Termite

Termites are eusocial insects that are classified at the taxonomic rank of infraorder Isoptera, or as epifamily Termitoidae within the order Blattodea (along with cockroaches). Termites were once classified in a separate order from cockroaches, but recent phylogenetic studies indicate that they evolved from cockroaches, as they are the sister group to wood eating cockroaches of the genus Cryptocercus. Previous estimates suggested the divergence took place during the Jurassic or Triassic. More recent estimates suggest they have an origin during the Late Jurassic,[3] with the first fossil records in the Early Cretaceous. About 3,106 species are currently described, with a few hundred more left to be described. Although these insects are often called "white ants",[4] they are not ants, and are not closely related to ants.

This article is about social insects. For other uses, see Termite (disambiguation).

Termite
Temporal range: Early Cretaceous–Recent
Formosan subterranean termite (Coptotermes formosanus)
Soldiers (red-coloured heads)
Workers (pale-coloured heads)
Scientific classification
Kingdom: Animalia
Phylum: Arthropoda
Class: Insecta
Cohort: Polyneoptera
Superorder: Dictyoptera
Order: Blattodea
Infraorder: Isoptera
Brullé, 1832
Families

† Cratomastotermitidae[1]
Mastotermitidae
† Termopsidae[2]
Archotermopsidae
Hodotermitidae
Stolotermitidae
Kalotermitidae
† Archeorhinotermitidae
Stylotermitidae
Rhinotermitidae
Serritermitidae
Termitidae

Like ants and some bees and wasps from the separate order Hymenoptera, termites divide as "workers" and "soldiers" that are usually sterile. All colonies have fertile males called "kings" and one or more fertile females called "queens". Termites mostly feed on dead plant material and cellulose, generally in the form of wood, leaf litter, soil, or animal dung. Termites are major detritivores, particularly in the subtropical and tropical regions, and their recycling of wood and plant matter is of considerable ecological importance.

Termites are among the most successful groups of insects on Earth, colonising most landmasses except Antarctica. Their colonies range in size from a few hundred individuals to enormous societies with several million individuals. Termite queens have the longest known lifespan of any insect, with some queens reportedly living up to 30 to 50 years. Unlike ants, which undergo a complete metamorphosis, each individual termite goes through an incomplete metamorphosis that proceeds through egg, nymph, and adult stages. Colonies are described as superorganisms because the termites form part of a self-regulating entity: the colony itself.[5]

Termites are a delicacy in the diet of some human cultures and are used in many traditional medicines. Several hundred species are economically significant as pests that can cause serious damage to buildings, crops, or plantation forests. Some species, such as the West Indian drywood termite (Cryptotermes brevis), are regarded as invasive species.

Etymology

The infraorder name Isoptera is derived from the Greek words iso (equal) and ptera (winged), which refers to the nearly equal size of the fore and hind wings.[6] "Termite" derives from the Latin and Late Latin word termes ("woodworm, white ant"), altered by the influence of Latin terere ("to rub, wear, erode") from the earlier word tarmes. A termite nest is also known as a termitary or termitarium (plural termitaria or termitariums).[7] In earlier English, termites were known as "wood ants" or "white ants".[8] The modern term was first used in 1781.[9]

Taxonomy and evolution
The external appearance of the giant northern termite Mastotermes darwiniensis is suggestive of the close relationship between termites and cockroaches.

Termites were formerly placed in the order Isoptera. As early as 1934 suggestions were made that they were closely related to wood-eating cockroaches (genus Cryptocercus, the woodroach) based on the similarity of their symbiotic gut flagellates.[10] In the 1960s additional evidence supporting that hypothesis emerged when F. A. McKittrick noted similar morphological characteristics between some termites and Cryptocercus nymphs.[11] In 2008 DNA analysis from 16S rRNA sequences[12] supported the position of termites being nested within the evolutionary tree containing the order Blattodea, which included the cockroaches.[13][14] The cockroach genus Cryptocercus shares the strongest phylogenetical similarity with termites and is considered to be a sister-group to termites.[15][16] Termites and Cryptocercus share similar morphological and social features: for example, most cockroaches do not exhibit social characteristics, but Cryptocercus takes care of its young and exhibits other social behaviour such as trophallaxis and allogrooming.[17] Termites are thought to be the descendants of the genus Cryptocercus.[13][18] Some researchers have suggested a more conservative measure of retaining the termites as the Termitoidae, an epifamily within the cockroach order, which preserves the classification of termites at family level and below.[19] Termites have long been accepted to be closely related to cockroaches and mantids, and they are classified in the same superorder (Dictyoptera).[20][21]

The oldest unambiguous termite fossils date to the early Cretaceous, but given the diversity of Cretaceous termites and early fossil records showing mutualism between microorganisms and these insects, they possibly originated earlier in the Jurassic or Triassic.[22][23][24] Possible evidence of a Jurassic origin is the assumption that the extinct Fruitafossor consumed termites, judging from its morphological similarity to modern termite-eating mammals.[25] The oldest termite nest discovered is believed to be from the Upper Cretaceous in West Texas, where the oldest known faecal pellets were also discovered.[26] Claims that termites emerged earlier have faced controversy. For example, F. M. Weesner indicated that the Mastotermitidae termites may go back to the Late Permian, 251 million years ago,[27] and fossil wings that have a close resemblance to the wings of Mastotermes of the Mastotermitidae, the most primitive living termite, have been discovered in the Permian layers in Kansas.[28] It is even possible that the first termites emerged during the Carboniferous.[29] The folded wings of the fossil wood roach Pycnoblattina, arranged in a convex pattern between segments 1a and 2a, resemble those seen in Mastotermes, the only living insect with the same pattern.[28] Krishna et al., though, consider that all of the Paleozoic and Triassic insects tentatively classified as termites are in fact unrelated to termites and should be excluded from the Isoptera.[30] Other studies suggest that the origin of termites is more recent, having diverged from Cryptocercus sometime during the Early Cretaceous.[3]

Macro image of a worker.

The primitive giant northern termite (Mastotermes darwiniensis) exhibits numerous cockroach-like characteristics that are not shared with other termites, such as laying its eggs in rafts and having anal lobes on the wings.[31] It has been proposed that the Isoptera and Cryptocercidae be grouped in the clade "Xylophagodea".[32] Termites are sometimes called "white ants" but the only resemblance to the ants is due to their sociality which is due to convergent evolution[33][34] with termites being the first social insects to evolve a caste system more than 100 million years ago.[35] Termite genomes are generally relatively large compared to that of other insects; the first fully sequenced termite genome, of Zootermopsis nevadensis, which was published in the journal Nature Communications, consists of roughly 500Mb,[36] while two subsequently published genomes, Macrotermes natalensis and Cryptotermes secundus, are considerably larger at around 1.3Gb.[37][34]

External phylogeny

Dictyoptera
 
 

Manipulatoridae (extinct)

 
 
 

Alienopteridae (extinct)

 
 

Mantodea (Mantises)

 
 
 
Blattodea
 

Blaberoidea

 
Solumblattodea
 

Corydiodea

 
Blattoidea
 

Blattoidae

 
Kittrickea
 

Lamproblattidae

 
Xylophagodea
 

Cryptocercidae (brown-hooded cockroaches)

 
 

Termitoidae (Termites)

 
 
 
 
 
 
 

Internal phylogeny[30]

Termitoidae
 

†Cratomastotermitidae

 
 
 

Mastotermitidae

 
Euisoptera
 

†Carinatermes

 
 
 

†Termopsidae

 
 
 

†Mariconitermes

 
 
 

Hodotermitidae

 
 
 

†Cratokalotermes

 
 
 

Archotermopsidae

 
 
 

Stolotermitidae

 
 
 

†Tanytermes

 
 
 

†Baissatermes

 
 
 

†Dharmatermes

 
 
 

Kalotermitidae

 
Neoisoptera
 

†Archeorhinotermitidae

 
 
 

Stylotermitidae

 
 
 

Rhinotermitidae

 
 
 

Serritermitidae

 
 

Termitidae

 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 

As of 2013, about 3,106 living and fossil termite species are recognised, classified in 12 families; reproductive and/or soldier castes are usually required for identification. The infraorder Isoptera is divided into the following clade and family groups, showing the subfamilies in their respective classification:[30]

Basal termite families
Epifamily Termitoidae
Family †Cratomastotermitidae
Family Mastotermitidae
   Parvorder Euisoptera
Family †Termopsidae
Family Archotermopsidae
Family Hodotermitidae
Family Stolotermitidae
Family Kalotermitidae

Neoisoptera

The Neoisoptera, literally meaning "newer termites" (in an evolutionary sense), are a recently coined nanorder that include families commonly referred-to as "higher termites", although some authorities only apply this term to the largest family Termitidae. The latter characteristically do not have Pseudergate nymphs (many "lower termite" worker nymphs have the capacity to develop into reproductive castes: see below). Cellulose digestion in "higher termites" has co-evolved with eukaryotic gut microbiota[38] and many genera have symbiotic relationships with fungi such as Termitomyces; in contrast, "lower termites" typically have flagellates and prokaryotes in their hindguts. Five families are now included here:

Distribution and diversity

Termites are found on all continents except Antarctica. The diversity of termite species is low in North America and Europe (10 species known in Europe and 50 in North America), but is high in South America, where over 400 species are known.[39] Of the 3,000 termite species currently classified, 1,000 are found in Africa, where mounds are extremely abundant in certain regions. Approximately 1.1 million active termite mounds can be found in the northern Kruger National Park alone.[40] In Asia, there are 435 species of termites, which are mainly distributed in China. Within China, termite species are restricted to mild tropical and subtropical habitats south of the Yangtze River.[39] In Australia, all ecological groups of termites (dampwood, drywood, subterranean) are endemic to the country, with over 360 classified species.[39]

Due to their soft cuticles, termites do not inhabit cool or cold habitats.[41] There are three ecological groups of termites: dampwood, drywood and subterranean. Dampwood termites are found only in coniferous forests, and drywood termites are found in hardwood forests; subterranean termites live in widely diverse areas.[39] One species in the drywood group is the West Indian drywood termite (Cryptotermes brevis), which is an invasive species in Australia.[42]

Diversity of Isoptera by continent:
Asia Africa North America South America Europe Australia
Estimated number of species 435 1,000 50 400 10 360

Description
Close-up view of a worker's head

Termites are usually small, measuring between 4 to 15 millimetres (0.16 to 0.59 in) in length.[39] The largest of all extant termites are the queens of the species Macrotermes bellicosus, measuring up to over 10 centimetres (4 in) in length.[43] Another giant termite, the extinct Gyatermes styriensis, flourished in Austria during the Miocene and had a wingspan of 76 millimetres (3.0 in) and a body length of 25 millimetres (0.98 in).[44][note 1]

Most worker and soldier termites are completely blind as they do not have a pair of eyes. However, some species, such as Hodotermes mossambicus, have compound eyes which they use for orientation and to distinguish sunlight from moonlight.[45] The alates (winged males and females) have eyes along with lateral ocelli. Lateral ocelli, however, are not found in all termites, absent in the families Hodotermitidae, Termopsidae, and Archotermopsidae.[46][47] Like other insects, termites have a small tongue-shaped labrum and a clypeus; the clypeus is divided into a postclypeus and anteclypeus. Termite antennae have a number of functions such as the sensing of touch, taste, odours (including pheromones), heat and vibration. The three basic segments of a termite antenna include a scape, a pedicel (typically shorter than the scape), and the flagellum (all segments beyond the scape and pedicel).[47] The mouth parts contain a maxillae, a labium, and a set of mandibles. The maxillae and labium have palps that help termites sense food and handling.[47]

Consistent with all insects, the anatomy of the termite thorax consists of three segments: the prothorax, the mesothorax and the metathorax.[47] Each segment contains a pair of legs. On alates, the wings are located at the mesothorax and metathorax. The mesothorax and metathorax have well-developed exoskeletal plates; the prothorax has smaller plates.[48]

Diagram showing a wing, along with the clypeus and leg

Termites have a ten-segmented abdomen with two plates, the tergites and the sternites.[49] The tenth abdominal segment has a pair of short cerci.[50] There are ten tergites, of which nine are wide and one is elongated.[51] The reproductive organs are similar to those in cockroaches but are more simplified. For example, the intromittent organ is not present in male alates, and the sperm is either immotile or aflagellate. However, Mastotermitidae termites have multiflagellate sperm with limited motility.[52] The genitals in females are also simplified. Unlike in other termites, Mastotermitidae females have an ovipositor, a feature strikingly similar to that in female cockroaches.[53]

The non-reproductive castes of termites are wingless and rely exclusively on their six legs for locomotion. The alates fly only for a brief amount of time, so they also rely on their legs.[49] The appearance of the legs is similar in each caste, but the soldiers have larger and heavier legs. The structure of the legs is consistent with other insects: the parts of a leg include a coxa, trochanter, femur, tibia and the tarsus.[49] The number of tibial spurs on an individual's leg varies. Some species of termite have an arolium, located between the claws, which is present in species that climb on smooth surfaces but is absent in most termites.[54]

Unlike in ants, the hind-wings and fore-wings are of equal length.[6] Most of the time, the alates are poor flyers; their technique is to launch themselves in the air and fly in a random direction.[55] Studies show that in comparison to larger termites, smaller termites cannot fly long distances. When a termite is in flight, its wings remain at a right angle, and when the termite is at rest, its wings remain parallel to the body.[56]

Caste system
Caste system of termites
A – King
B – Queen
C – Secondary queen
D – Tertiary queen
E – Soldiers
F – Worker

Worker termites undertake the most labour within the colony, being responsible for foraging, food storage, and brood and nest maintenance.[57][58] Workers are tasked with the digestion of cellulose in food and are thus the most likely caste to be found in infested wood. The process of worker termites feeding other nestmates is known as trophallaxis. Trophallaxis is an effective nutritional tactic to convert and recycle nitrogenous components.[59] It frees the parents from feeding all but the first generation of offspring, allowing for the group to grow much larger and ensuring that the necessary gut symbionts are transferred from one generation to another. Some termite species may rely on nymphs to perform work without differentiating as a separate caste.[58] Workers may be male or female and are usually sterile, especially in termites that have a nest site that is separate from their foraging site. Sterile workers are sometimes termed as true workers while those that are fertile, as in the wood-nesting Archotermopsidae, are termed as false workers.[60]

