Insect

For other uses, see Insect (disambiguation).

Insect
Temporal range: 396–0 Ma

Early Devonian[1] (but see text)–Present

Clockwise from top left: dance fly (Empis livida), long-nosed weevil (Rhinotia hemistictus), mole cricket (Gryllotalpa brachyptera), German wasp (Vespula germanica), emperor gum moth (Opodiphthera eucalypti), assassin bug (Harpactorinae)
A chorus of several Magicicada species
Scientific classification
Kingdom: Animalia
Phylum: Arthropoda
Clade: Pancrustacea
Subphylum: Hexapoda
(unranked): Ectognatha
Class: Insecta
Linnaeus, 1758
Subgroups

See text.

Insects (from Latin insectum, a calque of Greek ἔντομον [éntomon], "cut into sections") are a class of invertebrates within the arthropod phylum that have a chitinous exoskeleton, a three-part body (head, thorax and abdomen), three pairs of jointed legs, compound eyes and one pair of antennae. They are the most diverse group of animals on the planet, including more than a million described species and representing more than half of all known living organisms.[2][3] The number of extant species is estimated at between six and ten million,[2][4][5] and potentially represent over 90% of the differing animal life forms on Earth.[6] Insects may be found in nearly all environments, although only a small number of species reside in the oceans, a habitat dominated by another arthropod group, crustaceans.

The life cycles of insects vary but most hatch from eggs. Insect growth is constrained by the inelastic exoskeleton and development involves a series of molts. The immature stages can differ from the adults in structure, habit and habitat, and can include a passive pupal stage in those groups that undergo 4-stage metamorphosis (see holometabolism). Insects that undergo 3-stage metamorphosis lack a pupal stage and adults develop through a series of nymphal stages.[7] The higher level relationship of the Hexapoda is unclear. Fossilized insects of enormous size have been found from the Paleozoic Era, including giant dragonflies with wingspans of 55 to 70 cm (22–28 in). The most diverse insect groups appear to have coevolved with flowering plants.

Adult insects typically move about by walking, flying or sometimes swimming (see § Locomotion below). As it allows for rapid yet stable movement, many insects adopt a tripedal gait in which they walk with their legs touching the ground in alternating triangles. Insects are the only invertebrates to have evolved flight. Many insects spend at least part of their lives under water, with larval adaptations that include gills, and some adult insects are aquatic and have adaptations for swimming. Some species, such as water striders, are capable of walking on the surface of water. Insects are mostly solitary, but some, such as certain bees, ants and termites, are social and live in large, well-organized colonies. Some insects, such as earwigs, show maternal care, guarding their eggs and young. Insects can communicate with each other in a variety of ways. Male moths can sense the pheromones of female moths over great distances. Other species communicate with sounds: crickets stridulate, or rub their wings together, to attract a mate and repel other males. Lampyridae in the beetle order communicate with light.

Humans regard certain insects as pests, and attempt to control them using insecticides and a host of other techniques. Some insects damage crops by feeding on sap, leaves or fruits. A few parasitic species are pathogenic. Some insects perform complex ecological roles; blow-flies, for example, help consume carrion but also spread diseases. Insect pollinators are essential to the life-cycle of many flowering plant species on which most organisms, including humans, are at least partly dependent; without them, the terrestrial portion of the biosphere (including humans) would be devastated.[8] Many other insects are considered ecologically beneficial as predators and a few provide direct economic benefit. Silkworms and bees have been used extensively by humans for the production of silk and honey, respectively. In some cultures, people eat the larvae or adults of certain insects.

Etymology

The word "insect" comes from the Latin word insectum, meaning "with a notched or divided body", or literally "cut into", from the neuter singular perfect passive participle of insectare, "to cut into, to cut up", from in- "into" and secare "to cut";[9] because insects appear "cut into" three sections. Pliny the Elder introduced the Latin designation as a loan-translation of the Greek word ἔντομος (éntomos) or "insect" (as in entomology), which was Aristotle's term for this class of life, also in reference to their "notched" bodies. "Insect" first appears documented in English in 1601 in Holland's translation of Pliny. Translations of Aristotle's term also form the usual word for "insect" in Welsh (trychfil, from trychu "to cut" and mil, "animal"), Serbo-Croatian (zareznik, from rezati, "to cut"), Russian (насекомое nasekomoje, from seč'/-sekat', "to cut"), etc.[9]

Phylogeny and evolution

Evolution has produced enormous variety in insects. Pictured are some of the possible shapes of antennae.
Main article: Evolution of insects

The evolutionary relationship of insects to other animal groups remains unclear.

Although traditionally grouped with millipedes and centipedes—possibly on the basis of convergent adaptations to terrestrialisation[10]—evidence has emerged favoring closer evolutionary ties with crustaceans. In the Pancrustacea theory, insects, together with Entognatha, Remipedia, and Cephalocarida, make up a natural clade labeled Miracrustacea.[11]

A report in November 2014 unambiguously places the insects in one clade, with the crustaceans and myriapods, as the nearest sister clades.[12] This study resolved insect phylogeny of all extant insect orders, and provides "a robust phylogenetic backbone tree and reliable time estimates of insect evolution."[12]

Other terrestrial arthropods, such as centipedes, millipedes, scorpions, and spiders, are sometimes confused with insects since their body plans can appear similar, sharing (as do all arthropods) a jointed exoskeleton. However, upon closer examination, their features differ significantly; most noticeably, they do not have the six-legged characteristic of adult insects.[13]




Hexapoda (Insecta, Collembola, Diplura, Protura)



Crustacea (crabs, shrimp, isopods, etc.)



Myriapoda

Pauropoda



Diplopoda (millipedes)



Chilopoda (centipedes)



Symphyla



Chelicerata

Arachnida (spiders, scorpions and allies)



Eurypterida (sea scorpions: extinct)



Xiphosura (horseshoe crabs)



Pycnogonida (sea spiders)




Trilobites (extinct)



A phylogenetic tree of the arthropods and related groups[14]

The higher-level phylogeny of the arthropods continues to be a matter of debate and research. In 2008, researchers at Tufts University uncovered what they believe is the world's oldest known full-body impression of a primitive flying insect, a 300 million-year-old specimen from the Carboniferous period.[15] The oldest definitive insect fossil is the Devonian Rhyniognatha hirsti, from the 396-million-year-old Rhynie chert. It may have superficially resembled a modern-day silverfish insect. This species already possessed dicondylic mandibles (two articulations in the mandible), a feature associated with winged insects, suggesting that wings may already have evolved at this time. Thus, the first insects probably appeared earlier, in the Silurian period.[1][16]

Four super radiations of insects have occurred: beetles (evolved about 300 million years ago), flies (evolved about 250 million years ago), and moths and wasps (evolved about 150 million years ago).[17] These four groups account for the majority of described species. The flies and moths along with the fleas evolved from the Mecoptera.

The origins of insect flight remain obscure, since the earliest winged insects currently known appear to have been capable fliers. Some extinct insects had an additional pair of winglets attaching to the first segment of the thorax, for a total of three pairs. As of 2009, no evidence suggests the insects were a particularly successful group of animals before they evolved to have wings.[18]

Late Carboniferous and Early Permian insect orders include both extant groups, their stem groups,[19] and a number of Paleozoic groups, now extinct. During this era, some giant dragonfly-like forms reached wingspans of 55 to 70 cm (22 to 28 in), making them far larger than any living insect. This gigantism may have been due to higher atmospheric oxygen levels that allowed increased respiratory efficiency relative to today. The lack of flying vertebrates could have been another factor. Most extinct orders of insects developed during the Permian period that began around 270 million years ago. Many of the early groups became extinct during the Permian-Triassic extinction event, the largest mass extinction in the history of the Earth, around 252 million years ago.[20]

The remarkably successful Hymenoptera appeared as long as 146 million years ago in the Cretaceous period, but achieved their wide diversity more recently in the Cenozoic era, which began 66 million years ago. A number of highly successful insect groups evolved in conjunction with flowering plants, a powerful illustration of coevolution.[21]

Many modern insect genera developed during the Cenozoic. Insects from this period on are often found preserved in amber, often in perfect condition. The body plan, or morphology, of such specimens is thus easily compared with modern species. The study of fossilized insects is called paleoentomology.

Evolutionary relationships

Insects are prey for a variety of organisms, including terrestrial vertebrates. The earliest vertebrates on land existed 400 million years ago and were large amphibious piscivores. Through gradual evolutionary change, insectivory was the next diet type to evolve.[22]

Insects were among the earliest terrestrial herbivores and acted as major selection agents on plants.[21] 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.[23] This successful evolutionary pattern has also been used by mimics. Over time, this has led to complex groups of coevolved species. Conversely, some interactions between plants and insects, like pollination, are beneficial to both organisms. Coevolution has led to the development of very specific mutualisms in such systems.

Taxonomy

Classification
Insecta
Dicondylia
Pterygota

Cladogram of living insect groups,[24] with numbers of species in each group.[5] The Apterygota, Palaeoptera, and Exopterygota are possibly paraphyletic groups.

Traditional morphology-based or appearance-based systematics have usually given the Hexapoda the rank of superclass,[25]:180 and identified four groups within it: insects (Ectognatha), springtails (Collembola), Protura, and Diplura, the latter three being grouped together as the Entognatha on the basis of internalized mouth parts. Supraordinal relationships have undergone numerous changes with the advent of methods based on evolutionary history and genetic data. A recent theory is that the Hexapoda are polyphyletic (where the last common ancestor was not a member of the group), with the entognath classes having separate evolutionary histories from the Insecta.[26] Many of the traditional appearance-based taxa have been shown to be paraphyletic, so rather than using ranks like subclass, superorder, and infraorder, it has proved better to use monophyletic groupings (in which the last common ancestor is a member of the group). The following represents the best-supported monophyletic groupings for the Insecta.

