Araignées de Martinique
76 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
Référence | Total | Valides | Espèces | Taxons terminaux | ||||
---|---|---|---|---|---|---|---|---|
nb | % | nb | % | nb | % | nb | % | |
Dierkens (2010) | 13 | 9,09% | 11 | 17,46% | 11 | 17,46% | 11 | 17,46% |
Questel (2020) | 13 | 9,09% | 12 | 19,05% | 12 | 19,05% | 12 | 19,05% |
Yokoyama (2013) | 11 | 7,69% | 10 | 15,87% | 10 | 15,87% | 10 | 15,87% |
Sánchez-Ruiz & Maréchal (2020) | 10 | 6,99% | 9 | 14,29% | 9 | 14,29% | 9 | 14,29% |
Touroult et al. (2020) | 10 | 6,99% | 10 | 15,87% | 10 | 15,87% | 10 | 15,87% |
Vedel et al. (2013) | 10 | 6,99% | 10 | 15,87% | 10 | 15,87% | 10 | 15,87% |
Maréchal & Iinuma (2013) | 7 | 4,9% | 6 | 9,52% | 6 | 9,52% | 6 | 9,52% |
Questel & Le Quellec (2012) | 7 | 4,9% | 7 | 11,11% | 7 | 11,11% | 7 | 11,11% |
Cazanove (2022) | 6 | 4,2% | 6 | 9,52% | 6 | 9,52% | 6 | 9,52% |
Taczanowski (1873) | 6 | 4,2% | 4 | 6,35% | 4 | 6,35% | 4 | 6,35% |
Taczanowski (1874) | 6 | 4,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Berland (1933) | 5 | 3,5% | 3 | 4,76% | 3 | 4,76% | 3 | 4,76% |
Berland (1934) | 5 | 3,5% | 3 | 4,76% | 3 | 4,76% | 3 | 4,76% |
Berland (1942) | 5 | 3,5% | 2 | 3,17% | 2 | 3,17% | 2 | 3,17% |
Dierkens & Charlat (2011) | 5 | 3,5% | 5 | 7,94% | 5 | 7,94% | 5 | 7,94% |
Dierkens & Ramage (2016) | 5 | 3,5% | 5 | 7,94% | 5 | 7,94% | 5 | 7,94% |
Dierkens (2011) | 5 | 3,5% | 4 | 6,35% | 4 | 6,35% | 4 | 6,35% |
Ramage (2017) | 5 | 3,5% | 5 | 7,94% | 5 | 7,94% | 5 | 7,94% |
Souza et al. (2019) | 5 | 3,5% | 2 | 3,17% | 2 | 3,17% | 2 | 3,17% |
Dierkens (2021) | 4 | 2,8% | 4 | 6,35% | 4 | 6,35% | 4 | 6,35% |
Berland (1935) | 3 | 2,1% | 2 | 3,17% | 2 | 3,17% | 2 | 3,17% |
Caporiacco (1954) | 3 | 2,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Dierkens (2012) | 3 | 2,1% | 3 | 4,76% | 3 | 4,76% | 3 | 4,76% |
Fukushima & Bertani (2017) | 3 | 2,1% | 1 | 1,59% | 1 | 1,59% | 1 | 1,59% |
Ledoux & Hallé (1995) | 3 | 2,1% | 3 | 4,76% | 3 | 4,76% | 3 | 4,76% |
Simon (1896) | 3 | 2,1% | 1 | 1,59% | 1 | 1,59% | 1 | 1,59% |
Berland (1924) | 2 | 1,4% | 0 | 0% | 0 | 0% | 0 | 0% |
Brescovit (1991) | 2 | 1,4% | 1 | 1,59% | 1 | 1,59% | 1 | 1,59% |
Hervé & Garrouste (2009) | 2 | 1,4% | 2 | 3,17% | 2 | 3,17% | 2 | 3,17% |
Jourdan & Mille (2006) | 2 | 1,4% | 2 | 3,17% | 2 | 3,17% | 2 | 3,17% |
