Insect

Although traditionally grouped with millipedes and centipedes,[22] more recent analysis indicates closer evolutionary ties with crustaceans. In the Pancrustacea theory, insects, together with Entognatha, Remipedia, and Cephalocarida, form a clade, the Pancrustacea.[23] Insects form a single clade, closely related to crustaceans and myriapods.[24]

Other terrestrial arthropods, such as centipedes, millipedes, scorpions, spiders, woodlice, mites, and ticks are sometimes confused with insects since their body plans can appear similar, sharing (as do all arthropods) a jointed exoskeleton. However, upon closer examination, their features differ significantly; most noticeably, they do not have the six-legged characteristic of adult insects.[25]

A phylogenetic tree of the arthropods places the insects in the context of other hexapods and the crustaceans, and the more distantly-related myriapods and chelicerates.[26]

Evolution has produced enormous variety in insects. Pictured are some possible shapes of antennae.

The internal phylogeny is based on the works of Sroka, Staniczek & Bechly 2014,[27] Prokop et al. 2017[28] and Wipfler et al. 2019.[29]

Traditional morphology-based or appearance-based systematics have usually given the Hexapoda the rank of superclass,[30]^: 180 and identified four groups within it: insects (Ectognatha), springtails (Collembola), Protura, and Diplura, the latter three being grouped together as the Entognatha on the basis of internalized mouth parts. Supraordinal relationships have undergone numerous changes with the advent of methods based on evolutionary history and genetic data. A recent theory is that the Hexapoda are polyphyletic (where the last common ancestor was not a member of the group), with the entognath classes having separate evolutionary histories from the Insecta.[31] Many of the traditional appearance-based taxa are paraphyletic, so rather than using ranks like subclass, superorder, and infraorder, it has proved better to use monophyletic groupings (in which the last common ancestor is a member of the group). The following represents the best-supported monophyletic groupings for the Insecta.

Insects can be divided into two groups historically treated as subclasses: wingless insects, known as Apterygota, and winged insects, known as Pterygota. The Apterygota consisted of the primitively wingless orders Archaeognatha (jumping bristletails) and Zygentoma (silverfish). However, Apterygota is not a monophyletic group, as Archaeognatha are the sister group to all other insects, based on the arrangement of their mandibles, while Zygentoma and Pterygota are grouped together as Dicondylia. It was originally believed that Archaeognatha possessed a single phylogenetically primitive condyle each (thus the name "Monocondylia"), where all more derived insects have two, but this has since been shown to be incorrect; all insects, including Archaeognatha, have dicondylic mandibles, but archaeognaths possess two articulations that are homologous to those in other insects, though slightly different.[32] The Zygentoma themselves possibly are not monophyletic, with the family Lepidotrichidae being a sister group to the Dicondylia (Pterygota and the remaining Zygentoma).[33][34]

Paleoptera and Neoptera are the winged orders of insects differentiated by the presence of hardened body parts called sclerites, and in the Neoptera, muscles that allow their wings to fold flatly over the abdomen. Neoptera can further be divided into incomplete metamorphosis-based (Polyneoptera and Paraneoptera) and complete metamorphosis-based groups. It has proved difficult to clarify the relationships between the orders in Polyneoptera because of constant new findings calling for revision of the taxa. For example, the Paraneoptera have turned out to be more closely related to the Endopterygota than to the rest of the Exopterygota. The recent molecular finding that the traditional louse orders Mallophaga and Anoplura are derived from within Psocoptera has led to the new taxon Psocodea.[35] Phasmatodea and Embiidina have been suggested to form the Eukinolabia.[36] Mantodea, Blattodea, and Isoptera are thought to form a monophyletic group termed Dictyoptera.[37]

The Exopterygota likely are paraphyletic in regard to the Endopterygota. The Neuropterida are often lumped or split on the whims of the taxonomist. Fleas are now thought to be closely related to boreid mecopterans.[38] Many questions remain in the basal relationships among endopterygote orders, particularly the Hymenoptera.

