a large intestine, divers appendages, salivary, biliary, and urinary glands. The oesophagus is often not wider than a hair, and part of it in many species is enlarged into a pouch, which is called the crop, because it occupies the same position, and performs analogous functions with that organ in birds. It is enough to say that the food remains there some time before passing on to the other parts of the intestinal canal, and undergoes a certain amount of preparation. It is in the gizzard, when one exists, that the food, separated by the masticatory organs of the mouth, undergoes another and more complete grinding. Its structure is suited to its office. It is, in fact, very muscular, often half cartilaginous, and strongly contractile. Its interior walls are provided with a grinding apparatus, which varies according to the species, and consists of teeth, plates, spines, and notches, which convert the food into pulp. It only exists among insects which live on solid matters, hard vegetables, small animals, tough skin, &c. This apparatus is absent in sucking insects and those which live on soft substances, such as the pollen of flowers, &c. The chylific ventricle or stomach is never absent; it is the organ which performs the principal part in the act of digestion. Two kinds of appendages belong to the chylific ventricle, but only in certain families. The first are papillÆ, in the form of the fingers of a glove, which bristle over the exterior of this organ, and in which it is believed that the food begins to be converted into chyle. The second are cÆca, and larger and less numerous. They have been considered as secretory organs, answering to the pancreas in vertebrate animals. Fig. 10, which represents the digestive apparatus of Carabus auratus, a common beetle, presents to the eyes of the reader the different organs of which we are speaking. A is the mouth of the insect, B the oesophagus, C the crop, D the gizzard, E the chylific ventricle, F and G the small and large intestines, and H the anus. It is not necessary to consider the other parts of the alimentary canal in insects, but only to refer to some of the appendages of this apparatus. The salivary glands pour into the digestive tube a liquid, generally colourless, which, from the place where it is secreted, and its alkaline nature, corresponds to the saliva in vertebrate animals. It is this liquid which comes from the tongue of sucking insects in the form of drops. These glands are always two in number. Their form is as variable as complicated. The most simple is that of a closed flexible tube, generally rolled into a ball, and opening on the sides of the oesophagus. At the posterior extremity of the chylific ventricle are inserted a variable number of fine tubes, usually elongated and flexible, and terminating in culs-de-sac at one end. Their colour, which depends on the liquid they may contain, is sometimes white, but more frequently brown, blackish, or green. They appear to be composed of a very slight and delicate membrane, as they are very easily torn, and nothing is more difficult than to unroll and to disengage them from the fatty or other tissues by which they are enveloped. The function of these vessels is uncertain. Cuvier and LÉon Dufour supposed them to be analogous to the liver, and on that account they have been called biliary vessels; and they are often termed the Malpighian vessels, after the name of their discoverer. According to M. Lacordaire, their functions vary with their position. When they enter the chylific ventricle, they furnish only bile; bile and a urinary liquid when they enter the posterior part of the ventricle and the intestine; and urine alone when they are placed near the posterior extremity of the alimentary canal. Fig. 11 represents part of the preceding figure more highly magnified, showing the manner in which these tubes enter the chylific ventricle. In our rapid description of the digestive apparatus of insects, it only remains for us to mention certain purifying organs which secrete those fluids, generally blackish, caustic, or of peculiar smell, which some insects emit when they are irritated, and which cause a smarting when they get into one's eyes. Less well developed than the salivary organs, they are often of a very complicated structure. In Fig. 12 is represented the secretory apparatus of the Carabus auratus, which will serve for an example: A represents the secretory sacs aggregated together like a bunch of grapes, B the canal, C the pouch which receives the secretion, D the excretory duct. Sometimes the secretion is liquid, and has a foetid or ammoniacal odour; sometimes, as in the Bombardier beetle (Brachinus crepitans), it is gaseous, and is emitted, with an explosion, in the form of a whitish vapour, having a strong pungent odour analogous to that of nitric acid, and the same properties. It reddens litmus paper, and burns and reddens the skin, which after a time becomes brown, and continues so for a considerable time. About the middle of the seventeenth century Malpighi at Bologna, and Swammerdam at Utrecht, discovered a pulsatory organ occupying a median line of the back, which appeared to them to be a heart, in different insects. Nevertheless, Cuvier, having declared some time afterwards that there was no circula tion, properly so called, among insects, his opinion was universally adopted. But in 1827 a German naturalist named Carus discovered that there were real currents of blood circulating throughout the body, and returning to their point of departure. The observations of Carus were repeated and confirmed by many other naturalists, and we are thus enabled to form a sufficiently exact idea