Army ant

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"Army Ants" redirects here. For other uses, see Army Ants (disambiguation).
African Dorylus raid

The name army ant (or legionary ant or marabunta) is applied to over 200 ant species, in different lineages, due to their aggressive predatory foraging groups, known as "raids", in which huge numbers of ants forage simultaneously over a certain area.

Another shared feature is that, unlike most ant species, army ants do not construct permanent nests; an army ant colony moves almost incessantly over the time it exists. All species are members of the true ant family, Formicidae, but several groups have independently evolved the same basic behavioral and ecological syndrome. This syndrome is often referred to as "legionary behavior", and is an example of convergent evolution.[n 1]

Most New World army ants belong to the subfamily Ecitoninae, which contains two tribes: Cheliomyrmecini and Ecitonini. The former only contains the genus Cheliomyrmex, whereas the latter contains four genera: Neivamyrmex, Nomamyrmex, Labidus, and Eciton.[1] The largest genus is Neivamyrmex, which contains more than 120 species; the most predominant species is Eciton burchellii; its common name "army ant" is considered to be the archetype of the species. Old World army ants are divided between the Aenictini and Dorylini tribes. Aenictini contains more than 50 species of army ants in the single genus, Aenictus. However, the Dorylini contain the genus Dorylus, the most aggressive group of driver ants; 60 species are known.

Originally, the Old World and New World lineages of army ants were thought to have evolved independently, in an example of convergent evolution. In 2003, though, genetic analysis of various species suggests that they all evolved from a single common ancestor, which lived approximately 100 million years ago at the time of the separation of the continents of Africa and South America.[1] Army ant taxonomy remains in flux, and genetic analysis will likely continue to provide more information about the relatedness of the various taxa.

Morphology[edit]

Workers[edit]

The workers of army ants are usually blind or can have compound eyes that are reduced to a single lens. There are species of army ants where the worker caste may show polymorphism based on physical differences and job allocations; however, there are also species that show no polymorphism at all.[2] The worker caste is usually composed of sterile female worker ants.[3]

Queen[edit]

Colonies of real army ants always have only one queen, while some other ant species can have several queens. The queen is dichthadiigyne (a blind ant with large gaster) but may sometimes possess vestigial eyes.[2] The queens of army ants are unique in that they do not have wings, have an enlarged gaster size and an extended cylindrical abdomen.[4] They are significantly larger than worker army ants and possess 10–12 segments on their antennae.[2] Queens will mate with multiple males and because of their enlarged gaster, can produce 3 to 4 million eggs a month, resulting in synchronized brood cycles and colonies composed of millions of individuals all related to a single queen.[2][5]

Males[edit]

Males are large in size and have a large cylindrical abdomen, highly modified mandibles and uncommon genitalia not seen in other ants.[6] They have 13 segments on their antennae, are alated (have wings) and therefore can resemble wasps.[2] Males are born as part of a sexual brood.[6] As soon as they are born, they will fly off in search of a queen to mate with. In some instances where males seek to mate with a queen from an existing colony, the receiving workers will forcibly remove the wings in order to accommodate the large males into the colony for mating.[4] Because of their size, males are sometimes called "sausage flies" or "sausage ants."

Behavior[edit]

E. vagans with larvae of a raided wasp nest
Dorylus sp. in Cameroon, consuming a grasshopper
Safari ants (Dorylus sp.) on a march in Kakamega Forest, Kenya. The soldiers have created a tunnel through which the workers move, and clearly show their mandibles

Army ant syndrome[edit]

The army ant syndrome refers to behavioral and reproductive traits such as obligate collective foraging, nomadism and high specialized queens that allow these organisms to become the most ferocious social hunters.[1]

Most ant species will send individual scouts to find food sources and later recruit others from the colony to help; however, army ants dispatch a cooperative, leaderless group of foragers to detect and overwhelm the prey at once.[1][2] Army ants do not have a permanent nest but instead form many bivouacs as they travel. The constant traveling is due to the need to hunt large amounts of prey to feed its enormous colony population.[2] Their queens are wingless and have abdomens that expand significantly during egg production.[4] This allows for the production of 3-4 million eggs every month and often results in synchronized brood cycles, thus each colony will be formed of millions of individuals that descend from a single queen. All three of these traits are found to be in all army ant species and the defining traits of army ants.[1][7]

