.jpg){kind=logo}
Terataner
| Terataner | |
|---|---|
| |
| Terataner foreli | |
| Scientific classification | |
| Kingdom: | Animalia |
| Phylum: | Arthropoda |
| Class: | Insecta |
| Order: | Hymenoptera |
| Family: | Formicidae |
| Subfamily: | Myrmicinae |
| Tribe: | Crematogastrini |
| Alliance: | Cataulacus genus group |
| Genus: | Terataner Emery, 1912 |
| Type species | |
| Atopomyrmex foreli, now Terataner foreli | |
| Diversity | |
| 14 species (Species Checklist, Species by Country)
| |
| Synonyms | |
| |
Currently a small genus occurring in the Afrotropical and Malagasy regions, there are apparently many more undescribed species present in existing collections. Terataner are very conspicuous, heavily armoured, medium-sized to large arboreal or sub-arboreal ants that prey on ants, termites and other insects. (Bolton 1981a, Alpert 1992, Hita Garcia, Wiesel and Fischer 2013, Hita Garcia et al. 2017) Ergatoid (permanently wingless) queens occur in most species (Alpert 1992, Hita Garcia et al. 2017).
Identification
Bolton (1981) redescribed the genus based on twelve known species. This description is modified slightly to incorporate a number of additional forms that are as yet undescribed. Workers - Monomorphic arboreal and terrestrial myrmicine ants. Mandibles armed with 5 teeth and a basal angle. Postpetiole simple, armed with a transverse crest, crest bearing a short projection, or postpetiole armed with a single long or short spine.
Keys to Species in this Genus
Distribution
Distribution and Richness based on AntMaps
Species by Region
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 | 7 | 0 | 0 | 8 | 0 | 0 | 0 | 0 |
| Total Species | 2851 | 1736 | 3047 | 932 | 840 | 4391 | 1767 | 2925 |
Biology
Hita Garcia et al. (2017) - The currently known species can be divided into two groups with contrasting biological lifestyles. The first, smaller group with just the four species of the Terataner luteus complex is restricted in its distribution to the rainforests of West and Central Africa. All four species are strictly arboreal and nest in rotten parts of standing timber at a considerable distance from the ground. The female reproductives are morphologically typical ant queens with wings. The second and much larger group contains the remaining eight valid species (plus most undescribed species) and is predominantly found on Madagascar with few species on the Seychelles, Mayotte, the Comoros, and East and South Africa. They tend to nest subarboreally in the lower vegetation in preformed nest cavities, such as hollow twigs and burrows of wood-boring insects. Intriguingly, the female reproductives of the second group are wingless, ergatoid queens that are often difficult to distinguish from the workers.
With the relatively limited material available at the time, Alpert observed the presence of ergatoid reproductives in six species collected from Madagascar. Based on the extensive material presently available to us, we confirm that approximately 40 species (described plus undescribed) of Malagasy Terataner species produce ergatoid queens. The same is true for Terataner bottegoi from East Africa, from which we have two whole colonies available that each contains one ergatoid queen. We do not know the queen morphology of Terataner transvaalensis or of a few undescribed Malagasy species due to scarcity of available material, but based on the overall presence of ergatoid reproductives in these groups, we predict that these species will also have ergatoid queens. Our examination of approximately 4,000 Terataner specimens from over 200 localities suggest ergatoid queens are collected only by sampling entire nests from hollow sticks, branches or other plant material. Moreover, it also seems that colonies of Terataner are monogynous since all examined colonies contained only one ergatoid reproductive. Nevertheless, the ergatoid queen's role within the colony, mating behaviour, and colony establishment remain unknown. Considering that the ergatoid is wingless, the latter is thought to happen by colony fission. Observations of living colonies in Madagascar are required to shed light on the biology of these intriguing ants.
