The ants love Honey and Sugar water. Their young also eat small insects.
Found in London.
Small Black ant. Sometimes seen farming aphids. Similar to other Lasius ants.
Worker: 3-5mm
Extant: 1 valid subspecies
Formica nigra Linnaeus, 1758 PDF: 580 (w.) [Type-locality Sweden, after Linnaeus, 1761 PDF: 427.] SWEDEN. Palearctic. AntCat AntWiki HOLTaxonomic history
Latreille, 1798 PDF: 39 (q.m.); Wheeler & Wheeler, 1953c PDF: 148 (l.); Hauschteck, 1962 PDF: 219 (k.); Imai & Kubota, 1972 PDF: 196 (k.).Combination in Lasius: Fabricius, 1804 PDF: 415; Mayr, 1861 PDF: 49 (in key).Combination in Donisthorpea: Morice & Durrant, 1915 PDF: 423; Donisthorpe, 1915f: 200.Combination in Formicina (Donisthorpea): Emery, 1916a PDF: 240.Combination in Acanthomyops: Forel, 1916 PDF: 460; Kuznetsov-Ugamsky, 1927e PDF: 188.Combination in Formicina: Bondroit, 1918 PDF: 23.Combination in Lasius (Donisthorpea): Nadig, 1918 PDF: 340.Combination in Acanthomyops (Donisthorpea): Ruzsky, 1920 PDF: 78; Kiseleva, 1925 PDF: 74; Betrem, 1926 PDF: 215; Donisthorpe, 1927a PDF: 8; Donisthorpe, 1950e PDF: 1063.Combination in Lasius: Wheeler, 1916o PDF: 172; Ruzsky, 1916: 5; Stitz, 1917 PDF: 349; Menozzi, 1921 PDF: 32; Müller, 1923b PDF: 124; Kuznetsov-Ugamsky, 1929a PDF: 26.Combination in Lasius (Lasius): Ruzsky, 1912 PDF: 633; Forel, 1915d: 53; Emery, 1924c PDF: 170; Emery, 1925d PDF: 229; Karavaiev, 1936: 201; Wilson, 1955a PDF: 59.Status as species: Linnaeus, 1761 PDF: 427; Scopoli, 1763 PDF: 313; Linnaeus, 1767 PDF: 962; Fabricius, 1775 PDF: 392; Forskål, 1775: xxiii; Fabricius, 1782: 489; Retzius, 1783 PDF: 75; Geoffroy, in Fourcroy, 1785: 453; Fabricius, 1787 PDF: 308; Razoumowsky, 1789: 225; Christ, 1791 PDF: 510; Olivier, 1792: 492; Fabricius, 1793 PDF: 352; Latreille, 1798 PDF: 39; Fabricius, 1804 PDF: 415; Gravenhorst, 1807 PDF: 287; Latreille, 1809 PDF: 126; Billberg, 1820: 104; Latreille, 1802a PDF: 156; Walckenaer, 1802: 161; Fabricius, 1804 PDF: 415; Latreille, 1817a: 99; Lamarck, 1817 PDF: 96; Stephens, 1829b: 357; Brullé, 1833 PDF: 327; Losana, 1834 PDF: 317; Lepeletier de Saint-Fargeau, 1835 PDF: 206; Nylander, 1846a PDF: 920; Smith, 1851 PDF: 2; Schenck, 1852 PDF: 49; Mayr, 1855 PDF: 355 (redescription); Smith, 1855a PDF: 109; Nylander, 1856b PDF: 67; Gredler, 1858 PDF: 12; Smith, 1858a PDF: 6, 52; Mayr, 1861 PDF: 49 (in key); Meinert, 1861: 318; Roger, 1863b PDF: 11; Mayr, 1863a PDF: 426; Mayr, 1865 PDF: 55; Emery, 1869b PDF: 9; Smith, 1871c: 1; Dours, 1873 PDF: 165; Smith, 1874b PDF: 403; Forel, 1874 PDF: 46 (in