Colobopsis
Colobopsis Temporal range: 34–0 Ma Eocene – Recent | |
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Colobopsis cerberulus | |
Scientific classification | |
Kingdom: | Animalia |
Phylum: | Arthropoda |
Class: | Insecta |
Order: | Hymenoptera |
Family: | Formicidae |
Subfamily: | Formicinae |
Tribe: | Camponotini |
Genus: | Colobopsis Mayr, 1861 |
Type species | |
Formica truncata, now Colobopsis truncata | |
Diversity | |
117 species 1 fossil species (Species Checklist, Species by Country) | |
Synonyms | |
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Historical note on Colobopsis with respect to Camponotus, Wheeler (1904):
"Since 1889 Colobopsis has been used to include those species of Camponotus which have sharply truncated heads in the soldier caste ... species in which the anterior truncated surface of the head in the major workers and the females is distinctly marginate and in which even the mandibles have a sharp external ridge separating an anterior from a latero-ventral face. In these species the head presents a peculiar sculpture consisting of umbilicate punctures ... and there is an absence of a cocoon in the pupal stages of all the phases."
Historical notes on Colobopsis ethology, Emery (1925):
"Ethology. - The species of Colobopsis, as well as many subgenera of Camponotus, live in wood, small and large dead branches, galls, etc., in which they carve galleries; the which open to the surface of the wood always have the exact diameter of the anterior truncation of the head of majors and queens. A soldier, or the queen, keeps custody over the nest, that is to say, she seals the hole with her head, and retires into the nest tunnel to allow sisters to pass. Towards this end, the gallery widens immediately within the hole, which means that the doorman (i.e., the soldier or guard) can give passage to sisters and immediately close the opening by means of its plug-shaped head. Many species of various Camponotus subgenera Myrmamblys, Myrmogonia [now synonymized with Colobopsis], Myrmaphaenus, etc., as well as lignicolous ants in general, have pronounced plug-like heads in the major workers, and are likely to have a soldier act as gatekeeper for the colony."
(Translation of Emery 1925 by B. E. Boudinot, 19 February 2017.)
At a Glance | • Phragmotic |
Photo Gallery
Identification
Based on the dual phylogenies of Blaimer et al. (2015) which demonstrated that Colobopsis is sister to the remainder of the Camponotini, Ward et al. (2016) assiduously transferred all Colobopsis species out of Camponotus and proposed the following diagnosis for Colobopsis:
"Minor worker Generally small, HW 0.65–1.10 (exceptions: cylindrica group and the Fijian radiation, where HW 0.90–1.70), with rounded head and relatively small eyes, REL 0.20–0.32; head width three-quarters of more of head length (CI 0.75–0.98; except one Fijian species, C. polynesica, where CI ~0.72); antennal insertions—and hence also the frontal carinae—relatively relatively well separated, ASM/HW 0.36–0.47 (except cylindrica group, New Caledonia radiation and the Fijian radiation, where ASM/HW 0.31–0.39), ASM/CLW usually 0.66–0.98 (except some New Caledonian and most Fijian species where ASM/CLW is in the range of 0.60– 0.66); frontal carinae relatively short, usually not strongly sinuate, the antennal insertions occurring at about midlength of the frontal carinae; clypeus more or less subquadrate, as long as wide or slightly wider than long (CLW/CLL 0.96–1.32), with sides parallel or diverging moderately towards the anterior margin (clypeus broader in Fijian species of the bryani and dentata groups where CLW/CLL ~ 1.46, and in the conica and vitrea groups, sensu Emery (1925), where CLW/CLL 1.40–1.50 and clypeus more trapezoidal in form); anterolateral extremities of clypeus differentiated from rest of clypeus by a sulcus or impression running from the anterior tentorial pit to the clypeal margin, the suture between clypeus and malar region of head often weak here, so that the clypeus appears to lack the anterolateral extensions often conspicuous in Camponotus minors (compare Figures 2–5 with Figure 15).
Major worker Head generally phragmotic, varying from strongly truncate and marginate (Figure 6) to weakly truncate (Figure 7), the truncated portion incorporating part of the clypeus, the malar region of the head capsule and the upper surface of the mandibles. Clypeus elongate-rectangular, the anterolateral extremities separated from the clypeus by a well-marked sulcus and appearing to form an independent triangular sclerite.
