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Contents

  • (Top)
  • 1 Etymology
  • 2 Taxonomy and evolution
  • 3 Distribution and diversity
  • 4 Morphology
    • 4.1 Head
    • 4.2 Mesosoma
    • 4.3 Metasoma
    • 4.4 Polymorphism
    • 4.5 Genome size
  • 5 Life cycle
    • 5.1 Reproduction
    • 5.2 Nests, colonies, and supercolonies
  • 6 Behaviour and ecology
    • 6.1 Communication
    • 6.2 Defence
    • 6.3 Learning
    • 6.4 Nest construction
    • 6.5 Cultivation of food
    • 6.6 Navigation
    • 6.7 Locomotion
    • 6.8 Cooperation and competition
    • 6.9 Relationships with other organisms
  • 7 Relationship with humans
    • 7.1 As food
    • 7.2 As pests
    • 7.3 In science and technology
    • 7.4 As pets
    • 7.5 In culture
  • 8 See also
  • 9 References
    • 9.1 Cited texts
  • 10 Further reading
  • 11 External links

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From Wikipedia, the free encyclopedia
(Redirected from Ants)
Family of insects
This article is about the family of insects. For other uses, see Ant (disambiguation).

Ants
Temporal range: 113–0 Ma
PreꞒ
Ꞓ
O
S
D
C
P
T
J
K
Pg
N
Late Aptian – Present
Fire ants
Scientific classification Edit this classification
Kingdom: Animalia
Phylum: Arthropoda
Clade: Pancrustacea
Class: Insecta
Order: Hymenoptera
Infraorder: Aculeata
Superfamily: Formicoidea
Latreille, 1809[1]
Family: Formicidae
Latreille, 1809
Type species
Formica rufa
Linnaeus, 1761
Subfamilies
  • Agroecomyrmecinae
  • Amblyoponinae (incl. "Apomyrminae")
  • Aneuretinae
  • †Brownimeciinae
  • Dolichoderinae
  • Dorylinae
  • Ectatomminae
  • †Formiciinae
  • Formicinae
  • †Haidomyrmecinae
  • Leptanillinae
  • Martialinae
  • Myrmeciinae (incl. "Nothomyrmeciinae")
  • Myrmicinae
  • Paraponerinae
  • Ponerinae
  • Proceratiinae
  • Pseudomyrmecinae
  • †Sphecomyrminae
  • †Zigrasimeciinae
Diversity
21 subfamilies
Bright red ant, likely part of the Formica pallidefulva species group, on a flower

Ants are eusocial insects of the family Formicidae and, along with the related wasps and bees, belong to the order Hymenoptera.[2] Ants evolved from vespoid wasp ancestors in the Cretaceous period. More than 13,800 of an estimated total of 22,000 species have been described. They are easily identified by their geniculate (elbowed) antennae and the distinctive node-like structure that forms their slender waists.

Ants form colonies that range in size from a few dozen individuals often living in small natural cavities to highly organised colonies that may occupy large territories with a sizeable nest (or nests) that consist of millions of individuals. In some cases they reach hundreds of millions of individuals in super colonies. Typical colonies consist of various castes of sterile, wingless females, most of which are workers (ergates), as well as soldiers (dinergates) and other specialised groups. Nearly all ant colonies also have some fertile males called "drones" and one or more fertile females called "queens" (gynes). The colonies are described as superorganisms because the ants appear to operate as a unified entity, collectively working together to support the colony.

Ants have colonised almost every landmass on Earth. The only places lacking indigenous ants are Antarctica and a few remote or inhospitable islands. Ants thrive in moist tropical ecosystems and may exceed the combined biomass of wild birds and mammals. Their success in so many environments has been attributed to their social organisation and their ability to modify habitats, tap resources, and defend themselves. Their long co-evolution with other species has led to mimetic, commensal, parasitic, and mutualistic relationships.

