Vespidés
164 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
Référence | Total | Valides | Espèces | Taxons terminaux | ||||
---|---|---|---|---|---|---|---|---|
nb | % | nb | % | nb | % | nb | % | |
Carpenter (2023) | 18 | 1,98% | 18 | 4,58% | 9 | 2,7% | 16 | 4,62% |
Van et al. (2023) | 18 | 1,98% | 14 | 3,56% | 11 | 3,3% | 13 | 3,76% |
Dos Santos Junior et al. (2015) | 17 | 1,87% | 5 | 1,27% | 5 | 1,5% | 5 | 1,45% |
Bellmann (2019) | 16 | 1,76% | 15 | 3,82% | 15 | 4,5% | 11 | 3,18% |
Lopes et al. (2021) | 16 | 1,76% | 16 | 4,07% | 16 | 4,8% | 13 | 3,76% |
Spinola (1841) | 16 | 1,76% | 6 | 1,53% | 6 | 1,8% | 4 | 1,16% |
Linnaeus (1758) | 12 | 1,32% | 1 | 0,25% | 1 | 0,3% | 0 | 0% |
Carpenter & Madl (2009) | 11 | 1,21% | 9 | 2,29% | 9 | 2,7% | 9 | 2,6% |
Gereys (2016) | 11 | 1,21% | 10 | 2,54% | 5 | 1,5% | 9 | 2,6% |
Gusenleitner & Madl (2011) | 11 | 1,21% | 10 | 2,54% | 3 | 0,9% | 10 | 2,89% |
Ramage (2017) | 11 | 1,21% | 11 | 2,8% | 7 | 2,1% | 10 | 2,89% |
Schmid-Egger et al. (2017) | 11 | 1,21% | 9 | 2,29% | 9 | 2,7% | 9 | 2,6% |
Lepeletier (1841) | 10 | 1,1% | 4 | 1,02% | 4 | 1,2% | 4 | 1,16% |
Somavilla et al. (2018) | 10 | 1,1% | 10 | 2,54% | 10 | 3% | 9 | 2,6% |
Jennings et al. (2013) | 9 | 0,99% | 6 | 1,53% | 5 | 1,5% | 4 | 1,16% |
Olivier (1791-[1792]) | 9 | 0,99% | 0 | 0% | 0 | 0% | 0 | 0% |
Borsato (2006) | 8 | 0,88% | 8 | 2,04% | 2 | 0,6% | 8 | 2,31% |
Ducke (1904) | 8 | 0,88% | 1 | 0,25% | 1 | 0,3% | 1 | 0,29% |
Gusenleitner (1993) | 8 | 0,88% | 6 | 1,53% | 5 | 1,5% | 6 | 1,73% |
Paulian (1998) | 8 | 0,88% | 8 | 2,04% | 5 | 1,5% | 7 | 2,02% |
Richards (1978) | 8 | 0,88% | 1 | 0,25% | 0 | 0% | 1 | 0,29% |
Gusenleitner (2011) | 7 | 0,77% | 7 | 1,78% | 4 | 1,2% | 6 | 1,73% |
Selis et al. (2024) | 7 | 0,77% | 7 | 1,78% | 7 | 2,1% | 7 | 2,02% |
Rome (2016) | 6 | 0,66% | 6 | 1,53% | 6 | 1,8% | 4 | 1,16% |
Saussure (1854) | 6 | 0,66% | 0 | 0% | 0 | 0% | 0 | 0% |
Schulthess (1915) | 6 | 0,66% | 0 | 0% | 0 | 0% | 0 | 0% |
Carpenter (1996) | 5 | 0,55% | 5 | 1,27% | 4 | 1,2% | 5 | 1,45% |
Ducke (1910) | 5 | 0,55% | 3 | 0,76% | 3 | 0,9% | 3 | 0,87% |
Gusenleitner (1999) | 5 | 0,55% | 4 | 1,02% | 4 | 1,2% | 3 | 0,87% |
Jourdan (2020) | 5 | 0,55% | 5 | 1,27% | 4 | 1,2% | 3 | 0,87% |
Kuhlmann (2006) | 5 | 0,55% | 5 | 1,27% | 5 | 1,5% | 5 | 1,45% |
Turner (1919) | 5 | 0,55% | 0 | 0% | 0 | 0% | 0 | 0% |
Blüthgen (1953) | 4 | 0,44% | 2 | 0,51% | 1 | 0,3% | 2 | 0,58% |
Bousquet (2016) | 4 | 0,44% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1804) | 4 | 0,44% | 1 | 0,25% | 1 | 0,3% | 1 | 0,29% |
Grandinete et al. (2015) | 4 | 0,44% | 2 | 0,51% | 2 | 0,6% | 2 | 0,58% |
Panzer ([1797]) | 4 | 0,44% | 0 | 0% | 0 | 0% | 0 | 0% |
Remillet (1988) | 4 | 0,44% | 4 | 1,02% | 4 | 1,2% | 4 | 1,16% |
Saussure (1875) | 4 | 0,44% | 2 | 0,51% | 2 | 0,6% | 2 | 0,58% |
Schulthess et al. (1907) | 4 | 0,44% | 0 | 0% | 0 | 0% | 0 | 0% |