Life History Traits
- Mean colony size: 7-39 (Greer et al., 2021)
- Compound colony type: not parasitic (Greer et al., 2021)
- Nest site: hypogaeic; arboreal (Greer et al., 2021)
- Diet class: predator (Greer et al., 2021)
- Foraging stratum: subterranean/leaf litter; arboreal (Greer et al., 2021)
- Foraging behaviour: cooperative (Greer et al., 2021)
Castes
Morphology
Worker Morphology
Explore: Show all Worker Morphology data or Search these data. See also a list of all data tables or learn how data is managed.
• Antennal segment count: 12 • Antennal club: 3 • Palp formula: 5,3; 4,3 • Total dental count: 5-7 • Spur formula: 1 simple, 1 simple; 0, 0 • Eyes: >100 ommatidia • Pronotal Spines: absent • Mesonotal Spines: absent • Propodeal Spines: absent; dentiform • Petiolar Spines: dentiform; present • Caste: none or weak • Sting: present • Metaplural Gland: present • Cocoon: absent
Male Morphology
- Explore: Show all Male Morphology data or Search these data. See also a list of all data tables or learn how data is managed.
• Antennal segment count 13 • Antennal club 0 • Palp formula 4,3 • Total dental count 5-6 • Spur formula 1 simple, 1 simple
Phylogeny
| Myrmicinae |
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
See Phylogeny of Myrmicinae for details.
Nomenclature
The following information is derived from Barry Bolton's Online Catalogue of the Ants of the World.
- TERATANER [Myrmicinae: Formicoxenini]
- Terataner Emery, 1912b: 103. Type-species: Atopomyrmex foreli, by original designation.
- Terataner senior synonym of Tranetera: Bolton, 1981b: 288.
- TRANETERA [junior synonym of Terataner]
- Tranetera Arnold, 1952b: 130 [as subgenus of Terataner]. Type-species: Atopomyrmex bottegoi, by original designation.
- Tranetera junior synonym of Terataner: Bolton, 1981b: 288.
Taxonomic Notes
Bolton (1981) revised the genus in the Ethiopian region. He provided descriptions of the six African species, newly described velatus from West Africa and xaltus from Madagascar, provided keys to workers.
Description
Worker
Bolton (1981) - Monomorphic arboreal myrmicine ants. Mandibles armed with 5 or 6 teeth. Palp formula 5, 3 (alluaudi) or 4, 3 (bottegoi, elegans, luteus. piceus, scotti). Anterior clypeal margin with a median notch or impression. Median portion of clypeus broad and broadly inserted between the frontal lobes, bounded laterally by a pair of widely separated carinae which run to the anterior margin; lateral portions of clypeus unmodified. Frontal lobes narrow, continuing back into a pair of more or less straight frontal carinae which are usually roughly parallel and relatively close together on the dorsum of the head. Towards the occiput the frontal carinae either fade out or are sharply angled outwards as a ridge or row of tubercles which runs to the sides of the head. Antennal scrobes absent or at most the sides of the head below the frontal carinae with a broad and very shallow concavity. Antennae 12-segmented with a 3-segmented club, the scapes when laid back failing to reach the occipital margin. Eyes large and conspicuous, situated at or in front of the midlength of the head. Occipital corners tuberculate or denticulate in full-face view. Pronotum marginate laterally and usually also anteriorly, the lateral marginations generally simple but sometimes expanded into ornate lobes or flanges. Pronotal shoulders angulate, denticulate or tuberculate in dorsal view. Promesonotal suture absent on the dorsum or represented by a line or slight indentation, only rarely easily visible. Mesonotum usually marginate laterally and forming a low projecting angle or tubercle in dorsal view; rarely immarginate and armed with a sharp denticle laterally. Metanotal groove impressed, most frequently only shallowly so but deep in some species; very shallow indeed in some samples of elegans. Propodeum bluntly marginate to rounded laterally, unarmed or with a pair of denticles or teeth. Metapleural lobes large and strongly developed; ventral margin of metapleuron with a strong broad groove running forward from the orifice of the metapleural glands. Ventral surface of alitrunk between hind coxae entire, simple, without a broad deep circular pit. Middle and hind tibiae frequently with a distinct simple spur, the spur reduced in some and indistinguishable from the hairs of the tibial apex in others. Petiole with a short, stout anterior peduncle, the node narrow and tapering dorsally so that it appears triangular or conical in profile. In anterior or posterior view the narrow dorsum of the node either forms a transverse crest or is indented medially so that a pair of blunt prominences are formed laterally. In some these prominences are acute and dentiform, in others developed into quite long teeth; rarely the petiole is strongly bispinose. In one species (scotti) the petiole is developed into a very high plate dorsally which has a central emargination. Postpetiole simple or armed dorsally with a transverse crest or a single spine. Pilosity very variable, some species densely hairy, others almost hairless. Sculpture generally of coarse rugae or sulci, but reduced in the African species piceus, elegans, luteus and velatus.