Ant societies have division of labour, communication between individuals, and an ability to solve complex problems. These parallels with human societies have long been an inspiration and subject of study. Many human cultures make use of ants in cuisine, medication, and rites. Some species are valued in their role as biological pest control agents. Their ability to exploit resources may bring ants into conflict with humans, however, as they can damage crops and invade buildings. Some species, such as the red imported fire ant (Solenopsis invicta), Linepithema humile, Wasmannia auropunctata, Anoplolepis gracilipes, and Pheidole megacephala are regarded as invasive species in other parts of the world, establishing themselves in areas where they have been introduced accidentally.

Etymology

The word ant and the archaic word emmet[3] are derived from ante, emete of Middle English, which come from ǣmette of Old English; these are all related to Low Saxon e(e)mt, empe and varieties (Old Saxon emeta) and to German Ameise (Old High German āmeiza). All of these words come from West Germanic *ǣmaitjōn, and the original meaning of the word was "the biter" (from Proto-Germanic *ai-, "off, away" + *mait- "cut").[4][5]

The study of ants is called myrmecology, from Ancient Greek μύρμηξ mýrmēx ("ant"). It has been hypothesised that a Proto-Indo-European word *morwi- was the root for Sanskrit vamrah, Greek μύρμηξ mýrmēx, Latin formīca, Old Church Slavonic mraviji, Old Irish moirb, Old Norse maurr, Dutch mier, Swedish myra, Danish myre, Middle Dutch miere, and Crimean Gothic miera.[6][7]

Taxonomy and evolution

The family name Formicidae is derived from the Latin formīca ("ant")[8][page needed] from which the words in other Romance languages, such as the Portuguese formiga, Italian formica, Spanish hormiga, Romanian furnică, and French fourmi are derived. The family belongs to the order Hymenoptera, which also includes sawflies, bees, and wasps. Ants evolved from a lineage within the stinging wasps, and a 2013 study suggests that they are a sister group of the Apoidea.[9] However, since Apoidea is a superfamily, ants must be upgraded to the same rank.[10]

A more detailed basic taxonomy was proposed in 2020. Three species of the extinct mid-Cretaceous genera Camelomecia and Camelosphecia were placed outside of the Formicidae, in a separate clade within the general superfamily Formicoidea, which, together with Apoidea, forms the higher-ranking group Formicapoidina.[1] Fernández et al. (2021) suggest that the common ancestors of ants and apoids within the Formicapoidina probably existed as early as in the end of the Jurassic period, before divergence in the Cretaceous.[10]

Relationship of ants with aculeate wasp families
Aculeata

Chrysidoidea

Vespidae

Rhopalosomatidae

Pompilidae

Mutillidae

Tiphiidae

Chyphotidae

Scolioidea

Apoidea

Formicoidea

Phylogenetic position of the Formicidae as seen in Johnson et al. (2013)[9][10]
Relationships of ant subfamilies
Formicoidea
Formicoid

Myrmicinae

Ectatomminae

Formicinae

Dolichoderinae

Aneuretinae

Pseudomyrmecinae

Myrmeciinae

Dorylinae‡

Poneroid

Ponerinae

Agroecomyrmecinae

Paraponerinae

Proceratiinae

Amblyoponinae

Apomyrminae

Leptanilloid

Leptanillinae

Martialinae

(Formicidae)
A phylogeny of the extant ant subfamilies.[11][12][13]

*Cerapachyinae is paraphyletic

‡ The previous dorylomorph subfamilies – Ecitoninae, Aenictinae, Aenictogitoninae, Cerapachyinae, Leptanilloidinae – were synonymized under Dorylinae by Brady et al. in 2014[14]
Vulcanidris, one of the earliest ants ever known from the Early Cretaceous
Ants fossilised in Baltic amber

