Lasius alienus
Lasius alienus | |
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Scientific classification | |
Kingdom: | Animalia |
Phylum: | Arthropoda |
Class: | Insecta |
Order: | Hymenoptera |
Family: | Formicidae |
Subfamily: | Formicinae |
Tribe: | Lasiini |
Genus: | Lasius |
Section: | niger clade |
Species group: | alienus |
Species: | L. alienus |
Binomial name | |
Lasius alienus (Foerster, 1850) |
Common in Europe and Asia, rare in Japan. It shows a preference for habitats that are in open areas such as agricultural fields. It is a common species in Greece where it is known from all provinces. In Achaia and Aetolia-Acarnania, it has been observed in rural sites in tourist resorts, mixed and fir forests and mountain pastures. Nests were located under stones. (Borowiec & Salata, 2021)
At a Glance | • Limited invasive |
Common Name | |
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Hime-tobiiro-ke-ari | |
Language: | Japanese |
Cornfield Ant | |
Language: | English |
Identification
Seifert (2020) - Absolute size small (CS 823 µm). Scape length index small, head and maxillary palp length indices medium (SL/ CS900 0.946, CL/CW900 1.069, MP6/CS900 0.181). Number of mandibular dents medium (MaDe900 8.18). Clypeal pubescence moderately dense, intermediate between the situation in the Lasius paralienus and Lasius obscuratus species complexes (sqPDCL900 4.11). Pronotal setae relatively long (PnHL/CS900 0.152). Setae number on hind margin of head low (nOcc900 4.9). Gular setae absent or very few (nGu900 0.8). Dorsum of scape and extensor profile of hind tibia without or with very few semierect setae (nSc900 0.1, nHT900 0.9). The best separation from all other species with reduced scape and tibial pilosity is the strong setae reduction on metapleuron below propodeal spiracle (nSt900 0.3). Frequent coloration: Head, mesosoma, coxae and gaster medium brown; antenna, tibiae and tarsae light yellowish brown; mandibles light reddish brown.
Keys including this Species
- Key to Europe and Asia Minor Lasius alienus group species
- Key to Lasius Palaearctic workers
- Key to Lasius males
- Key to Lasius queens
- Key to Lasius species of the subgenus Lasius of Greece
- Key to New England Lasius
- Key to Palaearctic Lasius s. str.
- Key to Palaearctic Lasius subgenus Lasius s. st.
- Key to the Lasius of the Indian Himalayas
Distribution
This species occurs throughout Europe and Asia, from the British Isles and Scandinavia south to Morocco and Tunisia, east into Lebanon, northern Iraq, and southern China, and north into Russia, Central Asia, China, and Japan (Ellison et al., 2012). Recorded from Japan since the early 20th century (e.g. Wheeler, 1906; Teranishi 1915, 1930; Morisita,1945; Japanese Ant Image Database).
Lasius alienus was recorded from all Greek provinces but due to the recent revision of this genus (Seifert, 2020) its historical records should be reinvestigated (Borowiec et al., 2022).
Latitudinal Distribution Pattern
Latitudinal Range: 67.216667° to 22.952079°.
North Temperate |
North Subtropical |
Tropical | South Subtropical |
South Temperate |
- Source: AntMaps
Distribution based on Regional Taxon Lists
Oriental Region: India, Pakistan.
Palaearctic Region: Albania, Andorra, Armenia, Austria, Azerbaijan, Belarus, Belgium, Bulgaria, Channel Islands, China, Croatia, Czechia, Denmark, Estonia, Finland, France, Georgia, Germany (type locality), Greece, Hungary, Iberian Peninsula, Iran, Israel, Italy, Japan, Kazakhstan, Kyrgyzstan, Latvia, Lithuania, Malta, Mongolia, Montenegro, Netherlands, North Macedonia, Poland, Portugal, Republic of Korea, Republic of Moldova, Romania, Russian Federation, Slovakia, Slovenia, Spain, Sweden, Switzerland, Turkmenistan, Türkiye, United Kingdom of Great Britain and Northern Ireland.