key); André, 1874b (in key); Mayr, 1877a: 6; Emery, 1878a PDF: ix (in list); Emery, 1878: 47; Emery & Forel, 1879 PDF: 452; Mayr, 1880 PDF: 25; Saunders, 1880 PDF: 208; André, 1882c PDF: 192 (in key); Emery, 1882b PDF: 450; Costa, 1883: 60; White, 1884 PDF: 254; Mayr, 1886d PDF: 429; Forel, 1886h PDF: 206; Cresson, 1887 PDF: 257; Nasonov, 1889: 22; Forel, 1890b PDF: lxvii; Lameere, 1892: 64; Forel, 1892j PDF: 307; Emery, 1892c PDF: 162; Dalla Torre, 1893 PDF: 187; Emery, 1893e PDF: 85; Emery, 1893k PDF: 638; Medina, 1893 PDF: 105; Forel, 1894c PDF: 404; Forel, 1895e PDF: 227; Ruzsky, 1896 PDF: 71; Saunders, 1896 PDF: 25; Forel, 1899b PDF: 127; Forel, 1900h PDF: 269, 285; Wheeler, 1900c PDF: 47; Forel, 1901m PDF: 66; Ruzsky, 1902d PDF: 16; Ruzsky, 1903b PDF: 307; Ruzsky, 1903c PDF: 207; Ruzsky, 1904a PDF: 288; Forel, 1904c PDF: 386; Ruzsky, 1905b: 292; Wheeler, 1906h PDF: 321; Wheeler, 1906j PDF: 352; Wasmann, 1906 PDF: 114 (in key); Santschi, 1908 PDF: 517; Wheeler, 1908i PDF: 622; Bondroit, 1910 PDF: 485; Yano, 1910a PDF: 421; Karavaiev, 1912b PDF: 587; Krausse, 1912c PDF: 165; Stitz, 1914 PDF: 84; Emery, 1914c PDF: 159; Ruzsky, 1914a PDF: 61; Ruzsky, 1914b PDF: 105; Forel, 1915d: 53 (in key); Donisthorpe, 1915f: 200; Ruzsky, 1916: 5; Stitz, 1917 PDF: 349; Wheeler, 1917a PDF: 524; Emery, 1916a PDF: 240; Escherich, 1917: 332 (in key); Bondroit, 1918 PDF: 23; Nadig, 1918 PDF: 340; Menozzi, 1918 PDF: 87; Santschi, 1919e PDF: 246; Ruzsky, 1920 PDF: 78; Menozzi, 1922c PDF: 331; Kulmatycki, 1922 PDF: 80; Soudek, 1922b PDF: 69; Müller, 1923b PDF: 124; Emery, 1924c PDF: 170; Emery, 1925d PDF: 229; Kiseleva, 1925 PDF: 74; Ruzsky, 1925a PDF: 287; Santschi, 1925f PDF: 88; Santschi, 1925g PDF: 349; Lomnicki, 1925b PDF: 2; Soudek, 1925b PDF: 16; Wheeler, 1926a PDF: 5; Betrem, 1926 PDF: 215; Karavaiev, 1926e PDF: 193; Menozzi, 1926b PDF: 182; Santschi, 1926f PDF: 288; Stärcke, 1926a PDF: 123 (in key); Donisthorpe, 1927a PDF: 8; Donisthorpe, 1927c: 229; Karavaiev, 1927a PDF: 300; Karavaiev, 1927d: 280 (in key); Karavaiev, 1927e PDF: 347; Kuznetsov-Ugamsky, 1927e PDF: 188; Menozzi, 1927b PDF: 91; Wheeler, 1927e PDF: 3; Wheeler, 1927g PDF: 118; Lomnicki, 1928 PDF: 8; Kuznetsov-Ugamsky, 1928b PDF: 19; Wheeler, 1928c PDF: 38; Wheeler, 1928d PDF: 120; Wheeler, 1929g PDF: 10; Wheeler, 1929h PDF: 58; Kuznetsov-Ugamsky, 1929a PDF: 26; Kuznetsov-Ugamsky, 1929b PDF: 37; Karavaiev, 1930b PDF: 147; Wheeler, 1930k PDF: 80; Karavaiev, 1931b PDF: 32; Karavaiev, 1931c PDF: 109; Karavaiev, 1931e PDF: 214; Santschi, 1931a: 