In 1966, E. O. Wilson and his colleagues identified the fossil remains of an ant (Sphecomyrma) that lived in the Cretaceous period. The specimen, trapped in amber dating back to around 92 million years ago, has features found in some wasps, but not found in modern ants.[15] The oldest fossils of ants date to the mid-Cretaceous, around 113–100 million years ago, which belong to extinct stem-groups such as the Haidomyrmecinae, Sphecomyrminae and Zigrasimeciinae, with modern ant subfamilies appearing towards the end of the Cretaceous around 80–70 million years ago.[16][17] Ants diversified extensively during the Angiosperm Terrestrial Revolution[18] and assumed ecological dominance around 60 million years ago.[19][20][21][22] Some groups, such as the Leptanillinae and Martialinae, are suggested to have diversified from early primitive ants that were likely to have been predators underneath the surface of the soil.[13][23]

During the Cretaceous period, a few species of primitive ants ranged widely on the Laurasian supercontinent (the Northern Hemisphere). Their representation in the fossil record is poor, in comparison to the populations of other insects, representing only about 1% of fossil evidence of insects in the era. Ants became dominant after adaptive radiation at the beginning of the Paleogene period. By the Oligocene and Miocene, ants had come to represent 20–40% of all insects found in major fossil deposits. Of the species that lived in the Eocene epoch, around one in 10 genera survive to the present. Genera surviving today comprise 56% of the genera in Baltic amber fossils (early Oligocene), and 92% of the genera in Dominican amber fossils (apparently early Miocene).[19][24]

Termites live in colonies and are sometimes called "white ants", but termites are only distantly related to ants. They are the sub-order Isoptera, and together with cockroaches, they form the order Blattodea. Blattodeans are related to mantids, crickets, and other winged insects that do not undergo complete metamorphosis. Like ants, termites are eusocial, with sterile workers, but they differ greatly in the genetics of reproduction. The similarity of their social structure to that of ants is attributed to convergent evolution.[25] Velvet ants look like large ants, but are wingless female wasps.[26][27]

Distribution and diversity

RegionNumber of
species [28]
Neotropics2,162
Nearctic580
Europe180
Africa2,500
Asia2,080
Melanesia275
Australia985
Polynesia42

Ants have a cosmopolitan distribution. They are found on all continents except Antarctica, and only a few large islands, such as Greenland, Iceland, parts of Polynesia and the Hawaiian Islands lack native ant species.[29][30] Ants occupy a wide range of ecological niches and exploit many different food resources as direct or indirect herbivores, predators and scavengers. Most ant species are omnivorous generalists, but a few are specialist feeders. There is considerable variation in ant abundance across habitats, peaking in the moist tropics to nearly six times that found in less suitable habitats.[31] Their ecological dominance has been examined primarily using estimates of their biomass: myrmecologist E. O. Wilson had estimated in 2009 that at any one time the total number of ants was between one and ten quadrillion (short scale) (i.e., between 1015 and 1016) and using this estimate he had suggested that the total biomass of all the ants in the world was approximately equal to the total biomass of the entire human race.[32] More careful estimates made in 2022 which take into account regional variations puts the global ant contribution at 12 megatons of dry carbon, which is about 20% of the total human contribution, but greater than that of the wild birds and mammals combined. This study also puts a conservative estimate of the ants at about 20 × 1015 (20 quadrillion).[33][34][35]

Ants range in size from 0.75 to 52 millimetres (0.030–2.0 in),[36][37] the largest species being the fossil Titanomyrma giganteum, the queen of which was 6 cm (2+1⁄2 in) long with a wingspan of 15 cm (6 in).[38] Ants vary in colour; most ants are yellow to red or brown to black, but a few species are green and some tropical species have a metallic lustre. More than 13,800 species are currently known[39] (with upper estimates of the potential existence of about 22,000; see the article List of ant genera), with the greatest diversity in the tropics. Taxonomic studies continue to resolve the classification and systematics of ants. Online databases of ant species, including AntWeb and the Hymenoptera Name Server, help to keep track of the known and newly described species.[39] The relative ease with which ants may be sampled and studied in ecosystems has made them useful as indicator species in biodiversity studies.[40][41]

Morphology

Diagram of a worker ant (Neoponera verenae)

