| Anochetus hohenbergiae|
Feitosa & Delabie, 2012
The largest species in the genus, Anochetus hohenbergiae is an arboreal nesting ant.
- 1 Identification
- 2 Distribution
- 3 Biology
- 4 Castes
- 5 Nomenclature
- 6 References
Feitosa & Delabie (2012) - Size very large in comparison to the Neotropical species known in the genus (TL > 12.70); HL + ML > 4.30; posterior margin of head strongly concave; mandibles with a row of 13–16 teeth in the masticatory margin; propodeum unarmed; petiolar node with a single, reduced apical tooth.
Anochetus hohenbergiae shares its large size, elongate body and serially dentate mandibles with members of the emarginatus group, a Neotropical species-complex proposed by Brown (1978). This species can be guided to the couplet 3 of Brown’s key (1978: 572) where it is stranded due the petiolar characteristics which do not fit any of the alternatives. In fact, A. hohenbergiae is unlikely to be confounded with any other Anochetus species. This is the largest species in the genus, and the combination of abundant pilosity, posterior margin of head strongly concave, mandibles with a row of 13–16 teeth in the masticatory margin, propodeum unarmed, and petiolar node with a single, reduced apical tooth is unique in the genus. This species shares the exceptionally large body size with Anochetus elegans (TL 12.24–12.51 mm); however A. hohenbergiae is even larger (TL > 12.70) and lacks the pair of blunt petiolar spines of A. elegans.
Keys including this Species
Anochetus hohenbergiae is known only from three localities in southern state of Bahia, Northeastern Brazil.
Distribution based on Regional Taxon Lists
Check distribution from AntMaps.
Distribution based on specimens
Feitosa & Delabie (2012) - Several years ago (1992), three dealate gynes of Anochetus hohenbergiae were collected together at the base of an unidentified epiphyte on a 23 m high tree in the CEPLAC experimental areas at Ilheus, suggesting that pleometrotic colony founding may occur (Delabie, pers. obs.). During the following years a single gyne and two workers were collected in the same locality, but no information was obtained on their habits, except that at least one of the workers was collected foraging on the ground in a cocoa plantation.
Recently, a survey of canopy ants in native and introduced trees used to shade cocoa plantations at the same locality and in Una county (67 km S of Ilheus), revealed new specimens, all of them associated with epiphytic bromeliads. Six dealate gynes and two workers were found associated with several individuals belonging to two Bromeliaceae species: Hohenbergia blanchetii (Baker) E. Morren ex Mez, and Hohenbergia sp. At Ilheus, the bromeliads were fixed at 12–16 meters high to a single tree (24 meters high), Erythrina fusca Loureiro (Leguminosae, Fabaceae), an introduced species commonly used to shade cocoa plantations (Delabie et al. 2007). At Una, the ants were found at the base of Hohenbergia spp. on two different native trees, Enterolobium contortisiliquum (Vell.) Morong (Leguminosae, Mimosoideae) and Rollinia laurifolia Schlecht. (Annonaceae), at 14 and 19 meters high (the trees were 21 and 28 meters high, respectively). Each gyne was associated with a single bromeliad, which suggests that they were probably founding colonies.
An astigmatine mite (Acari: Sarcoptiformes: Astigmatina) was found attached to the body of one of the workers. The mite was in the hypopus stage, an heteromorphic deutonymph which is a resistant form that lacks mouthparts, has a closed gut, is highly resistant to environmental stress, and commonly has ventral suckers with which it secures attachment to insects and other animals when searching for suitable sites to achieve its full development. The relationship generally is restricted to phoretic dispersal in that these nymphs lack functional mouthparts (Walter & Krantz 2009).
The scarcity of A. hohenbergiae in collections is in part because colonies are restricted to the canopy of scattered trees in the forest. Given the large size of the individuals and restricted nesting habitat, colonies of this species are probably small (<100 individuals), as common for most Anochetus species.