References
- Alpert, G. D. 1992. Observations on the genus Terataner in Madagascar (Hymenoptera: Formicidae). Psyche (Camb.) 99: 117-127.
- Arnold, G. 1952b. The genus Terataner Emery (Formicidae). J. Entomol. Soc. South. Afr. 15: 129-131 (page 129, Review of genus)
- Blaimer, B.B., Ward, P.S., Schultz, T.R., Fisher, B.L., Brady, S.G. 2018. Paleotropical diversification dominates the evolution of the hyperdiverse ant tribe Crematogastrini (Hymenoptera: Formicidae). Insect Systematics and Diversity 2(5): 3; 1-14 (doi:10.1093/isd/ixy013).
- Bolton, B. 1981b. A revision of six minor genera of Myrmicinae (Hymenoptera: Formicidae) in the Ethiopian zoogeographical region. Bull. Br. Mus. (Nat. Hist.) Entomol. 43: 245-307 (page 288, Terataner senior synonym of Tranetera, and revision of genus)
- Bolton, B. 1994. Identification guide to the ant genera of the world. Cambridge, Mass.: Harvard University Press, 222 pp. (page 105, Terataner in Myrmicinae, Formicoxenini)
- Bolton, B. 2003. Synopsis and Classification of Formicidae. Mem. Am. Entomol. Inst. 71: 370pp (page 253, Terataner in Myrmicinae, Formicoxenini)
- 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).
- Dlussky, G. M.; Fedoseeva, E. B. 1988. Origin and early stages of evolution in ants. Pp. 70-144 in: Ponomarenko, A. G. (ed.) Cretaceous biocenotic crisis and insect evolution. Moskva: Nauka, 232 pp. (page 79, Terataner in Myrmicinae, Podomyrmini)
- Emery, C. 1912b. Études sur les Myrmicinae. [I-IV.]. Ann. Soc. Entomol. Belg. 56: 94-105 (page 103, 105, Terataner in Myrmicinae, Myrmecinini)
- Emery, C. 1914e. Intorno alla classificazione dei Myrmicinae. Rend. Sess. R. Accad. Sci. Ist. Bologna Cl. Sci. Fis. (n.s.) 18: 29-42 (page 41, Terataner in Myrmicinae, Myrmecinini)
- Emery, C. 1924f [1922]. Hymenoptera. Fam. Formicidae. Subfam. Myrmicinae. [concl.]. Genera Insectorum 174C: 207-397 (page 241, Terataner in Myrmicinae, Myrmecinini [subtribe Podomyrmini])
- Forel, A. 1917. Cadre synoptique actuel de la faune universelle des fourmis. Bull. Soc. Vaudoise Sci. Nat. 51: 229-253 (page 244, Terataner in Myrmicinae, Myrmecinini)
- Jansen, G., Savolainen, R. 2010. Molecular phylogeny of the ant tribe Myrmicini (Hymenoptera: Formicidae). Zoological Journal of the Linnean Society 160(3), 482–495 (doi:10.1111/j.1096-3642.2009.00604.x).
- 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 663, Terataner in Myrmicinae, Myrmecinini)