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Insect
Insect
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Insect
Temporal range: Carboniferous–Present
Insects have a three-part body: head with large compound eyes and antennae, a thorax with three pairs of legs, and a segmented abdomen. Many groups also have two pairs of wings.
Scientific classification Edit this classification
Kingdom: Animalia
Phylum: Arthropoda
Clade: Allotriocarida
Subphylum: Hexapoda
Class: Insecta
Linnaeus, 1758
Subgroups
Synonyms
  • Ectognatha
  • Entomida
Insects live in a world of motion. This leaf-footed bug climbs wind blown grass and flies off.

Insects (from Latin insectum) are hexapod invertebrates of the class Insecta. They are the largest group within the arthropod phylum. Insects have a chitinous exoskeleton, a three-part body (head, thorax and abdomen), three pairs of jointed legs, compound eyes, and a pair of antennae. Insects are the most diverse group of animals, with more than a million described species; they represent more than half of all animal species.

The insect nervous system consists of a brain and a ventral nerve cord. Most insects reproduce by laying eggs. Insects breathe air through a system of paired openings along their sides, connected to small tubes that take air directly to the tissues. The blood therefore does not carry oxygen; it is only partly contained in vessels, and some circulates in an open hemocoel. Insect vision is mainly through their compound eyes, with additional small ocelli. Many insects can hear, using tympanal organs, which may be on the legs or other parts of the body. Their sense of smell is via receptors, usually on the antennae and the mouthparts.

Nearly all insects hatch from eggs. Insect growth is constrained by the inelastic exoskeleton, so development involves a series of molts. The immature stages often differ from the adults in structure, habit, and habitat. Groups that undergo four-stage metamorphosis often have a nearly immobile pupa. Insects that undergo three-stage metamorphosis lack a pupa, developing through a series of increasingly adult-like nymphal stages. The higher level relationship of the insects is unclear. Fossilized insects of enormous size have been found from the Paleozoic Era, including giant dragonfly-like insects with wingspans of 55 to 70 cm (22 to 28 in). The most diverse insect groups appear to have coevolved with flowering plants.

Adult insects typically move about by walking and flying; some can swim. Insects are the only invertebrates that can achieve sustained powered flight; insect flight evolved just once. Many insects are at least partly aquatic, and have larvae with gills; in some species, the adults too are aquatic. Some species, such as water striders, can walk on the surface of water. Insects are mostly solitary, but some, such as bees, ants and termites, are social and live in large, well-organized colonies. Others, such as earwigs, provide 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 great distances. Other species communicate with sounds: crickets stridulate, or rub their wings together, to attract a mate and repel other males. Lampyrid beetles communicate with light.

Humans regard many insects as pests, especially those that damage crops, and attempt to control them using insecticides and other techniques. Others are parasitic, and may act as vectors of diseases. Insect pollinators are essential to the reproduction of many flowering plants and so to their ecosystems. Many insects are ecologically beneficial as predators of pest insects, while a few provide direct economic benefit. Two species in particular are economically important and were domesticated many centuries ago: silkworms for silk and honey bees for honey. Insects are consumed as food in 80% of the world's nations, by people in roughly 3,000 ethnic groups. Human activities are having serious effects on insect biodiversity.

Etymology

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The word insect comes from the Latin word insectum from in + sĕco, "cut up",[1] as insects appear to be cut into three parts. The Latin word was introduced by Pliny the Elder who calqued the Ancient Greek word ἔντομον éntomon "insect" (as in entomology) from ἔντομος éntomos "cut in pieces";[2] this was Aristotle's term for this class of life in his biology, also in reference to their notched bodies. The English word insect first appears in 1601 in Philemon Holland's translation of Pliny.[3][4]

Insects and other bugs

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Distinguishing features

[edit]

In common speech, insects and other terrestrial arthropods are often called bugs [a] or creepy crawlies. Entomologists to some extent reserve the name "bugs" for a narrow category of "true bugs", insects of the order Hemiptera, such as cicadas and shield bugs.[6] Other terrestrial arthropods, such as centipedes, millipedes, woodlice, spiders, mites and scorpions, are sometimes confused with insects, since they have a jointed exoskeleton.[7] Adult insects are the only arthropods that ever have wings, with up to two pairs on the thorax. Whether winged or not, adult insects can be distinguished by their three-part body plan, with head, thorax, and abdomen; they have three pairs of legs on the thorax.[8]

Diversity

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About half of all eukaryotes are insects (left side of diagram).

Estimates of the total number of insect species vary considerably, suggesting that there are perhaps some 5.5 million insect species in existence, of which about one million have been described and named.[9] These constitute around half of all eukaryote species, including animals, plants, and fungi.[10] The most diverse insect orders are the Hemiptera (true bugs), Lepidoptera (butterflies and moths), Diptera (true flies), Hymenoptera (wasps, ants, and bees), and Coleoptera (beetles), each with more than 100,000 described species.[9]

Distribution and habitats

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Insects are distributed over every continent and almost every terrestrial habitat. There are many more species in the tropics, especially in rainforests, than in temperate zones.[11] The world's regions have received widely differing amounts of attention from entomologists. The British Isles have been thoroughly surveyed, so that Gullan and Cranston 2014 state that the total of around 22,500 species is probably within 5% of the actual number there; they comment that Canada's list of 30,000 described species is surely over half of the actual total. They add that the 3,000 species of the American Arctic must be broadly accurate. In contrast, a large majority of the insect species of the tropics and the southern hemisphere are probably undescribed.[11] Some 30–40,000 species inhabit freshwater; very few insects, perhaps a hundred species, are marine.[12] Insects such as snow scorpionflies flourish in cold habitats including the Arctic and at high altitude.[13] Insects such as desert locusts, ants, beetles, and termites are adapted to some of the hottest and driest environments on earth, such as the Sonoran Desert.[14]

Phylogeny and evolution

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External phylogeny

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Insects form a clade, a natural group with a common ancestor, among the arthropods.[15] A phylogenetic analysis by Kjer et al. (2016) places the insects among the Hexapoda, six-legged animals with segmented bodies; their closest relatives are the Diplura (bristletails).[16]

Hexapoda

Collembola (springtails)

Protura (coneheads)

Diplura (two-pronged bristletails)

Insecta (=Ectognatha)

Internal phylogeny

[edit]

The internal phylogeny is based on the works of Wipfler et al. 2019 for the Polyneoptera,[17] Johnson et al. 2018 for the Paraneoptera,[18] and Kjer et al. 2016 for the Holometabola.[19] The numbers of described extant species (boldface for groups with over 100,000 species) are from Stork 2018.[9]

Insecta
Monocondylia

Archaeognatha (hump-backed/jumping bristletails, 513 spp)

Dicondylia

Zygentoma (silverfish, firebrats, fishmoths, 560 spp)

Pterygota
Palaeoptera

Odonata (dragonflies and damselflies, 5,899 spp)

Ephemeroptera (mayflies, 3,240 spp)

Neoptera
Polyneoptera

Zoraptera (angel insects, 37 spp)

Dermaptera (earwigs, 1,978 spp)

Plecoptera (stoneflies, 3,743 spp)

Orthoptera (grasshoppers, crickets, katydids, 23,855 spp)

Notoptera

Grylloblattodea (ice crawlers, 34 spp)

Mantophasmatodea (gladiators, 15 spp)

Phasmatodea (stick insects, 3,014 spp)

Embioptera (webspinners, 463 spp)

Dictyoptera

Mantodea (mantises, 2,400 spp)

Blattodea (cockroaches and termites, 7,314 spp)

Eumetabola
Paraneoptera

Psocodea (book lice, barklice and sucking lice, 11,000 spp)

Hemiptera (true bugs, 103,590 spp)

Thysanoptera (thrips, 5,864 spp)

Holometabola

Hymenoptera (sawflies, wasps, bees, ants, 116,861 spp)

Neuropteroidea
Coleopterida

Strepsiptera (twisted-wing flies, 609 spp)

Coleoptera (beetles, 386,500 spp)

Neuropterida

Raphidioptera (snakeflies, 254 spp)

Neuroptera (lacewings, 5,868 spp)

Megaloptera (alderflies and dobsonflies, 354 spp)

Panorpida
Amphiesmenoptera

Lepidoptera (butterflies and moths, 157,338 spp)

Trichoptera (caddisflies, 14,391 spp)

Antliophora

Diptera (true flies, 155,477 spp)

Mecoptera (scorpionflies, 757 spp)

Siphonaptera (fleas, 2,075 spp)

larvae, pupae
wings flex over abdomen
wings

Taxonomy

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Early

[edit]
Diagram of Linnaeus's key to his seven orders of insect, 1758[20]
Aptera

wingless
Diptera

2‑winged
Coleoptera

forewings fully hardened
Hemiptera

forewings partly hardened
dissimilar pairs
Lepidoptera

wings scaly
Neuroptera

no sting
Hymenoptera

sting
wings membranous
similar pairs
4‑winged
winged
Insecta

Aristotle was the first to describe the insects as a distinct group. He placed them as the second-lowest level of animals on his scala naturae, above the spontaneously generating sponges and worms, but below the hard-shelled marine snails. His classification remained in use for many centuries.[21]

In 1758, in his Systema Naturae,[22] Carl Linnaeus divided the animal kingdom into six classes including Insecta. He created seven orders of insect according to the structure of their wings. These were the wingless Aptera, the two-winged Diptera, and five four-winged orders: the Coleoptera with fully-hardened forewings; the Hemiptera with partly-hardened forewings; the Lepidoptera with scaly wings; the Neuroptera with membranous wings but no sting; and the Hymenoptera, with membranous wings and a sting.[20]