Additionally: Dimorphic worker caste, with few or no intermediates between major and minor workers, except in the cylindrica group (Emery 1925); larva with distinctive ventral trough (praesaepium), overhung posteriorly by a protruding welt of the second abdominal segment (Wheeler & Wheeler 1953, 1982); pupa naked (Wheeler 1904). Brendon Boudinot has recently found that male Colobopsis have distinctive genitalia,with the shape of the digitus distinguishing them from Camponotus males (Boudinot, in prep.)."
Distinguishing Colobopsis from Camponotus
To differentiate Colobopsis from Camponotus Ward et al. (2016) proposed the following global key:
1 Not occurring in Fiji or New Caledonia ... 2
- Occurring in Fiji ... 3
- Occurring New Caledonia ... 4
2 Generally small species, HW 0.65–1.10 (except cylindrica-group of Southeast Asia with HW 1.20–1.70, and facies as in Figures 4 and 5); either antennal insertions relatively well separated, such that ASM/HW 0.36–0.47 and ASM/CLW 0.66–0.98, and/or clypeus relatively narrow, such that CLW/CLL 0.96–1.32; antennal insertions occurring at about midlength of frontal carinae; anterolateral extremities of clypeus set off from rest of clypeus by a sulcus or impression, so clypeus appears to lack prominent anterolateral extensions (Figures 2–5) ... Colobopsis
- Small to large species, HW 0.70–3.00; antennal insertions less well separated, such that ASM/HW 0.22–0.35 and ASM/CLW 0.35–0.68; clypeus variable in shape but in smaller species with HW 0.70–1.35 (e.g., Camponotus (Myrmamblys), C. (Myrmentoma) and C. (Pseudocolobopsis)) clypeus tending to be relatively broad, such that CLW/CLL 1.25–1.62, although exceptions occur (e.g., in some C. (Pseudocolobopsis) species) (Figures 14–15); antennal insertions usually occurring in front of midlength of frontal carinae; clypeus typically with prominent anterolateral extensions (Figure 15) ... Camponotus
3 With conspicuous long setae, gracile legs, and a shield-shaped clypeus with prominent anterolateral extensions (Figure 16) ... Camponotus chloroticus
- Without the combination of conspicuous long setae and gracile legs; clypeus lacking prominent anterolateral extensions (Figures 8–11) ... Colobopsis
4 Small species, HW 0.68–1.04; antennal insertions more widely separated (ASM/HW 0.34–0.39 and ASM/CLW 0.64–0.77) (Figures 18–19); clypeus tending to be less broad (CLW/CLL 1.15–1.40) ... Colobopsis
- Small to medium-sized species, HW 0.75–2.10; antennal insertions less well separated (ASM/HW 0.25–0.29 and ASM/CLW 0.46–0.55); clypeus varying in shape, but if HW < 1.05 (e.g., Camponotus pulchellus complex) (Figure 17) then clypeus tending to be broader (CLW/CLL 1.25–1.60) ... Camponotus
See images of species within this genus |
Keys to Species in this Genus
- Key to Australian Camponotus majors of the southwestern Botanical Province
- Key to Australian Camponotus minors of the southwestern Botanical Province
Distribution
Ward et al. (2016) - Colobopsis occurs in the New World from southern United States to Costa Rica; across the southern and central Palearctic from the western Mediterranean to Japan; throughout the Oriental and Australian biogeographic regions as far south as Tasmania; and into the Pacific as far east as New Caledonia, Vanuatu, and Fiji. The genus is notably absent from the Afrotropics and most of the Neotropics.
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 | |
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Species | 0 | 12 | 82 | 1 | 7 | 9 | 19 | 8 |
Total Species | 2841 | 1736 | 3045 | 932 | 835 | 4379 | 1741 | 2862 |
Fossils
Fossils are known from: Bembridge Marls, Isle of Wight, UK (Priabonian, Late Eocene), Zhangpu amber, Zhangpu County, Fujian Province, China (Miocene) (an unidentified species, Wang et al., 2021).
