Linnaeus 1758 
The giant anteater (Myrmecophaga tridactyla), also known as the ant bear, is an insectivorous mammal native to Central and South America. It is one of four living species of anteaters, the only extant member of the genus Myrmecophaga, and is classified with sloths in the order Pilosa. This species is mostly terrestrial, in contrast to other living anteaters and sloths, which are arboreal or semiarboreal. The giant anteater is the biggest of its family, 182 to 217 cm (5.97 to 7.12 ft) in length, with weights of 33 to 50 kg (73 to 110 lb) for males and 27 to 47 kg (60 to 104 lb) for females. It is recognizable by its elongated snout, bushy tail, long fore claws, and distinctively colored pelage.
The giant anteater is found in multiple habitats, including grassland and rainforest. It forages in open areas and rests in more forested habitats. It feeds primarily on ants and termites, using its fore claws to dig them up and its long, sticky tongue to collect them. Though giant anteaters live in overlapping home ranges, they are mostly solitary except during mother-offspring relationships, aggressive interactions between males, and when mating. Mother anteaters carry their offspring on their backs until weaning them.
The giant anteater is listed as vulnerable by the International Union for Conservation of Nature. It has been extirpated from many parts of its former range. Threats to its survival include habitat destruction, fire, and poaching for fur and bushmeat, although some anteaters inhabit protected areas. With its distinctive appearance and habits, the anteater has been featured in pre-Columbian myths and folktales, as well as modern popular culture.
Taxonomy and phylogeny
The giant anteater got its binomial name from Carl Linnaeus in 1758. Its generic name, Myrmecophaga, and specific name, tridactyla, are both Greek, meaning "anteater" and "three fingers", respectively. Myrmecophaga jubata was used as a synonym. Three subspecies have been tentatively proposed: M. t. tridactyla (ranging from Venezuela and the Guianas to northern Argentina), M. t. centralis (native to Central America, northwestern Colombia, and northern Ecuador), and M. t. artata (native to northeastern Colombia and northwestern Venezuela). The giant anteater is grouped with the semiarboreal northern and southern tamanduas in the family Myrmecophagidae. Together with the family Cyclopedidae, whose only extant member is the arboreal silky anteater, the two families comprise the suborder Vermilingua.
|Phylogenetic tree of the living Xenarthra.|
Anteaters and sloths belong to order Pilosa and share superorder Xenarthra with the Cingulata (whose only extant members are armadillos). The two orders of Xenarthra split 66 million years ago (Mya) during the Late Cretaceous epoch. Anteaters and sloths diverged around 55 Mya, between the Paleocene and Eocene epochs. The Cyclopes lineage emerged around 30 Mya in the Oligocene epoch, while the Myrmecophaga and Tamandua lineages split 10 Mya in the Late Miocene subepoch. During most of the Cenozoic era, anteaters were confined to South America, which was formerly an island continent. Following the formation of the Isthmus of Panama about 3 Mya, anteaters of all three extant genera invaded Central America as part of the Great American Interchange.
The fossil record for anteaters is generally sparse. Known fossils include the Pliocene genus Palaeomyrmidon, a close relative to the silky anteater, Protamandua, the sister taxon to the clade that includes the giant anteater and the tamanduas from the Miocene, and Neotamandua, a sister taxon to Myrmecophaga. Protamandua was larger than the silky anteater, but smaller than a tamandua, while Neotamandua was larger, falling somewhere between a tamandua and a giant anteater. Protamandua did not appear to have feet specialized for terrestrial or arboreal locomotion, but it may have had a prehensile tail. Neotamandua, though, is unlikely to have had a prehensile tail and its feet were intermediate in form between those of the tamanduas and the giant anteater. The species Neotamandua borealis was suggested to be an ancestor of the latter. Another member of the genus Myrmecophaga has been recovered from the Montehermosan Monte Hermoso Formation in Argentina and was described by Kraglievitch in 1934 as Nunezia caroloameghinoi. The species was reclassified as Myrmecophaga caroloameghinoi by S. E. Hirschfeld in 1976.