10; Soudek, 1931 PDF: 13; Gösswald, 1932 PDF: 53; Santschi, 1932e PDF: 72; Santschi, 1932h PDF: 5; Teranishi, 1932 PDF: 52; Arnol'di, 1933a: 602 (in key); Finzi, 1933 PDF: 165; Santschi, 1933a PDF: 22; Stitz, 1934: 8; Grandi, 1935 PDF: 103; Karavaiev, 1935b PDF: 108; Zimmermann, 1935 PDF: 47; Finzi, 1936 PDF: 191; Karavaiev, 1936: 201 (redescription); Ruzsky, 1936 PDF: 90; Santschi, 1936c PDF: 208; Santschi, 1939c PDF: 5; Kôno & Sugihara, 1939 PDF: 10; Teranishi, 1940: 20; Novák & Sadil, 1941 PDF: 101 (in key); Eidmann, 1941a PDF: 24; Santschi, 1941 PDF: 277; Holgersen, 1943c PDF: 174 (in key); Stärcke, 1944b PDF: 157 (in key); Holgersen, 1944a PDF: 181; Morisita, 1945 PDF: 22; Ruzsky, 1946 PDF: 69; Van Boven, 1947b PDF: 185 (in key); Forsslund, 1947 PDF: 69; Röszler, 1950 PDF: 219; Schmitz, 1950 PDF: 14; Creighton, 1950a PDF: 420; Azuma, 1950a: 35; Azuma, 1951 PDF: 88; Chapman & Capco, 1951 PDF: 202; Consani & Zangheri, 1952 PDF: 44; Azuma, 1953 PDF: 4; Azuma, 1955 PDF: 80; Wellenius, 1955 PDF: 15; Wilson, 1955a PDF: 59 (redescription); Ceballos, 1956: 315; Bernard, 1956b PDF: 261; Smith, 1958c PDF: 148; Bernard, 1959a PDF: 351; Collingwood, 1961a PDF: 71; Collingwood, 1962c PDF: 219; Baroni Urbani, 1964b PDF: 63; Baroni Urbani, 1964c PDF: 165; Cagniant, 1964 PDF: 92; Cagniant, 1966b PDF: 281; Imai, 1966b PDF: 119; Beck et al., 1967: 70; Bernard, 1967a PDF: 355 (redescription); Yarrow, 1967 PDF: 30; Cagniant, 1968a PDF: 146; Kutter, 1968b: 60; Collingwood & Yarrow, 1969 PDF: 78; Pisarski, 1969b: 305; Yamauchi & Hayashida, 1970 PDF: 503; Dlussky & Pisarski, 1970 PDF: 87; Collingwood, 1970b: 380; Cagniant, 1970c PDF: 38; Baroni Urbani, 1971c PDF: 205; Collingwood, 1971 PDF: 165; Banert & Pisarski, 1972 PDF: 353; Bourne, 1973 PDF: 24; Baroni Urbani, 1974a PDF: 238; Bolton & Collingwood, 1975: 7 (in key); Hunt & Snelling, 1975 PDF: 22; Pisarski, 1975: 33; Tarbinsky, 1976 PDF: 134 (redescription); Collingwood, 1976a PDF: 305; Azuma, 1977a PDF: 117; Van Boven, 1977 PDF: 144; Kutter, 1977c: 227; Yensen et al., 1977 PDF: 184; Arnol'di & Dlussky, 1978: 555 (in key); Báez & Ortega, 1978: 189; Collingwood, 1978 PDF: 89 (in key); Collingwood, 1979 PDF: 99; Francoeur & Snelling, 1979 PDF: 6; Smith, 1979: 1436; Yamauchi, 1979 PDF: 152; Onoyama, 1980a PDF: 199; Barquín, 1981: 448; Pisarski & Krzysztofiak, 1981 PDF: 160; Schembri & Collingwood, 1981 PDF: 439; Collingwood, 1981 PDF: 27; Allred, 1982: 481; Collingwood, 1982 PDF: 287; Agosti & Collingwood, 1987a PDF: 58; Agosti & Collingwood, 1987b PDF: 282 (in key); Nilsson & Douwes, 1987: 70; MacKay et al., 1988: 118; Kupyanskaya, 1990a: 219; Casevitz-Weulersse, 1990c PDF: 430; Le Moli & Rosi, 1991: 36; Morisita et al., 1991: 27; Seifert, 1991b PDF: 71; Seifert, 1992b PDF: 27 (redescription); Wang, 1992: 680; Wu & Wang, 1992c PDF: 1312; Hohmann et al., 1993: 163; Arakelian, 1994 PDF: 121; Radchenko, 1994b: 114 (in key); Bolton, 1995b: 224; Douwes, 1995: 94; Poldi et al., 1995: 8; Tang et al., 1995: 110; Wu & Wang, 1995a: 153; Espadaler, 1997g PDF: 28; Collingwood & Prince, 1998: 23 (in key); Gallé et al., 1998: 216; Collingwood & Heatwole, 2002 PDF: 12; Czechowski et al., 2002 PDF: 100; Mackay & Mackay, 2002 PDF: 384; Zhang & Zheng, 2002 PDF: 219; Karaman & Karaman, 2003 PDF: 54; Lin & Wu, 2003: 61; Csosz & Markó, 2005 PDF: 227; Karaman & Karaman, 2005 PDF: 57; Ward, 2005 PDF: 64; Bračko, 2006 PDF: 149; Markó et al., 2006 PDF: 68; Petrov, 2006 PDF: 69, 107 (in key); Schultz et al., 2006 PDF: 205; Bračko, 2007 PDF: 20; Seifert, 2007: 274; Werner & Wiezik, 2007 PDF: 154; Zryanin & Zryanina, 2007 PDF: 234; Gratiashvili & Barjadze, 2008 PDF: 136; Casevitz-Weulersse & Galkowski, 2009 PDF: 484; Lapeva-Gjonova et al., 2010 PDF: 39; Boer, 2010: 43; Csosz et al., 2011 PDF: 58; Karaman, 2011a PDF: 88; Legakis, 2011 PDF: 27; Borowiec & Salata, 2012 PDF: 503; Czechowski et al., 2012: 253; Guénard & Dunn, 2012 PDF: 33; Kiran & Karaman, 2012 PDF: 13; Bharti & Gul, 2013a PDF: 57 (in key); Borowiec, 2014 PDF: 88 (see note in bibliography); Bračko et al., 2014 PDF: 20; Bharti et al., 2016 PDF: 28; Lebas et al., 2016: 220; Radchenko, 2016: 360; Salata & Borowiec, 2018c 10.5281/zenodo.2199191 PDF: 46; Schär et al., 2018 10.1111/jbi.13380 PDF: 6; Seifert, 2018: 273; Seifert, 2020 10.25674/so92iss1pp15 PDF: 63.Senior synonym of Lasius alienoniger: Wilson, 1955a PDF: 59; Bernard, 1967a PDF: 355; Baroni Urbani, 1971c PDF: 206; Van Boven, 1977 PDF: 144; Kutter, 1977c: 14; Smith, 1979: 1436; Yamauchi, 1979 PDF: 152; Onoyama, 1980a PDF: 199; Arakelian, 1994 PDF: 122; Bolton, 1995b: 224; Radchenko, 2016: 360.Senior synonym of Lasius emeryi: Wilson, 1955a PDF: 59; Smith, 1979: 1436; Bolton, 1995b: 224.Senior synonym of Lasius minimus: Wilson, 1955a PDF: 59; Smith, 1979: 1436; Bolton, 1995b: 224.Senior synonym of Lasius nigerrimus: Emery, 1892c PDF: 162; Dalla Torre, 1893 PDF: 188; Donisthorpe, 1915f: 200; Emery, 1925d PDF: 230; Donisthorpe, 1927c: 229; Karavaiev, 1936: 202; Bolton, 1995b: 224; Radchenko, 2016: 360.Senior synonym of Lasius nitidus: Wilson, 1955a PDF: 59; Smith, 