Insect morphology
Insect morphology is the study and description of the physical form of insects. The terminology used to describe insects is similar to that used for other arthropods due to their shared evolutionary history. Three physical features separate insects from other arthropods: they have a body divided into three regions , three pairs of legs, and mouthparts located outside of the head capsule. This position of the mouthparts divides them from their closest relatives, the non-insect hexapods, which include Protura, Diplura, and Collembola.
There is enormous variation in body structure amongst insect species. Individuals can range from 0.3 mm to 30 cm across ; have no eyes or many; well-developed wings or none; and legs modified for running, jumping, swimming, or even digging. These modifications allow insects to occupy almost every ecological niche except the deep ocean. This article describes the basic insect body and some variations of the different body parts; in the process, it defines many of the technical terms used to describe insect bodies.
Anatomy summary
Insects, like all arthropods, have no interior skeleton; instead, they have an exoskeleton, a hard outer layer made mostly of chitin that protects and supports the body. The insect body is divided into three parts: the head, thorax, and abdomen. The head is specialized for sensory input and food intake; the thorax, which is the anchor point for the legs and wings, is specialized for locomotion; and the abdomen is for digestion, respiration, excretion, and reproduction. Although the general function of the three body regions is the same across all insect species, there are major differences in basic structure, with wings, legs, antennae, and mouthparts being variable from group to group.External
Exoskeleton
The insect's outer skeleton, the cuticle, consists of two layers; the epicuticle, which is a thin, waxy, water-resistant outer layer that lacks chitin, and the layer under it is called the procuticle. This is chitinous and much thicker than the epicuticle and has two layers, the outer is the exocuticle while the inner is the endocuticle. The tough and flexible endocuticle is built from numerous layers of fibrous chitin and proteins, crisscrossing each other in a sandwich pattern, while the exocuticle is rigid and sclerotized. The exocuticle is greatly reduced in many soft-bodied insects, especially the larval stages. Chemically, chitin is a long-chain polymer of a N-acetylglucosamine, a derivative of glucose. In its unmodified form, chitin is translucent, pliable, and resilient. In arthropods, however, it is often modified, becoming embedded in a hardened proteinaceous matrix, which forms much of the exoskeleton. In its pure form, it is leathery, but when encrusted in calcium carbonate, it becomes much harder. The difference between the unmodified and modified forms is evident when comparing the body wall of a caterpillar to a beetle.From the embryonic stages, a layer of columnar or cuboidal epithelial cells gives rise to the external cuticle and an internal basement membrane. The majority of insect material is inside of the endocuticle. The cuticle provides muscular support and acts as a protective shield as the insect develops. However, since it cannot grow, the external sclerotized part of the cuticle is periodically shed in a process called "molting". As the time for molting approaches, most of the exocuticle material is reabsorbed. In molting, the old cuticle separates from the epidermis. Enzymatic molting fluid is then released between the old cuticle and epidermis, which separates the exocuticle by digesting the endocuticle and sequestering its material for the new cuticle. When the new cuticle has formed sufficiently, the epicuticle and reduced exocuticle are shed in ecdysis.
The four principal regions of an insect body segment are the tergum or dorsal, sternum or ventral, and the two pleura or laterals. Hardened plates in the exoskeleton are called sclerites, which are subdivisions of the major regions – tergites, sternites, and pleurites, for respective regions tergum, sternum, and pleuron.
Head
The head in most insects is enclosed in a hard, heavily sclerotized, exoskeletal head capsule. The main exception is in those species whose larvae are not fully sclerotized, mainly some holometabola; but even most unsclerotized or weakly sclerotized larvae tend to have well-sclerotized head capsules, for example, the larvae of Coleoptera and Hymenoptera. The larvae of Cyclorrhapha however, tend to have hardly any head capsule at all.The head capsule bears most of the sensory organs, including the antennae, ocelli, and compound eyes, along with the mouthparts. In the adult insect, the head capsule appears unsegmented, though embryological studies show it to consist of six segments that bear the paired head appendages, including the mouthparts, each pair on a specific segment. Each such pair occupies one segment, though not all segments in modern insects bear any visible appendages.