This name had long been applied to a morphologically similar North American form that is now know as Lasius americanus (Schär et al. 2018).
Distribution based on AntMaps
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. |
Habitat
Borowiec and Salata (2022) - In Greece, common species, inhabits a wide variety of habitats from sea level to 1590 m a.s.l. Observed in open areas inside tourist resorts, urban ruderal areas, on roadsides with bushes, on pastures, olive plantations, all types of forests, on higher altitudes in coniferous forests and on pastures with shrubs.
Biology
Wilson (1955) - In North Africa and France (Bernard, 1950; Scherdlin, 1909), Ireland (O’Rourke, 1950), England (Diver, 1940), Germany (Gosswald, 1932), East Prussia (Skwarra, 1929), and Daghestan (Kuznetzov-Ugamskij, 1929), Lasius alienus typically inhabits open dry situations, nesting under stones and occasionally constructing crater entrances in open soil. It shows much less latitude in nesting sites than its sister species Lasius niger, but is more successful in cultivated areas. Bernard notes that in France it is able to replace niger entirely in pastures, even at high elevations, but tends to give way in turn to Tapinoma simrothi and Tapinoma nigerrimum. Diver, in an intensive study of the comparative ecology of alienus and niger in a local area in Dorset, found alienus restricted mostly to dry heath, whereas niger occurred in every major habitat studied. In Daghestan, Kutznezov-Ugamskij found alienus to have more southern affinities than niger. Where the two occur together, alienus is limited mostly to the steppes and mountain meadows (up to 11,000 feet), while niger occurs mostly in the forests.
In Eurasia alienus is replaced in most habitats, including woodland, by its extremely successful and abundant sister species Lasius niger.
Lasius alienus probably does not differ much from niger in food habits and ethology. Several Europeans, including Gosswald and O'Rourke have independently observed that alienus tends to be the more secretive of the two species. This is possibly correlated with the preference of this species in Eurasia for more exposed situations.
Records of nuptial flights in this species are too sparse to allow a rigorous comparison with niger. In Europe winged forms are found in nido during about the same period as for niger. I have records ranging from June (Trieste, MCZ; no further date) to October 28 (Italy, MCZ) without evident preponderance during any part of this period; a single pair were preserved in copula in October (Trieste; MCZ; no further date).
Regional Notes
Europe
Guiliani et al. (2019) observed this species foraging on extrafloral nectaries of the invasive Reynoutria x bohemica (Polygonaceae) in Tuscany. The habitats examined were river banks and disturbed habitats.
Collingwood (1979) - This wide ranging species nests in the soil on sandy lowland heaths, dry open pasture, sea cliffs and rocky outcrops in North Europe. Its habits are mainly subterranean, feeding on the exudates of root aphids but also by scavenging and predating small insects. Workers are generally unobtrusive and non aggressive compared with Lasius niger. Nests are single queened founded by solitary fertilised queens. Mating swarms occur in August.
Flight Period
X | X | X | |||||||||
Jan | Feb | Mar | Apr | May | Jun | Jul | Aug | Sep | Oct | Nov | Dec |
Source: antkeeping.info.
- Check details at Worldwide Ant Nuptial Flights Data, AntNupTracker and AntKeeping.
- Explore: Show all Flight Month data or Search these data. See also a list of all data tables or learn how data is managed.
Association with Other Organisms
- Explore: Show all Associate data or Search these data. See also a list of all data tables or learn how data is managed.
Other Insects
- This species is a host for the temporary parasites Lasius carniolicus (de la Mora et al., 2021; Janda et al., 2004; Seifert, 2018; unconfirmed), Lasius claviger, Lasius distinguendus, Lasius interjectus, Lasius jensi, Lasius latipes, Lasius meridionalis (unconfirmed), Lasius reginae and Lasius umbratus (unconfirmed).