1979: 1436; Bolton, 1995b: 224.Senior synonym of Lasius pallescens: Roger, 1859 PDF: 238; Mayr, 1861 PDF: 49 (in key); Mayr, 1863a PDF: 425; Roger, 1863b PDF: 11; Mayr, 1865 PDF: 55; André, 1874c (in list); Emery & Forel, 1879 PDF: 452; Dalla Torre, 1893 PDF: 189; Donisthorpe, 1915f: 200; Emery, 1925d PDF: 230; Donisthorpe, 1927c: 229; Karavaiev, 1936: 202; Baroni Urbani, 1971c PDF: 205; Bolton, 1995b: 224; Radchenko, 2016: 360.Senior synonym of Lasius transylvanicus: Wilson, 1955a PDF: 59; Smith, 1979: 1436; Bolton, 1995b: 224.Syst. Piez. 415,1. Formica minor, Ray , Hist. Ins. 69.
Swamm. Bill. Nat. t. 16, f. 1 - 11. The small black Ant, Gould, Eng. Ants, ii. 5. La Fourmi toute noire, Geoff. Ins. Par. ii. 429, 6. Hab. - Britain, Banks.
Chine occidentale (Sze-tschwan, fl. Pasyn-kou, pres de Tschzumse, 2 [[ queen ]], 19. VII; vallee de Maon-jukou, 1 [[ queen ]], 20. VII. 1893. Potanin!); Ussuri merid. (Sidemi, 4 [[ worker ]], 20 - 30. VII. 1897. Jankovsku!); Region transcaspienne (As'- chabad, 1 [[ queen ]], 1896. Ahkger!); Transcaucasie (Borzom, Likani, attires par la lumiere electr., 3 [[ queen ]], 8 [[ male ]], 12. VII. 1901. R. Schmidt!; Gouv. Kutais, Artvin, 2 [[ worker ]], 23. VI. 1898. Derjugin!).
Pas de longs poils epais, couches, jaunes sur l'abdomen.
Tébessa (jardins).
[[ worker ]] et [[ queen ]] recoltes a Hakodate, Japon, par M. Hilgendorf (Musee de Berlin). Ces exemplaires sont absolument identiques a ceux d'Europe. — Comme cette espece si commune est deja connue comme habitant toute l'Europe, le Turkestan, le nord de l'Afrique, Madere et les Etats-Unis, on peut bien admettre maintenant qu'elle habite tout l'hemisphere nord jusqu'a environ 30 degres de latitude au sud.
— Canaria, Tenerife (M. Noualhier). Forme typique a scapes et tibias tres poilus.
Ces deux especes sont tres communes en Europe; la deuxieme a ete trouvee aussi dans le nord de l'Afrique, ou elle a ete probablement importee d'Europe.
Himalaya (Smythies); 6,000 ' a 9,000 '.
[[ worker ]]: - L: 3, 6 a 4, 2 mill. Sillon frontal tres distinct. Beaucoup plus large et plus robuste que lu precedent. Plus robuste et plus grand que la forme typique d'Europe. Pubescence un peu plus grossiere, comme chez le L. alienus . D'un brun assez fonce, avec les joues, les mandibules, les scapes, la base des funicules, les tarses, une partie du dessous de la tete et les articulations des pattes d'un jaunatre sale plus ou moins rougeatre on brunatre (chez le L. brunneus , i. st., la couleur est d'un rouge brunatre avec l'abdomen brun).
