Pheidole pallidula

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Pheidole pallidula
Scientific classification
Kingdom: Animalia
Phylum: Arthropoda
Class: Insecta
Order: Hymenoptera
Family: Formicidae
Subfamily: Myrmicinae
Tribe: Attini
Genus: Pheidole
Species: P. pallidula
Binomial name
Pheidole pallidula
(Nylander, 1849)

Pheidole pallidula casent0080858 profile 1.jpg

Pheidole pallidula casent0080858 dorsal 1.jpg

Specimen labels

Subspecies
Synonyms

Mostly a west-Mediterranean species, occurring from Italy to Spain and North Africa. Some closely related taxa occur from the Balkans eastwards (see Taylor & Sharaf 2010; Rigato & Toni, 2011). Pashaei Rad et al. (2018) found this species in Iran in moderate rainfall to dry areas. They prefer warm, open habitats such as rural sites in anthropogenic habitats, roadsides, pastures, mediterranean shrubs and forests. Members of this complex are pioneering species, as one of the first to inhabit disturbed habitats resulting from human activity, such as road investments, extensive excavations, but also areas after fires (Borowiec & Salata, 2021).

Mediterranean populations of the taxon named Pheidole pallidula have recently been divided into four species, three of them recorded in Greece (Seifert, 2016), but this revision is still under discussion owing to the great local variability of this very common Mediterranean ant. From the northern Aegean Islands was recorded Pheidole balcanica and Pheidole koshewnikovi (Borowiec et al., 2022).

At a Glance • Polygynous  • Limited invasive  

Identification

Sharaf et al. (2017) - Major worker. TL 3.4–3.9; Head in full-face view subrectangular with moderately deeply impressed posterior margin; clypeus smooth and shining with weak median longitudinal carina; frontal carinae short and feebly divergent; antennae elongate; eyes small and weakly circular; hypostoma with a pair of large lateral teeth; mesosoma in profile with a slightly domed promesonotum; metanotal groove impressed; propodeal spines with small triangular teeth. In profile, petiole with a relatively short pedicel; postpetiole small and globular; gaster distinctly smaller than head; pilosity long, fine and abundant. Body shining; sculpture absent except for fine longitudinal striations on anterior one third of head. Colour overall pale yellowish brown, mandibles dark brown.

Distribution

Pheidole pallidula has a broad distribution in the Mediterranean region (Bernard 1983) and has been recorded from the Iberian Peninsula (Espadaler 1986). Sharaf et al. (2017) report the first record from Socotra Island, Yemen.

Latitudinal Distribution Pattern

Latitudinal Range: 49° to 28.15°.

   
North
Temperate
North
Subtropical
Tropical South
Subtropical
South
Temperate

Distribution based on Regional Taxon Lists

Afrotropical Region: Socotra Archipelago, Yemen.
Palaearctic Region: Afghanistan, Albania, Algeria, Andorra, Armenia, Austria, Azerbaijan, Balearic Islands, Bulgaria, Canary Islands, Croatia, France, Georgia, Gibraltar, Greece, Iberian Peninsula, Iran, Israel, Italy (type locality), Kazakhstan, Kyrgyzstan, Malta, Monaco, Montenegro, Portugal (type locality), North Macedonia, Romania, Russian Federation, Slovenia, Spain, Türkiye, Turkmenistan.

Distribution based on AntMaps

AntMapLegend.png

Distribution based on AntWeb specimens

Check data from AntWeb

Countries Occupied

Number of countries occupied by this species based on AntWiki Regional Taxon Lists. In general, fewer countries occupied indicates a narrower range, while more countries indicates a more widespread species.
pChart

Biology

Obregon et al. 2015. Larva of Zizeeria knysna attended by Pheidole pallidula. Córdoba (Spain).

Behavior

Sempo et al. (2006) examined how the presence of brood influenced the spatial distribution of workers and soldiers within colonies of P. pallidula.

Morphology

Castro et al. (2016) described a stridulatory structure in this species. They used SEM photographs to discern the details they reported.

A pentagonal pars stridens, but in this case the pentagon is inverted, with the apex pointing to the gaster. This shape is much more marked in the major than in the minor forms. Width and length are quite similar, but it is slightly wider (0.08 mm width and 0.07 mm length). Striation is among the thinnest of all the considered species. Pillars are noticeable and thin, with scattered teeth situated mostly in the lateral parts of the stridulatory organs.

Beltra et al. (2017) found this ant forging on grape vines in Eastern Spain vineyards.

Association with Other Organisms

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Two mermithid-infected (nematode) soldiers (mermithostratiotes) (arrows) of Pheidole pallidula adjacent to smaller workers and an uninfected soldier (with large head). Note smaller heads on infected soldiers. Photo courtesy of Luc Passera (Poinar, 2012, Fig. 7).