The soldier caste has anatomical and behavioural specialisations, and their sole purpose is to defend the colony.[61] Many soldiers have large heads with highly modified powerful jaws so enlarged they cannot feed themselves. Instead, like juveniles, they are fed by workers.[61][62] Fontanelles, simple holes in the forehead that exude defensive secretions, are a feature of the family Rhinotermitidae.[63] Many species are readily identified using the characteristics of the soldiers' larger and darker head and large mandibles.[58][61] Among certain termites, soldiers may use their globular (phragmotic) heads to block their narrow tunnels.[64] Different sorts of soldiers include minor and major soldiers, and nasutes, which have a horn-like nozzle frontal projection (a nasus).[58] These unique soldiers are able to spray noxious, sticky secretions containing diterpenes at their enemies.[65] Nitrogen fixation plays an important role in nasute nutrition.[66] Soldiers are usually sterile but some species of Archotermopsidae are known to have neotenic forms with soldier-like heads while also having sexual organs.[67]

The reproductive caste of a mature colony includes a fertile female and male, known as the queen and king.[68] The queen of the colony is responsible for egg production for the colony. Unlike in ants, the king mates with her for life.[69] In some species, the abdomen of the queen swells up dramatically to increase fecundity, a characteristic known as physogastrism.[57][68] Depending on the species, the queen starts producing reproductive winged alates at a certain time of the year, and huge swarms emerge from the colony when nuptial flight begins. These swarms attract a wide variety of predators.[68]

Life cycle
A young termite nymph. Nymphs first moult into workers, but others may further moult to become soldiers or alates.
Termite, and shed wings from other termites, on an interior window sill. Shedding of wings is associated with reproductive swarming.[70]

Termites are often compared with the social Hymenoptera (ants and various species of bees and wasps), but their differing evolutionary origins result in major differences in life cycle. In the eusocial Hymenoptera, the workers are exclusively female. Males (drones) are haploid and develop from unfertilised eggs, while females (both workers and the queen) are diploid and develop from fertilised eggs. In contrast, worker termites, which constitute the majority in a colony, are diploid individuals of both sexes and develop from fertilised eggs. Depending on species, male and female workers may have different roles in a termite colony.[71]

The life cycle of a termite begins with an egg, but is different from that of a bee or ant in that it goes through a developmental process called incomplete metamorphosis, with egg, nymph and adult stages.[72] Nymphs resemble small adults, and go through a series of moults as they grow. In some species, eggs go through four moulting stages and nymphs go through three.[73] Nymphs first moult into workers, and then some workers go through further moulting and become soldiers or alates; workers become alates only by moulting into alate nymphs.[74]

The development of nymphs into adults can take months; the time period depends on food availability, temperature, and the general population of the colony. Since nymphs are unable to feed themselves, workers must feed them, but workers also take part in the social life of the colony and have certain other tasks to accomplish such as foraging, building or maintaining the nest or tending to the queen.[58][75] Pheromones regulate the caste system in termite colonies, preventing all but a very few of the termites from becoming fertile queens.[76]

Queens of the eusocial termite Reticulitermes speratus are capable of a long lifespan without sacrificing fecundity. These long-lived queens have a significantly lower level of oxidative damage, including oxidative DNA damage, than workers, soldiers and nymphs.[77] The lower levels of damage appear to be due to increased catalase, an enzyme that protects against oxidative stress.[77]

Reproduction
Alates swarming during nuptial flight after rain

Termite alates only leave the colony when a nuptial flight takes place. Alate males and females pair up together and then land in search of a suitable place for a colony.[78] A termite king and queen do not mate until they find such a spot. When they do, they excavate a chamber big enough for both, close up the entrance and proceed to mate.[78] After mating, the pair never go outside and spend the rest of their lives in the nest. Nuptial flight time varies in each species. For example, alates in certain species emerge during the day in summer while others emerge during the winter.[79] The nuptial flight may also begin at dusk, when the alates swarm around areas with many lights. The time when nuptial flight begins depends on the environmental conditions, the time of day, moisture, wind speed and precipitation.[79] The number of termites in a colony also varies, with the larger species typically having 100–1,000 individuals. However, some termite colonies, including those with many individuals, can number in the millions.[44]

The queen only lays 10–20 eggs in the very early stages of the colony, but lays as many as 1,000 a day when the colony is several years old.[58] At maturity, a primary queen has a great capacity to lay eggs. In some species, the mature queen has a greatly distended abdomen and may produce 40,000 eggs a day.[80] The two mature ovaries may have some 2,000 ovarioles each.[81] The abdomen increases the queen's body length to several times more than before mating and reduces her ability to move freely; attendant workers provide assistance.

The king grows only slightly larger after initial mating and continues to mate with the queen for life (a termite queen can live between 30 to 50 years); this is very different from ant colonies, in which a queen mates once with the male(s) and stores the gametes for life, as the male ants die shortly after mating.[69][75] If a queen is absent, a termite king produces pheromones which encourage the development of replacement termite queens.[82] As the queen and king are monogamous, sperm competition does not occur.[83]

Termites going through incomplete metamorphosis on the path to becoming alates form a subcaste in certain species of termite, functioning as potential supplementary reproductives. These supplementary reproductives only mature into primary reproductives upon the death of a king or queen, or when the primary reproductives are separated from the colony.[74][84] Supplementaries have the ability to replace a dead primary reproductive, and there may also be more than a single supplementary within a colony.[58] Some queens have the ability to switch from sexual reproduction to asexual reproduction. Studies show that while termite queens mate with the king to produce colony workers, the queens reproduce their replacements (neotenic queens) parthenogenetically.[85][86]

The neotropical termite Embiratermes neotenicus and several other related species produce colonies that contain a primary king accompanied by a primary queen or by up to 200 neotenic queens that had originated through thelytokous parthenogenesis of a founding primary queen.[87] The form of parthenogenesis likely employed maintains heterozygosity in the passage of the genome from mother to daughter, thus avoiding inbreeding depression.

Behaviour and ecology

Diet
Termite faecal pellets

Termites are detritivores, consuming dead plants at any level of decomposition. They also play a vital role in the ecosystem by recycling waste material such as dead wood, faeces and plants.[88][89][90] Many species eat cellulose, having a specialised midgut that breaks down the fibre.[91] Termites are considered to be a major source (11%) of atmospheric methane, one of the prime greenhouse gases, produced from the breakdown of cellulose.[92] Termites rely primarily upon symbiotic protozoa (metamonads) and other microbes such as flagellate protists in their guts to digest the cellulose for them, allowing them to absorb the end products for their own use.[93][94]The microbial ecosystem present in the termite gut contains many species found nowhere else on Earth. Termites hatch without these symbionts present in their guts, and develop them after fed a culture from other termites.[95] Gut protozoa, such as Trichonympha, in turn, rely on symbiotic bacteria embedded on their surfaces to produce some of the necessary digestive enzymes. Most higher termites, especially in the family Termitidae, can produce their own cellulase enzymes, but they rely primarily upon the bacteria. The flagellates have been lost in Termitidae.[96][97][98] Researches have found species of spirochetes living in termite guts capable of fixing atmospheric nitrogen to a form usable by the insect.[99] Scientists' understanding of the relationship between the termite digestive tract and the microbial endosymbionts is still rudimentary; what is true in all termite species, however, is that the workers feed the other members of the colony with substances derived from the digestion of plant material, either from the mouth or anus.[59][100] Judging from closely related bacterial species, it is strongly presumed that the termites' and cockroach's gut microbiota derives from their dictyopteran ancestors.[101]

Certain species such as Gnathamitermes tubiformans have seasonal food habits. For example, they may preferentially consume Red three-awn (Aristida longiseta) during the summer, Buffalograss (Buchloe dactyloides) from May to August, and blue grama Bouteloua gracilis during spring, summer and autumn. Colonies of G. tubiformans consume less food in spring than they do during autumn when their feeding activity is high.[102]

Various woods differ in their susceptibility to termite attack; the differences are attributed to such factors as moisture content, hardness, and resin and lignin content. In one study, the drywood termite Cryptotermes brevis strongly preferred poplar and maple woods to other woods that were generally rejected by the termite colony. These preferences may in part have represented conditioned or learned behaviour.[103]

Some species of termite practice fungiculture. They maintain a "garden" of specialised fungi of genus Termitomyces, which are nourished by the excrement of the insects. When the fungi are eaten, their spores pass undamaged through the intestines of the termites to complete the cycle by germinating in the fresh faecal pellets.[104][105] Molecular evidence suggests that the family Macrotermitinae developed agriculture about 31 million years ago. It is assumed that more than 90 percent of dry wood in the semiarid savannah ecosystems of Africa and Asia are reprocessed by these termites. Originally living in the rainforest, fungus farming allowed them to colonise the African savannah and other new environments, eventually expanding into Asia.[106]

Depending on their feeding habits, termites are placed into two groups: the lower termites and higher termites. The lower termites predominately feed on wood. As wood is difficult to digest, termites prefer to consume fungus-infected wood because it is easier to digest and the fungi are high in protein. Meanwhile, the higher termites consume a wide variety of materials, including faeces, humus, grass, leaves and roots.[107] The gut in the lower termites contains many species of bacteria along with protozoa, while the higher termites only have a few species of bacteria with no protozoa.[108]

Predators
Crab spider with a captured alate

Termites are consumed by a wide variety of predators. One termite species alone, Hodotermes mossambicus, was found in the stomach contents of 65 birds and 19 mammals.[109] Arthropods such as ants,[110][111] centipedes, cockroaches, crickets, dragonflies, scorpions and spiders,[112] reptiles such as lizards,[113] and amphibians such as frogs[114] and toads consume termites, with two spiders in the family Ammoxenidae being specialist termite predators.[115][116][117] Other predators include aardvarks, aardwolves, anteaters, bats, bears, bilbies, many birds, echidnas, foxes, galagos, numbats, mice and pangolins.[115][118][119][120] The aardwolf is an insectivorous mammal that primarily feeds on termites; it locates its food by sound and also by detecting the scent secreted by the soldiers; a single aardwolf is capable of consuming thousands of termites in a single night by using its long, sticky tongue.[121][122] Sloth bears break open mounds to consume the nestmates, while chimpanzees have developed tools to "fish" termites from their nest. Wear pattern analysis of bone tools used by the early hominin Paranthropus robustus suggests that they used these tools to dig into termite mounds.[123]

A Matabele ant (Megaponera analis) kills a Macrotermes bellicosus termite soldier during a raid.

Among all predators, ants are the greatest enemy to termites.[110][111] Some ant genera are specialist predators of termites. For example, Megaponera is a strictly termite-eating (termitophagous) genus that perform raiding activities, some lasting several hours.[124][125] Paltothyreus tarsatus is another termite-raiding species, with each individual stacking as many termites as possible in its mandibles before returning home, all the while recruiting additional nestmates to the raiding site through chemical trails.[110] The Malaysian basicerotine ants Eurhopalothrix heliscata uses a different strategy of termite hunting by pressing themselves into tight spaces, as they hunt through rotting wood housing termite colonies. Once inside, the ants seize their prey by using their short but sharp mandibles.[110] Tetramorium uelense is a specialised predator species that feeds on small termites. A scout recruits 10–30 workers to an area where termites are present, killing them by immobilising them with their stinger.[126] Centromyrmex and Iridomyrmex colonies sometimes nest in termite mounds, and so the termites are preyed on by these ants. No evidence for any kind of relationship (other than a predatory one) is known.[127][128] Other ants, including Acanthostichus, Camponotus, Crematogaster, Cylindromyrmex, Leptogenys, Odontomachus, Ophthalmopone, Pachycondyla, Rhytidoponera, Solenopsis and Wasmannia, also prey on termites.[118][110][129] In contrast to all these ant species, and despite their enormous diversity of prey, Dorylus ants rarely consume termites.[130]

Ants are not the only invertebrates that perform raids. Many sphecoid wasps and several species including Polybia and Angiopolybia are known to raid termite mounds during the termites' nuptial flight.[131]

Parasites, pathogens and viruses

Termites are less likely to be attacked by parasites than bees, wasps and ants, as they are usually well protected in their mounds.[132][133] Nevertheless, termites are infected by a variety of parasites. Some of these include dipteran flies,[134] Pyemotes mites, and a large number of nematode parasites. Most nematode parasites are in the order Rhabditida;[135] others are in the genus Mermis, Diplogaster aerivora and Harteria gallinarum.[136] Under imminent threat of an attack by parasites, a colony may migrate to a new location.[137] Fungal pathogens such as Aspergillus nomius and Metarhizium anisopliae are, however, major threats to a termite colony as they are not host-specific and may infect large portions of the colony;[138][139] transmission usually occurs via direct physical contact.[140] M. anisopliae is known to weaken the termite immune system. Infection with A. nomius only occurs when a colony is under great stress.