Insects are prey for a variety of organisms, including terrestrial vertebrates. The earliest vertebrates on land existed 400 million years ago and were large amphibious piscivores. Through gradual evolutionary change, insectivory was the next diet type to evolve.[39]

Insects were among the earliest terrestrial herbivores and acted as major selection agents on plants.[40] Plants evolved chemical defenses against this herbivory and the insects, in turn, evolved mechanisms to deal with plant toxins. Many insects make use of these toxins to protect themselves from their predators. Such insects often advertise their toxicity using warning colors.[41] This successful evolutionary pattern has also been used by mimics. Over time, this has led to complex groups of coevolved species. Conversely, some interactions between plants and insects, like pollination, are beneficial to both organisms. Coevolution has led to the development of very specific mutualisms in such systems.

The oldest possible insect is Leverhulmia known from the Early Devonian aged Windyfield chert, which may represent a primitive wingless insect.[42] The oldest known flying insects appeared during the mid-Carboniferous, around 328–324 million years ago, and the group subsequently underwent a rapid explosive diversification. Claims that they originated substantially earlier during the Silurian or Devonian based on molecular clock estimates are unlikely based on the fossil record, and are likely analytical artefacts.[43]

Four large-scale radiations of insects have occurred: beetles (from about 300 million years ago), flies (from about 250 million years ago), moths and wasps (both from about 150 million years ago).[44] These four groups account for the majority of described species.

The remarkably successful Hymenoptera (wasps, bees, and ants) appeared as long as 200 million years ago in the Triassic period, but achieved their wide diversity more recently in the Cenozoic era, which began 66 million years ago. Some highly successful insect groups evolved in conjunction with flowering plants, a powerful illustration of coevolution.[40]

Insect morphology
A- Head B- Thorax C- Abdomen

1. antenna
2. ocellus (lower)
3. ocellus (upper)
4. compound eye
5. brain (cerebral ganglia)
6. prothorax
7. dorsal blood vessel
8. tracheal tubes (trunk with spiracle)
9. mesothorax
10. metathorax
11. forewing
12. hindwing
13. midgut (stomach)
14. dorsal tube (Heart)
15. ovary
16. hindgut (intestine, rectum, anus)
17. anus
18. oviduct
19. nerve cord (abdominal ganglia)
20. Malpighian tubules
21. tarsal pads
22. claws
23. tarsus
24. tibia
25. femur
26. trochanter
27. foregut (crop, gizzard)
28. thoracic ganglion
29. coxa
30. salivary gland
31. subesophageal ganglion
32. mouthparts

Insects have segmented bodies supported by exoskeletons, the 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.[60] The head supports a pair of sensory antennae, a pair of compound eyes, zero to three simple eyes (or ocelli) and three sets of variously modified appendages that form the mouthparts. The thorax is made up of three segments: the prothorax, mesothorax and the metathorax. Each thoracic segment supports one pair of legs. The meso- and metathoracic segments may each have a pair of wings, depending on the insect. 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.[30]^: 22–48 Considerable variation and many adaptations in the body parts of insects occur, especially wings, legs, antenna and mouthparts.

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. Of all the insect orders, Orthoptera displays the most features found in other insects, including the sutures and sclerites.[61] 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° to become parallel to the primary axis of the body. In some species, this region is modified and assumes a different name.[61]^: 13

The thorax is a tagma 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 delineated by an intersegmental suture. Each segment has four basic regions. The dorsal surface is called the tergum (or notum) to distinguish it from the abdominal terga.[30] 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, the mesopleura and metapleura, as well as the mesosternum and metasternum, are used.[61]

The abdomen is the largest tagma 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 and sternum. Terga are separated from each other and from the adjacent sterna or pleura by membranes. 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.[61]

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 other in a sandwich pattern, while the exocuticle is rigid and hardened.[30]^: 22–24 The exocuticle is greatly reduced in many insects during their larval stages, e.g., caterpillars. It is also reduced in soft-bodied adult insects.

During growth insects goes through a various number of instars where the old exoskeleton is shed, but once they reach sexual maturity, they stop molting. The exceptions are apterygote (ancestrally wingless) insects. Mayflies are the only insects with a sexually immature instar with functional wings, called subimago.[62]

As an adaptation to life on land, insects have evolved a gene that creates an enzyme called multicopper oxidase-2 (MCO2), which uses atmospheric oxygen to harden their cuticle, unlike crustaceans which use calcium for the same purpose. This makes their exoskeleton into a lightweight material. The gene is insect specific and not found in any other groups of arthropods, including hexapods like springtails and diplurans.[63]

Insects are the only invertebrates to have developed active flight capability, and this has played an important role in their success.[30]^: 186 Their flight 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 efficient and allows more muscle connections.