- This species is associated with the aphids Aphis fabae, Aphis galliiscabri, Aphis gossypii, Aphis idaei, Aphis maidi-radicis, Aphis molluginis, Aphis nasturtii, Aphis pomi, Aphis pseudocardui, Aphis solanella, Aphis urticata, Aphis verbasci, Brachycaudus (Appelia) tragopogonis, Brachycaudus cardui, Capitophorus hippophaes, Chaitophorus kapuri, Cinara atlantica, Cinara palaestinesis, Cinara pini, Dysaphis foeniculus, Dysaphis pyri, Myzus cerasi, Neobetulaphis pusilla, Periphyllus bulgaricus, Rhopalosiphum cerasifoliae, Rhopalosiphum maidis, Rhopalosiphum nymphaeae, Sipha maydis and Toxoptera aurantii (Saddiqui et al., 2019 and included references).
- This ant has been associated with the butterflies Glaucopsyche alexis and a species that has recently been split into two species: Polyommatus icarus and Polyommatus celin (Obregon et al. 2015).
- This species is a host for the ichneumonid wasp Hybrizon buccatus (a parasitoid) (Quevillon, 2018) (encounter mode primary; direct transmission; transmission outside nest).
- This species is a host for the ichneumonid wasp Hybrizon rileyi (a parasitoid) (Quevillon, 2018) (encounter mode primary; direct transmission; transmission outside nest).
- This species is a host for the phorid fly Pseudacteon formicarum (a parasitoid) (Quevillon, 2018) (encounter mode primary; direct transmission; transmission outside nest).
- This species is a host for the tachinid fly Strongylogaster globula (a parasitoid) (Quevillon, 2018) (encounter mode primary; direct transmission; transmission outside nest).
- This species is a prey for the Microdon fly Microdon ruficrus (a predator) (Quevillon, 2018).
Mites
- This species is a host for the mite Imparipes obsoletus (a parasite) (Khaustov, 2015) (ectoparasite).
- This species is a host for the mite Petalomium carelitschensis (a parasite) (Khaustov, 2015) (ectoparasite).
- This species is a host for the mite Scutacarus longisetus (a parasite) (Khaustov, 2015) (ectoparasite).
Nematode
- This species is a host for the nematode "Mermis" (a parasite) in England (Oxford, Cornwal) (Crawley & Baylis, 1921).
- This species is a host for the nematode Mermithidae (unspecified "Mermix") (a parasite) in Germany (Wuerzburg) (Gösswald, 1938; Laciny, 2021).
- This species is a host for the nematode Mermis myrmecophila (a parasite) in Germany (Gosswald, 1929; Laciny, 2021).
Fungi
- This species is a host for the fungus Laboulbenia formicarum (a parasite) (Quevillon, 2018) (encounter mode primary; direct transmission; transmission within nest).
- This species is a host for the fungus Laboulbenia formicarum (a pathogen) (Espadaler & Santamaria, 2012).
The reported host/parasite relationship between Lasius distinguendus and Lasius alienus as reported by Janda et al. (2004) should be investigated in the field as Seifert (2018) could not corroborated this relationship (de la Mora et al., 2021).
Reports of Lasius fuliginosus invading Lasius alienus nests (Janda et al., 2004) are unlikely based on biology (Seifert, pers. comm., in de la Mora et al., 2021).
Reports of Lasius mixtus invading Lasius alienus nests (Janda et al., 2004) are a possible misidentification of the host due to subsequent taxonomic revision (de la Mora et al., 2021).
Life History Traits
- Queen number: monogynous (Frumhoff & Ward, 1992)
Castes
Queen
Images from AntWeb
Queen (alate/dealate). Specimen code casent0173158. Photographer April Nobile, uploaded by California Academy of Sciences. | Owned by CAS, San Francisco, CA, USA. |
Male
Images from AntWeb
Worker. Specimen code casent0172725. 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.
- alienus. Formica aliena Foerster, 1850a: 36 (w.m.) GERMANY.