The giant anteater is the most terrestrial of the living anteater species. Its ancestors may originally have been adapted to arboreal life; the transition to life on the ground could have been aided by the expansion of open habitats such as savanna in South America and the availability there of colonial insects, such as termites, that provided a larger potential food source. Both the giant anteater and the southern tamandua are well represented in the fossil record of the late Pleistocene and early Holocene.
The giant anteater can be identified by its large size, elongated muzzle, and long bushy tail. It has a total body length of 182 to 217 cm (5.97 to 7.12 ft). Males weigh 33 to 50 kg (73 to 110 lb) and females weigh 27 to 47 kg (60 to 104 lb), making the giant anteater the biggest extant species in its suborder. The head of the giant anteater, at 30 cm (12 in) long, is particularly elongated, even when compared to other anteaters. Its tubular snout, which ends in its tiny mouth opening and nostrils, takes up most of its head. Its eyes and ears are relatively small. It has poor eyesight, but its sense of smell is 40 times more sensitive than that of humans. Giant anteaters can live around 16 years in captivity.
Even for an anteater, the neck is especially thick compared to the back of the head, and a small hump is found at the back of the neck. The coat is mostly greyish, brown or black and salted with white. The forelimbs are white, with black bands around the wrists, while the hindlimbs are dark. Thick black bands with white outlines stretch from throat to shoulder, ending in triangular points. The body ends in a brown tail. The coat hairs are long, especially on the tail, which makes the tail look larger than it actually is. A stiff mane stretches along the back. The bold pattern was thought to be disruptive camouflage, but a 2009 study suggests it is warning coloration. While adult males are slightly larger and more muscular than females, with wider heads and necks, visual sex determination can be difficult. The penis and testes are located internally between the rectum and urinary bladder in males, and females have a single pair of mammary glands near the armpits.
The giant anteater has broad ribs. Despite its specific name, tridactyla, meaning three fingers, it has five toes on each foot. Four toes on the front feet have claws, which are particularly elongated on the second and third digits. It walks on its front knuckles similar to gorillas and chimpanzees. Doing this allows the giant anteater to keep its claws out of the way while walking. The middle digits, which support most of its weight, are extended at the metacarpophalangeal joints and bent at the interphalangeal joints. Unlike the front feet, the hind feet have short claws on all five toes and walk plantigrade. As a "hook-and-pull" digger, the giant anteater's enlarged supraspinous fossa gives the teres major more leverage—increasing the front limbs' pulling power—and the triceps muscle helps power the flexion of the thickened third digit of the front feet.
The giant anteater has a low body temperature for a mammal, about 33 °C (91 °F), a few degrees lower than a typical mammalian temperature of 36 to 38 °C (97 to 100 °F). Xenarthrans in general tend to have lower metabolic rates than most other mammals, a trend thought to correlate with their dietary specializations and low mobility.
The giant anteater has no teeth and is capable of only very limited jaw movement. It relies on the rotation of the two halves of its lower jaw, held together by a ligament at the tip, to open and close its mouth. This is accomplished by its masticatory muscles, which are relatively underdeveloped. Jaw depression creates an oral opening large enough for the slender tongue to flick out. It is typically 60 cm (24 in) long and is triangular posteriorly, rounded anteriorly, and ends in a small, rounded tip. The tongue is covered in backward-curving papillae and coated in thick, sticky saliva secreted from its enlarged salivary glands, which allows the giant anteater to collect insects with it.
The tube-like rostrum and small mouth opening restrict the tongue to protrusion-retraction movements. During feeding, the animal relies on the orientation of its head for aim. The tongue can reach up to 45 cm (18 in), longer than the length of the skull, and move in and out around 160 times per minute (nearly three times per second). The anteater's tongue has little to no attachments to the hyoid and this is what allows it to flick its tongue at such distances and speed. The long sternoglossus muscle, which is formed by the fusion of the sternohyoid and the hyoglossus, is directly anchored to the sternum. The hyoid apparatus is large, V-shaped and flexible and supports the tongue as it goes in and out of the mouth. The buccinators allow it to slide back in without losing attached food and tighten the mouth to prevent food from escaping as it extends. When retracted, the tongue is held in the oropharynx by the secondary palate, preventing it from blocking respiration.