Snelling (1983) | 4 | 0,44% | 1 | 0,25% | 1 | 0,3% | 1 | 0,29% |
Vachal (1907) | 4 | 0,44% | 0 | 0% | 0 | 0% | 0 | 0% |
Barroso et al. (2022) | 3 | 0,33% | 3 | 0,76% | 3 | 0,9% | 3 | 0,87% |
Buysson (1908) | 3 | 0,33% | 0 | 0% | 0 | 0% | 0 | 0% |
Cameron (1912) | 3 | 0,33% | 0 | 0% | 0 | 0% | 0 | 0% |
Carpenter & Glare (2010) | 3 | 0,33% | 3 | 0,76% | 3 | 0,9% | 3 | 0,87% |
Carpenter et al. (2004) | 3 | 0,33% | 3 | 0,76% | 3 | 0,9% | 3 | 0,87% |
Deleurance (1945) | 3 | 0,33% | 1 | 0,25% | 1 | 0,3% | 1 | 0,29% |
Jourdan & Mille (2006) | 3 | 0,33% | 2 | 0,51% | 2 | 0,6% | 1 | 0,29% |
Meurgey & Ramage (2020) | 3 | 0,33% | 3 | 0,76% | 3 | 0,9% | 3 | 0,87% |
Meurgey (2011) | 3 | 0,33% | 2 | 0,51% | 2 | 0,6% | 2 | 0,58% |
Nouvel & Ribaut (1956) | 3 | 0,33% | 0 | 0% | 0 | 0% | 0 | 0% |
Schulz (1906) | 3 | 0,33% | 0 | 0% | 0 | 0% | 0 | 0% |
Selis et al. (2023) | 3 | 0,33% | 2 | 0,51% | 2 | 0,6% | 2 | 0,58% |
Tussac (1996) | 3 | 0,33% | 0 | 0% | 0 | 0% | 0 | 0% |
Vidal (2023) | 3 | 0,33% | 2 | 0,51% | 2 | 0,6% | 2 | 0,58% |
Albouy et al. (2017) | 2 | 0,22% | 2 | 0,51% | 2 | 0,6% | 2 | 0,58% |
Alonso-zarazaga & Evenhuis (2017) | 2 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Bequaert (1948) | 2 | 0,22% | 2 | 0,51% | 2 | 0,6% | 2 | 0,58% |
Berland (1928) | 2 | 0,22% | 1 | 0,25% | 1 | 0,3% | 0 | 0% |
Carpenter & Brown (2021) | 2 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Christ (1791) | 2 | 0,22% | 1 | 0,25% | 0 | 0% | 1 | 0,29% |
De Geer (1773) | 2 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Dufour & Perris (1840) | 2 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1804) | 2 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Fox (1898) | 2 | 0,22% | 1 | 0,25% | 1 | 0,3% | 0 | 0% |
Fox (1899) | 2 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Gereys (2006) | 2 | 0,22% | 1 | 0,25% | 0 | 0% | 1 | 0,29% |
Gereys (2009) | 2 | 0,22% | 2 | 0,51% | 2 | 0,6% | 2 | 0,58% |
Gereys (2011) | 2 | 0,22% | 2 | 0,51% | 0 | 0% | 2 | 0,58% |
Gereys (2022) | 2 | 0,22% | 1 | 0,25% | 1 | 0,3% | 1 | 0,29% |
Giordani & Soika (1993) | 2 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Giordani Soika (1943) | 2 | 0,22% | 2 | 0,51% | 2 | 0,6% | 2 | 0,58% |
Giordani Soika (1978) | 2 | 0,22% | 1 | 0,25% | 1 | 0,3% | 1 | 0,29% |
Giordani Soika (1990) | 2 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Giraud (1866) | 2 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Gmelin (1790) | 2 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Gusenleitner et al. (1997) | 2 | 0,22% | 2 | 0,51% | 1 | 0,3% | 1 | 0,29% |
Gusenleitner (1972) | 2 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Gusenleitner (1987) | 2 | 0,22% | 2 | 0,51% | 2 | 0,6% | 2 | 0,58% |
Proceedings of the Zoological Society of London, 1907: 1035-1037.">Hopkinson (1907) | 2 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Kohl (1898) | 2 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Lepeletier (1836) | 2 | 0,22% | 1 | 0,25% | 1 | 0,3% | 0 | 0% |