Jean-Baptiste de Lamarck, in his 1809 Philosophie Zoologique, treated the insects as one of nine invertebrate phyla.[23] In his 1817 Le Règne Animal, Georges Cuvier grouped all animals into four embranchements ("branches" with different body plans), one of which was the articulated animals, containing arthropods and annelids.[24] This arrangement was followed by the embryologist Karl Ernst von Baer in 1828, the zoologist Louis Agassiz in 1857, and the comparative anatomist Richard Owen in 1860.[25] In 1874, Ernst Haeckel divided the animal kingdom into two subkingdoms, one of which was Metazoa for the multicellular animals. It had five phyla, including the articulates.[26][25]

Modern

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Traditional morphology-based systematics have usually given the Hexapoda the rank of superclass,[27] and identified four groups within it: insects (Ectognatha), Collembola, Protura, and Diplura, the latter three being grouped together as the Entognatha on the basis of internalized mouth parts.[28]

The use of phylogenetic data has brought about numerous changes in relationships above the level of orders.[28] Insects can be divided into two groups historically treated as subclasses: wingless insects or Apterygota, and winged insects or Pterygota. The Apterygota traditionally consisted of the primitively wingless orders Archaeognatha (jumping bristletails) and Zygentoma (silverfish). However, Apterygota is not monophyletic, as Archaeognatha are sister to all other insects, based on the arrangement of their mandibles, while the Pterygota, the winged insects, emerged from within the Dicondylia, alongside the Zygentoma.[29]

The Pterygota (Palaeoptera and Neoptera) are winged and have hardened plates on the outside of their body segments; the Neoptera have muscles that allow their wings to fold flat over the abdomen. Neoptera can be divided into groups with incomplete metamorphosis (Polyneoptera and Paraneoptera) and those with complete metamorphosis (Holometabola). The molecular finding that the traditional louse orders Mallophaga and Anoplura are within Psocoptera has led to the new taxon Psocodea.[30] Phasmatodea and Embiidina have been suggested to form the Eukinolabia.[31] Mantodea, Blattodea, and Isoptera form a monophyletic group, Dictyoptera.[32] Fleas are now thought to be closely related to boreid mecopterans.[33]

Evolutionary history

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The oldest fossil that may be a primitive wingless insect is Leverhulmia from the Early Devonian Windyfield chert.[34] The oldest known flying insects are from the mid-Carboniferous, around 328–324 million years ago. The group subsequently underwent a rapid explosive diversification. Claims that they originated substantially earlier, during the Silurian or Devonian (some 400 million years ago) based on molecular clock estimates, are unlikely to be correct, given the fossil record.[35]

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).[36]

The remarkably successful Hymenoptera (wasps, bees, and ants) appeared some 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. Insects were among the earliest terrestrial herbivores and acted as major selection agents on plants.[37] 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.[38]

Morphology and physiology

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External

[edit]
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

Three-part body

[edit]

Insects have a segmented body supported by an exoskeleton, the hard outer covering made mostly of chitin. The body is organized into three interconnected units: the head, thorax and abdomen. 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 carries the three pairs of legs and up to two pairs of wings. The abdomen contains most of the digestive, respiratory, excretory and reproductive structures.[8]

Segmentation

[edit]

The head is enclosed in a hard, heavily sclerotized, unsegmented head capsule, which contains most of the sensing organs, including the antennae, compound eyes, ocelli, and mouthparts.[40] The thorax is composed of three sections named (from front to back) the prothorax, mesothorax and metathorax. The prothorax carries the first pair of legs. The mesothorax carries the second pair of legs and the front wings. The metathorax carries the third pair of legs and the hind wings.[8][40] The abdomen is the largest part of the insect, typically with 11–12 segments, and is less strongly sclerotized than the head or thorax. Each segment of the abdomen has sclerotized upper and lower plates (the tergum and sternum), connected to adjacent sclerotized parts by membranes. Each segment carries a pair of spiracles.[40]

Exoskeleton

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The outer skeleton, the cuticle, is made up of two layers: the epicuticle, a thin and waxy water-resistant outer layer without chitin, and a lower layer, the thick chitinous procuticle. The procuticle has two layers: an outer exocuticle and an inner 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 sclerotized.[41][42] As an adaptation to life on land, insects have an enzyme that uses atmospheric oxygen to harden their cuticle, unlike crustaceans which use heavy calcium compounds for the same purpose. This makes the insect exoskeleton a lightweight material.[43]

Internal systems

[edit]

Nervous

[edit]

The nervous system of an insect consists of 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.[44] The thoracic segments have one ganglion on each side, connected into a pair per segment. This arrangement is also seen in the first eight segments of the abdomen. Many insects have fewer ganglia than this.[45] Insects are capable of learning.[46]

Digestive

[edit]

An insect uses its digestive system to extract nutrients and other substances from the food it consumes.[47] There is extensive variation among different orders, life stages, and even castes in the digestive system of insects.[48] The gut runs lengthwise through the body. It has three sections, with paired salivary glands and salivary reservoirs.[49] By moving its mouthparts the insect mixes its food with saliva.[50][51] Some insects, like flies, expel digestive enzymes onto their food to break it down, but most insects digest their food in the gut.[52] The foregut is lined with cuticule as protection from tough food. It includes the mouth, pharynx, and crop which stores food.[53] Digestion starts in the mouth with enzymes in the saliva. Strong muscles in the pharynx pump fluid into the mouth, lubricating the food, and enabling certain insects to feed on blood or from the xylem and phloem transport vessels of plants.[54] Once food leaves the crop, it passes to the midgut, where the majority of digestion takes place. Microscopic projections, microvilli, increase the surface area of the wall to absorb nutrients.[55] In the hindgut, undigested food particles are joined by uric acid to form fecal pellets; most of the water is absorbed, leaving a dry pellet to be eliminated. Insects may have one to hundreds of Malpighian tubules. These 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.[56]

Reproductive

[edit]

The reproductive system of female insects consist of a pair of ovaries, accessory glands, one or more spermathecae to store sperm, and ducts connecting these parts. The ovaries are made up of a variable number of egg tubes, ovarioles. Female insects make eggs, receive and store sperm, manipulate sperm from different males, and lay eggs. Accessory glands produce substances to maintain sperm and to protect the eggs. They can produce glue and protective substances for coating eggs, or tough coverings for a batch of eggs called oothecae.[57]

For males, the reproductive system consists of one or two testes, suspended in the body cavity by tracheae. The testes contain sperm tubes or follicles in a membranous sac. These connect to a duct that leads to the outside. The terminal portion of the duct may be sclerotized to form the intromittent organ, the aedeagus.[58]

Respiratory

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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, insects have 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 tracheae and tracheoles. In most insects, air is taken in through paired spiracles, openings on the sides of the abdomen and thorax. The respiratory system limits the size of insects. As insects get larger, gas exchange via spiracles becomes 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).[59] Gas exchange patterns in insects range from continuous and diffusive ventilation, to discontinuous.[60][61][62][63]

Circulatory

[edit]

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 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.[64][65] 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.[66]

Sensory

[edit]
Most insects have a pair of large compound eyes and other sensory organs such as antennae able to detect movements and chemical stimuli on their heads.

Many insects possess numerous specialized sensory organs able to detect stimuli including limb position (proprioception) by campaniform sensilla, light, water, chemicals (senses of taste and smell), sound, and heat.[67] Some insects such as bees can perceive ultraviolet wavelengths, or detect polarized light, while the antennae of male moths can detect the pheromones of female moths over distances of over a kilometer.[68] There is a trade-off between visual acuity and chemical or tactile acuity, such that most insects with well-developed eyes have reduced or simple antennae, and vice versa. Insects perceive sound by different mechanisms, such as thin vibrating membranes (tympana).[69] Insects were the earliest organisms to produce and sense sounds. Hearing has evolved independently at least 19 times in different insect groups.[70]

Most insects, except some cave crickets, are able to perceive light and dark. Many have acute vision capable of detecting small and rapid movements. The eyes may include simple eyes or ocelli as well as larger compound eyes. Many species can detect light in the infrared, ultraviolet and visible light wavelengths, with color vision. Phylogenetic analysis suggests that UV-green-blue trichromacy existed from at least the Devonian Period, some 400 million years ago.[71]

The individual lenses in compound eyes are immobile, but fruit flies have photoreceptor cells underneath each lens which move rapidly in and out of focus, in a series of movements called photoreceptor microsaccades. This gives them, and possibly many other insects, a much clearer image of the world than previously assumed.[72]

An insect's sense of smell is via chemical receptors, usually on the antennae and the mouthparts. These detect both airborne volatile compounds and odorants on surfaces, including pheromones from other insects and compounds released by food plants. Insects use olfaction to locate mating partners, food, and places to lay eggs, and to avoid predators. It is thus an extremely important sense, enabling insects to discriminate between thousands of volatile compounds.[73]

Some insects are capable of magnetoreception; ants and bees navigate using it both locally (near their nests) and when migrating.[74] The Brazilian stingless bee detects magnetic fields using the hair-like sensilla on its antennae.[75][76]

Reproduction and development

[edit]

Life-cycles

[edit]
Butterflies mating

The majority of insects hatch from eggs. The fertilization and development takes place inside the egg, enclosed by a shell (chorion) that consists of maternal tissue. In contrast to eggs of other arthropods, most insect eggs are drought resistant. This is because inside the chorion two additional membranes develop from embryonic tissue, the amnion and the serosa. This serosa secretes a cuticle rich in chitin that protects the embryo against desiccation.[77] Some species of insects, like aphids and tsetse flies, are ovoviviparous: their eggs develop entirely inside the female, and then hatch immediately upon being laid.[78] Some other species, such as in the cockroach genus Diploptera, are viviparous, gestating inside the mother and born alive.[79] Some insects, like parasitoid wasps, are polyembryonic, meaning that a single fertilized egg divides into many separate embryos.[80] Insects may be univoltine, bivoltine or multivoltine, having one, two or many broods in a year.[81]

Aphid giving birth to live female young by parthenogenesis from unfertilized eggs
A female leaf-footed bug deposits an egg before flying off.