Ants are distinct in their morphology from other insects in having geniculate (elbowed) antennae, metapleural glands, and a strong constriction of their second abdominal segment into a node-like petiole. The body is divided into three distinct sections (formally known as tagmata): the head, mesosoma, and metasoma. The petiole forms a narrow waist between their mesosoma (thorax plus the first abdominal segment, which is fused to it) and gaster (abdomen less the abdominal segments in the petiole). The petiole may be formed by one or two nodes (the second alone, or the second and third abdominal segments).[42] Tergosternal fusion, when the tergite and sternite of a segment fuse together, can occur partly or fully on the second, third and fourth abdominal segment and is used in identification. Fourth abdominal tergosternal fusion was formerly used as character that defined the poneromorph subfamilies, Ponerinae and relatives within their clade, but this is no longer considered a synapomorphic character.[43]

Like other arthropods, ants have an exoskeleton, an external covering that provides a protective casing around the body and a point of attachment for muscles, in contrast to the internal skeletons of humans and other vertebrates. Insects do not have lungs; oxygen and other gases, such as carbon dioxide, pass through their exoskeleton via tiny valves called spiracles. Insects also lack closed blood vessels; instead, they have a long, thin, perforated tube along the top of the body (called the "dorsal aorta") that functions like a heart, and pumps haemolymph toward the head, thus driving the circulation of the internal fluids. The nervous system consists of a ventral nerve cord that runs the length of the body, with several ganglia and branches along the way reaching into the extremities of the appendages.[44]

Head

Bull ant showing the powerful mandibles and the relatively large compound eyes that provide excellent vision

An ant's head contains many sensory organs. Like most insects, ants have compound eyes made from numerous tiny lenses attached together. Ant eyes are good for acute movement detection, but do not offer a high resolution image. They also have three small ocelli (simple eyes) on the top of the head that detect light levels and polarization.[45] Compared to vertebrates, ants tend to have blurrier eyesight, particularly in smaller species,[46] and a few subterranean taxa are completely blind.[12] However, some ants, such as Australia's bulldog ant, have excellent vision and are capable of discriminating the distance and size of objects moving nearly a meter away.[47] Based on experiments conducted to test their ability to differentiate between selected wavelengths of light, some ant species such as Camponotus blandus, Solenopsis invicta, and Formica cunicularia are thought to possess a degree of colour vision.[48]

Two antennae ("feelers") are attached to the head; these organs detect chemicals, air currents, and vibrations; they also are used to transmit and receive signals through touch. The head has two strong jaws, the mandibles, used to carry food, manipulate objects, construct nests, and for defence.[44] In some species, a small pocket (infrabuccal chamber) inside the mouth stores food, so it may be passed to other ants or their larvae.[49]

Mesosoma

Both the wings and the 6 legs of the ant are attached to the mesosoma ("thorax"). The legs terminate in a hooked claw which allows them to hook on and climb surfaces.[50] Only reproductive ants (queens and males) have wings. Queens shed their wings after the nuptial flight, leaving visible stubs, a distinguishing feature of queens. In a few species, wingless queens (ergatoids) and males occur.[44]

Metasoma

The metasoma (the "abdomen") of the ant houses important internal organs, including those of the reproductive, respiratory (tracheae), and excretory systems. Workers of many species have their egg-laying structures modified into stings that are used for subduing prey and defending their nests.[44]

Polymorphism

Seven leafcutter ant workers of various castes (left) and two queens (right)

In the colonies of a few ant species, there are physical castes—workers in distinct size-classes, called minor (micrergates), median, and major ergates (macrergates). Often, the larger ants have disproportionately larger heads, and correspondingly stronger mandibles. Although formally known as dinergates, such individuals are sometimes called "soldier" ants because their stronger mandibles make them more effective in fighting, although they still are workers and their "duties" typically do not vary greatly from the minor or median workers.[51] In a few species, the median workers are absent, creating a sharp divide between the minors and majors.[52] Weaver ants, for example, have a distinct bimodal size distribution.[53][54] Some other species show continuous variation in the size of workers. The smallest and largest workers in Carebara diversa show nearly a 500-fold difference in their dry weights.[55]