Giant anteaters swallow at a much higher rate than most other mammals; when feeding, they swallow almost continuously. Before being swallowed, insects are crushed against the palate. The giant anteater's stomach, similar to a bird's gizzard, has hardened folds and uses strong contractions to grind up the insects. The digestive process is assisted by small amounts of ingested sand and soil. The giant anteater cannot produce stomach acid of its own, but uses the formic acid of its prey for digestion.
Distribution and status
The giant anteater is native to Central and South America. Its known range stretches from Honduras to northern Argentina, and fossil remains have been found as far north as northwestern Sonora, Mexico. It is largely absent from the Andes and has been extirpated in Uruguay. It may also be extirpated in Belize, Costa Rica, and Guatemala. The species is found in a number of habitats including both tropical rainforest and xeric shrubland, provided enough prey is present to sustain it.
The species is listed as Vulnerable by the IUCN, due to the number of regional extirpations, and under Appendix II by CITES, tightly restricting trade in specimens of the animal. Between 2000 and 2010, the total population declined by 30%. In 1994, some 340 giant anteaters died due to wildfires at Emas National Park in Brazil. The animal is particularly vulnerable to fires due to its slow movement and flammable coat.
Human-induced threats include collision with vehicles, attacks by dogs, and destruction of habitat. The giant anteater is commonly hunted in Bolivia, both for sport and sustenance. The animal's thick, leathery hide is used to make equestrian equipment in the Chaco. In Venezuela, it is hunted for its claws. Giant anteaters are killed for safety reasons, due to their reputation as dangerous animals. The giant anteater remains widespread. Some populations are stable and the animal is found in various protected areas in the Amazon, Pantanal and the Cerrado. It is officially protected in some Argentine provinces as a national heritage species.
Behavior and ecology
The giant anteater may use multiple habitats. A 2007 study of giant anteaters in the Brazilian Pantanal found the animals generally forage in open areas and rest in forested areas, possibly because forests are warmer than grasslands on cold days and cooler on hot days. Giant anteaters can be either diurnal or nocturnal. A 2006 study in the Pantanal found those anteaters to be mostly nocturnal: they are most active during nighttime and early morning, and retire as the temperature rises. On colder days, they start and end periods of activity earlier, shifting them into daylight hours, and may become diurnal. Diurnal giant anteaters have been observed at Serra da Canastra. Nocturnality in anteaters may be a response to human disturbances.
Giant anteaters typically rest in dense brush, but may use tall grass on cooler days. They carve a shallow cavity in the ground for resting. The animal sleeps curled up with its bushy tail folded over its body. The tail serves both to conserve body heat and as camouflage. One anteater was recorded sleeping with its tail stretched out on a sunny morning with an ambient temperature of 17 °C (63 °F); possibly it was positioned this way to allow its body to absorb the sun's rays for warmth.
Giant anteaters are good swimmers and are capable of moving through wide rivers. They have been observed to bathe. They are also able to climb and have been recorded ascending both termite mounds and trees while foraging. One individual was observed holding onto a branch with its feet just touching the ground.
Giant anteaters' home ranges vary in size depending on the location. At Serra da Canastra National Park in Brazil, female anteaters have home ranges around 3.67 km2 (910 acres), while males live in home ranges of 2.74 km2 (680 acres). In other parts of Brazil, anteaters may have 9 km2 (2,200 acres) ranges. Anteaters from Venezuela have been recorded living in home ranges as large as 25 km2 (6,200 acres). Individuals mostly live alone, except for females that nurse their young and males courting females. Anteaters communicate their presence, status, and sexual condition with secretions from their anal glands. They also advertise their presence to other individuals though tree markings and urine. They appear to be able to recognize each other's saliva by scent.
Females appear to be more tolerant of females than males are of males, leading to greater overlap in female home ranges. Males are more likely to engage in agonistic behaviors, such as slowly circling each other, chasing, or actual fighting. Circling anteaters may cry a drawn-out "harrr". In combat, they slash at each other with their claws and wrestle each other to the ground. Fighting anteaters may emit roars or bellows. Males are possibly territorial.