Other developmental and reproductive variations include haplodiploidy, polymorphism, paedomorphosis or peramorphosis, sexual dimorphism, parthenogenesis, and more rarely hermaphroditism.[82][83] 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.[84]

Some insects are parthenogenetic, meaning that the female can reproduce and give birth without having the eggs fertilized by a male. Many aphids undergo a cyclical form of parthenogenesis in which they alternate between one or many generations of asexual and sexual reproduction.[85][86] 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 their haplodiploid system, diploid females spawn many females and a few haploid males.[78]

Metamorphosis

[edit]

Metamorphosis in insects is the process of development that converts young to adults. There are two forms of metamorphosis: incomplete and complete.

Incomplete

[edit]
Incomplete metamorphosis in a locust with multiple instars. Egg is not shown. The largest specimen is adult.

Hemimetabolous insects, those with incomplete metamorphosis, change gradually after hatching from the egg by undergoing a series of molts through stages called instars, until the final, adult, stage is reached. 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; this makes the old cuticle split along predefined weaknesses where it was thinnest.[87][88]

Complete

[edit]
Life-cycle of butterfly, undergoing complete metamorphosis from egg through caterpillar larvae to pupa and adult

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 can be 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. 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.[89] Insects undergo considerable change in form during the pupal stage, and emerge as adults. Butterflies are well-known for undergoing complete metamorphosis; 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.[82]

Communication

[edit]

Insects that produce sound can generally hear it. Most insects can hear only a narrow range of frequencies related to the frequency of the sounds they can produce. Mosquitoes can hear up to 2 kilohertz.[90] Certain predatory and parasitic insects can detect the characteristic sounds made by their prey or hosts, respectively. Likewise, some nocturnal moths can perceive the ultrasonic emissions of bats, which helps them avoid predation.[91]

Light production

[edit]

A few insects, such as 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.[92] 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.[93] The colors of emitted light vary from dull blue (Orfelia fultoni, Mycetophilidae) to the familiar greens and the rare reds (Phrixothrix tiemanni, Phengodidae).[94]

Sound production

[edit]

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).[95] 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.[96][97] Some moths produce ultrasonic clicks that warn predatory bats of their unpalatability (acoustic aposematism),[98] while some palatable moths have evolved to mimic these calls (acoustic Batesian mimicry).[99] 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.[100]

Very low sounds are produced in various species of Coleoptera, Hymenoptera, Lepidoptera, Mantodea and Neuroptera. These low sounds are produced by the insect's movement, amplified by stridulatory structures on the insect's muscles and joints; these sounds can be used to warn or communicate with other insects. Most sound-making insects also have tympanal organs that can perceive airborne sounds. Some hemipterans, such as the water boatmen, communicate via underwater sounds.[101]

Cricket in garage with familiar call

Communication using surface-borne vibrational signals is more widespread among insects because of size constraints in producing air-borne sounds.[102] 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.[103]

Some species use vibrations for communicating, such as to attract mates as in the songs of the shield bug Nezara viridula.[104] Vibrations can also be used to communicate between species; lycaenid caterpillars, which form a mutualistic association with ants communicate with ants in this way.[105] The Madagascar hissing cockroach has the ability to press air through its spiracles to make a hissing noise as a sign of aggression;[106] 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.[107]

Chemical communication

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Social insects such as ants have multiple types of pheromonal glands, producing different semiochemicals for communication with other insects.[108]

Many 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 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.[108] 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.[109]

Social behavior

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Honey bee's figure-eight waggle dance. An orientation 45° to the right of 'up' on the comb indicates food 45° to the right of the sun. The dancer's rapid waggling blurs her abdomen.

Social insects, such as termites, ants and many bees and wasps, are eusocial.[110] They live together in such large well-organized colonies of genetically similar individuals that they are sometimes considered superorganisms. In particular, reproduction is largely limited to a queen caste; other females are workers, prevented from reproducing by worker policing. Honey bees have evolved a system of abstract symbolic communication where a behavior is used to represent and convey specific information about the environment. In this communication system, called dance language, the angle at which a bee dances represents a direction relative to the sun, and the length of the dance represents the distance to be flown.[111] Bumblebees too have some social communication behaviors. Bombus terrestris, for example, more rapidly learns about visiting unfamiliar, yet rewarding flowers, when they can see a conspecific foraging on the same species.[112]

Only insects that live in nests or colonies possess fine-scale spatial orientation. Some can navigate unerringly to a single hole a few millimeters in diameter among thousands of similar holes, after a trip of several kilometers. In philopatry, insects that hibernate are able to recall a specific location up to a year after last viewing the area of interest.[113] A few insects seasonally migrate large distances between different geographic regions, as in the continent-wide monarch butterfly migration.[114]

Care of young

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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 provide parental care, where they at least guard their eggs, and sometimes guard their offspring until adulthood, possibly even feeding them. Many wasps and bees construct a nest or burrow, store provisions in it, and lay an egg upon those provisions, providing no further care.[115]

Locomotion

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Flight

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Insects such as hoverflies are capable of rapid and agile flight.

Insects are the only group of invertebrates to have developed flight. The ancient groups of insects in the Palaeoptera, the dragonflies, damselflies and mayflies, operate their wings directly by paired muscles attached to points on each wing base that raise and lower them. This can only be done at a relatively slow rate. All other insects, the Neoptera, have indirect flight, in which the flight muscles cause rapid oscillation of the thorax: there can be more wingbeats than nerve impulses commanding the muscles. One pair of flight muscles is aligned vertically, contracting to pull the top of the thorax down, and the wings up. The other pair runs longitudinally, contracting to force the top of the thorax up and the wings down.[116][117] Most insects gain aerodynamic lift by creating a spiralling vortex at the leading edge of the wings.[118] Small insects like thrips with tiny feathery wings gain lift using the clap and fling mechanism; the wings are clapped together and pulled apart, flinging vortices into the air at the leading edges and at the wingtips.[119][120]

The evolution of insect wings has been a subject of debate; it has been suggested they came from modified gills, flaps on the spiracles, or an appendage, the epicoxa, at the base of the legs.[121] More recently, entomologists have favored evolution of wings from lobes of the notum, of the pleuron, or more likely both.[122] In the Carboniferous age, the dragonfly-like Meganeura had as much as a 50 cm (20 in) wide wingspan. The appearance of gigantic insects is consistent with high atmospheric oxygen at that time, as the respiratory system of insects constrains their size.[123] 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).[124]

Unlike birds, small insects are swept along by the prevailing winds[125] although many larger insects migrate. Aphids are transported long distances by low-level jet streams.[126]

Walking

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Spatial and temporal stepping pattern of walking desert ants performing an alternating tripod gait. Recording rate: 500 fps, Playback rate: 10 fps.

Many adult insects use six legs for walking, with an alternating tripod gait. This allows for rapid walking with 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.[127] 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 (tetrapodal) or more feet (wave-gait) may be touching the ground.[128] Cockroaches are among the fastest insect runners and, at full speed, adopt a bipedal run. More sedate locomotion is seen in the well-camouflaged stick insects (Phasmatodea). A small number of species such as Water striders can move on the surface of water; their claws are recessed in a special groove, preventing the claws from piercing the water's surface film.[62] The ocean-skaters in the genus Halobates even live on the surface of open oceans, a habitat that has few insect species.[129]

Swimming

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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 aquatic. In some groups, such as water beetles, the adults too are aquatic.[62]

Many of these species are adapted for 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.[130] Other insects such as the rove beetle Stenus emit pygidial gland surfactant secretions that reduce surface tension; this enables them to move on the surface of water by Marangoni propulsion.[131][132]

Ecology

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Insects play many critical roles in ecosystems, including soil turning and aeration, dung burial, pest control, pollination and wildlife nutrition.[133] For instance, termites modify the environment around their nests, encouraging grass growth;[134] many beetles are scavengers; dung beetles recycle biological materials into forms useful to other organisms.[135][136] Insects are responsible for much of the process by which topsoil is created.[137]

Defense

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Reduvius personatus, the masked hunter bug nymph, camouflages itself with sand grains to avoid predators.

Insects are mostly small, soft bodied, and fragile compared to larger lifeforms. The immature stages are small, move slowly or are immobile, and so all stages are exposed to predation and parasitism. Insects accordingly employ multiple defensive strategies, including camouflage, mimicry, toxicity and active defense.[138] Many insects rely on camouflage to avoid being noticed by their predators or prey.[139] It is common among leaf beetles and weevils that feed on wood or vegetation.[138] Stick insects mimic the forms of sticks and leaves.[140] Many insects use mimicry to deceive predators into avoiding them. In Batesian mimicry, edible species, such as of hoverflies (the mimics), gain a survival advantage by resembling inedible species (the models).[138][141] In Müllerian mimicry, inedible species, such as of wasps and bees, resemble each other so as to reduce the sampling rate by predators who need to learn that those insects are inedible. Heliconius butterflies, many of which are toxic, form Müllerian complexes, advertising their inedibility.[142] Chemical defense is common among Coleoptera and Lepidoptera, usually being advertised by bright warning colors (aposematism), as in the monarch butterfly. As larvae, they obtain their toxicity by sequestering chemicals from the plants they eat into their own tissues. Some manufacture their own toxins. Predators that eat poisonous butterflies and moths may vomit violently, learning not to eat insects with similar markings; this is the basis of Müllerian mimicry.[143] Some ground beetles of the family Carabidae actively defend themselves, spraying chemicals from their abdomen with great accuracy, to repel predators.[138]

Pollination

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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.[144] Most flowering plants require an animal to do the transportation. The majority of pollination is by insects.[145] Because insects usually receive benefit for the pollination in the form of energy rich nectar it is a mutualism. The various flower traits, such as bright colors and pheromones that coevolved with their pollinators, have been called pollination syndromes, though around one third of flowers cannot be assigned to a single syndrome.[146]

Parasitism

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Many insects are parasitic. The largest group, with over 100,000 species[147] and perhaps over a million,[148] consists of a single clade of parasitoid wasps among the Hymenoptera.[149] These are parasites of other insects, eventually killing their hosts.[147] Some are hyper-parasites, as their hosts are other parasitoid wasps.[147][150] Several groups of insects can be considered as either micropredators or external parasites;[151][152] for example, many hemipteran bugs have piercing and sucking mouthparts, adapted for feeding on plant sap,[153][154] while species in groups such as fleas, lice, and mosquitoes are hematophagous, feeding on the blood of animals.[152]

Relationship to humans

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As pests

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Aedes aegypti, the yellow fever mosquito, is a vector of several diseases.