Of all the insect orders, Orthoptera displays the greatest variety of features found in the heads of insects, including the sutures and sclerites. Here, the vertex, or the apex, is situated between the compound eyes of insects with hypognathous and opisthognathous heads. In prognathous insects, the vertex is not found between the compound eyes, but rather where the ocelli are normally found. This is because the primary axis of the head is rotated 90° to become parallel to the primary axis of the body. In some species, this region is modified and assumes a different name.
The ecdysial suture is made of the coronal, frontal, and epicranial sutures plus the ecdysial and cleavage lines, which vary among different species of insects. The ecdysial suture is longitudinally placed on the vertex, separating the epicranial halves of the head to the left and right sides. Depending on the insect, the suture may come in different shapes: like either a Y, U or V. Those diverging lines that make up the ecdysial suture are called the frontal or frontogenal sutures. Not all species of insects have frontal sutures, but in those that do, the sutures split open during ecdysis, which provides an opening for the new instar to emerge from the integument.
The frons is that part of the head capsule that lies ventrad or anteriad of the vertex. The frons varies in size relative to the insect, and in many species, the definition of its borders is arbitrary, even in some insect taxa that have well-defined head capsules. In most species, though, the frons is bordered at its anterior by the frontoclypeal or epistomal sulcus above the clypeus. Laterally it is limited by the fronto-genal sulcus, if present, and the boundary with the vertex, by the ecdysial cleavage line, if it is visible. If there is a median ocellus, it generally is on the frons, though in some insects such as many Hymenoptera, all three ocelli appear on the vertex. A more formal definition is that it is the sclerite from which the pharyngeal dilator muscles arise, but in many contexts that too, is not helpful. In the anatomy of some taxa, such as many Cicadomorpha, the front of the head is fairly clearly distinguished and tends to be broad and sub-vertical; that median area commonly is taken to be the frons.
The clypeus is a sclerite between the face and labrum, which is dorsally separated from the frons by the frontoclypeal suture in primitive insects. The clypeogenal suture laterally demarcates the clypeus, with the clypeus ventrally separated from the labrum by the clypeolabral suture. The clypeus differs in shape and size, such as species of Lepidoptera with a large clypeus with elongated mouthparts. The cheek or gena forms the sclerotized area on each side of the head below the compound eyes extending to the gular suture. Like many parts making up the insect's head, the gena varies among species, with its boundaries difficult to establish. In dragonflies and damselflies, it is between the compound eyes, clypeus, and mouthparts. The postgena is the area immediately posteriad, or posterior or lower on the gena of pterygote insects, and forms the lateral and ventral parts of the occipital arch. The occipital arch is a narrow band forming the posterior edge of the head capsule arching dorsally over the foramen. The subgenal area is usually narrow, located above the mouthparts; this area also includes the hypostoma and pleurostoma. The vertex extends anteriorly above the bases of the antennae as a prominent, pointed, concave rostrum. The posterior wall of the head capsule is penetrated by a large aperture, the foramen. Through it passes the organ systems, such as the nerve cord, esophagus, salivary ducts, and musculature, connecting the head with the thorax.
On the posterior aspect of the head are the occiput, postgena, occipital foramen, posterior tentorial pit, gula, postgenal bridge, hypostomal suture and bridge, and the mandibles, labium, and maxilla. The occipital suture is well-founded in species of Orthoptera, but not so much in other orders. Where found, the occipital suture is the arched, horseshoe-shaped groove on the back of the head ending at the posterior of each mandible. The postoccipital suture is a landmark on the posterior surface of the head, and is typically near the occipital foremen. In pterygotes, the postocciput forms the extreme posterior, often U-shaped, which forms the rim of the head extending to the postoccipital suture. In pterygotes, such as those of Orthoptera, the occipital foramen and the mouth are not separated. The three types of occipital closures, or points under the occipital foramen that separate the two lower halves of the postgena, are the hypostomal bridge, the postgenal bridge, and the gula. The hypostomal bridge is usually found in insects with hypognathous orientation. The postgenal bridge is found in the adults of species of higher Diptera and aculeate Hymenoptera, while the gula is found on some Coleoptera, Neuroptera, and Isoptera, which typically display prognathous-oriented mouthparts.