Transcaucasie (Borzom, Likani, attires par la lumiere electr., l [[ male ]], 1 [[ queen ]], 12. VII; Gouv. Elisabethpol, Geok-tapa, 14 [[ worker ]], 26. VII. 1901. R. Schmidt!).
Lasius niger var. alienoniger Forel, 1874: Forel 1892 , Atanassov 1936 , 1952 (see Notes below)
Records
(Map 55): Bulgaria ( Agosti and Collingwood 1987a , Atanassov and Dlusskij 1992 , Seifert 1992 ); Western Predbalkan: Krapets vill. [ Atanassov 1936 (as Lasius alieno niger )]; Central Predbalkan: Dermantsi vill. (Lukovit) [ Atanassov 1934 , 1936 (as Lasius alieno niger )]; Western Stara Planina Mts: Chepan (Dragoman) ( Borisova et al. 2005 ); Eastern Stara Planina Mts: Sliven ( Forel 1892 ); Zemen Gorge: Skakavitsa waterfall ( Atanassov 1936 ); Vitosha Mt. [ Atanassov 1952 (as Lasius niger L. var. alieno-niger Forel), Hlaváč et al. 2007 ]; Sofia Basin: Sofia [ Atanassov 1936 (as Lasius alieno niger ), Antonova 2004 , 2005 , Lapeva-Gjonova 2004b , Lapeva-Gjonova and Atanasova 2004 , Antonova and Penev 2006 , 2008 , Hlaváč et al. 2007 ], the surroundings of Sofia near Vladaya vill. ( Antonova and Penev 2006 , 2008 ); Plana Mt.: Pasarel vill. ( Vagalinski and Lapeva-Gjonova in press ); Podbalkan Basins: Rose valley ( Atanassov et al. 1955 ); Lozenska Planina Mt. ( Vassilev and Evtimov 1973 ): near German monastery ( Antonova and Penev 2008 ); Belasitsa Mt. ( Atanassov 1964 ); Krupnik-Sandanski-Petrich Valley: around Mitino vill., Petrich plain ( Atanassov 1964 ); Rila Mt.: the valley of Rilska river [ Forel 1892 (as Lasius niger Rasse alienus var. alieno-niger)]; Western Rhodopi Mts: Asenovgrad [ Forel 1892 (as Lasius niger Rasse alienus var. alieno-niger)], Devin, Peshtera, Batak ( Lapeva-Gjonova in press (a) ); Southern Black Sea coast: Burgas, Sozopol [ Forel 1892 (as Lasius niger Rasse alienus var. alieno-niger)], Veselie vill. ( Forel 1892 ).
Notes:
Some of the above mentioned records most probably include also closely related Lasius platythorax . Lasius niger alienoniger Forel, 1874 has been considered by different authors to be a separate species or a junior synonym of Lasius niger , but Seifert (1992) proposed it should be considered as incertae sedis in Lasius (for details see Bolton 1995 , Bolton et al. 2006 ).
Transcaucasie orient. (Gouv. Baku, gorge de Bum, 1 [[ worker ]], 1892. Schelkovnikov!); Region transcaspienne (As'chabad, 1 [[ queen ]], 1896. Ahnger!).