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 either 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.[30]^: 57

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.[64] 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.[65]

At least some insects have nociceptors, cells that detect and transmit signals responsible for the sensation of pain.[66][67] This was discovered in 2003 by studying the variation in reactions of larvae of the common fruit-fly 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.[68] Although nociception has been demonstrated in insects, there is no consensus that insects feel pain consciously[69]

Insects are capable of learning.[70]

An insect uses its digestive system to extract nutrients and other substances from the food it consumes.[71] 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.

There is extensive variation among different orders, life stages, and even castes in the digestive system of insects.[72] This is the result of extreme adaptations to various lifestyles. The present description focuses on a generalized composition of the digestive system of an adult orthopteroid insect, which is considered basal to interpreting particularities of other groups.

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.[30]^: 70–77 The salivary glands (element 30 in numbered diagram) 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 (element 32 in numbered diagram) 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.[73][74] 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.[75]^: 31 The gut is where almost all of insects' digestion takes place. It can be divided into the foregut, midgut and hindgut.

Stylized diagram of insect digestive tract showing malpighian tubule, from an insect of the order Orthoptera

The first section of the alimentary canal is the foregut (element 27 in numbered diagram), 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.[30]^: 70

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.[75]^: 30–31

Once food leaves the crop, it passes to the midgut (element 13 in numbered diagram), 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.[75]^: 32

In the hindgut (element 16 in numbered diagram), 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 (element 17), completing the process of digestion. Envaginations at the anterior end of the hindgut form the Malpighian tubules, which form the main excretory system of insects.

Insects may have one to hundreds of Malpighian tubules (element 20). These tubules remove nitrogenous wastes from the hemolymph of the insect and regulate osmotic balance. Wastes and solutes are emptied directly into the alimentary canal, at the junction between the midgut and hindgut.[30]^{: 71–72, 78–80}

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 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.[61]^: 880

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.[61]^: 885

The tube-like heart (green) of the mosquito Anopheles gambiae extends horizontally across the body, interlinked with the diamond-shaped wing muscles (also green) and surrounded by pericardial cells (red). Blue depicts cell nuclei.

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 (element 8 in numbered diagram). In most insects, air is taken in through openings on the sides of the abdomen and thorax called spiracles.

The respiratory system is an important factor that limits the size of insects. As insects get larger, this type of oxygen transport is less efficient and thus the heaviest insect currently weighs less than 100 g. However, with increased atmospheric oxygen levels, as were present in the late Paleozoic, larger insects were possible, such as dragonflies with wingspans of more than two feet (60 cm).[76]

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.[30]^: 65–68 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.[77] 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.[78][79]

Because oxygen is delivered directly to tissues via tracheoles, the circulatory system is not used to carry oxygen, and is therefore greatly reduced. The insect circulatory system is open; it has no veins or arteries, and instead consists of little more than a single, perforated dorsal tube that pulses peristaltically. This dorsal blood vessel (element 14) is divided into two sections: the heart and aorta. The dorsal blood vessel circulates the hemolymph, arthropods' fluid analog of blood, from the rear of the body cavity forward.[30]^: 61–65[80] Hemolymph is composed of plasma in which hemocytes are suspended. Nutrients, hormones, wastes, and other substances are transported throughout the insect body in the hemolymph. Hemocytes include many types of cells that are important for immune responses, wound healing, and other functions. Hemolymph pressure may be increased by muscle contractions or by swallowing air into the digestive system to aid in molting.[81] Hemolymph is also a major part of the open circulatory system of other arthropods, such as spiders and crustaceans.[82][83]

Metamorphosis in insects is the biological process of development all insects must undergo. There are two forms of metamorphosis: incomplete metamorphosis and complete metamorphosis.

Hemimetabolous insects, those with 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 inside the old one. 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.[30]^: 142[92]

Immature insects that go through incomplete metamorphosis are called nymphs or in the case of dragonflies and damselflies, also 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.

This southern hawker dragonfly molts its exoskeleton several times during its life as a nymph; shown is the final molt to become a winged adult (eclosion).

Gulf fritillary life cycle, an example of holometabolism.

Holometabolism, or complete metamorphosis, is where the insect changes in four stages, an egg or embryo, a larva, a pupa and the adult or imago. In these species, an 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.[30]^: 151 Insects undergo considerable change in form during the pupal stage, and emerge as adults. Butterflies are a well-known example of insects that undergo complete metamorphosis, although most insects use this life cycle. Some insects have evolved this system to hypermetamorphosis.