According to Brown (1978: 560), members of the emarginatus group of Anochetus are arboreal or semiarboreal foragers that often nest in hollow branches or in epiphytes or between palm leaf bases well above ground level. This is also the case with A. hohenbergiae, which probably nest between the lateral leaves of bromeliads or in galleries along the Hohenbergia roots. Nevertheless, there are two species recently described for the group that are known to nest in the ground: A. elegans and A. miserabilis. In spite of shared morphological features, the emarginatus group is quite heterogeneous biologically.
Brown (1978: 553) mentions that ergatoid gynes are fairly common in Anochetus and are probably the only functional queens in some groups, including the emarginatus group. However, current studies report the occurrence of gamergates (reproductive workers) in Anochetus emarginatus (Fabricius 1804) (Chris Starr, in prep.). Longino (2007) suggests that another species in the group, A. striatulus Emery 1890, may also have gamergates, Gonzalez-Campero & Elizalde (2008) described winged gynes of Anochetus miserabilis, a species also placed in the emarginatus group.
DaRocha et al. (2015) studied the diversity of ants found in bromeliads of a single large tree of Erythrina, a common cocoa shade tree, at an agricultural research center in Ilhéus, Brazil. Forty-seven species of ants were found in 36 of 52 the bromeliads examined. Bromeliads with suspended soil and those that were larger had higher ant diversity. Anochetus hohenbergiae was found in 5 different bromeliads but was associated with twigs and bark cavities, rather than suspended soil or litter, of the plants.
Males have yet to be collected.
The following information is derived from Barry Bolton's New General Catalogue, a catalogue of the world's ants.
- hohenbergiae. Anochetus hohenbergiae Feitosa & Delabie, 2012: 254, figs. 1-5 (w.q.) BRAZIL.
Unless otherwise noted the text for the remainder of this section is reported from the publication that includes the original description.
Holotype: HL 2.39; HW 2.10; ML 1.95; SL 2.83; EL 0.49; WL 4.05; PL 0.93; GL 3.46; TL 12.78; CI 87.76; SI 134.88; OI 23.26. Color dark brown with head and gaster slightly darker than mesosoma and petiole; legs yellowish in the coxae and grading to dark brown towards tarsi. Pilosity whitish and relatively dense; body covered by long, flexuous, suberect hairs, except for the mesopleura which is entirely glabrous; antennae and legs with short, suberect hairs along a fine appressed pubescence in antennal funiculi and tarsi. Mandibles shiny, finely and densely covered by minute punctuation; cephalic capsule mostly smooth and shining, with oblique striae fanning out from frontal carinae to about two-thirds of head length, cleft medially by the posteromedian longitudinal impression; antennal scapes with the same pattern of sculpture that mandibles. Pronotum with anterior and lateral portions irregularly costulate, central disc smooth and shiny; central disc of mesonotum and mesopleura entirely smooth and shiny; metapleura with a smooth central area and coarse regulation along the margins; propodeal dorsum transversely costulate, except by its anterior area which presents short, irregular, longitudinal costulae; legs smooth and shiny; petiolar node sparsely rugose, with anterior and posterior faces predominantly smooth; gaster shiny and devoid of any conspicuous sculpture (figs. 1, 3).
Head subquadrate, with vertexal margin strongly concave, virtually U-shaped; posteromedian incision shallow, but conspicuous. Masticatory margins of mandibles with a row of 13–16 teeth (fig. 3B); intercalary tooth one fifth of the ventral apical tooth (fig. 3A). Antennal scapes thickened in midlength and fairly surpassing the posterolateral margins of vertex; funicular segments gradually thickened distally. Compound eyes well developed.
Mesosoma noticeably elongate. Pronotum evenly convex in lateral view, without projections; promesonotal suture relatively narrow and well impressed. Mesonotum elliptical in dorsal view; mesopleura forming a unique plate, without a transverse incision separating anepisternum and katepisternum; mesopleural tooth absent. Metanotal groove broad and well marked; metanotal spiracle distinct; metapleura ending in a rounded lobe, not projecting over petiolar peduncle; metapleural tooth vestigial.