Insects can be divided into two groups historically treated as subclasses: wingless insects, known as Apterygota, and winged insects, known as Pterygota. The Apterygota consist of the primitively wingless order of the silverfish (Thysanura). Archaeognatha make up the Monocondylia based on the shape of their mandibles, while Thysanura and Pterygota are grouped together as Dicondylia. The Thysanura themselves possibly are not monophyletic, with the family Lepidotrichidae being a sister group to the Dicondylia (Pterygota and the remaining Thysanura).[27][28]

Paleoptera and Neoptera are the winged orders of insects differentiated by the presence of hardened body parts called sclerites, and in the Neoptera, muscles that allow their wings to fold flatly over the abdomen. Neoptera can further be divided into incomplete metamorphosis-based (Polyneoptera and Paraneoptera) and complete metamorphosis-based groups. It has proved difficult to clarify the relationships between the orders in Polyneoptera because of constant new findings calling for revision of the taxa. For example, the Paraneoptera have turned out to be more closely related to the Endopterygota than to the rest of the Exopterygota. The recent molecular finding that the traditional louse orders Mallophaga and Anoplura are derived from within Psocoptera has led to the new taxon Psocodea.[29] Phasmatodea and Embiidina have been suggested to form the Eukinolabia.[30] Mantodea, Blattodea, and Isoptera are thought to form a monophyletic group termed Dictyoptera.[31]

The Exopterygota likely are paraphyletic in regard to the Endopterygota. Matters that have incurred controversy include Strepsiptera and Diptera grouped together as Halteria based on a reduction of one of the wing pairs – a position not well-supported in the entomological community.[32] The Neuropterida are often lumped or split on the whims of the taxonomist. Fleas are now thought to be closely related to boreid mecopterans.[33] Many questions remain in the basal relationships amongst endopterygote orders, particularly the Hymenoptera.

The study of the classification or taxonomy of any insect is called systematic entomology. If one works with a more specific order or even a family, the term may also be made specific to that order or family, for example systematic dipterology.

Diversity

Main article: Insect biodiversity

Though the true dimensions of species diversity remain uncertain, estimates range from 2.6–7.8 million species with a mean of 5.5 million.[34] This probably represents less than 20% of all species on Earth, and with only about 20,000 new species of all organisms being described each year, most species likely will remain undescribed for many years unless species descriptions increase in rate. About 850,000–1,000,000 of all described species are insects. Of the 24 orders of insects, four dominate in terms of numbers of described species, with at least 3 million species included in Coleoptera, Diptera, Hymenoptera and Lepidoptera. A recent study estimated the number of beetles at 0.9–2.1 million with a mean of 1.5 million.[34]

Comparison of the estimated number of species in the four most speciose insect orders
Described species Average description rate
(species per year)
Publication effort
Coleoptera 300,000–400,000 2308 0.01
Lepidoptera 110,000–120,000 642 0.03
Diptera 90,000–150,000 1048 0.04
Hymenoptera 100,000–125,000 1196 0.02

Morphology and physiology

External

Insect morphology
A- Head B- Thorax C- Abdomen
1. antenna
2. ocelli (lower)
3. ocelli (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. mid-gut (stomach)
14. dorsal tube (Heart)
15. ovary
16. hind-gut (intestine, rectum & anus)
17. anus
18. oviduct
19. nerve chord (abdominal ganglia)
20. Malpighian tubes
21. tarsal pads
22. claws
23. tarsus
24. tibia
25. femur
26. trochanter
27. fore-gut (crop, gizzard)
28. thoracic ganglion
29. coxa
30. salivary gland
31. subesophageal ganglion
32. mouthparts

Insects have segmented bodies supported by exoskeletons, the hard outer covering made mostly of chitin. The segments of the body are organized into three distinctive but interconnected units, or tagmata: a head, a thorax and an abdomen.[35] The head supports a pair of sensory antennae, a pair of compound eyes, and, if present, one to three simple eyes (or ocelli) and three sets of variously modified appendages that form the mouthparts. The thorax has six segmented legs—one pair each for the prothorax, mesothorax and the metathorax segments making up the thorax—and, none, two or four wings. The abdomen consists of eleven segments, though in a few species of insects, these segments may be fused together or reduced in size. The abdomen also contains most of the digestive, respiratory, excretory and reproductive internal structures.[25]:22–48 Considerable variation and many adaptations in the body parts of insects occur, especially wings, legs, antenna and mouthparts.

Segmentation

The head is enclosed in a hard, heavily sclerotized, unsegmented, exoskeletal head capsule, or epicranium, which contains most of the sensing organs, including the antennae, ocellus or eyes, and the mouthparts. Of all the insect orders, Orthoptera displays the most features found in other insects, including the sutures and sclerites.[36] Here, the vertex, or the apex (dorsal region), is situated between the compound eyes for insects with a hypognathous and opisthognathous head. In prognathous insects, the vertex is not found between the compound eyes, but rather, where the ocelli are normally. This is because the primary axis of the head is rotated 90° to become parallel to the primary axis of the body. In some species, this region is modified and assumes a different name.[36]:13

The thorax is a tagma composed of three sections, the prothorax, mesothorax and the metathorax. The anterior segment, closest to the head, is the prothorax, with the major features being the first pair of legs and the pronotum. The middle segment is the mesothorax, with the major features being the second pair of legs and the anterior wings. The third and most posterior segment, abutting the abdomen, is the metathorax, which features the third pair of legs and the posterior wings. Each segment is dilineated by an intersegmental suture. Each segment has four basic regions. The dorsal surface is called the tergum (or notum) to distinguish it from the abdominal terga.[25] The two lateral regions are called the pleura (singular: pleuron) and the ventral aspect is called the sternum. In turn, the notum of the prothorax is called the pronotum, the notum for the mesothorax is called the mesonotum and the notum for the metathorax is called the metanotum. Continuing with this logic, the mesopleura and metapleura, as well as the mesosternum and metasternum, are used.[36]

The abdomen is the largest tagma of the insect, which typically consists of 11–12 segments and is less strongly sclerotized than the head or thorax. Each segment of the abdomen is represented by a sclerotized tergum and sternum. Terga are separated from each other and from the adjacent sterna or pleura by membranes. Spiracles are located in the pleural area. Variation of this ground plan includes the fusion of terga or terga and sterna to form continuous dorsal or ventral shields or a conical tube. Some insects bear a sclerite in the pleural area called a laterotergite. Ventral sclerites are sometimes called laterosternites. During the embryonic stage of many insects and the postembryonic stage of primitive insects, 11 abdominal segments are present. In modern insects there is a tendency toward reduction in the number of the abdominal segments, but the primitive number of 11 is maintained during embryogenesis. Variation in abdominal segment number is considerable. If the Apterygota are considered to be indicative of the ground plan for pterygotes, confusion reigns: adult Protura have 12 segments, Collembola have 6. The orthopteran family Acrididae has 11 segments, and a fossil specimen of Zoraptera has a 10-segmented abdomen.[36]

Exoskeleton

The insect outer skeleton, the cuticle, is made up of two layers: the epicuticle, which is a thin and waxy water resistant outer layer and contains no chitin, and a lower layer called the procuticle. The procuticle is chitinous and much thicker than the epicuticle and has two layers: an outer layer known as the exocuticle and an inner layer known as the endocuticle. The tough and flexible endocuticle is built from numerous layers of fibrous chitin and proteins, criss-crossing each other in a sandwich pattern, while the exocuticle is rigid and hardened.[25]:22–24 The exocuticle is greatly reduced in many soft-bodied insects (e.g., caterpillars), especially during their larval stages.

Insects are the only invertebrates to have developed active flight capability, and this has played an important role in their success.[25]:186 Their muscles are able to contract multiple times for each single nerve impulse, allowing the wings to beat faster than would ordinarily be possible. Having their muscles attached to their exoskeletons is more efficient and allows more muscle connections; crustaceans also use the same method, though all spiders use hydraulic pressure to extend their legs, a system inherited from their pre-arthropod ancestors. Unlike insects, though, most aquatic crustaceans are biomineralized with calcium carbonate extracted from the water.[37][38]

Internal

Nervous system

The nervous system of an insect can be divided into a brain and a ventral nerve cord. The head capsule is made up of six fused segments, each with 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.[25]:57

The thoracic segments have one ganglion on each side, which are connected into a pair, one pair per segment. This arrangement is also seen in the abdomen but only in the first eight segments. Many species of insects have reduced numbers of ganglia due to fusion or reduction.[39] Some cockroaches have just six ganglia in the abdomen, whereas the wasp Vespa crabro has only two in the thorax and three in the abdomen. Some insects, like the house fly Musca domestica, have all the body ganglia fused into a single large thoracic ganglion.

At least a few insects have nociceptors, cells that detect and transmit signals responsible for the sensation of pain.[40] This was discovered in 2003 by studying the variation in reactions of larvae of the common fruitfly Drosophila to the touch of a heated probe and an unheated one. The larvae reacted to the touch of the heated probe with a stereotypical rolling behavior that was not exhibited when the larvae were touched by the unheated probe.[41] Although nociception has been demonstrated in insects, there is no consensus that insects feel pain consciously[42]

Insects are capable of learning.[43]

Digestive system

An insect uses its digestive system to extract nutrients and other substances from the food it consumes.[44] Most of this food is ingested in the form of macromolecules and other complex substances like proteins, polysaccharides, fats and nucleic acids. These macromolecules must be broken down by catabolic reactions into smaller molecules like amino acids and simple sugars before being used by cells of the body for energy, growth, or reproduction. This break-down process is known as digestion.

The main structure of an insect's digestive system is a long enclosed tube called the alimentary canal, which runs lengthwise through the body. The alimentary canal directs food unidirectionally from the mouth to the anus. It has three sections, each of which performs a different process of digestion. In addition to the alimentary canal, insects also have paired salivary glands and salivary reservoirs. These structures usually reside in the thorax, adjacent to the foregut.[25]:70–77

The salivary glands (element 30 in numbered diagram) in an insect's mouth produce saliva. The salivary ducts lead from the glands to the reservoirs and then forward through the head to an opening called the salivarium, located behind the hypopharynx. By moving its mouthparts (element 32 in numbered diagram) the insect can mix its food with saliva. The mixture of saliva and food then travels through the salivary tubes into the mouth, where it begins to break down.[45][46] Some insects, like flies, have extra-oral digestion. Insects using extra-oral digestion expel digestive enzymes onto their food to break it down. This strategy allows insects to extract a significant proportion of the available nutrients from the food source.[47]:31 The gut is where almost all of insects' digestion takes place. It can be divided into the foregut, midgut and hindgut.

