Poneracantha triangularis

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Poneracantha triangularis
Scientific classification
Kingdom: Animalia
Phylum: Arthropoda
Class: Insecta
Order: Hymenoptera
Family: Formicidae
Subfamily: Ectatomminae
Tribe: Ectatommini
Genus: Poneracantha
Species: P. triangularis
Binomial name
Poneracantha triangularis
(Mayr, 1887)

Gnamptogenys triangularis casent0103948 profile 1.jpg

Gnamptogenys triangularis casent0103948 dorsal 1.jpg

Specimen Label

Synonyms

A millipede feeder that is found in humid forests. The USA record (Deyrup, et. al. 1989:93) is undoubtedly a recent introduction and they have apparently found prey in the local species of millipedes, as they are well established. (Lattke 1995)

Poneracantha triangularis is a specialized predator on millipedes. In the laboratory, P. triangularis is especially fond of the invasive Asian millipede Oxidus gracilis (Koch), which is abundant on the Statesboro campus. Like many millipedes, O. gracilis defends itself against predators with a foul-smelling cocktail of toxic chemicals, including hydrogen cyanide (Taira et al. 2003). These defenses, however, are apparently ineffective against P. triangularis, which has been recorded attacking O. gracilis in the field and can survive for hours in cyanide killing jars that killed other ants within a few minutes (Lattke 1990). Poneracantha triangularis workers emit an odor similar to that of O. gracilis (Wang et al. 2021), suggesting that this ant can not only tolerate the millipede’s chemical weapons but perhaps also co-opt them for its own protection. Although P. triangularis is an invasive species (i.e., introduced by humans to a new area, from which it has subsequently spread), its apparent scarcity and specialized diet suggest that it is not likely to become a serious pest, as MacGown and Wetterer (2012) and Wang et al. (2021) have noted. (Harvey, 2022)

At a Glance • Invasive  

Photo Gallery

  • Figure. 1. Poneracantha triangularis workers subduing an Oxidus gracilis millipede in Pensacola, Florida. Photo by A.C. Stoll (Wang et al., 2022, Fig. 1).

Identification

A member of the rastrata complex (in the rastrata subgroup of the rastrata species group). Promesonotal suture weakly impressed; node dorsum with transverse costulae and subquadrate costulae and subquadrate subpetiolar process; first gastric sternum with transverse costulae; metacoxal tooth long and thin. Piceous body. (Lattke 1995)

Keys including this Species

Distribution

Introduced into Alabama and Florida (Dade and Escambia counties) from Central or South America. It is not as yet common there, but seems well established. First published Florida record: Deyrup et al. 1989; earlier specimens: 1985. (Deyrup, Davis & Cover, 2000.)

Latitudinal Distribution Pattern

Latitudinal Range: 25.68015° to -34.583333°.

     
North
Temperate
North
Subtropical
Tropical South
Subtropical
South
Temperate

Distribution based on Regional Taxon Lists

Nearctic Region: United States.
Neotropical Region: Argentina, Bolivia, Brazil, Colombia, Costa Rica, Ecuador, French Guiana, Peru, Uruguay (type locality).

Distribution based on AntMaps

AntMapLegend.png

Distribution based on AntWeb specimens

Check data from AntWeb

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.
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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.
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Biology

This species was studied in Venezuela by Lattke (1990). He found nests in fallen logs and branches, inhabited by 80-120 individuals. In the four nests examined he found only the remains of millipedes, in the form of disarticulated segmental rings, surrounding the area of the nest. Larvae were found with their heads thrust into the body of a dead millipede. Many millipedes secrete powerful defensive secretions, including cyanide. Lattke found that both adults and larvae of P. triangularis are resistant to cyanide, surviving for three hours in a potassium cyanide killing jar that killed other ants in less than five minutes. Even the P. triangularis were dead in twelve hours.

A colony from Homestead, Florida, had many millipede fragments in the nest (Gary Umphrey 1987, pers. comm.; Deyrup, Davis & Cover, 2000).

The following notes are from Wang et al. (2021):

Poneracantha triangularis records in the southeastern United States are uncommon, but come from a wide range of habitats, from relatively intact forest to highly disturbed urban sites. It is known distribution in Texas, Louisiana, Mississippi, Alabama, Florida, Georgia and South Carolina. Our northernmost site records come from 34.1°N in South Carolina. However, based on its South American range extending to 38.1°S, P. triangularis may have the potential to spread further north in the US, perhaps as far as Richmond, Virginia (37.5°N) and Lexington, Kentucky (38.0°N) (MacGown & Wetterer 2012). A large portion of records of P. triangularis in the southeastern US come from specimens and photographs of alate queens and males. This may indicate that this species is more common than generally appreciated, but simply overlooked.

