Observed on open, sunny locations: forest edges, lawns, fields with scattered shrubs, urban areas. Nest in soil, mostly sheltered by stones; workers are individual foragers on the ground, in herbs and bases of trees and shrubs. Fast moving after disturbance. Aphaenogaster senilis is an important seed disperser.
|At a Glance||• Brachypterous Queen|
- 1 Identification
- 2 Distribution
- 3 Biology
- 4 Castes
- 5 Nomenclature
- 6 References
A member of the A. testaceopilosa group. Boer (2013) - Workers and gynes have one funiculus segment more than the other species of the A. testaceopilosa-group, just as in Aphaenogaster gemella. Antennal club of male is 6–8-segmented (indistinct club), instead of a distinct 5-segmented club, again just as in A. gemella. The species resembles A. gemella very much. The main difference in all castes is the absence of propodeal spines or knobs in A. gemella.
Keys including this Species
- Key to Aphaenogaster European testaceopilosa-group males
- Key to Aphaenogaster European testaceopilosa-group queens
- Key to Aphaenogaster European testaceopilosa-group workers
- Key to Aphaenogaster workers of Europe
- Key to Iberian Peninsula Aphaenogaster species
The original description of this species was based on Sardinian specimens (Mayr 1853). On the island it seems confined to the southernmost provinces, where it is often abundant. However, it is a West-Mediterranean taxon, widespread from the Canary Islands to southern France and especially common in the Iberian Peninsula (Cagniant et al. 1991; Rigato & Toni, 2011).
Distribution based on Regional Taxon Lists
Distribution based on AntMaps
Distribution based on AntWeb specimens
Check data from AntWeb
Worker numbers average 1.260 ± 69 (mean ± SE, n=168, range 121-3.906) (Boulay et al. 2007). Nest density was found to be 174 nests ha-1 at a site in southern Spain. Foraging is strictly diurnal and occurs from February to November. Colonies move their nests frequently, occupying open areas in spring and fall and shady sites during the heat of the summer (Barroso et al. 2013)
Aphaenogaster senilis produces new colonies via fission. Monogynous. Sex ratios are highly male biased (172:1, numerically). Workers can have functional ovaries and are likely able to produce males from their eggs, provided these are allowed to develop. Queens are hypothesized to produce pheromones that suppress the production of new sexuals (Boulay et al. 2007).
Microsatellite markers revealed that the single queen mates with only one foreign male (Chéron et al. 2009). Thirty colonies were experimentally orphaned, and workers reared 2.0 ± 1.1 brachypterous gynes from the previous queen’s diploid brood, with 10 groups producing one gyne and 20 groups producing two to five gynes. The firstborn gyne emerged on average 17 days before the second. Behavioural observations showed that gynes interacted aggressively and the firstborn gyne was always dominant. She was usually the only one to survive, even though gynes did not differ in weight (Chéron et al. 2009). Such low colonial investment in gyne production is consistent with colony fission (Cronin et al. 2013).
The contents of the Dufours gland and postpharyngeal gland have been examined for workers and queens (Boulay et al. 2007)
Pekár et al. (2018) - This ant is preyed upon by numerous spider species in the genus Zodarion (Araneae: Zodariidae). All members of this genus are specialized ant predators that exclusively prey on ants.
Gynes are brachypterous (Tinaut & Ruano 1992). Males can fly between nests, hence mating occurs in or near the natal nest of gynes.
The following information is derived from Barry Bolton's New General Catalogue, a catalogue of the world's ants.
- senilis. Aphaenogaster senilis Mayr, 1853b: 108 (w.q.) ITALY. Emery, 1916b: 140 (m.). Junior synonym of testaceopilosa: Nylander, 1856b: 86; Smith, F. 1858b: 165 (misspelled as similis); Roger, 1859: 255; Dalla Torre, 1893: 107. Subspecies of testaceopilosa: Emery, 1878b: 53; Emery, 1916b: 131; Santschi, 1919e: 245. Revived status as species: Bondroit, 1918: 161; Santschi, 1933c: 396; Cagniant, 1964: 100; Bernard, 1967: 132. Baroni Urbani, 1971c: 44. Senior synonym of acoreensis: Yarrow, 1967: 26; of fuentei: Collingwood, 1978: 67; of occidua: Casevitz-Weulerrse & Galkowski, 2009: 486; of grata, occidua: Boer, 2013: 81. Current subspecies: nominal plus disjuncta.