Many insects are considered pests by humans. These include parasites of people and livestock, such as lice and bed bugs; mosquitoes act as vectors of several diseases. Other pests include insects like termites that damage wooden structures; herbivorous insects such as locusts, aphids, and thrips that destroy agricultural crops, or like wheat weevils damage stored agricultural produce. Farmers have often attempted to control insects with chemical insecticides, but increasingly rely on biological pest control. This uses one organism to reduce the population density of a pest organism; it is a key element of integrated pest management.[156][157] Biological control is favored because insecticides can cause harm to ecosystems far beyond the intended pest targets.[158][159]

In beneficial roles

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Silkworms were domesticated for silk over 5,000 years ago.[160][161] Here, silk cocoons are being unrolled.

Pollination of flowering plants by insects including bees, butterflies, flies, and beetles, is economically important.[162] The value of insect pollination of crops and fruit trees was estimated in 2021 to be about $34 billion in the US alone.[163]

Insects produce useful substances such as honey,[164] wax,[165][166] lacquer[167] and silk.[168] Honey bees have been cultured by humans for thousands of years for honey.[169] Beekeeping in pottery vessels began about 9,000 years ago in North Africa.[170] The silkworm has greatly affected human history, as silk-driven trade established relationships between China and the rest of the world.[171][172]

Insects that feed on or parasitise other insects are beneficial to humans if they thereby reduce damage to agriculture and human structures. For example, aphids feed on crops, causing economic loss, but ladybugs feed on aphids, and can be used to control them. Insects account for the vast majority of insect consumption.[173][174][175]

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. Insects have gained attention as potential sources of drugs and other medicinal substances.[176] Adult insects, such as crickets and insect larvae of various kinds, are commonly used as fishing bait.[177]

Population declines

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At least 66 insect species extinctions have been recorded since 1500, many of them on oceanic islands.[178] Declines in insect abundance have been attributed to human activity in the form of artificial lighting,[179] land use changes such as urbanization or farming,[180][181] pesticide use,[182] and invasive species.[183][184] A 2019 research review suggested that a large proportion of insect species is threatened with extinction in the 21st century,[185] though the details have been disputed.[186] A larger 2020 meta-study, analyzing data from 166 long-term surveys, suggested that populations of terrestrial insects are indeed decreasing rapidly, by about 9% per decade.[187][188]

In research

[edit]
The fruit fly Drosophila melanogaster is a widely used model organism.

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, including 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.[189] 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 theory of evolution.[190]

As food

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Witchetty grubs are prized as high-protein foods by Aboriginal Australians.[191]

Insects are consumed as food in 80% of the world's nations, by people in roughly 3,000 ethnic groups.[192][193] In Africa, locally abundant species of locusts and termites are a common traditional human food source.[194] 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.[195] In most first-world countries, however, entomophagy (the eating of insects), is taboo.[196] They are also recommended by armed forces as a survival food for troops in adversity.[194] Because of the abundance of insects and a worldwide concern of food shortages, the Food and Agriculture Organization of the United Nations considers that people throughout the world may have to eat insects as a food staple. Insects are noted for their nutrients, having a high content of protein, minerals and fats and are already regularly eaten by one-third of the world's population.[197]

In other products

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Black soldier fly larvae can provide protein and fats for use in cosmetics.[198] Insect cooking oil, insect butter and fatty alcohols can be made from such insects as the superworm (Zophobas morio).[199] Insect species including the black soldier fly or the housefly in their maggot forms, and beetle larvae such as mealworms, can be processed and used as feed for farmed animals including chicken, fish and pigs.[200] Many species of insects are sold and kept as pets.[201]

In religion and folklore

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Ancient Egyptian scarab with separate wings, c. 712-342 BC

Scarab beetles held religious and cultural symbolism in ancient 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. 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.[202]

See also

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Notes

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References

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Sources

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Revisions and contributorsEdit on WikipediaRead on Wikipedia
from Grokipedia
Insects are a class of hexapod within the phylum Arthropoda, subphylum , characterized by a chitinous , three distinct body regions or tagmata (head, , and ), a single pair of antennae, compound eyes (often supplemented by ocelli), three pairs of jointed legs attached to the , and typically one or two pairs of wings arising from the . This body plan enables remarkable adaptability, with insects undergoing incomplete or complete during development, involving molting of the and transformation through larval, pupal (in holometabolous orders), and adult stages. With over 1 million described species—representing approximately 80% of all known animal species—insects are the most diverse group of multicellular organisms on Earth, and estimates suggest a total of 5.5 million species may exist, though many remain undiscovered due to their small size and vast habitats. They are divided into about 29 orders, with the most species-rich being Coleoptera (beetles, over 350,000 species), Lepidoptera (butterflies and moths, over 180,000 species), and Hymenoptera (ants, bees, and wasps, over 150,000 species). Insects have evolved over 400 million years, originating in the Devonian period, and now inhabit nearly every terrestrial and freshwater ecosystem, from deserts and rainforests to urban areas, though they are absent from the deep ocean and extreme polar regions. Insects play pivotal roles in global ecosystems, serving as primary pollinators for about 75% of flowering and major crops, decomposers that recycle nutrients through scavenging and dung burial, predators and parasitoids that regulate pest populations, and a foundational food source for vertebrates and other . Their activities support , , and , yet some species act as vectors for diseases (e.g., mosquitoes transmitting ) or agricultural pests, leading to significant economic impacts estimated in billions annually. Despite their ecological indispensability, insect populations face widespread declines due to habitat loss, pesticides, and , threatening and ecosystem stability.

Definition and Basics

Etymology and nomenclature

The word insect derives from the Latin insectum, the neuter past participle of insecare ("to cut into" or "to notch"), reflecting the apparent segmentation of the animal's body into distinct parts. This term appeared in classical texts, such as Pliny the Elder's Natural History (circa 77 CE), where it translated the Greek entomon ("notched" or "cut up"), but it gained systematic usage in modern taxonomy through Carl Linnaeus's Systema Naturae (10th edition, 1758), in which he established Insecta as a class encompassing arthropods like insects, arachnids, and crustaceans. Linnaeus's introduction of in the same 1758 edition revolutionized insect naming by assigning each species a unique two-word Latinized identifier: the name (capitalized) followed by the specific (lowercase), such as Musca domestica for the . This system, applied uniformly to insects as part of zoological , includes the designation of for each to anchor stability; for example, the for the Apis (bees) is Apis mellifera, the Western honeybee. The (ICZN), founded in 1895 and revised through its fourth edition in 1999, governs these rules specifically for animals, including insects, addressing revisions like updates to publication requirements and digital naming to maintain nomenclatural consistency. Prior to Linnaeus, insect naming lacked , with vernacular terms like "" used broadly in English from the late to denote any small, creepy, or pesty creature, originating from Middle English bugge (possibly from Welsh bwgan, meaning "" or "," evoking of the unknown). In contrast, modern entomological classifications under the ICZN distinguish scientific binomina from common names; for instance, the "ladybug" is formally , while "honeybee" corresponds to Apis mellifera. This shift from folk terminology to precise, universal has enabled global collaboration in entomological research.

Distinguishing features

Insects are distinguished by their tripartite body plan, consisting of a head, , and , which represents a specialized tagmosis unique among arthropods. The head typically arises from the fusion of six embryonic segments, the comprises three distinct segments (, mesothorax, and metathorax), and the usually features eleven segments, though modifications occur across . This segmentation pattern supports specialized functions, with the head housing sensory and feeding structures, the bearing locomotion appendages, and the dedicated to visceral organs. A hallmark of insects is their hexapod nature, characterized by exactly three pairs of jointed legs attached to the thoracic segments, setting them apart from other arthropods such as arachnids with eight legs or crustaceans with variable limb counts exceeding six. These legs, each composed of segments including coxa, , , , tarsus, and pretarsus, enable diverse adaptations like running, jumping, or grasping. Many insects also possess one or two pairs of wings emerging from the meso- and metathorax, facilitating flight and dispersal, though wingless forms exist in primitive or specialized groups. Sensory structures further define insects, including paired compound eyes on the head that provide panoramic vision through thousands of ommatidia and one pair of antennae serving as primary chemoreceptors and mechanosensors. The entire body is encased in a chitinous , or , which offers protection, structural support, and sites for muscle attachment while preventing . Physiologically, insects exhibit an open circulatory system where bathes tissues directly, pumped by a dorsal vessel acting as a heart, contrasting with the closed systems of vertebrates. Respiration occurs via a tracheal system of branching tubes that deliver oxygen directly to cells, entering through spiracles on the and , an efficient for their small size and high metabolic demands. These traits collectively underscore the class Insecta's evolutionary specialization within the phylum Arthropoda.

