Pogonomyrmex vermiculatus Emery 1906

 

Pogonomyrmex vermiculatus Emery, 1906: 157 (worker). Syntypes examined: 1 worker [MSNG], ARGENTINA, Santa Cruz Province: near the Santa Cruz River, 5-7 station (southern Patagonia). See also Gallardo, 1932: 138, fig. 24 (MSNG worker is the HOLOTYPE, by monotypy).

 

Pogonomyrmex vermiculatus var. joergenseni Forel, 1915: 353 (worker). Syntypes examined: 12 workers [MLPA], 2 workers [MACN], 6 workers [MHNG], 1 worker [USNM], #284, ARGENTINA, Santa Cruz Province: to the east of Lago Argentina (Jörgensen leg.). Kusnezov, 1951: 253 [synonomy under chubutensis, not confirmed here] (MACN worker here designated LECTOTYPE). NEW STATUS

 

Worker

Diagnosis.  First gastric tergite usually smooth to moderately coriarious, occasionally with faint striae at base or anterior one-half of tergite.  Cephalic interrugae punctate-granulate, etc.

Measurements (mm) - holotype (n = 12). HL 1.49 (1.40-1.63); HW 1.61 (1.42-1.69); MOD 0.35 (0.30-0.37); OMD 0.35 (0.32-0.41); SL 1.27 (1.04-1.35); PNW 1.12 (0.95-1.12); HFL 1.53 (1.37-1.61); ML 1.82 (1.52-2.01); PW 0.45 (0.37-0.47); PPW * (0.50-0.61).  Indices: SI 78.88 (65.09-80.50); CI 108.05 (99.34-106.96); OI 21.74 (18.34-24.03); HFI 95.03 (86.39-103.90).

* =postpetiole missing.

Description.  Head subquadrate to quadrate (CI = 99.34-106.96), broadest just posterior to eye; posterior margin flat to slightly convex in full-face view.  Longitudinal cephalic rugae prominent, in full-face view, median rugae diverging slightly toward posterior corners of head.  Vertex rugose, interrugal spaces smooth and shining to weakly granulate, sub-shining.  Cephalic interrugal spaces moderately to strongly granulate, dull.  Anterior margin of clypeus strongly concave, medial portion incised to depth of lateral lobes, dorsum with numerous subparallel longitudinal rugae.  Mandible with six teeth; mandibular dorsum coarsely striated.  MOD ranging from 0.19-0.25x HL.  Eyes in profile situated slightly anterior to middle of head, OMD = 0.91-1.23x MOD.  In full-face view, eyes protruding slightly beyond lateral margins of head.  Antennal scapes (SI = 65.09-80.50) failing to reaching posterior corner of head by less than length of basal funicular segment.  Antennal scapes with weak longitudinal striae, sub-shining to shining; basal flange well developed, flattened, partly translucent with carinate margin.  Psammophore well developed. 

Mesosomal profile convex.  In dorsal view, humeral portion of pronotum enlarged, slightly to distinctly angulate.  All mesosomal surfaces with prominent subparallel irregular rugae, occasionally rugoreticulate on pronotal sides.  Dorsum of promesonotum with longitudinal rugae that diverge anteriorly toward humeral angles.  Irregular rugae on pronotal sides traverse ventrally or posterioventrally; rugae on mesopleura angle posteriodorsally; irregular transverse rugae on dorsum of propodeum traverse ventrally or anterioventrally on sides.  Promesonotal suture often slightly to moderately impressed.  Superior propodeal spines well developed, slightly shorter than width between their bases, connected by a well-defined keel; inferior propodeal spines well developed, slightly broader than high, tapering to a slightly blunt to acute tip.  Propodeal spiracles narrowly ovate.  Interrugal spaces on mesosoma smooth and shining to strongly granulate, slightly dull to sub-shining.  Legs smooth and shining to weakly coriarious, sub-shining to shining.

