coevolved with flowering plants. Insects typically move about by walking, flying or occasionally swimming. As it allows for rapid yet stable movement, many insects adopt a tripedal gait in which they walk with their legs touching the ground in alternating triangles. Insects are the only invertebrates to have evolved flight. Many insects spend at least part of their life underwater, with larval adaptations that include gills and some adult insects are aquatic and have adaptations for swimming. Some species, like water striders, are capable of walking on the surface of water. Insects are mostly solitary, but some insects, such as certain bees, ants, and termites are social and live in large, well-organized colonies. Some insects, like earwigs, show maternal care, guarding their eggs and young. Insects can communicate with each other in a variety of ways. Male moths can sense the pheromones of female moths over distances of many kilometers. Other species communicate with sounds: crickets stridulate, or rub their wings together, to attract a mate and repel other males. Lampyridae in the beetle order Coleoptera communicate with light. Humans regard certain insects as pests and attempt to control them using insecticides and a host of other techniques. Some insects damage crops by feeding on sap, leaves or fruits, a few bite humans and livestock, alive and dead, to feed on blood and some are capable of transmitting diseases to humans, pets and livestock. Nevertheless, without insects to pollinate flowering plants, a necessary process in their reproduction, the terrestrial portion of the biosphere (including humans) would be devastated as a great many organisms rely on flowering plants.Many other insects are considered ecologically beneficial as predators and a few provide direct economic benefit. Silkworms and bees have been used extensively by humans for the production of silk and honey, respectively.
Etymology
The word insect dates back to 1600, from the Latin word insectum meaning "with a notched or divided body," literally "cut into," from neuter plural of insectare "to cut into, to cut up," from in- "into" + secare "to cut"; from the fact that insects are "cut into" three sections. The word created by Pliny the Elder's loan-translation of the Greek word ἔντομος or "insect" (as in entomology), which was Aristotle's term for this class of life, also in reference to their "notched" bodies, first documented in English in 1601 in Holland's translation of Pliny. Translations of Aristotle's term also form the usual word for "insect" in Welsh (trychfil, from trychu "cut" + mil "animal"), Serbo-Croatian (zareznik, from rezati "cut"), Russian (насекомое nasekomoe, from sekat "cut"), etc.
Distribution and Diversity
Even though the true dimensions of species diversity remain uncertain, estimates are ranging from 1.4 to 1.8 million species. This probably represents less than 20% of all species on Earth, and with only about 20,000 new species of all organisms being described each year, it seems that most species will remain undescribed for many years unless there is a rapid increase in species descriptions. About 850,000–1,000,000 of all described species are insects. Of the 30 or so orders of insects, four dominate in terms of numbers of described species, with an estimated 600,000–795,000 species include Coleoptera, Diptera, Hymenoptera, and Lepidoptera. There are almost as many named species of beetle as there are of all other insects added together, or all other non-insects (plants and animals).
Morphology and Phisiology
Insect Morphology
A- Head B- Thorax C- Abdomen
1
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antenna
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17
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anus
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2
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ocelli (lower)
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18
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oviduct
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3
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ocelli (upper)
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19
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nerve chord (abdominal ganglia)
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4
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compound eye
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20
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Malpighian tubes
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5
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brain (cerebral ganglia)
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21
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tarsal pads
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6
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prothorax
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22
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claws
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7
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dorsal blood vessel
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23
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tarsus
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8
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tracheal tubes (trunk with spiracle)
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24
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tibia
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9
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mesothorax
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25
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femur
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10
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metathorax
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26
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trochanter
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11
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forewing
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27
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fore-gut (crop, gizzard)
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12
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hindwing
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28
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thoracic ganglion
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13
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mid-gut (stomach)
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29
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coxa
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14
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dorsal tube (Heart)
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30
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salivary gland
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15
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ovary
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31
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subesophageal ganglion
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16
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hind-gut (intestine, rectum & anus)
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32
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mouthparts
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External
Insects have segmented bodies supported by an exoskeleton, a hard outer covering made mostly of chitin. The segments of the body are organized into three distinctive but interconnected units, or tagmata: a head, a thorax, and an abdomen.The head supports a pair of sensory antennae, a pair of compound eyes, and, if present, one to three simple eyes (or ocelli) and three sets of variously modified appendages that form the mouthparts. The thorax has six segmented legs—one pair each for the prothorax, mesothorax and the metathorax segments making up the thorax—and, if present in the species, two or four wings. The abdomen consists of eleven segments, though in a few species of insects these segments may be fused together or reduced in size. The abdomen also contains most of the digestive, respiratory, excretory and reproductive internal structures.There is considerable variation and many adaptations in the body parts of insects especially wings, legs, antenna, mouth-parts etc.