Diversity and distribution

Insects represent one of the most species-rich groups on , with approximately 1 million formally described and estimates suggesting a total of 5 to 10 million species worldwide. Among the described , the order Coleoptera (beetles) exhibits the highest diversity, with over 400,000 species, while (butterflies and moths) follows with approximately 180,000 species. These figures underscore the immense undescribed , particularly in understudied tropical regions where new species discoveries continue at a steady pace. Insects are distributed across nearly all terrestrial and freshwater habitats globally, achieving ubiquity except in the deep and polar caps, where extreme conditions preclude their presence. Their highest densities and occur in tropical rainforests, which harbor the majority of global insect diversity due to stable climates and abundant resources fostering . Biogeographic patterns reveal pronounced in isolated regions; for instance, Madagascar's insect includes a high proportion of unique species, with over 90% in well-studied groups like and mayflies, resulting from the island's long geological isolation. Diversity patterns are shaped by environmental factors, including , which can reduce local by isolating populations and limiting , while climate influences rates through variations in and that drive adaptive radiations. These dynamics highlight how connectivity and climatic stability in biodiverse hotspots like the promote evolutionary divergence, contributing to the overall global mosaic of insect distributions.

Evolutionary Origins

Phylogenetic relationships

Insects belong to the phylum Arthropoda, where they are classified within the subphylum , encompassing all six-limbed arthropods including true insects and their close relatives such as springtails and proturans. Within Arthropoda, forms the alongside Crustacea, with molecular phylogenomic analyses of nuclear protein-coding sequences strongly supporting as the to a derived lineage of crustaceans known as Xenocarida (comprising remipeds, cephalocarids, and branchiopods). Recent phylogenomic studies using extensive genomic data continue to affirm this relationship. This relationship positions insects as nested within a paraphyletic Crustacea, rejecting earlier hypotheses that linked insects more closely to myriapods (centipedes and millipedes). Broader phylogeny places the as sister to within the , a grouping defined by shared mandibular mouthparts, while (including spiders, scorpions, and horseshoe crabs) branches basally from , supported by extensive phylogenomic data from over 60 nuclear genes across 178 species. as a whole resides within the superphylum , a molting of protostome bilaterians that also includes nematodes and onychophorans, distinguishing from lophotrochozoan bilaterians such as annelids and mollusks through molecular markers like sequences. Molecular evidence robustly affirms the of Insecta (or more broadly ), with analyses of 18S rRNA genes from multiple taxa revealing shared derived substitutions that unite hexapods exclusive of other arthropods, as demonstrated in combined datasets of ribosomal and protein-coding loci. Similarly, cluster comparisons across arthropods, including sequences from basal hexapods like , support hexapod monophyly through conserved genomic organization and expression patterns, such as the duplication and divergence of the and fushi tarazu genes specific to insects. Within , the major clades contrast the wingless —comprising (bristletails) and (silverfish and firebrats), which form a paraphyletic grade of primitive, ametabolous insects—with the monophyletic , encompassing all winged insects and secondarily wingless forms like fleas. Mitochondrial genome phylogenies from basal lineages confirm as the immediate sister group to (forming the ), while diverges earlier, underscoring the evolutionary transition from wingless ancestors to the dominant winged radiation. This division highlights the origin of flight as a key innovation within , with fossil evidence from the period aligning with molecular divergence estimates around 400 million years ago.

Fossil record and timeline

The fossil record of insects begins in the period, approximately 407 to 396 million years ago, with the fragmentary remains of Rhyniognatha hirsti from the in , representing a potential early insect based on its dicondylic mandibles suggestive of a pterygote affinity. This specimen, consisting primarily of preserved mouthparts, indicates that insects may have originated near the base of the Ectognatha clade, though its exact placement remains debated due to limited material and possible affinities with other arthropods. Subsequent evidence is scarce, highlighting a significant "Hexapod Gap" spanning much of this period to the early , during which few definitive insect traces appear, likely reflecting preservational biases rather than absence. The period, particularly its later stages around 328 to 324 million years ago, marks a major diversification of winged insects (), with fossils documenting the rapid emergence of diverse orders such as and early odonatans featuring large, veined wings adapted for flight. This radiation coincided with expanding terrestrial forests and elevated atmospheric oxygen levels, enabling larger body sizes and aerial capabilities, as evidenced by compressions and impressions from coal-bearing deposits. By the Pennsylvanian subperiod (roughly 323 to 299 million years ago), winged forms dominated the record, with over 1,000 described illustrating a burst in morphological disparity. In the Mesozoic era, insect diversification accelerated further, particularly during the Cretaceous period (145 to 66 million years ago), aligning with the radiation of angiosperms that provided new ecological niches through floral resources and pollination mutualisms. This era saw the proliferation of holometabolous insects, including bees, butterflies, and beetles, with family-level diversity stabilizing at modern levels by the mid-Cretaceous, driven by angiosperm expansion that mitigated extinctions and boosted originations. Key evidence comes from lagerstätten preserving soft tissues, such as the Mazon Creek deposits in Illinois (late Carboniferous, ~308 million years ago), which yield exceptionally preserved insects like orthopterans and palaeodictyopterans in siderite concretions, offering insights into early terrestrial ecosystems. Similarly, the Crato Formation in Brazil's Araripe Basin (Aptian stage, ~113 million years ago) has produced over 2,000 insect specimens, including odonates and hemipterans with mineralized cuticles, revealing high-fidelity taphonomic windows into Cretaceous biodiversity. Despite these rich assemblages, the insect fossil record remains highly incomplete, primarily due to the small size, soft-bodied nature, and terrestrial habits of most species, which favor rapid decay over mineralization. Estimates suggest that the documented fossil diversity captures only a fraction of past insect richness, as indicated by sampling biases in lagerstätten and the underrepresentation of immature stages or non-aquatic forms. This incompleteness underscores the need for continued exploration of exceptional deposits to refine timelines of .

Key evolutionary adaptations

Insects achieved remarkable success through several pivotal evolutionary innovations that enhanced their survival, dispersal, and diversification. One of the most transformative adaptations was the development of powered flight in the clade, which originated approximately 350 million years ago during the early period. This innovation predated vertebrate flight by approximately 130 million years and enabled insects to escape predators, overcome geographic barriers for migration, access new food resources, and locate mates more effectively, contributing to their rapid diversification into over 15 orders by the end of the . Another critical adaptation was the of , particularly the complete (holometabolous) form, which emerged around 350 million years ago in the early . This developmental strategy involves distinct larval, pupal, and adult stages, allowing for niche separation where larvae specialize in feeding and growth in protected or aquatic environments, while adults focus on and dispersal in often contrasting habitats. The hormonal regulation, involving ecdysteroids for molting and juvenile hormones for stage specification, facilitated this separation, reducing and enhancing overall ecological adaptability. Holometaboly, seen in over 60% of insect today, such as beetles and , underscores its role in driving insect dominance. Refinements to the , particularly the incorporation of cuticular hydrocarbons (CHCs) into the , were essential for resisting and conquering terrestrial environments. This layer evolved as arthropods, including early insects, transitioned to around 400 million years ago, with CHCs forming a barrier that minimizes loss through the epicuticle. In species, variations in CHC chain length and branching explain much of the differences in desiccation tolerance, with longer methyl-branched CHCs in arid-adapted lineages enhancing survival in dry conditions. These modifications, building on the basic chitin-protein structure, provided mechanical support and protection while enabling insects to thrive in diverse terrestrial habitats without constant access to . The co-evolution of insects with angiosperms following the Cretaceous period further propelled insect diversification through specialized herbivory and pollination interactions. Angiosperm radiation during the Early Cretaceous (125–90 million years ago) initiated the Cretaceous Terrestrial Revolution, but post-Cretaceous dynamics, particularly the Angiosperm Terrestrial Revolution (100–50 million years ago), amplified insect origination rates while mitigating extinctions. Fossil evidence from around 99 million years ago shows early pollination syndromes, with insects like bees and butterflies developing morphological and behavioral specializations for angiosperm pollen transfer, while herbivorous clades adapted to exploit new plant tissues and defenses. This reciprocal evolution, evident in orders such as Lepidoptera and Diptera, linked insect family richness peaks to angiosperm dominance, fostering biodiversity through mutual dependencies.

Physical Structure

External morphology

The external morphology of insects is characterized by a chitinous exoskeleton that provides support and protection, divided into three main tagmata: the head, thorax, and abdomen. This exoskeleton, known as the cuticle, consists of multiple layers and is periodically shed during molting to allow for growth. The head is a hardened capsule formed by sclerites, which are chitinous plates fused together, enclosing sensory organs and mouthparts. Insect mouthparts exhibit diverse modifications adapted to feeding habits; for instance, chewing mouthparts feature laterally moving mandibles for biting and grinding solid food, as seen in grasshoppers, while piercing-sucking types involve stylets that penetrate tissues to extract liquids, typical in aphids. Antennae, paired appendages on the head, vary in shape for sensory functions; filiform antennae are thread-like with uniform segments, common in ground beetles, whereas clubbed forms widen distally, as in butterflies with capitate or clavate types. The thorax comprises three segments—the prothorax, mesothorax, and metathorax—each bearing a pair of legs and, in pterygotes, wings attached to the meso- and metathorax. Legs are segmented appendages consisting of the coxa (basal segment attached to the ), trochanter, femur (largest segment), tibia, and tarsus (distal foot-like portion, often with claws). Wings, when present, are typically membranous with intricate venation patterns formed by chitinous veins that reinforce the structure and aid in species identification; for example, dragonflies display extensive branching veins, while have reduced venation in scaled wings. The is a flexible region typically composed of 11 segments, each with dorsal terga and ventral sclerites connected by intersegmental membranes for expansion during feeding or . In many , the terminal segments bear cerci, sensory appendages that detect vibrations or chemicals, and females often possess an , a specialized for depositing eggs into substrates. The , the outermost layer enveloping the body, is secreted by the underlying epidermal cells and divided into the epicuticle and procuticle. The epicuticle is a thin, waxy outer coating with sublayers including a layer, layer, and inner epicuticle, primarily functioning to prevent ; studies show variations in wax composition influence water loss rates across species and habitats. The procuticle, beneath the epicuticle, comprises an exocuticle (sclerotized for rigidity via protein tanning) and endocuticle (flexible, containing microfibrils in a protein matrix), providing mechanical strength. Molting, or , occurs when the old splits along predetermined lines, allowing the insect to emerge and expand a new, soft that hardens over hours to days, enabling growth in a rigid .