Termites are infected by viruses including Entomopoxvirinae and the Nuclear Polyhedrosis Virus.[141][142]

Locomotion and foraging

Because the worker and soldier castes lack wings and thus never fly, and the reproductives use their wings for just a brief amount of time, termites predominantly rely upon their legs to move about.[49]

Foraging behaviour depends on the type of termite. For example, certain species feed on the wood structures they inhabit, and others harvest food that is near the nest.[143] Most workers are rarely found out in the open, and do not forage unprotected; they rely on sheeting and runways to protect them from predators.[57] Subterranean termites construct tunnels and galleries to look for food, and workers who manage to find food sources recruit additional nestmates by depositing a phagostimulant pheromone that attracts workers.[144] Foraging workers use semiochemicals to communicate with each other,[145] and workers who begin to forage outside of their nest release trail pheromones from their sternal glands.[146] In one species, Nasutitermes costalis, there are three phases in a foraging expedition: first, soldiers scout an area. When they find a food source, they communicate to other soldiers and a small force of workers starts to emerge. In the second phase, workers appear in large numbers at the site. The third phase is marked by a decrease in the number of soldiers present and an increase in the number of workers.[147] Isolated termite workers may engage in Lévy flight behaviour as an optimised strategy for finding their nestmates or foraging for food.[148]

Competition

Competition between two colonies always results in agonistic behaviour towards each other, resulting in fights. These fights can cause mortality on both sides and, in some cases, the gain or loss of territory.[149][150] "Cemetery pits" may be present, where the bodies of dead termites are buried.[151]

Studies show that when termites encounter each other in foraging areas, some of the termites deliberately block passages to prevent other termites from entering.[145][152] Dead termites from other colonies found in exploratory tunnels leads to the isolation of the area and thus the need to construct new tunnels.[153] Conflict between two competitors does not always occur. For example, though they might block each other's passages, colonies of Macrotermes bellicosus and Macrotermes subhyalinus are not always aggressive towards each other.[154] Suicide cramming is known in Coptotermes formosanus. Since C. formosanus colonies may get into physical conflict, some termites squeeze tightly into foraging tunnels and die, successfully blocking the tunnel and ending all agonistic activities.[155]

Among the reproductive caste, neotenic queens may compete with each other to become the dominant queen when there are no primary reproductives. This struggle among the queens leads to the elimination of all but a single queen, which, with the king, takes over the colony.[156]

Ants and termites may compete with each other for nesting space. In particular, ants that prey on termites usually have a negative impact on arboreal nesting species.[157]

Communication
Hordes of Nasutitermes on a march for food, following and leaving trail pheromones

Most termites are blind, so communication primarily occurs through chemical, mechanical and pheromonal cues.[46][145] These methods of communication are used in a variety of activities, including foraging, locating reproductives, construction of nests, recognition of nestmates, nuptial flight, locating and fighting enemies, and defending the nests.[46][145] The most common way of communicating is through antennation.[145] A number of pheromones are known, including contact pheromones (which are transmitted when workers are engaged in trophallaxis or grooming) and alarm, trail and sex pheromones. The alarm pheromone and other defensive chemicals are secreted from the frontal gland. Trail pheromones are secreted from the sternal gland, and sex pheromones derive from two glandular sources: the sternal and tergal glands.[46] When termites go out to look for food, they forage in columns along the ground through vegetation. A trail can be identified by the faecal deposits or runways that are covered by objects. Workers leave pheromones on these trails, which are detected by other nestmates through olfactory receptors.[62] Termites can also communicate through mechanical cues, vibrations, and physical contact.[62][145] These signals are frequently used for alarm communication or for evaluating a food source.[145][158]

When termites construct their nests, they use predominantly indirect communication. No single termite would be in charge of any particular construction project. Individual termites react rather than think, but at a group level, they exhibit a sort of collective cognition. Specific structures or other objects such as pellets of soil or pillars cause termites to start building. The termite adds these objects onto existing structures, and such behaviour encourages building behaviour in other workers. The result is a self-organised process whereby the information that directs termite activity results from changes in the environment rather than from direct contact among individuals.[145]

Termites can distinguish nestmates and non-nestmates through chemical communication and gut symbionts: chemicals consisting of hydrocarbons released from the cuticle allow the recognition of alien termite species.[159][160] Each colony has its own distinct odour. This odour is a result of genetic and environmental factors such as the termites' diet and the composition of the bacteria within the termites' intestines.[161]

Defence
See also: Insect defences
Termites rush to a damaged area of the nest.

Termites rely on alarm communication to defend a colony.[145] Alarm pheromones can be released when the nest has been breached or is being attacked by enemies or potential pathogens. Termites always avoid nestmates infected with Metarhizium anisopliae spores, through vibrational signals released by infected nestmates.[162] Other methods of defence include intense jerking and secretion of fluids from the frontal gland and defecating faeces containing alarm pheromones.[145][163]

In some species, some soldiers block tunnels to prevent their enemies from entering the nest, and they may deliberately rupture themselves as an act of defence.[164] In cases where the intrusion is coming from a breach that is larger than the soldier's head, soldiers form a phalanx-like formation around the breach and bite at intruders.[165] If an invasion carried out by Megaponera analis is successful, an entire colony may be destroyed, although this scenario is rare.[165]

To termites, any breach of their tunnels or nests is a cause for alarm. When termites detect a potential breach, the soldiers usually bang their heads, apparently to attract other soldiers for defence and to recruit additional workers to repair any breach.[62] Additionally, an alarmed termite bumps into other termites which causes them to be alarmed and to leave pheromone trails to the disturbed area, which is also a way to recruit extra workers.[62]

Nasute termite soldiers on rotten wood

The pantropical subfamily Nasutitermitinae has a specialised caste of soldiers, known as nasutes, that have the ability to exude noxious liquids through a horn-like frontal projection that they use for defence.[166] Nasutes have lost their mandibles through the course of evolution and must be fed by workers.[65] A wide variety of monoterpene hydrocarbon solvents have been identified in the liquids that nasutes secrete.[167] Similarly, Formosan subterranean termites have been known to secrete naphthalene to protect their nests.[168]

Soldiers of the species Globitermes sulphureus commit suicide by autothysis – rupturing a large gland just beneath the surface of their cuticles. The thick, yellow fluid in the gland becomes very sticky on contact with the air, entangling ants or other insects that are trying to invade the nest.[169][170] Another termite, Neocapriterme taracua, also engages in suicidal defence. Workers physically unable to use their mandibles while in a fight form a pouch full of chemicals, then deliberately rupture themselves, releasing toxic chemicals that paralyse and kill their enemies.[171] The soldiers of the neotropical termite family Serritermitidae have a defence strategy which involves front gland autothysis, with the body rupturing between the head and abdomen. When soldiers guarding nest entrances are attacked by intruders, they engage in autothysis, creating a block that denies entry to any attacker.[172]

Workers use several different strategies to deal with their dead, including burying, cannibalism, and avoiding a corpse altogether.[173][174][175] To avoid pathogens, termites occasionally engage in necrophoresis, in which a nestmate carries away a corpse from the colony to dispose of it elsewhere.[176] Which strategy is used depends on the nature of the corpse a worker is dealing with (i.e. the age of the carcass).[176]

Relationship with other organisms
Rhizanthella gardneri is the only orchid known to be pollinated by termites.

A species of fungus is known to mimic termite eggs, successfully avoiding its natural predators. These small brown balls, known as "termite balls", rarely kill the eggs, and in some cases the workers tend to them.[177] This fungus mimics these eggs by producing a cellulose-digesting enzyme known as glucosidases.[178] A unique mimicking behaviour exists between various species of Trichopsenius beetles and certain termite species within Reticulitermes. The beetles share the same cuticle hydrocarbons as the termites and even biosynthesize them. This chemical mimicry allows the beetles to integrate themselves within the termite colonies.[179] The developed appendages on the physogastric abdomen of Austrospirachtha mimetes allows the beetle to mimic a termite worker.[180]

Some species of ant are known to capture termites to use as a fresh food source later on, rather than killing them. For example, Formica nigra captures termites, and those who try to escape are immediately seized and driven underground.[181] Certain species of ants in the subfamily Ponerinae conduct these raids although other ant species go in alone to steal the eggs or nymphs.[157] Ants such as Megaponera analis attack the outside of mounds and Dorylinae ants attack underground.[157][182] Despite this, some termites and ants can coexist peacefully. Some species of termite, including Nasutitermes corniger, form associations with certain ant species to keep away predatory ant species.[183] The earliest known association between Azteca ants and Nasutitermes termites date back to the Oligocene to Miocene period.[184]

An ant raiding party collecting Pseudocanthotermes militaris termites after a successful raid

54 species of ants are known to inhabit Nasutitermes mounds, both occupied and abandoned ones.[185] One reason many ants live in Nasutitermes mounds is due to the termites' frequent occurrence in their geographical range; another is to protect themselves from floods.[185][186] Iridomyrmex also inhabits termite mounds although no evidence for any kind of relationship (other than a predatory one) is known.[127] In rare cases, certain species of termites live inside active ant colonies.[187] Some invertebrate organisms such as beetles, caterpillars, flies and millipedes are termitophiles and dwell inside termite colonies (they are unable to survive independently).[62] As a result, certain beetles and flies have evolved with their hosts. They have developed a gland that secrete a substance that attracts the workers by licking them. Mounds may also provide shelter and warmth to birds, lizards, snakes and scorpions.[62]

Termites are known to carry pollen and regularly visit flowers,[188] so are regarded as potential pollinators for a number of flowering plants.[189] One flower in particular, Rhizanthella gardneri, is regularly pollinated by foraging workers, and it is perhaps the only Orchidaceae flower in the world to be pollinated by termites.[188]

Many plants have developed effective defences against termites. However, seedlings are vulnerable to termite attacks and need additional protection, as their defence mechanisms only develop when they have passed the seedling stage.[190] Defence is typically achieved by secreting antifeedant chemicals into the woody cell walls.[191] This reduces the ability of termites to efficiently digest the cellulose. A commercial product, "Blockaid", has been developed in Australia that uses a range of plant extracts to create a paint-on nontoxic termite barrier for buildings.[191] An extract of a species of Australian figwort, Eremophila, has been shown to repel termites;[192] tests have shown that termites are strongly repelled by the toxic material to the extent that they will starve rather than consume the food. When kept close to the extract, they become disoriented and eventually die.[192]

Relationship with the environment

Termite populations can be substantially impacted by environmental changes including those caused by human intervention. A Brazilian study investigated the termite assemblages of three sites of Caatinga under different levels of anthropogenic disturbance in the semi-arid region of northeastern Brazil were sampled using 65 x 2 m transects.[193] A total of 26 species of termites were present in the three sites, and 196 encounters were recorded in the transects. The termite assemblages were considerably different among sites, with a conspicuous reduction in both diversity and abundance with increased disturbance, related to the reduction of tree density and soil cover, and with the intensity of trampling by cattle and goats. The wood-feeders were the most severely affected feeding group.

Nests
An arboreal termite nest in Mexico
Termite nest in a Banksia, Palm Beach, Sydney.

A termite nest can be considered as being composed of two parts, the inanimate and the animate. The animate is all of the termites living inside the colony, and the inanimate part is the structure itself, which is constructed by the termites.[194] Nests can be broadly separated into three main categories: subterranean (completely below ground), epigeal (protruding above the soil surface), and arboreal (built above ground, but always connected to the ground via shelter tubes).[195] Epigeal nests (mounds) protrude from the earth with ground contact and are made out of earth and mud.[196] A nest has many functions such as providing a protected living space and providing shelter against predators. Most termites construct underground colonies rather than multifunctional nests and mounds.[197] Primitive termites of today nest in wooden structures such as logs, stumps and the dead parts of trees, as did termites millions of years ago.[195]

To build their nests, termites primarily use faeces, which have many desirable properties as a construction material.[198] Other building materials include partly digested plant material, used in carton nests (arboreal nests built from faecal elements and wood), and soil, used in subterranean nest and mound construction. Not all nests are visible, as many nests in tropical forests are located underground.[197] Species in the subfamily Apicotermitinae are good examples of subterranean nest builders, as they only dwell inside tunnels.[198] Other termites live in wood, and tunnels are constructed as they feed on the wood. Nests and mounds protect the termites' soft bodies against desiccation, light, pathogens and parasites, as well as providing a fortification against predators.[199] Nests made out of carton are particularly weak, and so the inhabitants use counter-attack strategies against invading predators.[200]

Arboreal carton nests of mangrove swamp-dwelling Nasutitermes are enriched in lignin and depleted in cellulose and xylans. This change is caused by bacterial decay in the gut of the termites: they use their faeces as a carton building material. Arboreal termites nests can account for as much as 2% of above ground carbon storage in Puerto Rican mangrove swamps. These Nasutitermes nests are mainly composed of partially biodegraded wood material from the stems and branches of mangrove trees, namely, Rhizophora mangle (red mangrove), Avicennia germinans (black mangrove) and Laguncularia racemose (white mangrove).[201]

Some species build complex nests called polycalic nests; this habitat is called polycalism. Polycalic species of termites form multiple nests, or calies, connected by subterranean chambers.[118] The termite genera Apicotermes and Trinervitermes are known to have polycalic species.[202] Polycalic nests appear to be less frequent in mound-building species although polycalic arboreal nests have been observed in a few species of Nasutitermes.[202]

Mounds
Main article: Mound-building termites

Nests are considered mounds if they protrude from the earth's surface.[198] A mound provides termites the same protection as a nest but is stronger.[200] Mounds located in areas with torrential and continuous rainfall are at risk of mound erosion due to their clay-rich construction. Those made from carton can provide protection from the rain, and in fact can withstand high precipitation.[198] Certain areas in mounds are used as strong points in case of a breach. For example, Cubitermes colonies build narrow tunnels used as strong points, as the diameter of the tunnels is small enough for soldiers to block.[203] A highly protected chamber, known as the "queens cell", houses the queen and king and is used as a last line of defence.[200]

Species in the genus Macrotermes arguably build the most complex structures in the insect world, constructing enormous mounds.[198] These mounds are among the largest in the world, reaching a height of 8 to 9 metres (26 to 29 feet), and consist of chimneys, pinnacles and ridges.[62] Another termite species, Amitermes meridionalis, can build nests 3 to 4 metres (9 to 13 feet) high and 2.5 metres (8 feet) wide. The tallest mound ever recorded was 12.8 metres (42 ft) long found in the Democratic Republic of the Congo.[204]

The sculptured mounds sometimes have elaborate and distinctive forms, such as those of the compass termite (Amitermes meridionalis and A. laurensis), which builds tall, wedge-shaped mounds with the long axis oriented approximately north–south, which gives them their common name.[205][206] This orientation has been experimentally shown to assist thermoregulation. The north–south orientation causes the internal temperature of a mound to increase rapidly during the morning while avoiding overheating from the midday sun. The temperature then remains at a plateau for the rest of the day until the evening.[207]

Shelter tubes
Nasutiterminae shelter tubes on a tree trunk provide cover for the trail from nest to forest floor.