of the manner in which the blood circulates. The following summary of the phenomena of circulation among insects is borrowed from "LeÇons sur la Physiologie et l'Anatomie comparÉe," by M. Milne-Edwards:— The tube which passes under the skin of the back of the head, and front part of the body, above the alimentary canal, has been known for a long time as the dorsal vessel. It is composed of two very distinct portions: the anterior, which is tubular and not contractile; and the posterior, which is larger, of more complicated structure, and which contracts and dilates at regular intervals. This latter part constitutes, then, more particularly the heart of the insect. Generally it occupies the whole length of the abdomen, and is fixed to the vault of the tegumentary skeleton by membranous expansions, in such a manner as to leave a free space around it, but shut above and below, so as to form a reservoir into which the blood pours before penetrating to the heart. This reservoir is often called the auricle, for it seems to act as an instrument of impulsion, and to drive the blood into the ventricle or heart, properly so called. The heart is fusiform, and is divided by numerous constrictions into chambers. These chambers have exits placed in pairs, and membranous folds which divide the cavity in the manner of a portcullis. The lips of the orifices, instead of terminating in a clean edge, penetrate into the interior of the heart in the form of the mouth-piece of a flute. The double membranous folds thus formed on each side of the dorsal vessel are in the shape of a half moon, and separate from each other when this organ dilates; but the contrary movement taking place, the passage is closed. By the aid of this valvular apparatus, the blood can penetrate into the heart from the pericardic chamber, the empty space surrounding the heart, but cannot flow back from the heart into that reservoir. The anterior or aortic portion of the dorsal vessels shows neither fan-shaped lateral expansions, nor orifices, and consists of a single membranous tube. The whole of the blood set in motion by the contractions of the cardial portion of the dorsal vessel runs into the cavity of the head, and circulates afterwards in irregular channels formed by the empty spaces left between the different organs. It is the unoccupied portions of the great visceral cavity which serve as channels for the blood, and through them run the main currents to the lateral and lower parts of the body. These currents regain the back part of the abdomen, and enter the heart after having passed over the internal organs. These principal channels are in continuity with other gaps between the muscles, or between the bundles of fibres of which these muscles are composed. The principal currents send into the network thus formed, minor branches, which having ramified in their turn among the principal parts of the organism, re-enter some main current to regain the dorsal vessel. In the transparent parts of the body the blood may be seen circulating in this way to a number of inter-organic channels, penetrating the limbs and the wings, when these appendages are not horny, and, in short, diffusing itself everywhere. "If, by means of coloured injections," says M. Milne-Edwards, "one studies the connections which exist between the cavities in which sanguineous currents have been found to exist and the rest of the economy, it is easy to see that the irrigatory system thus formed penetrates to the full depth of every organ, and should cause the rapid renewal of the nourishing fluid in all the parts where the process of vitality renders the passage of this fluid necessary." We shall see presently, in speaking of respiration, that the relations between the nourishing fluid and the atmospheric air are more direct and regular than was for a long time supposed. In short, insects possess an active circulation, although we find neither arteries nor veins, and although the blood put in motion by the contractions of the heart, and carried to the head by the aortic portion of the dorsal vessel, can only distribute itself in the different parts of the system to return to the heart, by the gaps left between the different organs, or between the membranes and fibres of which these organs are composed. Fig. 13 (page 14), which shows both the circulating and breathing systems of an insect, enables us to recognise the different organs which we have described, as helping to keep up both respiration and circulation. The knowledge of the respiration of the insect is comparatively a modern scientific acquisition. Malpighi was the first to prove, in 1669, that insects are provided with organs of respiration, and that air is as indispensable to them as it is to other living beings. But the opinion of this celebrated naturalist has been contradicted, and his views were long contested. Now, however, one can easily recognise the apparatus by the aid of which the respiration of the insect is effected. Fig. 13.