- Foerster, 1850a: 71 (q.); Wheeler, G.C. & Wheeler, J. 1953c: 147 (l.); Hauschteck, 1962: 219 (k.).
- Combination in Lasius: Mayr, 1861: 49 (in key);
- Combination in Lasius (Lasius): Ruzsky, 1912: 633; Forel, 1915d: 53; Wheeler, W.M. 1916k: 172; Karavaiev, 1936: 205;
- Combination in Donisthorpea: Donisthorpe, 1915d: 212;
- Combination in Formicina (Donisthorpea): Emery, 1916b: 240;
- Combination in Formicina: Bondroit, 1918: 25;
- Combination in Lasius (Donisthorpea): Nadig, 1918: 340;
- Combination in Acanthomyops: Ruzsky, 1925b: 44;
- Combination in Acanthomyops (Donisthorpea): Betrem, 1926: 215; Donisthorpe, 1927a: 8; Donisthorpe, 1950e: 1063;
- Combination in Lasius: Ruzsky, 1916: 5; Wheeler, W.M. 1917i: 463; Menozzi, 1921: 32; Müller, 1923b: 125; Emery, 1925b: 230; Kuznetsov-Ugamsky, 1929a: 27.
- Combination in Lasius (Lasius): Wilson, 1955a: 77.
- Subspecies of niger: Forel, 1874: 46 (in key); Mayr, 1877: 20 (in list); Emery & Forel, 1879: 452; Mayr, 1886d: 429; Forel, 1886e: clxvii; Provancher, 1887: 236 (in key); Cresson, 1887: 255; Forel, 1889: 256; Forel, 1890a: lxvii; Emery, 1891b: 16; Forel, 1892i: 307; Lameere, 1892: 64; Emery, in Dalla Torre, 1893: 187 (footnote); Forel, 1894c: 404; Forel, 1894d: 12; Ruzsky, 1896: 71; Saunders, E. 1896: 25; Ruzsky, 1902a: 233; Ruzsky, 1903b: 306; Forel, 1904b: 386; Ruzsky, 1905b: 304; Wheeler, W.M. 1906c: 322; Forel, 1906b: 85; Forel, 1906c: 189; Wasmann, 1906: 114 (in key); Forel, 1909c: 105; Yano, 1910: 421; Bondroit, 1910: 485; Forel, 1910a: 23; Karavaiev, 1910a: 268; Forel, 1911d: 352; Karavaiev, 1912b: 588; Krausse, 1912b: 165; Forel, 1913d: 438; Ruzsky, 1914a: 61; Stitz, 1914: 84; Emery, 1914d: 159; Ruzsky, 1915a: 434; Forel, 1915d: 53 (in key); Emery, 1916b: 240; Ruzsky, 1916: 5; Wheeler, W.M. 1916k: 172; Escherich, 1917: 332 (in key); Wheeler, W.M. 1917a: 525; Wheeler, W.M. 1917i: 463; Nadig, 1918: 340; Santschi, 1919e: 246; Menozzi, 1921: 32; Menozzi, 1922b: 331; Soudek, 1922: 69; Kulmatycki, 1922: 80; Finzi, 1923: 4; Kuznetsov-Ugamsky, 1923: 243; Emery, 1925b: 230; Ruzsky, 1925a: 288; Ruzsky, 1925b: 44; Santschi, 1925g: 349; Soudek, 1925b: 16; Santschi, 1926f: 289; Menozzi, 1926b: 182; Karavaiev, 1927a: 300; Karavaiev, 1927c: 280 (in key); Karavaiev, 1927d: 347; Kuznetsov-Ugamsky, 1927e: 188; Menozzi, 1927b: 91; Kuznetsov-Ugamsky, 1928b: 20; Lomnicki, 1928: 8; Wheeler, W.M. 1928c: 38; Kuznetsov-Ugamsky, 1929a: 27; Kuznetsov-Ugamsky, 1929b: 37; Karavaiev, 1930b: 147; Wheeler, W.M. 1930h: 80; Karavaiev, 1931e: 214; Soudek, 1931: 13; Gösswald, 1932: 57; Menozzi, 1932b: 311; Wheeler, W.M. 1932a: 16; Arnol’di, 1933b: 603 (in key); Grandi, 1935: 103; Karavaiev, 1935b: 108; Menozzi, 1936d: 305; Karavaiev, 1936: 205 (redescription); Karavaiev, 1937: 175; Menozzi, 1939a: 312; Morisita, 1945: 22; Ruzsky, 1946: 69; Azuma, 1951: 88; Smith, M.R. 1951a: 850; Chapman & Capco, 1951: 202; Azuma, 1953: 4; Azuma, 1955: 80; Ceballos, 1956: 316.
