(Species Checklist, Species by Country)
|Based on Ward et al. 2016.|
Myrmoteras is unique among the Formicinae in having the mandibles specialized as trap-jaws. This feature has evolved independently several times in ants and is also found in the ponerines Odontomachus and Anochetus, as well as a few myrmicine genera such as Strumigenys. Species are found largely in forested areas where they forage singly on the surface of the ground and in leaf litter. Nests are tiny, with a single queen and less than 10 workers, in soil or small twigs on the ground. These ants are relatively rare, or at least uncommonly encountered. The genus is primarily Oriental, occurring from India to the Philippines, Sulawesi and Lombok but is especially rich in Borneo and Sulawesi.
|At a Glance||• Trap-Jaw|
Ward et al. (2016) - An isolated genus in its subfamily with numerous distinctive features including elongate, trap-jaw mandibles and very large eyes.
Moffett (1985) - Formicine ants with a distinctive transverse occipital lobe present in all castes. Female castes very similar in appearance, with very large heads; huge, convex eyes; and very long, linear mandibles with well-developed teeth. Males with heads small relative to females; eyes large, convex; scapes long, SI values within range of females; mandibles greatly reduced and without teeth.
Worker. Small to moderately sized (TL 3.9 to 7.0 mm) monomorphic ants belonging to the subfamily Formicinae. Head very large, broader than trunk or gaster, and at least half as long as trunk. Head strongly constricted in back of ocelli so as to form a clearly demarcated occipital lobe which extends transversely across the back of the head; the lobe is narrowed medially above the foramen magnum. Eyes huge, oval and strongly convex, well over half as long as the head length; taking up most of lateral surfaces of head. Ocelli invariably present. A hair originating beneath each compound eye projects forward to either side of clypeus and is usually visible in full face view. Antennae 12-merous; scapes long, gently curved and incrassate distad, invariably extending well beyond occiput; funiculus with segments III generally shortest, terminal segment the longest by far. Antennal fossae positioned dorsally between eyes rather than anterior to eyes as in Gesomyrmex; insertions far apart near eye margins and some distance behind the clypeus. Frontal carinae absent, although margins of antennal fossae somewhat raised.
Mandibles slender and extremely elongate, usually longer than head (at minimum 85% as long as head), with the toothed margin running virtually parallel with lateral margins (never subtriangular as in most formicines); somewhat wider than deep in cross section. Mandibular teeth well separated, numbering 8 to 14. The proximal teeth are tiny, but distally the teeth become longer, slender and sharp. There are invariably one or (more commonly) two apical denticles between the apical and penultimate teeth. Mandibles articulated laterally, not relatively close together along anterior margin as in Odontomachus (where the front of the head is strongly constricted); nevertheless, the mandibular bases are more approximate than in other formicines because the front of the head is relatively narrow. Clypeus about 25 to 50% wider than long, lacking a feeble medial ridge; generally having a well-developed clypeal tooth at each forward corner and with more or less conspicuous lateral flanges. Clypeus not conspicuously produced, leaving mandible bases and labrum exposed. Labrum elongate, with a small, dorsalmost portion visible in full face view; the remainder projects downward between mandible bases. Palpal formula variable: maxillary 3 to 6; labial 2 to 4 segments.
Trunk elongate, widest at pronotum, and somewhat dumbbell-shaped, as the mesothorax is constricted and narrow, with its dorsal and ventral surfaces virtually straight and parallel in profile; pronotum and propodeum relatively massive, convex to flattened above. Metathoracic spiracles raised on conspicuous tubercles. Petiole with prominent peduncles; node broad in front view (usually widest near crown), thick and more or less rounded in profile; never strongly anteroposteriorly compressed. Sternum of petiole virtually without hairs except for a pair of ventrolaterally placed hairs near the base of each peduncle. Caster rounded, with a prominent circlet of hairs around the acidopore; about the size of the head or smaller. Legs long, with tibiae distinctly thicker than femora; middle and hind tibiae often conspicuously dilated.
Queen. Virtually identical to workers in size (including WL and gaster size), proportions and morphology, but alate. Trunk high and convex, having a full complement of flight sclerites, and often sculptured somewhat differently than in the worker.