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

The first section of the alimentary canal is the foregut (element 27 in numbered diagram), or stomodaeum. The foregut is lined with a cuticular lining made of chitin and proteins as protection from tough food. The foregut includes the buccal cavity (mouth), pharynx, esophagus and crop and proventriculus (any part may be highly modified) which both store food and signify when to continue passing onward to the midgut.[25]:70

Digestion starts in buccal cavity (mouth) as partially chewed food is broken down by saliva from the salivary glands. As the salivary glands produce fluid and carbohydrate-digesting enzymes (mostly amylases), strong muscles in the pharynx pump fluid into the buccal cavity, lubricating the food like the salivarium does, and helping blood feeders, and xylem and phloem feeders.

From there, the pharynx passes food to the esophagus, which could be just a simple tube passing it on to the crop and proventriculus, and then onward to the midgut, as in most insects. Alternately, the foregut may expand into a very enlarged crop and proventriculus, or the crop could just be a diverticulum, or fluid-filled structure, as in some Diptera species.[47]:30–31

Bumblebee defecating. Note the contraction of the abdomen to provide internal pressure
Midgut

Once food leaves the crop, it passes to the midgut (element 13 in numbered diagram), also known as the mesenteron, where the majority of digestion takes place. Microscopic projections from the midgut wall, called microvilli, increase the surface area of the wall and allow more nutrients to be absorbed; they tend to be close to the origin of the midgut. In some insects, the role of the microvilli and where they are located may vary. For example, specialized microvilli producing digestive enzymes may more likely be near the end of the midgut, and absorption near the origin or beginning of the midgut.[47]:32

Hindgut

In the hindgut (element 16 in numbered diagram), or proctodaeum, undigested food particles are joined by uric acid to form fecal pellets. The rectum absorbs 90% of the water in these fecal pellets, and the dry pellet is then eliminated through the anus (element 17), completing the process of digestion. The uric acid is formed using hemolymph waste products diffused from the Malpighian tubules (element 20). It is then emptied directly into the alimentary canal, at the junction between the midgut and hindgut. The number of Malpighian tubules possessed by a given insect varies between species, ranging from only two tubules in some insects to over 100 tubules in others.[25]:71–72, 78–80

Reproductive system

The reproductive system of female insects consist of a pair of ovaries, accessory glands, one or more spermathecae, and ducts connecting these parts. The ovaries are made up of a number of egg tubes, called ovarioles, which vary in size and number by species. The number of eggs that the insect is able to make vary by the number of ovarioles with the rate that eggs can be develop being also influenced by ovariole design. Female insects are able make eggs, receive and store sperm, manipulate sperm from different males, and lay eggs. Accessory glands or glandular parts of the oviducts produce a variety of substances for sperm maintenance, transport and fertilization, as well as for protection of eggs. They can produce glue and protective substances for coating eggs or tough coverings for a batch of eggs called oothecae. Spermathecae are tubes or sacs in which sperm can be stored between the time of mating and the time an egg is fertilized.[36]:880

For males, the reproductive system is the testis, suspended in the body cavity by tracheae and the fat body. Most male insects have a pair of testes, inside of which are sperm tubes or follicles that are enclosed within a membranous sac. The follicles connect to the vas deferens by the vas efferens, and the two tubular vasa deferentia connect to a median ejaculatory duct that leads to the outside. A portion of the vas deferens is often enlarged to form the seminal vesicle, which stores the sperm before they are discharged into the female. The seminal vesicles have glandular linings that secrete nutrients for nourishment and maintenance of the sperm. The ejaculatory duct is derived from an invagination of the epidermal cells during development and, as a result, has a cuticular lining. The terminal portion of the ejaculatory duct may be sclerotized to form the intromittent organ, the aedeagus. The remainder of the male reproductive system is derived from embryonic mesoderm, except for the germ cells, or spermatogonia, which descend from the primordial pole cells very early during embryogenesis.[36]:885

Respiratory system

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

Insect respiration is accomplished without lungs. Instead, the insect respiratory system uses a system of internal tubes and sacs through which gases either diffuse or are actively pumped, delivering oxygen directly to tissues that need it via their trachea (element 8 in numbered diagram). Since oxygen is delivered directly, the circulatory system is not used to carry oxygen, and is therefore greatly reduced. The insect circulatory system has no veins or arteries, and instead consists of little more than a single, perforated dorsal tube which pulses peristaltically. Toward the thorax, the dorsal tube (element 14) divides into chambers and acts like the insect's heart. The opposite end of the dorsal tube is like the aorta of the insect circulating the hemolymph, arthropods' fluid analog of blood, inside the body cavity.[25]:61–65[48] Air is taken in through openings on the sides of the abdomen called spiracles.

The respiratory system is an important factor that limits the size of insects. As insects get bigger, this type of oxygen transport gets less efficient and thus the heaviest insect currently weighs less than 100 g. However, with increased atmospheric oxygen levels, as happened in the late Paleozoic, larger insects were possible, such as dragonflies with wingspans of more than two feet.[49]

There are many different patterns of gas exchange demonstrated by different groups of insects. Gas exchange patterns in insects can range from continuous and diffusive ventilation, to discontinuous gas exchange.[25]:65–68 During continuous gas exchange, oxygen is taken in and carbon dioxide is released in a continuous cycle. In discontinuous gas exchange, however, the insect takes in oxygen while it is active and small amounts of carbon dioxide are released when the insect is at rest.[50] Diffusive ventilation is simply a form of continuous gas exchange that occurs by diffusion rather than physically taking in the oxygen. Some species of insect that are submerged also have adaptations to aid in respiration. As larvae, many insects have gills that can extract oxygen dissolved in water, while others need to rise to the water surface to replenish air supplies which may be held or trapped in special structures.[51][52]

Circulatory system

The insect circulatory system utilizes hemolymph, a tissue analogous to blood that circulates in the interior of the insect body, while remaining in direct contact with the animal's tissues. It is composed of plasma in which hemocytes are suspended. In addition to hemocytes, the plasma also contains many chemicals. It is also the major tissue type of the open circulatory system of arthropods, characteristic of spiders, crustaceans and insects.[53][54]

Reproduction and development

A pair of Simosyrphus grandicornis hoverflies mating in flight.
A pair of grasshoppers 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. In Schizophora however the serosa does not develop, but these flies lay their eggs in damp places, such as rotting matter.[55] Some species of insects, like the cockroach Blaptica dubia, as well as juvenile aphids and tsetse flies, are ovoviviparous. The eggs of ovoviviparous animals develop entirely inside the female, and then hatch immediately upon being laid.[7] Some other species, such as those in the genus of cockroaches known as Diploptera, are viviparous, and thus gestate inside the mother and are born alive.[25]:129, 131, 134–135 Some insects, like parasitic wasps, show polyembryony, where a single fertilized egg divides into many and in some cases thousands of separate embryos.[25]:136–137 Insects may be univoltine, bivoltine or multivoltine, i.e. they may have one, two or many broods (generations) in a year.[56]

The different forms of the male (top) and female (bottom) tussock moth Orgyia recens is an example of sexual dimorphism in insects.

Other developmental and reproductive variations include haplodiploidy, polymorphism, paedomorphosis or peramorphosis, sexual dimorphism, parthenogenesis and more rarely hermaphroditism.[25]:143 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.[57] Polymorphism is where a species may have different morphs or forms, as in the oblong winged katydid, which has four different varieties: green, pink and yellow or tan. Some insects may retain phenotypes that are normally only seen in juveniles; this is called paedomorphosis. In peramorphosis, an opposite sort of phenomenon, insects take on previously unseen traits after they have matured into adults. Many insects display sexual dimorphism, in which males and females have notably different appearances, such as the moth Orgyia recens as an exemplar of sexual dimorphism in insects.

Some insects use parthenogenesis, a process in which the female can reproduce and give birth without having the eggs fertilized by a male. Many aphids undergo a form of parthenogenesis, called cyclical parthenogenesis, in which they alternate between one or many generations of asexual and sexual reproduction.[58][59] In summer, aphids are generally female and parthenogenetic; in the autumn, males may be produced for sexual reproduction. Other insects produced by parthenogenesis are bees, wasps and ants, in which they spawn males. However, overall, most individuals are female, which are produced by fertilization. The males are haploid and the females are diploid.[7] More rarely, some insects display hermaphroditism, in which a given individual has both male and female reproductive organs.

Insect life-histories show adaptations to withstand cold and dry conditions. Some temperate region insects are capable of activity during winter, while some others migrate to a warmer climate or go into a state of torpor.[60] Still other insects have evolved mechanisms of diapause that allow eggs or pupae to survive these conditions.[61]

Metamorphosis

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

Incomplete metamorphosis

Main article: Hemimetabolism

Hemimetabolous insects, those with incomplete metamorphosis, change gradually by undergoing a series of molts. An insect molts when it outgrows its exoskeleton, which does not stretch and would otherwise restrict the insect's growth. The molting process begins as the insect's epidermis secretes a new epicuticle inside the old one. After this new epicuticle is secreted, the epidermis releases a mixture of enzymes that digests the endocuticle and thus detaches the old cuticle. When this stage is complete, the insect makes its body swell by taking in a large quantity of water or air, which makes the old cuticle split along predefined weaknesses where the old exocuticle was thinnest.[25]:142[62]

Immature insects that go through incomplete metamorphosis are called nymphs or in the case of dragonflies and damselflies, also naiads. Nymphs are similar in form to the adult except for the presence of wings, which are not developed until adulthood. With each molt, nymphs grow larger and become more similar in appearance to adult insects.

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

Complete metamorphosis

Main article: Holometabolism
Gulf Fritillary life cycle, an example of holometabolism.

