Leafcutter ant

Atta colombica workers transporting leaves
Two leafcutter ants

Leafcutter ants, a non-generic name, are any of 47 species[1] of leaf-chewing ants belonging to the two genera Atta and Acromyrmex. These species of tropical, fungus-growing ants are all endemic to South and Central America, Mexico, and parts of the southern United States. [2] Leafcutter ants can carry more than 5000 times their body weight and cut and process fresh vegetation (leaves, flowers, and grasses) to serve as the nutritional substrate for their fungal cultivars."[3]

Acromyrmex and Atta ants have much in common anatomically; however, the two can be identified by their external differences. Atta ants have three pairs of spines and a smooth exoskeleton on the upper surface of the thorax, while Acromyrmex ants have four pairs and a rough exoskeleton.[4]

Next to humans, leafcutter ants form the largest and most complex animal societies on Earth. In a few years, the central mound of their underground nests can grow to more than 30 m (98 ft) across, with smaller, radiating mounds extending out to a radius of 80 m (260 ft), taking up 30 to 600 m2 (320 to 6,460 sq ft) and containing eight million individuals.[2]

The lifecycle of a leafcutter ant colony

Reproduction and colony founding

Atta colombica, queen with larvae and workers on substrate

Winged females and males leave their respective nests en masse and engage in a nuptial flight known as the revoada. Each female mates with multiple males to collect the 300 million sperm she needs to set up a colony.[5]

Once on the ground, the female loses her wings and searches for a suitable underground lair in which to found her colony. The success rate of these young queens is very low, and only 2.5% will go on to establish a long-lived colony. To start her own fungus garden, the queen stores bits of the parental fungus garden mycelium in her infrabuccal pocket, which is located within her oral cavity.[6]

Colony hierarchy

In a mature leafcutter colony, ants are divided into castes, based mostly on size, that perform different functions. Acromyrmex and Atta exhibit a high degree of biological polymorphism, four castes being present in established colonies — minims, minors, mediae, and majors. Majors are also known as soldiers or dinergates. Atta ants are more polymorphic than Acromyrmex, meaning comparatively less difference occurs in size from the smallest to largest types of Acromymex.

Leafcutter ant Atta cephalotes

Ant-fungus mutualism

Their societies are based on an ant-fungus mutualism, and different species of ants use different species of fungus, but all of the fungi the ants use are members of the Lepiotaceae family. The ants actively cultivate their fungus, feeding it with freshly cut plant material and keeping it free from pests and molds. This mutualistic relationship is further augmented by another symbiotic partner, a bacterium that grows on the ants and secretes chemicals; essentially, the ants use portable antimicrobials. Leaf cutter ants are sensitive enough to adapt to the fungi's reaction to different plant material, apparently detecting chemical signals from the fungus. If a particular type of leaf is toxic to the fungus, the colony will no longer collect it. The only two other groups of insects to use fungus-based agriculture are ambrosia beetles and termites. The fungus cultivated by the adults is used to feed the ant larvae, and the adult ants feed on leaf sap. The fungus needs the ants to stay alive, and the larvae need the fungus to stay alive, so the mutualism is obligatory.

The fungus used by the higher attine ants do no longer produce spores. These ants fully domesticated their fungal partner 15 million years ago, a process that took 30 million years to complete.[7] Their fungus produce nutritious and swollen hyphal tips (gongylidia) that grow in bundles called staphylae, to specifically feed the ants.[8]

Waste management

Workers of Atta colombica at work
Leafcutter ant in Costa Rica

Leafcutter ants have very specific roles in taking care of the fungal garden and dumping the refuse. Waste management is a key role for each colony's longevity. The necrotrophic parasitic fungus Escovopsis threatens the ants' food source and thus is a constant danger to the ants. The waste transporters and waste-heap workers are the older, more dispensable leafcutter ants, ensuring the healthier and younger ants can work on the fungal garden. The Atta colombica species, unusually for the Attine tribe, have an external waste heap. Waste transporters take the waste, which consists of used substrate and discarded fungus, to the waste heap. Once dropped off at the refuse dump, the heap workers organise the waste and constantly shuffle it around to aid decomposition. A compelling observation of A. colombica was the dead ants placed around the perimeter of the waste heap. [9][10]

In addition to feeding the fungal garden with foraged food, mainly consisting of leaves, it is protected from Escovopsis by the antibiotic secretions of Actinobacteria' (genus Pseudonocardia). This mutualistic micro-organism lives in the metapleural glands of the ant.[11] Actinobacteria are responsible for producing the majority of the world's antibiotics today.