Segmentation
The head: is enclosed in a hard, heavily sclerotized, unsegmented, exoskeletal head capsule, or epicranium, which contains most of the sensing organs, including the antennae, ocellus or eyes, and the mouthparts. Out of all the insect orders, Orthoptera displays the most features found in other insects, including the sutures and sclerites. here, the vertex, or the apex (dorsal region), is situated between the compound eyes for insects with a hypognathous and opisthognathous head. In prognathous insects, the vertex is not found between the compound eyes, but rather, where the ocelli are normally. This is because the primary axis of the head is rotated 90 degrees to become parallel to the primary axis of the body. In some species this region is modified and assumes a different name. The thorax: is a segment composed of three sections, the prothorax, mesothorax, and the metathorax. The anterior segment, closest to the head, is the prothorax, with the major features being the first pair of legs and the pronotum. The middle segment is the mesothorax with the major features being the second pair of legs and the anterior wings. The third and most posterior segment, abutting the abdomen, is the metathorax, which features the third pair of legs and the posterior wings. Each segment is dilineated by an intersegmental suture. Each segment has four basic regions. The dorsal surface is called the tergum (or notum) to distinguish them from the abdominal terga.The two lateral regions are called the pleura (singular: pleuron) and the ventral aspect is called the sternum. In turn, the notum of the prothorax is called the pronotum, the notum for the mesothorax is called the mesonotum and the notum for the metathorax is called the metanotum. Continuing with this logic, there is also the mesopleura and metapleura as well as the mesosternum and metasternum. The abdomen: is a the last segment of the insect, which typically consists of 11–12 segments and is less strongly sclerotized than the head or thorax. Each segment of the abdomen is represented by a sclerotized tergum, sternum, and perhaps a pleurite. Terga are separated from each other and from the adjacent sterna or pleura by a membrane. Spiracles are located in the pleural area. Variation of this ground plan includes the fusion of terga or terga and sterna to form continuous dorsal or ventral shields or a conical tube. Some insects bear a sclerite in the pleural area called a laterotergite. Ventral sclerites are sometimes called laterosternites. During the embryonic stage of many insects and the postembryonic stage of primitive insects, 11 abdominal segments are present. In modern insects there is a tendency toward reduction in the number of the abdominal segments, but the primitive number of 11 is maintained during embryogenesis.Variation in abdominal segment number is considerable. If the Apterygota are considered to be indicative of the ground plan for pterygotes, confusion reigns: adult Protura have 12 segments, Collembola have 6. The orthopteran family Acrididae has 11 segments, and a fossil specimen of Zoraptera has a 10-segmented abdomen.
Exoskeleton
The insect outer skeleton, the cuticle, is made up of two layers: the epicuticle, which is a thin and waxy water resistant outer layer and contains no chitin, and a lower layer called the procuticle. The procuticle is chitinous and much thicker than the epicuticle and has two layers: an outer layer known as the exocuticle and an inner layer known as the endocuticle. The tough and flexible endocuticle is built from numerous layers of fibrous chitin and proteins, criss-crossing each others in a sandwich pattern, while the exocuticle is rigid and hardened.The exocuticle is greatly reduced in many soft-bodied insects (e.g., caterpillars), especially during their larval stages. Insects are the only invertebrates to have developed active flight capability, and this has played an important role in their success. Their muscles are able to contract multiple times for each single nerve impulse, allowing the wings to beat faster than would ordinarily be possible. Having their muscles attached to their exoskeletons is more efficient and allows more muscle connections; crustaceans also use the same method, though all spiders use hydraulic pressure to extend their legs, a system inherited from their pre-arthropod ancestors. Unlike insects, though, most aquatic crustaceans are biomineralized with calcium carbonate extracted from the water.