Workers cannot mate; however, because of the haplodiploid sex-determination system in ants, workers of a number of species can lay unfertilised eggs that become fully fertile, haploid males. The role of workers may change with their age and in some species, such as honeypot ants, young workers are fed until their gasters are distended, and act as living food storage vessels. These food storage workers are called repletes.[56] For instance, these replete workers develop in the North American honeypot ant Myrmecocystus mexicanus. Usually the largest workers in the colony develop into repletes; and, if repletes are removed from the colony, other workers become repletes, demonstrating the flexibility of this particular polymorphism.[57] This polymorphism in morphology and behaviour of workers initially was thought to be determined by environmental factors such as nutrition and hormones that led to different developmental paths; however, genetic differences between worker castes have been noted in Acromyrmex sp.[58] These polymorphisms are caused by relatively small genetic changes; differences in a single gene of Solenopsis invicta can decide whether the colony will have single or multiple queens.[59] The Australian jack jumper ant (Myrmecia pilosula) has only a single pair of chromosomes (with the males having just one chromosome as they are haploid), the lowest number known for any animal, making it an interesting subject for studies in the genetics and developmental biology of social insects.[60][61]

Genome size

Genome size is a fundamental characteristic of an organism. Ants have been found to have tiny genomes, with the evolution of genome size suggested to occur through loss and accumulation of non-coding regions, mainly transposable elements, and occasionally by whole genome duplication.[62] This may be related to colonisation processes, but further studies are needed to verify this.[62]

Life cycle

Meat ant nest during swarming

The life of an ant starts from an egg. If the egg is fertilized, the progeny will be female diploid; if not, it will be male haploid. Ants develop by complete metamorphosis with the larva stages passing through a pupal stage before emerging as an adult. The larva is largely immobile and is fed and cared for by workers. Food is given to the larvae by trophallaxis, a process in which an ant regurgitates liquid food held in its crop. This is also how adults share food, stored in the "social stomach". Larvae, especially in the later stages, may also be provided solid food, such as trophic eggs, pieces of prey, and seeds brought by workers.[63]

The larvae grow through a series of four or five moults and enter the pupal stage. The pupa has the appendages free and not fused to the body as in a butterfly pupa.[64] The differentiation into queens and workers (which are both female), and different castes of workers, is influenced in some species by the nutrition the larvae obtain. Genetic influences and the control of gene expression by the developmental environment are complex and the determination of caste continues to be a subject of research.[65] Winged male ants, called drones (termed "aner" in old literature[51]), emerge from pupae along with the usually winged breeding females. Some species, such as army ants, have wingless queens. Larvae and pupae need to be kept at fairly constant temperatures to ensure proper development, and so often are moved around among the various brood chambers within the colony.[66]

A new ergate (worker) spends the first few days of its adult life caring for the queen and young. She then graduates to digging and other nest work, and later to defending the nest and foraging. These changes are sometimes fairly sudden, and define what are called temporal castes. Such age-based task-specialization or polyethism has been suggested as having evolved due to the high casualties involved in foraging and defence, making it an acceptable risk only for ants who are older and likely to die sooner from natural causes.[67][68] In the Brazilian ant Forelius pusillus, the nest entrance is closed from the outside to protect the colony from predatory ant species at sunset each day. One to eight workers seal the nest entrance from the outside, in effect sacrificing themselves, as they have no chance of returning to the nest.[69] Whether these seemingly suicidal workers are older workers has not been determined.[70]

Ant colonies can be long-lived. The queens can live for up to 30 years, and workers live from 1 to 3 years. Males, however, are more transitory, being quite short-lived and surviving for only a few weeks.[71] Ant queens are estimated to live 100 times as long as solitary insects of a similar size.[72]