Parasitism

When the ants are out collecting leaves, they are at risk of attack by some species of phorid flies, parasitoids that lay eggs into the crevices of the worker ants' heads. Often, a minim will sit on a worker ant and ward off any attack.[12]

Also, the wrong type of fungus can grow during cultivation. Escovopsis, a highly virulent fungus, has the potential to devastate an ant garden, as it is horizontally transmitted. Escovopsis was cultured, during colony foundation, in 6.6% of colonies.[13] However, in one- to two-year-old colonies, almost 60% had Escovopsis growing in the fungal garden.[14]

Interactions with humans

In some parts of their range, leafcutter ants can be a serious agricultural pest, defoliating crops and damaging roads and farmland with their nest-making activities.[5] For example, some Atta species are capable of defoliating an entire citrus tree in less than 24 hours. A promising approach to deterring attacks of the leafcutter ant Acromyrmex lobicornis on crops has been demonstrated. Collecting the refuse from the nest and placing it over seedlings or around crops resulted in a deterrent effect over a period of 30 days.[15]

See also

References

  1. Speight, Martin R.; Watt, Allan D.; Hunter, Mark D. (1999). Ecology of Insects. Blackwell Science. p. 156. ISBN 0-86542-745-3..
  2. 1 2 Ross 2002, pp. 11–13.
  3. Schultz, T. R.; Brady, S. G. (2008). "Major evolutionary transitions in ant agriculture". Proceedings of the National Academy of Sciences of the United States of America. 105 (14): 5435–5440. Bibcode:2008PNAS..105.5435S. doi:10.1073/pnas.0711024105. PMC 2291119Freely accessible. PMID 18362345.
  4. Hedlund, Kye S. (March 2005), Diagnoses of the North American: Ant Genera (Hymenoptera: Formicidae).
  5. 1 2 Piper, Ross (2007), Extraordinary Animals: An Encyclopedia of Curious and Unusual Animals, Greenwood Press, p. 298, ISBN 0-313-33922-8.
  6. Weber, Neal A. (1972), Gardening Ants, The Attines, The American Philosophical Society, pp. 14, 34, ISBN 0-87169-092-6.
  7. Crop Domestication Is a Balancing Act
  8. For Leaf-Cutter Ants, Farm Life Isn't So Simple
  9. Hart, A. G. & Ratnieks, F. L. W. (2002), "Waste management in the leaf-cutting ant Atta colombica", Behavioural Ecology, 13 (2): 224–231, doi:10.1093/beheco/13.2.224.
  10. Bot, A. N. M.; Currie, C. R.; Hart, A. G. & Boomsma, J. J. (2001), "Waste Management in Leaf-cutting Ants", Ethology Ecology and Evolution, 13 (3): 225–237, doi:10.1080/08927014.2001.9522772.
  11. Zhang, M. M.; Poulsen, M. & Currie, C. R. (2007), "Symbiont recognition of mutualistic bacteria by Acromyrmex leaf-cutting ants", The ISME Journal, 1 (4): 313–320, doi:10.1038/ismej.2007.41.
  12. "Leafcutter Ants", Lincoln Park Zoo.
  13. Currie, C. R.; Mueller, U. G. & Malloch, D. (1999), "The agricultural pathology of ant fungus gardens", PNAS, 96 (14): 7998–8002, Bibcode:1999PNAS...96.7998C, doi:10.1073/pnas.96.14.7998.
  14. Reynolds, H. T. & Currie, C. R. (2004), "Pathogenicity of Escovopsis weberi: The parasite of the attine ant-microbe symbiosis directly consumes the ant-cultivated fungus", Mycologia, 96 (5): 955–959, doi:10.2307/3762079.
  15. Ballari, S. A. & Farji-Brener, A. G. (2006), "Refuse dumps of the leaf-cutting ants as a deterrent for ant herbivory: does refuse age matter?", The Netherlands Entomological Society, 121 (3): 215–219, doi:10.1111/j.1570-8703.2006.00475.x.

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