Anochetus altisquamis

Anochetus altisquamis
Scientific classification
Kingdom:	Animalia
Phylum:	Arthropoda
Class:	Insecta
Order:	Hymenoptera
Family:	Formicidae
Subfamily:	Ponerinae
Tribe:	Ponerini
Genus:	Anochetus
Species:	A. altisquamis
Binomial name
Anochetus altisquamis Mayr, 1887 Specimen labels
Synonyms
Anochetus fumata Luederwaldt, 1918

Identification

Keys including this Species

• Key to the Anochetus species of the Neotropics

Distribution

Latitudinal Distribution Pattern

Latitudinal Range: -15.4375° to -34.378°.

North Temperate	North Subtropical	Tropical	South Subtropical	South Temperate

• Source: AntMaps

Distribution based on Regional Taxon Lists

Neotropical Region: Argentina, Brazil (type locality), Paraguay, Uruguay.

Distribution based on AntMaps

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Distribution based on AntWeb specimens

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Countries Occupied

Number of countries occupied by this species based on AntWiki Regional Taxon Lists. In general, fewer countries occupied indicates a narrower range, while more countries indicates a more widespread species.

Estimated Abundance

Relative abundance based on number of AntMaps records per species (this species within the purple bar). Fewer records (to the left) indicates a less abundant/encountered species while more records (to the right) indicates more abundant/encountered species.

Biology

Explore Overview of Anochetus biology  Not much is known about the the biology of Anochetus altisquamis but we can presume that its biology is similar to other Anochetus species. The following account of Anochetus biology is modified from Brown (1968): Habitat. The places where Anochetus live are varied. Where they penetrate into the temperate zone, most species excavate nests in the earth. Occasionally the nest is dug under a covering rock. In the tropics, many nests are also dug in the soil, but in moist forested areas, a common site is the soil beneath a rotting log or other large mass of rotting wood, with extensions of the nest into the log itself. Another frequent nesting site in tropical forest is in the humus and leaf litter at the base of large trees, particularly between buttress roots. Anochetus species of medium or small size often nest in small pieces of rotting wood or bark, or even small rotting twigs or seeds and nuts lying in or on the forest litter. Some species tend to choose more arboreal nest sites. Diet. Foraging for living animal prey takes place on the soil surface, within the soil-humus-log mold matrix, or on the trunks, branches and foliage of trees and plants wherever these are available. Fragmentary evidence indicates that most epigaeically foraging tropical Anochetus tend to do their foraging at dusk, at night, or during dawn hours. I found Anochetus africanus walking on tree trunks only at night in the Ivory Coast. Some species, particularly those with red heads or other aposematic coloration, apparently forage in the open more during the day. No systematic comparative study has yet been made of foraging hours for different species. The food of Anochetus consists principally of living arthropods caught and killed or incapacitated by the ants. The smaller and more delicate species Anochetus inermis has been observed by me in a laboratory nest. The colony came from a piece of rotten wood from the floor of a wet ravine near Bucay in western Ecuador. The colony was fed with small tenebrionid beetle larvae (Tribolium castaneum), comparable in size to the A. inermis workers, and the latter attacked the prey with their mandibles in the familiar snapping manner, but very cautiously and nervously, with stealthy approach, extremely rapid strike, and instant recoil-retreat. After several attacks of this kind, with intervening periods of waiting, during which the beetle larvae fled, rested, or writhed about in distress, an ant would finally attack with its mandibles and hold them closed on the prey for long enough to deliver a quick sting in the intersegmental membrane. After this, the prey appeared to be paralyzed, or at least subdued, and sooner or later was carried off by the ant to the nest, and eventually placed on an ant larva. Frequent delays and excursions before the prey are finally immobilized and brought to the ant larvae in the nest may well have the function of allowing time for protective allomones of the prey to dissipate. Many tenebrionid adults, including Tribofium, possess potent quinonoid defensive allomones, but the larva is not known to possess quinones in this genus. Nuptial flight. Although males of different species of Anochetus are commonly taken at light, other species are not. Stewart and Jarmila Peck gave me Malaise trap samples taken in western Ecuador that contained males of several species, but Malaise traps capture both day- and night-flying insects. Defense. When a nest of any of the larger Anochetus species is breached, some of the workers immediately hide beneath leaves or other objects, while other workers rush about with open jaws, which they snap at foreign objects, or even at leaves and twigs, with an audible tick. On human skin or clothing, a worker will snap her jaws and hold fast to the surface with them, at the same time quickly bringing her gaster around to sting. The sting is long and strong, and to me the effect is shocking and quickly painful. Most of the smaller and medium-sized Anochetus species feign death when disturbed, crouching flat against the surface, or rolling themselves into a ball and remaining still, often for a minute or more. Only when held do they sting. Their stings can be felt in most cases, but the effect is usually trifling. ‎

Nomenclature

The following information is derived from Barry Bolton's Online Catalogue of the Ants of the World.