Complete metamorphosis is a trait of the most diverse insect group, the Endopterygota.[30]^: 143 Endopterygota includes 11 Orders, the largest being Diptera (flies), Lepidoptera (butterflies and moths), and Hymenoptera (bees, wasps, and ants), and Coleoptera (beetles). This form of development is exclusive to insects and not seen in any other arthropods.

Most insects have compound eyes and two antennae.

A few insects, such as members of the families Poduridae and Onychiuridae (Collembola), Mycetophilidae (Diptera) and the beetle families Lampyridae, Phengodidae, Elateridae and Staphylinidae are bioluminescent. The most familiar group are the fireflies, beetles of the family Lampyridae. Some species are able to control this light generation to produce flashes. The function varies with some species using them to attract mates, while others use them to lure prey. Cave dwelling larvae of Arachnocampa (Mycetophilidae, fungus gnats) glow to lure small flying insects into sticky strands of silk.[97] Some fireflies of the genus Photuris mimic the flashing of female Photinus species to attract males of that species, which are then captured and devoured.[98] The colors of emitted light vary from dull blue (Orfelia fultoni, Mycetophilidae) to the familiar greens and the rare reds (Phrixothrix tiemanni, Phengodidae).[99]

Most insects, except some species of cave crickets, are able to perceive light and dark. Many species have acute vision capable of detecting minute movements. The eyes may include simple eyes or ocelli as well as compound eyes of varying sizes. Many species are able to detect light in the infrared, ultraviolet and visible light wavelengths. Color vision has been demonstrated in many species and phylogenetic analysis suggests that UV-green-blue trichromacy existed from at least the Devonian period between 416 and 359 million years ago.[100]

The individual lenses in compound eyes are immobile, and it was therefore presumed that insects were not able to focus. But research on fruit flies, which is the only insects studied so far, has shown that photoreceptor cells underneath each lens move rapidly in and out of focus in a series of movements called photoreceptor microsaccades. This gives them a much clearer image of the world than previously assumed.[101]

Insects were the earliest organisms to produce and sense sounds. Hearing has evolved independently at least 19 times in different insect groups.[102] Insects make sounds mostly by mechanical action of appendages. In grasshoppers and crickets, this is achieved by stridulation. Cicadas make the loudest sounds among the insects by producing and amplifying sounds with special modifications to their body to form tymbals and associated musculature. The African cicada Brevisana brevis has been measured at 106.7 decibels at a distance of 50 cm (20 in).[103] Some insects, such as the Helicoverpa zea moths, hawk moths and Hedylid butterflies, can hear ultrasound and take evasive action when they sense that they have been detected by bats.[104][105] Some moths produce ultrasonic clicks that were once thought to have a role in jamming bat echolocation. The ultrasonic clicks were subsequently found to be produced mostly by unpalatable moths to warn bats, just as warning colorations are used against predators that hunt by sight.[106] Some otherwise palatable moths have evolved to mimic these calls.[107] More recently, the claim that some moths can jam bat sonar has been revisited. Ultrasonic recording and high-speed infrared videography of bat-moth interactions suggest the palatable tiger moth really does defend against attacking big brown bats using ultrasonic clicks that jam bat sonar.[108]

Very low sounds are also produced in various species of Coleoptera, Hymenoptera, Lepidoptera, Mantodea and Neuroptera. These low sounds are simply the sounds made by the insect's movement. Through microscopic stridulatory structures located on the insect's muscles and joints, the normal sounds of the insect moving are amplified and can be used to warn or communicate with other insects. Most sound-making insects also have tympanal organs that can perceive airborne sounds. Some species in Hemiptera, such as the corixids (water boatmen), are known to communicate via underwater sounds.[109] Most insects are also able to sense vibrations transmitted through surfaces.

Communication using surface-borne vibrational signals is more widespread among insects because of size constraints in producing air-borne sounds.[110] Insects cannot effectively produce low-frequency sounds, and high-frequency sounds tend to disperse more in a dense environment (such as foliage), so insects living in such environments communicate primarily using substrate-borne vibrations.[111] The mechanisms of production of vibrational signals are just as diverse as those for producing sound in insects.