Foraging and predation
This animal is an insectivore, feeding mostly on ants or termites. In areas that experience seasonal flooding, like the grassy plains of the Venezuelan-Colombian Llanos, anteaters mainly feed on ants, because termites are less available. Conversely, anteaters at Emas National Park eat mainly termites, which occur in high density on the grasslands. At Serra da Canastra, anteaters switch between eating mainly ants during the wet season (October to March) and termites during the dry season (May to September).
Anteaters track prey by their scent. After finding a nest, the animal tears it open with its long fore claws and inserts its long, sticky tongue to collect its prey. An anteater spends one minute on average feeding at a nest, visiting up to 200 nests in one day and consuming as many as 30,000 insects. The anteater may be driven away from a nest by the chemical or biting attacks of soldiers. Some termite species rely on their fortified mounds for protection and many individuals escape while the predator digs. These modes of defense prevent the entire colony from being eaten in one anteater attack.
Other prey include the larvae of beetles and western honey bees that have located their hives in termite mounds. Anteaters may target termite mounds with bee hives. In captivity, anteaters are fed mixtures made of milk, eggs, mealworms, and ground beef. To drink, an anteater may dig for water when no surface water is available, creating waterholes for other animals. Giant anteaters are primarily prey for jaguars and pumas. They typically flee from danger by galloping, but if cornered, will rear up on their hind legs and slash at the attacker. The front claws of the giant anteater are formidable weapons, capable of killing a jaguar. The giant anteater is a host of the Acanthocephalan intestinal parasites Gigantorhynchus echinodiscus and Moniliformis monoechinus.
Reproduction and parenting
Giant anteaters can mate throughout the year. During courtship, a male consorts with an estrous female, following and sniffing her. Male and female pairs are known to feed at the same insect nest. While mating, the female lies on her side as the male crouches over her. A couple may stay together for up to three days and mate several times during that period. Gestation lasts around 190 days and ends with the birth of a single pup, which typically weighs around 1.4 kg (3.1 lb). Females give birth standing upright.
Pups are born with eyes closed and begin to open them after six days. The mother carries its dependent pup on its back. The pup's black and white band aligns with its mother's, camouflaging it. The young communicate with their mothers with sharp whistles and use their tongues during nursing. After three months, the pup begins to eat solid food and is fully weaned by ten months. The mother grooms her offspring during rest periods lasting up to an hour. Grooming peaks during the first three months and declines as the young reaches nine months of age, ending by ten months. The decline mirrors that of the weakening bond between mother and offspring; young anteaters usually become independent by nine or ten months. Anteaters are sexually mature in 2.5–4 years.
Interactions with humans
Although they are shy and typically attempt to avoid humans, giant anteaters can inflict severe wounds with their front claws and have been known to seriously injure or kill humans who corner and threaten them. Between 2010 and 2012, two hunters were killed by giant anteaters in Brazil; in both cases, the hunters were agitating and wounding cornered animals and the attacks appeared to be defensive behaviors. In April 2007, an anteater at the Florencio Varela Zoo mauled and killed a zookeeper with its front claws. The animal in question, a male named Ramon, had a reputation for aggressiveness.
In the mythology and folklore of the indigenous peoples of the Amazon Basin, the giant anteater is depicted as a trickster foil to the jaguar, as well as a humorous figure due to its long snout. In one Shipib tale, an anteater challenged a jaguar to a breath-holding contest under water, which the jaguar accepted. After the two removed their pelts and submerged, the anteater jumped out of the water and stole the jaguar's pelt, leaving the jaguar with the anteater's pelt. In a Yarabara myth, the evil ogre Ucara is transformed into one by the sun. This myth emphasizes the nearly immobile nature of the anteater's mouth, which was considered a burden. The Kayapo people wear masks of various animals and spirits, including the anteater, during naming and initiation ceremonies. They believe women who touched anteater masks or men who stumbled while wearing them would die or receive some sort of physical disorder.