Propodeum unarmed; dorsal face meeting the declivous face in a slight curve; in lateral view, dorsal profile only minimally convex; propodeal spiracle minute, elliptical, and directed posterad. Legs long and slender; pretarsal claws with a short basal lobe (fig. 3C).
Petiole subtriangular and thick, slightly inclined posteriorly; in lateral view, anterior and posterior faces gently convex medially; node with a single, reduced apical tooth, faintly curved posterad, but not overhanging posterior face of petiole in dorsal view; anterior ventral process rounded and weakly developed.
Gaster elongate. First gastral segment (abdominal III) evenly convex dorsally and laterally, with sternite nearly straight; constriction between segments I and II of gaster (abdominal III and IV) only feebly impressed.
Paratypes (n=5): HL 2.49–2.63; HW 2.15–2.24; ML 1.95–2.05; SL 2.83–2.93; EL 0.49–0.59; WL 4.20–4.39; PL 1.02–1.12; GL 4.29–4.93; TL 14.05–15.02; CI 83.33–88.46; SI 128.89–131.82; OI 22.22–26.09. Similar to conspecific worker, but not ergatoid. Body size larger and color slightly darker than in worker. Dorsal surface of head with three distinct ocelli; eyes moderately larger than in worker. Pronotum relatively narrow; scutum large and rounded; notauli indistinct; parapsidial lines feebly visible and subparallel; regulae reduced and lighter than adjacent integument; scutoscutellar sulcus broad and weakly impressed; scutellum rounded and placed at the same level as the scutum; axillae subtriangular; anepisternum clearly separated of katepisternum by a S-shaped suture; propodeum only moderately convex.
Holotype worker. Brasil: Bahia, Ilheus, Areas Exp. CEPEC, 14o46’30”S 39o03’03”W, X.1996, Carmo, J.C.S., #5119 Laboratório de Mirmecologia CEPEC / CPDC.
Paratypes. Same locality as holotype, #4586, 18.XI.1992, E. Silveira col. (1 gyne) [CPDC]; #4586C, 28.I.1993, P.A.O. Soares col. (1 gyne) [CPDC]; #5537, III.2007, Wesley D. da Rocha col., PD0700104/ PD700209 (2 gynes) [CPDC]; same information, PD700318/PD700319 (2 gynes) Museu de Zoologia da Universidade de Sao Paulo; same information, PD700195 (1 gyne) California Academy of Sciences; no further data (1 worker) Musee National d'Histoire Naturelle; Una, Fazenda Ararauna, “cabruca” cacao plantation, 15°18’S 39°09’W, 22.II.2009, Wesley D. da Rocha col., C1E6FA (1 gyne) [CPDC]; same information, 05.III.2009 Wesley D. da Rocha col., C5E2FA (2 workers) [CPDC, MZSP]; #5680, Una, REBIO, XI.2011-II.2012, col. Daniela Uzel Sena (3 workers) [CPDC].
The holotype worker of A. hohenbergiae lacks the tibia and tarsus of the left mid- and hind legs, and of the right mid leg.
The specific epithet is a reference to the observed association of this species with epiphytes of the genus Hohenbergia Schult.f. (Bromeliaceae: Bromelioideae).
- DaRocha, W. D., S. P. Ribeiro, F. S. Neves, G. W. Fernandes, M. Leponce, and J. H. C. Delabie. 2015. How does bromeliad distribution structure the arboreal ant assemblage (Hymenoptera: Formicidae) on a single tree in a Brazilian Atlantic forest agroecosystem? Myrmecological News. 21:83-92.
- Feitosa, R.M., Lacau, S., Da Rocha, W.D., Oliveira, A.R. & Delabie, J.H.C. 2012. A giant new arboreal species of the ant genus Anochetus from Brazil (Formicidae: Ponerinae). Ann. Soc. Entomol. France (n.s.)48, 253-259. PDF