Internal
Nervous System
The nervous system of an insect can be divided into a brain and a ventral nerve cord. The head capsule is made up of six fused segments, each with a pair of ganglia, or a cluster of nerve cells outside of the brain. The first three pairs of ganglia are fused into the brain, while the three following pairs are fused into a structure of three pairs of ganglia under the insect's esophagus, called the subesophageal ganglion.
The thoracic segments have one ganglion on each side, which are connected into a pair, one pair per segment. This arrangement is also seen in the abdomen but only in the first eight segments. Many species of insects have reduced numbers of ganglia due to fusion or reduction. Some cockroaches have just six ganglia in the abdomen, whereas the wasp Vespa crabro has only two in the thorax and three in the abdomen. Some insects, like the house fly Musca domestica, have all the body ganglia fused into a single large thoracic ganglion.
At least a few insects have nociceptors, cells that detect and transmit sensations of pain. This was discovered in 2003 by studying the variation in reactions of larvae of the common fruitfly Drosophila to the touch of a heated probe and an unheated one. The larvae reacted to the touch of the heated probe with a stereotypical rolling behavior that was not exhibited when the larvae were touched by the unheated probe. Although nociception has been demonstrated in insects, there is not a consensus that insects feel pain consciously but see Pain in invertebrates.
Digestive System
An insect uses its digestive system to extract nutrients and other substances from the food it consumes. Most of this food is ingested in the form of macromolecules and other complex substances like proteins, polysaccharides, fats, and nucleic acids. These macromolecules must be broken down by catabolic reactions into smaller molecules like amino acids and simple sugars before being used by cells of the body for energy, growth, or reproduction. This break-down process is known as digestion. The main structure of an insect's digestive system is a long enclosed tube called the alimentary canal, which runs lengthwise through the body. The alimentary canal directs food unidirectionally from the mouth to the anus. It has three sections, each of which performs a different process of digestion. In addition to the alimentary canal, insects also have paired salivary glands and salivary reservoirs. These structures usually reside in the thorax, adjacent to the foregut. The salivary glands in an insect's mouth produce saliva. The salivary ducts lead from the glands to the reservoirs and then forward through the head to an opening called the salivarium, located behind the hypopharynx. By moving its mouthparts the insect can mix its food with saliva. The mixture of saliva and food then travels through the salivary tubes into the mouth, where it begins to break down. Some insects, like flies, have extra-oral digestion. Insects using extra-oral digestion expel digestive enzymes onto their food to break it down. This strategy allows insects to extract a significant proportion of the available nutrients from the food source. The gut is where almost all of insects' digestion takes place. It can be divided into the foregut, midgut and hindgut.
Foregut
The first section of the alimentary canal is the foregut, or stomodaeum. The foregut is lined with a cuticular lining made of chitin and proteins as protection from tough food. The foregut includes the buccal cavity (mouth), pharynx, esophagus, and Crop and proventriculus (any part may be highly modified) which both store food and signify when to continue passing onward to the midgut.
Digestion starts in buccal cavity (mouth) as partially chewed food is broken down by saliva from the salivary glands. As the salivary glands produce fluid and carbohydrate-digesting enzymes (mostly amylases), strong muscles in the pharynx pump fluid into the buccal cavity, lubricating the food like the salivarium does, and helping blood feeders, and xylem and phloem feeders.
From there, the pharynx passes food to the esophagus, which could be just a simple tube passing it on to the crop and proventriculus, and then onward to the midgut, as in most insects. Alternately, the foregut may expand into a very enlarged crop and proventriculus, or the crop could just be a diverticulum, or fluid filled structure, as in some Diptera species.
Midgut
Once food leaves the crop, it passes to the midgut, also known as the mesenteron, where the majority of digestion takes place. Microscopic projections from the midgut wall, called microvilli, increase the surface area of the wall and allow more nutrients to be absorbed; they tend to be close to the origin of the midgut. In some insects, the role of the microvilli and where they are located may vary. For example, specialized microvilli producing digestive enzymes may more likely be near the end of the midgut, and absorption near the origin or beginning of the midgut.
Hindgut
In the hindgut, or proctodaeum, undigested food particles are joined by uric acid to form fecal pellets. The rectum absorbs 90% of the water in these fecal pellets, and the dry pellet is then eliminated through the anus, completing the process of digestion. The uric acid is formed using hemolymph waste products diffused from the Malpighian tubules. It is then emptied directly into the alimentary canal, at the junction between the midgut and hindgut. The number of Malpighian tubules possessed by a given insect varies between species, ranging from only two tubules in some insects to over 100 tubules in others.