In both its native and exotic range, P. triangularis preys on millipedes (Lattke 1990, 1995, Deyrup et al. 2000). Millipedes are often particularly common in disturbed environments, so potential prey for P. triangularis is plentiful. The greenhouse millipede, O. gracilis, a cosmopolitan species originally from Asia, is now very common in the southeastern US. Millipedes produce a wide range of defensive chemicals that protect them from most potential predators. Although O. gracilis produces several highly toxic defensive chemicals, including hydrogen cyanide (Taira et al. 2003), P. triangularis has overcome these defensives. Poneracantha triangularis may even be able to use these chemicals to make themselves toxic to potential predators.

There have been no studies examining potential impacts of P. triangularis. Even if this species were having a localized impact on millipede populations, this might be difficult to detect. Nonetheless, it seems unlikely that P. triangularis will ever become a significant pest.

Flight Period

X
Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec

Source: antkeeping.info.

Castes

Worker

Images from AntWeb

Gnamptogenys triangularis casent0179951 h 1 high.jpgGnamptogenys triangularis casent0179951 p 1 high.jpgGnamptogenys triangularis casent0179951 d 1 high.jpgGnamptogenys triangularis casent0179951 l 1 high.jpg
Worker. Specimen code casent0179951. Photographer Erin Prado, uploaded by California Academy of Sciences. Owned by MIZA, Maracay, Venezuela.
Gnamptogenys triangularis casent0006087 head 1.jpgGnamptogenys triangularis casent0006087 profile 1.jpgGnamptogenys triangularis casent0006087 dorsal 1.jpgGnamptogenys triangularis casent0006087 label 1.jpg
Worker. Specimen code casent0006087. Photographer April Nobile, uploaded by California Academy of Sciences. Owned by CAS, San Francisco, CA, USA.
Gnamptogenys triangularis casent0246690 h 1 high.jpgGnamptogenys triangularis casent0246690 p 1 high.jpgGnamptogenys triangularis casent0246690 d 1 high.jpgGnamptogenys triangularis casent0246690 l 1 high.jpg
Worker. Specimen code casent0246690. Photographer Andrea Walker, uploaded by California Academy of Sciences. Owned by USNM, Washington, DC, USA.
Gnamptogenys triangularis casent0281234 h 1 high.jpgGnamptogenys triangularis casent0281234 p 1 high.jpgGnamptogenys triangularis casent0281234 d 1 high.jpgGnamptogenys triangularis casent0281234 l 1 high.jpg
Worker. Specimen code casent0281234. Photographer Estella Ortega, uploaded by California Academy of Sciences. Owned by PSWC, Philip S. Ward Collection.
Gnamptogenys triangularis casent0907186 h 1 high.jpgGnamptogenys triangularis casent0907186 p 1 high.jpgGnamptogenys triangularis casent0907186 d 1 high.jpgGnamptogenys triangularis casent0907186 l 1 high.jpg
Syntype of Ectatomma triangulare richteriWorker. Specimen code casent0907186. Photographer Will Ericson, uploaded by California Academy of Sciences. Owned by MHNG, Geneva, Switzerland.

Queen

Images from AntWeb

Gnamptogenys triangularis casent0104851 head 1.jpgGnamptogenys triangularis casent0104851 profile 1.jpgGnamptogenys triangularis casent0104851 dorsal 1.jpgGnamptogenys triangularis casent0104851 label 1.jpg
Queen (alate/dealate). Specimen code casent0104851. Photographer April Nobile, uploaded by California Academy of Sciences. Owned by CAS, San Francisco, CA, USA.

