Anteaters after the Flood



Chad Arment (2025)





Giant anteater (Myrmecophaga tridactyla)



The suborder Vermilingua contains two families of the toothless anteaters: the Cyclopedidae and Myrmecophagidae. Systematically, it is placed within the order Pilosa (which also includes the sloths), which in turn is placed within the superorder Xenarthra (which also includes the armadillos). Xenarthrans first show up in the post-Flood Cenozoic in South America, indicating that they were part of the early trans-Atlantic migration via rafting from the Old World as animal populations spread out from the Ark’s landing site in the Middle East. The Vermilingua is likely a monobaramin, but whether it has a common ancestor with sloths or even armadillos is undetermined. Because the oldest anteater is an early Miocene, as-yet-undescribed specimen from Argentina (Bargo et al. 2012), it may be a hyperspecialized pilosan, or it may represent a distinct lineage that simply wasn’t fossilized before that time period after the Flood.



All xenarthrans share, genetically, “five independent insertions of retroposed elements (U6, U5-L1MB2-L1MB4-chimer, L1MB4, L1MB5, L1ME3a)”, while the Vermilingua exclusively share a “LINE element (L1MB8) and a 24 nt deletion”, and “four indels present in Myrmecophaga and Tamandua indicate a common ancestry of these species to the exclusion of Cyclopes” (Möller-Krull, et al. 2007). In reviewing shared pseudogenes and inactivating mutations that accompany morphological adaptations to myrmecophagy (ant- and termite-feeding), Emerling et al. (2025), noted that pseudogene patterns in living anteaters suggest the inactivation of ODAM, ODAPH, and DSPP (Dento-gingival junction genes) in the stem vermilinguans, and the inactivation of MYH16 (a masticatory muscle gene) and AMBN (a tooth enamel gene) in stem Myrmecophagidae, along with ‘incipient pseudogenization’ of TAS1R3 (a gustatory gene) in Myrmecophaga tridactyla. Cyclopes didactylus also had inactivation of MYH16 and AMBN, but via different mutations, and ‘incipient loss’ of PKD2L1 (a gustatory gene). The latter study is particularly interesting, as it demonstrates that baraminic kinds are created for change—that change may occur via separate genes or different mutations on the same gene. When adaptational convergence occurs, as with anteaters, aardvarks, and pangolins, many of the affected genes are responsible for the same areas. This suggests the Creator set up similar, but not rigorously exact, pathways (perhaps mutational hotspots, as some creationists have suggested) for change in different baraminic lineages.



The Cyclopedidae are the pygmy or silky anteaters, including the living Cyclopes and its sister taxon, the late Miocene-Pliocene fossil Palaeomyrmidon. This family is considered an early offshoot of the anteater lineage (Barros et al. 2003). Cyclopes is small, squirrel-sized, and arboreal with a prehensile tail (Hirshfeld 1976), and has a proportionally shorter face and larger braincase than is seen in myrmecophagids (Hayssen et al. 2012). While traditionally considered monotypic with numerous subspecies (Coimbra et al. 2017), at least seven species are now recognized, with several subspecies elevated (Miranda et al. 2017).



The Myrmecophagidae includes the extant tamanduas (Tamandua) and the giant anteater (Myrmecophaga), along with the fossil Neotamandua and Protamandua. The two species of tamanduas are semi-arboreal, have prehensile tails, and have normal grasping clawed digits. Tamandua is known from Pleistocene fossils (Hayssen 2011).


Myrmecophaga is monotypic today, M. tridactyla, though at least one Miocene-Pliocene fossil species is known, M. caroloameghinoi (Gaudin et al. 2018). Giant anteaters are large, terrestrial, with a rigid tail, and knuckle-walk on their front clawed digits (Hirschfeld 1976). While they typically engage in plantigrade ‘knuckle-walking’, when disturbed they can rise erect on their hind legs and defend themselves with their powerful claws, with sometimes fatal results to attackers (Haddad, Jr., et al. 2014; Grillo et al. 2022). Giant anteaters are on the extreme end of specialized myrmecophagy, with a highly elongated skull that is toothless and incapable of chewing, and a long, sticky tongue that works through rapid protrusion/retraction. Tamanduas have a similar feeding strategy, while pygmy anteaters are behaviorally similar in feeding while exhibiting biomechanical differences due to dissimilar skull shape and masticatory apparatus (Naples 1999; Ferreira-Cardoso et al. 2020).