- Status as species: Schenck, 1852: 51; Mayr, 1855: 360 (redescription); Nylander, 1856b: 68; Gredler, 1858: 13; Smith, F. 1858b: 7; Mayr, 1861: 49 (in key); Roger, 1861b: 165; Roger, 1863b: 11; Mayr, 1863: 425; Smith, F. 1871b: 2; André, 1874: 180 (in key); Mayr, 1877: 6; Emery, 1878b: 47; Saunders, E. 1880: 209; Mayr, 1880: 26; André, 1882b: 192 (in key); White, W.F. 1884: 255; Nasonov, 1889: 22; Emery, 1891b: 16; Dalla Torre, 1893: 181; Emery, 1897f: 238; Ruzsky, 1902d: 16; Ruzsky, 1903c: 207; Bingham, 1903: 342; Viehmeyer, 1906: 56; Emery, 1908d: 24; Bondroit, 1911: 11; Donisthorpe, 1915d: 212; Bondroit, 1918: 25; Crawley, 1920b: 177; Müller, 1923a: 74; Müller, 1923b: 125; Lomnicki, 1925b: 3; Betrem, 1926: 215; Stärcke, 1926: 124 (in key); Donisthorpe, 1927a: 8; Donisthorpe, 1927b: 242; Finzi, 1933: 165; Stitz, 1934: 9; Zimmermann, 1935: 48; Ruzsky, 1936: 90; Finzi, 1939c: 160; Stitz, 1939: 279; Novák & Sadil, 1941: 101 (in key); Röszler, 1942a: 53; Stärcke, 1944a: 153; van Boven, 1947: 186 (in key); Arnol'di, 1948: 212 (in list); Creighton, 1950a: 419; Röszler, 1951: 91; Consani & Zangheri, 1952: 44; Wilson, 1955a: 77 (redescription); Bernard, 1956b: 261; Bernard, 1959: 351; Dlussky, 1962: 182; Baroni Urbani, 1964a: 7; Baroni Urbani, 1964b: 63; Baroni Urbani, 1964c: 166; Cagniant, 1964: 92; Cagniant, 1966b: 281; Bernard, 1967: 356 (redescription); Baroni Urbani, 1968b: 488; Cagniant, 1968a: 146; Kutter, 1968a: 61; Baroni Urbani, 1969a: 334; Collingwood & Yarrow, 1969: 79; Pisarski, 1969a: 231; Pisarski, 1969b: 306; Dlussky & Pisarski, 1970: 87; Cagniant, 1970c: 38; Baroni Urbani, 1971c: 200; Bourne, 1973: 24; Pisarski, 1975: 34; Tarbinsky, 1976: 138 (redescription); Collingwood, 1976: 305; Aktaç, 1977: 126; Azuma, 1977: 117; van Boven, 1977: 144; Kutter, 1977c: 227; Arnol’di & Dlussky, 1978: 555 (in key); Collingwood, 1978: 89 (in key); Wheeler, G.C. & Wheeler, J. 1978: 393; Smith, D.R. 1979: 1435; Collingwood, 1979: 97; Yamauchi, 1979: 156; Pisarski & Krzysztofiak, 1981: 160; Schembri & Collingwood, 1981: 438; Collingwood, 1981: 27; Allred, 1982: 479; Collingwood, 1982: 285; Wheeler, G.C. & Wheeler, J. 1986g: 65; Agosti & Collingwood, 1987b: 282 (in key); Nilsson & Douwes, 1987: 70; DuBois & LaBerge, 1988: 149; Deyrup, et al. 1989: 99; Kupyanskaya, 1990: 218; Dlussky, Soyunov & Zabelin, 1990: 159; Casevitz-Weulersse, 1990c: 428; Morisita, et al. 1991: 27; Wu, J. & Wang, 1992: 1312; Atanassov & Dlussky, 1992: 237; Seifert, 1992b: 13 (redescription); Arakelian, 1994: 116; Radchenko, 1994b: 115 (in key); Douwes, 1995: 94; Bolton, 1995b: 221; Wu, J. & Wang, 1995: 155; Tang, Li, et al. 1995: 108; Collingwood & Prince, 1998: 23 (in