Strumigenys maynei

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Strumigenys maynei
Scientific classification
Kingdom: Animalia
Phylum: Arthropoda
Class: Insecta
Order: Hymenoptera
Family: Formicidae
Subfamily: Myrmicinae
Tribe: Attini
Genus: Strumigenys
Species: S. maynei
Binomial name
Strumigenys maynei
Forel, 1916

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Specimen Labels

Synonyms

Often found nesting in rotten wood in the leaf litter layer, but also in rot holes in trees some distance above the ground. In Ghana, Bolton (1983) found a nest in a cocoa branch about 1.7 m above the ground. In Ivory Coast, S. maynei (2.5 mm long) nests together with Platythyrea conradti (15 mm long) in hollow branches (Yéo et al. 2006), while in Benin Taylor et al. (2018) found it mainly nesting in rotten wood on trees or in the leaf litter.

Identification

Bolton (2000) - A member of the Strumigenys lujae-group. Upper scrobe margin broad; apicoscrobal hair absent. Pronotal humeral hair absent. Pronotum dorsally (and usually also laterally) with dense costulate sculpture that is longitudinal to oblique; spaces between costulae smooth and glossy. Pleurae and side of propodeum reticulate-punctate. Dorsum of head and alitrunk with conspicuous short broadly spatulate ground-pilosity.

Bolton (1983) - S. maynei is characterized by its absence of flagellate hairs, generally strong costulate pronotal sculpture, broad upper scrobe margins and conspicuous ground-pilosity; it is unlikely to be confused with any other species. In distribution it appears to be restricted to the forest zones of West and central Africa, and Uganda. Georges Terron's collection has yielded a couple of small workers from Cameroun in which the pronotal sculpture is very reduced indeed. These may represent a separate sibling species but I suspect that they are more likely to be members of the first brood of a new colony.

The closest relative of maynei is Strumigenys geoterra, a species which shares the characters of broad upper scrobe margins, lack of flagellate hairs and very broad conspicuous ground-pilosity. However, in geoterra the entire alitrunk is glassy smooth and without trace of sculpture, the upper scrobe margins are very broad and strikingly convex, the cephalic ground-pilosity is even coarser than in maynei, there is an obvious impression separating the pronotum and mesonotum, the pronotal dorsal pilosity is strong and elevated, and the petiole node is smooth dorsally.

Keys including this Species

Distribution

Latitudinal Distribution Pattern

Latitudinal Range: 6.5° to -28.66667°.

   
North
Temperate 		North
Subtropical 		Tropical South
Subtropical 		South
Temperate

Distribution based on Regional Taxon Lists

Afrotropical Region: Angola, Benin, Burundi, Cameroun, Democratic Republic of Congo (type locality), Equatorial Guinea, Gabon, Gambia, Ghana, Guinea, Guinea-Bissau, Ivory Coast, Kenya, Nigeria, South Africa, Uganda, United Republic of Tanzania, Zimbabwe.
Malagasy Region: Madagascar.

Distribution based on AntMaps

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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

In Ivory Coast, Strumigenys (=Pyramica) maynei (2.5 mm long) enjoys a commensal relationship with Platythyrea conradti (15 mm long) (Yéo et al. 2006). The two species frequently nest together in hollow branches. P. maynei has its own network of small galleries in the rotten sapwood, with connections to chambers inhabited by Platythyrea conradti. The brood of both species are kept completely separate. In the laboratory, S. maynei scavenged food from P. conradti 's chambers (Yéo et al. 2006). One of the workers returning to this nest was carrying a small nematoceran fly (Bolton 1983)

Commensal association between Strumigenys maynei and Platythyrea conradti. Photo by Patrick Landmann.

Parmentier et al. (2017) investigated the mutual benefits for the two partner species. S. maynei was highly efficient at nest defense against intranidal arthropods and alien ant intruders, whereas they took advantage of small prey thriving in the organic nest material collected by large P. conradti.


Workers and brood of Strumigenys maynei'. Photo by Patrick Landmann.

Castes

Male

Strumigenys maynei fmnhins0000083130 h 1 high.jpgStrumigenys maynei fmnhins0000083130 p 1 high.jpgStrumigenys maynei fmnhins0000083130 d 1 high.jpgStrumigenys maynei fmnhins0000083130 l 1 high.jpg
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Nomenclature

  • maynei. Strumigenys (Trichoscapa) maynei Forel, 1916: 427 (w.q.m.) DEMOCRATIC REPUBLIC OF CONGO. Combination in S. (Cephaloxys): Wheeler, W.M. 1922a: 920; Emery, 1924d: 324; in Serrastruma: Brown, 1952e: 77; in Pyramica: Bolton, 1999: 1673; in Strumigenys: Baroni Urbani & De Andrade, 2007: 123. Senior synonym of latiuscula: Brown, 1952e: 77. See also: Bolton, 1983: 347; Bolton, 2000: 316.

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

Description

Worker

Bolton (1983) - TL 2.3-3.0, HL 0.52-0.66, HW 0.44-0.54, CI 78-86, ML 0.18-0.24, MI 32-39, SL 0.34-0.42, SI 73-83, PW 0·31-0·41, AL 0·62-0·82 (45 measured).