- acoreensis. Aphaenogaster senilis var. acoreensis Santschi, 1933a: 21 (q.) AZORES IS. [Also described as new by Santschi, 1933c: 397.] Junior synonym of senilis: Yarrow, 1967: 26.
- fuentei. Aphaenogaster testaceopilosa var. fuentei Medina, 1893: 105 (w.) SPAIN. Junior synonym of senilis: Collingwood, 1978: 67.
- grata. Aphaenogaster senilis var. grata Santschi, 1933c: 397, fig. 34 (m.) SPAIN. Junior synonym of senilis: Boer, 2013: 81.
- occidua. Aphaenogaster senilis var. occidua Santschi, 1933c: 396, fig. 26 (w.m.) FRANCE. Junior synonym of senilis: Casevitz-Weulerrse & Galkowski, 2009: 486, Boer, 2013: 81.
Holotype: male of A. senilis grata: Spain: Parla (Madrid), 28.v.1927 (Dusmet, Naturhistorisches Museum, Basel). Syntypes: of A. senilis occidua: France: Banyuls (Pyr. Or.), vii.1932, 5 workers, 4 males (Denis, NHMB). Unless otherwise noted the text for the remainder of this section is reported from the publication that includes the original description.
Boer (2013) :
Lateral sides of pronotum and metanotum without or with weak longitudinal rugulae, propodeum with distinct longitidinal rugulae. Rugulose sculpture on dorsal side absent. Head in full-face view with longitudinal rugulae, here and there with some cross-connections. Mesosoma, head in full-face view, dorsal and lateral sides of petioles punctate. Legs of different individuals are showing a transition from punctulation to microreticulation. Ventral to the propodeal spines punctate and sometimes transversely costulate. Dorsal side of postpetiole with longitudinal costulae. Dorsal side of base of gaster with transverse microstriae. Head, pronotum, terminal side of propodeum, beneath the propodeal spines, lateral sides of petioles and dorsal side of the gaster matt. Dorsum postpetiole wax gloss to matt. Lateral sides of gaster satin. Dorsal side of petiole matt to wax gloss. Antennal club 5-segmented. Petiolar node with rounded top. Petiole equal in height as postpetiole or somewhat higher. Spur of hind tibia with minute dentation.
Measurements (n = 33). CI 71–84 (76); CW 1.18–1.46 (1.29) mm; CL 1.50–1.87 (1.71) mm; PHI 31–35 (32); PI 72–93 (81); PPPI: 43–54 (48); PSI 112–167 (135); PSLWI 95–188 (121); PWI 20–43 (24); RPH 121–153 (139); RPSI 11–44 (30); SI 129–149 (141); SL 1.70–1.89 (1.83) mm; SPD 1–3 (1.7); SPL 4–6 (4.9).
Head in full-face view, including occiput, with longitudinal rugulae with cross-connections. Longitudinal rugulae on clypeus, head and anterior side of the postpetiole and lateral sides of the mesosoma. Transverse rugulae on pronotum (partly), propodeum and terminal sides of petioles. Pronotum (partly), mesoscutum and scutellum scabriculous. Punctation on head, mesosoma and petioles (including anterior part of the petiole). About 30 transverse microstriae in the midline of the first gastral tergite near the base. Mesosoma dorsally matt, gaster dorsally matt satin to satin. Antennal club 5-segmented. Wings with a light yellowish tint. Scutellum rises weakly above the mesoscutum and does not bend over themetanotum.