Termites construct shelter tubes, also known as earthen tubes or mud tubes, that start from the ground. These shelter tubes can be found on walls and other structures.[208] Constructed by termites during the night, a time of higher humidity, these tubes provide protection to termites from potential predators, especially ants.[209] Shelter tubes also provide high humidity and darkness and allow workers to collect food sources that cannot be accessed in any other way.[208] These passageways are made from soil and faeces and are normally brown in colour. The size of these shelter tubes depends on the number of food sources that are available. They range from less than 1 cm to several cm in width, but may be dozens of metres in length.[209]

Relationship with humans

As pests
Termite mound as an obstacle on a runway at Khorixas (Namibia)
Termite damage on external structure

Owing to their wood-eating habits, many termite species can do significant damage to unprotected buildings and other wooden structures.[210] Termites play an important role as decomposers of wood and vegetative material, and the conflict with humans occurs where structures and landscapes containing structural wood components, cellulose derived structural materials and ornamental vegetation provide termites with a reliable source of food and moisture.[211] Their habit of remaining concealed often results in their presence being undetected until the timbers are severely damaged, with only a thin exterior layer of wood remaining, which protects them from the environment.[212] Of the 3,106 species known, only 183 species cause damage; 83 species cause significant damage to wooden structures.[210] In North America, 18 subterranean species are pests;[213] in Australia, 16 species have an economic impact; in the Indian subcontinent 26 species are considered pests, and in tropical Africa, 24. In Central America and the West Indies, there are 17 pest species.[210] Among the termite genera, Coptotermes has the highest number of pest species of any genus, with 28 species known to cause damage.[210] Less than 10% of drywood termites are pests, but they infect wooden structures and furniture in tropical, subtropical and other regions. Dampwood termites only attack lumber material exposed to rainfall or soil.[210]

Drywood termites thrive in warm climates, and human activities can enable them to invade homes since they can be transported through contaminated goods, containers and ships.[210] Colonies of termites have been seen thriving in warm buildings located in cold regions.[214] Some termites are considered invasive species. Cryptotermes brevis, the most widely introduced invasive termite species in the world, has been introduced to all the islands in the West Indies and to Australia.[42][210]

Termite damage in wooden house stumps

In addition to causing damage to buildings, termites can also damage food crops.[215] Termites may attack trees whose resistance to damage is low but generally ignore fast-growing plants. Most attacks occur at harvest time; crops and trees are attacked during the dry season.[215]

The damage caused by termites costs the southwestern United States approximately $1.5 billion each year in wood structure damage, but the true cost of damage worldwide cannot be determined.[210][216] Drywood termites are responsible for a large proportion of the damage caused by termites.[217] The goal of termite control is to keep structures and susceptible ornamental plants free from termites.;[218] Structures may be homes or business, or elements such as wooden fence posts and telephone poles. Regular and thorough inspections by a trained professional may be necessary to detect termite activity in the absence of more obvious signs like termite swarmers or alates inside or adjacent to a structure. Termite monitors made of wood or cellulose adjacent to a structure may also provide indication of termite foraging activity where it will be in conflict with humans. Termites can be controlled by application of Bordeaux mixture or other substances that contain copper such as chromated copper arsenate.[219]

To better control the population of termites, various methods have been developed to track termite movements.[216] One early method involved distributing termite bait laced with immunoglobulin G (IgG) marker proteins from rabbits or chickens. Termites collected from the field could be tested for the rabbit-IgG markers using a rabbit-IgG-specific assay. More recently developed, less expensive alternatives include tracking the termites using egg white, cow milk, or soy milk proteins, which can be sprayed on termites in the field. Termites bearing these proteins can be traced using a protein-specific ELISA test.[216]

As food
See also: Entomophagy
Mozambican boys from the Yawo tribe collecting flying termites
These flying alates were collected as they came out of their nests in the ground during the early days of the rainy season.

43 termite species are used as food by humans or are fed to livestock.[220] These insects are particularly important in impoverished countries where malnutrition is common, as the protein from termites can help improve the human diet. Termites are consumed in many regions globally, but this practice has only become popular in developed nations in recent years.[220]

Termites are consumed by people in many different cultures around the world. In many parts of Africa, the alates are an important factor in the diets of native populations.[221] Groups have different ways of collecting or cultivating insects; sometimes collecting soldiers from several species. Though harder to acquire, queens are regarded as a delicacy.[222] Termite alates are high in nutrition with adequate levels of fat and protein. They are regarded as pleasant in taste, having a nut-like flavour after they are cooked.[221]

Alates are collected when the rainy season begins. During a nuptial flight, they are typically seen around lights to which they are attracted, and so nets are set up on lamps and captured alates are later collected. The wings are removed through a technique that is similar to winnowing. The best result comes when they are lightly roasted on a hot plate or fried until crisp. Oil is not required as their bodies usually contain sufficient amounts of oil. Termites are typically eaten when livestock is lean and tribal crops have not yet developed or produced any food, or if food stocks from a previous growing season are limited.[221]

In addition to Africa, termites are consumed in local or tribal areas in Asia and North and South America. In Australia, Indigenous Australians are aware that termites are edible but do not consume them even in times of scarcity; there are few explanations as to why.[221][222] Termite mounds are the main sources of soil consumption (geophagy) in many countries including Kenya, Tanzania, Zambia, Zimbabwe and South Africa.[223][224][225][226] Researchers have suggested that termites are suitable candidates for human consumption and space agriculture, as they are high in protein and can be used to convert inedible waste to consumable products for humans.[227]

In agriculture
Scientists have developed a more affordable method of tracing the movement of termites using traceable proteins.[216]

Termites can be major agricultural pests, particularly in East Africa and North Asia, where crop losses can be severe (3–100% in crop loss in Africa).[228] Counterbalancing this is the greatly improved water infiltration where termite tunnels in the soil allow rainwater to soak in deeply, which helps reduce runoff and consequent soil erosion through bioturbation.[229] In South America, cultivated plants such as eucalyptus, upland rice and sugarcane can be severely damaged by termite infestations, with attacks on leaves, roots and woody tissue. Termites can also attack other plants, including cassava, coffee, cotton, fruit trees, maize, peanuts, soybeans and vegetables.[21] Mounds can disrupt farming activities, making it difficult for farmers to operate farming machinery; however, despite farmers' dislike of the mounds, it is often the case that no net loss of production occurs.[21] Termites can be beneficial to agriculture, such as by boosting crop yields and enriching the soil. Termites and ants can re-colonise untilled land that contains crop stubble, which colonies use for nourishment when they establish their nests. The presence of nests in fields enables larger amounts of rainwater to soak into the ground and increases the amount of nitrogen in the soil, both essential for the growth of crops.[230]

In science and technology
See also: Renewable energy, Termite-inspired robots, and Sustainable architecture

The termite gut has inspired various research efforts aimed at replacing fossil fuels with cleaner, renewable energy sources.[231] Termites are efficient bioreactors, capable of producing two litres of hydrogen from a single sheet of paper.[232] Approximately 200 species of microbes live inside the termite hindgut, releasing the hydrogen that was trapped inside wood and plants that they digest.[231][233] Through the action of unidentified enzymes in the termite gut, lignocellulose polymers are broken down into sugars and are transformed into hydrogen. The bacteria within the gut turns the sugar and hydrogen into cellulose acetate, an acetate ester of cellulose on which termites rely for energy.[231] Community DNA sequencing of the microbes in the termite hindgut has been employed to provide a better understanding of the metabolic pathway.[231] Genetic engineering may enable hydrogen to be generated in bioreactors from woody biomass.[231]

The development of autonomous robots capable of constructing intricate structures without human assistance has been inspired by the complex mounds that termites build.[234] These robots work independently and can move by themselves on a tracked grid, capable of climbing and lifting up bricks. Such robots may be useful for future projects on Mars, or for building levees to prevent flooding.[235]

Termites use sophisticated means to control the temperatures of their mounds. As discussed above, the shape and orientation of the mounds of the Australian compass termite stabilises their internal temperatures during the day. As the towers heat up, the solar chimney effect (stack effect) creates an updraft of air within the mound.[236] Wind blowing across the tops of the towers enhances the circulation of air through the mounds, which also include side vents in their construction. The solar chimney effect has been in use for centuries in the Middle East and Near East for passive cooling, as well as in Europe by the Romans.[237] It is only relatively recently, however, that climate responsive construction techniques have become incorporated into modern architecture. Especially in Africa, the stack effect has become a popular means to achieve natural ventilation and passive cooling in modern buildings.[236]

In culture
The pink-hued Eastgate Centre

The Eastgate Centre is a shopping centre and office block in central Harare, Zimbabwe, whose architect, Mick Pearce, used passive cooling inspired by that used by the local termites.[238] It was the first major building exploiting termite-inspired cooling techniques to attract international attention. Other such buildings include the Learning Resource Center at the Catholic University of Eastern Africa and the Council House 2 building in Melbourne, Australia.[236]

Few zoos hold termites, due to the difficulty in keeping them captive and to the reluctance of authorities to permit potential pests. One of the few that do, the Zoo Basel in Switzerland, has two thriving Macrotermes bellicosus populations – resulting in an event very rare in captivity: the mass migrations of young flying termites. This happened in September 2008, when thousands of male termites left their mound each night, died, and covered the floors and water pits of the house holding their exhibit.[239]

African tribes in several countries have termites as totems, and for this reason tribe members are forbidden to eat the reproductive alates.[240] Termites are widely used in traditional popular medicine; they are used as treatments for diseases and other conditions such as asthma, bronchitis, hoarseness, influenza, sinusitis, tonsillitis and whooping cough.[220] In Nigeria, Macrotermes nigeriensis is used for spiritual protection and to treat wounds and sick pregnant women. In Southeast Asia, termites are used in ritual practices. In Malaysia, Singapore and Thailand, termite mounds are commonly worshiped among the populace.[241] Abandoned mounds are viewed as structures created by spirits, believing a local guardian dwells within the mound; this is known as Keramat and Datok Kong. In urban areas, local residents construct red-painted shrines over mounds that have been abandoned, where they pray for good health, protection and luck.[241]

See also

Notes
  1. It is unknown whether the termite was female or male. If it was a female, the body length would be far greater than 25 millimetres when mature.