Some species use vibrations for communicating within members of the same species, such as to attract mates as in the songs of the shield bug Nezara viridula.[112] Vibrations can also be used to communicate between entirely different species; lycaenid (gossamer-winged butterfly) caterpillars, which are myrmecophilous (living in a mutualistic association with ants) communicate with ants in this way.[113] The Madagascar hissing cockroach has the ability to press air through its spiracles to make a hissing noise as a sign of aggression;[114] the death's-head hawkmoth makes a squeaking noise by forcing air out of their pharynx when agitated, which may also reduce aggressive worker honey bee behavior when the two are close.[115]

Chemical communications in animals rely on a variety of aspects including taste and smell. Chemoreception is the physiological response of a sense organ (i.e. taste or smell) to a chemical stimulus where the chemicals act as signals to regulate the state or activity of a cell. A semiochemical is a message-carrying chemical that is meant to attract, repel, and convey information. Types of semiochemicals include pheromones and kairomones. One example is the butterfly Phengaris arion which uses chemical signals as a form of mimicry to aid in predation.[116]

In addition to the use of sound for communication, a wide range of insects have evolved chemical means for communication. These semiochemicals are often derived from plant metabolites including those meant to attract, repel and provide other kinds of information. Pheromones, a type of semiochemical, are used for attracting mates of the opposite sex, for aggregating conspecific individuals of both sexes, for deterring other individuals from approaching, to mark a trail, and to trigger aggression in nearby individuals. Allomones benefit their producer by the effect they have upon the receiver. Kairomones benefit their receiver instead of their producer. Synomones benefit the producer and the receiver. While some chemicals are targeted at individuals of the same species, others are used for communication across species. The use of scents is especially well-developed in social insects.[30]^: 96–105 Cuticular hydrocarbons are nonstructural materials produced and secreted to the cuticle surface to fight desiccation and pathogens. They are important, too, as pheromones, especially in social insects.[117]

The eusocial insects build nests, guard eggs, and provide food for offspring full-time. Most insects, however, lead short lives as adults, and rarely interact with one another except to mate or compete for mates. A small number exhibit some form of parental care, where they will at least guard their eggs, and sometimes continue guarding their offspring until adulthood, and possibly even feeding them. Another simple form of parental care is to construct a nest (a burrow or an actual construction, either of which may be simple or complex), store provisions in it, and lay an egg upon those provisions. The adult does not contact the growing offspring, but it nonetheless does provide food. This sort of care is typical for most species of bees and various types of wasps.[121]

Basic motion of the insect wing in insect with an indirect flight mechanism scheme of dorsoventral cut through a thorax segment with a wings, b joints, c dorsoventral muscles, d longitudinal muscles.

Insects are the only group of invertebrates to have developed flight. The evolution of insect wings has been a subject of debate. Some entomologists suggest that the wings are from paranotal lobes, or extensions from the insect's exoskeleton called the nota, called the paranotal theory. Other theories are based on a pleural origin. Another theory suggest the wings are actually made up of both the notum and the pleuron.[122] These theories include suggestions that wings originated from modified gills, spiracular flaps or as from an appendage of the epicoxa. The epicoxal theory suggests the insect wings are modified epicoxal exites, a modified appendage at the base of the legs or coxa.[123] In the Carboniferous age, some of the Meganeura dragonflies had as much as a 50 cm (20 in) wide wingspan. The appearance of gigantic insects has been found to be consistent with high atmospheric oxygen. The respiratory system of insects constrains their size, however the high oxygen in the atmosphere allowed larger sizes.[124] The largest flying insects today are much smaller, with the largest wingspan belonging to the white witch moth (Thysania agrippina), at approximately 28 cm (11 in).[125]

Insect flight has been a topic of great interest in aerodynamics due partly to the inability of steady-state theories to explain the lift generated by the tiny wings of insects. But insect wings are in motion, with flapping and vibrations, resulting in churning and eddies, and the misconception that physics says "bumblebees can't fly" persisted throughout most of the twentieth century.