Nomadic and stationary phase[edit]

Army ants have two phases of activity—a nomadic (wandering) phase and a stationary (statary) phase—that constantly cycle, and can be found throughout all army ants species.[4]

The nomadic phase begins around 10 days after the queen lays her eggs. This phase will last approximately 15 days to let the larvae develop. The ants move during the day, capturing insects, spiders, and small vertebrates to feed their brood. At dusk, they will form their nests or bivouac, which they change almost daily.[4] Among the army ants are some species that only venture out at night, but no adequate studies of their activities have been made. At the end of the nomadic phase, the larvae will spin pupal cases and no longer require food. The colony can then live in the same bivouac site for around 20 days, foraging only on approximately two-thirds of these days.[4][8]

The stationary phase, which lasts about two to three weeks, begins when the larvae pupate. From this point on, the prey that were previously fed to the larvae are now fed exclusively to the queen.[4] The abdomen (gaster) of the queen swells significantly, and she lays her eggs. At the end of the stationary phase, both the pupae emerge from their cocoons (eclosion) and the next generation of eggs hatch so the colony has a new group of workers and larvae. After this, the ants resume the nomadic phase.[2][4]

Colony fission[edit]

Army ants will split into groups when the size of the colony has reached a size threshold which happens approximately every three years.[9] Wingless virgin queens will hatch among a male sexual brood that will hatch at a later date. When the colony fissions, there are two ways new queens are decided. A possible outcome is a new queen will stay at the original nest with a portion of the workers and the male brood while the old queen will leave with the other portion of workers and find a new nest. Another possibility is that the workers will reject the old queen and new queens will head the two new colonies.[4][8] The workers will affiliate with individual queens based on the pheromone cues that are unique to each queen. When new bivouacs are formed, communication between the original colony and the new bivouacs will cease to exist.[4]

Queen behavior[edit]

Being the largest ants on Earth, army ants, such as African Dorylus queens hold the world record in reproductive potential among the insects, with an egg-laying capacity of several millions per month. Army ant queens never have to leave the protection of the colony, where they mate with foreign incoming males which disperse on nuptial flights. The exact mating behavior of the army ant queen is still unknown, but observations seem to imply that queens may be fertilized by multiple males.[10] Due to the queen's large reproductive potential, one colony of army ants can be related to a single queen.[5]

When the queen ant passes away, there is no replacement and army ants cannot rear emergency queens. Most of the time, if the queen passes away, the colony will most likely die too. Queen loss can occur due to accidents during emigrations, predator attack, old age or illness.[9] However, there are possibilities to avoid colony death. When a colony loses its queen, the worker ants will usually fuse with another colony that has a queen in a few days.,[3][11] Sometimes, the workers will backtrack along the paths of prior emigrations to search for a queen that has been lost or merge with a sister colony.[11][12] By merging with a related colony, the workers would increase their overall inclusive fitness.[9] The workers that merge into a new colony may cause the a colony to increase in size by 50%.

Sexual selection by workers[edit]

Workers in army ant species have a unique role in selecting both the queen and the male mate.

When the queens emerge, the workers in the colony will form two ‘systems’ or arms in opposite directions. These queens that are hatched will move down either the arms and only two queens will succeed, one for each branch. The remaining new queens will be left in the middle and are abandoned to die. Two new bivouacs will be formed and break off into different directions. The workers will surround the two to-be queens and ensure they reach the arms and survive. These workers that surround the queens are affected by the CHC (pheromone) profile emitted from the new queen.[4]

When males hatch from their brood, they will fly off to find a mate. For males to access the queen and mate, they must run through the workers in the colony. Males that are favored are superficially similar in size and shape to the queen. The males also produce large quantities of pheromones to pacify the worker ants.[4]

Reproduction responsibilities[edit]