References
  1. Behrensmeyer, A. K.; Turner, A. "Fossilworks, Gateway to the Paleobiology Database".
  2. Engel, M.S.; Grimaldi, D.A.; Krishna, K. (2009). "Termites (Isoptera): their phylogeny, classification, and rise to ecological dominance". American Museum Novitates. 2009 (3650): 1–27. doi:10.1206/651.1. hdl:2246/5969. ISSN 0003-0082. S2CID 56166416.
  3. Evangelista, Dominic A.; Wipfler, Benjamin; Béthoux, Olivier; Donath, Alexander; Fujita, Mari; Kohli, Manpreet K.; Legendre, Frédéric; Liu, Shanlin; Machida, Ryuichiro; Misof, Bernhard; Peters, Ralph S. (2019-01-30). "An integrative phylogenomic approach illuminates the evolutionary history of cockroaches and termites (Blattodea)". Proceedings of the Royal Society B: Biological Sciences. 286 (1895): 20182076. doi:10.1098/rspb.2018.2076. ISSN 0962-8452. PMC 6364590. PMID 30963947.
  4. "Termite". Merriam-Webster.com.
  5. Bignell, Roisin & Lo 2010, p. 2.
  6. Cranshaw, W. (2013). "11". Bugs Rule!: An Introduction to the World of Insects. Princeton, New Jersey: Princeton University Press. p. 188. ISBN 978-0-691-12495-7.
  7. Lobeck, A. Kohl (1939). Geomorphology; an Introduction to the Study of Landscapes (1st ed.). University of California: McGraw Hill Book Company, Incorporated. pp. 431–432. ASIN B002P5O9SC.
  8. Harper, Douglas. "Termite". Online Etymology Dictionary.
  9. "Termite". Merriam-Webster Online Dictionary. Retrieved 5 January 2015.
  10. Cleveland, L.R.; Hall, S.K.; Sanders, E.P.; Collier, J. (1934). "The Wood-Feeding Roach Cryptocercus, its protozoa, and the symbiosis between protozoa and roach". Memoirs of the American Academy of Arts and Sciences. 17 (2): 185–382. doi:10.1093/aesa/28.2.216.
  11. McKittrick, F.A. (1965). "A contribution to the understanding of cockroach-termite affinities". Annals of the Entomological Society of America. 58 (1): 18–22. doi:10.1093/aesa/58.1.18. PMID 5834489.
  12. Ware, J.L.; Litman, J.; Klass, K.-D.; Spearman, L.A. (2008). "Relationships among the major lineages of Dictyoptera: the effect of outgroup selection on dictyopteran tree topology". Systematic Entomology. 33 (3): 429–450. doi:10.1111/j.1365-3113.2008.00424.x. S2CID 86777253.
  13. Inward, D.; Beccaloni, G.; Eggleton, P. (2007). "Death of an order: a comprehensive molecular phylogenetic study confirms that termites are eusocial cockroaches". Biology Letters. 3 (3): 331–5. doi:10.1098/rsbl.2007.0102. PMC 2464702. PMID 17412673.
  14. Eggleton, P.; Beccaloni, G.; Inward, D. (2007). "Response to Lo et al.". Biology Letters. 3 (5): 564–565. doi:10.1098/rsbl.2007.0367. PMC 2391203.
  15. Ohkuma, M.; Noda, S.; Hongoh, Y.; Nalepa, C.A.; Inoue, T. (2009). "Inheritance and diversification of symbiotic trichonymphid flagellates from a common ancestor of termites and the cockroach Cryptocercus". Proceedings of the Royal Society B: Biological Sciences. 276 (1655): 239–245. doi:10.1098/rspb.2008.1094. PMC 2674353. PMID 18812290.
  16. Lo, N.; Tokuda, G.; Watanabe, H.; Rose, H.; Slaytor, M.; Maekawa, K.; Bandi, C.; Noda, H. (June 2000). "Evidence from multiple gene sequences indicates that termites evolved from wood-feeding cockroaches". Current Biology. 10 (13): 801–814. doi:10.1016/S0960-9822(00)00561-3. PMID 10898984. S2CID 14059547.
  17. Grimaldi, D.; Engel, M.S. (2005). Evolution of the insects (1st ed.). Cambridge: Cambridge University Press. p. 237. ISBN 978-0-521-82149-0.
  18. Klass, K.D.; Nalepa, C.; Lo, N. (2008). "Wood-feeding cockroaches as models for termite evolution (Insecta: Dictyoptera): Cryptocercus vs. Parasphaeria boleiriana". Molecular Phylogenetics & Evolution. 46 (3): 809–817. doi:10.1016/j.ympev.2007.11.028. PMID 18226554.
  19. Lo, N.; Engel, M.S.; Cameron, S.; Nalepa, C.A.; Tokuda, G.; Grimaldi, D.; Kitade, O..; Krishna, K.; Klass, K.-D.; Maekawa, K.; Miura, T.; Thompson, G.J. (2007). "Comment. Save Isoptera: a comment on Inward et al.". Biology Letters. 3 (5): 562–563. doi:10.1098/rsbl.2007.0264. PMC 2391185. PMID 17698448.
  20. Costa, James (2006). The other insect societies. Harvard University Press. pp. 135–136. ISBN 978-0-674-02163-1.
  21. Capinera, J.L. (2008). Encyclopedia of Entomology (2nd ed.). Dordrecht: Springer. pp. 3033–3037, 3754. ISBN 978-1-4020-6242-1.
  22. Vrsanky, P.; Aristov, D. (2014). "Termites (Isoptera) from the Jurassic/Cretaceous boundary: Evidence for the longevity of their earliest genera". European Journal of Entomology. 111 (1): 137–141. doi:10.14411/eje.2014.014.
  23. Poinar, G.O. (2009). "Description of an early Cretaceous termite (Isoptera: Kalotermitidae) and its associated intestinal protozoa, with comments on their co-evolution". Parasites & Vectors. 2 (1–17): 12. doi:10.1186/1756-3305-2-12. PMC 2669471. PMID 19226475.
  24. Legendre, F.; Nel, A.; Svenson, G.J.; Robillard, T.; Pellens, R.; Grandcolas, P.; Escriva, H. (2015). "Phylogeny of Dictyoptera: Dating the Origin of Cockroaches, Praying Mantises and Termites with Molecular Data and Controlled Fossil Evidence". PLOS ONE. 10 (7): e0130127. Bibcode:2015PLoSO..1030127L. doi:10.1371/journal.pone.0130127. PMC 4511787. PMID 26200914.
  25. Luo, Z.X.; Wible, J.R. (2005). "A Late Jurassic digging mammal and early mammalian diversification". Science. 308 (5718): 103–107. Bibcode:2005Sci...308..103L. doi:10.1126/science.1108875. PMID 15802602. S2CID 7031381.
  26. Rohr, D.M.; Boucot, A. J.; Miller, J.; Abbott, M. (1986). "Oldest termite nest from the Upper Cretaceous of west Texas". Geology. 14 (1): 87. Bibcode:1986Geo....14...87R. doi:10.1130/0091-7613(1986)14<87:OTNFTU>2.0.CO;2.
  27. Weesner, F.M. (1960). "Evolution and Biology of the Termites". Annual Review of Entomology. 5 (1): 153–170. doi:10.1146/annurev.en.05.010160.001101.
  28. Tilyard, R.J. (1937). "Kansas Permian insects. Part XX the cockroaches, or order Blattaria". American Journal of Science. 34 (201): 169–202, 249–276. Bibcode:1937AmJS...34..169T. doi:10.2475/ajs.s5-34.201.169.
  29. Henry, M.S. (2013). Symbiosis: Associations of Invertebrates, Birds, Ruminants, and Other Biota. New York, New York: Elsevier. p. 59. ISBN 978-1-4832-7592-5.
  30. Krishna, K.; Grimaldi, D.A.; Krishna, V.; Engel, M.S. (2013). "Treatise on the Isoptera of the world" (PDF). Bulletin of the American Museum of Natural History. 1. 377 (7): 1–200. doi:10.1206/377.1. S2CID 87276148.
  31. Bell, W.J.; Roth, L.M.; Nalepa, C.A. (2007). Cockroaches: ecology, behavior, and natural history. Baltimore, Md.: Johns Hopkins University Press. p. 161. ISBN 978-0-8018-8616-4.
  32. Engel, M. (2011). "Family-group names for termites (Isoptera), redux". ZooKeys (148): 171–184. doi:10.3897/zookeys.148.1682. PMC 3264418. PMID 22287896.
  33. Thorne, Barbara L (1997). "Evolution of eusociality in termites" (PDF). Annual Review of Ecology and Systematics. 28 (5): 27–53. doi:10.1146/annurev.ecolsys.28.1.27. PMC 349550. Archived from the original (PDF) on 2010-05-30.
  34. Harrison, Mark C.; Jongepier, Evelien; Robertson, Hugh M.; Arning, Nicolas; Bitard-Feildel, Tristan; Chao, Hsu; Childers, Christopher P.; Dinh, Huyen; Doddapaneni, Harshavardhan; Dugan, Shannon; Gowin, Johannes; Greiner, Carolin; Han, Yi; Hu, Haofu; Hughes, Daniel S. T.; Huylmans, Ann-Kathrin; Kemena, Carsten; Kremer, Lukas P. M.; Lee, Sandra L.; Lopez-Ezquerra, Alberto; Mallet, Ludovic; Monroy-Kuhn, Jose M.; Moser, Annabell; Murali, Shwetha C.; Muzny, Donna M.; Otani, Saria; Piulachs, Maria-Dolors; Poelchau, Monica; Qu, Jiaxin; Schaub, Florentine; Wada-Katsumata, Ayako; Worley, Kim C.; Xie, Qiaolin; Ylla, Guillem; Poulsen, Michael; Gibbs, Richard A.; Schal, Coby; Richards, Stephen; Belles, Xavier; Korb, Judith; Bornberg-Bauer, Erich (2018). "Hemimetabolous genomes reveal molecular basis of termite eusociality". Nature Ecology & Evolution. 2 (3): 557–566. doi:10.1038/s41559-017-0459-1. PMC 6482461. PMID 29403074.
  35. "Termites had first castes". Nature. 530 (7590): 256. 2016. Bibcode:2016Natur.530Q.256.. doi:10.1038/530256a. S2CID 49905391.
  36. Terrapon, Nicolas; Li, Cai; Robertson, Hugh M.; Ji, Lu; Meng, Xuehong; Booth, Warren; Chen, Zhensheng; Childers, Christopher P.; Glastad, Karl M.; Gokhale, Kaustubh; et al. (2014). "Molecular traces of alternative social organization in a termite genome". Nature Communications. 5: 3636. Bibcode:2014NatCo...5.3636T. doi:10.1038/ncomms4636. PMID 24845553.
  37. Poulsen, Michael; Hu, Haofu; Li, Cai; Chen, Zhensheng; Xu, Luohao; Otani, Saria; Nygaard, Sanne; Nobre, Tania; Klaubauf, Sylvia; Schindler, Philipp M .; et al. (2014). "Complementary symbiont contributions to plant decomposition in a fungus-farming termite". Proceedings of the National Academy of Sciences. 111 (40): 14500–14505. Bibcode:2014PNAS..11114500P. doi:10.1073/pnas.1319718111. PMC 4209977. PMID 25246537.
  38. Kohler, T; Dietrich, C; Scheffrahn, RH; Brune, A (2012). "High‐resolution analysis of gut environment and bacterial microbiota reveals functional compartmentation of the gut in wood‐feeding higher termites (Nasutitermes spp.)". Applied and Environmental Microbiology. 78 (13): 4691–4701. doi:10.1128/aem.00683-12. PMC 3370480. PMID 22544239.
  39. "Termite Biology and Ecology". Division of Technology, Industry and Economics Chemicals Branch. United Nations Environment Programme. Archived from the original on 10 November 2014. Retrieved 12 January 2015.
  40. Meyer, V.W.; Braack, L.E.O.; Biggs, H.C.; Ebersohn, C. (1999). "Distribution and density of termite mounds in the northern Kruger National Park, with specific reference to those constructed by Macrotermes Holmgren (Isoptera: Termitidae)". African Entomology. 7 (1): 123–130.
  41. Sanderson, M.G. (1996). "Biomass of termites and their emissions of methane and carbon dioxide: A global database". Global Biogeochemical Cycles. 10 (4): 543–557. Bibcode:1996GBioC..10..543S. doi:10.1029/96GB01893.
  42. Heather, N.W. (1971). "The exotic drywood termite Cryptotermes brevis (Walker) (Isoptera : Kalotermitidae) and endemic Australian drywood termites in Queensland". Australian Journal of Entomology. 10 (2): 134–141. doi:10.1111/j.1440-6055.1971.tb00022.x.
  43. Claybourne, Anna (2013). A colony of ants, and other insect groups. Chicago, Ill.: Heinemann Library. p. 38. ISBN 978-1-4329-6487-0.
  44. Engel, M.S.; Gross, M. (2008). "A giant termite from the Late Miocene of Styria, Austria (Isoptera)". Naturwissenschaften. 96 (2): 289–295. Bibcode:2009NW.....96..289E. doi:10.1007/s00114-008-0480-y. PMID 19052720. S2CID 21795900.
  45. Heidecker, J.L.; Leuthold, R.H. (1984). "The organisation of collective foraging in the harvester termite Hodotermes mossambicus (Isoptera)". Behavioral Ecology and Sociobiology. 14 (3): 195–202. doi:10.1007/BF00299619. S2CID 22158321.
  46. Costa-Leonardo, A.M.; Haifig, I. (2010). "Pheromones and exocrine glands in Isoptera". Vitamins and Hormones. 83: 521–549. doi:10.1016/S0083-6729(10)83021-3. ISBN 9780123815163. PMID 20831960.
  47. Bignell, Roisin & Lo 2010, p. 7.
  48. Bignell, Roisin & Lo 2010, pp. 7–9.
  49. Bignell, Roisin & Lo 2010, p. 11.
  50. Robinson, W.H. (2005). Urban Insects and Arachnids: A Handbook of Urban Entomology. Cambridge: Cambridge University Press. p. 291. ISBN 978-1-139-44347-0.
  51. Bignell, Roisin & Lo 2010, p. 12.
  52. Riparbelli, M.G; Dallai, R; Mercati, D; Bu, Y; Callaini, G (2009). "Centriole symmetry: a big tale from small organisms". Cell Motility and the Cytoskeleton. 66 (12): 1100–5. doi:10.1002/cm.20417. PMID 19746415.
  53. Nalepa, C.A.; Lenz, M. (2000). "The ootheca of Mastotermes darwiniensis Froggatt (Isoptera: Mastotermitidae): homology with cockroach oothecae". Proceedings of the Royal Society B: Biological Sciences. 267 (1454): 1809–1813. doi:10.1098/rspb.2000.1214. PMC 1690738. PMID 12233781.
  54. Crosland, M.W.J.; Su, N.Y.; Scheffrahn, R.H. (2005). "Arolia in termites (Isoptera): functional significance and evolutionary loss". Insectes Sociaux. 52 (1): 63–66. doi:10.1007/s00040-004-0779-4. S2CID 26873138.
  55. Bignell, Roisin & Lo 2010, p. 9.
  56. Bignell, Roisin & Lo 2010, p. 10.
  57. Bignell, Roisin & Lo 2010, p. 13.
  58. "Termites". Australian Museum. Retrieved 8 January 2015.
  59. Machida, M.; Kitade, O.; Miura, T.; Matsumoto, T. (2001). "Nitrogen recycling through proctodeal trophallaxis in the Japanese damp-wood termite Hodotermopsis japonica (Isoptera, Termopsidae)". Insectes Sociaux. 48 (1): 52–56. doi:10.1007/PL00001745. ISSN 1420-9098. S2CID 21310420.