• altisquamis. Anochetus altisquamis Mayr, 1887: 529 (w.) BRAZIL (Santa Catarina).
  • Type-material: syntype workers (number not stated).
  • Type-locality: Brazil: Santa Catarina (L. Hetschko).
  • Type-depository: NHMW.
  • Status as species: Dalla Torre, 1893: 47; Emery, 1894c: 187 (in key); Emery, 1894e: 4; Forel, 1895b: 117; Emery, 1906c: 117; Emery, 1911d: 110; Bruch, 1914: 213; Forel, 1915c: 352; Gallardo, 1918b: 90; Luederwaldt, 1918: 36; Borgmeier, 1923: 75; Kusnezov, 1953b: 336; Kempf, 1972a: 20; Kempf & Lenko, 1976: 58; Brown, 1978c: 556, 619; Zolessi, et al. 1988: 3; Brandão, 1991: 325; Bolton, 1995b: 63; Wild, 2007b: 38 González-Campero & Elizalde, 2008: 98 (in key); Feitosa, 2015c: 98.
  • Senior synonym of fumata: Kempf & Lenko, 1976: 58; Brown, 1978c: 556; Brandão, 1991: 325.
  • Distribution: Argentina, Brazil, Paraguay, Uruguay.
• fumata. Anochetus altisquamis forma fumata Luederwaldt, 1918: 53 (w.) BRAZIL (Minas Gerais).
  • Type-material: syntype workers (number not stated, “numerous examples”).
  • [Note: Baroni Urbani, 1973b: 143, cites 11w syntypes NHMB.]
  • Type-localities: Brazil: Minas Gerais, Ypiranga (H. Luederwaldt) (invalid restriction of type-locality by Kempf, 1972a: 20; no lectotype designated), Brazil: Minas Gerais, Christina (H. Luederwaldt).
  • Type-depositories: MZSP, NHMB.
  • [Also described as new by Luederwaldt,1920: 3.]
  • Subspecies of altisquamis: Borgmeier, 1923: 75; Kempf, 1972a: 20.
  • Junior synonym of altisquamis: Kempf & Lenko, 1976: 58; Brown, 1978c: 556; Brandão, 1991: 325; Bolton, 1995b: 64.

Description

Karyotype

• See additional details at the Ant Chromosome Database.

 Explore: Show all Karyotype data or Search these data. See also a list of all data tables or learn how data is managed.

• n = 15, 2n = 30, karyotype = 16M + 14A (Brazil) (Santos et al., 2010) (karyotype originally as 12M+6SM+2ST+10T).

References

• Aguiar, H.J.A.C., Barros, L.A.C., Silveira, L.I., Petitclerc, F., Etienne, S., Orivel, J. 2020. Cytogenetic data for sixteen ant species from North-eastern Amazonia with phylogenetic insights into three subfamilies. Comparative Cytogenetics 14(1): 43–60 (doi:10.3897/CompCytogen.v14i1.46692).
• Albuquerque, E., Prado, L., Andrade-Silva, J., Siqueira, E., Sampaio, K., Alves, D., Brandão, C., Andrade, P., Feitosa, R., Koch, E., Delabie, J., Fernandes, I., Baccaro, F., Souza, J., Almeida, R., Silva, R. 2021. Ants of the State of Pará, Brazil: a historical and comprehensive dataset of a key biodiversity hotspot in the Amazon Basin. Zootaxa 5001, 1–83 (doi:10.11646/zootaxa.5001.1.1).
• Camargo, K.S. de. 2011. Composicao e diversidade de "Poneromorfas" (Hymenoptera, Formicidae) em duas fitofisionomias de cerrado e padroes de distribuicao de "Poneromorfas", Pseudomyrmecinae e Cephalotini (Myrmicinae) para o Brasil. Thesis, Universidade de Brasilia.
• Esteves, F.A., Fisher, B.L. 2021. Corrieopone nouragues gen. nov., sp. nov., a new Ponerinae from French Guiana (Hymenoptera, Formicidae). ZooKeys 1074, 83–173 (doi:10.3897/zookeys.1074.75551).
• Feitosa, R.M., Silva, R.R.da, Aguiar, A.P. 2016. Diurnal flight periodicity of a Neotropical ant assemblage (Hymenoptera, Formicidae) in the Atlantic Forest. Revista Brasileira de Entomologia 60, 241–247. (doi:10.1016/j.rbe.2016.05.006).
• Kempf, W. W.; Lenko, K. 1976. Levantamento da formicifauna no litoral norte e ilhas adjacentes do Estado de Sa~o Paulo, Brasil. I. Subfamilias Dorylinae, Ponerinae e Pseudomyrmecinae (Hym., Formicidae). Stud. Entomol. 19: 45-66 (page 58, senior synonym of fumata)
• Mariano, C.S.F., Santos, I.S., Silva, J.G., Costa, M.A., Pompolo, S.G. 2015. Citogenética e evolução do cariótipo em formigas poneromorfas. In: Delabie, J.H.C., Feitosa, R.M., Serrao, J.E., Mariano, C.S.F., Majer, J.D. (eds) As formigas poneromorfas do Brasil, 1st edn. Ilhéus, Brasil, pp 102–125 (doi:10.7476/9788574554419.0010).
• Mayr, G. 1887. Südamerikanische Formiciden. Verh. K-K. Zool.-Bot. Ges. Wien 37: 511-632 (page 529, worker described)

