Biology:Myrmecophagy

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Short description: Feeding on termites or ants
The snout and the scientific name of the giant anteater (Myrmecophaga tridactyla) reflect its feeding habits.

Myrmecophagy is a feeding behavior defined by the consumption of termites or ants, particularly as pertaining to those animal species whose diets are largely or exclusively composed of said insect types. Literally, myrmecophagy means "ant-eating" (Ancient Greek: murmēx, "ants" and phagein, "to eat") rather than "termite eating" (for which the strict term is termitophagy). The two habits often overlap, as both of these eusocial insect types often live in large, densely populated nests requiring similar adaptations in the animal species that exploit them.[1]

Vertebrates

Juvenile Iberian green woodpecker eating ants

Myrmecophagy is found in several land-dwelling vertebrate taxa, including reptiles and amphibians (horned lizards and blind snakes, narrow-mouthed toads of the family Microhylidae and poison frogs of the Dendrobatidae), a number of New World bird species (Antbirds, Antthrushes, Antpittas, flicker of genus Colaptes), and multiple mammalian groups including anteaters, aardvarks, aardwolves, armadillos, echidnas, numbats, pangolins, and sloth bears.

The extinct alvarezsaurids, a group of theropod dinosaurs from the Cretaceous period, have been interpreted as myrmecophagous, with their short, robustly built arms with a single claw being interpreted as being used to break into colonial insect nests.[2]

Mammals that specialize in myrmecophagy often display similar adaptations for this niche.[3][4] Many have powerful forelimbs and claws adapted to excavating the nests of ant or termite colonies from the earth or from wood or under bark. Most have reduced teeth and some have reduced jaws as well. Many have low basal body temperatures resulting from the low caloric content of ants and termites,[5][6] and most have advanced olfaction to help them find prey.[7][4] Practically all have long, sticky tongues. In the nineteenth and early twentieth century many zoologists saw these shared features as evidence of relatedness, and accordingly they regarded the various species as a single order of Mammalia, the Edentata. It quite early became clear that such a classification was hard to sustain, and there was a growing trend to see the features as examples of convergent evolution. For example, at the start of the 20th century Frank Evers Beddard, writing in The Cambridge Natural History, Vol 10, Mammalia, having discussed some discrepant features, said: "The fact is, that we have here a polymorphic order which contains in all probability representatives of at least two separate orders. We have at present a very few, and these perhaps highly modified, descendants of a large and diverse group of mammals."[8] As genome sequences for various former members of Edentata have been published,[9][7] all genetic evidence has confirmed that its members are taxonomically distant.[10]

Invertebrates

Myrmarachne spider eating a queen ant. The spider mimics the ant (Wasmannian mimicry) both to avoid predators (Batesian mimicry) and to deceive its ant prey (aggressive mimicry).

Ants are dangerous, small, and rich in distasteful and harmful compounds, making them difficult prey and favouring ant mimicry for defence among invertebrates. Ants are plentiful, so members of several invertebrate taxa do feed on ants. Such ant predators include some spiders, such as species in the family Salticidae (jumping spiders), spiders in the family Oecobiidae and the family Theridiidae. While exclusive myrmecophagy is not very common, there are some striking examples, such as the Australian ant-slayer spider Euryopis umbilicata that feeds almost exclusively on one species of ant.[11] Other examples include some myrmecomorphs (ant mimics) and myrmecophiles. Myrmecomorphs are Batesian mimics, giving them protection against predators which avoid ants, and access to abundant food.[12]

Various Hemipteran bugs, in the family Reduviidae feed largely or exclusively on ants. Examples include the genera Paredocla and Acanthaspis.[13]

Some insects that feed on ants do so because they are opportunistic predators of small insects that run on the ground surface, of which ants are a large proportion. Remarkable examples of convergent evolution are certain species of the Neuropteran family Myrmeleontidae, largely Myrmeleon, the so-called ant lions, and the Dipteran family Vermileonidae, in particular the genera Lampromyia and Vermilio, the so-called worm lions. Both of them are regarded with interest for their habit of constructing conical pit traps in fine sand or dust, at the bottom of which they await prey that has fallen in. Both throw sand to interfere with any attempts on the part of the prey to escape.[14]

Myrmecophagy takes more forms than just eating adult ants; the later instars of caterpillars of many butterflies in the family Lycaenidae enter the nests of particular species of ants and eat the ants' eggs and larvae.[15] Larvae of some species of flies, such as the genus Microdon in the family Syrphidae spend their entire immature lives in the nests of ants, feeding largely or entirely on the ant brood. Some beetles specialise in feeding on the brood of particular species of ants. An example is the coccinellid Diomus; larvae of Diomus thoracicus in French Guiana specialise in the nests of the invasive ant species Wasmannia auropunctata.[16]

One of the predominant predators on ants are other ants, especially the army ants and their close relatives.[17][18] Some ants such as the raider ant Oocerea biroi and the new world army ant Nomamyrmex esenbecki are obligate myrmecophages, that is they eat exclusively other ants,[18][19] while other ants like the infamous swarm-raiding Eciton burchellii eat more or less all arthropods in their paths, including any ants they can get.[17][18] Primarily it is the highly nutritious pupae and larvae, rather than the adult ants, that are taken and eaten.[17][18]