  60. Higashi, Masahiko; Yamamura, Norio; Abe, Takuya; Burns, Thomas P. (1991-10-22). "Why don't all termite species have a sterile worker caste?". Proceedings of the Royal Society B: Biological Sciences. 246 (1315): 25–29. doi:10.1098/rspb.1991.0120. ISSN 0962-8452. PMID 1684665. S2CID 23067349.
  61. Bignell, Roisin & Lo 2010, p. 18.
  62. Krishna, K. "Termite". Encyclopædia Britannica. Retrieved 11 September 2015.
  63. Busvine, J.R. (2013). Insects and Hygiene The biology and control of insect pests of medical and domestic importance (3rd ed.). Boston, MA: Springer US. p. 545. ISBN 978-1-4899-3198-6.
  64. Meek, S.P. (1934). Termite Control at an Ordnance Storage Depot. American Defense Preparedness Association. p. 159.
  65. Prestwich, G.D. (1982). "From tetracycles to macrocycles". Tetrahedron. 38 (13): 1911–1919. doi:10.1016/0040-4020(82)80040-9.
  66. Prestwich, G. D.; Bentley, B.L.; Carpenter, E.J. (1980). "Nitrogen sources for neotropical nasute termites: Fixation and selective foraging". Oecologia. 46 (3): 397–401. Bibcode:1980Oecol..46..397P. doi:10.1007/BF00346270. ISSN 1432-1939. PMID 28310050. S2CID 6134800.
  67. Thorne, B. L.; Breisch, N. L.; Muscedere, M. L. (2003-10-28). "Evolution of eusociality and the soldier caste in termites: Influence of intraspecific competition and accelerated inheritance". Proceedings of the National Academy of Sciences. 100 (22): 12808–12813. Bibcode:2003PNAS..10012808T. doi:10.1073/pnas.2133530100. ISSN 0027-8424. PMC 240700. PMID 14555764.
  68. Horwood, M.A.; Eldridge, R.H. (2005). Termites in New South Wales Part 1. Termite biology (PDF) (Technical report). Forest Resources Research. ISSN 0155-7548. 96-38.
  69. Keller, L. (1998). "Queen lifespan and colony characteristics in ants and termites". Insectes Sociaux. 45 (3): 235–246. doi:10.1007/s000400050084. S2CID 24541087.
  70. Srinivasan, Amia (September 10, 2018). "What Termites Can Teach Us". The New Yorker. Archived from the original on March 7, 2020.
  71. Korb, J. (2008). "Termites, hemimetabolous diploid white ants?". Frontiers in Zoology. 5 (1): 15. doi:10.1186/1742-9994-5-15. PMC 2564920. PMID 18822181.
  72. Davis, P. "Termite Identification". Entomology at Western Australian Department of Agriculture. Archived from the original on 2009-06-12.
  73. Neoh, K.B.; Lee, C.Y. (2011). "Developmental stages and caste composition of a mature and incipient colony of the drywood termite, Cryptotermes dudleyi (Isoptera: Kalotermitidae)". Journal of Economic Entomology. 104 (2): 622–8. doi:10.1603/ec10346. PMID 21510214. S2CID 23356632.
  74. "Native subterranean termites". University of Florida. Retrieved 8 January 2015.
  75. Schneider, M.F. (1999). "Termite Life Cycle and Caste System". University of Freiburg. Retrieved 8 January 2015.
  76. Simpson, S.J.; Sword, G.A.; Lo, N. (2011). "Polyphenism in Insects". Current Biology. 21 (18): 738–749. doi:10.1016/j.cub.2011.06.006. PMID 21959164. S2CID 656039.
  77. Tasaki E, Kobayashi K, Matsuura K, Iuchi Y (2017). "An Efficient Antioxidant System in a Long-Lived Termite Queen". PLOS ONE. 12 (1): e0167412. Bibcode:2017PLoSO..1267412T. doi:10.1371/journal.pone.0167412. PMC 5226355. PMID 28076409.
  78. Miller, D.M. (5 March 2010). "Subterranean Termite Biology and Behavior". Virginia Tech (Virginia State University). Retrieved 8 January 2015.
  79. Gouge, D.H.; Smith, K.A.; Olson, C.; Baker, P. (2001). "Drywood Termites". Cooperative Extension, College of Agriculture & Life Sciences. University of Arizona. Retrieved 16 September 2015.
  80. Kaib, M.; Hacker, M.; Brandl, R. (2001). "Egg-laying in monogynous and polygynous colonies of the termite Macrotermes michaelseni (Isoptera, Macrotermitidae)". Insectes Sociaux. 48 (3): 231–237. doi:10.1007/PL00001771. S2CID 35656795.
  81. Gilbert, executive editors, G.A. Kerkut, L.I. (1985). Comprehensive insect physiology, biochemistry, and pharmacology (1st ed.). Oxford: Pergamon Press. p. 167. ISBN 978-0-08-026850-7.
  82. Wyatt, T.D. (2003). Pheromones and animal behaviour: communication by smell and taste (Repr. with corrections 2004. ed.). Cambridge: Cambridge University Press. p. 119. ISBN 978-0-521-48526-5.
  83. Morrow, E.H. (2004). "How the sperm lost its tail: the evolution of aflagellate sperm". Biological Reviews of the Cambridge Philosophical Society. 79 (4): 795–814. doi:10.1017/S1464793104006451. PMID 15682871. S2CID 25878093.
  84. "Supplementary reproductive". University of Hawaii. Archived from the original on 30 October 2014. Retrieved 16 September 2015.
  85. Yashiro, T.; Matsuura, K. (2014). "Termite queens close the sperm gates of eggs to switch from sexual to asexual reproduction". Proceedings of the National Academy of Sciences. 111 (48): 17212–17217. Bibcode:2014PNAS..11117212Y. doi:10.1073/pnas.1412481111. PMC 4260566. PMID 25404335.
  86. Matsuura, K.; Vargo, E.L.; Kawatsu, K.; Labadie, P. E.; Nakano, H.; Yashiro, T.; Tsuji, K. (2009). "Queen Succession Through Asexual Reproduction in Termites". Science. 323 (5922): 1687. Bibcode:2009Sci...323.1687M. doi:10.1126/science.1169702. PMID 19325106. S2CID 21785886.
  87. Fougeyrollas R, Dolejšová K, Sillam-Dussès D, Roy V, Poteaux C, Hanus R, Roisin Y (June 2015). "Asexual queen succession in the higher termite Embiratermes neotenicus". Proc. Biol. Sci. 282 (1809): 20150260. doi:10.1098/rspb.2015.0260. PMC 4590441. PMID 26019158.
  88. Bignell, Roisin & Lo 2010, pp. 13–14.
  89. Freymann, B.P.; Buitenwerf, R.; Desouza, O.; Olff (2008). "The importance of termites (Isoptera) for the recycling of herbivore dung in tropical ecosystems: a review". European Journal of Entomology. 105 (2): 165–173. doi:10.14411/eje.2008.025.
  90. de Souza, O.F.; Brown, V.K. (2009). "Effects of habitat fragmentation on Amazonian termite communities". Journal of Tropical Ecology. 10 (2): 197–206. doi:10.1017/S0266467400007847.
  91. Tokuda, G.; Watanabe, H.; Matsumoto, T.; Noda, H. (1997). "Cellulose digestion in the wood-eating higher termite, Nasutitermes takasagoensis (Shiraki): distribution of cellulases and properties of endo-beta-1,4-glucanase". Zoological Science. 14 (1): 83–93. doi:10.2108/zsj.14.83. PMID 9200983. S2CID 2877588.
  92. Ritter, Michael (2006). The Physical Environment: an Introduction to Physical Geography. University of Wisconsin. p. 450. Archived from the original on 18 May 2007.
  93. Ikeda-Ohtsubo, W.; Brune, A. (2009). "Cospeciation of termite gut flagellates and their bacterial endosymbionts: Trichonympha species and Candidatus Endomicrobium trichonymphae". Molecular Ecology. 18 (2): 332–342. doi:10.1111/j.1365-294X.2008.04029.x. PMID 19192183. S2CID 28048145.
  94. Slaytor, M. (1992). "Cellulose digestion in termites and cockroaches: What role do symbionts play?". Comparative Biochemistry and Physiology B. 103 (4): 775–784. doi:10.1016/0305-0491(92)90194-V.
  95. "The Termite Gut and its Symbiotic Microbes". iBiology. Retrieved 2020-05-16.
  96. Watanabe, H..; Noda, H.; Tokuda, G.; Lo, N. (1998). "A cellulase gene of termite origin". Nature. 394 (6691): 330–331. Bibcode:1998Natur.394..330W. doi:10.1038/28527. PMID 9690469. S2CID 4384555.
  97. Tokuda, G.; Watanabe, H. (2007). "Hidden cellulases in termites: revision of an old hypothesis". Biology Letters. 3 (3): 336–339. doi:10.1098/rsbl.2007.0073. PMC 2464699. PMID 17374589.
  98. Li, Z.-Q.; Liu, B.-R.; Zeng, W.-H.; Xiao, W.-L.; Li, Q.-J.; Zhong, J.-H. (2013). "Character of Cellulase Activity in the Guts of Flagellate-Free Termites with Different Feeding Habits". Journal of Insect Science. 13 (37): 37. doi:10.1673/031.013.3701. PMC 3738099. PMID 23895662.
  99. "The Termite Gut and its Symbiotic Microbes". iBiology. Retrieved 2020-05-16.
  100. Geetha Iyer Scroll.in (Mar 09, 2017) Why Indians worship the mound of the much-hated termite "[The soldier termites] and the reproductive castes obtain their nutrients from the workers through oral or anal trophallaxis."
  101. Dietrich, C.; Kohler, T.; Brune, A. (2014). "The Cockroach origin of the termite gut microbiota: patterns in bacterial community structure reflect major evolutionary events". Applied and Environmental Microbiology. 80 (7): 2261–2269. doi:10.1128/AEM.04206-13. PMC 3993134. PMID 24487532.
  102. Allen, C.T.; Foster, D.E.; Ueckert, D.N. (1980). "Seasonal Food Habits of a Desert Termite, Gnathamitermes tubiformans, in West Texas". Environmental Entomology. 9 (4): 461–466. doi:10.1093/ee/9.4.461.
  103. McMahan, E.A. (1966). "Studies of Termite Wood-feeding Preferences" (PDF). Hawaiian Entomological Society. 19 (2): 239–250. ISSN 0073-134X.
  104. Aanen, D.K.; Eggleton, P.; Rouland-Lefevre, C.; Guldberg-Froslev, T.; Rosendahl, S.; Boomsma, J.J. (2002). "The evolution of fungus-growing termites and their mutualistic fungal symbionts". Proceedings of the National Academy of Sciences. 99 (23): 14887–14892. Bibcode:2002PNAS...9914887A. doi:10.1073/pnas.222313099. JSTOR 3073687. PMC 137514. PMID 12386341.
  105. Mueller, U.G.; Gerardo, N. (2002). "Fungus-farming insects: Multiple origins and diverse evolutionary histories". Proceedings of the National Academy of Sciences. 99 (24): 15247–15249. Bibcode:2002PNAS...9915247M. doi:10.1073/pnas.242594799. PMC 137700. PMID 12438688.
  106. Roberts, E.M.; Todd, C.N.; Aanen, D.K.; Nobre, T.; Hilbert-Wolf, H.L.; O'Connor, P.M.; Tapanila, L.; Mtelela, C.; Stevens, N.J. (2016). "Oligocene termite nests with in situ fungus gardens from the Rukwa Rift Basin, Tanzania, support a paleogene African origin for insect agriculture". PLOS ONE. 11 (6): e0156847. Bibcode:2016PLoSO..1156847R. doi:10.1371/journal.pone.0156847. PMC 4917219. PMID 27333288.
  107. Radek, R. (1999). "Flagellates, bacteria, and fungi associated with termites: diversity and function in nutrition – a review" (PDF). Ecotropica. 5: 183–196.
  108. Breznak, J.A.; Brune, A. (1993). "Role of microorganisms in the digestion of lignocellulose by termites". Annual Review of Entomology. 39 (1): 453–487. doi:10.1146/annurev.en.39.010194.002321.
  109. Kok, O.B.; Hewitt, P.H. (1990). "Bird and mammal predators of the harvester termite Hodotermes mossambicus (Hagen) in semi-arid regions of South Africa". South African Journal of Science. 86 (1): 34–37. ISSN 0038-2353.
  110. Hölldobler, B.; Wilson, E.O. (1990). The Ants. Cambridge, Massachusetts: Belknap Press of Harvard University Press. pp. 559–566. ISBN 978-0-674-04075-5.
  111. Culliney, T.W.; Grace, J.K. (2000). "Prospects for the biological control of subterranean termites (Isoptera: Rhinotermitidae), with special reference to Coptotermes formosanus". Bulletin of Entomological Research. 90 (1): 9–21. doi:10.1017/S0007485300000663. PMID 10948359.
  112. Dean, W.R.J.; Milton, S.J. (1995). "Plant and invertebrate assemblages on old fields in the arid southern Karoo, South Africa". African Journal of Ecology. 33 (1): 1–13. doi:10.1111/j.1365-2028.1995.tb00777.x.
  113. Wade, W.W. (2002). Ecology of Desert Systems. Burlington: Elsevier. p. 216. ISBN 978-0-08-050499-5.
  114. Reagan, D.P.; Waide, R.B. (1996). The food web of a tropical rain forest. Chicago: University of Chicago Press. p. 294. ISBN 978-0-226-70599-6.
  115. Bardgett, R.D.; Herrick, J.E.; Six, J.; Jones, T.H.; Strong, D.R.; van der Putten, W.H. (2013). Soil ecology and ecosystem services (1st ed.). Oxford: Oxford University Press. p. 178. ISBN 978-0-19-968816-6.
  116. Bignell, Roisin & Lo 2010, p. 509.
  117. Choe, J.C.; Crespi, B.J. (1997). The evolution of social behavior in insects and arachnids (1st ed.). Cambridge: Cambridge university press. p. 76. ISBN 978-0-521-58977-2.
  118. Abe, Y.; Bignell, D.E.; Higashi, T. (2014). Termites: Evolution, Sociality, Symbioses, Ecology. Springer. pp. 124–149. doi:10.1007/978-94-017-3223-9. ISBN 978-94-017-3223-9. S2CID 30804981.
  119. Wilson, D.S.; Clark, A.B. (1977). "Above ground defence in the harvester termite, Hodotermes mossambicus". Journal of the Entomological Society of South Africa. 40: 271–282.
  120. Lavelle, P.; Spain, A.V. (2001). Soil ecology (2nd ed.). Dordrecht: Kluwer Academic. p. 316. ISBN 978-0-306-48162-8.
  121. Richardson, P.K.R.; Bearder, S.K. (1984). "The Hyena Family". In MacDonald, D. (ed.). The Encyclopedia of Mammals. New York, NY: Facts on File Publication. pp. 158–159. ISBN 978-0-87196-871-5.
  122. Mills, G.; Harvey, M. (2001). African Predators. Washington, D.C.: Smithsonian Institution Press. p. 71. ISBN 978-1-56098-096-4.
