Insectes sociaux de Nouvelle-Calédonie
Kalotermitidae, Rhinotermitidae, Formicidae, Termitidae, Serritermitidae, Polistinae, Apis, Bombus, Meliponini et Vespinae de Nouvelle-Calédonie
179 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
| Référence | Total | Valides | Espèces | Taxons terminaux | ||||
|---|---|---|---|---|---|---|---|---|
| nb | % | nb | % | nb | % | nb | % | |
| Jennings et al. (2013) | 123 | 19,94% | 109 | 63,01% | 99 | 63,46% | 105 | 65,22% |
| Emery (1914) | 115 | 18,64% | 47 | 27,17% | 40 | 25,64% | 44 | 27,33% |
| Taylor (1987) | 112 | 18,15% | 96 | 55,49% | 87 | 55,77% | 93 | 57,76% |
| Wheeler (1935) | 110 | 17,83% | 51 | 29,48% | 46 | 29,49% | 49 | 30,43% |
| Ramage (2017) | 41 | 6,65% | 41 | 23,7% | 40 | 25,64% | 41 | 25,47% |
| Ramage (2014) | 39 | 6,32% | 38 | 21,97% | 38 | 24,36% | 38 | 23,6% |
| Perrault (1988) | 38 | 6,16% | 36 | 20,81% | 36 | 23,08% | 36 | 22,36% |
| Wilson & Taylor (1967) | 38 | 6,16% | 26 | 15,03% | 26 | 16,67% | 26 | 16,15% |
| Jourdan & Mille (2006) | 32 | 5,19% | 29 | 16,76% | 27 | 17,31% | 28 | 17,39% |
| Morrison (1996) | 30 | 4,86% | 25 | 14,45% | 25 | 16,03% | 25 | 15,53% |
| Morrison (1997) | 28 | 4,54% | 24 | 13,87% | 24 | 15,38% | 24 | 14,91% |
| Wetterer (2002) | 27 | 4,38% | 24 | 13,87% | 24 | 15,38% | 24 | 14,91% |
| Wheeler (1932) | 27 | 4,38% | 14 | 8,09% | 14 | 8,97% | 14 | 8,7% |
| Wilson & Hunt (1967) | 26 | 4,21% | 25 | 14,45% | 25 | 16,03% | 25 | 15,53% |
| Wheeler (1936) | 25 | 4,05% | 9 | 5,2% | 9 | 5,77% | 9 | 5,59% |
| Meurgey & Ramage (2020) | 24 | 3,89% | 24 | 13,87% | 23 | 14,74% | 23 | 14,29% |
| Jaffe & Lattke (1994) | 23 | 3,73% | 20 | 11,56% | 20 | 12,82% | 20 | 12,42% |
| Ramage et al. (2023) | 23 | 3,73% | 23 | 13,29% | 23 | 14,74% | 23 | 14,29% |
| Cheesman (1928) | 21 | 3,4% | 21 | 12,14% | 21 | 13,46% | 21 | 13,04% |
| Franco et al. (2019) | 19 | 3,08% | 18 | 10,4% | 18 | 11,54% | 18 | 11,18% |
| Galkowski (2016) | 19 | 3,08% | 19 | 10,98% | 19 | 12,18% | 19 | 11,8% |
| Wheeler (1932) | 19 | 3,08% | 11 | 6,36% | 11 | 7,05% | 11 | 6,83% |
| Blard et al. (2003) | 16 | 2,59% | 16 | 9,25% | 16 | 10,26% | 16 | 9,94% |
| Jourdan (2020) | 16 | 2,59% | 16 | 9,25% | 14 | 8,97% | 14 | 8,7% |
| Lebas et al. (2016) | 16 | 2,59% | 16 | 9,25% | 16 | 10,26% | 16 | 9,94% |
| Meurgey (2011) | 15 | 2,43% | 13 | 7,51% | 12 | 7,69% | 13 | 8,07% |
| Wheeler (1933) | 14 | 2,27% | 5 | 2,89% | 5 | 3,21% | 5 | 3,11% |
| Fisher & Fong (2020) | 12 | 1,94% | 12 | 6,94% | 12 | 7,69% | 11 | 6,83% |
| Casevitz-Weulersse & Galkowski (2009) | 11 | 1,78% | 10 | 5,78% | 10 | 6,41% | 10 | 6,21% |