Ants are active all year long in the tropics; however, in cooler regions, they survive the winter in hibernation. The forms of inactivity are varied and some temperate species have larvae going into the inactive state (diapause), while in others, the adults alone pass the winter in a state of reduced activity.[73]

Reproduction

Winter ant (Prenolepis imparis) mating, the drone is much smaller than the queen

A wide range of reproductive strategies have been noted in ant species. Females of many species are known to be capable of reproducing asexually through thelytokous parthenogenesis.[74] Secretions from the male accessory glands in some species can plug the female genital opening and prevent females from re-mating.[75] Most ant species have a system in which only the queen and breeding females have the ability to mate. Contrary to popular belief, some ant nests have multiple queens, while others may exist without queens. Workers with the ability to reproduce are called "gamergates" and colonies that lack queens are then called gamergate colonies; colonies with queens are said to be queen-right.[76]

In the ant Cataglyphis hispanica, workers are produced by hybridization of two distinct lineages while the male and female reproductives are produced through (asexual) parthenogenesis.[77] The production of hybrid workers with the existence of non-hybrid queens and males has been termed as "social hybridogenesis".[78] This has been noted in the genera Messor, Pogonomyrmex, Cataglyphis and Solenopsis.[79] The use of sperm of another species by females has been termed as sperm parasitism.[80] A more complex situation was discovered in 2025 where Messor ibericus queens were shown to lay some eggs that developed into workers which match genetically with a different species of ant, Messor structor. Although the two species overlap in some parts of their range, the colonies studied were on the island of Sicily where M. ibericus alone is found. Queen M. ibericus in this region were able to produce M. structor males through cloning of sperms stored in their spermatheca and producing hybrid workers by fertilizing her eggs with the cloned sperm. The hybrid workers have a M. structor phenotype with mitochondrial DNA of M. ibericus. This reproductive mode has been termed as "xenoparous", defined by one species being able to produce the offspring of another species.[81]

Drones can enter a foreign colony and mate with existing queens in some species such as in army ants. When the drone is initially attacked by the workers, it releases a mating pheromone. If recognized as a mate, it will be carried to the queen to mate.[82] Males may also patrol the nest and fight others by grabbing them with their mandibles, piercing their exoskeleton and then marking them with a pheromone. The marked male is interpreted as an invader by worker ants and is killed.[83]

A Hypoponera worker, likely H. opacior, crawls around in soil under leaf litter.
A Hypoponera worker, likely H. opacior.

Most ants are univoltine, producing a new generation each year.[84] During the species-specific breeding period, winged females and winged males, known to entomologists as alates, leave the colony in what is called a nuptial flight. The nuptial flight usually takes place in the late spring or early summer when the weather is hot and humid. Heat makes flying easier, and freshly fallen rain makes the ground softer for mated queens to dig nests.[85] Males typically take flight before the females. Males then use visual cues to find a common mating ground, for example, a landmark such as a pine tree to which other males in the area converge. Males secrete a mating pheromone that females follow. Males will mount females in the air, but the actual mating process usually takes place on the ground. Females of some species mate with just one male but in others they may mate with as many as ten or more different males, storing the sperm in their spermathecae.[86] The genus Cardiocondyla have species with both winged and wingless males, where the latter will only mate with females living in the same nest. Some species in the genus have lost winged males completely, and only produce wingless males.[87] In C. elegans, workers may transport newly emerged queens to other conspecific nests where the wingless males from unrelated colonies can mate with them, a behavioural adaptation that may reduce the chances of inbreeding.[88]

Hypoponera opacior produces both winged and wingless queens and males. Winged alates mate through nuptial flights in June,[89] but wingless queens and males have a different way of reproduction. During the fall, the wingless queens mate inside the nest. Then, the colony splits and the queen departs with a portion of the colony's workers, in order to start a new colony. The queen must leave the nest, as the workers will try to kill her if she does not.[90] The wingless males mate with the queens while they are still in cocoons, and, unlike Cardiocondyla, do not fight. The males mate with the queens for up to 40 hours, and it is thought that they guard the queens in order to prevent other males from mating with them.[91]