Borowiec and Salata (2015) found that the specimens of the previously described species Pheidole symbiotica were simply workers of Pheidole pallidula that were infested with mermithid nematodes.

Other Insects

This species is associated with the aphids Aphis davletshinae, Aphis frangulae, Aphis umbrella, Cinara palaestinesis, Myzus persicae, Aphis nerii, Thelaxes suberis (Saddiqui et al., 2019 and included references).

Pheidole pallidula worker and a male Paussus favieri.

Di Giulio et al. (2015) showed the beetle Paussus favieri uses sounds they generate to allow them to live unmolested in colonies of P. pallidula. It had been known that Paussus posses stridulatory organs and while it was suspected this served some role in ant interactions, their purpose had never been investigated. Di Giulio et al. reported "We first characterized the acoustic signals of Paussus favieri and worker, soldier and queen castes of its host ant, Pheidole pallidula. We next analysed ants’ responses to Paussus stridulations by playback experiments and found that the ants react to Paussus sounds, which demonstrates that Paussus stridulations convey an interspecific message. More unexpected, however, was the finding that Paussus beetles were able to produce at least three different acoustical signals that elicited different responses in the ants. We show that Paussus favieri is not only able to mimic ants’ stridulations but can also “speak” three different “languages”, each corresponding to sounds produced by different ant castes, including the queen, to direct host ant behaviours. In effect, Paussus utilizes modular acoustical mimicry to achieve the highest hierarchical status of the colony."

Obregon et al. 2015 - This ant has been associated with the butterflies Favonius quercus and Zizeeria knysna.

This species is a host for the cricket Myrmecophilus balcanicus (a myrmecophile) in Macedonia.

Nematode

  • This species is a host for the nematode Mermithidae (unspecified "Mermix") (a parasite) in France (Wheeler, 1928; Laciny, 2021).
  • This species is a host for the nematode Hexamermis (a parasite) in France (Passera, 1976; Laciny, 2021).

Platyhelminthes

  • This species is a host for the cestode Raillietina circumvalata (a parasitoid) (Quevillon, 2018) (encounter mode secondary; indirect transmission; transmission outside nest).
  • This species is a host for the cestode Raillietina echinobothrida (a parasitoid) (Quevillon, 2018) (encounter mode secondary; indirect transmission; transmission outside nest).

Fungi

This species is a host for the fungus Myrmicinosporidium durum (a pathogen) in Portugal, Slovenia, Spain (García, F., Espadaler, X. 2010; Espadaler & Roig, 2012; Espadaler & Santamaria, 2012; Gonçalves et al., 2012).

Flight Period

X X X X
Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec

Source: antkeeping.info.

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Life History Traits

  • Queen number: polygynous (Frumhoff & Ward, 1992)
  • Mean colony size: 5,000 (Beckers et al., 1989)
  • Foraging behaviour: mass recruiter (Beckers et al., 1989)

Castes

Worker

Minor

Images from AntWeb

Pheidole pallidula casent0080859 head 1.jpgPheidole pallidula casent0080859 profile 1.jpgPheidole pallidula casent0080859 dorsal 1.jpgPheidole pallidula casent0080859 label 1.jpg
Worker. Specimen code casent0080859. Photographer April Nobile, uploaded by California Academy of Sciences. Owned by CAS, San Francisco, CA, USA.

Major

Images from AntWeb

Pheidole pallidula casent0080860 head 1.jpgPheidole pallidula casent0080860 profile 1.jpgPheidole pallidula casent0080860 dorsal 1.jpgPheidole pallidula casent0080860 label 1.jpg
Worker (major/soldier). Specimen code casent0080860. Photographer April Nobile, uploaded by California Academy of Sciences. Owned by CAS, San Francisco, CA, USA.

Nomenclature

The following information is derived from Barry Bolton's Online Catalogue of the Ants of the World.