Petiolar peduncle long, ventral surface with a well developed rounded process.  In side view, posterior face of petiole weakly convex; petiolar node asymmetrical with anterior surface notably longer than posterior surface, apex subangulate to angulate.  In dorsal view, petiole longer than broad, widest near spatulate anterior margin, gradually tapering to posterior margin.  Posterior face of petiole with regular to irregular transverse or obligue rugae.  Dorsum of postpetiole convex in side view; in dorsal view, widest at or near posterior margin, tapering to anterior margin, maximum width and length about equal.  Transverse rugae on dorsum of postpetiole only slightly finer and denser than those on petiole; interrugal spaces on petiole and postpetiole smooth and shining to weakly coriarious, sub-shining.  Dorsum of first gastric tergite variable, most commonly smooth and shining to weakly or moderately coriarious at and near base, sub-shining (62 of 71; 87.3%), with striae at base (7 of 71; 9.9%), or with striae continuing onto anterior one-half or more of tergite (2 of 71; 2.8%).

Erect, short to medium-length, white pilosity moderately abundant on head, longest occasionally approaching MOD.  Moderately abundant suberect to semidecumbent pilosity on scape; abundant decumbent hairs on funicular segments.  Legs with moderately abundant suberect to decumbent white setae.  Mesosoma, petiole, postpetiole, and gastric tergites with moderately dense, erect, white setae, longest on mesosoma and petiole.  Head a dark reddish-brown to reddish-black, rest of body black except for antenna, mandibles and lateral lobes of clypeus blackish with a slight reddish infusion; dorsum of promesonotum sometimes with a reddish infusion.

      Queen

Diagnosis.  As in worker diagnosis, but with caste-specific morphology of the mesosoma related to wing-bearing and presence of small ocelli on the head, except with longitudinal striae present on the first gastric tergite.  The combination of: (1) dark reddish head and a black body, (2) … uniquely characterize this species.

Measurements (mm) – (n = 12). HL 1.42-1.83; HW 1.59-1.87; MOD 0.34-0.41; OMD 0.34-0.42; SL 1.16-1.38; PNW 1.24-1.50; HFL 1.47-1.79; ML 2.19-3.01; PW 0.47-0.61; PPW 0.69-0.84.  Indices: SI 65.19-78.86; CI 100.55-117.53; OI 18.58-23.27; HFI 85.25-98.16.

Description.  As in worker diagnosis, but with caste-specific morphology of the mesosoma related to wing-bearing and presence of small ocelli on head, except with longitudinal striae present on the first gastric tergite, and as illustrated in Figure xx.  In full face view, head quadrate to slightly broader than long (CI = 100.55-117.53), broadest just posterior to eyes, posterior margin flat to very weakly convex.  Longitudinal cephalic rugae prominent, wavy; in full-face view median rugae diverging towards posterior corners of head, interrugal spaces moderately granulate-punctate, sub-shining; vertex rugose, interrugal spaces smooth and shining.  Mandible with six teeth, dorsal surface coarsely rugose.  Psammophore moderately well-developed.

All mesosomal surfaces except pronotal sides with subparallel, regular to wavy rugae, rugae irregular to rugoreticulate on pronotal sides, interrugal spaces smooth and shining to weakly granulate-punctate, sub-shining; superior propodeal spines acuminate, ranging from short and triangular to moderately well developed, elongate; inferior propodeal spines moderately well developed, wider than tall, broadly rounded to subangulate.  Petiolar peduncle long, ventral surface with a weak rounded process.  In side view, petiolar node asymmetrical with anterior surface notably shorter than posterior surface, apex of node subangulate to angulate.  Posterior face of petiole with wavy transverse to oblique rugae, interrugal spaces weakly granulate-punctate, sub-shining.  In dorsal view, postpetiole slightly wider than long; dorsum with wavy, transverse rugae that are weaker and more dense than those on petiole, interrugal spaces weakly granulate-punctate, sub-shining.  First gastric tergite striate along base, striae sometimes extending over anterior one-half of tergite, dull.  Most body surfaces with moderately abundant suberect to erect, medium-length, whitish setae, one to two longer hairs along posterior margin of head approach MOD.  Head reddish-brown, rest of body black, but mesoscutum, scutellum, and first gastric tergite sometimes with an orangish infusion.  

