A small number of collections have been made, with most from litter sampling in rainforest.
- 1 Identification
- 2 Distribution
- 3 Biology
- 4 Castes
- 5 Nomenclature
- 6 References
- 7 References based on Global Ant Biodiversity Informatics
Bolton (2000) - A member of the Strumigenys loriae-group. The shape of the mandible in chyzeri often varies between populations and in some samples even varies between workers from the same nest-series. In particular, variation in the maximum width of the mandible in relation to its length in full-face view, is apparent. Also there is variation in the relative length and thickness of the preapical tooth, and the degree to which it overhangs the inner mandibular margin. To some extent the first of these seems usually to be size-related as larger individuals frequently have more slender mandibles and smaller individuals have stouter mandibles. These variations appear to have no significance in the species-rank taxonomy.
Newly synonymised above are Mann’s Solomon Islands species Strumigenys antaeus and the infraspecific Strumigenys foscior. Mann (1919) recognised that antaeus was very close to chyzeri but said that the “deeply excavated clypeus readily distinguishes antaeus from chyzeri Emery which has the anterior border arcuate.” In fact, type-material and all other samples of chyzeri have the clypeal margin the same shape as in antaeus. Series of antaeus are paler in colour than is usual, being dull brownish yellow where samples of chyzeri from most of its range are mid-brown to blackish brown, though paler samples are not unknown in both New Guinea and Australia. In fact, the type-series of foscior is considerably darker than antaeus and more closely approximates the usual shades seen in chyzeri.
In the regional fauna there are two other groups in which the preapical tooth of the mandible arises from the dorsal surface of the mandible rather than from its usual location on the inner margin, the wallacei-group and the fuarda-group. Neither of these has the complex shape of cephalic dorsolateral margin and head capsule possessed by chyzeri (see group diagnosis, above). There are other striking differences. For instance in the wallacei-group the ventral surface of head anteriorly has a single broad deep transverse trench that in profile occupies all the space between the posterior margin of the buccal cavity and the level of the eye; this represents a fusion of the postbuccal groove and the ventral preocular impression into a single exaggerated trench. In chyzeri the postbuccal groove and the preocular impression are separate. In fuarda the ventral surface of the head bears no impressions at all except for an extremely shallow feeble postbuccal groove.
Within the loriae-group the oddly placed and shaped preapical tooth is immediately diagnostic. In several collections workers of chyzeri have been found mounted upon the same pins as specimens of loriae, the two should not be confused.
Keys including this Species
Distribution based on Regional Taxon Lists
Distribution based on AntMaps
Distribution based on AntWeb specimens
Check data from AntWeb
Strumigenys were once thought to be rare. The development and increased use of litter sampling methods has led to the discovery of a tremendous diversity of species. Many species are specialized predators (e.g. see Strumigenys membranifera and Strumigenys louisianae). Collembola (springtails) and other tiny soil arthropods are typically favored prey. Species with long linear mandibles employ trap-jaws to sieze their stalked prey (see Dacetine trap-jaws). Larvae feed directly on insect prey brought to them by workers. Trophallaxis is rarely practiced. Most species live in the soil, leaf litter, decaying wood or opportunistically move into inhabitable cavities on or under the soil. Colonies are small, typically less than 100 individuals but in some species many hundreds. Moist warm habitats and micro-habitats are preferred. A few better known tramp and otherwise widely ranging species tolerate drier conditions. Foraging is often in the leaf litter and humus. Workers of many species rarely venture above ground or into exposed, open areas. Individuals are typically small, slow moving and cryptic in coloration. When disturbed individuals freeze and remain motionless. Males are not known for a large majority of species.
The following information is derived from Barry Bolton's Online Catalogue of the Ants of the World.
- chyzeri. Strumigenys chyzeri Emery, 1897c: 576, pl. 14, figs. 4-6 (w.q.m.) NEW GUINEA. Senior synonym of antaeus, fuscior: Bolton, 2000: 859.