Internal organ systems

Insects possess a diverse array of internal organ systems adapted for efficient physiological function within their exoskeleton-constrained bodies. These systems facilitate essential processes such as nutrient processing, , circulation, neural coordination, and , often differing markedly from those in vertebrates due to the insects' open circulatory design and segmented architecture. The of insects is decentralized and comprises a dorsal located in the head, a ventral nerve cord running along the ventral body surface, and segmental ganglia that serve as local processing centers. The integrates sensory inputs and coordinates complex behaviors, while the ventral nerve cord connects the to fused thoracic and abdominal ganglia, allowing for rapid reflex responses in each body segment. This structure enables efficient control over locomotion and environmental interactions without a centralized . Visual processing is handled by compound eyes and ocelli, which interface directly with the . Compound eyes consist of numerous ommatidia, each functioning as an independent optical unit with a corneal lens, crystalline , and photoreceptor cells that detect light via rhabdomeric phototransduction, providing wide-angle vision suited for motion detection. Ocelli, simpler dorsal eyes with a single lens and fewer photoreceptors, primarily sense light intensity and horizon orientation to aid in flight stabilization. The digestive system forms a complete tubular alimentary canal divided into , , and regions, each with specialized roles in , nutrient absorption, and waste elimination. The , lined with , includes the , , , crop for storage, and proventriculus for grinding; the is the primary site of enzymatic and absorption, often protected by a peritrophic membrane; and the reabsorbs water and ions from wastes before expulsion via the . Malpighian tubules, blind-ending structures arising at the midgut-hindgut junction, function in by filtering to remove nitrogenous wastes like , which are then processed in the for efficient in terrestrial environments. Circulation relies on an open system where nutrient-rich hemolymph bathes tissues directly within the hemocoel cavity, pumped by a dorsal vessel that acts as both heart and aorta. The posterior abdominal portion functions as the heart, with ostia (valved openings) allowing hemolymph entry during diastole, while muscular contractions propel it anteriorly through the vessel; the anterior thoracic aorta distributes it forward before it diffuses back. Hemolymph, comprising plasma, hemocytes for immunity, and minimal respiratory pigments, lacks hemoglobin and relies on body movements and accessory pumps for circulation, ensuring oxygen and nutrient delivery despite low pressure. Respiration occurs via a tracheal system of air-filled tubes that deliver oxygen directly to cells, bypassing blood transport. External spiracles on the and open into tracheae, which branch into finer tracheoles penetrating tissues; gas exchange happens by across thin tracheole walls, driven by concentration gradients and enhanced in active insects by abdominal pumping or spiracle . This system supports high metabolic rates during flight, with spiracles often valved to minimize water loss, achieving efficient O₂ uptake comparable to lungs in small-bodied insects. The includes paired ovaries or testes in the , producing gametes, along with accessory glands that secrete supportive fluids. In females, ovaries consist of ovarioles where oocytes develop, maturing into eggs released via oviducts to a genital chamber; accessory glands produce proteins, adhesives, or protective coatings. Males have testes forming spermatocytes that mature into sperm stored in , transferred via ejaculatory ducts with contributions from accessory glands for formation. Endocrine regulation involves , a from prothoracic glands that triggers and egg maturation, and juvenile hormone from corpora allata, which modulates reproductive development and prevents premature in adults.

Reproduction and Growth

Mating and fertilization

While the majority of insects reproduce sexually, some species are capable of through , in which unfertilized eggs develop into offspring, typically females. This mode is common in , which use cyclical to rapidly increase populations during favorable conditions, and in certain stick insects (), where females produce all-female broods without males. Insects exhibit diverse behaviors that ensure successful , primarily involving where sperm is transferred from males to females during copulation. rituals play a crucial role in mate attraction and selection, often relying on chemical, visual, or auditory signals to synchronize . These behaviors vary widely across , reflecting adaptations to environmental and ecological pressures. Courtship in many insects begins with pheromones, volatile chemicals released by one sex to attract over distances. For instance, moths release sex pheromones that guide males to potential mates using olfactory cues. In honey bees (Apis mellifera), virgin queens produce pheromones during nuptial flights that draw drones to mating congregations, facilitating airborne copulation. Visual and behavioral displays complement these signals; male fireflies (Photinus species) emit species-specific bioluminescent flashes in patterned sequences to court females, with receptive females responding via flashes to indicate acceptance. Similarly, male fruit flies (Drosophila melanogaster) perform elaborate dances involving wing vibrations and leg taps to stimulate females during . Insect mating systems range from to , though —where individuals mate with multiple partners—is predominant, allowing for higher reproductive output in resource-limited environments. occurs rarely, often in species with high paternal investment like certain burying beetles, but most insects, such as and , engage in promiscuous mating to maximize in . transfer typically occurs via direct through genitalia or indirectly via a , a proteinaceous packet containing and nutrients produced by . In lepidopterans like moths, the is deposited in the female's reproductive tract during copulation, providing both genetic material and sustenance to enhance egg production. Fertilization is invariably internal in insects, with stored in spermathecae for delayed use in egg fertilization. A notable variation is , observed in bed bugs (), where males pierce the 's abdominal wall with a specialized paramere to inject directly into the hemocoel, bypassing the genital tract. This coercive strategy incurs costs to females, including injury and , but has led to counter-adaptations like the spermalege, a specialized organ that reduces damage. Variations in during mating include short-term mate guarding and nuptial gifts, which provide immediate benefits to females without extending to prolonged offspring care. In some bush crickets, males transfer spermatophores containing nutritious that females digest to boost , representing a form of paternal investment that influences female remating decisions. Males in species like the green lacewing may guard females post-copulation to prevent from rival males, ensuring higher paternity success. These strategies highlight the evolutionary trade-offs in insect reproduction, balancing male reproductive assurance with female control over fertilization.

Developmental stages and metamorphosis

Insects exhibit a remarkable diversity in their developmental processes, primarily categorized into three types of metamorphosis: ametabolous, hemimetabolous, and holometabolous. These variations reflect evolutionary adaptations in life cycle strategies, allowing insects to occupy diverse ecological niches. Ametabolous development represents the most primitive form, with no distinct metamorphic stages, while hemimetabolous and holometabolous forms involve increasing degrees of transformation between juvenile and adult phases. Ametabolous development, seen in primitive orders such as (e.g., ), involves direct growth without significant morphological changes between juveniles and adults. Juveniles hatch from eggs resembling miniature adults and undergo multiple molts throughout life, with adults continuing to molt periodically to replace worn exoskeletons. This pattern lacks a pupal stage or major restructuring, emphasizing continuous growth rather than transformation. Hemimetabolous, or incomplete, metamorphosis occurs in orders like (e.g., grasshoppers) and (e.g., true bugs), featuring , , and stages. Nymphs emerge from and closely resemble adults in form and habitat but are wingless and sexually immature initially. Through successive molts—typically 4 to 8 —nymphs gradually develop wings, genitalia, and other adult features, with each becoming progressively more -like. The final molt produces a fully winged, reproductive , without a quiescent pupal phase. Holometabolous, or complete, metamorphosis is the most derived and widespread pattern, found in over 80% of insect species, including Coleoptera (beetles) and (butterflies). It encompasses four distinct stages: , , , and . Larvae hatch as worm-like, feeding specialists often dissimilar to adults, undergoing several molts to grow while remaining in the larval form. The prepupal molt leads to the pupal stage, a non-feeding, immobile phase where extensive tissue remodeling occurs—larval structures histolyze, and adult organs differentiate from imaginal discs. The ecloses from the fully formed, with wings, reproductive organs, and other mature features. For instance, in butterflies like Danaus plexippus (), the feeds voraciously before pupating into a chrysalis, emerging as a winged capable of migration. This separation of feeding (larval) and reproductive () phases enhances resource partitioning. These metamorphic processes are tightly regulated by hormones, primarily and (JH). , a produced by the prothoracic glands, initiates molting and metamorphic changes by triggering cascades that lead to apolysis ( separation) and new formation. In all insect types, pulses of drive each molt. JH, a sesquiterpenoid secreted by the corpora allata, modulates the response to : high levels maintain juvenile characteristics and prevent premature , while declining levels allow to promote differentiation. In ametabolous and hemimetabolous insects, JH persists through most molts but drops before the final molt; in holometabolous forms, JH is low during the larval-to-pupal transition, enabling complete restructuring. Disruptions in this hormonal balance, such as altered JH titers, can lead to developmental anomalies like extra larval instars or failed .

Behavioral Patterns

Communication methods

Insects employ a diverse array of communication methods to interact with conspecifics, including chemical, visual, auditory, and tactile signals, which facilitate coordination in , , and social behaviors. These modalities are adapted to the insects' sensory capabilities and environmental constraints, often overlapping in function to enhance signal reliability. Pheromones represent the primary chemical communication channel in insects, consisting of volatile or contact semiochemicals that elicit specific behavioral or physiological responses. pheromones, such as those released by or during threats, trigger rapid escape or defensive aggregation among nearby individuals. Sex pheromones, crucial for mate attraction, are exemplified by bombykol (E,Z)-10,12-hexadecadien-1-ol, a 16-carbon alcohol produced by female silkworms () that stimulates males to initiate flights over long distances. Trail pheromones, laid by social insects like , guide colony members to food sources; for instance, the (Linepithema humile) uses a blend of hydrocarbons to mark persistent foraging paths. These pheromones are detected via specialized antennal sensilla, with structures varying by type—e.g., bombykol binds to odorant receptors in antennae to activate neural signaling. Visual signals in insects often rely on color patterns and movements visible under daylight or low-light conditions, serving to attract mates or deter rivals. Wing patterns, such as the iridescent scales on wings or the eyespots on hindwings, convey species identity or warning signals during courtship displays. provides a striking visual cue in certain beetles, notably fireflies (family Lampyridae), where light is produced through the oxidation of catalyzed by in photocytes, emitting flashes in species-specific patterns to synchronize . This reaction yields a cold light peaking at around 560 nm, efficient for nocturnal communication without significant heat loss. Auditory communication involves the production and detection of airborne sounds or substrate-borne vibrations, enabling interactions over short to medium ranges. , a common mechanism, occurs when body parts are rubbed together; in crickets (), males rub their forewings to produce chirps via file-and-scraper structures, with the song's frequency and pulse rate signaling fitness to females. Substrate vibrations, transmitted through or soil, are used by insects like leafhoppers, where organs generate pulses detected by subgenual organs in the legs, facilitating mate location or aggregation. These signals are particularly effective in dense vegetation where visual cues are obscured. Tactile communication manifests through direct physical contact, often involving antennae or body grooming to exchange information in close proximity. Antennation, where insects touch antennae to one another, allows social species like bees to transfer pheromonal cues or assess colony status, as seen in honeybees (Apis mellifera) during trophallaxis. Grooming behaviors, such as mutual antennal cleaning in termites, reinforce social bonds and distribute alarm signals within nests. These methods are integral to maintaining cohesion in eusocial groups, though they also play roles in broader interactions like mating recognition.