| Ward (1984) | 11 | 1,78% | 11 | 6,36% | 11 | 7,05% | 11 | 6,83% |
| Wheeler (1908) | 11 | 1,78% | 5 | 2,89% | 5 | 3,21% | 5 | 3,11% |
| Blatrix et al. (2018) | 10 | 1,62% | 10 | 5,78% | 10 | 6,41% | 10 | 6,21% |
| Brown (1958) | 10 | 1,62% | 6 | 3,47% | 6 | 3,85% | 6 | 3,73% |
| Perrault (1993) | 10 | 1,62% | 8 | 4,62% | 8 | 5,13% | 8 | 4,97% |
| Questel (2020) | 10 | 1,62% | 10 | 5,78% | 10 | 6,41% | 9 | 5,59% |
| Bolton (2000) | 9 | 1,46% | 9 | 5,2% | 9 | 5,77% | 9 | 5,59% |
| Fabres (1974) | 9 | 1,46% | 4 | 2,31% | 4 | 2,56% | 4 | 2,48% |
| Guilbert & Casevitz-Weulersse (1997) | 8 | 1,3% | 7 | 4,05% | 6 | 3,85% | 7 | 4,35% |
| Holmgren & Holmgren (1915) | 8 | 1,3% | 2 | 1,16% | 2 | 1,28% | 2 | 1,24% |
| Ortiz-Sepulveda et al. (2019) | 7 | 1,13% | 6 | 3,47% | 6 | 3,85% | 6 | 3,73% |
| Questel & Le Quellec (2012) | 7 | 1,13% | 7 | 4,05% | 6 | 3,85% | 6 | 3,73% |
| Sparks et al. (2019) | 7 | 1,13% | 7 | 4,05% | 6 | 3,85% | 6 | 3,73% |
| Talaga et al. (2015) | 7 | 1,13% | 7 | 4,05% | 7 | 4,49% | 7 | 4,35% |
| Ramage et al. (2019) | 6 | 0,97% | 6 | 3,47% | 6 | 3,85% | 6 | 3,73% |
| Wetterer (2012) | 6 | 0,97% | 6 | 3,47% | 6 | 3,85% | 6 | 3,73% |
| Wetterer (2014) | 6 | 0,97% | 6 | 3,47% | 6 | 3,85% | 6 | 3,73% |
| Bernard (1968) | 5 | 0,81% | 4 | 2,31% | 4 | 2,56% | 4 | 2,48% |
| Fouquet (2000) | 5 | 0,81% | 5 | 2,89% | 5 | 3,21% | 5 | 3,11% |
| Rageau (1958) | 5 | 0,81% | 5 | 2,89% | 3 | 1,92% | 5 | 3,11% |
| Wetterer (2012) | 5 | 0,81% | 5 | 2,89% | 5 | 3,21% | 5 | 3,11% |
| Wetterer (2013) | 5 | 0,81% | 5 | 2,89% | 5 | 3,21% | 5 | 3,11% |
| Bolton (2012) | 4 | 0,65% | 0 | 0% | 0 | 0% | 0 | 0% |
| Borowiec (2016) | 4 | 0,65% | 1 | 0,58% | 1 | 0,64% | 1 | 0,62% |
| Ward et al. (2016) | 4 | 0,65% | 2 | 1,16% | 1 | 0,64% | 2 | 1,24% |
| Allen et al. (2022) | 3 | 0,49% | 3 | 1,73% | 3 | 1,92% | 3 | 1,86% |
| Dalla Torre (1893) | 3 | 0,49% | 0 | 0% | 0 | 0% | 0 | 0% |
| Donisthorpe (1932) | 3 | 0,49% | 0 | 0% | 0 | 0% | 0 | 0% |
| Forel (1899) | 3 | 0,49% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gusenleitner & Madl (2011) | 3 | 0,49% | 3 | 1,73% | 2 | 1,28% | 3 | 1,86% |
| Heterick et al. (2011) | 3 | 0,49% | 3 | 1,73% | 3 | 1,92% | 3 | 1,86% |
| Jerdon (1851) | 3 | 0,49% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jourdan et al. (2014) | 3 | 0,49% | 3 | 1,73% | 2 | 1,28% | 3 | 1,86% |
| Lowe et al. (2007) | 3 | 0,49% | 3 | 1,73% | 3 | 1,92% | 3 | 1,86% |
| Mayr (1870) | 3 | 0,49% | 3 | 1,73% | 3 | 1,92% | 3 | 1,86% |
| Nève de Mévergnies et al. (2024) | 3 | 0,49% | 3 | 1,73% | 3 | 1,92% | 3 | 1,86% |
| Salata & Fisher (2022) | 3 | 0,49% | 3 | 1,73% | 3 | 1,92% | 3 | 1,86% |