Holometabolism, or complete metamorphosis, is where the insect changes in four stages, an egg or embryo, a larva, a pupa and the adult or imago. In these species, an egg hatches to produce a larva, which is generally worm-like in form. This worm-like form can be one of several varieties: eruciform (caterpillar-like), scarabaeiform (grub-like), campodeiform (elongated, flattened and active), elateriform (wireworm-like) or vermiform (maggot-like). The larva grows and eventually becomes a pupa, a stage marked by reduced movement and often sealed within a cocoon. There are three types of pupae: obtect, exarate or coarctate. Obtect pupae are compact, with the legs and other appendages enclosed. Exarate pupae have their legs and other appendages free and extended. Coarctate pupae develop inside the larval skin.[25]:151 Insects undergo considerable change in form during the pupal stage, and emerge as adults. Butterflies are a well-known example of insects that undergo complete metamorphosis, although most insects use this life cycle. Some insects have evolved this system to hypermetamorphosis.

Some of the oldest and most successful insect groups, such Endopterygota, use a system of complete metamorphosis.[25]:143 Complete metamorphosis is unique to a group of certain insect orders including Diptera, Lepidoptera and Hymenoptera. This form of development is exclusive and not seen in any other arthropods.

Senses and communication

Many insects possess very sensitive and, or specialized organs of perception. 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 many kilometers.[63] The yellow paper wasp (Polistes versicolor) is known for its wagging movements as a form of communication within the colony; it can waggle with a frequency of 10.6±2.1 Hz (n=190). These wagging movements can signal the arrival of new material into the nest and aggression between workers can be used to stimulate others to increase foraging expeditions.[64] There is a pronounced tendency for there to be 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. There are a variety of different mechanisms by which insects perceive sound, while the patterns are not universal, insects can generally hear sound if they can produce it. Different insect species can have varying hearing, though most insects can hear only a narrow range of frequencies related to the frequency of the sounds they can produce. Mosquitoes have been found to hear up to 2 kHz, and some grasshoppers can hear up to 50 kHz.[65] Certain predatory and parasitic insects can detect the characteristic sounds made by their prey or hosts, respectively. For instance, some nocturnal moths can perceive the ultrasonic emissions of bats, which helps them avoid predation.[25]:87–94 Insects that feed on blood have special sensory structures that can detect infrared emissions, and use them to home in on their hosts.

Some insects display a rudimentary sense of numbers,[66] such as the solitary wasps that prey upon a single species. The mother wasp lays her eggs in individual cells and provides each egg with a number of live caterpillars on which the young feed when hatched. Some species of wasp always provide five, others twelve, and others as high as twenty-four caterpillars per cell. The number of caterpillars is different among species, but always the same for each sex of larva. The male solitary wasp in the genus Eumenes is smaller than the female, so the mother of one species supplies him with only five caterpillars; the larger female receives ten caterpillars in her cell.

Light production and vision

Most insects have compound eyes and two antennae.

A few insects, such as members of the families Poduridae and Onychiuridae (Collembola), Mycetophilidae (Diptera) and the beetle families Lampyridae, Phengodidae, Elateridae and Staphylinidae are bioluminescent. The most familiar group are the fireflies, beetles of the family Lampyridae. Some species are able to control this light generation to produce flashes. The function varies with some species using them to attract mates, while others use them to lure prey. Cave dwelling larvae of Arachnocampa (Mycetophilidae, Fungus gnats) glow to lure small flying insects into sticky strands of silk.[67] 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.[68] The colors of emitted light vary from dull blue (Orfelia fultoni, Mycetophilidae) to the familiar greens and the rare reds (Phrixothrix tiemanni, Phengodidae).[69]

Most insects, except some species of cave crickets, are able to perceive light and dark. Many species have acute vision capable of detecting minute movements. The eyes may include simple eyes or ocelli as well as compound eyes of varying sizes. Many species are able to detect light in the infrared, ultraviolet and the visible light wavelengths. Color vision has been demonstrated in many species and phylogenetic analysis suggests that UV-green-blue trichromacy existed from at least the Devonian period between 416 and 359 million years ago.[70]

Sound production and hearing

Insects were the earliest organisms to produce and sense sounds. 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 and musculature. The African cicada Brevisana brevis has been measured at 106.7 decibels at a distance of 50 cm (20 in).[71] 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.[72][73] Some moths produce ultrasonic clicks that were once thought to have a role in jamming bat echolocation. The ultrasonic clicks were subsequently found to be produced mostly by unpalatable moths to warn bats, just as warning colorations are used against predators that hunt by sight.[74] Some otherwise palatable moths have evolved to mimic these calls.[75] More recently, the claim that some moths can jam bat sonar has been revisited. Ultrasonic recording and high-speed infrared videography of bat-moth interactions suggest the palatable tiger moth really does defend against attacking big brown bats using ultrasonic clicks that jam bat sonar.[76]

Grasshopper stridulation
Several unidentified grasshoppers stridulating

Problems playing this file? See media help.

Very low sounds are also produced in various species of Coleoptera, Hymenoptera, Lepidoptera, Mantodea and Neuroptera. These low sounds are simply the sounds made by the insect's movement. Through microscopic stridulatory structures located on the insect's muscles and joints, the normal sounds of the insect moving are amplified and can be used to warn or communicate with other insects. Most sound-making insects also have tympanal organs that can perceive airborne sounds. Some species in Hemiptera, such as the corixids (water boatmen), are known to communicate via underwater sounds.[77] Most insects are also able to sense vibrations transmitted through surfaces.

Communication using surface-borne vibrational signals is more widespread among insects because of size constraints in producing air-borne sounds.[78] 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.[79] The mechanisms of production of vibrational signals are just as diverse as those for producing sound in insects.

Some species use vibrations for communicating within members of the same species, such as to attract mates as in the songs of the shield bug Nezara viridula.[80] Vibrations can also be used to communicate between entirely different species; lycaenid (gossamer-winged butterfly) caterpillars which are myrmecophilous (living in a mutualistic association with ants) communicate with ants in this way.[81] The Madagascar hissing cockroach has the ability to press air through its spiracles to make a hissing noise as a sign of aggression;[82] 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 in close proximity.[83]

Chemical communication

Chemical communications in animals rely on a variety of aspects including taste and smell. Chemoreception is the physiological response of a sense organ (i.e. taste or smell) to a chemical stimulus where the chemicals act as signals to regulate the state or activity of a cell. A semiochemical is a message-carrying chemical that is meant to attract, repel, and convey information. Types of semiochemicals include pheromones and kairomones. One example is the butterfly Phengaris arion which uses chemical signals as a form of mimicry to aid in predation.[84]

In addition to the use of sound for communication, a wide range of insects have evolved chemical means for communication. These chemicals, termed semiochemicals, are often derived from plant metabolites include those meant to attract, repel and provide other kinds of information. Pheromones, a type of semiochemical, are used for attracting mates of the opposite sex, for aggregating conspecific individuals of both sexes, for deterring other individuals from approaching, to mark a trail, and to trigger aggression in nearby individuals. Allomonea 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 known to have developed in social insects.[25]:96–105

Social behavior

A cathedral mound created by termites (Isoptera).

Social insects, such as termites, ants and many bees and wasps, are the most familiar species of eusocial animal.[85] They live together in large well-organized colonies that may be so tightly integrated and genetically similar that the colonies of some species are sometimes considered superorganisms. It is sometimes argued that the various species of honey bee are the only invertebrates (and indeed one of the few non-human groups) to have evolved a system of abstract symbolic communication where a behavior is used to represent and convey specific information about something in 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.[25]:309–311 Though perhaps not as advanced as honey bees, bumblebees also potentially have some social communication behaviors. Bombus terrestris, for example, exhibit a faster learning curve for visiting unfamiliar, yet rewarding flowers, when they can see a conspecific foraging on the same species.[86]

Only insects which live in nests or colonies demonstrate any true capacity for fine-scale spatial orientation or homing. This can allow an insect to return unerringly to a single hole a few millimeters in diameter among thousands of apparently identical holes clustered together, after a trip of up to several kilometers' distance. In a phenomenon known as philopatry, insects that hibernate have shown the ability to recall a specific location up to a year after last viewing the area of interest.[87] A few insects seasonally migrate large distances between different geographic regions (e.g., the overwintering areas of the Monarch butterfly).[25]:14

Care of young

The eusocial insects build nest, guard eggs, and provide food for offspring full-time (see Eusociality). Most insects, however, lead short lives as adults, and rarely interact with one another except to mate or compete for mates. A small number exhibit some form of parental care, where they will at least guard their eggs, and sometimes continue guarding their offspring until adulthood, and possibly even feeding them. Another simple form of parental care is to construct a nest (a burrow or an actual construction, either of which may be simple or complex), store provisions in it, and lay an egg upon those provisions. The adult does not contact the growing offspring, but it nonetheless does provide food. This sort of care is typical for most species of bees and various types of wasps.[88]

Locomotion

Flight

Main article: Insect wing
White-lined sphinx moth feeding in flight
Basic motion of the insect wing in insect with an indirect flight mechanism scheme of dorsoventral cut through a thorax segment with
a wings
b joints
c dorsoventral muscles
d longitudinal muscles.

Insects are the only group of invertebrates to have developed flight. The evolution of insect wings has been a subject of debate. Some entomologists suggest that the wings are from paranotal lobes, or extensions from the insect's exoskeleton called the nota, called the paranotal theory. Other theories are based on a pleural origin. These theories include suggestions that wings originated from modified gills, spiracular flaps or as from an appendage of the epicoxa. The epicoxal theory suggests the insect wings are modified epicoxal exites, a modified appendage at the base of the legs or coxa.[89] In the Carboniferous age, some of the Meganeura dragonflies had as much as a 50 cm (20 in) wide wingspan. The appearance of gigantic insects has been found to be consistent with high atmospheric oxygen. The respiratory system of insects constrains their size, however the high oxygen in the atmosphere allowed larger sizes.[90] The largest flying insects today are much smaller and include several moth species such as the Atlas moth and the White Witch (Thysania agrippina).

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

Unlike birds, many small insects are swept along by the prevailing winds[91] although many of the larger insects are known to make migrations. Aphids are known to be transported long distances by low-level jet streams.[92] As such, fine line patterns associated with converging winds within weather radar imagery, like the WSR-88D radar network, often represent large groups of insects.[93]

Walking

Many adult insects use six legs for walking and have adopted a tripedal gait. The tripedal gait allows for rapid walking while always having a stable stance and has been studied extensively in cockroaches. The legs are used in alternate triangles touching the ground. For the first step, the middle right leg and the front and rear left legs are in contact with the ground and move the insect forward, while the front and rear right leg and the middle left leg are lifted and moved forward to a new position. When they touch the ground to form a new stable triangle the other legs can be lifted and brought forward in turn and so on.[94] 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, or avoiding obstacles, four or more feet may be touching the ground. Insects can also adapt their gait to cope with the loss of one or more limbs.