Biology
Ward et al. (2016) - Most species of Colobopsis are strictly arboreal, nesting in cavities in dead branches or twigs and employing phragmotic major workers to block the nest entrance (Forel 1892; Wheeler 1904; Creighton 1967). In some Fijian species, with reduced phragmosis, nests can also be found in rotten wood and in epiphytic ant-plants (Sarnat & Economo 2012). Phragmosis is also reduced in some Southeast Asian species nesting in live stems; at least one species, Colobopsis macarangae, apparently lacks a major worker subcaste (Dumpert 1996). In the field, collections of Colobopsis can be readily distinguished from those of Camponotus if pupae are available: these are always naked in Colobopsis (Wheeler 1904; Ward, pers. obs.), while those of Camponotus are enclosed in cocoons.
The Colobopsis cylindrica group employs a novel defensive strategy. Minor workers of these so called exploding ants will, when threatened, flex their gasters so hard that they rupture. This releases a toxic chemical mixture that they then attempt to smear on their antagonists.
Association with Other Organisms
- Explore: Show all Associate data or Search these data. See also a list of all data tables or learn how data is managed.
Species Uncertain
- This species is a host for the nematode Mermithidae (unspecified taxon) (a parasite) in Brunei, KBFSC (Laciny et al., 2017) (ant identified as Colobopsis sp. nrSA).
- This species is a host for the nematode Mermithidae (unspecified "Mermis") (a parasite) in Papua New Guinea (Maeyama et al., 1994 Laciny, 2021).
All Associate Records for Genus
Taxon | Relationship | Associate Type | Associate Taxon | Associate Relationship | Locality | Source | Notes |
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Colobopsis | host | nematode | Mermithidae (unspecified "Mermis") | parasite | Papua New Guinea | Maeyama et al., 1994 Laciny, 2021 | |
Colobopsis | host | nematode | Mermithidae (unspecified taxon) | parasite | Brunei, KBFSC | Laciny et al., 2017 | ant identified as ''Colobopsis'' sp. nrSA |
Colobopsis leonardi | host | fungus | Ophiocordyceps camponoti-leonardi | parasitoid | Quevillon, 2018 | encounter mode primary; direct transmission; transmission outside nest | |
Colobopsis leonardi | host | fungus | Ophiocordyceps camponoti-leonardi | pathogen | Andersen, Ferrari et al., 2012; Andersen, Hughes et al., 2012; Araujo et al., 2018; Shrestha et al., 2017 | ||
Colobopsis leonardi | host | fungus | Ophiocordyceps camponoti-saundersi | parasitoid | Quevillon, 2018 | encounter mode primary; direct transmission; transmission outside nest | |
Colobopsis leonardi | host | fungus | Ophiocordyceps formicarum | parasitoid | Quevillon, 2018 | encounter mode primary; direct transmission; transmission outside nest | |
Colobopsis leonardi | host | fungus | Ophiocordyceps unilateralis | parasitoid | Quevillon, 2018 | encounter mode primary; direct transmission; transmission outside nest | |
Colobopsis saundersi | host | fungus | Ophiocordyceps camponoti-saundersi | pathogen | Araujo et al., 2018 | ||
Colobopsis vitrea praerufa | host | fungus | Ophiocordyceps formicarum | parasitoid | Quevillon, 2018 | encounter mode primary; direct transmission; transmission outside nest | |
Colobopsis vitrea praerufa | host | fungus | Ophiocordyceps unilateralis | parasitoid | Quevillon, 2018 | encounter mode primary; direct transmission; transmission outside nest |
Flight Period
All Flight Records for Genus
- Explore: Show all Flight Month data or Search these data. See also a list of all data tables or learn how data is managed.
Taxon | Month | Source | Notes |
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Colobopsis impressa | Apr • May • Jun • Jul | antkeeping.info | |
Colobopsis mississippiensis | Jun • Jul | antkeeping.info | |
Colobopsis nipponica | Jun • Jul | Japan | |
Colobopsis obliqua | May • Jun | antkeeping.info | |
Colobopsis truncata | Jun • Jul • Aug | antkeeping.info |
Life History Traits
- Compound colony type: not parasitic (Greer et al., 2021)
- Nest site: arboreal (Greer et al., 2021)
- Diet class: herbivore (Greer et al., 2021)
- Foraging stratum: arboreal (Greer et al., 2021)
Castes
Major and minor castes, majors with phragmotic heads.
Morphology
Phylogeny
Formicinae |
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See Phylogeny of Formicinae for details.
Nomenclature
The following information is derived from Barry Bolton's Online Catalogue of the Ants of the World.