Male. Known only for subgenus Myrmoteras. Head small relative to females, widest immediately behind eyes. Occipital lobe present, well developed. Eyes very large and convex, but relatively smaller than in workers (about half as long as head length); ocelli conspicuous. Antennae 13-merous; relative to head size scape about as long as in females; funiculus long and filiform. Mandibles greatly reduced and edentate, subtriangular with blunt tips; barely extending forward of labrum when opened and not capable of meeting apically at full closure. Forward margin of clypeus rounded, lacking teeth. Palpal segmentation variable as in females.
Trunk similar to that of queen. Node of petiole broader than in females; pairs of ventrolateral hairs near bases of peduncles present. Middle and hind tibiae slender relative to females, about as thick as femora. Parameres simple in outline, with narrow, blunt tips and having numerous setae. Pygostyles present. Digitus of volsella heavily sclerotized and strongly curved downwards, coming to a sharp terminal point, and finely serrate along dorsal margin; cuspidal lobes small, rounded. Aedeagus a pair of broad subrectangular plates. (Description of male genitalia based largely on Myrmoteras indicum.)
Fore wings with Mf1 present, and with Rs + M present but somewhat contracted (Brown and Nutting, 1949).
|See images of species within this genus|
Keys to Species in this Genus
- Key to Myrmoteras of the Indo-Chinese peninsula
- Key to Philippine species of Myrmoteras
- Key to Myrmoteras
- Key to Myrmoteras of India
Primarily an Oriental distribution from India to the Philippines, Sulawesi, and Lombok of the Lesser Sunda Islands; limited to the east by Weber’s Line (Zettel and Sorger 2011).
Distribution and Richness based on AntMaps
Number of species within biogeographic regions, along with the total number of species for each region.
|Afrotropical Region||Australasian Region||Indo-Australian Region||Malagasy Region||Nearctic Region||Neotropical Region||Oriental Region||Palaearctic Region|
Species of the genus Myrmoteras are among the most bizarre ant forms and unique among Formicinae by having mandibles that form into a specialized trap-jaw mechanism – a character that, however, has convergently evolved in other subfamilies (Odontomachus and Anochetus in Ponerinae; Dacetini in Myrmicinae). Myrmoteras have cryptic living habits in leaf litter, and specialized collecting methods have yielded a relatively high species diversity, especially on Borneo and Sulawesi (Agosti 1992).
Life History Traits
- Mean colony size: 8-22 (Greer et al., 2021)
- Compound colony type: not parasitic (Greer et al., 2021)
- Nest site: hypogaeic (Greer et al., 2021)
- Diet class: predator (Greer et al., 2021)
- Foraging stratum: subterranean/leaf litter (Greer et al., 2021)
- Foraging behaviour: solitary (Greer et al., 2021)
Queen-worker dimorphism in body size is exceedingly small, and so is ovarian dimorphism (4 vs. 2 ovarioles). Flight thorax of queens has a large pronotum (dorsum of first segment), indicating worker-like neck muscles, hence queens are able to hunt during independent foundation (non-claustral ICF).
• Antennal segment count: 12 • Antennal club: absent-gradual weak • Palp formula: 6,4; 5,4; 5,5; 4,3; 4,2; 3,3 • Total dental count: 8-16 • Spur formula: 1 simple, 1 simple; 0, 0 • Eyes: >100 ommatidia • Scrobes: absent • Pronotal Spines: absent • Mesonotal Spines: absent • Propodeal Spines: absent • Petiolar Spines: absent • Caste: none or weak • Sting: absent • Metaplural Gland: present • Cocoon: present
• Antennal segment count 13 • Antennal club 0 • Palp formula 6,4; 3,3 • Total dental count 0 • Spur formula 1 simple, 1 simple
The following information is derived from Barry Bolton's Online Catalogue of the Ants of the World.
- MYRMOTERAS [Formicinae: Myrmoteratini]
- Myrmoteras Forel, 1893f: 607. Type-species: Myrmoteras binghamii Forel, 1893f: 608, by monotypy.
- [Myrmoteras also described as new by Forel, 1894c: 418.]
- Myrmoteras in Camponotinae: Forel, 1894c: 420; Emery, 1896e: 187; in Camponotinae, Myrmoteratini: Emery, 1895j: 772; Wheeler, W.M. 1910g: 143; Forel, 1917: 248; in Gesomyrmicinae, Myrmoteratini: Ashmead, 1905b: 384; in Formicinae, Myrmoteratini: Wheeler, W.M. 1922a: 694; Emery, 1925b: 36; subsequent authors; in Oecophylla genus group: Agosti, 1991: 295.