—Organs of circulation and breathing in an insect. A, abdominal portion of the dorsal vessel. B, aortic or thoracic portion. C, air-vessels of the head; D, of the abdomen. The respiratory apparatus is essentially composed of membranous ducts of great tenuity, their ramifications spread everywhere in incalculable numbers, and bury themselves in the different organs, much in the same way as the fibrous roots of plants bury themselves in the soil. These vessels are called tracheÆ. Their communications with the air are established externally in different ways, according to the character of the medium in which the insect lives. It is well known that a vast number of insects live in the air. The air penetrates into the tracheÆ by a number of orifices placed at the sides of the body, which are termed spiracles. On close examination these may be seen in the shape of button-holes in a number of different species. Let us dwell for a moment on the breathing apparatus of the insect, that is to say, on the tracheÆ. This apparatus is sometimes composed of elastic tubes only, sometimes of a collection of tubes and membranous pouches. We will first treat of the former. The coats of these breathing tubes are very elastic, and always preserve a cylindrical form, even when not distended. This state of things is maintained by the existence, throughout the whole length of the tracheÆ, of a thread of half horny consistency, rolled up in a spiral, and covered externally by a very delicate membranous sheath. The external membrane is thin, smooth, and generally colourless, or of a pearly white. The cartilaginous spiral is sometimes cylindrical and sometimes flat. It only adheres slightly to the external membrane, but is, on the other hand, closely united to the internal one. This spiral thread is only continuous in the same trunk; it breaks off when it branches, and each branch then possesses its own thread, in such a way that it is not joined to the thread of the trunk from which it issued, except by continuity, just as the branch of a tree is attached to the stem which supports it. This thread is prolonged, without interruption, to the extreme points of the finest ramifications. The number of tracheÆ in the body of an insect is very great. That patient anatomist, Lyonet, has proved this in his great work on the Goat-moth Caterpillar, Cossus ligniperda. Lyonet, who congratulated himself with having finished his long labours without having had to destroy more than eight or nine of the species he wished to describe, had the patience to count the different air-tubes in that caterpillar. He found that there were 256 longitudinal and 1,336 transverse branches; in short, that the body of this creature is traversed in all directions by 1,572 aeriferous tubes which are visible to the eye by the aid of a magnifying glass, without taking into account those which may be imperceptible. The complicated system of the breathing apparatus which we are describing is sometimes composed of an assemblage of tubes and membranous pouches, besides the elastic tubes which we have already mentioned. These pouches vary in size, and are very elastic, expanding when the air enters, and contracting when it leaves them, as they are altogether without the species of framework formed by the spiral thread of the tubular tracheÆ, of which they are only enlargements. Fig. 13 is explanatory of these organs of respiration. The respiratory mechanism of an insect is easily understood. "The abdominal cavity," says M. Milne-Edwards, "in which is placed the greater part of the respiratory apparatus, is susceptible of being contracted and dilated alternately by the play of the different segments of which the skeleton is composed, and which are placed in such a manner that they can be drawn into each other to a greater or less extent. When the insect contracts its body, the tracheÆ are compressed and the air driven out. But when, on the other hand, the visceral cavity assumes its normal size, or dilates, these channels become larger, and the air with which they are filled being rarefied by this expansion, is no longer in equilibrium with the outer air with which it is in communication through the medium of the spiracles. The exterior air is then impelled into the interior of the respiratory tubes, and the inspiration is effected." The respiratory movements can be accelerated or diminished, according to the wants of the animal; in general, there are from thirty to fifty to the minute. In a state of repose the spiracles are open, and all the tracheÆ are free to receive air whenever the visceral cavity is dilated, but those orifices may be closed, and the insect thus possesses the faculty of stopping all communication between the respiratory apparatus and the surrounding atmosphere. Some insects live in the water; they are therefore obliged to come to the surface to take the air they are in need of, or else to possess themselves of the small amount contained in the water. Both these methods of respiration exist under different forms in aquatic insects. To inhale atmospheric air, which is necessary for respiration, above the water, certain insects employ their elytra [2] as a sort of reservoir; others make use of their antennÆ, the hairs of which retain the globules of air. In this case it is brought under the thorax, whence a groove carries it to the spiracles. Sometimes the same result is obtained by a more complicated arrangement, consisting of respiratory tubes which can be thrust into the air, which it is their function to introduce into the organisation. Insects which breathe in the water without rising to the surface are provided with gills—organs which, though variable in form, generally consist of foliaceous or fringed expansions, in the midst of which the tracheÆ ramify in considerable numbers. These vessels are filled with air, but it does not disseminate itself in them directly, and it is only through the walls of these tubes that the contained gas is exchanged for the air held in suspension by the surrounding water. The oxygen contained in the water passes through certain very permeable membranes of the gill, and penetrates the tracheÆ, which discharge, in exchange, carbonic acid, which is the gaseous product of respiration. Fig. 14 represents the gills or breathing apparatus in an aquatic insect. We take as an example Ephemera. [3] It