Linnaeus (1761) | 2 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Mocsáry (1883) | 2 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Panzer ([1799]) | 2 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Parnaudeau & Madl (2009) | 2 | 0,22% | 1 | 0,25% | 1 | 0,3% | 1 | 0,29% |
Questel (2020) | 2 | 0,22% | 2 | 0,51% | 2 | 0,6% | 2 | 0,58% |
Rageau (1958) | 2 | 0,22% | 2 | 0,51% | 2 | 0,6% | 2 | 0,58% |
Rome et al. (2009) | 2 | 0,22% | 2 | 0,51% | 1 | 0,3% | 1 | 0,29% |
Rome et al. (2011) | 2 | 0,22% | 2 | 0,51% | 1 | 0,3% | 1 | 0,29% |
Rome et al. (2013) | 2 | 0,22% | 2 | 0,51% | 1 | 0,3% | 1 | 0,29% |
Rortais et al. (2010) | 2 | 0,22% | 2 | 0,51% | 1 | 0,3% | 1 | 0,29% |
Rossi (1790) | 2 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Seurat (1934) | 2 | 0,22% | 2 | 0,51% | 1 | 0,3% | 2 | 0,58% |
Silveira (2006) | 2 | 0,22% | 2 | 0,51% | 2 | 0,6% | 2 | 0,58% |
Villemant et al. (2010) | 2 | 0,22% | 2 | 0,51% | 1 | 0,3% | 1 | 0,29% |
Villemant et al. (2011) | 2 | 0,22% | 2 | 0,51% | 1 | 0,3% | 1 | 0,29% |
Zilli (2021) | 2 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
André (1886) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Beggs et al. (2011) | 1 | 0,11% | 1 | 0,25% | 1 | 0,3% | 1 | 0,29% |
Berland (1927) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Bitsch et al. (2010) | 1 | 0,11% | 1 | 0,25% | 1 | 0,3% | 1 | 0,29% |
Bitsch et al. (2010) | 1 | 0,11% | 1 | 0,25% | 1 | 0,3% | 1 | 0,29% |
Blüthgen (1937) | 1 | 0,11% | 1 | 0,25% | 1 | 0,3% | 1 | 0,29% |
Buck et al. (2008) | 1 | 0,11% | 1 | 0,25% | 1 | 0,3% | 1 | 0,29% |
Carpenter et al. (1991) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Carpenter (2011) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Castro & Dvorak (2009) | 1 | 0,11% | 1 | 0,25% | 1 | 0,3% | 1 | 0,29% |
Chrétien (1896) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Dejean et al. (2011) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Dilman (2013) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Dos et al. (2020) | 1 | 0,11% | 1 | 0,25% | 1 | 0,3% | 1 | 0,29% |
Dumbardon-Martial & Delblond (2019) | 1 | 0,11% | 1 | 0,25% | 1 | 0,3% | 1 | 0,29% |
Fabricius (1781) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1787) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1798) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Fourcroy (1785) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Gereys & Perrard (2023) | 1 | 0,11% | 1 | 0,25% | 1 | 0,3% | 1 | 0,29% |
Gereys et al. (2021) | 1 | 0,11% | 1 | 0,25% | 1 | 0,3% | 0 | 0% |
Gereys (2005) | 1 | 0,11% | 1 | 0,25% | 1 | 0,3% | 1 | 0,29% |
Giordani & Soika (1958) | 1 | 0,11% | 1 | 0,25% | 1 | 0,3% | 1 | 0,29% |
Giordani Soika (1971) | 1 | 0,11% | 1 | 0,25% | 1 | 0,3% | 1 | 0,29% |