key); Czechowski, et al. 2002: 105; Mackay & Mackay, 2002: 379; Deyrup, 2003: 45; Imai, et al. 2003: 63; Coovert, 2005: 120; Csösz, & Markó, 2005: 230; Karaman, G.S. & Karaman, 2005: 56; MacGown & Forster, 2005: 64; Bračko, 2006: 148; Bračko, 2007: 20; Seifert, 2007: 272; Werner & Wiezik, 2007: 153; Zryanin & Zryanina, 2007: 234; Gratiashvili & Barjadze, 2008: 136; Casevitz-Weulersse & Galkowsky, 2009: 483; Lapeva-Gjonova, et al. 2010: 35; Boer, 2010: 42; Csösz, et al. 2011: 58; Legakis, 2011: 26; Borowiec, L. & Salata, 2012: 498; Czechowski, et al. 2012: 263; Ellison, et al. 2012: 189; Borowiec, L. 2014: 83; Seifert & Galkowski, 2016: 52 (in key); Radchenko, 2016: 362; Deyrup, 2017: 206; Schar et al., 2018: 6.
- Senior synonym of pannonica: Wilson, 1955a: 77; Radchenko, 2016: 362.
- Material of the unavailable names alienoamericanus, flavidus, turkmenus referred here by Wilson, 1955a: 77.
Type Material
- Neotype worker plus 10 workers from the neotype nest labelled GER: Eifel, 7.9. 1991, 37 km SE Aachen, Schleiden ; depositories SMN Görlitz, BMNH London (Seifert, 2020).
Wilson (1955) - Dr. H. Bischoff has informed me that no syntypes of Lasius alienus can be located in the Foerster Collection in the Berlin Museum. What may be part of the type series has been found instead in the Mayr Collection and lent me by Dr. M. Beier. This consists of two pins, one holding two workers and the other a single male, labelled "Aach. Forst/Las. alienus det. Mayr." The workers are identifiable as typical alienus.
Unless otherwise noted the text for the remainder of this section is reported from the publication that includes the original description.
Description
Worker
Wilson (1955) - Within the PW range of 0.53-0.70 mm., the seta count is always less than 20 and usually less than 10. The seta count is strongly allometric, making it advisable to determine individual specimens by comparing them with the regression zones of Figure 6. In Europe the regression zones of Lasius niger and Lasius alienus are parallel but well segregated; the alienus line is set so that the great majority of workers have seta counts of less than 5, while most niger exceed 20. In eastern Asia, on the other hand, alienus evidently becomes scarcer, and the niger zone shifts down and forward to become contiguous with that of alienus. As a result, a small number of individuals cannot be safely determined to either species.
Size ranging and averaging smaller than in niger. In a sample of 147, with no more than 2 per nest series, mean with standard error 0.56 ± 0.004 mm., standard deviation 0.054 mm, Color averaging lighter than niger, although total variation in both species shows complete overlap.