Cockroaches are among the fastest insect runners and, at full speed, adopt a bipedal run to reach a high velocity in proportion to their body size. As cockroaches move very quickly, they need to be video recorded at several hundred frames per second to reveal their gait. More sedate locomotion is seen in the stick insects or walking sticks (Phasmatodea). A few insects have evolved to walk on the surface of the water, especially members of the Gerridae family, commonly known as water striders. A few species of ocean-skaters in the genus Halobates even live on the surface of open oceans, a habitat that has few insect species.[95]

Use in robotics

Insect walking is of particular interest as an alternative form of locomotion in robots. The study of insects and bipeds has a significant impact on possible robotic methods of transport. This may allow new robots to be designed that can traverse terrain that robots with wheels may be unable to handle.[94]

Swimming

Main article: Aquatic insects
The backswimmer Notonecta glauca underwater, showing its paddle-like hindleg adaptation

A large number of insects live either part or the whole of their lives underwater. In many of the more primitive orders of insect, the immature stages are spent in an aquatic environment. Some groups of insects, like certain water beetles, have aquatic adults as well.[51]

Many of these species have adaptations to help in under-water locomotion. Water beetles and water bugs have legs adapted into paddle-like structures. Dragonfly naiads use jet propulsion, forcibly expelling water out of their rectal chamber.[96] Some species like the water striders are capable of walking on the surface of water. They can do this because their claws are not at the tips of the legs as in most insects, but recessed in a special groove further up the leg; this prevents the claws from piercing the water's surface film.[51] Other insects such as the Rove beetle Stenus are known to emit pygidial gland secretions that reduce surface tension making it possible for them to move on the surface of water by Marangoni propulsion (also known by the German term Entspannungsschwimmen).[97][98]

Ecology

See also: Insect ecology

Insect ecology is the scientific study of how insects, individually or as a community, interact with the surrounding environment or ecosystem.[99]:3 Insects play one of the most important roles in their ecosystems, which includes many roles, such as soil turning and aeration, dung burial, pest control, pollination and wildlife nutrition. An example is the beetles, which are scavengers that feed on dead animals and fallen trees and thereby recycle biological materials into forms found useful by other organisms.[100] These insects, and others, are responsible for much of the process by which topsoil is created.[25]:3, 218–228

Defense and predation

Perhaps one of the most well-known examples of mimicry, the viceroy butterfly (top) appears very similar to the noxious-tasting monarch butterfly (bottom).[101]

Insects are mostly soft bodied, fragile and almost defenseless compared to other, larger lifeforms. The immature stages are small, move slowly or are immobile, and so all stages are exposed to predation and parasitism. Insects then have a variety of defense strategies to avoid being attacked by predators or parasitoids. These include camouflage, mimicry, toxicity and active defense.[102]

Camouflage is an important defense strategy, which involves the use of coloration or shape to blend into the surrounding environment.[103] This sort of protective coloration is common and widespread among beetle families, especially those that feed on wood or vegetation, such as many of the leaf beetles (family Chrysomelidae) or weevils. In some of these species, sculpturing or various colored scales or hairs cause the beetle to resemble bird dung or other inedible objects. Many of those that live in sandy environments blend in with the coloration of the substrate.[102] Most phasmids are known for effectively replicating the forms of sticks and leaves, and the bodies of some species (such as O. macklotti and Palophus centaurus) are covered in mossy or lichenous outgrowths that supplement their disguise. Some species have the ability to change color as their surroundings shift (B. scabrinota, T. californica). In a further behavioral adaptation to supplement crypsis, a number of species have been noted to perform a rocking motion where the body is swayed from side to side that is thought to reflect the movement of leaves or twigs swaying in the breeze. Another method by which stick insects avoid predation and resemble twigs is by feigning death (catalepsy), where the insect enters a motionless state that can be maintained for a long period. The nocturnal feeding habits of adults also aids Phasmatodea in remaining concealed from predators.[104]

Another defense that often uses color or shape to deceive potential enemies is mimicry. A number of longhorn beetles (family Cerambycidae) bear a striking resemblance to wasps, which helps them avoid predation even though the beetles are in fact harmless.[102] Batesian and Müllerian mimicry complexes are commonly found in Lepidoptera. Genetic polymorphism and natural selection give rise to otherwise edible species (the mimic) gaining a survival advantage by resembling inedible species (the model). Such a mimicry complex is referred to as Batesian and is most commonly known by the mimicry by the limenitidine Viceroy butterfly of the inedible danaine Monarch. Later research has discovered that the Viceroy is, in fact more toxic than the Monarch and this resemblance should be considered as a case of Müllerian mimicry.[105] In Müllerian mimicry, inedible species, usually within a taxonomic order, find it advantageous to resemble each other so as to reduce the sampling rate by predators who need to learn about the insects' inedibility. Taxa from the toxic genus Heliconius form one of the most well known Müllerian complexes.[106]

Chemical defense is another important defense found amongst species of Coleoptera and Lepidoptera, usually being advertised by bright colors, such as the Monarch butterfly. They obtain their toxicity by sequestering the chemicals from the plants they eat into their own tissues. Some Lepidoptera manufacture their own toxins. Predators that eat poisonous butterflies and moths may become sick and vomit violently, learning not to eat those types of species; this is actually the basis of Müllerian mimicry. A predator who has previously eaten a poisonous lepidopteran may avoid other species with similar markings in the future, thus saving many other species as well.[107] Some ground beetles of the Carabidae family can spray chemicals from their abdomen with great accuracy, to repel predators.[102]

Pollination

See also: Pollination
European honey bee carrying pollen in a pollen basket back to the hive

Pollination is the process by which pollen is transferred in the reproduction of plants, thereby enabling fertilisation and sexual reproduction. Most flowering plants require an animal to do the transportation. While other animals are included as pollinators, the majority of pollination is done by insects.[108] Because insects usually receive benefit for the pollination in the form of energy rich nectar it is a grand example of mutualism. The various flower traits (and combinations thereof) that differentially attract one type of pollinator or another are known as pollination syndromes. These arose through complex plant-animal adaptations. Pollinators find flowers through bright colorations, including ultraviolet, and attractant pheromones. The study of pollination by insects is known as anthecology.

Parasitism

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

Relationship to humans

As pests

See also: Pest insect
Aedes aegypti, a parasite, is the vector of dengue fever and yellow fever

Many insects are considered pests by humans. Insects commonly regarded as pests include those that are parasitic (e.g. lice, bed bugs), transmit diseases (mosquitoes, flies), damage structures (termites), or destroy agricultural goods (locusts, weevils). Many entomologists are involved in various forms of pest control, as in research for companies to produce insecticides, but increasingly rely on methods of biological pest control, or biocontrol. Biocontrol uses one organism to reduce the population density of another organism — the pest — and is considered a key element of integrated pest management.[109][110]

Despite the large amount of effort focused at controlling insects, human attempts to kill pests with insecticides can backfire. If used carelessly, the poison can kill all kinds of organisms in the area, including insects' natural predators, such as birds, mice and other insectivores. The effects of DDT's use exemplifies how some insecticides can threaten wildlife beyond intended populations of pest insects.[111][112]

In beneficial roles

Because they help flowering plants to cross-pollinate, some insects are critical to agriculture. This European honey bee is gathering nectar while pollen collects on its body.
A robberfly with its prey, a hoverfly. Insectivorous relationships such as these help control insect populations.

Although pest insects attract the most attention, many insects are beneficial to the environment and to humans. Some insects, like wasps, bees, butterflies and ants, pollinate flowering plants. Pollination is a mutualistic relationship between plants and insects. As insects gather nectar from different plants of the same species, they also spread pollen from plants on which they have previously fed. This greatly increases plants' ability to cross-pollinate, which maintains and possibly even improves their evolutionary fitness. This ultimately affects humans since ensuring healthy crops is critical to agriculture. As well as pollination ants help with seed distribution of plants. This helps to spread the plants which increases plant diversity. This leads to an overall better environment.[113] A serious environmental problem is the decline of populations of pollinator insects, and a number of species of insects are now cultured primarily for pollination management in order to have sufficient pollinators in the field, orchard or greenhouse at bloom time.[114]:240–243 Another solution, as shown in Delaware, has been to raise native plants to help support native pollinators like L. vierecki.[115] Insects also produce useful substances such as honey, wax, lacquer and silk. Honey bees have been cultured by humans for thousands of years for honey, although contracting for crop pollination is becoming more significant for beekeepers. The silkworm has greatly affected human history, as silk-driven trade established relationships between China and the rest of the world.

Insectivorous insects, or insects which feed on other insects, are beneficial to humans because they eat insects that could cause damage to agriculture and human structures. For example, aphids feed on crops and cause problems for farmers, but ladybugs feed on aphids, and can be used as a means to get significantly reduce pest aphid populations. While birds are perhaps more visible predators of insects, insects themselves account for the vast majority of insect consumption. Ants also help control animal populations by consuming small vertebrates.[116] Without predators to keep them in check, insects can undergo almost unstoppable population explosions.[25]:328–348[25]:400[117][118]

Insects are also used in medicine, for example fly larvae (maggots) were formerly used to treat wounds to prevent or stop gangrene, as they would only consume dead flesh. This treatment is finding modern usage in some hospitals. Recently insects have also gained attention as potential sources of drugs and other medicinal substances.[119] Adult insects, such as crickets and insect larvae of various kinds, are also commonly used as fishing bait.[120]

In research

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

Insects play important roles in biological research. For example, because of its small size, short generation time and high fecundity, the common fruit fly Drosophila melanogaster is a model organism for studies in the genetics of higher eukaryotes. D. melanogaster has been an essential part of studies into principles like genetic linkage, interactions between genes, chromosomal genetics, development, behavior and evolution. Because genetic systems are well conserved among eukaryotes, understanding basic cellular processes like DNA replication or transcription in fruit flies can help to understand those processes in other eukaryotes, including humans.[121] The genome of D. melanogaster was sequenced in 2000, reflecting the organism's important role in biological research. It was found that 70% of the fly genome is similar to the human genome, supporting the evolution theory.[122]

As food

Main article: Entomophagy

In some cultures, insects, especially deep-fried cicadas, are considered to be delicacies, whereas in other places they form part of the normal diet. Insects have a high protein content for their mass, and some authors suggest their potential as a major source of protein in human nutrition.[25]:10–13 In most first-world countries, however, entomophagy (the eating of insects), is taboo.[123] Since it is impossible to entirely eliminate pest insects from the human food chain, insects are inadvertently present in many foods, especially grains. Food safety laws in many countries do not prohibit insect parts in food, but rather limit their quantity. According to cultural materialist anthropologist Marvin Harris, the eating of insects is taboo in cultures that have other protein sources such as fish or livestock.