Unlike birds, many small insects are swept along by the prevailing winds[126] although many of the larger insects are known to make migrations. Aphids are known to be transported long distances by low-level jet streams.[127] As such, fine line patterns associated with converging winds within weather radar imagery, like the WSR-88D radar network, often represent large groups of insects.[128] Radar can also be deliberately used to monitor insects.[129]

Many adult insects use six legs for walking, with an alternating tripod gait. This allows for rapid walking while always having a stable stance; it has been studied extensively in cockroaches and ants. For the first step, the middle right leg and the front and rear left legs are in contact with the ground and move the insect forward, while the front and rear right leg and the middle left leg are lifted and moved forward to a new position. When they touch the ground to form a new stable triangle the other legs can be lifted and brought forward in turn and so on.[130] The purest form of the tripedal gait is seen in insects moving at high speeds. However, this type of locomotion is not rigid and insects can adapt a variety of gaits. For example, when moving slowly, turning, avoiding obstacles, climbing or slippery surfaces, four (tetrapod) or more feet (wave-gait[131]) may be touching the ground. Insects can also adapt their gait to cope with the loss of one or more limbs.

Cockroaches are among the fastest insect runners and, at full speed, adopt a bipedal run to reach a high velocity in proportion to their body size. As cockroaches move very quickly, they need to be video recorded at several hundred frames per second to reveal their gait. More sedate locomotion is seen in the stick insects or walking sticks (Phasmatodea). A few insects have evolved to walk on the surface of the water, especially members of the Gerridae family, commonly known as water striders. A few species of ocean-skaters in the genus Halobates even live on the surface of open oceans, a habitat that has few insect species.[132]

Insect walking is of particular interest as practical form of robot locomotion. The study of insects and bipeds has a significant impact on possible robotic methods of transport. This may allow new hexapod robots to be designed that can traverse terrain that robots with wheels may be unable to handle.[130]

The backswimmer Notonecta glauca underwater, showing its paddle-like hindleg adaptation

A large number of insects live either part or the whole of their lives underwater. In many of the more primitive orders of insect, the immature stages are spent in an aquatic environment. Some groups of insects, like certain water beetles, have aquatic adults as well.[78]

Many of these species have adaptations to help in under-water locomotion. Water beetles and water bugs have legs adapted into paddle-like structures. Dragonfly naiads use jet propulsion, forcibly expelling water out of their rectal chamber.[133] Some species like the water striders are capable of walking on the surface of water. They can do this because their claws are not at the tips of the legs as in most insects, but recessed in a special groove further up the leg; this prevents the claws from piercing the water's surface film.[78] Other insects such as the Rove beetle Stenus are known to emit pygidial gland secretions that reduce surface tension making it possible for them to move on the surface of water by Marangoni propulsion (also known by the German term Entspannungsschwimmen).[134][135]

Perhaps one of the most well-known examples of mimicry, the viceroy butterfly (top) appears very similar to the monarch butterfly (bottom).[138]

Insects are mostly soft bodied, fragile and almost defenseless compared to other, larger lifeforms. The immature stages are small, move slowly or are immobile, and so all stages are exposed to predation and parasitism. Insects then have a variety of defense strategies to avoid being attacked by predators or parasitoids. These include camouflage, mimicry, toxicity and active defense.[139]

Camouflage is an important defense strategy, which involves the use of coloration or shape to blend into the surrounding environment.[140] This sort of protective coloration is common and widespread among beetle families, especially those that feed on wood or vegetation, such as many of the leaf beetles (family Chrysomelidae) or weevils. In some of these species, sculpturing or various colored scales or hairs cause the beetle to resemble bird dung or other inedible objects. Many of those that live in sandy environments blend in with the coloration of the substrate.[139] Most phasmids are known for effectively replicating the forms of sticks and leaves, and the bodies of some species (such as O. macklotti and Palophus centaurus) are covered in mossy or lichenous outgrowths that supplement their disguise. Very rarely, a species may have the ability to change color as their surroundings shift (Bostra scabrinota). In a further behavioral adaptation to supplement crypsis, a number of species have been noted to perform a rocking motion where the body is swayed from side to side that is thought to reflect the movement of leaves or twigs swaying in the breeze. Another method by which stick insects avoid predation and resemble twigs is by feigning death (catalepsy), where the insect enters a motionless state that can be maintained for a long period. The nocturnal feeding habits of adults also aids Phasmatodea in remaining concealed from predators.[141]