During the Spanish colonization of the Americas, the giant anteater was one of many native fauna taken to Europe for display. At first, Europeans believed all anteaters were female and mated with their noses, a misconception corrected by naturalist Félix de Azara. In the 20th century, Salvador Dalí wrote imaginatively that the giant anteater "reaches sizes bigger than the horse, possesses enormous ferocity, has exceptional muscle power, is a terrifying animal." Dalí depicted an anteater in the style of The Great Masturbator. It was used as a bookplate for André Breton, who compared the temptations a man experiences in life to what "the tongue of the anteater must offer to the ant."
The 1940 Max Fleischer cartoon Ants in the Plants features a colony of ants fighting off a villainous anteater. Released during the Phoney War, the film may have alluded to France's Maginot Line. An anteater is also a recurring character in the comic strip B.C.. This character was the inspiration for Peter the Anteater, the University of California, Irvine team mascot. In the Stephen King miniseries Kingdom Hospital, the character Antubis appears in the form of an anteater-like creature with razor-sharp teeth.
- Gardner, A.L. (2005). "Order Pilosa". In Wilson, D.E.; Reeder, D.M (eds.). Mammal Species of the World: A Taxonomic and Geographic Reference (3rd ed.). Johns Hopkins University Press. p. 102. ISBN 978-0-8018-8221-0. OCLC 62265494.
- Miranda, F.; Bertassoni, A. & Abba, A.M. (2014). "Myrmecophaga tridactyla". IUCN Red List of Threatened Species. 2014: e.T14224A47441961. doi:10.2305/IUCN.UK.2014-1.RLTS.T14224A47441961.en. Retrieved 3 January 2018.
- Linnæus, Carl (1758). Systema naturæ per regna tria naturæ, secundum classes, ordines, genera, species, cum characteribus, differentiis, synonyms, locis. Tomus I (in Latin) (10th ed.). Holmiæ: Laurentius Salvius. p. 35. Retrieved 23 November 2012.
- Smith, P. (2007). Giant anteater Myrmecophaga tridactyla Linnaeus, 1758 FAUNA Paraguay. Handbook of the Mammals of Paraguay 2. pp. 1–18. Retrieved 7 March 2019.
- Smith, P. (2 November 2007). "Giant Anteater Myrmecophaga tridactyla Linnaeus, 1758" (PDF). Fauna Paraguay.com. Retrieved 13 June 2012.
- Gardner, A. L. (2008). Mammals of South America: Marsupials, xenarthrans, shrews, and bats. University of Chicago Press. pp. 168–75. ISBN 978-0-226-28240-4. OCLC 124031828.
- Delsuc, F.; Vizcaíno, S. F.; Douzery E. J. P. (2004). "Influence of Tertiary paleoenvironnemental changes on the diversification of South American mammals: a relaxed molecular clock study within xenarthrans". BMC Evolutionary Biology. 4: 11. doi:10.1186/1471-2148-4-11. PMC 419338. PMID 15115541.
- Shaw C. A.; McDonald, H. G. (1987). "First Record of Giant Anteater (Xenarthra, Myrmecophagidae) in North America". Science. AAAS. 236 (4798): 186–188. Bibcode:1987Sci...236..186S. doi:10.1126/science.236.4798.186. JSTOR 1698387. PMID 17789783. S2CID 27112941.
- McDonald, H. G.; Vizcaíno, S. F.; Bargo, M. S. (2008). "Skeletal anatomy and fossil history of the Vermilingua". In Vizcaíno, S. F.; Loughry, W. J. (eds.). The Biology of the Xenarthra. pp. 64–72. ISBN 978-0-8130-3165-1. OCLC 741613153.
- Gaudin, T. J.; Branham, D. G. (1998). "The phylogeny of the Myrmecophagidae (Mammalia, Xenarthra, Vermilingua) and the relationship of Eurotamandua to the Vermilingua". Journal of Mammalian Evolution. 5 (3): 237–65. doi:10.1023/A:1020512529767. S2CID 29173495.
- Hirschfeld, S. E. (1976). "A New Fossil Anteater (Edentata, Mammalia) from Colombia, S. A. and Evolution of the Vermilingua". Journal of Paleontology. 50 (3): 419–32. JSTOR 1303522.