Mandibular denticles regular, without a suddenly enlarged series of 4-8 denticles basally but often with the basalmost denticle larger than those preceding. Upper scrobe margins strongly developed into broad projecting flanges which run the length of the scrobe and do not peter out posteriorly, the margins without flagellate hairs present. Clypeus sculptured, finely punctulate to granular, with short but broad spatulate ground-pilosity and a row of longer spatulate hairs projecting forwards over the bases of the mandibles from the false anterior clypeal margin. Dorsum of head strongly reticulate-punctate, with conspicuous short but broad spatulate ground-pilosity. In profile the cephalic dorsum behind the highest point of the vertex with 4-6 stout standing hairs which are narrowly to moderately clavate apically, the variation in number occurring in single nest-series. Usually 4 such hairs are present, situated in a row in front of the occipital margin; rarely a pair is present anterior to this row. Alitrunk in profile with promesonotum shallowly convex and sloping more steeply posteriorly to the impressed metanotal groove. Propodeum convex dorsally, on a lower level than the promesonotum and terminating posteriorly in a pair of triangular teeth which are subtended by conspicuous spongiform infradental lamellae. Sides of pronotum longitudinally costulate, usually distinctly so but sometimes the costulae effaced in places or becoming weaker lower down the sides; the spaces between the costulae smooth. Pleurae and sides of propodeum densely reticulate-punctate. Pronotal dorsum longitudinally to obliquely strongly costulate, the spaces between the costulae smooth; this sculpture usually weaker in small workers than in large. Remainder of dorsal alitrunk strongly reticulate-punctate. Flagellate hairs usually absent from pronotal humeri (present in only a single specimen of those examined). Mesonotum with a single pair of curved standing clavate hairs. Ground pilosity of dorsal alitrunk dense spatulate and very conspicuous. Spongiform appendages of pedicel segments moderately developed in profile. The petiole with a ventral lamella and small lateral processes, the postpetiole with a well developed ventral lobe and smaller lateral lobe. Petiole in dorsal view reticulate-punctate, sometimes only superficially so, with a narrow transverse spongiform strip posteriorly. Postpetiole dorsally smooth to superficially punctulate, sometimes with a suggestion of minute longitudinal striae; with a narrow posterior spongiform strip which abuts a similar strip on the base of the first gastral tergite. Basigastral costulae short. Dorsal surfaces of petiole, postpetiole and gaster with stout apically clavate hairs. Colour dull brownish yellow to mid-brown.

Type Material

Bolton (1983) - Syntype workers, female, male, ZAIRE: Stanleyville (= Kisangani) (Kohl) (Musee d'Histoire Naturelle Genève; Musee Royal de I' Afrique Centrale; Museum of Comparative Zoology) [examined].

References

References based on Global Ant Biodiversity Informatics

  • Bolton B. 1983. The Afrotropical dacetine ants (Formicidae). Bulletin of the British Museum (Natural History). Entomology 46: 267-416.
  • Bolton, B. 2000. The Ant Tribe Dacetini. Memoirs of the American Entomological Institute 65
  • Borowiec L., and S. Salata. 2018. Notes on ants (Hymenoptera: Formicidae) from Gambia (Western Africa). Annals of the Upper Silesian Museum in Bytom Entomology 26: 1-13.
  • CSIRO Collection
  • Field Museum Collection, Chicago, Illinois (C. Moreau)
  • Garcia F.H., Wiesel E. and Fischer G. 2013.The Ants of Kenya (Hymenoptera: Formicidae)—Faunal Overview, First Species Checklist, Bibliography, Accounts for All Genera, and Discussion on Taxonomy and Zoogeography. Journal of East African Natural History, 101(2): 127-222
  • IZIKO South Africa Museum Collection
  • Kone M., S. Konate, K. Yeo, P. K. Kouassi, and K. E. Linsenmair. 2012. Changes in ant communities along an age gradient of cocoa cultivation in the Oumé region, central Côte d’Ivoire. Entomological Science 15: 324–339.
  • Siqueira de Castro F., A. B. Gontijo, P. de Tarso Amorim Castro, and S. Pontes Ribeiro. 2012. Annual and Seasonal Changes in the Structure of Litter-Dwelling Ant Assemblages (Hymenoptera: Formicidae) in Atlantic Semideciduous Forests. Psyche doi:10.1155/2012/959715
  • Siqueira de Castro F., A. B. Gontijo, W. Duarte da Rocha, and S. Pontes Ribeiro. 2011. As comunidades de formigas de serapilheira nas florestas semidecíduas do Parque Estadual do Rio Doce, Minas Gerais. MG.BIOTA, Belo Horizonte 3(5): 5-24.
  • Taylor B., N. Agoinon, A. Sinzogan, A. Adandonon, Y. N'Da Kouagou, S. Bello, R. Wargui, F. Anato, I. Ouagoussounon, H. Houngbo, S. Tchibozo, R. Todjhounde, and J. F. Vayssieres. 2018. Records of ants (Hymenoptera: Formicidae) from the Republic of Benin, with particular reference to the mango farm ecosystem. Journal of Insect Biodiversity 8(1): 006–029.
  • Yanoviak S. P., B. L. Fisher, and A. Alonso. 2007. Arboreal ant diversity (Hymenoptera: Formicidae) in a central African forest. African Journal of Ecology. 46(1): 60-66.
  • Yeo K., S. Konate, S. Tiho, and S. K. Camara. 2011. Impacts of land use types on ant communities in a tropical forest margin (Oumé - Cote d'Ivoire). African Journal of Agricultural Research 6(2): 260-274.
  • Yeo, K., M. Molet and C. Peeters. 2006. When David and Goliath share a home: Compound nesting of Pyramica and Platythyrea ants. Insectes Sociaux 53:435-438
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