Male.

Diagnosis.

Measurements (mm) - (n = 12). HL 1.10-1.29; HW 1.16-1.37; MOD 0.42-0.51; OMD 0.13-0.21; SL 0.41-0.52; HFL 1.45-1.81; ML 2.23-2.59; PW 0.48-0.61; PPW 0.68-0.82.  Indices: SI 31.54-40.52; CI 98.35-114.66; OI 33.08-37.23; HFI 114.60-137.12. 

Description.

Additional material examined. ARGENTINA: CHUBUT: 17.4 km S Dr Ricardo Rojas, 1870’ (RAJC); Rt 26 at 2.3 km E Alto Río Mayo, 2050’ (RAJC). SANTA CRUZ: 2.3 km S Cuevos de los Manos, 2100’ (RAJC); 53.7 km S Jct Rt 40 & 29, 2080’ (RAJC); Rt 11 at 10.9 km E El Calafete, 830’ (RAJC); Rt 11 at 19.3 km W El Calafete, 720’ (RAJC); Rt 25 at 0.9 km E Tamil Aike, 1760’ (RAJC); Rt 40 at 2.6 km  N Bajo Caracoles, 1940’ (RAJC); Rt 40 at 20.6 km S Bajo Caracoles, 2380’ (RAJC); Rt 40 at 58.2 km S Bajo Caracoles, 2350’ (RAJC); Rt 40 at 94.8 km S Bajo Caracoles, 2000’ (RAJC); Rt 40 at 30.9 km S Perito Moreno, 1970’ (RAJC); Rt 40 at 48.0 km S Perito Moreno, 1970’ (RAJC); Rt 40 at 76.9 km S Perito Moreno, 2260’ (RAJC). CHILE: Magdallenes: Río Bagueles, Estancia Cerro Guido (LACM).

Etymology.  In his description, Emery (1906) indicated that the mesosoma was covered with rugae that meander irregularly – hence the name vermiculatus (see also Kusnezov, 1951).

 

Discussion.  Pogonomyrmex vermiculatus is only known to co-occur with one P. rastratus-group species, P. carbonarius.  Pogonomyrmex vermiculatus can be distinguished from P. carbonarius based on: (1) its bicolored body (dark red head, rest of body black), (2) longitudinal striae usually absent on base of gaster, and (3) irregular longitudinal rugae on the dorsum of the mesosoma.  In P. carbonarius, the color is uniformly black (rarely with dark reddish coloration), longitudinal striae cover most of the first gastric tergite, and the longitudinal rugae on the dorsum of the mesosoma are very regular. 

The identity of P. vermiculatus has been misunderstood since its description due to the paucity of verified material combined with the fact that no one examined the syntype worker (holotype, by monotypy).  For example, Kusnezov (1951) only examined material from Meseta de las Vizcachas, Santa Cruz Province (#6756), and his description of P. vermiculatus followed that of Emery (1906), indicating that fine longitudinal striae were present along the base of the first gastric tergite, with the rest of the tergite smooth and shiny.  Kuznesov also used “fine longitudinal striae along the base of the first gastric tergite” to key out P. vermiculatus.  Unfortunately, the holotype is not informative because it is missing the postpetiole and gaster. 

The description of one syntype worker also resulted in misunderstanding intra- and internidal variation in characters such as striae on the first gastric tergite.  However, this variation is significant as material collected during this study shows that within one colony workers can display a range of states (see above).  These collections also demonstrate that the holotype worker was not representative because most workers of P. vermiculatus lack striae along the base of the first gastric tergite (see above).