Fertilised meat ant queen beginning to dig a new colony

Mated females then seek a suitable place to begin a colony. There, they break off their wings using their tibial spurs and begin to lay and care for eggs. The females can selectively fertilise future eggs with the sperm stored to produce diploid workers or lay unfertilized haploid eggs to produce drones. The first workers to hatch, known as nanitics,[92] are weaker and smaller than later workers but they begin to serve the colony immediately. They enlarge the nest, forage for food, and care for the other eggs. Species that have multiple queens may have a queen leaving the nest along with some workers to found a colony at a new site,[86] a process akin to swarming in honeybees.

Nests, colonies, and supercolonies

The typical ant species has a colony occupying a single nest, housing one or more queens, where the brood is raised. There are however more than 150 species of ants in 49 genera that are known to have colonies consisting of multiple spatially separated nests. These polydomous (as opposed to monodomous) colonies have food and workers moving between the nests.[93] Membership to a colony is identified by the response of worker ants which identify whether another individual belongs to their own colony or not. A signature cocktail of body surface chemicals (also known as cuticular hydrocarbons or CHCs) forms the so-called colony odor which other members can recognize.[94] Some ant species appear to be less discriminating; in the Argentine ant Linepithema humile, workers carried from a colony anywhere in the southern US and Mexico are acceptable within other colonies in the same region. Similarly, workers from colonies established in Europe are accepted by any other colonies within Europe, but not by the colonies in the Americas. The interpretation of these observations has been debated and some have been termed these large populations as supercolonies[95][96][97] while others have termed the populations as unicolonial.[98]

Behaviour and ecology

Communication

See also: Ant communication
Two Camponotus sericeus workers communicating through touch and pheromones
Ants find a dying white cabbage larvae that parasitoid wasps larvae exited two days earlier.

Ants communicate with each other using pheromones, sounds, and touch.[99] Since most ants live on the ground, they use the soil surface to leave pheromone trails that may be followed by other ants. In species that forage in groups, a forager that finds food marks a trail on the way back to the colony; this trail is followed by other ants, these ants then reinforce the trail when they head back with food to the colony. When the food source is exhausted, no new trails are marked by returning ants and the scent slowly dissipates. This behaviour helps ants deal with changes in their environment. For instance, when an established path to a food source is blocked by an obstacle, the foragers leave the path to explore new routes. If an ant is successful, it leaves a new trail marking the shortest route on its return. Successful trails are followed by more ants, reinforcing better routes and gradually identifying the best path.[99][100]

Ants use pheromones for more than just making trails. A crushed ant emits an alarm pheromone that sends nearby ants into an attack frenzy and attracts more ants from farther away. Several ant species even use "propaganda pheromones" to confuse enemy ants and make them fight among themselves.[101] Pheromones are produced by a wide range of structures including Dufour's glands, poison glands and glands on the hindgut, pygidium, rectum, sternum, and hind tibia.[72] Pheromones also are exchanged, mixed with food, and passed by trophallaxis, transferring information within the colony.[102] This allows other ants to detect what task group (e.g., foraging or nest maintenance) other colony members belong to.[103] In ant species with queen castes, when the dominant queen stops producing a specific pheromone, workers begin to raise new queens in the colony.[104]

Some ants produce sounds by stridulation, using the gaster segments and their mandibles. Sounds may be used to communicate with colony members or with other species.[105][106]

Defence

See also: Defense in insects
A Plectroctena sp. attacks another of its kind to protect its territory.

Ants attack and defend themselves by biting and, in many species, by stinging often injecting or spraying chemicals. Bullet ants (Paraponera), located in Central and South America, are considered to have the most painful sting of any insect, although it is usually not fatal to humans. This sting is given the highest rating on the Schmidt sting pain index.[107]

The sting of jack jumper ants can be lethal for humans,