may be observed that the gills or foliaceous laminÆ are placed at the circumference of the body, and at its smallest parts. We have now seen that the respiratory apparatus is considerably developed in insects; it is, therefore, easy to foresee that those functions are most actively employed by them. In fact, if one compares the oxygen they imbibe with the heavy organic matter of which their body is composed, the amount is enormous. Before finishing this rapid examination of the body of an insect, we shall have to say a few words on the nervous system. This system is chiefly composed of a double series of ganglions, or collections of nerves, which are united together by longitudinal cords. The number of these ganglions corresponds with that of the segments. Sometimes they are at equal distances, and extend in a chain from one end of the body to the other; at others they are many of them close together, so as to form a single mass. The cephalic ganglions are two in number; they have been described by anatomists under the name of brain. "This expression," says M. Lacordaire, "would be apt to mislead the reader, as it would induce him to suppose the existence of a concentration of faculties to control the feelings and excite the movements, which is not the case." [4] The same naturalist observes, "All the ganglions of the ventral chain are endowed with nearly the same properties, and represent each other uniformly." The ganglion situated above the oesophagus gives rise to the optic nerves, which are the most considerable of all those of the body, and to the nerves of the antennÆ. The ganglion beneath the oesophagus provides the nerves of the mandibles, of the jaws, and of the lower lip. The three pairs of ganglions which follow those placed immediately below the oesophagus, belong to the three segments of the thorax, and give rise to the nerves of the feet and wings. They are in general more voluminous than the following pairs, which occupy the abdomen. Fig. 15 represents the nervous system of the Carabus auratus: A is the cephalic ganglion; B, the sub-oesophagian ganglion; C, the prothoracic ganglion; D and E are the ganglions of the mesothorax and metathorax. The remainder, F F, are the abdominal ganglions. Before finishing these preliminary observations, it is necessary to say that the preceding remarks only apply absolutely to insects arrived at the perfect state. It is important to make this remark, as insects, before arriving at that state, pass through various other stages. These stages are often so different from each other, that it would be difficult to imagine that they are only modifications of the same animal; one would suppose that they were as many different kinds of animals, if there was not abundant proof of the contrary. The successive stages through which an insect passes are four in number:—the egg; the larva; the pupa, nymph, or chrysalis; and the perfect insect, or imago. The egg state, which is common to them, as to all other articulate animals, it is unnecessary to explain. Nearly all insects lay eggs, though some few are viviparous. There often exists in the extremity of the abdomen of the female a peculiar organ, called the ovipositor, which is destined to make holes for the reception of the eggs. By a wonderful instinct the mother always lays her eggs in a place where her young, on being hatched, can find an abundance of nutritious substances. It will not be needless to observe that in most cases, these aliments are quite different to those which the mother seeks for herself. In the second stage, that is to say, on leaving the egg—the larva period—the insect presents itself in a soft state, without wings, and resembles a worm. In ordinary language, it is nearly always called a worm, or grub, and in certain cases, a caterpillar. LinnÆus was the first to use the term "larva"—taken from the Latin word larva, "a mask"—as he considered that, in this form, the insect was as it were masked. During this period of its life the insect eats voraciously, and often changes its skin. At a certain period it ceases to eat, retires to some hidden spot, and, after changing its skin for the last time, enters the third stage of its existence, and becomes a chrysalis. In this state it resembles a mummy enveloped in bandages, or a child in its swaddling clothes. It is generally incapable of either moving or nourishing itself. It continues so for days, weeks, months, and sometimes even for years. While the insect is thus apparently dead, a slow but certain change is going on in the interior of its body. A marvellous work, though not visible outside, is being effected, for the different organs of the insect are developing by degrees under the covering which surrounds them. When their formation is complete, the insect disengages itself from the narrow prison in which it was enclosed, and makes its appearance, provided with wings, and capable of propagating its kind; in short, of enjoying all the faculties which Nature has accorded to its species. It has thrown off the mask; the larva and pupa has disappeared, and given place to the perfect insect. To show the reader the four states through which the insect passes in succession, in Fig. 16 is represented the insect known as the Hydrophilus, [5] firstly, in the egg state; secondly, as the larva, or caterpillar; thirdly in the pupa; and fourthly as the perfect insect or imago. The different degrees of transformation and evolution which we have just described, are those which take place either completely or incompletely in all insects. Their metamorphoses are then at an end. There are certain insects, however, that show no difference in their