In the colony, instead of having both queen and workers producing off spring, the queen is the sole reproductive in the colony. With queens mating with multiple males, workers are on average more closely related to the offspring of the queen that to the offspring of other workers.[13] Both the queen and the daughter workers would benefit from producing sons, because worker reproduction has a colony cost or each worker is more related to the queen’s son than to other worker’s sons, the worker caste will oppose worker reproduction and pull their resources to only raise the queen’s offspring. Three factors have been suggested to rationalize the loss of worker reproduction in the presence of a queen. First, if the worker reproduces, it lowers the general performance of the colony because it is not working. Second, workers increase their inclusive fitness by policing other workers because they themselves are more related to the queen’s offspring than other worker’s offspring.[13] Lastly, male larvae have a larger body size relative to workers, the larvae become too large to be transported so colonies with a sexual brood must remain in a nest for a period of 41–56 days as compared to non-reproductive colonies that remain in the nest an average of 17 days. This suggests that if workers produced sons, it would be produced asynchronously with the queen's sexual brood and not likely to be reared to adulthood as it would be hard for the worker to predict when the queen would reproduce.[13]

Colony fusion[edit]

When the queen of an army-ant colony dies, the workers may join another colony. In other cases, when two colonies of the same species meet, they usually change the marching direction to avoid conflicts.

Foraging[edit]

The whole colony of army ants can consume up to 500,000 prey animals each day, so can have a significant influence on the population, diversity, and behavior of their prey.[14] The prey selection differs with the species. Underground species prey primarily on ground-dwelling arthropods and their larvae, earthworms, and occasionally also the young of vertebrates, turtle eggs, or oily seeds. A majority of the species, the "colony robbers", specialize in the offspring of other ants and wasps. Only a few species seem to have the very broad spectrum of prey seen in the raiding species. Even these species do not eat every kind of animal. Although small vertebrates that get caught in the raid will be killed, the jaws of the American Eciton are not suited to this type of prey, in contrast to the African Dorylus. These undesired prey are simply left behind and consumed by scavengers or by the flies that accompany the ant swarm. Only a few species hunt primarily on the surface of the earth; they seek their prey mainly in leaf litter and in low vegetation. About five species hunt in higher trees, where they can attack birds and their eggs, although they focus on hunting other social insects along with their eggs and larvae. Colonies of army ants are large compared to the colonies of other Formicidae. Colonies can have over 15 million workers and can transport 3000 prey (items) per hour during the raid period.[10][15]

When army ants forage, the trails that are formed can be over 20m wide and over 100m long.[15] They stay on the path through the use of a concentration gradient of pheromones. The concentration of pheromone is highest in the middle of the trail, splitting the trail into two distinct regions: area with high concentration and two areas with low concentrations of pheromones. The outbound ants will occupy the outer two lanes and the returning ants will occupy the central lane.[15] The returning worker ants have also to be found to emit more pheromones than those leaving the nest, causing the difference in concentration of pheromone in the trails.[16] The pheromones will allow foraging to be much more efficient by allowing the army ants to avoid their own former paths and those of their conspecifics.[14]

Nesting[edit]

Eciton sp. forming a bridge

Army ants do not build a nest like most other ants. Instead, they build a living nest with their bodies, known as a bivouac. Bivouacs tend to be found in tree trunks or in burrows dug by the ants. The members of the bivouac hold onto each other's legs and so build a sort of ball, which may look unstructured to a layman's eyes, but is actually a well-organized structure.[17] The older female workers are located on the exterior; in the interior are the younger female workers. At the smallest disturbance, soldiers gather on the top surface of the bivouac, ready to defend the nest with powerful pincers and (in the case of the Aenictinae and Ecitoninae) stingers. The interior of the nest is filled with numerous passages and contains many chambers with food, the queen, the larvae, and the eggs.

Symbionts[edit]

Many species of army ant are widely considered to be keystone species, due to the high number of vertebrate and invertebrate associates that rely on army ant colonies for nutrition or protection.[18] During their hunt, many surface-raiding army ants are accompanied by various birds, such as antbirds, thrushes, ovenbirds and wrens, which devour the insects that are flushed out by the ants, a behavior known as cleptoparasitism.[19] A wide variety of arthropods including staphylinid beetles and mites also follow colonies. The Neotropical army ant Eciton burchellii has an estimated 350 to 500 animal associates, the most of any one species known to science.[20]

Taxonomy[edit]

Historically, "army ant" in the broad sense, referred to various members of five different ant subfamilies: in two of these cases, the Ponerinae and Myrmicinae, only a few species and genera exhibit legionary behavior; in the other three lineages, Ecitoninae, Dorylinae, and Leptanillinae, all of the constituent species are legionary. More recently, ant classifications now recognize an additional New World subfamily, Leptanilloidinae, which also consists of obligate legionary species, so is another group now included among the army ants.