References based on Global Ant Biodiversity Informatics

• Borgmeier T. 1923. Catalogo systematico e synonymico das formigas do Brasil. 1 parte. Subfam. Dorylinae, Cerapachyinae, Ponerinae, Dolichoderinae. Archivos do Museu Nacional (Rio de Janeiro) 24: 33-103.
• Brandao, C.R.F. 1991. Adendos ao catalogo abreviado das formigas da regiao neotropical (Hymenoptera: Formicidae). Rev. Bras. Entomol. 35: 319-412.
• Drose W., L. R. Podgaiski, C. Fagundes Dias, M. de Souza Mendonca. 2019. Local and regional drivers of ant communities in forest-grassland ecotones in South Brazil: A taxonomic and phylogenetic approach. Plos ONE 14(4): e0215310.
• Emery C. 1894. Viaggio del dottor Alfredo Borelli nella Repubblica Argentina e nel Paraguay. VIII. Formiche. Bollettino dei Musei di Zoologia ed Anatomia Comparata della Reale Università di Torino 9(186): 1-4.
• Emery C. 1911. Hymenoptera. Fam. Formicidae. Subfam. Ponerinae. Genera Insectorum 118: 1-125.
• Favretto M. A., E. Bortolon dos Santos, and C. J. Geuster. 2013. Entomofauna from West of Santa Catarina State, South of Brazil. EntomoBrasilis 6 (1): 42-63.
• Fernandes T. T., R. R. Silva, D. Rodrigues de Souza-Campana, O. Guilherme Morais da Silva, and M. Santina de Castro Morini. 2019. Winged ants (Hymenoptera: Formicidae) presence in twigs on the leaf litter of Atlantic Forest. Biota Neotropica 19(3): http://dx.doi.org/10.1590/1676-0611-bn-2018-0694
• Fernandes T. T., W. Dattilo, R. R. Silva, P. Luna, C. M. Oliveira, and M. Santina de Castro Morini. 2019. Ant occupation of twigs in the leaf litter of the Atlantic Forest: influence of the environment and external twig structure. Tropical Conservation Science 12: 1-9.
• Fernández, F. and S. Sendoya. 2004. Lista de las hormigas neotropicales. Biota Colombiana Volume 5, Number 1.
• Fleck M. D., E. Bisognin Cantarelli, and F. Granzotto. 2015. Register of new species of ants (Hymenoptera: Formicidae) in Rio Grande do Sul state. Ciencia Florestal, Santa Maria 25(2): 491-499.
• Kempf W. W. 1978. A preliminary zoogeographical analysis of a regional ant fauna in Latin America. 114. Studia Entomologica 20: 43-62.
• Kempf W. W., and K. Lenko. 1976. Levantamento da formicifauna no litoral norte e ilhas adjacentes do Estado de São Paulo, Brasil. I. Subfamilias Dorylinae, Ponerinae e Pseudomyrmecinae (Hym., Formicidae). Studia Entomologica 19: 45-66.
• Kempf, W.W. 1972. Catalago abreviado das formigas da regiao Neotropical (Hym. Formicidae) Studia Entomologica 15(1-4).
• Luederwaldt H. 1918. Notas myrmecologicas. Rev. Mus. Paul. 10: 29-64.
• Luederwaldt H. 1920. Neue Brasilianische Ameisen. Sa~o Paulo: Weiszflog Irmaos, 14 pp
• Mentone T. O., E. A. Diniz, C. B. Munhae, O. C. Bueno, and M. S. C. Morini. 2011. Composition of ant fauna (Hymenoptera: Formicidae) at litter in areas of semi-deciduous forest and Eucalyptus spp., in Southeastern Brazil. Biota Neotrop. 11(2): http://www.biotaneotropica.org.br/v11n2/en/abstract?inventory+bn00511022011.
• Oliveira Mentone T. de, E. A. Diniz, C. de Bortoli Munhae, O. Correa Bueno and M. S. de Castro Morini. 2012. Composition of ant fauna (Hymenoptera: Formicidae) at litter in areas of semi-deciduous forest and Eucalyptus spp., in Southeastern Brazil. Biota Neotrop 11(2): 237-246.