  123. d'Errico, F.; Backwell, L. (2009). "Assessing the function of early hominin bone tools". Journal of Archaeological Science. 36 (8): 1764–1773. doi:10.1016/j.jas.2009.04.005.
  124. Lepage, M.G. (1981). "Étude de la prédation de Megaponera foetens (F.) sur les populations récoltantes de Macrotermitinae dans un ecosystème semi-aride (Kajiado-Kenya)". Insectes Sociaux (in Spanish). 28 (3): 247–262. doi:10.1007/BF02223627. S2CID 28763771.
  125. Levieux, J. (1966). "Note préliminaire sur les colonnes de chasse de Megaponera fœtens F. (Hyménoptère Formicidæ)". Insectes Sociaux (in French). 13 (2): 117–126. doi:10.1007/BF02223567. S2CID 2031222.
  126. Longhurst, C.; Baker, R.; Howse, P.E. (1979). "Chemical crypsis in predatory ants". Experientia. 35 (7): 870–872. doi:10.1007/BF01955119. S2CID 39854106.
  127. Wheeler, W.M. (1936). "Ecological relations of Ponerine and other ants to termites". Proceedings of the American Academy of Arts and Sciences. 71 (3): 159–171. doi:10.2307/20023221. JSTOR 20023221.
  128. Shattuck, S.O.; Heterick, B.E. (2011). "Revision of the ant genus Iridomyrmex (Hymenoptera : Formicidae)" (PDF). Zootaxa. 2845: 1–74. doi:10.11646/zootaxa.2743.1.1. ISBN 978-1-86977-676-3. ISSN 1175-5334.
  129. Traniello, J.F.A. (1981). "Enemy deterrence in the recruitment strategy of a termite: Soldier-organized foraging in Nasutitermes costalis". Proceedings of the National Academy of Sciences. 78 (3): 1976–1979. Bibcode:1981PNAS...78.1976T. doi:10.1073/pnas.78.3.1976. PMC 319259. PMID 16592995.
  130. Schöning, C.; Moffett, M.W. (2007). "Driver Ants Invading a Termite Nest: why do the most catholic predators of all seldom take this abundant prey?" (PDF). Biotropica. 39 (5): 663–667. doi:10.1111/j.1744-7429.2007.00296.x.
  131. Mill, A.E. (1983). "Observations on Brazilian termite alate swarms and some structures used in the dispersal of reproductives (Isoptera: Termitidae)". Journal of Natural History. 17 (3): 309–320. doi:10.1080/00222938300770231.
  132. Schmid-Hempel 1998, p. 61.
  133. Schmid-Hempel 1998, p. 75.
  134. Wilson, E.O. (1971). The Insect Societies. 76 (5th ed.). Cambridge, Massachusetts: Belknap Press of Harvard University Press. p. 398. ISBN 978-0-674-45495-8.
  135. Schmid-Hempel 1998, p. 59.
  136. Schmid-Hempel 1998, pp. 301–302.
  137. Schmid-Hempel 1998, p. 19.
  138. Weiser, J.; Hrdy, I. (2009). "Pyemotes – mites as parasites of termites". Zeitschrift für Angewandte Entomologie. 51 (1–4): 94–97. doi:10.1111/j.1439-0418.1962.tb04062.x.
  139. Chouvenc, T.; Efstathion, C.A.; Elliott, M.L.; Su, N.Y. (2012). "Resource competition between two fungal parasites in subterranean termites". Die Naturwissenschaften. 99 (11): 949–58. Bibcode:2012NW.....99..949C. doi:10.1007/s00114-012-0977-2. PMID 23086391. S2CID 16393629.
  140. Schmid-Hempel 1998, pp. 38, 102.
  141. Chouvenc, T.; Mullins, A.J.; Efstathion, C.A.; Su, N.-Y. (2013). "Virus-like symptoms in a termite (Isoptera: Kalotermitidae) field colony". Florida Entomologist. 96 (4): 1612–1614. doi:10.1653/024.096.0450. S2CID 73570814.
  142. Al Fazairy, A.A.; Hassan, F.A. (2011). "Infection of Termites by Spodoptera littoralis Nuclear Polyhedrosis Virus". International Journal of Tropical Insect Science. 9 (1): 37–39. doi:10.1017/S1742758400009991. S2CID 84743428.
  143. Traniello, J.F.A.; Leuthold, R.H. (2000). Behavior and Ecology of Foraging in Termites. Springer Netherlands. pp. 141–168. doi:10.1007/978-94-017-3223-9_7. ISBN 978-94-017-3223-9.
  144. Reinhard, J.; Kaib, M. (2001). "Trail communication during foraging and recruitment in the subterranean termite Reticulitermes santonensis De Feytaud (Isoptera, Rhinotermitidae)". Journal of Insect Behavior. 14 (2): 157–171. doi:10.1023/A:1007881510237. S2CID 40887791.
  145. Costa-Leonardo, A.M.; Haifig, I. (2013). Termite communication during different behavioral activities in Biocommunication of Animals. Springer Netherlands. pp. 161–190. doi:10.1007/978-94-007-7414-8_10. ISBN 978-94-007-7413-1.
  146. Costa-Leonardo, A.M. (2006). "Morphology of the sternal gland in workers of Coptotermes gestroi (Isoptera, Rhinotermitidae)". Micron. 37 (6): 551–556. doi:10.1016/j.micron.2005.12.006. PMID 16458523.
  147. Traniello, J.F.; Busher, C. (1985). "Chemical regulation of polyethism during foraging in the neotropical termite Nasutitermes costalis". Journal of Chemical Ecology. 11 (3): 319–32. doi:10.1007/BF01411418. PMID 24309963. S2CID 27799126.
  148. Miramontes, O.; DeSouza, O.; Paiva, L.R.; Marins, A.; Orozco, S.; Aegerter, C.M. (2014). "Lévy flights and self-similar exploratory behaviour of termite workers: beyond model fitting". PLOS ONE. 9 (10): e111183. arXiv:1410.0930. Bibcode:2014PLoSO...9k1183M. doi:10.1371/journal.pone.0111183. PMC 4213025. PMID 25353958.
  149. Jost, C.; Haifig, I.; de Camargo-Dietrich, C.R.R.; Costa-Leonardo, A.M. (2012). "A comparative tunnelling network approach to assess interspecific competition effects in termites". Insectes Sociaux. 59 (3): 369–379. doi:10.1007/s00040-012-0229-7. S2CID 14885485.
  150. Polizzi, J.M.; Forschler, B.T. (1998). "Intra- and interspecific agonism in Reticulitermes flavipes (Kollar) and R. virginicus (Banks) and effects of arena and group size in laboratory assays". Insectes Sociaux. 45 (1): 43–49. doi:10.1007/s000400050067. S2CID 36235510.
  151. Darlington, J.P.E.C. (1982). "The underground passages and storage pits used in foraging by a nest of the termite Macrotermes michaelseni in Kajiado, Kenya". Journal of Zoology. 198 (2): 237–247. doi:10.1111/j.1469-7998.1982.tb02073.x.
  152. Cornelius, M.L.; Osbrink, W.L. (2010). "Effect of soil type and moisture availability on the foraging behavior of the Formosan subterranean termite (Isoptera: Rhinotermitidae)". Journal of Economic Entomology. 103 (3): 799–807. doi:10.1603/EC09250. PMID 20568626. S2CID 23173060.
  153. Toledo Lima, J.; Costa-Leonardo, A.M. (2012). "Subterranean termites (Isoptera: Rhinotermitidae): Exploitation of equivalent food resources with different forms of placement". Insect Science. 19 (3): 412–418. doi:10.1111/j.1744-7917.2011.01453.x. S2CID 82046133.
  154. Jmhasly, P.; Leuthold, R.H. (1999). "Intraspecific colony recognition in the termites Macrotermes subhyalinus and Macrotermes bellicosus (Isoptera, Termitidae)". Insectes Sociaux. 46 (2): 164–170. doi:10.1007/s000400050128. S2CID 23037986.
  155. Messenger, M.T.; Su, N.Y. (2005). "Agonistic behavior between colonies of the Formosan subterranean termite (Isoptera: Rhinotermitidae) from Louis Armstrong Park, New Orleans, Louisiana". Sociobiology. 45 (2): 331–345.
  156. Korb, J.; Weil, T.; Hoffmann, K.; Foster, K.R.; Rehli, M. (2009). "A gene necessary for reproductive suppression in termites". Science. 324 (5928): 758. Bibcode:2009Sci...324..758K. doi:10.1126/science.1170660. PMID 19423819. S2CID 31608071.
  157. Mathew, T.T.G.; Reis, R.; DeSouza, O.; Ribeiro, S.P. (2005). "Predation and interference competition between ants (Hymenoptera: Formicidae) and arboreal termites (Isoptera: Termitidae)" (PDF). Sociobiology. 46 (2): 409–419.
  158. Evans, T.A.; Inta, R.; Lai, J.C.S.; Lenz, M. (2007). "Foraging vibration signals attract foragers and identify food size in the drywood termite, Cryptotermes secundus". Insectes Sociaux. 54 (4): 374–382. doi:10.1007/s00040-007-0958-1. S2CID 40214049.
  159. Costa-Leonardo, A.M.; Casarin, F.E.; Lima, J.T. (2009). "Chemical communication in isoptera". Neotropical Entomology. 38 (1): 747–52. doi:10.1590/S1519-566X2009000100001. PMID 19347093.
  160. Richard, F.-J.; Hunt, J.H. (2013). "Intracolony chemical communication in social insects" (PDF). Insectes Sociaux. 60 (3): 275–291. doi:10.1007/s00040-013-0306-6. S2CID 8108234.
  161. Dronnet, S.; Lohou, C.; Christides, J.P.; Bagnères, A.G. (2006). "Cuticular hydrocarbon composition reflects genetic relationship among colonies of the introduced termite Reticulitermes santonensis Feytaud". Journal of Chemical Ecology. 32 (5): 1027–1042. doi:10.1007/s10886-006-9043-x. PMID 16739021. S2CID 23956394.
  162. Rosengaus, R.B.; Traniello, J.F.A.; Chen, T.; Brown, J.J.; Karp, R.D. (1999). "Immunity in a social insect". Naturwissenschaften. 86 (12): 588–591. Bibcode:1999NW.....86..588R. doi:10.1007/s001140050679. S2CID 10769345.
  163. Wilson, D.S. (1977). "Above ground predator defense in the harvester termite, Hodotermes mossambicus (Hagen)". Journal of the Entomological Society of Southern Africa. 40: 271–282.
  164. Belbin, R.M. (2013). The Coming Shape of Organization. New York: Routledge. p. 27. ISBN 978-1-136-01553-3.
  165. Wilson, E.O. (2014). A window on eternity: a biologist's walk through Gorongosa National Park (First ed.). Simon & Schuster. pp. 85, 90. ISBN 978-1-4767-4741-5.
  166. Miura, T.; Matsumoto, T. (2000). "Soldier morphogenesis in a nasute termite: discovery of a disc-like structure forming a soldier nasus". Proceedings of the Royal Society B: Biological Sciences. 267 (1449): 1185–1189. doi:10.1098/rspb.2000.1127. PMC 1690655. PMID 10902684.
  167. Prestwich, G.D.; Chen, D. (1981). "Soldier defense secretions of Trinervitermes bettonianus (Isoptera, Nasutitermitinae): Chemical variation in allopatric populations". Journal of Chemical Ecology. 7 (1): 147–157. doi:10.1007/BF00988642. PMID 24420434. S2CID 27654745.
  168. Chen, J.; Henderson, G.; Grimm, C. C.; Lloyd, S. W.; Laine, R. A. (1998-04-09). "Termites fumigate their nests with naphthalene". Nature. 392 (6676): 558–559. Bibcode:1998Natur.392..558C. doi:10.1038/33305. S2CID 4419882.
  169. Piper, Ross (2007), Extraordinary Animals: An Encyclopedia of Curious and Unusual Animals, Greenwood Press, p. 26, ISBN 978-0-313-33922-6
  170. Bordereau, C.; Robert, A.; Van Tuyen, V.; Peppuy, A. (1997). "Suicidal defensive behaviour by frontal gland dehiscence in Globitermes sulphureus Haviland soldiers (Isoptera)". Insectes Sociaux. 44 (3): 289–297. doi:10.1007/s000400050049. S2CID 19770804.
  171. Sobotnik, J.; Bourguignon, T.; Hanus, R.; Demianova, Z.; Pytelkova, J.; Mares, M.; Foltynova, P.; Preisler, J.; Cvacka, J.; Krasulova, J.; Roisin, Y. (2012). "Explosive backpacks in old termite workers". Science. 337 (6093): 436. Bibcode:2012Sci...337..436S. doi:10.1126/science.1219129. PMID 22837520. S2CID 206540025.
  172. ŠobotnÍk, J.; Bourguignon, T.; Hanus, R.; Weyda, F.; Roisin, Y. (2010). "Structure and function of defensive glands in soldiers of Glossotermes oculatus (Isoptera: Serritermitidae)". Biological Journal of the Linnean Society. 99 (4): 839–848. doi:10.1111/j.1095-8312.2010.01392.x.
  173. Ulyshen, M.D.; Shelton, T.G. (2011). "Evidence of cue synergism in termite corpse response behavior". Naturwissenschaften. 99 (2): 89–93. Bibcode:2012NW.....99...89U. doi:10.1007/s00114-011-0871-3. PMID 22167071. S2CID 2616753.
  174. Su, N.Y. (2005). "Response of the Formosan subterranean termites (Isoptera: Rhinotermitidae) to baits or nonrepellent termiticides in extended foraging arenas". Journal of Economic Entomology. 98 (6): 2143–2152. doi:10.1603/0022-0493-98.6.2143. PMID 16539144. S2CID 196618597.
  175. Sun, Q.; Haynes, K.F.; Zhou, X. (2013). "Differential undertaking response of a lower termite to congeneric and conspecific corpses". Scientific Reports. 3: 1650. Bibcode:2013NatSR...3E1650S. doi:10.1038/srep01650. PMC 3629736. PMID 23598990.
  176. Neoh, K.-B.; Yeap, B.-K.; Tsunoda, K.; Yoshimura, T.; Lee, C.Y.; Korb, J. (2012). "Do termites avoid carcasses? behavioral responses depend on the nature of the carcasses". PLOS ONE. 7 (4): e36375. Bibcode:2012PLoSO...736375N. doi:10.1371/journal.pone.0036375. PMC 3338677. PMID 22558452.
  177. Matsuura, K. (2006). "Termite-egg mimicry by a sclerotium-forming fungus". Proceedings of the Royal Society B: Biological Sciences. 273 (1591): 1203–1209. doi:10.1098/rspb.2005.3434. PMC 1560272. PMID 16720392.
  178. Matsuura, K.; Yashiro, T.; Shimizu, K.; Tatsumi, S.; Tamura, T. (2009). "Cuckoo fungus mimics termite eggs by producing the cellulose-digesting enzyme β-glucosidase". Current Biology. 19 (1): 30–36. doi:10.1016/j.cub.2008.11.030. PMID 19110429. S2CID 18604426.
  179. Howard, R.W.; McDaniel, C.A.; Blomquist, G.J. (1980). "Chemical mimicry as an integrating mechanism: cuticular hydrocarbons of a termitophile and its host". Science. 210 (4468): 431–433. Bibcode:1980Sci...210..431H. doi:10.1126/science.210.4468.431. PMID 17837424. S2CID 33221252.