A 2003 study of 30 species (by Sean Brady of Cornell University) indicates that army ants of subfamilies Ecitoninae (South America), Dorylinae (Africa) and Aenictinae (Asia) together formed a monophyletic group, based on data from three molecular genes and one mitochondrial gene. Brady concluded that these two groups are, therefore, a single lineage that evolved in the mid-Cretaceous period in Gondwana,[n 2] so the two subfamilies are now generally united into a single subfamily Ecitoninae, though this is still not universally recognized.[22]

Accordingly, the army ants as presently recognized consist of these genera:

Subfamily Aenictinae
Subfamily Dorylinae
Subfamily Ecitoninae
Subfamily Leptanillinae
Subfamily Leptanilloidinae
Subfamily Myrmicinae
Subfamily Ponerinae

Human beings and army ants[edit]

Notes[edit]

  1. ^ "There are also interesting [evolutionary] convergences within the ants. Although most ant colonies live a settled existence in a fixed nest, there seems to be a successful living to be made by wandering in enormous pillaging armies. This is called the legionary habit." (Dawkins 1986)
  2. ^ "Because army ants are found almost everywhere, scientists postulated that they evolved many times after the break-up and dispersal of the supercontinent Gondwana just over 100 million years ago. The conventional view of the evolution of army ants needs a revision because of new data obtained by Sean Brady, a Cornell University, US, entomologist who has discovered that these ants evolved from a common ancestor."(Whitehouse 2003)[21]

References[edit]