Measurements (n = 3). CI: 83–87; CL: 1.82–1.86 mm; CW: 1.50–1.61 mm; OCI: 29–37 (33); PHI 44–47; PI 64–68; PPPI 78–88; PSI 208–280; PSLWI 104–110; PWI 30–35; RPH 135–157; RPSI 57–67; SI 114; SI/CI: 132–138; SL 1.70–1.84 mm; SPD 1; SPL 4–5.5.
Rugulae are absent on the whole body. Whole body punctate, except the propodeum and gaster. No microstriae on first gastral tergite. Clypeus with transverse rugulae. Head, pronotum and mesonotum matt. Lateral sides of mesosoma (partly) and propodeum shiny. Petioles and dorsal side of gaster glossy to shiny. Lateral sides of gaster shiny. Antennal club 6–8-segmented (indistinct club). Pubescence on hind tibia suberect, their length longer than the diameter of the tibia. Wings clear. Scutellum slightly erect above mesoscutum, partly bent over metanotum. Mandible with one large apical tooth, tooth 2 and or 3 relatively large, rest of the masticatory margin of the mandibles distinctly dentate. A longitudinal groove between the two knobs at the terminal side of the propodeum. These knobs are dorsally flattened, diagonally to the rear. Ventral to the propodeal stigma are the metapleural gland bullae, which are extremely developed into broad discus-like, sharp ending knobs, bowed in the lateral direction, and slightly deflected in the more ventral direction.
Measurements (n = 7). CI 85–91 (89); CL 0.90–1.08 (1.03) mm; CW: 0.81–1.00 (0.91) mm; EYI 37–43 (39); OCI 44–56 (51); SL/CL 32–36 (33); SL 0.29–0.37 (34) mm.
- n = 16, 2n = 32, karyotype = 6M+6SM+20ST (Spain) (Palomeque et al., 1993a; Palomeque et al., 1993b; Lorite et al., 2000).
- Baroni Urbani, C. 1971c. Catalogo delle specie di Formicidae d'Italia (Studi sulla mirmecofauna d'Italia X). Mem. Soc. Entomol. Ital. 50: 5-287 (page 44, Revived status as species)
- Barroso, Á., F. Amor, X. Cerdá, and R. R. Boulay. 2013. Dispersal of non-myrmecochorous plants by a “keystone disperser” ant in a Mediterranean habitat reveals asymmetric interdependence. Insect. Soc. 60:75-86.
- Bernard, F. 1967a . Faune de l'Europe et du Bassin Méditerranéen. 3. Les fourmis (Hymenoptera Formicidae) d'Europe occidentale et septentrionale. Paris: Masson, 411 pp. (page 132, Revived status as species)
- Boer, P. 2013. Revision of the European ants of the Aphaenogaster testaceopilosa-group (Hymenoptera: Formicidae). Tijdschrift voor Entomologie 156, 57–93.
- Bondroit, J. 1918. Les fourmis de France et de Belgique. Ann. Soc. Entomol. Fr. 87: 1-174 (page 161, Revived status as species)
- Boulay, R., A. Hefetz, et al. (2007). Production of sexuals in a fission-performing ant: dual effects of queen pheromones and colony size. Behavioral Ecology and Sociobiology 61(10): 1531-1541.