- Nunezia caroloameghinoi at Fossilworks.org
- Hirschfeld, S.E. (1976). "A New Fossil Anteater (Edentata, Mammalia) from Colombia, S.A. and Evolution of the Vermilingua". Journal of Vertebrate Paleontology. 50: 419–432. Retrieved 7 March 2019.
- Eisenberg, J. F.; Redford, K. H. (2000). Mammals of the Neotropics: The Central Neotropics: Ecuador, Peru, Bolivia, Brazil. University of Chicago Press. pp. 92–93. ISBN 0-226-19542-2. OCLC 493329394.
- Mutlow, A. C. (2006). "Flea (Pulex simulans) Infestation in Captive Giant Anteaters (Myrmecophaga tridactyla)". Journal of Zoo and Wildlife Medicine. 37 (3): 427–29. doi:10.1638/06-026.1. PMID 17319150. S2CID 40236152.
- Loughry, W. J. (1997). "Survey of the Xenarthrans inhabiting Po~ odas Antas Biological Reserve" (PDF). Edentata. 3 (1): 5–7.
- Naples, V. (2001). "Anteaters". In MacDonald, D (ed.). The Encyclopedia of Mammals (2nd ed.). Oxford University Press. pp. 788–91. ISBN 0-7607-1969-1.
- Naples, V. L. (1999). "Morphology, evolution and function of feeding in the giant anteater (Myrmecophaga tridactyla)". Journal of Zoology. 249 (1): 19–41. doi:10.1111/j.1469-7998.1999.tb01057.x.
- Rodrigues, F. H. G.; Medri, Í. M.; Miranda Mourão, G. de; Camilo-Alves, C. de S. e; Mourão, G. (2008). "Anteater behavior and ecology". In Vizcaíno, S. F.; Loughry, W. J. (eds.). The Biology of the Xenarthra. pp. 257–68. ISBN 978-0-8130-3165-1. OCLC 741613153.
- Gaudin, T. J.; Hicks, P.; Blanco, Y. D. (2018). "Myrmecophaga tridactyla (Pilosa: Myrmecophagidae)". Mammalian Species. 50 (956): 1–13. doi:10.1093/mspecies/sey001.CS1 maint: multiple names: authors list (link)
- Caro, T.; Vanuytsel, L; Van Den Bogaert, W; Van Der Schueren, E (2009). "Contrasting coloration in terrestrial mammals". Philosophical Transactions of the Royal Society B. 364 (1516): 537–48. doi:10.1098/rstb.2008.0221. PMC 2674080. PMID 18990666.
- Naugher, K. B. (2004). "Anteaters (Myrmecophagidae)". In Hutchins, M.; Kleiman, D. G.; Geist, V.; McDade, M. С. (eds.). Grzimek's Animal Life Encyclopedia. 13 (2nd ed.). Gale. pp. 171–79. ISBN 0-7876-7750-7.
- Orr C. M. (2005). "Knuckle-walking anteater: a convergence test of adaptation for purported knuckle-walking features of African Hominidae". American Journal of Physical Anthropology. 128 (3): 639–58. doi:10.1002/ajpa.20192. PMID 15861420.
- Hall, B. K. (2007). Fins Into Limbs: Evolution, Development, And Transformation. University of Chicago Press. p. 304. ISBN 978-0-226-31337-5.
- Lovegrove, B. G. (August 2000). "The Zoogeography of Mammalian Basal Metabolic Rate". The American Naturalist. The University of Chicago Press. 156 (2): 201–219, see 214–215. doi:10.1086/303383. JSTOR 3079219. PMID 10856202. S2CID 4436119.
- Endo, H.; et al. (2007). "Three-Dimensional CT Examination of the Mastication System in the Giant Anteater" (PDF). Zoological Science. 24 (10): 1005–11. doi:10.2108/zsj.24.1005. hdl:2433/108571. PMID 18088164. S2CID 25864310.