Due to the abundance of insects and a worldwide concern of food shortages, the Food and Agriculture Organisation of the United Nations considers that the world may have to, in the future, regard the prospects of eating insects as a food staple. Insects are noted for their nutrients, having a high content of protein, minerals and fats and are eaten by one-third of the global population.[124]

In culture

Main article: Insects in culture

Scarab beetles held religious and cultural symbolism in Old Egypt, Greece and some shamanistic Old World cultures. The ancient Chinese regarded cicadas as symbols of rebirth or immortality. In Mesopotamian literature, the epic poem of Gilgamesh has allusions to Odonata which signify the impossibility of immortality. Amongst the Aborigines of Australia of the Arrernte language groups, honey ants and witchety grubs served as personal clan totems. In the case of the 'San' bush-men of the Kalahari, it is the praying mantis which holds much cultural significance including creation and zen-like patience in waiting.[25]:9

See also

Listen to this article (info/dl)


This audio file was created from a revision of the "Insect" article dated 2010-10-30, and does not reflect subsequent edits to the article. (Audio help)
More spoken articles

References

  1. 1 2 Engel, Michael S.; David A. Grimaldi (2004). "New light shed on the oldest insect". Nature. 427 (6975): 627–630. Bibcode:2004Natur.427..627E. doi:10.1038/nature02291. PMID 14961119.
  2. 1 2 Chapman, A. D. (2006). Numbers of living species in Australia and the World. Canberra: Australian Biological Resources Study. ISBN 978-0-642-56850-2.
  3. Wilson, E.O. "Threats to Global Diversity". Archived from the original on 20 February 2015. Retrieved 17 May 2009.
  4. Novotny, Vojtech; Basset, Yves; Miller, Scott E.; Weiblen, George D.; Bremer, Birgitta; Cizek, Lukas; Drozd, Pavel (2002). "Low host specificity of herbivorous insects in a tropical forest". Nature. 416 (6883): 841–844. Bibcode:2002Natur.416..841N. doi:10.1038/416841a. PMID 11976681.
  5. 1 2 Erwin, Terry L. (1997). Biodiversity at its utmost: Tropical Forest Beetles. pp. 27–40. In: Reaka-Kudla, M. L.; Wilson, D. E.; Wilson, E. O. (eds.). Biodiversity II. Joseph Henry Press, Washington, D.C.
  6. Erwin, Terry L. (1982). "Tropical forests: their richness in Coleoptera and other arthropod species". Coleopt. Bull. 36: 74–75.
  7. 1 2 3 "insect physiology" McGraw-Hill Encyclopedia of Science and Technology, Ch. 9, p. 233, 2007
  8. Vincent Brian Wigglesworth. "Insect". Encyclopædia Britannica online. Retrieved 19 April 2012.
  9. 1 2 Harper, Douglas; Dan McCormack (November 2001). "Online Etymological Dictionary". Online Etymological Dictionary. LogoBee.com. p. 1. Retrieved 1 November 2011.
  10. Russell Garwood; Gregory Edgecombe (2011). "Early terrestrial animals, evolution and uncertainty". Evolution, Education, and Outreach. 4 (3): 489–501. doi:10.1007/s12052-011-0357-y.
  11. "Palaeos invertebrates:Arthropoda". Palaeos Invertebrates. 3 May 2002. Archived from the original on 15 February 2009. Retrieved 6 May 2009.
  12. 1 2 Misof, et.al., Bernhard (7 November 2014). "Phylogenomics resolves the timing and pattern of insect evolution". Science. 346 (6210): 763–767. Bibcode:2014Sci...346..763M. doi:10.1126/science.1257570. PMID 25378627.
  13. "Evolution of insect flight". Malcolm W. Browne. 25 October 1994. Retrieved 6 May 2009.
  14. "Tree of Life Web Project. Version 1 January 1995 (temporary) of Arthropoda". Tree of Life Web Project. 1995. Retrieved 9 May 2009.
  15. "Researchers Discover Oldest Fossil Impression of a Flying Insect". Newswise. 14 October 2008. Retrieved 21 September 2014.
  16. Rice, C. M.; Ashcroft, W. A.; Batten, D. J.; Boyce, A. J.; Caulfield, J. B. D.; Fallick, A. E.; Hole, M. J.; Jones, E.; Pearson, M. J.; Rogers, G.; Saxton, J. M.; Stuart, F. M.; Trewin, N. H.; Turner, G. (1995). "A Devonian auriferous hot spring system, Rhynie, Scotland". Journal of the Geological Society, London. 152 (2): 229–250. doi:10.1144/gsjgs.152.2.0229.
  17. Wiegmann BM, Trautwein MD, Winkler IS, Barr NB, Kim JW, Lambkin C, Bertone MA, Cassel BK, Bayless KM, Heimberg AM, Wheeler BM, Peterson KJ, Pape T, Sinclair BJ, Skevington JH, Blagoderov V, Caravas J, Kutty SN, Schmidt-Ott U, Kampmeier GE, Thompson FC, Grimaldi DA, Beckenbach AT, Courtney GW, Friedrich M, Meier R, Yeates DK (2011). "Episodic radiations in the fly tree of life". Proceedings of the National Academy of Sciences. 108 (14): 5690–5695. Bibcode:2011PNAS..108.5690W. doi:10.1073/pnas.1012675108. PMC 3078341Freely accessible. PMID 21402926.
  18. Grimaldi, D.; Engel, M. S. (2005). Evolution of the Insects. Cambridge University Press. ISBN 0-521-82149-5.
  19. Garwood, Russell J.; Sutton, Mark D. (2010). "X-ray micro-tomography of Carboniferous stem-Dictyoptera: New insights into early insects". Biology Letters. 6 (5): 699–702. doi:10.1098/rsbl.2010.0199. PMC 2936155Freely accessible. PMID 20392720. Retrieved 9 June 2015.
  20. Rasnitsyn, A. P.; Quicke, D. L. J. (2002). History of Insects. Kluwer Academic Publishers. ISBN 1-4020-0026-X.
  21. 1 2 J. Stein Carter (29 March 2005). "Coevolution and Pollination". University of Cincinnati. Archived from the original on 30 April 2009. Retrieved 9 May 2009.
  22. Sahney, S.; Benton, M. J.; Falcon-Lang, H. J. (2010). "Rainforest collapse triggered Pennsylvanian tetrapod diversification in Euramerica". Geology. 38 (12): 1079–1082. Bibcode:2010Geo....38.1079S. doi:10.1130/G31182.1.
  23. "Coevolution and Pollination". University of Cincinnati. Archived from the original on 30 April 2009. Retrieved 9 May 2009.
  24. "Insecta". Tree of Life Web Project. 2002. Retrieved 12 May 2009.
  25. 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 Gullan, P.J.; Cranston, P.S. (2005). The Insects: An Outline of Entomology (3 ed.). Oxford: Blackwell Publishing. ISBN 1-4051-1113-5.
  26. Kendall, David A. (2009). "Classification of Insect". Retrieved 9 May 2009.
  27. Gilliott, Cedric (1995). Entomology (2 ed.). Springer-Verlag New York, LLC. p. 96. ISBN 0-306-44967-6.
  28. Kapoor, V.C. C. (1998). Principles and Practices of Animal Taxonomy. 1 (1 ed.). Science Publishers. p. 48. ISBN 1-57808-024-X.
  29. Johnson, K. P.; Yoshizawa, K.; Smith, V. S. (2004). "Multiple origins of parasitism in lice". Proceedings of the Royal Society of London. 271 (1550): 1771–1776. doi:10.1098/rspb.2004.2798. PMC 1691793Freely accessible. PMID 15315891.
  30. Terry, M. D.; Whiting, M. F. (2005). "Mantophasmatodea and phylogeny of the lower neopterous insects". Cladistics. 21 (3): 240–257. doi:10.1111/j.1096-0031.2005.00062.x.
  31. Lo, Nathan; Tokuda, Gaku; Watanabe, Hirofumi; Rose, Harley; Slaytor, Michael; Maekawa, Kiyoto; Bandi, Claudio; Noda, Hiroaki (2000). "Evidence from multiple gene sequences indicates that termites evolved from wood-feeding cockroaches". Current Biology. 10 (13): 801–804. doi:10.1016/S0960-9822(00)00561-3. PMID 10898984.
  32. Bonneton, F.; Brunet, F. G.; Kathirithamby J. & Laudet, V. (2006). "The rapid divergence of the ecdysone receptor is a synapomorphy for Mecopterida that clarifies the Strepsiptera problem". Insect Molecular Biology. 15 (3): 351–362. doi:10.1111/j.1365-2583.2006.00654.x. PMID 16756554.
  33. Whiting, M.F. (2002). "Mecoptera is paraphyletic: multiple genes and phylogeny of Mecoptera and Siphonaptera". Zoologica Scripta. 31 (1): 93–104. doi:10.1046/j.0300-3256.2001.00095.x.
  34. 1 2 Stork, N. E.; McBroom, J; Gely, C; Hamilton, A. J. (2015). "New approaches narrow global species estimates for beetles, insects, and terrestrial arthropods". Proceedings of the National Academy of Sciences. 112 (24): 7519–23. doi:10.1073/pnas.1502408112. PMC 4475949Freely accessible. PMID 26034274.
  35. "O. Orkin Insect zoo". The University of Nebraska Department of Entomology. Archived from the original on 2 June 2009. Retrieved 3 May 2009.
  36. 1 2 3 4 5 6 Resh, Vincent H.; Ring T. Carde (2009). Encyclopedia of Insects (2 ed.). U. S. A.: Academic Press. ISBN 0-12-374144-0.
  37. Barnes, R.S.K.; Calow, P.; Olive, P.; Golding, D.; and Spicer, J. (2001). "Invertebrates with Legs: the Arthropods and Similar Groups". The Invertebrates: A Synthesis. Blackwell Publishing. p. 168. ISBN 0-632-04761-5.