Social structures

Insects exhibit a range of social structures, from solitary living to highly organized colonial societies, with representing the most complex form observed primarily in the orders (, , and wasps) and Isoptera (). species are characterized by cooperative brood care, overlapping generations, and a reproductive division of labor where most individuals forgo personal reproduction to support the . In these societies, distinct castes emerge, including queens or kings dedicated to reproduction, sterile workers focused on , nest maintenance, and brood rearing, and soldiers specialized for defense against intruders. For instance, in , soldiers possess enlarged mandibles for combat, while in and , workers often display morphological adaptations like reduced wings or enhanced sensory organs suited to their tasks. The evolution of altruism in eusocial insects, where non-reproductive castes sacrifice their fitness to benefit relatives, is explained by theory, as formalized by . This theory posits that such behaviors spread if the genetic relatedness (rr) between altruist and beneficiary, multiplied by the fitness benefit (BB) to the beneficiary, exceeds the fitness cost (CC) to the altruist, expressed as Hamilton's rule: rB>CrB > C. In , haplodiploid sex determination results in sisters sharing 75% of their genes on average, elevating rr and favoring worker sterility to promote queens' offspring production. This mechanism underpins the stability of castes, as workers gain indirect fitness through aiding close kin rather than reproducing themselves. While many insects are solitary, relying on individual efforts for survival and reproduction without cooperative interactions, colonial species like honeybees (Apis mellifera) demonstrate advanced eusocial organization through temporal division of labor. In honeybee hives, workers progress from in-hive duties such as nursing larvae and cleaning to foraging outside as they age, optimizing colony efficiency and resource allocation. This contrasts with solitary bees, which lack castes and perform all tasks independently, highlighting how eusociality enhances colony resilience against environmental pressures. Beyond , non-eusocial insects form temporary aggregations for mutual benefit, as seen in bark beetles (family , subfamily Scolytinae). These beetles, which are otherwise solitary, release aggregation pheromones during host colonization, drawing conspecifics to amplify attack success on defended by overwhelming tree defenses through mass infestation. Such groupings facilitate and exploitation without permanent castes or reproductive suppression, relying instead on chemical signals to coordinate transient assemblies.

Modes of locomotion

Insects employ diverse modes of locomotion adapted to terrestrial, aerial, and aquatic environments, leveraging specialized anatomical features for efficient movement. These include walking on varied surfaces, for escape or predation, through water via mechanisms, and flight powered by oscillatory wing motions. Each mode relies on integrated musculoskeletal systems that enable rapid, energy-efficient travel across scales from millimeters to meters. Flight in insects is primarily achieved through the rapid oscillation of wings, driven by two main muscle types: synchronous and asynchronous. In synchronous flight muscles, each contraction is directly triggered by a neural impulse, limiting wingbeat frequencies to 5–50 Hz in larger insects like and locusts. Asynchronous muscles, prevalent in flies and bees, operate via stretch-activation where a single neural input initiates multiple contractions through mechanical feedback, enabling wingbeat frequencies exceeding 100 Hz and up to 200 Hz in species such as . For instance, fruit fly motor neurons fire at approximately 5 Hz, yet asynchronous muscles generate 200 Hz oscillations for sustained flight. Wing morphology, with flexible hinges and varying vein patterns, further optimizes aerodynamic forces during these beats. Walking is the most common in insects, often utilizing an alternating for stability and speed. In this pattern, three legs—one foreleg and hindleg from one side, plus the middle leg from the opposite side—remain in contact with the substrate while the other three swing forward, maintaining balance even on uneven terrain. exemplify this , transitioning from slow ambling to fast trotting while sustaining the tripod coordination up to speeds of 1.5 body lengths per second. For vertical on smooth surfaces, many insects rely on adhesive setae—microscopic, hair-like structures on their tarsi that exploit van der Waals forces for attachment. These setae, angled and compliant in flies and beetles, allow reversible without residue, supporting body weights on ceilings or walls. Aquatic locomotion varies by species, with surface-dwelling insects like water striders (Gerridae) using hydrofuge hairs to exploit . These hydrophobic microhairs, numbering thousands per square millimeter on legs and body, trap air and repel , enabling the insects to stride across films at speeds up to 1.5 meters per second without breaking the surface. In submerged environments, certain larvae employ for rapid movement. larvae (Anisoptera), for example, fill a rectal chamber with and expel it forcefully through the anus at frequencies up to 2.2 cycles per second, achieving bursts of for predation or evasion. Jumping serves as a burst locomotion mode for escaping threats or capturing prey, often powered by elastic energy storage. Fleas (Siphonaptera) utilize a catapult mechanism in their hind legs, where the trochanteral extensor muscle compresses a pad—a rubber-like protein with high elasticity—storing energy before rapid release. This enables jumps up to 150 times body length, with launch accelerations exceeding 100 g, far surpassing direct muscle-powered leaps.

Ecological Roles

Habitats and environmental adaptations

Insects predominantly occupy terrestrial habitats, where their serves as a primary barrier against , particularly in arid environments. The is coated with hydrocarbons and waxes that form a hydrophobic layer, drastically reducing evaporative loss through . In desert-dwelling tenebrionid beetles, such as Onymacris plana, this cuticular permeability is exceptionally low, enabling the insects to prioritize hemolymph dehydration over vital tissue loss during prolonged exposure to dry conditions. Similarly, species like Rhytinota praelonga regulate body fluid volumes effectively in hyper-arid zones through enhanced wax deposition, which correlates with their survival in environments where relative humidity often falls below 20%. These adaptations underscore the terrestrial dominance of insects, with over 90% of known species restricted to land-based ecosystems despite their ancient aquatic origins. Aquatic habitats host a diverse array of insects, especially in larval stages, supported by specialized respiratory mechanisms to extract oxygen from water. nymphs (: Anisoptera) feature internal -like structures within the rectal chamber, where jet-propelled water currents facilitate passive of dissolved oxygen across thin epithelial linings. This not only sustains respiration but also aids in rapid escape from predators via abdominal pumping. Predaceous diving beetles (Coleoptera: ), in contrast, rely on air bubbles trapped beneath their elytra or by hydrofuge hairs on the ventral surface, creating a "physical " that allows oxygen replenishment from surrounding water until the bubble diminishes due to . Such innovations enable these insects to exploit freshwater systems ranging from stagnant ponds to fast-flowing streams, where oxygen levels vary widely. Insects exhibit profound thermal and altitudinal tolerances, often through physiological and biochemical defenses against cold stress. , a hormonally induced in development, allows overwintering by suppressing , ceasing feeding, and directing toward protective sites like or ; for example, the (Ostrinia nubilalis) enters as a fifth-instar to endure subzero temperatures. Freeze-tolerant species, such as the (Eurosta solidaginis), accumulate cryoprotectants like and proteins—comprising up to 30% of body weight—to nucleate extracellular ice while preserving in intracellular fluids, preventing lethal crystal damage at temperatures as low as -40°C. These mechanisms facilitate colonization of high-altitude montane zones and polar fringes, where seasonal extremes challenge survival. Urban and extreme anthropogenic habitats have become refugia for resilient insect species, particularly invasive peridomestic pests. (Blattodea), such as the (Blattella germanica), thrive in human structures by exploiting warm, humid microenvironments like kitchen crevices and basements, where they navigate cracks as narrow as 1/16 inch and forage nocturnally on organic debris. Their rapid —yielding over 30,000 offspring per female annually—and tolerance to fluctuating temperatures and low humidity enable persistence in diverse built environments, from apartments to hospitals. This adaptability highlights insects' capacity to invade novel, resource-rich niches altered by human activity.