| Schulthess (1915) | 3 | 0,49% | 1 | 0,58% | 0 | 0% | 1 | 0,62% |
| Seifert (2003) | 3 | 0,49% | 2 | 1,16% | 2 | 1,28% | 2 | 1,24% |
| Shattuck (2011) | 3 | 0,49% | 3 | 1,73% | 3 | 1,92% | 3 | 1,86% |
| Touroult et al. (2018) | 3 | 0,49% | 3 | 1,73% | 3 | 1,92% | 3 | 1,86% |
| Ward et al. (2015) | 3 | 0,49% | 1 | 0,58% | 1 | 0,64% | 1 | 0,62% |
| Wetterer & Hita Garcia (2015) | 3 | 0,49% | 3 | 1,73% | 3 | 1,92% | 3 | 1,86% |
| Baroni Urbani & De Andrade (2007) | 2 | 0,32% | 1 | 0,58% | 1 | 0,64% | 1 | 0,62% |
| Bellmann (2019) | 2 | 0,32% | 2 | 1,16% | 2 | 1,28% | 1 | 0,62% |
| Bolton (2007) | 2 | 0,32% | 1 | 0,58% | 1 | 0,64% | 1 | 0,62% |
| Bondroit (1916) | 2 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
| Czechowski et al. (2002) | 2 | 0,32% | 2 | 1,16% | 2 | 1,28% | 2 | 1,24% |
| Emery (1883) | 2 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
| Emery (1900) | 2 | 0,32% | 1 | 0,58% | 1 | 0,64% | 1 | 0,62% |
| Emery (1911) | 2 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fabricius (1793) | 2 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
| Garrouste & Hervé (2009) | 2 | 0,32% | 2 | 1,16% | 2 | 1,28% | 2 | 1,24% |
| Kuhlmann (2006) | 2 | 0,32% | 2 | 1,16% | 1 | 0,64% | 2 | 1,24% |
| Le Breton et al. (2005) | 2 | 0,32% | 2 | 1,16% | 2 | 1,28% | 2 | 1,24% |
| Leponce et al. (2019) | 2 | 0,32% | 2 | 1,16% | 2 | 1,28% | 2 | 1,24% |
| Linnaeus (1758) | 2 | 0,32% | 1 | 0,58% | 1 | 0,64% | 0 | 0% |
| Mann (1921) | 2 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
| Meurgey & Dumbardon-Martial (2015) | 2 | 0,32% | 2 | 1,16% | 1 | 0,64% | 1 | 0,62% |
| Meurgey (2014) | 2 | 0,32% | 2 | 1,16% | 2 | 1,28% | 0 | 0% |
| Parnaudeau & Madl (2009) | 2 | 0,32% | 2 | 1,16% | 2 | 1,28% | 2 | 1,24% |
| Paulian (1998) | 2 | 0,32% | 2 | 1,16% | 1 | 0,64% | 2 | 1,24% |
| Remillet (1988) | 2 | 0,32% | 2 | 1,16% | 2 | 1,28% | 1 | 0,62% |
| Smith (1857) | 2 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
| Smith (1858) | 2 | 0,32% | 2 | 1,16% | 2 | 1,28% | 2 | 1,24% |
| Taylor (2018) | 2 | 0,32% | 2 | 1,16% | 2 | 1,28% | 2 | 1,24% |
| Touroult et al. (2020) | 2 | 0,32% | 2 | 1,16% | 2 | 1,28% | 2 | 1,24% |
| Turner (1919) | 2 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
| Wheeler (1923) | 2 | 0,32% | 2 | 1,16% | 2 | 1,28% | 2 | 1,24% |
| Zakardjian et al. (2023) | 2 | 0,32% | 2 | 1,16% | 0 | 0% | 2 | 1,24% |
| Albouy et al. (2017) | 1 | 0,16% | 1 | 0,58% | 1 | 0,64% | 0 | 0% |
| André (1889) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Beggs et al. (2011) | 1 | 0,16% | 1 | 0,58% | 1 | 0,64% | 1 | 0,62% |
| Blight et al. (2023) | 1 | 0,16% | 1 | 0,58% | 1 | 0,64% | 1 | 0,62% |