Borowiec and Salata (2022) - Small to moderately large, HL 0.742-1.035 (mean 0.836), HW 0.663-0.977 (mean 0.807), ML 0.80-1.06. Scape moderately elongate, SL 0.684-0.926 (mean 0.788). Color. Body unicolor with head, mesosoma, coxae and gaster medium brown. Antennae, tibiae and tarsi light yellowish brown, mandibles light reddish brown. Sometimes whole body and appendages are yellowish brown. Structure and setation. Head oval, always longer than wide, lateral surfaces above eyes convex, occipital margin of head straight to slightly concave. Occipital part of head with less than 15 (usually 8-12) erected setae, ventral part of head lacking erected setae, mesosomal dorsum with numerous, long erected setae. Below propodeal spiracle usually no erected setae or at most single short seta. Mandibles usually with 8 dents. Antennal scapi with smooth pubescence lacking erected setae, at most with few semierect hair, hind tibiae lacking erected setae or at most with 1-2, occasionally 3-4, short setae in basal part. Ventral surface of fore femora with 4-6 and mid femora 2-4 erected setae, of hind femora without or 1-2 setae close to base of femur, anterior surface of fore coxa with several long erected setae. Pubescence on the whole body with rather dense, appressed pubescence, surface with weak microreticulation, appears rather shining. Pubescence of clypeus dense, not as dense as in Lasius paralienus or Lasius bombycina but denser than in Lasius psammophilus or Lasius creticus. First gastral tergite on the whole surface with numerous erected setae. Propodeum in lateral view with straight anterior and posterior surface, conical and equal in height or slightly higher to mesonotum, metanotal groove deep.
Queen
Wilson (1955) - Seta count never exceeding 10 and usually 0.
Size averaging smaller than niger when the North American populations are included.
Male
Wilson (1955) - Seta count almost always 0.
Size range about the same as in Lasius niger and showing parallel geographic variation. Mandibles typically of niger type, but in two series (Engadin, Switzerland, Kutter leg. and Coll., Hornet, Beltrami Co., Minn., A. Achenbach leg., G. C. Wheeler Coll.) the mandible type is closer to the intermediate type of Lasius brunneus. Subgenital plate showing the same wide variation as in Lasius niger; series from Godinne, Belgium (A. Raignier leg.; MCZ) and the Engadin Valley, Switzerland (Kutter) encompass within themselves the full variation from the unilobed to bilobed condition.
Karyotype
- See additional details at the Ant Chromosome Database.
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- n = 15, 2n = 30 (Germany; Switzerland) (Hauschteck-Jungen & Jungen, 1983) (n=14 was also reported, Lorite and Palomeque 2010 suggested that such karyotype is due Robertsonian polymorphism).
- 2n = 28 (Switzerland) (Hauschteck, 1962).
Worker Morphology
- Explore: Show all Worker Morphology data or Search these data. See also a list of all data tables or learn how data is managed.
References
- Seifert, B. 1992b. A taxonomic revision of the Palaearctic members of the ant subgenus Lasius s.str. (Hymenoptera: Formicidae). Abh. Ber. Naturkundemus. Görlitz 66(5): 1-67.
- Alatorre-Bracamontes, C.E., Vásquez-Bolaños, M. 2010. Lista comentada de las hormigas (Hymenoptera: Formicidae) del norte de México. Dugesiana 17(1): 9-36.
- André, E. 1882c. Les fourmis. [part]. Pp. 153-232 in: André, Edm. 1881-1886. Species des Hyménoptères d'Europe et d'Algérie. Tome Deuxième. Beaune: Edmond André, 919 + 48 pp. (page 192, Status as species)
- Atanassov, N.; Dlussky, G. M. 1992. Fauna of Bulgaria. Hymenoptera, Formicidae. Fauna Bûlg. 22: 1-310 (page 237, Status as species)
- Baer, B. 2011. The copulation biology of ants (Hymenoptera: Formicidae). Myrmecological News 14: 55-68.