  180. Watson, J.A.L. (1973). "Austrospirachtha mimetes a new termitophilous corotocine from Northern Australia (Coleoptera: Staphylinidae)". Australian Journal of Entomology. 12 (4): 307–310. doi:10.1111/j.1440-6055.1973.tb01678.x.
  181. Forbes, H.O. (1878). "Termites Kept in Captivity by Ants". Nature. 19 (471): 4–5. Bibcode:1878Natur..19....4F. doi:10.1038/019004b0. S2CID 4125839. (subscription required)
  182. Darlington, J. (1985). "Attacks by doryline ants and termite nest defences (Hymenoptera; Formicidae; Isoptera; Termitidae)". Sociobiology. 11: 189–200.
  183. Quinet Y, Tekule N & de Biseau JC (2005). "Behavioural Interactions Between Crematogaster brevispinosa rochai Forel (Hymenoptera: Formicidae) and Two Nasutitermes Species (Isoptera: Termitidae)". Journal of Insect Behavior. 18 (1): 1–17. doi:10.1007/s10905-005-9343-y. S2CID 33487814.
  184. Coty, D.; Aria, C.; Garrouste, R.; Wils, P.; Legendre, F.; Nel, A.; Korb, J. (2014). "The First Ant-Termite Syninclusion in Amber with CT-Scan Analysis of Taphonomy". PLOS ONE. 9 (8): e104410. Bibcode:2014PLoSO...9j4410C. doi:10.1371/journal.pone.0104410. PMC 4139309. PMID 25140873.
  185. Santos, P.P.; Vasconcellos, A.; Jahyny, B.; Delabie, J.H.C. (2010). "Ant fauna (Hymenoptera, Formicidae) associated to arboreal nests of Nasutitermes spp: (Isoptera, Termitidae) in a cacao plantation in southeastern Bahia, Brazil". Revista Brasileira de Entomologia. 54 (3): 450–454. doi:10.1590/S0085-56262010000300016.
  186. Jaffe, K.; Ramos, C.; Issa, S. (1995). "Trophic Interactions Between Ants and Termites that Share Common Nests". Annals of the Entomological Society of America. 88 (3): 328–333. doi:10.1093/aesa/88.3.328.
  187. Trager, J.C. (1991). "A Revision of the fire ants, Solenopsis geminata group (Hymenoptera: Formicidae: Myrmicinae)". Journal of the New York Entomological Society. 99 (2): 141–198. doi:10.5281/zenodo.24912. JSTOR 25009890.
  188. Cingel, N.A. van der (2001). An atlas of orchid pollination: America, Africa, Asia and Australia. Rotterdam: Balkema. p. 224. ISBN 978-90-5410-486-5.
  189. McHatton, R. (2011). "Orchid Pollination: exploring a fascinating world" (PDF). The American Orchid Society. p. 344. Retrieved 5 September 2015.
  190. Cowie, R. (2014). Journey to a Waterfall a biologist in Africa. Raleigh, North Carolina: Lulu Press. p. 169. ISBN 978-1-304-66939-1.
  191. Tan, K.H. (2009). Environmental Soil Science (3rd ed.). Boca Raton, Florida: CRC Press. pp. 105–106. ISBN 978-1-4398-9501-6.
  192. Clark, Sarah (15 November 2005). "Plant extract stops termites dead". ABC. Archived from the original on 15 June 2009. Retrieved 8 February 2014.
  193. Vasconcellos, Alexandre; Bandeira, Adelmar G.; Moura, Flávia Maria S.; Araújo, Virgínia Farias P.; Gusmão, Maria Avany B.; Reginaldo, Constantino (February 2010). "Termite assemblages in three habitats under different disturbance regimes in the semi-arid Caatinga of NE Brazil". Journal of Arid Environments. Elsevier. 74 (2): 298–302. Bibcode:2010JArEn..74..298V. doi:10.1016/j.jaridenv.2009.07.007. ISSN 0140-1963.
  194. Bignell, Roisin & Lo 2010, p. 3.
  195. Noirot, C.; Darlington, J.P.E.C. (2000). Termite Nests: Architecture, Regulation and Defence in Termites: Evolution, Sociality, Symbioses, Ecology. Springer. pp. 121–139. doi:10.1007/978-94-017-3223-9_6. ISBN 978-94-017-3223-9.
  196. Bignell, Roisin & Lo 2010, p. 20.
  197. Eggleton, P.; Bignell, D.E.; Sands, W.A.; Mawdsley, N. A.; Lawton, J. H.; Wood, T.G.; Bignell, N.C. (1996). "The Diversity, Abundance and Biomass of Termites under Differing Levels of Disturbance in the Mbalmayo Forest Reserve, Southern Cameroon". Philosophical Transactions of the Royal Society B: Biological Sciences. 351 (1335): 51–68. Bibcode:1996RSPTB.351...51E. doi:10.1098/rstb.1996.0004.
  198. Bignell, Roisin & Lo 2010, p. 21.
  199. De Visse, S.N.; Freymann, B.P.; Schnyder, H. (2008). "Trophic interactions among invertebrates in termitaria in the African savanna: a stable isotope approach". Ecological Entomology. 33 (6): 758–764. doi:10.1111/j.1365-2311.2008.01029.x. S2CID 33877331.
  200. Bignell, Roisin & Lo 2010, p. 22.
  201. Vane, C.H.; Kim, A.W.; Moss-Hayes, V.; Snape, C.E.; Diaz, M.C.; Khan, N.S.; Engelhart, S.E.; Horton, B.P. (2013). "Degradation of mangrove tissues by arboreal termites (Nasutitermes acajutlae) and their role in the mangrove C cycle (Puerto Rico): Chemical characterization and organic matter provenance using bulk δ13C, C/N, alkaline CuO oxidation-GC/MS, and solid-state" (PDF). Geochemistry, Geophysics, Geosystems. 14 (8): 3176–3191. Bibcode:2013GGG....14.3176V. doi:10.1002/ggge.20194.
  202. Roisin, Y.; Pasteels, J. M. (1986). "Reproductive mechanisms in termites: Polycalism and polygyny in Nasutitermes polygynus and N. costalis". Insectes Sociaux. 33 (2): 149–167. doi:10.1007/BF02224595. S2CID 41799894.
  203. Perna, A.; Jost, C.; Couturier, E.; Valverde, S.; Douady, S.; Theraulaz, G. (2008). "The structure of gallery networks in the nests of termite Cubitermes spp. revealed by X-ray tomography". Die Naturwissenschaften. 95 (9): 877–884. Bibcode:2008NW.....95..877P. doi:10.1007/s00114-008-0388-6. PMID 18493731. S2CID 15326313.
  204. Glenday, Craig (2014). Guinness World Records 2014. pp. 33. ISBN 978-1-908843-15-9.
  205. Jacklyn, P. (1991). "Evidence for Adaptive Variation in the Orientation of Amitermes (Isoptera, Termitinae) Mounds From Northern Australia". Australian Journal of Zoology. 39 (5): 569. doi:10.1071/ZO9910569.
  206. Jacklyn, P.M.; Munro, U. (2002). "Evidence for the use of magnetic cues in mound construction by the termite Amitermes meridionalis (Isoptera : Termitinae)". Australian Journal of Zoology. 50 (4): 357. doi:10.1071/ZO01061.
  207. Grigg, G.C. (1973). "Some Consequences of the Shape and Orientation of 'magnetic' Termite Mounds" (PDF). Australian Journal of Zoology. 21 (2): 231–237. doi:10.1071/ZO9730231.
  208. Hadlington, P. (1996). Australian Termites and Other Common Timber Pests (2nd ed.). Kensington, NSW, Australia: New South Wales University Press. pp. 28–30. ISBN 978-0-86840-399-1.
  209. Kahn, L.; Easton, B. (2010). Shelter II. Bolinas, California: Shelter Publications. p. 198. ISBN 978-0-936070-49-0.
  210. Su, N.Y.; Scheffrahn, R.H. (2000). Termites as Pests of Buildings in Termites: Evolution, Sociality, Symbioses, Ecology. Springer Netherlands. pp. 437–453. doi:10.1007/978-94-017-3223-9_20. ISBN 978-94-017-3223-9.
  211. Thorne, Ph.D, Barbara L. (1999). NPMA Research Report On Subterranean Termites. Dunn Loring, VA: NPMA. p. 22.
  212. "Termites". Victorian Building Authority. Government of Victoria. 2014. Retrieved 20 September 2015.
  213. Thorne, Ph.D, Barbara L. (1999). NPMA Research Report On Subterranean Termites. Dunn Loring, VA: NPMA. p. 2.
  214. Grace, J.K.; Cutten, G.M.; Scheffrahn, R.H.; McEkevan, D.K. (1991). "First infestation by Incisitermes minor of a Canadian building (Isoptera: Kalotermitidae)". Sociobiology. 18: 299–304.
  215. Sands, W.A. (1973). "Termites as Pests of Tropical Food Crops". Tropical Pest Management. 19 (2): 167–177. doi:10.1080/09670877309412751.
  216. Flores, A. (17 February 2010). "New Assay Helps Track Termites, Other Insects". Agricultural Research Service. United States Department of Agriculture. Retrieved 15 January 2015.
  217. Su, N.Y.; Scheffrahn, R.H. (1990). "Economically important termites in the United States and their control" (PDF). Sociobiology. 17: 77–94. Archived from the original (PDF) on 2011-08-12.
  218. Thorne, Ph.D, Barbara L. (1999). NPMA Research Report On Subterranean Termites. Dunn Loring, VA: NPMA. p. 40.
  219. Elliott, Sara (26 May 2009). "How can copper keep termites at bay?". HowStuffWorks.
  220. Figueirêdo, R.E.C.R.; Vasconcellos, A.; Policarpo, I.S.; Alves, R.R.N. (2015). "Edible and medicinal termites: a global overview". Journal of Ethnobiology and Ethnomedicine. 11 (1): 29. doi:10.1186/s13002-015-0016-4. PMC 4427943. PMID 25925503.
  221. Nyakupfuka, A. (2013). Global Delicacies: Discover Missing Links from Ancient Hawaiian Teachings to Clean the Plaque of your Soul and Reach Your Higher Self. Bloomington, Indiana: BalboaPress. pp. 40–41. ISBN 978-1-4525-6791-4.
  222. Bodenheimer, F.S. (1951). Insects as Human Food: A Chapter of the Ecology of Man. Netherlands: Springer. pp. 331–350. ISBN 978-94-017-6159-8.
  223. Geissler, P.W. (2011). "The significance of earth-eating: social and cultural aspects of geophagy among Luo children". Africa. 70 (4): 653–682. doi:10.3366/afr.2000.70.4.653. S2CID 145754470.
  224. Knudsen, J.W. (2002). "Akula udongo (earth eating habit): a social and cultural practice among Chagga women on the slopes of Mount Kilimanjaro". African Journal of Indigenous Knowledge Systems. 1 (1): 19–26. doi:10.4314/indilinga.v1i1.26322. ISSN 1683-0296. OCLC 145403765.
  225. Nchito, M.; Wenzel Geissler, P.; Mubila, L.; Friis, H.; Olsen, A. (2004). "Effects of iron and multimicronutrient supplementation on geophagy: a two-by-two factorial study among Zambian schoolchildren in Lusaka". Transactions of the Royal Society of Tropical Medicine and Hygiene. 98 (4): 218–227. doi:10.1016/S0035-9203(03)00045-2. PMID 15049460.
  226. Saathoff, E.; Olsen, A.; Kvalsvig, J.D.; Geissler, P.W. (2002). "Geophagy and its association with geohelminth infection in rural schoolchildren from northern KwaZulu-Natal, South Africa". Transactions of the Royal Society of Tropical Medicine and Hygiene. 96 (5): 485–490. doi:10.1016/S0035-9203(02)90413-X. PMID 12474473.
  227. Katayama, N.; Ishikawa, Y.; Takaoki, M.; Yamashita, M.; Nakayama, S.; Kiguchi, K.; Kok, R.; Wada, H.; Mitsuhashi, J. (2008). "Entomophagy: A key to space agriculture" (PDF). Advances in Space Research. 41 (5): 701–705. Bibcode:2008AdSpR..41..701S. doi:10.1016/j.asr.2007.01.027.
  228. Mitchell, J.D. (2002). "Termites as pests of crops, forestry, rangeland and structures in Southern Africa and their control". Sociobiology. 40 (1): 47–69. ISSN 0361-6525.
  229. Löffler, E.; Kubiniok, J. (1996). "Landform development and bioturbation on the Khorat plateau, Northeast Thailand" (PDF). Natural History Bulletin of the Siam Society. 44: 199–216.
  230. Evans, T.A.; Dawes, T.Z.; Ward, P.R.; Lo, N. (2011). "Ants and termites increase crop yield in a dry climate". Nature Communications. 2: 262. Bibcode:2011NatCo...2..262E. doi:10.1038/ncomms1257. PMC 3072065. PMID 21448161.
  231. "Termite Power". DOE Joint Genome Institute. United States Department of Energy. 14 August 2006. Archived from the original on 22 September 2006. Retrieved 11 September 2015.CS1 maint: unfit URL (link)
  232. Hirschler, B. (22 November 2007). "Termites' gut reaction set for biofuels". ABC News. Retrieved 8 January 2015.
  233. Roach, J. (14 March 2006). "Termite Power: Can Pests' Guts Create New Fuel?". National Geographic News. Retrieved 11 September 2015.
  234. Werfel, J.; Petersen, K.; Nagpal, R. (2014). "Designing Collective Behavior in a Termite-Inspired Robot Construction Team". Science. 343 (6172): 754–758. Bibcode:2014Sci...343..754W. doi:10.1126/science.1245842. PMID 24531967. S2CID 38776920.
  235. Gibney, E. (2014). "Termite-inspired robots build castles". Nature. doi:10.1038/nature.2014.14713. S2CID 112117767.
  236. "Termites Green Architecture in the Tropics". The Architect. Architectural Association of Kenya. Retrieved 17 October 2015.
  237. Tan, A.; Wong, N. (2013). "Parameterization Studies of Solar Chimneys in the Tropics". Energies. 6 (1): 145–163. doi:10.3390/en6010145.
  238. Tsoroti, S. (15 May 2014). "What's that building? Eastgate Mall". Harare News. Retrieved 8 January 2015.
  239. "Im Zoo Basel fliegen die Termiten aus". Neue Zürcher Zeitung (in German). 8 February 2014. Retrieved 21 May 2011.
  240. Van-Huis, H. (2003). "Insects as food in Sub-Saharan Africa" (PDF). Insect Science and Its Application. 23 (3): 163–185. doi:10.1017/s1742758400023572.
  241. Neoh, K.B. (2013). "Termites and human society in Southeast Asia" (PDF). The Newsletter. 30 (66): 1–2.

Cited literature
  • Bignell, D.E.; Roisin, Y.; Lo, N. (2010). Biology of Termites: a Modern Synthesis (1st ed.). Dordrecht: Springer. ISBN 978-90-481-3977-4.
  • Schmid-Hempel, P. (1998). Parasites in Social Insects. New Jersey: Princeton University Press. ISBN 978-0-691-05924-2.
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