One of the few Oxyepoecus that has been collected from a nest that is not associated with another ant species.
Kempf (1974) - As regards mandibular shape, i. e. the basal tooth stout and separated from the remaining teeth by a deep cleft, punctifrons resembles Oxyepoecus mandibularis, which differs in having the entire cephalic and thoracic dorsum sculptured and opaque. The predominantly smooth and shining integument and the large eyes remind of Oxyepoecus inquilinus, the latter having, however, long, subfalcate mandibles, more sharply denticulate clypeus, a heavier, thick-set thorax, a well developed propodeal armature with prominent spines, strongly antero-posteriorly compressed and laterally expanded petiolar node, and the posterior surface of postpetiole heavily transversely costulate.
Finally, punctifrons diverges from Oxyepoecus crassinodus by lighter color, larger eyes, longer scape, the only shallowly impressed metanotal groove, the weak to often obsolete sculpture on sides of thorax and basal face of propodeum, the lack of transverse costulae on posterior surface of postpetiole.
Keys including this Species
Known from several localities within southeast and south Brazil, all in the “Mata Atlântica” Domain (Albuquerque and Brandão 2004).
Distribution based on Regional Taxon Lists
Distribution based on AntMaps
Distribution based on AntWeb specimens
Check data from AntWeb
While scant, the biological information about this species has been helpful in revealing that species within the genus, as noted below, can exist in their own nests.
Known O. punctifrons specimens were collected mainly in the leaf litter, however two workers and one gyne were founded interestingly in the canopy of an “Angico” tree Anandenanthera (Leguminosae) (Albuquerque and Brandão 2004).
The following account of the biology of species within the genus is based on, and modified from, Kempf (1974) and Albuquerque and Brandão (2009).
Our knowledge of Oxyepoecus ants still rests exclusively on chance discoveries. Since about 95% of the known specimens were taken as strays in berlesates of forest floor cover, very little may be said about the biology of Oxyepoecus species except for being denizens or at least foragers in this particular habitat. The minute size of Oxyepoecus, their color and cryptic habits hamper direct observation of their habits in natural conditions (especially inside shaded forest where light rarely reaches the ground).
Oxyepoecus has been considered very rare in collections, but our studies show that they are rather common in the leaf litter of most localities where recent surveys have been conducted in the Mata Atlântica (see Comments in Albuquerque & Brandão, 2004). It is interesting to note that one of these localities we recently surveyed, Cunha, São Paulo state has four Oxyepoecus species (Oxyepoecus myops, Oxyepoecus rastratus, Oxyepoecus longicephalus and Oxyepoecus rosai), three of which were found in one square meter of leaf-litter (sample 48; all but O. rosai). In Salesópolis, SP, we recorded five of the 17 known Oxyepoecus species (O. myops, Oxyepoecus punctifrons, O. rastratus, O. rosai and Oxyepoecus vezenyii). Both Cunha and Salesópolis are localities circa 1000 m above sea level, covered by pristine evergreen dense forest.
Although Oxyepoecus samples come mostly from forested localities, workers have been less frequently collected in places with more open vegetation, as open “cerrados” (savannas). Comparing the examined material of most species, one can see that the specimens mostly come from the same localities. This is because these localities we surveyed recently, extracting ants from the leaf-litter, or localities where careful collectors lived most of their lifes (Seara, SC, for instance, where F. Plaumann worked many years).
Kusnezov (1952) put forward the hypothesis that Oxyepoecus ants are inquilines of Pheidole and Solenopsis nests. Evidence exists for their being symbiotic relationships between several Oxyepoecus species and other Myrmicinae ants (details provided here). Independent colonies seem to be vouched for by Oxyepoecus punctifrons and Oxyepoecus rastratus. The types of the former, collected at Rio Negro, Paraná State, Brazil, came from a nest that had over 60 workers living by themselves, but no further information is available. A few workers of the same species, at Campos do Jordão, São Paulo State, Brazil, were also found on a dead twig, between the bark and an overgrown cover consisting of lichens and mosses. The types of the var. luederwaldti (= rastratus) are from a very small colony nesting under the bark in a simple cavity within the alburnum of a tree (Luederwaldt, 1926: 275). Lenko's rastratus specimens from Caraça, Minas Gerais State, had their nest within a decaying log on the ground in a forest. A similar nesting situation was found from a more recent collection from Paraguay (col A. Wild).