Interactions in ecosystems

Insects serve as pivotal agents in ecosystem dynamics, particularly through their roles in pollination, where they facilitate the reproduction of numerous plant species via mutualistic interactions. Approximately 85–90% of the world's angiosperms depend on animal pollinators, with insects such as bees comprising the majority of these vectors, transferring pollen between flowers in exchange for nectar and pollen rewards. This process underpins food webs by enabling seed and fruit production, supporting higher trophic levels. However, ongoing insect population declines, driven by habitat loss and climate change as of 2025, are reducing pollination services and threatening plant diversity. Coevolutionary mutualisms between insects and plants have shaped biodiversity, with specialized floral traits evolving alongside pollinator behaviors over millions of years, as evidenced in tropical communities where functional specialization is pronounced. Decomposition by insects accelerates cycling, transforming organic into forms accessible to and microorganisms. and together, particularly in tropical ecosystems, represent about one-third of animal and drive bioturbation, mobilizing carbon, , and through the breakdown of and , thereby enhancing . Flies, including blowflies and flesh flies, act as primary colonizers of carrion, with their larvae rapidly consuming tissues and releasing s into the , which alters local and concentrations to support microbial activity and growth. Overall, insect-mediated can increase rates by up to 44% in tropical rainforests, preventing lockup and maintaining . In food webs, insects occupy diverse trophic positions, with herbivory and predation influencing across levels. Herbivorous insects like function as primary consumers, feeding on sap and exerting selective pressure on , often acting as pests that reduce yields while channeling energy upward. Predators such as ladybird beetles (ladybugs) occupy higher trophic levels as secondary consumers, effectively controlling populations by consuming over 50% in controlled settings, thereby stabilizing herbivore outbreaks and preserving . These interactions exemplify top-down regulation, where predators mitigate impacts, fostering balanced energy flow from producers to consumers. Symbiotic relationships further amplify insects' ecosystem contributions, notably in where gut microbes enable the digestion of recalcitrant . In wood-feeding like Nasutitermes species, diverse bacterial communities—including Firmicutes such as Clostridium termitidis and Spirochaetes—produce lignocellulolytic enzymes that break down cell walls, converting up to 45% of substrates like wheat straw into bioavailable carboxylates such as . This mutualism allows to access nutrients from lignocellulose, recycling them into soil via , and highlights the prokaryotic microbiome's role in sustaining detrital pathways.

Defense mechanisms

Insects employ a diverse array of defense mechanisms to deter predators and evade threats, enhancing their in competitive environments. These strategies range from physical concealment and behavioral s to and visual warnings, often evolving in response to specific ecological pressures. Such mechanisms not only protect individuals but also contribute to the resilience of insect populations across taxa. Cryptic allows insects to blend seamlessly into their surroundings, reducing detection by predators. For instance, many katydids exhibit leaf mimicry, where their body morphology and coloration imitate foliage, including veins and edges, to avoid visual predation. This is particularly effective in diurnal , as evidenced by studies on Panacanthus in neotropical forests. , another form of , involves darker dorsal surfaces and lighter ventral ones, creating a flattened appearance against backgrounds and minimizing shadows that could reveal the insect's outline. This principle is observed in stick insects and grasshoppers, where it counters the overhead light typical of open habitats. Chemical defenses provide insects with potent means to repel or harm attackers through the production or sequestration of toxins. Monarch butterflies (Danaus plexippus) exemplify this by sequestering cardenolides from milkweed plants during their larval stage, rendering adults unpalatable or toxic to vertebrates like birds. This sequestration not only deters predation but also persists through , with empirical tests showing reduced attack rates on dosed models. Other insects, such as bombardier beetles, synthesize their own irritants, ejecting hot sprays from abdominal glands to startle predators. Behavioral defenses enable rapid responses to immediate threats without relying on morphology or chemistry. Autotomy, the voluntary detachment of appendages like legs, is common in spiders and insects such as , allowing escape from grasping predators while the discarded limb distracts the attacker. Regrowth occurs in subsequent molts, though at an energetic cost. Thanatosis, or feigning death, involves insects like certain ground beetles assuming a rigid, immobile posture to mimic carrion, exploiting predators' aversion to spoiled prey; this tactic is triggered by tactile or vibrational cues and can last minutes to hours. Aposematism uses conspicuous warning signals to advertise defenses, promoting predator learning and avoidance. Ladybugs (Coccinellidae) display bold red-and-black patterns paired with alkaloid-based unpalatability, where bitter deters feeding; field experiments confirm that predators like birds quickly associate these colors with distastefulness after initial encounters. This strategy often evolves alongside , where harmless species copy the signals of defended models to gain protection. Chemical signals, such as alarm pheromones, may reinforce by alerting conspecifics to dangers.

Human Interactions

Agricultural and medical impacts

Insects exert profound negative influences on global agriculture through direct crop damage, post-harvest losses, and ecosystem disruptions caused by invasive species. Among the most devastating are locust swarms, which can rapidly consume vast areas of vegetation; the 2020 East African desert locust upsurge, the worst in decades, affected over 21 million people by destroying crops and pastures across Ethiopia, Kenya, Somalia, and other nations, leading to vegetation and crop losses of 42% to 69% in vulnerable regions. Similarly, the boll weevil (Anthonomus grandis) has historically ravaged cotton production in the southeastern United States; following its arrival in 1892, it caused cotton yields to plummet by up to 50% within five years of infestation in affected counties, reducing total acreage from 5.2 million to 2.6 million acres between 1914 and 1923. Stored product pests, such as grain weevils ( spp.), further compound agricultural losses by infesting harvested commodities during storage, resulting in quality degradation and quantity reductions. These insects are responsible for an estimated 10% of global production losses annually, with developing countries experiencing up to one-third of their stored destroyed each year due to such infestations. The economic toll is substantial, contributing to billions in global losses through direct damage, contamination, and the costs of control measures. Invasive insect species amplify these agricultural threats by targeting native and resources. The (Agrilus planipennis), introduced from , has killed hundreds of millions of ash trees across since its detection in 2002, with larval feeding tissue and causing mortality in as little as two years for infested trees. This devastation threatens urban and rural landscapes, with potential losses to the U.S. timber industry alone exceeding $10 billion from the estimated 7.5 billion ash trees at risk. Beyond agriculture, insects pose significant medical risks as vectors for debilitating diseases, transmitting pathogens that affect human health on a massive scale. Mosquitoes, particularly Anopheles species, are primary vectors for malaria, caused by Plasmodium parasites; in 2023, this disease resulted in 263 million cases and 597,000 deaths worldwide, predominantly in sub-Saharan Africa. Ticks, such as the blacklegged tick (Ixodes scapularis), transmit Lyme disease via Borrelia burgdorferi bacteria during prolonged feeding, with transmission typically requiring 24-48 hours of attachment; in the United States, this leads to over 476,000 estimated cases annually, causing symptoms ranging from fever and rash to severe neurological complications if untreated. These vector-borne illnesses not only strain healthcare systems but also incur substantial economic burdens through treatment, lost productivity, and preventive efforts.

Beneficial uses and conservation

Insects provide essential services to human agriculture and ecosystems, most notably through pollination, which supports the production of fruits, vegetables, and nuts. Globally, insect pollinators, particularly bees, contribute an estimated $235–$577 billion annually (as of 2025) to crop values by facilitating the reproduction of approximately 75% of leading food crops. This economic valuation underscores the irreplaceable role of insects in sustaining food security, as their decline could disrupt yields of key commodities like coffee, cocoa, and almonds. Another critical beneficial use involves biological control, where predatory or parasitic insects are deployed to manage pest populations without synthetic chemicals. Trichogramma wasps, tiny egg parasitoids, exemplify this approach by targeting the eggs of lepidopteran pests such as moths and butterflies that damage crops like corn, , and . These wasps have been mass-reared and released in biological control programs worldwide, including in and the , reducing pest infestations by up to 90% in some field trials while minimizing environmental harm from pesticides. Despite these benefits, insect populations face severe conservation challenges, with over 40% of threatened by due primarily to loss from and , as well as exposure. As of 2025, studies continue to report that over 40% of insect face extinction risks due to these factors. insecticides, widely used in farming, exacerbate these declines by impairing insect navigation, reproduction, and immunity, leading to reduced abundances of bees, , and even at sublethal doses. The 2019 IPBES Global Assessment highlighted that around 1 million overall, including a significant portion of insects, are at risk of within decades, driven by these anthropogenic pressures. Conservation initiatives aim to mitigate these threats through habitat protection and restoration. For instance, the in , a spanning over 56,000 hectares, safeguards critical overwintering grounds for monarch butterflies (Danaus plexippus), supporting their migration and breeding while promoting sustainable . In , programs like those from the U.S. Fish and Wildlife Service and provide incentives for landowners to create milkweed-rich habitats, helping counter the 80-90% decline in eastern monarch populations since the . These efforts emphasize integrated strategies, such as reducing use and enhancing connectivity between protected areas, to bolster insect resilience amid ongoing environmental changes.

Cultural and scientific significance

Insects have held profound cultural significance across civilizations, often symbolizing transformation, rebirth, and the divine. In , the () represented the sun god , embodying the cycle of renewal as the beetle was observed rolling dung balls, mirroring the sun's daily journey across the sky. , with their metamorphic life cycle, have appeared in global folklore as emblems of the soul and spiritual change; in tradition, the term "psyche" denoted both the human soul and the , linking the insect to immortality and the afterlife. Humans have long derived valuable products from insects, integrating them into economies and industries. Silkworms () produce , a harvested from cocoons that has been central to production for millennia, originating in ancient around 3500 BCE. Honeybees (Apis mellifera) yield and , used since prehistoric times for food, medicine, and candles, with serving as a natural sweetener and antimicrobial agent. Cochineal insects (Dactylopius coccus) provide , extracted to create the vibrant red dye , which colored textiles, cosmetics, and foods in Mesoamerican cultures and later globally. Lac bugs (Kerria lacca) secrete resin processed into , a versatile coating for wood finishes, pharmaceuticals, and varnishes, dating back to ancient . Over 2,200 insect are consumed worldwide as , offering a sustainable protein source amid growing global demand. Crickets (Acheta domesticus), for instance, contain approximately 60-70% protein by dry weight, surpassing many traditional meats in completeness and providing essential micronutrients like iron and . In scientific research, insects serve as pivotal model organisms; the fruit fly has been instrumental in since Thomas Hunt Morgan's 1910 experiments, enabling discoveries in , , and that earned Nobel Prizes. Recent advances in , such as CRISPR-Cas9 applications in mosquitoes (), have progressed in 2025 to develop self-limiting gene drives that induce female sterility to curb transmission without permanent ecological alteration. Biomimicry draws from insect behaviors for innovation, with — inspired by trails in like Argentine ants (Linepithema humile)—applied in for efficient path planning and swarm coordination since their introduction in 1992.

References

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