- [Note: combinations in Colobopsis by McArthur, 2012: 234 pp. are ignored, but his page references to species are included. This is because his concept of Colobopsis included, without argument or justification, a selection of species from 21 other subgenera of Camponotus, including the type-species of six of those subgenera.]
References
- André, E. 1882c. Les fourmis. [part]. Pp. 153-232 in: André, Edm. 1881-1886. Species des Hyménoptères d'Europe et d'Algérie. Tome Deuxième. Beaune: Edmond André, 919 + 48 pp. (page 159, Colobopsis as genus)
- Arnold, G. 1922. A monograph of the Formicidae of South Africa. Part V. Myrmicinae. Ann. S. Afr. Mus. 14: 579-674 (page 613, Colobopsis as subgenus of Camponotus)
- 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, Colobopsis in Camponotinae, Camponotini; as genus)
- Barden, P. 2017. Fossil ants (Hymenoptera: Formicidae): ancient diversity and the rise of modern lineages. Myrmecological News 24: 1-30.
- Bingham, C. T. 1903. The fauna of British India, including Ceylon and Burma. Hymenoptera, Vol. II. Ants and Cuckoo-wasps. London: Taylor and Francis, 506 pp. (page 342, Colobopsis as genus; Type-species: Formica truncata; by subsequent designation)
- Blaimer, B.B., Brady, S.G., Schultz, T.R., Lloyd, M.W., Fisher, B.L., & Ward, P.S. 2015. Phylogenomic methods outperform traditional multi-locus approaches in resolving deep evolutionary history: a case study of formicine ants. BMC Evolutionary Biology, 15:271 (DOI 10.1186/s12862-015-0552-5).
- Bolton, B. 2003. Synopsis and Classification of Formicidae. Mem. Am. Entomol. Inst. 71: 370pp (page 113, 268, Colobopsis as subgenus of Camponotus)
- Bondroit, J. 1918. Les fourmis de France et de Belgique. Ann. Soc. Entomol. Fr. 87: 1-174 (page 65, 66, Colobopsis in Formicinae, Camponotini; as genus)
- Brassard, F., Leong, C.-M., Chan, H.-H., Guénard, B. 2021. High diversity in urban areas: How comprehensive sampling reveals high ant species richness within one of the most urbanized regions of the world. Diversity 13, 358 (doi:10.3390/d13080358).
- Burger, H.F., Vondráčková, K., Skłodowski, M., Qian-Qun Koid, Dent, D.H., Wallace, K., Fayle, T.M. 2021. Protection from herbivores varies among ant genera for the myrmecophilic plant Leea aculeata in Malaysian Borneo. Asian Myrmecology 14, e014002 (doi:10.20362/am.014002).
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- Creighton, W. S. 1950a. The ants of North America. Bulletin of the Museum of Comparative Zoology 104: 1-585 (page 390, Colobopsis as subgenus of Camponotus)
- Dalla Torre, K. W. von. 1893. Catalogus Hymenopterorum hucusque descriptorum systematicus et synonymicus. Vol. 7. Formicidae (Heterogyna). Leipzig: W. Engelmann, 289 pp. (page 219, Colobopsis as subgenus of Camponotus)
- Donisthorpe, H. 1943g. A list of the type-species of the genera and subgenera of the Formicidae. [part]. Ann. Mag. Nat. Hist. 11(10): 617-688 (page 634, Colobopsis as subgenus of Camponotus)
- Emery, C. 1889d. Formiche di Birmania e del Tenasserim raccolte da Leonardo Fea (1885-87). [concl.]. Ann. Mus. Civ. Stor. Nat. 27[=(2)(7): 513-520 (page 517, Colobopsis as subgenus of Camponotus)
- 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, Colobopsis in Camponotinae, Camponotini; Colobopsis as subgenus of Camponotus)
- Emery, C. 1920b. Le genre Camponotus Mayr. Nouvel essai de la subdivision en sous-genres. Rev. Zool. Afr. (Bruss.) 8: 229-260 (page 247, Colobopsis as subgenus of Camponotus)
- Emery, C. 1925d. Hymenoptera. Fam. Formicidae. Subfam. Formicinae. Genera Insectorum 183: 1-302 (page 144, Colobopsis in Formicinae, Camponotini; Colobopsis as subgenus of Camponotus)
- Emery, C.; Forel, A. 1879. Catalogue des Formicides d'Europe. Mitt. Schweiz. Entomol. Ges. 5: 441-481 (page 449, Colobopsis in Camponotinae [Camponotidae]; as genus)
- Fernandez, F., Guerrero, R.J., Sánchez-Restrepo, A.F. 2021. Sistemática y diversidad de las hormigas neotropicales. Revista Colombiana de Entomología 47, 1–20 (doi:10.25100/socolen.v47i1.11082).