Rather than simply tearing apart a termite or ant nest, the giant anteater makes a small breach, focuses on rapidly ingesting the trickle of ants that pour out for a minute or two, then leaves once the soldiers arrive to protect the nest. The anteater moves on to another nest and repeats the process, taking only a small percent of insects from any given nest, and not causing too much damage (Naples 1999). Up to 35,000 ants/termites may be eaten in a day (Gaudin et al. 2018). Giant anteaters are South American, but at least one Pleistocene specimen has been discovered in Sonora, Mexico, demonstrating northward expansion after the Isthmus of Panama connected the two continents (Shaw and McDonald 1987). Pleistocene specimens of the modern species are also known from Brazil and Uruguay (Gaudin et al. 2018).


Protamandua was an early Miocene sister taxon to the other myrmecophagids, with a skull that was elongated similar to the modern Cyclopes and a body length about half the size of modern Tamandua (Bargo et al. 2012). It was likely a good climber, had a prehensile tail (as does Cyclopes and Tamandua), and strong claws for tearing into social insect nests, along with cranial specializations for myrmecophagy. The middle Miocene-Pliocene Neotamandua “is most likely part of an anagenetic line of descent leading to Myrmecophaga” (De Melo Casali et al. 2020). Neotamandua was intermediate in size between Tamandua and Myrmecophaga (Hirshfeld 1976).





Myrmecophaga tridactyla skull

(CC BY 3.0 Dr. Mirko Junge)



references



Bargo, M. S., N. Toledo, and S. F. Vizcaíno. 2012. Paleobiology of the Santacrucian sloths and anteaters (Xenarthra, Pilosa). in: Vizcaíno, S. F., et al. (eds.) Early Miocene Paleobiology in Patagonia. Chapter 13. Cambridge, UK: Cambridge University Press.


Barros, M. C., I. Sampaio, and H. Schneider. 2003. Phylogenetic analysis of 16S mitochondrial DNA data in sloths and anteaters. Genetics and Molecular Biology 26(1): 5-11.


Coimbra, R. T. F., et al. 2017. Phylogeographic history of South American populations of the silky anteater Cyclopes didactylus (Pilosa: Cyclopedidae). Genetics and Molecular Biology 40(1): 40-49.


De Melo Casali, D., et al. 2020. Total-evidence phylogeny and divergence times of Vermilingua (Mammalia: Pilosa). Systematics and Biodiversity 18(3): 216-227.


Emerling, C. A., et al. 2025. Pseudogenes document protracted parallel regression of oral anatomy in myrmecophagous mammals. Pre-print. https://doi.org/10.1101/2025.02.21.639456 [CC BY-NC 4.0]


Ferreira-Cardoso, S., et al. 2020. Comparative masticatory myology in anteaters and its implications for interpreting morphological convergence in myrmecophagous placentals. PeerJ 8:e9690.


Gaudin, T. J., P. Hicks, and Y. Di Blanco. 2018. Myrmecophaga tridactyla (Pilosa: Myrmecophagidae). Mammalian Species 50(956): 1-13.


Grillo, V. T. R. S., et al. 2022. Repair of non-lethal vascular injury caused by giant anteater (Myrmecophaga tridactyla) in Brazil. Jornal Vascular Brasileiro 21: e20210081.


Haddad, V., Jr., et al. 2014. Human death caused by a giant anteater (Myrmecophaga tridactyla) in Brazil. Wilderness & Environmental Medicine 25: 446-449.


Hayssen, V. 2011. Tamandua tetradactyla (Pilosa: Myrmecophagidae). Mammalian Species 43(875): 64-74.


Hayssen, V., F. Miranda, and B. Pasch. 2012. Cyclopes didactylus (Pilosa: Cyclopedidae). Mammalian Species 44(895): 51-58.


Hirschfeld, S. E. 1976. A new fossil anteater (Edentata, Mammalia) from Colombia, S.A. and evolution of the Vermilingua. Journal of Paleontology 50(3): 419-432.


Miranda, F. R., et al. 2017. Taxonomic review of the genus Cyclopes Gray, 1821 (Xenarthra, Pilosa), with the revalidation and description of new species. Zoological Journal of the Linnean Society 20: 1-35.


Möller-Krull, M., et al. 2007. Retroposed elements and their flanking regions resolve the evolutionary history of xenarthran mammals (armadillos, anteaters, and sloths). Molecular Biology and Evolution 24(11): 2573-2582.


Naples, V. L. 1999. Morphology, evolution and function of feeding in the giant anteater (Myrmecophaga tridactyla). Journal of Zoology, London 249: 19-41.


Shaw, C. A., and H. G. McDonald. 1987. First record of giant anteater (Xenarthra, Myrmecophagidae) in North America. Science 236: 186-188.