various stages, except by absence of wings in the larva; and in these the chrysalis is only characterised by the growth of the wings, which, at first folded back and hidden under the skin, afterwards become free, but are not wholly developed till the last skin is cast. These insects are said to undergo incomplete metamorphoses, the former complete metamorphoses. Some never possess wings; indeed, there are others which undergo no metamorphosis, and are born possessed of all the organs with which it is necessary they should be provided. Some curious researches have been lately made on the strength of insects. M. Felix Plateau, of Brussels, has published some observations on this point, which we think of sufficient interest to reproduce here. In order to measure the muscular strength of man, or of animals—as the horse, for instance—many different dynamometric apparatuses have been invented, composed of springs, or systems of unequal levers. The Turks' heads which are seen at fairs, or in the Champs ÉlysÉes, at Paris, and on which the person who wishes to try his strength gives a strong blow with his fist, represent a dynamometer of this kind. The one which Buffon had constructed by RÉgnier the mechanician, and which is known by the name of RÉgnier's Dynamometer, is much more precise. It consists of an oval spring, of which the two ends approach each other; when they are pulled in opposite directions, a needle, which works on a dial marked with figures, indicates the force exercised on the spring. It has been proved, with this instrument, that the muscular effort of a man pulling with both hands is about 124 lbs., and that of a woman only 74 lbs. The ordinary effort of strength of a man in lifting a weight is 292 lbs.; and a horse, in pulling, shows a strength of 675 lbs.; a man, under the same circumstances, exhibiting a strength of 90 lbs. Physiologists have not as yet given their attention to the strength of invertebrate animals. It is, relatively speaking, immense. Many people have observed how out of proportion a jump of a flea is to its size. A flea is not more than an eighth of an inch in length, and it jumps a yard; in proportion, a lion ought to jump two-thirds of a mile. Pliny shows, in his "Natural History," that the weights carried by ants appear exceedingly great when they are compared with the size of these indefatigable labourers. The strength of these insects is still more striking, when one considers the edifices they are able to construct, and the devastations they occasion. The Termes, or White Ant,[6] constructs habitations many yards in height, which are so firmly and solidly built, that the buffaloes are able to mount them, and use them as observatories; they are made of particles of wood joined together by a gummy substance, and are able to resist even the force of a hurricane. There is another circumstance which is worth being noted. Man is proud of his works; but what are they, after all, in comparison with those of the ant, taking the relative heights into consideration? The largest pyramid in Egypt is only 146 yards high, that is, about ninety times the average height of man; whereas, the nests of the Termites are a thousand times the height of the insects which construct them. Their habitations are thus twelve times higher than the largest specimen of architecture raised by human hands. We are, therefore, far beneath these little insects, as far as strength and the spirit of working go. The destructive power of these creatures, so insignificant in appearance, are still more surprising. During the spring of a single year they can effect the ruin of a house by destroying the beams and planks. The town of La Rochelle, to which the Termites were imported by an American ship, is menaced with being eventually suspended on catacombs, like the town of Valencia in New Grenada. It is well known what destruction is caused when a swarm of locusts alight in a cultivated field; and it is certain that even their larvÆ do as severe injury as the perfect insect. All this sufficiently proves the destructive capabilities of these little animals, which we are accustomed to despise. M. Plateau has studied the power of traction in some insects, the power of pushing in the digging insects, and the lifting power of others during flight. He has thus been able to make some most interesting comparisons, of some of which we will relate the results. The average weight of man being 142 lbs., and his power of traction, according to RÉgnier, being 124 lbs., the proportion of the weight he can draw to the weight of his body is only as 87 to 100. With the horse the proportion is not more than 67 to 100, a horse 1,350 lbs. in weight only drawing about 900 lbs. The horse, therefore, can draw little more than half his own weight, and a man cannot draw the weight of his own body. This is a very poor result, if compared with the strength of the cockchafer. This insect, in fact, possesses a power of traction equal to more than fourteen times its own weight. If you amuse yourself with the children's game of making a cockchafer draw small cargoes of stones, you will be surprised at the great weight which this insignificant looking animal is able to manage. To test the power of traction in insects, M. Plateau attached them to a weight by means of a thread fastened to one of their feet. The Coleoptera (Beetles) are the best adapted for these experiments. The following are some of the results obtained by the Belgian physician:—Carabus auratus can draw seven times the weight of its body; Nebria brevicollis, twenty-five times; Necrophorus vespillo, fifteen times; Trichius fasciatus, forty-one times; and Oryctes nasicornis, four