- Myrmoteras as genus: all authors.
- Subgenera of Myrmoteras: nominal plus Myagroteras.
- Myrmoteras catalogues: Emery, 1925b: 36; Chapman & Capco, 1951: 209 (Asia); Bolton, 1995b: 287.
- Myrmoteras references: Bingham, 1903: 313 (diagnosis); Emery, 1925b: 36 (diagnosis); Creighton, 1930a: 184 (all species key); Wheeler, W.M. 1933e: 75 (all species key); Gregg, 1954: 25 (all species key); Moffett, 1985b: 17 (diagnosis, all species revision, key); Dlussky & Fedoseeva, 1988: 77 (synoptic classification); Agosti, 1992: 405 (diagnosis, review of genus, Malesian species key); Bolton, 2003: 23, 107 (diagnosis, synopsis); Zettel & Sorger, 2011: 62 (Philippines species key); Bui, et al. 2013: 545 (Indo-Chinese Peninsula species key); Bharti & Akbar, 2014d: 79 (India species key).
Bui et al 2013 - Myrmoteras is in the tribe Myrmoteratini Emery, 1895 (Bolton, 2003). Its geographical range is the Oriental region and the Austro-Malayan subregion of the Australian region (Moffett, 1985; Xu, 1998; Agosti, 1992; Zettel & Sorger, 2011). Creighton (1930) revised the genus for the first time, listing six species including two new species. Moffett (1985) recognised a total of 18 species including 10 new species in two morphologically distinct subgenera: Myrmoteras with seven species and the new subgenus Myagroteras with eleven species. Later Agosti (1992) revised the species in the Malay archipelago including the Malay peninsula south of the Kra isthmus, the Philippines, New Guinea, the Islands of New Britain and New Ireland, and added 13 new species. Xu (1998) described one new species from Yunnan province, southwestern China, and recently Zettel & Sorger (2011) revised the Philippine taxa, adding 2 new species, and gave a list of 34 valid species names from the whole range of the genus.
- Agosti, D. 1991. Revision of the oriental ant genus Cladomyrma, with an outline of the higher classification of the Formicinae (Hymenoptera: Formicidae). Syst. Entomol. 16: 293-310 (page 295, Myrmoteras in Formicinae, Oecophylla genus group)
- Agosti, D. 1992. Revision of the ant genus Myrmoteras of the Malay Archipelago (Hymenoptera, Formicidae). Rev. Suisse Zool. 99: 405-429.(page 405, Revision of genus)
- Ashmead, W. H. 1905c. A skeleton of a new arrangement of the families, subfamilies, tribes and genera of the ants, or the superfamily Formicoidea. Can. Entomol. 37: 381-384 (page 384, Myrmoteras in Gesomyrmicinae, Myrmoteratini)
- Bingham, 1903: 313 (diagnosis); Emery, 1925b: 36 (diagnosis, catalogue); Creighton, 1930a: 184 (all species key); Wheeler, W.M. 1933e: 75 (all species key); Chapman & Capco, 1951: 209 (Asia checklist); Gregg, 1954: 25 (all species key); Moffett, 1985b: 17 (diagnosis, all species revision, key); Dlussky & Fedoseeva, 1988: 77 (synoptic classification); Agosti, 1992: 405 (diagnosis, review of genus, Malesian species key); Bolton, 1994: 51 (synoptic classification); Bolton, 1995a: 1051 (census); Bolton, 1995b: 287 (catalogue); Bolton, 2003: 23, 107 (diagnosis, synopsis).
- Bolton, B. 2003. Synopsis and Classification of Formicidae. Mem. Am. Entomol. Inst. 71: 370pp (page 107, Myrmoteras in Formicinae, Myrmoteratini)
- Boudinot, B.E., Borowiec, M.L., Prebus, M.M. 2022. Phylogeny, evolution, and classification of the ant genus Lasius, the tribe Lasiini and the subfamily Formicinae (Hymenoptera: Formicidae). Systematic Entomology 47, 113-151 (doi:10.1111/syen.12522).