- antaeus. Strumigenys antaeus Mann, 1919: 355, fig. 34 (w.) SOLOMON IS. Junior synonym of chyzeri: Bolton, 2000: 859.
- fuscior. Strumigenys antaeus var. fuscior Mann, 1919: 357 (w.) SOLOMON IS. Junior synonym of chyzeri: Bolton, 2000: 860.
Unless otherwise noted the text for the remainder of this section is reported from the publication that includes the original description.
TL 2.5-3.2, HL 0.78-1.00, HW 0.65-0.87, CI 80-87, ML 0.36-0.50, MI 45-52, SL 0.44-0.59, SI 63-75, PW 0.30-0.39, AL 0.68-0.88 (35 measured). In full-face view preapical tooth of mandible arises from about the midwidth of the dorsal surface, at or close to the point where the mandible is broadest; preapical tooth very obviously not arising from the inner margin. From its origin the preapical tooth arcs medially across the mandible and up to half its length projects beyond the inner mandibular margin. In full-face view side of head in front of preocular impression convex but not expanded into a triangular or conical projecting process. Apical antennomere spindle-shaped, strongly constricted basally and narrowly articulated to preapical antennomere. In profile cephalic dorsum at highest point of vertex and near occipital margin with short stiff standing hairs; such hairs absent from concavity of transverse dorsal impression. Promesonotal standing pilosity stiff and short, restricted to a pair on pronotum close to anterodorsal margin, the humeral pair, and a single mesonotal pair. Pleurae and side of propodeum densely reticulate-punctate. Propodeal spines slender, straight or very shallowly upcurved. Dorsal (outer) surfaces of middle and hind basitarsi without erect long fine hairs. Lateral spongiform lobe of petiole little more than an extension of the collar. Ventral spongiform strip on petiole very reduced, in some samples present only beneath node, petering out beneath peduncle; in others present as a narrow crest that extends the length of the segment. Petiole node in dorsal view varying from broader than long to slightly longer than broad. Disc of postpetiole sometimes mostly smooth, varying from this to uniformly reticulate-punctate. Basigastral costulae shorter than to about equal to length of disc of postpetiole. Standing hairs on first gastral tergite short and stiff.
Syntype workers, queen and male, PAPUA NEW GUINEA: Madang ( = Friedrich-Wilhelmshafen), and near Aitape ( = Berlinhafen) (L. Biro) (Hungarian Natural History Museum, Museo Civico di Storia Naturale, Genoa, Naturhistorisches Museum Wien, Vienna) [examined].
- Syntype, workers, queen(s), male(s), Madang (as Friedrich-Wilhelmshafen) and near Aitape (as Berlinhafen), Papua New Guinea, Museo Civico di Storia Naturale, Genoa.
- Syntype, workers, queen(s), male(s), Madang (as Friedrich-Wilhelmshafen) and near Aitape (as Berlinhafen), Papua New Guinea, Naturhistorisches Museum Wien, Vienna.
- Bolton, B. 2000. The ant tribe Dacetini. Memoirs of the American Entomological Institute. 65:1-1028. (page 859, figs. 459, 503 redescription of worker, senior synonym of antaeus ( and its var. fuscior))
- Emery, C. 1897c. Formicidarum species novae vel minus cognitae in collectione Musaei Nationalis Hungarici quas in Nova-Guinea, colonia germanica, collegit L. Biró. Természetr. Füz. 20: 571-599. (page 576, pl. 14, figs. 4-6 worker, queen, male described)
- Emery, C. 1924f . Hymenoptera. Fam. Formicidae. Subfam. Myrmicinae. [concl.]. Genera Insectorum 174C: 207-397 (page 321, catalogue)
- Wheeler, W. M. 1935g. Check list of the ants of Oceania. Occas. Pap. Bernice P. Bishop Mus. 11(1 11: 1-56 (page 32, checklist)
References based on Global Ant Biodiversity Informatics
- Andersen A. N., M. Houadria, M. Berman, and M. van der Geest. Rainforest ants of the Tiwi Islands: a remarkable centr of endemism in Australia's monsoonal tropics. Insectes Sociaux 59: 433-441.