• Pacheco, R., R.R. Silva, M.S. de C. Morini, C.R.F. Brandao. 2009. A Comparison of the Leaf-Litter Ant Fauna in a Secondary Atlantic Forest with an Adjacent Pine Plantation in Southeastern Brazil. Neotropical Entomology 38(1):055-065
• Rosa da Silva R. 1999. Formigas (Hymenoptera: Formicidae) do oeste de Santa Catarina: historico das coletas e lista atualizada das especies do Estado de Santa Catarina. Biotemas 12(2): 75-100.
• Scott-Santos, C.P., F.A. Esteves, C.R.F. Brandao. 2008. Catalogue of "Poneromorph" ant type specimens (Hymenoptera, Formicidae) deposited in the Museu de Zoologia da Universidade de Sao Paulo, Brazil. Papeis Avulsos de Zoologia 48(11):75-88.
• Silva R.R., and C. R. F. Brandao. 2014. Ecosystem-Wide Morphological Structure of Leaf-Litter Ant Communities along a Tropical Latitudinal Gradient. PLoSONE 9(3): e93049. doi:10.1371/journal.pone.0093049
• Suguituru S. S., D. R. de Souza, C. de Bortoli Munhae, R. Pacheco, and M. S. de Castro Morini. 2011. Diversidade e riqueza de formigas (Hymenoptera: Formicidae) em remanescentes de Mata Atlântica na Bacia Hidrográfica do Alto Tietê, SP. Biota Neotrop. 13(2): 141-152.
• Suguituru S. S., M. Santina de Castro Morini, R. M. Feitosa, and R. Rosa da Silva. 2015. Formigas do Alto Tiete. Canal 6 Editora 458 pages
• Suguituru S. S., R. Rosa Silva, D. R. de Souza, C. de Bortoli Munhae, and M. Santina de Castro Morini. Ant community richness and composition across a gradient from Eucalyptus plantations to secondary Atlantic Forest. Biota Neotrop. 11(1): 369-376.
• Ulyssea M.A., C. E. Cereto, F. B. Rosumek, R. R. Silva, and B. C. Lopes. 2011. Updated list of ant species (Hymenoptera, Formicidae) recorded in Santa Catarina State, southern Brazil, with a discussion of research advances and priorities. Revista Brasileira de Entomologia 55(4): 603-–611.
• Wild, A. L. "A catalogue of the ants of Paraguay (Hymenoptera: Formicidae)." Zootaxa 1622 (2007): 1-55.
• Zolessi L. C. de, Y. P. Abenante, and M. E. de Philippi. 1988. Lista sistematica de las especies de Formicidos del Uruguay. Comun. Zool. Mus. Hist. Nat. Montev. 11: 1-9.
• Zolessi L. C. de; Y. P. de Abenante, and M. E. Philippi. 1989. Catálogo sistemático de las especies de Formícidos del Uruguay (Hymenoptera: Formicidae). Montevideo: ORCYT Unesco, 40 + ix pp.
• da Silva R. R., and R. Silvestre. 2000. Diversidade de formigas (Hymenoptera: Formicidae) em Seara, oeste de Santa Catarina. Biotemas 13(2): 85-105.
• da Silva, R.R. and R. Silvestre. 2004. Riqueza da fauna de formigas (Hymenoptera: Formicidae) que habita as camadas superficiais do solo em Seara, Santa Catarina. Papéis Avulsos de Zoologia (São Paulo) 44(1): 1-11
• de Souza D. R., S. G. dos Santos, C. de B. Munhae, and M. S. de C. Morini. 2012. Diversity of Epigeal Ants (Hymenoptera: Formicidae) in Urban Areas of Alto Tietê. Sociobiology 59(3): 703-117.
• de Zolessi, L.C., Y.P. de Abenante and M.E. Philippi. 1987. Lista sistemática de las especies de formícidos del Uruguay. Comunicaciones Zoologicas del Museo de Historia Natural de Montevideo 11(165):1-9