[[ worker ]]. L. 3 a 3,5 mill. Pilosite dressee du corps, des pattes et des scapes, ainsi que la grandeur des yeux identiques au niger typique. Mais la sculpture est plus faible, surtout sur la tete, qui est luisante, ponctuee, l'epistome meme tres luisant, plus luisant encore que chez le flavus . Les mandibules sont aussi luisantes et tres faiblement sculptees. La couleur varie d'un jaune brunatre aussi clair que chez les exemplaires fonces du Lasius flavus d'Europe a un brun plus clair que celui des exemplaires les plus clairs des Lasius niger et alienus , a peu pres comme chez les formes bruneo-emarginatus et brunneus , mais uniforme (le thorax n'etant pas plus clair que l'abdomen et la tete), et plus luisant
Du reste identique au L. niger . Les variations de couleur de cette forme rappellent celles de l´alieno-flavus Bingham, do l'Inde septentrionale, mais la pilosite, les yeux plus grands et la taille plus grande l'en distinguent.
Buchara oriental (Schugnan, fl. Gunt, Sardym, 10 [[ worker ]], 16. VIII; Kara-gurum-Mazar, 3 [[ worker ]], 24. VII; Roschan, Col de Mardzanai, 4 [[ worker ]], 19. VIII. 1897. Kaznakov!).
The black garden ant (Lasius niger), also known as the common black ant, is a formicine ant, the type species of the subgenus Lasius, which is found across Europe and in some parts of North America, South America, Asia and Australasia. The European species was split into two species; L. niger, which are found in open areas; and L. platythorax, which is found in forest habitats.[1] It is monogynous, meaning colonies contain a single queen.
Lasius niger colonies normally range from 4,000 to 7,000 workers, but can reach 40,000 in rare cases. A Lasius niger queen can live for up to 29 years[2] the longest recorded lifespan for any eusocial insect.[3] Lasius niger queens in the early stages of founding can have two to three other queens in the nest. They will tolerate each other until the first workers come, then it is most likely they will fight until one queen remains. Under laboratory conditions, workers can live at least 4 years.[4]
Lasius niger is host to a number of temporary social parasites of the Lasius mixtus group including Lasius mixtus and Lasius umbratus.
Ants mate on the wing, so "flying ants" are alates (reproductive individuals), which includes males and gynes (virgin queens). The mating (or nuptial) flights of Lasius niger usually occur around June to September throughout the species' range; in North America flights usually occur during the autumn, whereas in Europe they generally take place during the hot summer months of July and August. Flights can contain thousands of winged males and females.[5]
Disparities between local weather conditions can cause nuptial flights to be out of phase amongst widespread populations of L. niger. During long-lasting, hot summers, flights can take place simultaneously across the country, but overcast weather with local patches of sunshine results in a far less synchronized emergence of alates.
Once the queens have mated they will land and discard their wings and begin to find a suitable place to dig a tunnel. Meanwhile, males generally only live for a day or two after the mating flights and will then die.
After removing her wings, a queen will move quickly to find moist ground, then start digging a tunnel. Once the tunnel has been completed, the queen will block the entrance and retreat to the bottom. Subsequently, she will dig out a small chamber. This will serve as the claustral chamber of the new colony. Generally, a queen will begin to lay eggs immediately after the construction of the chamber, and the eggs will hatch after 8–10 weeks. Until the eggs hatch and the larvae grow to maturity, a Lasius niger queen will not eat, relying on the protein of her wing muscles to be broken down and digested. In some cases, a Lasius niger queen may eat her own eggs in order to survive.
Lasius niger, like other ants, have four stages of development: egg, larva, pupa, and adult. Lasius niger lay tiny, white, kidney-shaped eggs with a smooth sticky surface which helps them to be carried in a group instead of one by one. After hatching Lasius niger proceed onto the larva stage resembling tiny maggots. The larvae need to be fed by the queen (or workers in the case of an established colony) if they are to mature; as they feed the larvae grow, shedding their skin, doing so usually three times in total. With each molt, the larvae grow hooked hairs which allow them to be carried in groups. When Lasius niger larvae reach the last molt they are generally too big to be carried as part of a group and so are carried individually. Once the larva grows big enough it spins a cocoon around itself. To aid this process a queen (or workers) may bury the larva so that it can spin its cocoon undisturbed, and begin a process of metamorphosis. Once the process is complete the Lasius niger worker emerges from the cocoon. At this stage, the callow worker is completely white but will darken over the course of an hour until it has turned black.