- Cagniant, H. 1964 . Étude de quelques fourmis marocaines. Statistique provisoire des Formicidae du Maroc. Bull. Soc. Hist. Nat. Afr. Nord 53: 83-118 (page 100, Revived status as species)
- Chéron B, Doums C, Fédérici P, Monnin T (2009) Queen replacement in the monogynous ant Aphaenogaster senilis: supernumerary queens as life insurance. Animal Behaviour 78:1317-1325
- Collingwood, C. A. 1978. A provisional list of Iberian Formicidae with a key to the worker caste (Hym. Aculeata). EOS. Rev. Esp. Entomol. 52: 65-95 (page 67, Senior synonym of fuentei)
- Dalla Torre, K. W. von. 1893. Catalogus Hymenopterorum hucusque descriptorum systematicus et synonymicus. Vol. 7. Formicidae (Heterogyna). Leipzig: W. Engelmann, 289 pp. (page 107, Junior synonym of testaceopilosa)
- Emery, C. 1878c. Catalogo delle formiche esistenti nelle collezioni del Museo Civico di Genova. Parte seconda. Formiche dell'Europa e delle regioni limitrofe in Africa e in Asia. [concl.]. Ann. Mus. Civ. Stor. Nat. 12: 49-59 (page 53, Variety/subspecies of testaceopilosa)
- Emery, C. 1916a . Fauna entomologica italiana. I. Hymenoptera.-Formicidae. Bull. Soc. Entomol. Ital. 47: 79-275 (page 140, male described)
- Emery, C. 1916a . Fauna entomologica italiana. I. Hymenoptera.-Formicidae. Bull. Soc. Entomol. Ital. 47: 79-275 (page 131, Variety/subspecies of testaceopilosa)
- Galarza, J.A., Jovani, R., Cerda, X., Rico, C., Barros, A., Boulay, R.2012. Frequent colony relocations do not result in effective dispersal in the gypsy ant Aphaenogaster senilis. Oikos, 121:605-613. PDF
- Gomez, K., Martinez, D., Espadaler, X. 2018. Phylogeny of the ant genus Aphaenogaster (Hymenoptera: Formicidae) in the Iberian Peninsula, with the description of a new species. Sociobiology 65(2): 215-224 (DOI: 10.13102/sociobiology.v65i2.2099).
- Mayr, G. 1853c. Beiträge zur Kenntniss der Ameisen. Verh. Zool.-Bot. Ver. Wien 3: 101-114 (page 108, worker, queen described)
- Nylander, W. 1856b. Synopsis des Formicides de France et d'Algérie. Ann. Sci. Nat. Zool. (4) 5: 51-109 (page 86, Junior synonym of testaceopilosa)
- Oms, C.S., Cerdá, X., Boulay, R. 2017. Is phenotypic plasticity a key mechanism for responding to thermal stress in ants? The Science of Nature 104: 42 (DOI 10.1007/s00114-017-1464-6).
- Pekar, S., L. Petrakova, O. Sedo, S. Korenko, and Z. Zdrahal. 2018. Trophic niche, capture efficiency and venom profiles of six sympatric ant-eating spider species (Araneae: Zodariidae). Molecular Ecology. 27:1053-1064. doi:10.1111/mec.14485
- Rigato, F.; Toni, I. 2011. Short notes 21. Hymenoptera, Formicidae. Pp. 873-882 in: Nardi, G.; Whitmore, D.; Bardiani, M.; Birtele, D.; Mason, F.; Spada, L.; Cerretti, P. (eds.) 2011. Biodiversity of Marganai and Montimannu (Sardinia). Research in the framework of the ICP Forests network. Conservazione Habitat Invertebrati, 5. Sommacampagna, Verona: Cierre Edizioni, 896 pp.
- Roger, J. 1859. Beiträge zur Kenntniss der Ameisenfauna der Mittelmeerländer. I. Berl. Entomol. Z. 3: 225-259 (page 255, Junior synonym of testaceopilosa)
- Santschi, F. 1919e. Fourmis d'Espagne et des Canaries. Bol. R. Soc. Esp. Hist. Nat. 19: 241-248 (page 245, Variety/subspecies of testaceopilosa)
- Santschi, F. 1933d. Étude sur le sous-genre Aphaenogaster Mayr. Rev. Suisse Zool. 40: 389-408 (page 396, Revived status as species)
- Smith, F. 1858a. Catalogue of hymenopterous insects in the collection of the British Museum. Part VI. Formicidae. London: British Museum, 216 pp. (page 165, Junior synonym of testaceopilosa)
- Tinaut, A. & Ruano, F. 1992. Braquipterismo y apterismo en Formícidos. Morfología y biometría en las hembras de especies ibéricas de vida libre (Hymenoptera Formicidae). Graellsia 48: 121-131.
- Yarrow, I. H. H. 1967. On the Formicidae of the Azores. Bol. Mus. Munic. Funchal 21: 24-32 (page 26, Senior synonym of acoreensis)