| Bolton & Fisher (2011) | 1 | 0,16% | 1 | 0,58% | 1 | 0,64% | 1 | 0,62% |
| Boyd et al. (2006) | 1 | 0,16% | 1 | 0,58% | 1 | 0,64% | 0 | 0% |
| Brown (1963) | 1 | 0,16% | 1 | 0,58% | 1 | 0,64% | 1 | 0,62% |
| Camacho et al. (2022) | 1 | 0,16% | 1 | 0,58% | 1 | 0,64% | 1 | 0,62% |
| Carpenter & Madl (2009) | 1 | 0,16% | 1 | 0,58% | 1 | 0,64% | 1 | 0,62% |
| Carpenter (1996) | 1 | 0,16% | 1 | 0,58% | 1 | 0,64% | 1 | 0,62% |
| Célini et al. (2020) | 1 | 0,16% | 1 | 0,58% | 1 | 0,64% | 1 | 0,62% |
| Cohic (1959) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Colindre (2016) | 1 | 0,16% | 1 | 0,58% | 1 | 0,64% | 1 | 0,62% |
| Colindre (2017) | 1 | 0,16% | 1 | 0,58% | 1 | 0,64% | 1 | 0,62% |
| Colindre (2021) | 1 | 0,16% | 1 | 0,58% | 1 | 0,64% | 1 | 0,62% |
| Conte et al. (2007) | 1 | 0,16% | 1 | 0,58% | 1 | 0,64% | 0 | 0% |
| Darlington (1992) | 1 | 0,16% | 1 | 0,58% | 1 | 0,64% | 1 | 0,62% |
| De Geer (1773) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Delabie & Blard (2002) | 1 | 0,16% | 1 | 0,58% | 1 | 0,64% | 1 | 0,62% |
| Delabie et al. (2011) | 1 | 0,16% | 1 | 0,58% | 1 | 0,64% | 1 | 0,62% |
| Dumbardon-Martial & Delblond (2019) | 1 | 0,16% | 1 | 0,58% | 1 | 0,64% | 0 | 0% |
| Emery (1869) | 1 | 0,16% | 1 | 0,58% | 1 | 0,64% | 1 | 0,62% |
| Emery (1892) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Emery (1893) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Emery (1894) | 1 | 0,16% | 1 | 0,58% | 1 | 0,64% | 1 | 0,62% |
| Emery (1897) | 1 | 0,16% | 1 | 0,58% | 1 | 0,64% | 1 | 0,62% |
| Emery (1897) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fabricius (1804) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Forel (1874) | 1 | 0,16% | 1 | 0,58% | 1 | 0,64% | 1 | 0,62% |
| Forel (1881) | 1 | 0,16% | 1 | 0,58% | 1 | 0,64% | 1 | 0,62% |
| Forel (1886) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Forel (1890) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Forel (1901) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Forel (1907) | 1 | 0,16% | 1 | 0,58% | 1 | 0,64% | 1 | 0,62% |
| Friese (1907) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Groom et al. (2016) | 1 | 0,16% | 1 | 0,58% | 1 | 0,64% | 0 | 0% |
| Gusenleitner (2011) | 1 | 0,16% | 1 | 0,58% | 1 | 0,64% | 1 | 0,62% |
| Gutierrez (1981) | 1 | 0,16% | 1 | 0,58% | 1 | 0,64% | 1 | 0,62% |
| Kohout (2013) | 1 | 0,16% | 1 | 0,58% | 1 | 0,64% | 1 | 0,62% |
| LaPolla et al. (2010) | 1 | 0,16% | 1 | 0,58% | 1 | 0,64% | 1 | 0,62% |
| Latreille (1802) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lenoir et al. (2023) | 1 | 0,16% | 1 | 0,58% | 1 | 0,64% | 1 | 0,62% |