Graf (1961) | 1 | 0,11% | 1 | 0,25% | 1 | 0,3% | 1 | 0,29% |
Gribodo (1891) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Griffin (1939) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Gusenleitner (1994) | 1 | 0,11% | 1 | 0,25% | 1 | 0,3% | 1 | 0,29% |
Gusenleitner (2010) | 1 | 0,11% | 1 | 0,25% | 1 | 0,3% | 1 | 0,29% |
Hermes & Oliveira (2016) | 1 | 0,11% | 1 | 0,25% | 1 | 0,3% | 1 | 0,29% |
Jourdan et al. (2014) | 1 | 0,11% | 1 | 0,25% | 1 | 0,3% | 1 | 0,29% |
Kojima & Achterberg (1997) | 1 | 0,11% | 1 | 0,25% | 1 | 0,3% | 1 | 0,29% |
Lacoeuilhe et al. (2023) | 1 | 0,11% | 1 | 0,25% | 1 | 0,3% | 1 | 0,29% |
Latreille (1810) | 1 | 0,11% | 1 | 0,25% | 1 | 0,3% | 1 | 0,29% |
Lepeletier de Saint Fargeau & Audinet-Serville (1825) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Linnaeus (1767) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Linné (1771) | 1 | 0,11% | 1 | 0,25% | 1 | 0,3% | 0 | 0% |
Lowe et al. (2007) | 1 | 0,11% | 1 | 0,25% | 1 | 0,3% | 1 | 0,29% |
Magis (2003) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Phytoma, 677: 18-22.">Martinez et al. (2014) | 1 | 0,11% | 1 | 0,25% | 0 | 0% | 1 | 0,29% |
Morawitz (1867) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Neumeyer et al. (2014) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Olivier (1792) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Packard (1870) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Provancher (1888) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Questel & Le Quellec (2012) | 1 | 0,11% | 1 | 0,25% | 1 | 0,3% | 1 | 0,29% |
Rageau (1956) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Ramage et al. (2023) | 1 | 0,11% | 1 | 0,25% | 1 | 0,3% | 1 | 0,29% |
Reder & Weitzel (2012) | 1 | 0,11% | 1 | 0,25% | 1 | 0,3% | 1 | 0,29% |
Richards & Richards (1951) | 1 | 0,11% | 1 | 0,25% | 1 | 0,3% | 1 | 0,29% |
Saussure (de) (1852) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Saussure (1853-58) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Saussure (1857) | 1 | 0,11% | 1 | 0,25% | 1 | 0,3% | 0 | 0% |
Saussure (1857) | 1 | 0,11% | 1 | 0,25% | 1 | 0,3% | 1 | 0,29% |
Saussure (1867) | 1 | 0,11% | 1 | 0,25% | 0 | 0% | 1 | 0,29% |
Schulz (1906) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Somavilla et al. (2023) | 1 | 0,11% | 1 | 0,25% | 1 | 0,3% | 1 | 0,29% |
Spinola (1808) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Touroult et al. (2015) | 1 | 0,11% | 1 | 0,25% | 1 | 0,3% | 1 | 0,29% |
Tussac (1985) | 1 | 0,11% | 1 | 0,25% | 1 | 0,3% | 1 | 0,29% |
Villemant (2008) | 1 | 0,11% | 1 | 0,25% | 0 | 0% | 1 | 0,29% |
Villers (1789) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Waltl (1835) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Yamane et al. (1996) | 1 | 0,11% | 1 | 0,25% | 1 | 0,3% | 1 | 0,29% |
Yokoyama (2013) | 1 | 0,11% | 1 | 0,25% | 1 | 0,3% | 1 | 0,29% |