  38. Lowenstam, H.A.; Weiner, S. (1989). On biomineralization. Oxford University Press US. p. 111. ISBN 0-19-504977-2.
  39. Schneiderman, Howard A. (1960). "Discontinuous respiration in insects: role of the spiracles". Biol. Bull. 119 (3): 494–528. doi:10.2307/1539265. JSTOR 1539265.
  40. Eisemann, C. H.; Jorgensen, W. K.; Merritt, D. J.; Rice, M. J.; Cribb, B. W.; Webb, P. D.; Zalucki, M. P. (1984). "Do insects feel pain? — A biological view". Cellular and Molecular Life Sciences. 40 (2): 1420–1423. doi:10.1007/BF01963580.
  41. Tracey, J; Wilson, RI; Laurent, G; Benzer, S (2003). "painless, a Drosophila gene essential for nociception". Cell. 113 (2): 261–273. doi:10.1016/S0092-8674(03)00272-1. PMID 12705873.
  42. Sømme, LS (14 January 2005). "Sentience and pain in invertebrates" (PDF). Norwegian Scientific Committee for Food Safety. Retrieved 30 September 2009.
  43. Annual Review of Entomology, Evolutionary Biology of Insect Learning, Vol. 53: 145-160
  44. "General Entomology – Digestive and Excritory system". NC state University. Retrieved 3 May 2009.
  45. "General Entomology – Digestive and Excretory system". NC state University. Retrieved 3 May 2009.
  46. Duncan, Carl D. (1939). A Contribution to The Biology of North American Vespine Wasps (1 ed.). Stanford: Stanford University Press. pp. 24–29.
  47. 1 2 3 Nation, James L. (2001). "Digestion". Insect Physiology and Biochemistry (1st ed.). CRC Press. ISBN 0-8493-1181-0.
  48. Meyer, John R. (17 February 2006). "Circulatory System". NC State University: Department of Entomology, NC State University. p. 1. Retrieved 11 October 2009.
  49. "What Keeps Bugs from Being Bigger?". Argonne National Laboratory. 8 August 2007. Retrieved 15 July 2013.
  50. Chown, S.L.; S.W. Nicholson (2004). Insect Physiological Ecology. New York: Oxford University Press. ISBN 0-19-851549-9.
  51. 1 2 3 Richard W. Merritt; Kenneth W. Cummins; Martin B. Berg (editors) (2007). An Introduction to the Aquatic Insects of North America (4th ed.). Kendall Hunt Publishers. ISBN 978-0-7575-5049-2.
  52. Merritt, RW; KW Cummins & MB Berg (2007). An Introduction To The Aquatic Insects Of North America. Kendall Hunt Publishing Company. ISBN 0-7575-4128-3.
  53. Chapman, R.F. (1998). The Insects; Structure and Function (4th ed.). Cambridge, UK: Cambridge University Press. ISBN 0521578906.
  54. Wyatt, G. R. (1961). "The Biochemistry of Insect Hemolymph". Annual Review of Entomology. 6: 75–102. doi:10.1146/annurev.en.06.010161.000451.
  55. Jacobs, C.G.; Rezende, G.L.; Lamers, G.E.; van der Zee, M. (2013). "The extraembryonic serosa protects the insect egg against desiccation". Proceedings of the Royal Society – Biological series. 280 (1764): 20131082. doi:10.1098/rspb.2013.1082. PMID 23782888.
  56. "Glossary of Lepidopteran and Odonate anatomy". Rare species atlas. Virginia Department of Conservation and Recreation. 2013. Retrieved 14 June 2013.
  57. Hughes, William O. H.; Oldroyd, Benjamin P.; Beekman, Madeleine; Ratnieks, Francis L. W. (2008). "Ancestral Monogamy Shows Kin Selection Is Key to the Evolution of Eusociality". Science. American Association for the Advancement of Science. 320 (5880): 1213–1216. Bibcode:2008Sci...320.1213H. doi:10.1126/science.1156108. PMID 18511689.
  58. Nevo, E.; Coll, M. (2001). "Effect of nitrogen fertilization on Aphis gossypii (Homoptera: Aphididae): variation in size, color, and reproduction". J. Econ. Entomol. 94 (1): 27–32. doi:10.1603/0022-0493-94.1.27. PMID 11233124.
  59. Jahn, G. C.; Almazan, L. P.; Pacia, J. (2005). "Effect of nitrogen fertilizer on the intrinsic rate of increase of the rusty plum aphid, Hysteroneura setariae (Thomas) (Homoptera: Aphididae) on rice (Oryza sativa L.)" (PDF). Environmental Entomology. 34 (4): 938–943. doi:10.1603/0046-225X-34.4.938.
  60. Debbie Hadley. "Where do insects go in winter?". About.com. Retrieved 19 April 2012.
  61. Lee, Richard E Jr. (1989). "Insect Cold-Hardiness: To Freeze or Not to Freeze" (PDF). BioScience. 39 (5): 308–313. doi:10.2307/1311113. JSTOR 1311113.
  62. Ruppert, E.E.; Fox, R.S. & Barnes, R.D. (2004). Invertebrate Zoology (7 ed.). Brooks / Cole. pp. 523–524. ISBN 0-03-025982-7.
  63. "Insects" (PDF). Alien Life Forms. p. 4. Retrieved 17 May 2009.
  64. Esch, Harald (1971). "Wagging Movements in the Wasp Polistes versicolor Vulgaris Bequaert". Zeitschrift für Vergleichende Physiologie. 72 (3): 221–25. doi:10.1007/bf00297781.
  65. Cator, L. J.; Arthur, BJ; Harrington, LC; Hoy, RR (2009). "Harmonic convergence in the love songs of the dengue vector mosquito". Science. 323 (5917): 1077–1079. Bibcode:2009Sci...323.1077C. doi:10.1126/science.1166541. PMC 2847473Freely accessible. PMID 19131593.
  66. Möller, R. (2002). A Biorobotics Approach to the Study of Insect Visual Homing Strategies (PDF) (in German). p. 11.
  67. Pugsley, Chris W. (1983). "Literature review of the New Zealand glowworm Arachnocampa luminosa (Diptera: Keroplatidae) and related cave-dwelling Diptera" (PDF). New Zealand Entomologist. 7 (4): 419–424. doi:10.1080/00779962.1983.9722435.
  68. Lloyd, James E. (1984). "Occurrence of Aggressive Mimicry in Fireflies". The Florida Entomologist. 67 (3): 368–376. doi:10.2307/3494715. JSTOR 3494715.
  69. Lloyd, James E.; Erin C. Gentry (2003). The Encyclopedia of Insects. Academic Press. pp. 115–120. ISBN 0-12-586990-8.
  70. Briscoe, AD; Chittka, L (2001). "The evolution of color vision in insects". Annu. Rev. Entomol. 46: 471–510. doi:10.1146/annurev.ento.46.1.471. PMID 11112177.
  71. Walker, T.J., ed. (2001). University of Florida Book of Insect Records.
  72. Kay, Robert E. (1969). "Acoustic signalling and its possible relationship to assembling and navigation in the moth, Heliothis zea". Journal of Insect Physiology. 15 (6): 989–1001. doi:10.1016/0022-1910(69)90139-5.
  73. Spangler, Hayward G. (1988). "Moth hearing, defense, and communication". Annual Review of Entomology. 33 (1): 59–81. doi:10.1146/annurev.ento.33.1.59.
  74. Hristov, N.I.; Conner, W.E. (2005). "Sound strategy: acoustic aposematism in the bat–tiger moth arms race". Naturwissenschaften. 92 (4): 164–169. Bibcode:2005NW.....92..164H. doi:10.1007/s00114-005-0611-7. PMID 15772807.
  75. Barber, J. R.; W. E. Conner (2007). "Acoustic mimicry in a predator–prey interaction". Proc. Natl. Acad. Sci. 104 (22): 9331–9334. Bibcode:2007PNAS..104.9331B. doi:10.1073/pnas.0703627104. PMC 1890494Freely accessible. PMID 17517637.
  76. Corcoran, Aaron J.; Jesse R. Barber; William E. Conner (2009). "Tiger Moth Jams Bat Sonar". Science. 325 (5938): 325–327. Bibcode:2009Sci...325..325C. doi:10.1126/science.1174096.
  77. Theiss, Joachim (1982). "Generation and radiation of sound by stridulating water insects as exemplified by the corixids". Behavioral Ecology and Sociobiology. 10 (3): 225–235. doi:10.1007/BF00299689.
  78. Virant-Doberlet, M.; Čokl A. (2004). "Vibrational communication in insects". Neotropical Entomology. 33 (2): 121–134. doi:10.1590/S1519-566X2004000200001.
  79. Bennet-Clark, H.C. (1998). "Size and scale effects as constraints in insect sound communication". Phil. Trans. R. Soc. Lond. B. 353 (1367): 407–419. doi:10.1098/rstb.1998.0219.
  80. Miklas, Nadège; Stritih, Nataša; Čokl, Andrej; Virant-Doberlet, Meta; Renou, Michel (2001). "The Influence of Substrate on Male Responsiveness to the Female Calling Song in Nezara viridula". Journal of Insect Behavior. 14 (3): 313–332. doi:10.1023/A:1011115111592.
  81. DeVries, P. J. (1990). "Enhancement of symbiosis between butterfly caterpillars and ants by vibrational communication". Science. 248 (4959): 1104–1106. Bibcode:1990Sci...248.1104D. doi:10.1126/science.248.4959.1104. PMID 17733373.
  82. Nelson, Margaret C.; Jean Fraser (1980). "Sound production in the cockroach, Gromphadorhina portentosa: evidence for communication by hissing". Behavioral Ecology and Sociobiology. 6 (4): 305–314. doi:10.1007/BF00292773.
  83. Moritz, R. F. A.; Kirchner, W. H.; Crewe, R. M. (1991). "Chemical camouflage of the death's head hawkmoth (Acherontia atropos L.) in honeybee colonies". Naturwissenschaften. 78 (4): 179–182. Bibcode:1991NW.....78..179M. doi:10.1007/BF01136209.