Endocrine System
The salivary glands in an insect's mouth produce saliva. The salivary ducts lead from the glands to the reservoirs and then forward through the head to an opening called the salivarium, located behind the hypopharynx. By moving its mouthparts the insect can mix its food with saliva. The mixture of saliva and food then travels through the salivary tubes into the mouth, where it begins to break down. Some insects, like flies, have extra-oral digestion. Insects using extra-oral digestion expel digestive enzymes onto their food to break it down. This strategy allows insects to extract a significant proportion of the available nutrients from the food source.
Reproductive System
The reproductive system of female insects consist of a pair of ovaries, accessory glands, one or more spermathecae, and ducts connecting these parts. The ovaries are made up of a number of egg tubes, called ovarioles, which vary in size and number by species. The number of eggs that the insect is able to make vary by the number of ovarioles with the rate that eggs can be develop being also influenced by ovariole design. Female insects are able make eggs, receive and store sperm, manipulate sperm from different males, and lay eggs. Accessory glands or glandular parts of the oviducts produce a variety of substances for sperm maintenance, transport, and fertilization, as well as for protection of eggs. They can produce glue and protective substances for coating eggs or tough coverings for a batch of eggs called oothecae. Spermathecae are tubes or sacs in which sperm can be stored between the time of mating and the time an egg is fertilized.
For males, the reproductive system is the testis, suspended in the body cavity by tracheae and the fat body. Most male insects have a pair of testes, inside of which are sperm tubes or follicles that are enclosed within a membranous sac. The follicles connect to the vas deferens by the vas efferens, and the two tubular vasa deferentia connect to a median ejaculatory duct that leads to the outside. A portion of the vas deferens is often enlarged to form the seminal vesicle, which stores the sperm before they are discharged into the female. The seminal vesicles have glandular linings that secrete nutrients for nourishment and maintenance of the sperm. The ejaculatory duct is derived from an invagination of the epidermal cells during development and, as a result, has a cuticular lining. The terminal portion of the ejaculatory duct may be sclerotized to form the intromittent organ, the aedeagus. The remainder of the male reproductive system is derived from embryonic mesoderm, except for the germ cells, or spermatogonia, which descend from the primordial pole cells very early during embryogenesis.
Respirotary and Circulatory System
Insect respiration is accomplished without lungs. Instead, the insect respiratory system uses a system of internal tubes and sacs through which gases either diffuse or are actively pumped, delivering oxygen directly to tissues that need it via their trachea. Since oxygen is delivered directly, the circulatory system is not used to carry oxygen, and is therefore greatly reduced. The insect circulatory system has no veins or arteries, and instead consists of little more than a single, perforated dorsal tube which pulses peristaltically. Toward the thorax, the dorsal tube divides into chambers and acts like the insect's heart. The opposite end of the dorsal tube is like the aorta of the insect circulating the hemolymph, arthropods' fluid analog of blood, inside the body cavity. Air is taken in through openings on the sides of the abdomen called spiracles.There are many different patterns of gas exchange demonstrated by different groups of insects. Gas exchange patterns in insects can range from continuous and diffusive ventilation, to discontinuous gas exchange. During continuous gas exchange, oxygen is taken in and carbon dioxide is released in a continuous cycle. In discontinuous gas exchange, however, the insect takes in oxygen while it is active and small amounts of carbon dioxide are released when the insect is at rest. Diffusive ventilation is simply a form of continuous gas exchange that occurs by diffusion rather than physically taking in the oxygen. Some species of insect that are submerged also have adaptations to aid in respiration. As larvae, many insects have gills that can extract oxygen dissolved in water, while others need to rise to the water surface to replenish air supplies which may be held or trapped in special structures.
Reproduction and Development
The majority of insects hatch from eggs, but not all insects lay eggs. The fertilization and development takes place inside the egg, enclosed by a shell (chorion). Some species of insects, like the cockroach Blaptica dubia, as well as juvenile aphids and tsetse flies, are ovoviviparous. The eggs of ovoviviparous animals develop entirely inside the female, and then hatch immediately upon being laid. Some other species, such as those in the genus of cockroaches known as Diploptera, are viviparous, and thus gestate inside the mother and are born alive. Some insects, like parasitic wasps, show polyembryony, where a single fertilized egg divides into many and in some cases thousands of separate embryos.