The fact that Oxyepoecus workers are relatively abundant in material extracted from leaf litter samples, while dealate gynes are seldom found in the litter and larvae have never been found in litter samples, suggests that they nest in the soil, where the gynes and larvae live, but workers leave the nest periodically to search for food. Oxyepoecus has been attracted to honey or sardine baits set over the ground in different habitats, which suggests they are generalist foragers. In just one case, a gyne and two workers of O. punctifrons (Vezenyii group) were found by Rogerio R. da Silva under the bark of a the canopy branch in a recently fallen Leguminoseae (Albuquerque & Brandão, 2004).
Males have not been collected.
The following information is derived from Barry Bolton's New General Catalogue, a catalogue of the world's ants.
- punctifrons. Monomorium punctifrons Borgmeier, 1927b: 63 (w.) BRAZIL. [Also described as new by Borgmeier, 1928a: 39.] Wheeler, G.C. & Wheeler, J. 1977: 586 (l.). Albuquerque & Brandão, 2004: 71 (q.). Combination in Martia: Kusnezov, 1952h: 722; in Oxyepoecus: Ettershank, 1966: 146. See also: Kempf, 1974b: 495.
Unless otherwise noted the text for the remainder of this section is reported from the publication that includes the original description.
Kempf (1974) - (lectotype). Total length 3.2 (2.7-3.4) mm; head length 0.73 (0.64-0.79) mm; head width 0.59 (0.49-0.67) mm; scape length 0.53 (0.48-0.57) mm; maximum diameter of eyes 0.14 (0.11-0.15) mm; Weber's length of thorax 0.89 (0.77-0.98) mm; maximum width of pronotum 0.40 (0.36-0.47) mm; hind femur length 0.63 (0.55-0.68) mm; petiole width 0.20 (0.16-0.21) mm; postpetiole width 0.27 (0.23-0:32) mm; cephalic index 80 (77-85). Color reddish yellow. Integument smooth and shining with the following exceptions: frontal carinae laterad of posteromedian extension of clypeus finally costulate, the costulae not extending posteriorly beyond the frontal carinae; cheeks finely costulate, the costulae not attaining the anterior border of the eyes; mesopleura and inferior half of metapleura finely and superficially horizontally costulate; basal face of propodeum superficially, nearly indistinctly, transversely costulate. Piligerous punctures quite conspicuous on dorsum of head. Hairs abundant, long standing hairs on dorsum of head, thorax, petiole, postpetiole and on gaster; shorter, inclined hairs interspersed with the long hairs principally on head and on gaster; short, oblique hairs on sides of head, on antennae and legs.
Head. Mandibles subtriangular, the basal border as long as chewing border; basal tooth stout, separated from the subbasal tooth by a deep cleft. Antero-median apron of clypeus protruding, laterally carinate, the carinae diverging cephalad, terminating in front in a short, relatively little projecting tooth which is flanked laterally by a minute, obtuse, lobelike denticle. Frontal area impressed, smooth and shining, well delimited from clypeus. Frontal carinae little expanded laterad, short, terminating at level of anterior orbit of eyes, the distance between the subparallel outer edges subequal to one fourth of the maximum head width. Eyes relatively large, moderately convex, their distance from the mandibular insertion equal to thejr greatest diameter which has approximately 11 facets in a row, the total number being about 50 ommatidia in all. Antennal scapes relatively long, their apex attaining the occipital corner when laid back-over the head as much as possible. Funicular segment I longer than VIII and IX taken individually, as long as II-IV combined, segment II as long as broad, segment III-VII nearly as long as broad, segments VIII and IX slightly longer than broad.
Thorax. Shoulders absolutely rounded, not marked, dorsum of pronotum not marginate on sides, promesonotal suture absent. Metanotal groove slightly impressed in profile, metanotal suture present. Basal face of propodeum about twice as long as broad, laterally immarginate, posterior corner with a small, not prominent, rectangular tooth; sides of declivous face submarginate, not carinate. The costulae and striae on metapleura extend over the distinct bulla of the metasternal gland.
Petiole and postpetiole. Petiole briefly pedunculate, club-shaped in dorsal view, the node proper not compressed antero-posteriorly nor laterally expanded, anterior surface of node strictly oblique in profile. Subpetiolar carina sharp, terminating in front in a small tooth. Postpetiole likewise scarcely compressed antero-posteriorly and little expanded laterad, the lateral projections short, blunt and bulky, the posterior surface nearly devoid of transverse costulae or rugae, except for one or two vestigial ones just above the articular collar. Gaster scarcely excised in front.