Nomenclature

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

  • triangularis. Ectatomma (Gnamptogenys) triangulare Mayr, 1887: 544 (q.) URUGUAY.
    • Type-material: holotype queen.
    • Type-locality: Uruguay: (no further data) (C. Berg).
    • Type-depository: NHMW.
    • Emery, 1906c: 113 (w.).
    • Combination in E. (Parectatomma): Emery, 1911d: 44;
    • combination in Gnamptogenys: Brown, 1958g: 230;
    • combination in Poneracantha: Camacho, Franco, Branstetter, et al. 2022: 11.
    • Status as species: Dalla Torre, 1893: 26; Emery, 1896g: 46 (in key); Emery, 1906c: 113; Emery, 1911d: 44; Bruch, 1914: 213; Santschi, 1916e: 366; Gallardo, 1918b: 39; Luederwaldt, 1918: 34; Borgmeier, 1923: 59; Kusnezov, 1953b: 336; Brown, 1958g: 229, 323; Kusnezov, 1969: 35 (in key); Kempf, 1972a: 116; Zolessi, et al. 1988: 2; Bolton, 1995b: 211; Lattke, 1995: 190; Deyrup, 2003: 45; Lattke, et al. 2004: 349; MacGown & Forster, 2005: 68; Lattke, et al. 2007: 263 (in key); Lattke, et al. 2008: 100; MacGown & Wetterer, 2011: 1; Feitosa, 2015c: 98; Guénard & Economo, 2015: 226; Deyrup, 2017: 21; Feitosa & Prada-Achiardi, 2019: 673; Camacho, et al. 2020: 461 (in key); Camacho, Franco, Branstetter, et al. 2022: 11.
    • Senior synonym of aculeaticoxae: Lattke, 1995: 190; Camacho, Franco, Branstetter, et al. 2022: 11.
    • Senior synonym of richteri: Brown, 1958g: 230, 323; Kempf, 1972a: 116; Bolton, 1995b: 211; Lattke, 1995: 190; Camacho, Franco, Branstetter, et al. 2022: 11.
    • Distribution: Argentina, Bolivia, Brazil, Colombia, Costa Rica, Ecuador, French Guiana, Guyana, Panama, Peru, Suriname, Uruguay, U.S.A., Venezuela.
  • aculeaticoxae. Ectatomma (Parectatomma) aculeaticoxae Santschi, 1921g: 82 (w.m.) FRENCH GUIANA.
    • Type-material: 2 syntype workers, 1 syntype male.
    • Type-locality: French Guiana: Haute Carsevenne, 1898 (F. Geay).
    • Type-depositories: MNHN, NHMB.
    • Wheeler, G.C. & Wheeler, J. 1971b: 1201 (l.).
    • Combination in E. (Poneracantha): Santschi, 1929h: 476;
    • combination in Gnamptogenys: Brown, 1958g: 227.
    • Status as species: Santschi, 1929h: 476; Brown, 1958g: 227, 300; Kempf, 1961b: 491; Kempf, 1972a: 111; Deyrup, et al. 1989: 93; Lattke, 1990b: 5; Brandão, 1991: 345; Bolton, 1995b: 208; Deyrup, et al. 2000: 295 (error).
    • Junior synonym of triangularis: Lattke, 1995: 190; Camacho, Franco, Branstetter, et al. 2022: 11.
  • richteri. Ectatomma (Parectatomma) triangulare r. richteri Forel, 1913l: 203 (w.) ARGENTINA (Buenos Aires).
    • Type-material: syntype workers (number not stated).
    • Type-localities: Argentina: Buenos Aires, Belgrano (Richter), Buenos Aires, Rojas (Weiser).
    • Type-depositories: MHNG, NHMB.
    • Forel, 1914d: 265 (q.).
    • Subspecies of triangularis: Forel, 1914d: 265; Bruch, 1914: 213; Gallardo, 1918b: 41.
    • Junior synonym of triangularis: Brown, 1958g: 230, 323; Kempf, 1972a: 116; Bolton, 1995b: 210; Lattke, 1995: 190; Camacho, Franco, Branstetter, et al. 2022: 11.

Unless otherwise noted the text for the remainder of this section is reported from the publication that includes the original description.

Lattke (1995) - The number of transverse costulae on the petiolar dorsum can vary from 8 to 14, and those on the pronotum from 13 to 23. Specimens from Argentina tend to have a higher count but there is no gap separating the values. The length of the coxal teeth is variable and bears no relation to the number of petiolar costulae. Propodeal teeth also show variation form a low mound to the usual low, sharp teeth. Occasional specimens can have up to 4 transverse costulae on the anterior pronotal face, and rarely longitudinal costulae on the petiolar node. Other traits used by Santschi to separate Gnamptogenys aculeaticoxae, such as degree of impression of the promesonotal suture, gastric constriction and gauge of hairs, length vs. width of petiolar node and the mandibular costulation all show continuous variation that is best described as infraspecific.

Description

Karyotype

  • 2n = 24, karyotype = 18m + 6sm (Brazil) (Teixeira et al., 2019).
  • n = 10, 2n = 20 (French Guiana) (Mariano et al. 2015).