- Baroni Urbani, C. 1971c. Catalogo delle specie di Formicidae d'Italia (Studi sulla mirmecofauna d'Italia X). Memorie della Societa Entomologica Italiana 50: 5-287 (page 200, Status as species)
- Bernadou, A., Fourcassié, V., Espadaler, X. 2013. A preliminary checklist of the ants (Hymenoptera, Formicidae) of Andorra. ZooKeys 277, 13–23 (doi:10.3897/zookeys.277.4684).
- Bondroit, J. 1911a. Contribution à la faune de Belgique. Notes diverses. Ann. Soc. Entomol. Belg. 55: 8-13 (page 11, Status as species)
- Bondroit, J. 1918. Les fourmis de France et de Belgique. Ann. Soc. Entomol. Fr. 87: 1-174 (page 25, Status as species)
- Borowiec, L. 2014. Catalogue of ants of Europe, the Mediterranean Basin and adjacent regions (Hymenoptera: Formicidae). Genus (Wroclaw) 25(1-2): 1-340.
- Borowiec, L., Lebas, C., Salata, S. 2022. Notes on ants (Hymenoptera: Formicidae) from three northern Aegean islands – Lemnos, Samothraki and Thasos. Annals of the Upper Silesian Museum in Bytom, Entomology 31: 1-14 (doi:10.5281/ZENODO.7346453).
- Borowiec, L., Salata, S. 2017. First certain record of Lasius alienus (F RSTER, 1850) (Hymenoptera: Formicidae) and three ant species new to the Republic of Macedonia. Acta Entomologica Silesiana 25(online 019): 1–4.
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- Pages using DynamicPageList3 parser function
- Limited invasive
- Common Name
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- North subtropical
- Tropical
- FlightMonth
- Ant Associate
- Host of Lasius carniolicus
- Host of Lasius claviger
- Host of Lasius distinguendus
- Host of Lasius interjectus
- Host of Lasius jensi
- Host of Lasius latipes
- Host of Lasius meridionalis
- Host of Lasius reginae
- Host of Lasius umbratus
- Aphid Associate
- Host of Aphis fabae
- Host of Aphis galliiscabri
- Host of Aphis gossypii
- Host of Aphis idaei
- Host of Aphis maidi-radicis
- Host of Aphis molluginis
- Host of Aphis nasturtii
- Host of Aphis pomi
- Host of Aphis pseudocardui
- Host of Aphis solanella
- Host of Aphis urticata
- Host of Aphis verbasci
- Host of Brachycaudus (Appelia) tragopogonis
- Host of Brachycaudus cardui
- Host of Capitophorus hippophaes
- Host of Chaitophorus kapuri
- Host of Cinara atlantica
- Host of Cinara palaestinesis
- Host of Cinara pini
- Host of Dysaphis foeniculus
- Host of Dysaphis pyri
- Host of Myzus cerasi
- Host of Neobetulaphis pusilla
- Host of Periphyllus bulgaricus
- Host of Rhopalosiphum cerasifoliae
- Host of Rhopalosiphum maidis
- Host of Rhopalosiphum nymphaeae
- Host of Sipha maydis
- Host of Toxoptera aurantii
- Butterfly Associate
- Host of Glaucopsyche alexis
- Ichneumonid wasp Associate
- Host of Hybrizon buccatus
- Host of Hybrizon rileyi
- Phorid fly Associate
- Host of Pseudacteon formicarum
- Tachinid fly Associate
- Host of Strongylogaster globula
- ''Microdon'' fly Associate
- Host of Microdon ruficrus
- Mite Associate
- Host of Imparipes obsoletus
- Host of Petalomium carelitschensis
- Host of Scutacarus longisetus
- Nematode Associate
- Host of "Mermis"
- Host of Mermithidae (unspecified "Mermix")
- Host of Mermis myrmecophila
- Fungus Associate
- Host of Laboulbenia formicarum
- Photo Gallery
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