Another defense that often uses color or shape to deceive potential enemies is mimicry. A number of longhorn beetles (family Cerambycidae) bear a striking resemblance to wasps, which helps them avoid predation even though the beetles are in fact harmless.[139] Batesian and Müllerian mimicry complexes are commonly found in Lepidoptera. Genetic polymorphism and natural selection give rise to otherwise edible species (the mimic) gaining a survival advantage by resembling inedible species (the model). Such a mimicry complex is referred to as Batesian. One of the most famous examples, where the viceroy butterfly was long believed to be a Batesian mimic of the inedible monarch, was later disproven, as the viceroy is more toxic than the monarch, and this resemblance is now considered to be a case of Müllerian mimicry.[138] In Müllerian mimicry, inedible species, usually within a taxonomic order, find it advantageous to resemble each other so as to reduce the sampling rate by predators who need to learn about the insects' inedibility. Taxa from the toxic genus Heliconius form one of the most well known Müllerian complexes.[142]

Chemical defense is another important defense found among species of Coleoptera and Lepidoptera, usually being advertised by bright colors, such as the monarch butterfly. They obtain their toxicity by sequestering the chemicals from the plants they eat into their own tissues. Some Lepidoptera manufacture their own toxins. Predators that eat poisonous butterflies and moths may become sick and vomit violently, learning not to eat those types of species; this is actually the basis of Müllerian mimicry. A predator who has previously eaten a poisonous lepidopteran may avoid other species with similar markings in the future, thus saving many other species as well.[143] Some ground beetles of the family Carabidae can spray chemicals from their abdomen with great accuracy, to repel predators.[139]

European honey bee carrying pollen in a pollen basket back to the hive

Pollination is the process by which pollen is transferred in the reproduction of plants, thereby enabling fertilisation and sexual reproduction. Most flowering plants require an animal to do the transportation. While other animals are included as pollinators, the majority of pollination is done by insects.[144] Because insects usually receive benefit for the pollination in the form of energy rich nectar it is a grand example of mutualism. The various flower traits (and combinations thereof) that differentially attract one type of pollinator or another are known as pollination syndromes. These arose through complex plant-animal adaptations. Pollinators find flowers through bright colorations, including ultraviolet, and attractant pheromones. The study of pollination by insects is known as anthecology.

Many insects are parasites of other insects such as the parasitoid wasps. These insects are known as entomophagous parasites. They can be beneficial due to their devastation of pests that can destroy crops and other resources. Many insects have a parasitic relationship with humans such as the mosquito. These insects are known to spread diseases such as malaria and yellow fever and because of such, mosquitoes indirectly cause more deaths of humans than any other animal.

Aedes aegypti, a parasite, is the vector of dengue fever and yellow fever

Many insects are considered pests by humans. Insects commonly regarded as pests include those that are parasitic (e.g. lice, bed bugs), transmit diseases (mosquitoes, flies), damage structures (termites), or destroy agricultural goods (locusts, weevils). Many entomologists are involved in various forms of pest control, as in research for companies to produce insecticides, but increasingly rely on methods of biological pest control, or biocontrol. Biocontrol uses one organism to reduce the population density of another organism—the pest—and is considered a key element of integrated pest management.[145][146]

Despite the large amount of effort focused at controlling insects, human attempts to kill pests with insecticides can backfire. If used carelessly, the poison can kill all kinds of organisms in the area, including insects' natural predators, such as birds, mice and other insectivores. The effects of DDT's use exemplifies how some insecticides can threaten wildlife beyond intended populations of pest insects.[147][148]

Because they help flowering plants to cross-pollinate, some insects are critical to agriculture. This European honey bee is gathering nectar while pollen collects on its body.

A robberfly with its prey, a hoverfly. Insectivorous relationships such as these help control insect populations.

Although pest insects attract the most attention, many insects are beneficial to the environment and to humans. Some insects, like wasps, bees, butterflies and ants, pollinate flowering plants. Pollination is a mutualistic relationship between plants and insects. As insects gather nectar from different plants of the same species, they also spread pollen from plants on which they have previously fed. This greatly increases plants' ability to cross-pollinate, which maintains and possibly even improves their evolutionary fitness. This ultimately affects humans since ensuring healthy crops is critical to agriculture. As well as pollination ants help with seed distribution of plants. This helps to spread the plants, which increases plant diversity. This leads to an overall better environment.[149] A serious environmental problem is the decline of populations of pollinator insects, and a number of species of insects are now cultured primarily for pollination management in order to have sufficient pollinators in the field, orchard or greenhouse at bloom time.[150]^{: 240–243} Another solution, as shown in Delaware, has been to raise native plants to help support native pollinators like L. vierecki.[151]

The economic value of pollination by insects has been estimated to be about $34 billion in the US alone.[152]

Products made by insects. Insects also produce useful substances such as honey, wax, lacquer and silk. Honey bees have been cultured by humans for thousands of years for honey, although contracting for crop pollination is becoming more significant for beekeepers. The silkworm has greatly affected human history, as silk-driven trade established relationships between China and the rest of the world.