Variation. The divergence in size is noticeable as borne out by the measurements of the type series already given above. The additional specimens keep themselves more or less within the same limits, as shown by the range of the following measurements: head length 0.60-0.81 mm; head width 0.48-0.67 mm; scape length 0.44-0.55 mm; thorax length 0.76-0.96 mm; hind femur length 0.49-0.63 mm.
The development of the propodeal armature varies from merely obtuse or feebly tuberculate propodeal corners (smaller specimens) to neatly denticulate ones (larger specimens). The longitudinal costulae inside of the frontal carinae are quite constant with the exception of the Campos do Jordão (São Paulo State) specimens, which have them extended further back, in the fashion of crassinodus. The sculpture on the sides of thorax may be nearly absent (especially on mesopleura), or as in the description, or even stronger, as in the Campos do Jordão series. The same applies to the transverse costulae on basal face of propodeum, which vary between sharply expressed and nearly absent, the condition being to some extent dependent on overall size.
Albuquerque and Brandao (2004) - (ergatomorphic): t.l.= 3.32; h.l.= 0.67; h.w.= 0.55; s.l.= 0.55; m.l.e.= 0.15; m.w.pr.= 0.50; a.l.= 0.95; h.f.l.= 0.46; m.w.p.= 0.18; m.w.pp.= 0.35; c.i. 82. Resembling worker, with the head similar except for the presence of minute occelli, their diameter less than the minimum thickness of the antennal scape. Compound eyes almost equal to the worker, somewhat convex, with some 13 facets r.g.d., total number of ommatidia circa 60. Antennal segments (scape and funiculus) equal to the workers. Mesosoma with blunt marked shoulders; pronotum smooth and shining. Mesonotum (scutum and scutellum) relatively large, 2/3 of the mesosoma; scutum smooth and shining with some piligerous punctulae; scutellum entirely smooth. Mesopleuron with the anepisternum and katepisternum separated by a shallow groove, both with some very fine, almost imperceptible and oblique costulae. Dorsal face of the propodeum transversely costate, with 13-15 fine costulae, which continue downwards and obliquely forwards on the sides. Propodeal teeth short and blunt. Petiole not much compressed, almost club shaped, the subpetiolar process straight, ending anteriorly as a blunt and small denticle. Postpetiole twice broader than the petiole node, subpostpetiolar process somewhat developed as two small and transverse crests.
Kempf (1974) - 64 workers from the same colony, taken by the late Father Miguel Witte, O.F.M., at Rio Negro, Paraná State, Brazil, in April 1925 (TB n. 424, lectotype and paratypes).
- Albuquerque, N. L. d. and C. R. F. Brandão. 2004. A revision of the Neotropical Solenopsidini ant genus Oxyepoecus Santschi, 1926 (Hymenoptera: Formicidae: Myrmicinae). 1. The Vezenyii species-group. Papéis Avulsos de Zoologia (São Paulo). 44:55-80. DOI: 10.1590/S0031-10492004000400001 (page 71, worker, queen (ergatomorph) described)
- Albuquerque, N. L. d. and C. R. F. Brandão. 2009. A revision of the Neotropical Solenopsidini ant genus Oxyepoecus Santschi, 1926 (Hymenoptera: Formicidae: Myrmicinae): 2. Final. Key for species and revision of the Rastratus species-group. Papéis Avulsos de Zoologia (São Paulo). 49:289-309.
- Borgmeier, T. 1927b. Algumas novas formigas brasileiras. Arch. Mus. Nac. (Rio J.) 29: 57-65 PDF (page 63, worker described)
- Ettershank, G. 1966. A generic revision of the world Myrmicinae related to Solenopsis and Pheidologeton (Hymenoptera: Formicidae). Aust. J. Zool. 14: 73-171 (page 146, Combination in Oxyepoecus)
- Kempf, W. W. 1974b. A review of the Neotropical ant genus Oxyepoecus Santschi (Hymenoptera: Formicidae). Stud. Entomol. 17: 471-512 (page 495, see also)
- Kusnezov, N. 1952k . Acerca de las hormigas simbióticas del género Martia Forel (Hymenoptera, Formicidae). Acta Zool. Lilloana 10: 717-722 (page 722, Combination in Martia)
- Wheeler, G. C.; Wheeler, J. 1977a. Supplementary studies on ant larvae: Myrmicinae. Trans. Am. Entomol. Soc. 103: 581-602 (page 586, larva described)