| Light & Zimmerman (1936) | 1 | 0,16% | 1 | 0,58% | 1 | 0,64% | 1 | 0,62% |
| Light (1932) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Light (1932) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Linnaeus (1761) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lowne (1865) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lucas (1872) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Matos-Maraví et al. (2018) | 1 | 0,16% | 1 | 0,58% | 1 | 0,64% | 1 | 0,62% |
| Mayr (1855) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mayr (1866) | 1 | 0,16% | 1 | 0,58% | 1 | 0,64% | 1 | 0,62% |
| Mayr (1876) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mayr (1886) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mayr (1887) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mera-Rodríguez et al. (2023) | 1 | 0,16% | 1 | 0,58% | 1 | 0,64% | 1 | 0,62% |
| Meurgey & Questel (2015) | 1 | 0,16% | 1 | 0,58% | 1 | 0,64% | 0 | 0% |
| Pauly & Munzinger (2003) | 1 | 0,16% | 1 | 0,58% | 0 | 0% | 1 | 0,62% |
| Pauly et al. (2001) | 1 | 0,16% | 1 | 0,58% | 0 | 0% | 1 | 0,62% |
| Pierre et al. (2017) | 1 | 0,16% | 1 | 0,58% | 1 | 0,64% | 0 | 0% |
| Reverté et al. (2023) | 1 | 0,16% | 1 | 0,58% | 1 | 0,64% | 0 | 0% |
| Roger (1859) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Roger (1863) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sadlier et al. (2012) | 1 | 0,16% | 1 | 0,58% | 1 | 0,64% | 1 | 0,62% |
| Santschi (1920) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Santschi (1928) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Scheffrahn & Křeček (2001) | 1 | 0,16% | 1 | 0,58% | 1 | 0,64% | 1 | 0,62% |
| Schmidt & Shattuck (2014) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Seifert et al. (2017) | 1 | 0,16% | 1 | 0,58% | 1 | 0,64% | 1 | 0,62% |
| Seifert (2022) | 1 | 0,16% | 1 | 0,58% | 1 | 0,64% | 1 | 0,62% |
| Smith (1859) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Smith (1860) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Taylor & Wilson (1961) | 1 | 0,16% | 1 | 0,58% | 1 | 0,64% | 1 | 0,62% |
| Touroult et al. (2015) | 1 | 0,16% | 1 | 0,58% | 1 | 0,64% | 1 | 0,62% |
| Vachal (1907) | 1 | 0,16% | 1 | 0,58% | 1 | 0,64% | 0 | 0% |
| Vantaux et al. (2010) | 1 | 0,16% | 1 | 0,58% | 1 | 0,64% | 1 | 0,62% |
| Vayssières et al. (2001) | 1 | 0,16% | 1 | 0,58% | 1 | 0,64% | 1 | 0,62% |
| Viehmeyer (1924) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Walker (1859) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Wheeler (1929) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Zakardjian et al. (2020) | 1 | 0,16% | 1 | 0,58% | 1 | 0,64% | 0 | 0% |