- Bolton, B. 2000. The Ant Tribe Dacetini. Memoirs of the American Entomological Institute 65
- CSIRO Collection
- Chapman, J. W., and Capco, S. R. 1951. Check list of the ants (Hymenoptera: Formicidae) of Asia. Monogr. Inst. Sci. Technol. Manila 1: 1-327
- Dahl F. 1901. Das Leben der Ameisen im Bismarck-Archipel, nach eigenen Beobachtungen vergleichend dargestellt. Mitt. Zool. Mus. Berl. 2: 1-70.
- Emery C. 1897. Formicidarum species novae vel minus cognitae in collectione Musaei Nationalis Hungarici quas in Nova-Guinea, colonia germanica, collegit L. Biró. Természetrajzi Füzetek 20: 571-599.
- Forel A. 1901. Formiciden aus dem Bismarck-Archipel, auf Grundlage des von Prof. Dr. F. Dahl gesammelten Materials. Mitt. Zool. Mus. Berl. 2: 4-37.
- Janda M., G. D. Alpert, M. L. Borowiec, E. P. Economo, P. Klimes, E. Sarnat, and S. O. Shattuck. 2011. Cheklist of ants described and recorded from New Guinea and associated islands. Available on http://www.newguineants.org/. Accessed on 24th Feb. 2011.
- Lucky A., L. E. Alonso, E. Sarnat, and J. Hulr. 2015. Ants and scolytine beetles. In: Richards, S.J. and N. Whitmore (editors) 2015. A rapid biodiversity assessment of Papua New Guinea's Hindenburg Wall region. Wildlife Conservation Society Papua New Guinea Program. Goroka, PNG.
- Mann W. M. 1919. The ants of the British Solomon Islands. Bulletin of the Museum of Comparative Zoology 63:273-391.
- Mann William. 1916. The Ants of the British Solomon Islands. Bulletin of the Museum of Comparative Zoology at Harvard College 63(7): 273-391
- Mann, W.M. 1919. The ants of the British Solomon Islands. Bulletin of the Museum of Comparative Zoology of Harvard College 63: 273-391
- Room P. M. 1975. Diversity and organization of the ground foraging ant faunas of forest, grassland and tree crops in Papua Nez Guinea. Aust. J. Zool. 23: 71-89.
- Room, P.M. 1975. Relative Distributions of Ant Species in Cocoa Plantations in Papua New Guinea Relative Distributions of Ant Species in Cocoa Plantations in Papua New Guinea. Journal of Applied Ecology 12(1):47-61
- Snelling R. R. 2000. Ants of the Wapoga river area, Irian Jaya, Indonesia. In Mack, Andrew L. and Leeanne E. Alonso (eds.). 2000. A Biological Assessment of the Wapoga River Area of Northwestern Irian Jaya, Indonesia. RAP Bulletin of Biological Assessment 14, Conservation International, Washington, DC.
- Viehmeyer H. 1912. Ameisen aus Deutsch Neuguinea gesammelt von Dr. O. Schlaginhaufen. Nebst einem Verzeichnisse der papuanischen Arten. Abhandlungen und Berichte des Königlichen Zoologischen und Anthropologische-Ethnographischen Museums zu Dresden 14: 1-26.
- Viehmeyer H. 1914. Papuanische Ameisen. Deutsche Entomologische Zeitschrift 1914: 515-535.
- Wheeler W.M. 1935. Check list of the ants of Oceania. Occasional Papers of the Bernice Pauahi Bishop Museum 11(11):1-56.
- Wheeler, William Morton.1935.Checklist of the Ants of Oceania.Occasional Papers 11(11): 3-56