- Casali, D. M.; Martins-Santos, E.; Santos, A. L. Q.; Miranda, F. R.; Mahecha, G. A. B.; Perini, F. A. (2017). "Morphology of the tongue of Vermilingua (Xenarthra: Pilosa) and evolutionary considerations". Journal of Morphology. 278 (10): 1380–1399. doi:10.1002/jmor.20718. PMID 28643449. S2CID 13644895.CS1 maint: multiple names: authors list (link)
- Reiss, K. Z. (1997). "Myology of the Feeding Apparatus of Myrmecophagid Anteaters (Xenarthra: Myrmecophagidae)". Journal of Mammalian Evolution. 4 (2): 87–117. doi:10.1023/A:1027366129277. S2CID 42891487.
- Reiss, K. Z. (2000). "Feeding in Myrmecophagous Mammals". In Schwenk, K. (ed.). Feeding: Form, Function and Evolution in Tetrapod Vertebrates. pp. 464–474. ISBN 0-12-632590-1.
- Feldhamer, G. A.; et al. (2007). Mammalogy: Adaptation, Diversity, Ecology. Johns Hopkins University Press. p. 121. ISBN 978-0-8018-8695-9.
- Borges, N. C.; Nardotto, J. R. B.; Oliveira, R. S. L.; Rüncos, L. H. E.; Ribeiro, R. E.; Bogoevich, A M. (2017). "Anatomy description of cervical region and hyoid apparatus in living giant anteaters Myrmecophaga tridactyla Linnaeus, 1758". Pesquisa Veterinária Brasileira. 37 (11): 1345–1351. doi:10.1590/s0100-736x2017001100025.CS1 maint: multiple names: authors list (link)
- Aguiar, J. M.; Fonseca, G. A. B. (2008). "Conservation status of the Xenarthra". In Vizcaíno, S. F.; Loughry, W. J. (eds.). The Biology of the Xenarthra. pp. 219–22. ISBN 978-0-8130-3165-1. OCLC 741613153.
- "CITES species database: Myrmecophaga tridactyla". Convention on International Trade in Endangered Species of Wild Fauna and Flora. Retrieved 3 July 2012.
- Silveira, L.; et al. (1999). "Impact of wildfires on the megafauna of Emas National Park, central Brazil". Oryx. 33 (2): 108–14. doi:10.1046/j.1365-3008.1999.00039.x.
- Mourão, G.; Medri, Í. M. (2007). "Activity of a specialized insectivorous mammal (Myrmecophaga tridactyla) in the Pantanal of Brazil". Journal of Zoology. 271 (2): 187–92. doi:10.1111/j.1469-7998.2006.00198.x.
- Camilo-Alves, C. de S. e. P.; Miranda Mourão, G. de (2006). "Responses of a Specialized Insectivorous Mammal (Myrmecophaga tridactyla) to Variation in Ambient Temperature". Biotropica. 38 (1): 52–56. doi:10.1111/j.1744-7429.2006.00106.x.
- Shaw, J. H.; Machado-Neto, J.; Carter, T. J. (1987). "Behavior of Free-Living Giant Anteaters (Myrmecophaga tridactyla)". Biotropica. 19 (9): 255–59. doi:10.2307/2388344. JSTOR 2388344.
- Nowak, R. M. (1999). Walker's Mammals of the World, Volume 1. Johns Hopkins University Press. pp. 155–56. ISBN 0-8018-5789-9.
- Medri, Í. M.; Mourão, G. (2005). "A brief note on the sleeping habits of the giant anteater – Myrmecophaga tridactyla Linnaeus (Xenarthra, Myrmecophagidae)". Revista Brasileira de Zoologia. 22 (4): 1213–15. doi:10.1590/S0101-81752005000400061.
- Emmons, L. H.; Flores, Roly Peña; Alpirre, Sixto Angulo; Swarner, Matthew J. (2004). "Bathing Behavior of Giant Anteaters (Myrmecophaga tridactyla)". Edentata. 6: 41–43. doi:10.1896/1413-4418.104.22.168. S2CID 84283058.
- Young, R. J.; Coelho, C. M.; Wieloch, D. R. (2003). "A note on the climbing abilities of giant anteaters, Myrmecophaga tridactyla (Xenarthra , Myrmecophagidae)" (PDF). Boletim do Museu de Biologia Mello Leitão. 15 (15): 41–46. Archived from the original (PDF) on 2 July 2013. CS1 maint: discouraged parameter (link)
- Braga, F. G.; Santos, R. E. F.; Batista, A. C. (2010). "Marking behavior of the giant anteater Myrmecophaga tridactyla (Mammalia: Myrmecophagidae) in Southern Brazil" (PDF). Sociedade Brasileira de Zoologia. 27 (1): 7–12. doi:10.1590/s1984-46702010000100002.