Pest control. Insectivorous insects, or insects that feed on other insects, are beneficial to humans if they eat insects that could cause damage to agriculture and human structures. For example, aphids feed on crops and cause problems for farmers, but ladybugs feed on aphids, and can be used as a means to significantly reduce pest aphid populations. While birds are perhaps more visible predators of insects, insects themselves account for the vast majority of insect consumption. Ants also help control animal populations by consuming small vertebrates.[153] Without predators to keep them in check, insects can undergo almost unstoppable population explosions.[30]^{: 328–348}[30]^: 400[154][155]

Medical uses. Insects are also used in medicine, for example fly larvae (maggots) were formerly used to treat wounds to prevent or stop gangrene, as they would only consume dead flesh. This treatment is finding modern usage in some hospitals. Recently insects have also gained attention as potential sources of drugs and other medicinal substances.[156] Adult insects, such as crickets and insect larvae of various kinds, are also commonly used as fishing bait.[157]

The common fruit fly Drosophila melanogaster is one of the most widely used organisms in biological research.

Insects play important roles in biological research. For example, because of its small size, short generation time and high fecundity, the common fruit fly Drosophila melanogaster is a model organism for studies in the genetics of eukaryotes. D. melanogaster has been an essential part of studies into principles like genetic linkage, interactions between genes, chromosomal genetics, development, behavior and evolution. Because genetic systems are well conserved among eukaryotes, understanding basic cellular processes like DNA replication or transcription in fruit flies can help to understand those processes in other eukaryotes, including humans.[158] The genome of D. melanogaster was sequenced in 2000, reflecting the organism's important role in biological research. It was found that 70% of the fly genome is similar to the human genome, supporting the evolution theory.[159]

In some cultures, insects form part of the normal diet. In Africa, for instance, locally abundant species of both locusts and termites are a common traditional human food source.[160] Some, especially deep-fried cicadas, are considered to be delicacies. Insects have a high protein content for their mass, and some authors suggest their potential as a major source of protein in human nutrition.[30]^: 10–13 In most first-world countries, however, entomophagy (the eating of insects), is taboo.[161] They are also recommended by militaries as a survival food for troops in adversity.[160] Since it is impossible to eliminate pest insects from the human food chain, insects are inadvertently present in many foods, especially grains. Food safety laws in many countries do not prohibit insect parts in food, but rather limit their quantity. According to cultural materialist anthropologist Marvin Harris, the eating of insects is taboo in cultures that have other protein sources such as fish or livestock.

Because of the abundance of insects and a worldwide concern of food shortages, the Food and Agriculture Organization of the United Nations considers that the world may have to, in the future, regard the prospects of eating insects as a food staple. Insects are noted for their nutrients, having a high content of protein, minerals and fats and are eaten by one-third of the global population.[162]

Several insect species such as the black soldier fly or the housefly in their maggot forms, as well as beetle larvae such as mealworms can be processed and used as feed for farmed animals such as chicken, fish and pigs.[163]

Black soldier fly larvae can provide protein, fats for use in cosmetics,[164] and chitin.

Also, insect cooking oil, insect butter and fatty alcohols can be made from such insects as the superworm (Zophobas morio).[165][166]

Many species of insects are sold and kept as pets. There are special hobbyist magazines such as "Bugs" (now discontinued).[167]

Scarab beetles held religious and cultural symbolism in Old Egypt, Greece and some shamanistic Old World cultures. The ancient Chinese regarded cicadas as symbols of rebirth or immortality. In Mesopotamian literature, the epic poem of Gilgamesh has allusions to Odonata that signify the impossibility of immortality. Among the Aborigines of Australia of the Arrernte language groups, honey ants and witchetty grubs served as personal clan totems. In the case of the 'San' bush-men of the Kalahari, it is the praying mantis that holds much cultural significance including creation and zen-like patience in waiting.[30]^: 9