  1. ^ a b c d e Brady, Seán G. (May 2003). "Evolution of the army ant syndrome: The origin and long-term evolutionary stasis of a complex of behavioral and reproductive adaptations". Proceedings of the National Academy of Sciences of the United States of America 100 (11): 6575–9. doi:10.1073/pnas.1137809100. PMC 164488. PMID 12750466.  open access publication - free to read
  2. ^ a b c d e f g h Gotwald, William H., Jr. "Army Ants". pp. 157–254.  in Hermann 1982
  3. ^ a b Bourke, Andrew F. G; Franks, Nigel R. (1995). Social Evolution in Ants. Monographs in Behavior and Ecology. Princeton, NJ: Princeton University Press. ISBN 9780691044262. OCLC 32087436. 
  4. ^ a b c d e f g h i j k l Franks, Nigel R.; Hölldobler, Bert (1987). "Sexual competition during colony reproduction in army ants". Biological Journal of the Linnean Society 30 (3): 229–43. doi:10.1111/j.1095-8312.1987.tb00298.x.  Closed access
  5. ^ a b Kronauer, Daniel J. C.; Schöning, Caspar; Pedersen, Jes S. S.; Boomsma, Jacobus J.; Gadau, Jurgen R. (2004). "Extreme queen-mating frequency and colony fission in African army ants". Molecular Ecology 13 (8): 2381–8. doi:10.1111/j.1365-294X.2004.02262.x. PMID 15245410.  Closed access
  6. ^ a b Trager, James C., ed. (1988). Advances in Myrmecology. Leiden, NL: E.J. Brill. ISBN 9780916846381. OCLC 468279677. 
  7. ^ Wilson, Edward. O.; Hölldobler, Bert (September 2005). "Eusociality: Origin and consequences". Proceedings of the National Academy of Sciences 102 (38): 13367–71. doi:10.1073/pnas.0505858102. PMC 1224642. PMID 16157878.  open access publication - free to read
  8. ^ a b Schneirla, Theodore Christian (1971). Topoff, Howard R., ed. Army Ants: A Study in Social Organization. San Francisco: W. H. Freeman and Company. ISBN 9780716709336. OCLC 210501. 
  9. ^ a b c Kronauer, Daniel J. C. (2009). "Recent advances in army ant biology (Hymenoptera: Formicidae)". Myrmecological News 12: 51–65.  open access publication - free to read
  10. ^ a b Kronauer, Daniel J. C.; Johnson, Robert A.; Boomsma, Jacobus J. (2007). "The Evolution of multiple mating in army ants". Evolution 61 (2): 413–22. doi:10.1111/j.1558-5646.2007.00040.x. PMID 17348950.  Closed access
  11. ^ a b Kronauer, Daniel J. C.; Schöning, Caspar; d'Ettorre, Patricia; Boomsma, Jacobus J. (2010). "Colony fusion and worker reproduction after queen loss in army ants". Proceedings of the Royal Society B: Biological Sciences 277 (1682): 755–63. doi:10.1098/rspb.2009.1591. PMC 2842746. PMID 19889701.  open access publication - free to read
  12. ^ Schneirla, Theodore Christian. "Army-ant Life and Behavior under Dry-season Conditions. 3, The Course of Reproduction and Colony Behavior". Bulletin of the AMNH 94. hdl:2246/407.  open access publication - free to read
  13. ^ a b c Kronauer, Daniel J. C.; Schöning, Caspar; Boomsma, Jacobus J. (2006). "Male parentage in army ants". Molecular Ecology 15 (4): 1147–51. doi:10.1111/j.1365-294X.2005.02850.x. PMID 16599973.  Closed access
  14. ^ a b Franks, Nigel R.; Fletcher, Charles R. (July 1983). "Spatial Patterns in Army Ant Foraging and Migration: Eciton Burchelli on Barro Colorado Island, Panama". Behavioral Ecology and Sociobiology 12 (4): 261–70. doi:10.1007/BF00302894.  Closed access
  15. ^ a b c Couzin, Iain D.; Franks, Nigel R. (January 2003). "Self-organized lane formation and optimized traffic flow in army ants". Proceedings of the Royal Society B: Biological Sciences 270 (1511): 139–146. doi:10.1098/rspb.2002.2210. PMC 1691225. PMID 12590751. open access publication - free to read
  16. ^ Deneubourg, Jean-Louis; Goss, S.; Franks, Nigel R.; Pasteels, Jacques M. (1989). "The blind leading the blind: Modeling chemically mediated army ant raid patterns". Journal of Insect Behavior 2 (5): 719–25. doi:10.1007/BF01065789.  Closed access
  17. ^ Dawkins, Richard (1996) [1986]. "4. Making Tracks Through Animal Space". The Blind Watchmaker: Why the Evidence of Evolution Reveals a Universe Without Design. W. W. Norton & Company. p. 107. ISBN 9780393315707. 
  18. ^ Boswell, Graeme P.; Britton, Nicholas F.; Franks, Nigel R. (22 October 1998). "Habitat fragmentation, percolation theory and the conservation of a keystone species". Proceedings of the Royal Society B 265 (1409): 1921–25. doi:10.1098/rspb.1998.0521. 
  19. ^ Wrege, Peter H.; Wikelski, M.; Mandel, J. T.; Rassweiler, T.; Couzin, I. D. (2005). "Antbirds parasitize foraging army ants". Ecology 8 (3): 555–559. 
  20. ^ Rettenmeyer, C. W.; Rettenmeyer, M. E.; Joseph, J.; Berghoff, S. M (2011). "The largest animal association centered on one species: the army ant Eciton burchellii and its more than 300 associates". Insectes Sociaux 58: 281–292. doi:10.1007/s00040-010-0128-8. 
  21. ^ Whitehouse, David (2003-05-10). "Ant history revealed". Science & Environment. BBC News Online. Retrieved 2009-01-14. 
  22. ^ Engel, Michael S.; Grimaldi, David A. (2005). "Primitive new ants in Cretaceous amber from Myanmar, New Jersey, and Canada (Hymenoptera: Formicidae)". American Museum Novitates (New York: American Museum of Natural History) 3485: 1–24. doi:10.1206/0003-0082(2005)485[0001:PNAICA]2.0.CO;2. hdl:2246/5676.  open access publication - free to read

Bibliography[edit]

External links[edit]