- Redford, K. H. (1985). "Feeding and food preference in captive and wild Giant anteaters (Myrmecophaga tridactyla)". Journal of Zoology. 205 (4): 559–72. doi:10.1111/j.1469-7998.1985.tb03544.x.
- Vaughan, T. A.; Ryan, J. M.; Czaplewski, N. J. (2011). Mammalogy. Jones & Bartlett Learning. pp. 155–56. ISBN 978-0-7637-6299-5.
- "Mammals: Giant Anteater". San Diego Zoo Animal Bytes. San Diego Zoo. Archived from the original on 12 February 2007. Retrieved 3 May 2020.
- Nascimento Gomes, Ana Paula; Cesário, Clarice Silva; Olifiers, Natalie; de Cassia Bianchi, Rita; Maldonado, Arnaldo; Vilela, Roberto do Val (December 2019). "New morphological and genetic data of Gigantorhynchus echinodiscus (Diesing, 1851) (Acanthocephala: Archiacanthocephala) in the giant anteater Myrmecophaga tridactyla Linnaeus, 1758 (Pilosa: Myrmecophagidae)". International Journal for Parasitology: Parasites and Wildlife. 10: 281–288. doi:10.1016/j.ijppaw.2019.09.008. PMC 6906829. PMID 31867208.
- Amin, Omar M.; Heckmann, Richard A.; Osama, Mohammed; Evans, R. Paul (2016). "Morphological and molecular descriptions of Moniliformis saudi sp. n. (Acanthocephala: Moniliformidae) from the desert hedgehog, Paraechinus aethiopicus (Ehrenberg) in Saudi Arabia, with a key to species and notes on histopathology". Folia Parasitologica. 63. doi:10.14411/fp.2016.014. ISSN 0015-5683. PMID 27189420.
- "Giant anteaters kill two hunters in Brazil". Yahoo! News. 25 July 2014. Retrieved 3 May 2020.
- "Argentine zookeeper dies after anteater attack". Reuters. 12 April 2007. Retrieved 3 May 2020.
- Lalaurette, S. (13 April 2007). "Young woman dies after attack by anteater". La Nacion. Retrieved 3 March 2013.
- Roe, P. G. (1982). The Cosmic Zygote: Cosmology in the Amazon Basin. Rutgers University Press. pp. 189–91. ISBN 0-8135-0896-7.
- Mascia-Lees, F. E. (2011). A Companion to the Anthropology of the Body and Embodiment. John Wiley & Sons. ISBN 978-1-4051-8949-1.
- Cowie, H (2011). "Sloth bones and anteater tongues: Collecting American nature in the Hispanic world (1750–1808)". Atlantic Studies. 8 (1): 5–27. doi:10.1080/14788810.2011.540864. S2CID 164122848.
- Fanés, F. (2007). Salvador Dali: The Construction of the Image, 1925–1930. Yale University Press. p. 132. ISBN 978-0-300-09179-3.
- Shull, M. S.; Wilt, D. E. (2004). Doing Their Bit: Wartime American Animated Short Films, 1939–1945. McFarland. p. 98. ISBN 0-7864-1555-X.
- "The Anteater Mascot". Anteater Chronicles: The UC Irvine Story. Retrieved 25 June 2012.
- Browning, M. (2011). Stephen King on the Small Screen. Intellect Books. p. 122. ISBN 978-1-84150-412-4.
|Wikimedia Commons has media related to:|
|Wikispecies has information related to Myrmecophaga tridactyla.|
- The Online Anteater: information, images, fun facts, and other stuff about the giant anteater
- ARKive – images and movies of the giant anteater.
- Anteater, Sloth & Armadillo Specialist Group – Giant anteater
- Animal Diversity Web – Myrmecophaga tridactyla Giant anteater