times only. The bee can draw twenty times the weight of its body; Donacia nymphÆ [7] forty-two times its own weight. From this it follows that if the horse possessed the same strength as this last insect, or if the insect were the size of a horse, they would either of them be able to draw 155,250 lbs. M. Plateau has ascertained the pushing power in insects, by introducing them into a pasteboard tube, the interior of which was made rough, and in which was fixed a glass plate, which allowed the light to penetrate into the prison. The animal, if excited, struggled with all its strength against the transparent plate, which, on being pushed forward, turned a lever adapted to a miniature dynamometer, which indicated the amount of effort exercised. The results thus obtained prove that the pushing power, like the power of traction, is greater in inverse proportion to the size and weight of the animal. A few figures will better explain this curious law. In Oryctes nasicornis the proportion of the pushing power to the weight of the insect is only three to two; in Geotrupes stercorarius it is sixteen to two; and in Onthophagus nuchicornis seventy-nine to six. Experiments have been made on the lifting power of insects by fastening a ball of soft wax to a thread attached to the hind legs. The proportion of the weight lifted has been found equal to that of the body. That is to say, that the insect, when flying, can lift its own weight. This is proved by the following calculations:—In the Neuroptera the proportion is 1 in the Dragon-fly (Libellula vulgata), ·7 in Lestes sponsa. In the order Hymenoptera it is ·78 in the bee, and ·63 in Bombus terrestris, the humble-bee. In the Diptera it is ·9 in Calliphora vomitoria, [8] 1·84 in the Syrphus corollÆ, and 1·77 in the house-fly. These results show that insects have only sufficient power to sustain their own weight when flying, as the above calculations exhibit the maximum of which they are capable, and at the utmost this strength would only compensate for the fatigue occasioned by the action of flight. At the same time it is to be observed that the Diptera, and among others the house-fly, can sustain their flight longer than the Hymenoptera and Neuroptera, although one would not think so from their appearance. In conclusion, if an insect's power of flying is not considerable, its power of traction and propulsion are immense, compared with the vertebrate animals; and, in the same group of insects, those that are the smallest and lightest are the strongest. The proportion between the muscular strength of insects and the dimensions of their bodies, would not appear to be on account of their muscles being more numerous than those of vertebrate animals, but on account of greater intrinsic energy and muscular activity. The articulations of insects may be considered as solid cases which envelop the muscles, and the thickness of these cases appears to decrease in a singular manner according to the size of the creature. The relative bulk of the muscles being less in the smaller species than in the larger, it is necessary to explain the superior relative strength of the former by supposing them to possess a greater amount of vital energy. These astonishing phenomena will perhaps be better understood if we consider the obstacles which insects have to overcome to satisfy their wants, to seek their food, to defend themselves against their enemies, &c. To meet these requirements they are marvellously constructed for both labour and warfare, and their strength is superior to that displayed by all other animals. It is also much greater than that of the machines we construct to replace manual labour. They represent strength itself. God's workmen are infinitely more powerful than those invented by the genius of man, which we call machines. We think it necessary, in closing this chapter, to give a sort of general outline of the great class of animals which we are about to study. If we wished to characterise insects by their exterior aspect, we might consider them as articulate animals, whose bodies, covered with tough and membranous integuments, are divided into three distinct parts: the head, provided with two antennÆ, and eyes and mouth of very variable form; a trunk or thorax, composed of three segments, which has underneath it always six articulated limbs, and often above it two or four wings; and an abdomen, composed of nine segments, although some may not appear to exist at first sight. If, in addition to these characteristics, one considers that these animals are not provided with interior skeletons—that their nervous system is formed of a double cord, swelling at intervals, and placed along the under-side of the body, with the exception of the first swellings or ganglions which are under the head—that they are not provided with a complete circulating system—that they breathe by particular organs, termed tracheÆ, extending parallel to each other along each side of the body, and communicating with the exterior air by lateral openings termed spiracles—that their sexes are distinct—that they are reproduced from eggs—and, in conclusion, that the different parts we have mentioned are not complete until the creature has passed through several successive changes, called metamorphoses, a general idea may be formed of what is meant in zoology by the word "insect." Insects, whose general organisation we have briefly traced, have been classed by naturalists as follows:— 1. Aptera (Fleas and Lice). We shall commence the history of the various orders by examining the Aptera. | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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