References

  1. Crompton, John (1954). Ways of the Ant. Collins. ISBN 9780941130844. 
  2. Qin, Zichuan; Zhao, Qi; Choiniere, Jonah N.; Clark, James M.; Benton, Michael J.; Xu, Xing (July 2021). "Growth and miniaturization among alvarezsauroid dinosaurs" (in en). Current Biology 31 (16): 3687–3693.e5. doi:10.1016/j.cub.2021.06.013. PMID 34233160. 
  3. Reiss, Karen Zich (June 2001). "Using Phylogenies to Study Convergence: The Case of the Ant-Eating Mammals". American Zoologist 41 (3): 507–525. doi:10.1093/icb/41.3.507. ISSN 0003-1569. 
  4. 4.0 4.1 Reiss, Karen Zich (2000). "Feeding in Myrmecophagous Mammals". in Schwenk, Kurt. Feeding. Elsevier. pp. 459–485. doi:10.1016/b978-012632590-4/50016-2. ISBN 978-012632590-4. 
  5. Barker, J. M.; Cooper, C. E.; Withers, P. C.; Nicol, S. C. (May 2016). "Reexamining Echidna Physiology: The Big Picture forTachyglossus aculeatus acanthion". Physiological and Biochemical Zoology 89 (3): 169–181. doi:10.1086/686716. ISSN 1522-2152. PMID 27153127. http://ecite.utas.edu.au/116924. 
  6. McNab, Brian K. (August 1984). "Physiological convergence amongst ant‐eating and termite‐eating mammals". Journal of Zoology 203 (4): 485–510. doi:10.1111/j.1469-7998.1984.tb02345.x. 
  7. 7.0 7.1 Choo, Siew Woh; Rayko, Mike; Tan, Tze King; Hari, Ranjeev; Komissarov, Aleksey et al. (2016-08-10). "Pangolin genomes and the evolution of mammalian scales and immunity". Genome Research 26 (10): 1312–1322. doi:10.1101/gr.203521.115. ISSN 1088-9051. PMID 27510566. 
  8. Beddard, Frank Evers (1902). Harmer, Sir Sidney Frederic; Shipley, Arthur Everett; Gadow, Hans. eds. Mammalia. The Cambridge Natural History. 10. Macmillan Company. 
  9. Cheng, Shao-Chen; Liu, Chun-Bing; Yao, Xue-Qin; Hu, Jing-Yang; Yin, Ting-Ting et al. (2022-08-24). "Hologenomic insights into mammalian adaptations to myrmecophagy". National Science Review 10 (4): nwac174. doi:10.1093/nsr/nwac174. ISSN 2095-5138. PMID 37124465. 
  10. Gaubert, Philippe; Wible, John R.; Heighton, Sean P.; Gaudin, Timothy J. (2020). "Phylogeny and systematics". Pangolins. Elsevier. pp. 25–39. doi:10.1016/b978-0-12-815507-3.00002-2. ISBN 978-0-12-815507-3. 
  11. Aceves-Aparicio, Alfonso; Narendra, Ajay; McLean, Donald James; Lowe, Elizabeth C.; Christian, Marcelo; Wolff, Jonas O.; Schneider, Jutta M.; Herberstein, Marie E. (2022-10-04). "Fast acrobatic maneuvers enable arboreal spiders to hunt dangerous prey". Proceedings of the National Academy of Sciences 119 (40): e2205942119. doi:10.1073/pnas.2205942119. ISSN 0027-8424. PMID 36122198. 
  12. Cushing, Paula E. (2012). "Spider-Ant Associations: An Updated Review of Myrmecomorphy, Myrmecophily, and Myrmecophagy in Spiders". Psyche 2012: Article ID 151989. doi:10.1155/2012/151989. 
  13. Brandt, Miriam; Mahsberg, Dieter (February 2002). "Bugs with a backpack: the function of nymphal camouflage in the West African assassin bugs Paredocla and Acanthaspis spp.". Animal Behaviour 63 (2): 277–284. doi:10.1006/anbe.2001.1910. 
  14. Wilson, Edward O. (2000). Sociobiology: the new synthesis. Harvard University Press. pp. 172–. ISBN 978-0-674-00089-6. https://books.google.com/books?id=v7lV9tz8fXAC&pg=PA172. Retrieved 24 May 2013. 
  15. Ballmer, Gregory R.; Pratt, Gordon F. (1988). A Survey of the Last Instar Larvae of the Lycaenidae (Lepidoptera) of California. https://books.google.com/books?id=JbxHXwAACAAJ. Retrieved 25 May 2013. 
  16. Vantaux, Amélie; Roux, Olivier; Magro, Alexandra; Ghomsi, Nathan Tene; Gordon, Robert D.; Dejean, Alain; Orivel, Jérôme (September 2010). "Host-Specific Myrmecophily and Myrmecophagy in the Tropical Coccinellid Diomus thoracicus in French Guiana". Biotropica 42 (5): 622–629. doi:10.1111/j.1744-7429.2009.00614.x. 
  17. 17.0 17.1 17.2 Gotwald, William (1995). Army Ants: the Biology of Social Predation. Comstock Publishing Associates. ISBN 0801426332. https://archive.org/details/armyantsbiologyo00gotw. 
  18. 18.0 18.1 18.2 18.3 Hölldobler, Bert; Wilson, Edward O. (1990). The Ants. Belknap Press of Harvard University Press. ISBN 0-674-04075-9. 
  19. Powell, Scott; Clark, Ellie (1 November 2004). "Combat between large derived societies: a subterranean army ant established as a predator of mature leaf-cutting ant colonies". Insectes Sociaux 51 (4): 342–351. doi:10.1007/s00040-004-0752-2.