  84. Thomas, Jeremy; Schönrogge, Karsten; Bonelli, Simona; Barbero, Francesca; Balletto, Emilio (2010). "Corruption of ant acoustical signals by mimetic social parasites". Communicative and Integrative Biology. 3 (2): 169–171. doi:10.4161/cib.3.2.10603. PMC 2889977Freely accessible. PMID 20585513.
  85. Brewer, Gary. "Social insects". North Dakota State University. Archived from the original on 21 March 2008. Retrieved 6 May 2009.
  86. Leadbeater, E.; L. Chittka (2007). "The dynamics of social learning in an insect model, the bumblebee (Bombus terrestris)". Behavioral Ecology and Sociobiology. 61 (11): 1789–1796. doi:10.1007/s00265-007-0412-4.
  87. Salt, R.W. (1961). "Principles of Insect Cold-Hardiness". Annual Review of Entomology. Lethbirdge, Alberta, Canada. 6: 55–74. doi:10.1146/annurev.en.06.010161.000415.
  88. "Social Insects". North Dakota State University. Archived from the original on 21 March 2008. Retrieved 12 October 2009.
  89. Jockusch, EL; Ober, KA (September 2004). "Hypothesis testing in evolutionary developmental biology: a case study from insect wings". Journal of Heredity. 95 (5): 382–396. doi:10.1093/jhered/esh064. PMID 15388766.
  90. Dudley, R (1998). "Atmospheric oxygen, giant Paleozoic insects and the evolution of aerial locomotor performance" (PDF). Journal of Experimental Biology. 201 (8): 1043–1050.
  91. Yates, Diana (2008). Birds migrate together at night in dispersed flocks, new study indicates. University of Illinois at Urbana – Champaign. Retrieved on 26 April 2009.
  92. Drake, V. A.; R. A. Farrow (1988). "The Influence of Atmospheric Structure and Motions on Insect Migration". Annual Review of Entomology. 33: 183–210. doi:10.1146/annurev.en.33.010188.001151.
  93. Bart Geerts and Dave Leon (2003). P5A.6 Fine-Scale Vertical Structure of a Cold Front As Revealed By Airborne 95 GHZ Radar. University of Wyoming. Retrieved on 26 April 2009.
  94. 1 2 Biewener, Andrew A (2003). Animal Locomotion. Oxford University Press. ISBN 0-19-850022-X.
  95. Ikawa, Terumi; Okabe, Hidehiko; Hoshizaki, Sugihiko; Kamikado, Takahiro; Cheng, Lanna (2004). "Distribution of the oceanic insects Halobates (Hemiptera: Gerridae) off the south coast of Japan". Entomological Science. 7 (4): 351–357. doi:10.1111/j.1479-8298.2004.00083.x.
  96. Mill, P. J.; R. S. Pickard (1975). "Jet-propulsion in anisopteran dragonfly larvae". Journal of Comparative Physiology A. 97 (4): 329–338. doi:10.1007/BF00631969.
  97. Linsenmair, K.; Jander R. (1976). "Das "entspannungsschwimmen" von Velia and Stenus". Naturwissenschaften. 50 (6): 231. Bibcode:1963NW.....50..231L. doi:10.1007/BF00639292.
  98. Bush, J. W. M.; David L. Hu (2006). "Walking on Water: Biolocomotion at the Interface" (PDF). Annu. Rev. Fluid Mech. 38: 339–369. Bibcode:2006AnRFM..38..339B. doi:10.1146/annurev.fluid.38.050304.092157. Archived from the original (PDF) on 10 July 2007.
  99. Schowalter, Timothy Duane (2006). Insect ecology: an ecosystem approach (2(illustrated) ed.). Academic Press. p. 572. ISBN 978-0-12-088772-9.
  100. Losey, John E.; Vaughan, Mace (2006). "The Economic Value of Ecological Services Provided by Insects". BioScience. 56 (4): 311–323(13). doi:10.1641/0006-3568(2006)56[311:TEVOES]2.0.CO;2.
  101. Ritland, D.; L. P. Brower (1991). "The viceroy butterfly is not a Batesian mimic". Nature. 350 (6318): 497–498. Bibcode:1991Natur.350..497R. doi:10.1038/350497a0. Viceroys are as unpalatable as monarchs, and significantly more unpalatable than queens from representative Florida populations.
  102. 1 2 3 4 Evans, Arthur V.; Charles Bellamy (2000). An Inordinate Fondness for Beetles. University of California Press. ISBN 978-0-520-22323-3.
  103. "Photos: Masters of Disguise—Amazing Insect Camouflage". Retrieved 11 June 2015.
  104. Bedford, Geoffrey O. (1978). "Biology and Ecology of the Phasmatodea". Annual Review of Entomology. 23: 125–149. doi:10.1146/annurev.en.23.010178.001013.
  105. Ritland, D. B.; L. P. Brower (1991). "The viceroy butterfly is not a Batesian mimic". Nature. 350 (6318): 497–498. Bibcode:1991Natur.350..497R. doi:10.1038/350497a0. Viceroys are as unpalatable as monarchs, and significantly more unpalatable than queens from representative Florida populations
  106. Meyer, A. (2006). "Repeating Patterns of Mimicry". PLoS Biology. 4 (10): e341. doi:10.1371/journal.pbio.0040341. PMC 1617347Freely accessible. PMID 17048984.
  107. Kricher, John (1999). "6". A Neotropical Companion. Princeton University Press. pp. 157–158. ISBN 978-0-691-00974-2.
  108. "Pollinator Factsheet" (PDF). United States Forest Service. Archived from the original (PDF) on 10 April 2008. Retrieved 19 April 2012.
  109. Bale, JS; van Lenteren, JC; Bigler, F. (27 February 2008). "Biological control and sustainable food production". Philosophical Transactions of the Royal Society of London. Series B: Biological Sciences. 363 (1492): 761–776. doi:10.1098/rstb.2007.2182. PMC 2610108Freely accessible. PMID 17827110.
  110. Davidson, E. (2006). Big Fleas Have Little Fleas: How Discoveries of Invertebrate Diseases Are Advancing Modern Science. Tucson, Ariz.: University of Arizona Press. ISBN 0-8165-2544-7.
  111. Colborn, T; vom Saal, FS; Soto, AM (October 1993). "Developmental effects of endocrine-disrupting chemicals in wildlife and humans". Environmental Health Perspectives. 101 (5): 378–384. doi:10.2307/3431890. JSTOR 3431890. PMC 1519860Freely accessible. PMID 8080506.
  112. Nakamaru, M; Iwasab, Y; Nakanishic, J (October 2003). "Extinction risk to bird populations caused by DDT exposure". Chemosphere. 53 (4): 377–387. doi:10.1016/S0045-6535(03)00010-9. PMID 12946395.
  113. Holldobler, Wilson (1994). Journey to the ants: a story of scientific exploration. Westminster college McGill Library: Cambridge, Mass.:Belknap Press of Haravard University Press, 1994. pp. 196–199. ISBN 0-674-48525-4.
  114. Smith, Deborah T (1991). Agriculture and the Environment: The 1991 Yearbook of Agriculture (1991 ed.). United States Government Printing. ISBN 0-16-034144-2.
  115. Kuehn, F. Coordinator. (2015). "Farming for native bees". World Wide Web electronic publication. (Accessed: September 22, 2015).
  116. Camargo, Rafael; Paulo Oliveira (2011). "Natural history of the Neotrobical arboreal ant, Odontomachus hastatus: Nest sites, foraging schedule, and diet". Journal of Insect Science. 12 (18): 1–9. doi:10.1673/031.012.4801. PMC 3476954Freely accessible. PMID 22957686.
  117. "Biocontrol Network – Beneficial Insects". Biocontrol Network. Retrieved 9 May 2009.
  118. Davidson, RH; William F. Lyon (1979). Insect Pests of Farm, Garden, and Orchard. Wiley, John & Sons. p. 38. ISBN 0-471-86314-9.
  119. Dossey, Aaron T. (December 2010). "Insects and their chemical weaponry: New potential for drug discovery". Natural Product Reports. Royal Society of Chemistry (RSC Publishing). 27 (12): Pages 1737–1757. doi:10.1039/c005319h. PMID 20957283.
  120. Sherman, Ronald A.; Pechter, Edward A. (1987). "Maggot therapy: a review of the therapeutic applications of fly larvae in human medicine, especially for treating osteomyelitis". Medical and Veterinary Entomology. 2 (3): Pages 225–230. doi:10.1111/j.1365-2915.1988.tb00188.x.
  121. Pierce, BA (2006). Genetics: A Conceptual Approach (2nd ed.). New York: W.H. Freeman and Company. p. 87. ISBN 0-7167-8881-0.
  122. Adams, MD; Celniker, SE; Holt, RA; Evans, CA; Gocayne, JD; Amanatides, PG; Scherer, SE; Li, PW; et al. (24 March 2000). "The genome sequence of Drosophila melanogaster". Science. 287 (5461): 2185–2195. Bibcode:2000Sci...287.2185.. doi:10.1126/science.287.5461.2185. PMID 10731132.
  123. Michels, John (1880). John Michels, ed. Science. 1. American Association for the Advance of Science. 229 Broadway ave., N.Y.: American Association for the Advance of Science. pp. 2090pp. ISBN 1-930775-36-9.
  124. Maierbrugger, Arno (14 May 2013). "UN: Insects are 'food of the future' (video)". Inside Investor. Retrieved 17 May 2013.

External links

Wikisource has original works on the topic: Insects
External identifiers for Insect
Encyclopedia of Life 344
NCBI 50557

This article is issued from Wikipedia - version of the 11/28/2016. The text is available under the Creative Commons Attribution/Share Alike but additional terms may apply for the media files.