References

References based on Global Ant Biodiversity Informatics

  • Basset Y., L. Cizek, P. Cuenoud, R. K. Didham, F. Guilhaumon, O. Missa, V. Novotny, F. Odegaards, T. Roslin, J. Schmidl et al. 2012. Arthropod diversity in a tropical forest. Science 338(6113): 1481-1484.
  • 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.
  • Brown W. L., Jr. 1958. Contributions toward a reclassification of the Formicidae. II. Tribe Ectatommini (Hymenoptera). Bulletin of the Museum of Comparative Zoology 118: 173-362.
  • Cuezzo, F. 1998. Formicidae. Chapter 42 in Morrone J.J., and S. Coscaron (dirs) Biodiversidad de artropodos argentinos: una perspectiva biotaxonomica Ediciones Sur, La Plata. Pages 452-462.
  • Donoso D. A., G. Onore, G. Ramon, and J. E. Lattke. 2014. Invasive ants of continental Ecuador, a first account. REMCB 35: 133-141.
  • 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.
  • Fernández, F. and S. Sendoya. 2004. Lista de las hormigas neotropicales. Biota Colombiana Volume 5, Number 1.
  • Forster J.A. 2005. The Ants (hymenoptera: Formicidae) of Alabama. Master of Science, Auburn University. 242 pages.
  • Franco W., N. Ladino, J. H. C. Delabie, A. Dejean, J. Orivel, M. Fichaux, S. Groc, M. Leponce, and R. M. Feitosa. 2019. First checklist of the ants (Hymenoptera: Formicidae) of French Guiana. Zootaxa 4674(5): 509-543.
  • Gallardo A. 1918. Las hormigas de la República Argentina. Subfamilia Ponerinas. Anales del Museo Nacional de Historia Natural de Buenos Aires 30: 1-112.
  • INBio Collection (via Gbif)
  • Kaspari M., D. Donoso, J. A. Lucas, T. Zumbusch, and A. D. Kay. 2012. Using nutritional ecology to predict community structure: a field test in Neotropical ants. Ecosphere 3(11): art.93.
  • Kempf W. W. 1961. A survey of the ants of the soil fauna in Surinam (Hymenoptera: Formicidae). Studia Entomologica 4: 481-524.
  • Kempf, W.W. 1972. Catalago abreviado das formigas da regiao Neotropical (Hym. Formicidae) Studia Entomologica 15(1-4).
  • Kusnezov N. 1953. La fauna mirmecológica de Bolivia. Folia Universitaria. Cochabamba 6: 211-229.
  • Lattke J. E. 1995. Revision of the ant genus Gnamptogenys in the New World (Hymenoptera: Formicidae). Journal of Hymenoptera Research 4: 137-193
  • Lattke J. E., F. Fernández, T. M. Arias-Penna, E. E. Palacio, W. Mackay, and E. MacKay. 2008. Género Gnamptogenys Roger. Pp. 66-100 in: Jiménez, E.; Fernández, F.; Arias, T.M.; Lozano-Zambrano, F. H. (eds.) 2008. Sistemática, biogeografía y conservación de las hormigas cazadoras de Colombia. Bogotá: Instituto de Investigación de Recursos Biológicos Alexander von Humboldt, xiv + 609 pp.
  • Lattke, J. E. 1990b. Revisión del género Gnamptogenys Roger en Venezuela (Hymenoptera: Formicidae). Acta Terramaris 2: 1-47
  • Luederwaldt H. 1918. Notas myrmecologicas. Rev. Mus. Paul. 10: 29-64.
  • MacGown J. A., and J. K. Wetterer. 2011. Geographic spread of Gnamptogenys triangularis (Hymenoptera: Formicidae: Ectatomminae). Psyche 2012: Article ID 571430, (doi:10.1155/2012/571430):4 pp.
  • Pires de Prado L., R. M. Feitosa, S. Pinzon Triana, J. A. Munoz Gutierrez, G. X. Rousseau, R. Alves Silva, G. M. Siqueira, C. L. Caldas dos Santos, F. Veras Silva, T. Sanches Ranzani da Silva, A. Casadei-Ferreira, R. Rosa da Silva, and J. Andrade-Silva. 2019. An overview of the ant fauna (Hymenoptera: Formicidae) of the state of Maranhao, Brazil. Pap. Avulsos Zool. 59: e20195938.
  • 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.
  • Salazar F., and D. A. Donoso. 2013. New ant (Hymenoptera: Formicidae) records for Ecuador deposited at the Carl Rettenmeyer ant collection in the QCAZ Museum. Boletín Tecnico 11, Serie Zoológica 8-9: 151 – 177.
  • Santoandre S., J. Filloy, G. A. Zurita, and M. I. Bellocq. 2019. Ant taxonomic and functional diversity show differential response to plantation age in two contrasting biomes. Forest Ecology and Management 437: 304-313.
  • Santschi F. 1921. Ponerinae, Dorylinae et quelques autres formicides néotropiques. Bulletin de la Société Vaudoise des Sciences Naturelles 54: 81-103.
  • Santschi F. 1929. Révision du genre Holcoponera Mayr. Zoologischer Anzeiger. 82: 437-477.
  • 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.