Confusion over the identity of P. vermiculatus continued into recent times, when Snelling & Hunt (1975) erroneously synonomized two Chilean species, P. semistriata and P. intermedia, under P. vermiculatus without knowing the true identity of P. vermiculatus.  In reality, P. vermiculatus appears to be rare in Chile, where it is only recorded from the extreme south (Magdallenes Region), which contrasts with the variable morphology and broad geographic distribution described by Snelling & Hunt (1975).  Other studies have examined foraging and recruitment biology of P. vermiculatus in Chile (Medel & Fuentes, 1995; Torres-Contreras et al., 2007, 2009); vouchers from these studies have not been examined, but it is doubtful that P. vermiculatus was the species investigated because workers were in these studies were collected in central Chile (Las Chinchillas National Reserve and Fray Jorge National Park), hundreds of kilometers north of the known range.

The lack of material to examine likely resulted in Forel (1913) describing P. vermiculatus var. joergenseni from workers that were collected at or very near the type locality of P. vermiculatus.  Forel was apparently unaware of the proximity of these type localities given that he compared P. vermiculatus var. joergenseni to P. vermiculatus var. chubutensis, but not to P. vermiculatus.  This omission may also have occurred because Forel assumed that striae along the base of the first gastric tergite were diagnostic for P. vermiculatus.  Consequently, P. vermiculatus var. joergenseni and P. vermiculatus var. chubutensis were compared because both forms were described to have a smooth and shining first gastric tergite (i.e., lacking striae near the base). 

I examined 15 syntype workers of P. vermiculatus var. joergenseni, finding that the first gastric tergite was not uniform, but rather that workers varied in a manner similar to that described above for P. vermiculatus: the base of the first gastric tergite was smooth and shining on seven workers, weakly coriarious on six workers, with weak longitudinal striae on one worker, and with longitudinal striae extending to the mid-section on one worker.

Gallardo (1932) was the only study that directly compared P. vermiculatus and P. vermiculatus var. joergenseni, noting that the former form had punctures between the cephalic rugae whereas the latter form lacked depressed punctures between the cephalic rugae.  However, this character also varied among the syntypes of P. vermiculatus var. joergenseni, with the degree of interrugal punctures ranging from weak and sub-shining to strong and dull.  Thus, P. vermiculatus var. joergenseni is synonomized under P. vermiculatus.

REFERENCES

Emery, C. (1906) Studi sulle formiche della fauna Neotropica. Bollettino della Società Entomologica Italiana, 37, 107-194.

Forel, A. (1913) Fourmis d'Argentine, du Brésil, du Guatémala and de Cuba. Recues de M.M. Bruch, Prof. v. Ihering, Mlle Baez, M. Peper et M. Rovereto. Bulletin de la Société Vaudoise des Sciences Naturelles, 49, 203-250.

Gallardo, A. (1932) Las hormigas de la República Argentina. Subfamilia Mirmicinas, segunda sección Eumyrmicinae, tribu Myrmicini (F. Smith), género Pogonomyrmex Mayr. Anales del Museo Nacional de Historia Natural "Bernardino Rivadavia", 37, 89-170.

Kusnezov, N. (1951) El género Pogonomyrmex Mayr (Hym., Formicidae). Acta Zoologica Lilloana, 11, 227-333.

Medel, R.G. & Fuentes, J.E. (1995) Notes on the individual activity, diet, and abundance of the ants Pogonomyrmex vermiculatus and Solenopsis gayi (Hymenoptera: Formicidae) in a semiarid ecosystem on northern Chile. Revista Chilena de Entomologia, 33, 81-84.

Snelling, R.R. & Hunt, J.H. (1975) The ants of Chile (Hymenoptera: Formicidae). Revista Chilena de Entomologia, 9, 63-129.

Torres-Contreras, H., Olivares-Donoso, R. & Niemeyer, H.M. (2007) Solitary foraging in the ancestral South American ant, Pogonomyrmex vermiculatus.  Is it due to constraints in the production or perception of trail pheromones? Journal of Chemical Ecology, 33, 435-440.

Torres-Contreras, H., Olivares-Donoso, R. & Niemeyer, H.M. (2009) Fasting and chemical signals affect recruitment and foraging efficiency in the harvester ant, Pogonomyrmex vermiculatus. Behaviour, 146, 923-938.