The first worker ants that emerge are very small compared to later generations. At this point the workers immediately begin to expand the nest and care for the queen and brood; they eventually remove the seal from the entrance to the nest and begin to forage above ground. This is a critical time for the colony as they need to gather food quickly to support future growth and particularly to feed the starved queen, who would have lost around 50% of her body weight. From this point on the queen's egg laying output will increase significantly, becoming the queen's sole function. The later generations of worker ants will be bigger, stronger and more aggressive because there is more nutrition for them at the larval stage. The initial brood being fed only by the scarce resources available to a queen will be much smaller than brood supported by a team of foraging and nursing workers. Provided workers are able to find food, at this stage the colony will see an exponential rise in population. After several years, once the colony is well established, the queen will lay eggs that will become queens and males. Black ants often make large nests with extensive tunnel connections.
When building their colony, the ants structure it so as to inhibit the transmission of different contagions.[6] Different communities within the colony are segregated by a limited number of connective nodes, allowing for greater protection of vulnerable hive members, such as larvae and pupae, and the queen.[6]
Additionally, individual infected ants have been observed as spending more time foraging outside of the hive, venturing farther than other ants, and limiting their interactions once within the hive again.[6]
Although worker ants live for a couple of months, queens typically survive for almost 15 years but there have been instances of queens living up to 29 years,[2] the longest recorded lifespan for any eusocial insect.[3] Understanding the basis for the greater longevity of queens has a bearing on the general unsolved problem in biology of the causes of aging. In the study of long-lived queen ants it was found that queens have a higher expression than genetically identical workers of genes involved in processing damaged macromolecules.[2] Genes with higher expression included those that are necessary for repair of DNA damage (see DNA damage theory of aging) and genes involved in proteasome-mediated, ubiquitin-dependent, protein catabolic processes.
Lasius niger removes predators such as ladybirds from the vicinity of black bean aphid thus keeping their "milch cows" safe.[7] On a test plot of field beans (Vicia faba), plants without black bean aphids yielded an average of 56 seeds per plant, those with aphids and no ants yielded 17 seeds, and those with both ants and aphids averaged eight seeds per plant.[8] Vicia faba also produces extrafloral nectaries that Lasius niger can feed from directly.[9]
The Plebejus argus butterfly lays eggs near nests of L. niger, forming a mutualistic relationship.[10][11] This mutualistic relationship benefits the adult butterfly by reducing the need for parental investment.[10] Once the eggs hatch, the ants chaperone the larvae, averting the attacks of predatory organisms like wasps and spiders as well as parasites. In return, the ants receive a saccharine secretion fortified with amino acids from an eversible gland on the larvae's back.[10][11] As first instar larvae prepare to pupate, the ants carry the larvae into their nests.[10] Once the larvae become pupae, the ants continue to provide protection against predation and parasitism.[11][10] The butterfly leaves the nest when it emerges in June.[11]
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(help) The black garden ant (Lasius niger), also known as the common black ant, is a formicine ant, the type species of the subgenus Lasius, which is found across Europe and in some parts of North America, South America, Asia and Australasia. The European species was split into two species; L. niger, which are found in open areas; and L. platythorax, which is found in forest habitats. It is monogynous, meaning colonies contain a single queen.
Lasius niger colonies normally range from 4,000 to 7,000 workers, but can reach 40,000 in rare cases. A Lasius niger queen can live for up to 29 years the longest recorded lifespan for any eusocial insect. Lasius niger queens in the early stages of founding can have two to three other queens in the nest. They will tolerate each other until the first workers come, then it is most likely they will fight until one queen remains. Under laboratory conditions, workers can live at least 4 years.
Lasius niger is host to a number of temporary social parasites of the Lasius mixtus group including Lasius mixtus and Lasius umbratus.