- Forel, A. 1878c. Études myrmécologiques en 1878 (première partie) avec l'anatomie du gésier des fourmis. Bull. Soc. Vaudoise Sci. Nat. 15: 337-392 (page 368, Colobopsis in Camponotinae [Camponotidae]; as genus)
- Forel, A. 1879a. Études myrmécologiques en 1879 (deuxième partie [1re partie en 1878]). Bull. Soc. Vaudoise Sci. Nat. 16: 53-128 (page 125, Colobopsis as genus)
- Forel, A. 1886h. Études myrmécologiques en 1886. Ann. Soc. Entomol. Belg. 30: 131-215 (page 193, Colobopsis in Camponotinae, Camponotini; as genus)
- Forel, A. 1893b. Sur la classification de la famille des Formicides, avec remarques synonymiques. Ann. Soc. Entomol. Belg. 37: 161-167 (page 165, Colobopsis as subgenus of Camponotus)
- Forel, A. 1893c. Les Formicides de l'Empire des Indes et de Ceylan. Part II. J. Bombay Nat. Hist. Soc. 7: 430-439 (page 435, Colobopsis as subgenus of Camponotus)
- Forel, A. 1912j. Formicides néotropiques. Part VI. 5me sous-famille Camponotinae Forel. Mém. Soc. Entomol. Belg. 20: 59-92 (page 90, Colobopsis as subgenus of Camponotus)
- Forel, A. 1914a. Le genre Camponotus Mayr et les genres voisins. Rev. Suisse Zool. 22: 257-276 (page 263, Colobopsis as subgenus of Camponotus)
- Forel, A. 1917. Cadre synoptique actuel de la faune universelle des fourmis. Bull. Soc. Vaudoise Sci. Nat. 51: 229-253 (page 251, Colobopsis as subgenus of Camponotus)
- Greer, J. A., Moreau, C. S. 2021. Phylogenetic analysis and trait evolution of ant cocoons. Insect Systematics & Evolution 53(1), 60–77 (doi:10.1163/1876312x-bja10008).
- Jaffe, K. 1993. El mundo de las hormigas. Baruta, Venezuela: Equinoccio (Ediciones de la Universidad Simón Bolívar), 188 pp. (page 14, Colobopsis as genus (anachronism))
- Kempf, W. W. 1972b. Catálogo abreviado das formigas da regia~o Neotropical. Stud. Entomol. 15: 3-344 (page 42, Colobopsis as subgenus of Camponotus)
- Klimeš, P., Drescher, J., Buchori, D., Hidayat, P., Nazarreta, R., Potocký, P., Rimandai, M., Scheu, S., Matos-Maraví, P. 2022. Uncovering cryptic diversity in the enigmatic ant genus Overbeckia and insights into the phylogeny of Camponotini (Hymenoptera:Formicidae:Formicinae). Invertebrate Systematics, 36(6), 557-579 (doi:10.1071/is21067).
- Laciny, A., Zettel, H., Metscher, B., Kamariah, A.S., Kopchinskiy, A., Pretzer, C., Druzhinina, I.S. 2017. Morphological variation and mermithism in female castes of Colobopsis sp. nrSA, a Bornean “exploding ant” of the Colobopsis cylindrica group (Hymenoptera: Formicidae). Myrmecological News 24:91-106.
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- Mayr, G. 1870b. Neue Formiciden. Verh. K-K. Zool.-Bot. Ges. Wien 20: 939-996 (page 940, Colobopsis as genus)
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- Zettel, H., Laciny, A., Jaitrong, W., Syaukani, S., Kopchinskiy, A., Druzhinina, I.S. 2018. Evidence of predation in two species of the Colobopsis cylindrica group (Hymenoptera Formicidae Camponotini). Asian Myrmecology 10 e010011 (DOI 10.20362am.010011).
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