- Burchill, A.T., Moreau, C.S. 2016. Colony size evolution in ants: macroevolutionary trends. Insectes Sociaux 63, 291–298 (doi:10.1007/s00040-016-0465-3).
- Cantone S. 2018. Winged Ants, The queen. Dichotomous key to genera of winged female ants in the World. The Wings of Ants: morphological and systematic relationships (self-published).
- Emery, C. 1895l. Die Gattung Dorylus Fab. und die systematische Eintheilung der Formiciden. Zool. Jahrb. Abt. Syst. Geogr. Biol. Tiere 8: 685-778 (page 772, Myrmoteras in Camponotinae, Myrmoteratini)
- Emery, C. 1925d. Hymenoptera. Fam. Formicidae. Subfam. Formicinae. Genera Insectorum 183: 1-302 (page 36, Myrmoteras in Formicinae, Myrmoteratini)
- Forel, A. 1893i. Note préventive sur un nouveau genre et une nouvelle espèce de Formicide (Camponotide). Ann. Soc. Entomol. Belg. 37: 607-608 (page 607, Type-species: Myrmoteras binghamii, by monotypy)
- Forel, A. 1894c. Les Formicides de l'Empire des Indes et de Ceylan. Part IV. J. Bombay Nat. Hist. Soc. 8: 396-420 (page 418,420: Myrmoteras described as new)
- Forel, A. 1917. Cadre synoptique actuel de la faune universelle des fourmis. Bull. Soc. Vaudoise Sci. Nat. 51: 229-253 (page 248, Myrmoteras in Camponotinae, Myrmoteratini)
- Ito F., Miyazaki S. Hashim R. & Billen J. 2017. Colony composition and behavioral characteristics of Myrmoteras iriodum and M. jaitrongi in Ulu Gombak, Peninsular Malaysia (Hymenoptera: Formicidae). Asian Myrmecology 9: e009010 (1-9).
- Kreider, J.J., Chen, T.W., Hartke, T.R., Buchori, D., Hidayat, P., Nazarreta, R., Scheu, S., Drescher, J. 2021. Rainforest conversion to monocultures favors generalist ants with large colonies. Ecosphere 12 (doi:10.1002/ecs2.3717).
- Larabee, F.J., Gronenberg, W., Suarez, A.V., 2017. Performance, morphology and control of power-amplified mandibles in the trap-jaw ant Myrmoteras (Hymenoptera: Formicidae). Journal of Experimental Biology 220, 3062–3071 (DOI 10.1242/jeb.156513).
- Larabee, F.J., Suarez, A.V. 2014. The evolution and functional morphology of trap-jaw ants (Hymenoptera: Formicidae). Myrmecological News 20: 25-36.
- Moffett MW, 1986. Trap-jaw predation and other observations on two species of Myrmoteras (Hymenoptera: Formicidae). Insectes Sociaux 33: 85 – 99.
- Moffett, M.W. 1985. Revision of the genus Myrmoteras. Bulletin of the Museum of Comparative Zoology 151: 1-53. (page 1, Revision of genus)
- Paul, J. 2001. Mandible movements in ants. Comparative Biochemistry and Physiology Part A: Molecular, Integrative Physiology 131, 7–20 (doi:10.1016/s1095-6433(01)00458-5).
- Ward, P.S., Blaimer, B.B., Fisher, B.L. 2016. A revised phylogenetic classification of the ant subfamily Formicinae (Hymenoptera: Formicidae), with resurrection of the genera Colobopsis and Dinomyrmex. Zootaxa. 4072(3):343–357. (doi 10.11646/zootaxa.4072.3.4).
- Wheeler, W. M. 1910b. Ants: their structure, development and behavior. New York: Columbia University Press, xxv + 663 pp. (page 143, Myrmoteras in Camponotinae, Myrmoteratini)
- Wheeler, W. M. 1922i. Ants of the American Museum Congo expedition. A contribution to the myrmecology of Africa. VII. Keys to the genera and subgenera of ants. Bull. Am. Mus. Nat. Hist. 45: 631-710 (page 694, Myrmoteras in Formicinae, Myrmoteratini)
- Zettel, H. and Sorger, D.M. 2011. New Myrmoteras ants from the southeastern Philippines. Raffles Bulletin of Zoology. 59:61-67.