Other developmental and reproductive variations include haplodiploidy, polymorphism, paedomorphosis or peramorphosis, sexual dimorphism, parthenogenesis and more rarely hermaphroditism. In haplodiploidy, which is a type of sex-determination system, the offspring's sex is determined by the number of sets of chromosomes an individual receives. This system is typical in bees and wasps. Polymorphism is the where a species may have different morphs or forms, as in the oblong winged katydid, which has four different varieties: green, pink, and yellow or tan. Some insects may retain phenotypes that are normally only seen in juveniles; this is called paedomorphosis. In peramorphosis, an opposite sort of phenomenon, insects take on previously unseen traits after they have matured into adults. Many insects display sexual dimorphism, in which males and females have notably different appearances, such as the moth Orgyia recens as an exemplar of sexual dimorphism in insects. Some insects use parthenogenesis, a process in which the female can reproduce and give birth without having the eggs fertilized by a male. Many aphids undergo a form of parthenogenesis, called cyclical parthenogenesis, in which they alternate between one or many generations of asexual and sexual reproduction. In summer, aphids are generally female and parthenogenetic; in the autumn, males may be produced for sexual reproduction. Other insects produced by parthenogenesis are bees, wasps, and ants, in which they spawn males. However, overall, most individuals are female, which are produced by fertilization. The males are haploid and the females are diploid. More rarely, some insects display hermaphroditism, in which a given individual has both male and female reproductive organs. Insect life-histories show adaptations to withstand cold and dry conditions. Some temperate region insects are capable of activity during winter, while some others migrate to a warmer climate or go into a state of torpor. Still other insects have evolved mechanisms of diapause that allow eggs or pupae to survive these conditions.
Metamorphosis
Metamorphosis in insects is the biological process of development all insects must undergo. There are two forms of metamorphosis: incomplete metamorphosis and complete metamorphosis
Incomplete Metamorphosis
Insects that show hemimetabolism, or incomplete metamorphosis, change gradually by undergoing a series of molts. An insect molts when it outgrows its exoskeleton, which does not stretch and would otherwise restrict the insect's growth. The molting process begins as the insect's epidermis secretes a new epicuticle. After this new epicuticle is secreted, the epidermis releases a mixture of enzymes that digests the endocuticle and thus detaches the old cuticle. When this stage is complete, the insect makes its body swell by taking in a large quantity of water or air, which makes the old cuticle split along predefined weaknesses where the old exocuticle was thinnest. Other arthropods have a much different process and only molt; though must accommodate for the difference in exoskeleton structure and make up with other enzymes.
Immature insects that go through incomplete metamorphosis are called nymphs or in the case of dragonflies and damselflies as naiads. Nymphs are similar in form to the adult except for the presence of wings, which are not developed until adulthood. With each molt, nymphs grow larger and become more similar in appearance to adult insects.
Complete Metamorphosis
Holometabolism, or complete metamorphosis, is where the insect changes all in four stages, an egg or embryo, a larva, a pupa, and the adult or imago. In these species, egg hatches to produce a larva, which is generally worm-like in form. This worm-like form can be one of several varieties: eruciform (caterpillar-like), scarabaeiform (grub-like), campodeiform (elongated, flattened, and active), elateriform (wireworm-like) or vermiform (maggot-like). The larva grows and eventually becomes a pupa, a stage marked by reduced movement and often sealed within a cocoon. There are three types of pupae: obtect, exarate or coarctate. Obtect pupae are compact, with the legs and other appendages enclosed. Exarate pupae have their legs and other appendages free and extended. Coarctate pupae develop inside the larval skin. Insects undergo considerable change in form during the pupal stage, and emerge as adults. Butterflies are a well known example of an insects that undergo complete metamorphosis, although most insects use this life cycle. Some insects have evolved this system to hypermetamorphosis. Some of the oldest and most successful insect groups, such Endopterygota, use a system of complete metamorphosis. Complete metamorphosis is unique to a group of certain insect orders including Diptera, Lepidoptera, and Hymenoptera. This form of development is exclusive and not seen in any other arthropods.
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