  • pallidula. Myrmica pallidula Nylander, 1849: 42 (w.) ITALY (Sicily).
    • [Misspelled as pallidcela by Wheeler, W.M. 1937c: 38, figure caption.].
    • Mayr, 1855: 457 (s.q.m.); Vandel, 1931: 114 (gynandromorph); Hauschteck, 1961: 221 (k.).
    • Combination in Oecophthora: Mayr, 1855: 455.
    • Combination in Pheidole: Smith, 1858b: 173.
    • Junior synonym of megacephala: Mayr, 1861: 70 (in key).
    • Subspecies of megacephala: Emery & Forel, 1879: 463; Forel, 1890a: lxxvi; Emery, 1891b: 13; Dalla Torre, 1893: 94.
    • Status as species: Mayr, 1855: 455; Nylander, 1856b: 97; Roger, 1863b: 30; Mayr, 1863: 441; Emery, 1869b: 19; Forel, 1874: 81 (in key); André, 1874: 198 (in key); André, 1881b: 76; André, 1883b: 383 (in key); Nasonov, 1889: 39; Ruzsky, 1902d: 26; Ruzsky, 1903b: 310; Ruzsky, 1905b: 643; Karavaiev, 1910b: 61; Forel, 1915d: 33 (in key); Emery, 1915j: 226; Wheeler, W.M. & Mann, 1916: 170; Stitz, 1917: 339; Bondroit, 1918: 166; Menozzi, 1921: 26; Emery, 1921f: 86; Müller, 1923a: 69; Müller, 1923b: 67; Wheeler, W.M. 1926: 3; Karavaiev, 1927a: 288; Finzi, 1936: 162; Wheeler, W.M. 1937c: 38; Finzi, 1940: 159; Bernard, 1945: 133; Bernard, 1956b: 258; Bernard, 1959: 346; Baroni Urbani, 1964a: 3; Baroni Urbani, 1964b: 42; Baroni Urbani, 1964c: 152; Cagniant, 1964: 88; Pisarski, 1967: 385; Bernard, 1967: 153 (redescription); Baroni Urbani, 1968b: 446; Pisarski, 1970: 307; Cagniant, 1970a: 417; Baroni Urbani, 1971c: 70; Baroni Urbani, 1976: 211; Tarbinsky, 1976: 68 (redescription); Aktaç, 1977: 121; Arnol'di & Dlussky, 1978: 537 (in key); Collingwood, 1978: 77 (in key); Schembri & Collingwood, 1981: 427; Bolton, 1987: 291; Agosti & Collingwood, 1987b: 272 (in key); Dlussky, Soyunov & Zabelin, 1990: 229; Atanassov & Dlussky, 1992: 123; Arakelian, 1994: 41; Bolton, 1995b: 327; Mei, 1995: 762; Cagniant, 2006a: 197; Radchenko, 2007: 33; Seifert, 2016b: 13.
    • Senior synonym of subdentata: Mayr, 1855: 456.
    • Senior synonym of inquilina: Bolton, 1987: 291.
    • Senior synonym of symbiotica: Borowiec, L. & Salata, 2015: 183.
    • Senior synonym of obscura: Seifert, 2016b: 13.
    • Current subspecies: nominal plus selenia, tasdelenia.
  • subdentata. Oecophthora subdentata Mayr, 1853a: 145 (s.w.) AUSTRIA. Junior synonym of pallidula: Mayr, 1855: 456.
  • symbiotica. Pheidole symbiotica Wasmann, 1909: 693 (footnote), figs. 1, 2 (w.) PORTUGAL. Wasmann, 1910: 515 (q.m.). Junior synonym of pallidula: Forel, 1913d: 430. Revived from synonymy as subspecies of pallidula: Emery, 1915j: 226. Revived status as species: Collingwood, 1978: 68. Junior synonym of pallidula: Borowiec & Salata, 2015: 183.
  • inquilina. Xenoaphaenogaster inquilina Baroni Urbani, 1964b: 50, figs. 15, 16 (w.) ITALY (Sicily). [Unresolved junior secondary homonym of Epipheidole inquilina Wheeler, W.M. 1903f: 664.] Junior synonym of pallidula: Bolton, 1987: 291.
  • emeryi. Pheidole pallidula var. emeryi Krausse, 1912a: 169 (s.w.) ITALY (Sardinia).
    • [Junior primary homonym of Pheidole emeryi Mayr, 1887: 589.]
    • Subspecies of pallidula: Emery, 1921f: 86.
    • Replacement name: Pheidole pallidula var. obscura Santschi, 1936c: 200.
  • obscura. Pheidole pallidula var. obscura Santschi, 1936c: 200.
    • Replacement name for Pheidole pallidula var. emeryi Krausse, 1912a: 169. [Junior primary homonym of Pheidole emeryi Mayr, 1887: 589.]
    • Subspecies of pallidula: Bolton, 1995b: 326.
    • Junior synonym of pallidula: Seifert, 2016b: 13.

Description

Karyotype

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  • n = 10, 2n = 20 (Greece; Spain; Switzerland; Tunisia) (Hauschteck-Jungen & Jungen, 1983).
  • n = 10, 2n = 20, karyotype = 8M+12SM (Spain) (Palomeque et al., 1987; Palomeque et al., 1990b; Lorite et al., 2000).
  • 2n = 24 (Switzerland) (Hauschteck, 1961).

References

References based on Global Ant Biodiversity Informatics

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