Lopez (1994) | 2 | 1,4% | 2 | 3,17% | 2 | 3,17% | 2 | 3,17% |
Nentwig et al. (2019) | 2 | 1,4% | 2 | 3,17% | 2 | 3,17% | 2 | 3,17% |
Passanha & Brescovit (2018) | 2 | 1,4% | 2 | 3,17% | 2 | 3,17% | 2 | 3,17% |
Platnick & Berniker (2014) | 2 | 1,4% | 2 | 3,17% | 2 | 3,17% | 2 | 3,17% |
Platnick et al. (2012) | 2 | 1,4% | 2 | 3,17% | 2 | 3,17% | 2 | 3,17% |
Platnick (1993) | 2 | 1,4% | 2 | 3,17% | 2 | 3,17% | 2 | 3,17% |
Rheims & Jäger (2022) | 2 | 1,4% | 2 | 3,17% | 2 | 3,17% | 2 | 3,17% |
Taczanowski (1872) | 2 | 1,4% | 0 | 0% | 0 | 0% | 0 | 0% |
UICN Comité français, OFB, MNHN & AsFrA (2023) | 2 | 1,4% | 2 | 3,17% | 2 | 3,17% | 2 | 3,17% |
Walckenaer ([1841]) | 2 | 1,4% | 0 | 0% | 0 | 0% | 0 | 0% |
Archer (1965) | 1 | 0,7% | 0 | 0% | 0 | 0% | 0 | 0% |
Berland (1927) | 1 | 0,7% | 1 | 1,59% | 1 | 1,59% | 1 | 1,59% |
Berland (1929) | 1 | 0,7% | 0 | 0% | 0 | 0% | 0 | 0% |
Berland (1934) | 1 | 0,7% | 1 | 1,59% | 1 | 1,59% | 1 | 1,59% |
Bigot (1992) | 1 | 0,7% | 1 | 1,59% | 1 | 1,59% | 1 | 1,59% |
Crews (2011) | 1 | 0,7% | 1 | 1,59% | 1 | 1,59% | 1 | 1,59% |
Déjean et al. (2023) | 1 | 0,7% | 1 | 1,59% | 1 | 1,59% | 1 | 1,59% |
Déjean (2015) | 1 | 0,7% | 1 | 1,59% | 1 | 1,59% | 1 | 1,59% |
Dierkens (2011) | 1 | 0,7% | 1 | 1,59% | 1 | 1,59% | 1 | 1,59% |
Emerit & Ledoux (2008) | 1 | 0,7% | 1 | 1,59% | 1 | 1,59% | 1 | 1,59% |
European Nucleotide Archive (2019) | 1 | 0,7% | 1 | 1,59% | 1 | 1,59% | 1 | 1,59% |
Exline & Levi (1962) | 1 | 0,7% | 0 | 0% | 0 | 0% | 0 | 0% |
Ferreira-sousa et al. (2023) | 1 | 0,7% | 1 | 1,59% | 1 | 1,59% | 1 | 1,59% |
Gabriel (2020) | 1 | 0,7% | 0 | 0% | 0 | 0% | 0 | 0% |
Gillespie (2003) | 1 | 0,7% | 1 | 1,59% | 1 | 1,59% | 1 | 1,59% |
Gillespie (2003) | 1 | 0,7% | 1 | 1,59% | 1 | 1,59% | 1 | 1,59% |
Hentz (1850) | 1 | 0,7% | 0 | 0% | 0 | 0% | 0 | 0% |
Jäger (2002) | 1 | 0,7% | 0 | 0% | 0 | 0% | 0 | 0% |
Koch (1836) | 1 | 0,7% | 0 | 0% | 0 | 0% | 0 | 0% |
Levi (1986) | 1 | 0,7% | 1 | 1,59% | 1 | 1,59% | 1 | 1,59% |
Linnaeus (1758) | 1 | 0,7% | 0 | 0% | 0 | 0% | 0 | 0% |
Marples (1957) | 1 | 0,7% | 1 | 1,59% | 1 | 1,59% | 1 | 1,59% |
Nibouche et al. (202X) | 1 | 0,7% | 1 | 1,59% | 1 | 1,59% | 1 | 1,59% |
Petrunkevitch (1929) | 1 | 0,7% | 0 | 0% | 0 | 0% | 0 | 0% |
Pocock (1903) | 1 | 0,7% | 0 | 0% | 0 | 0% | 0 | 0% |
Questel (2023) | 1 | 0,7% | 1 | 1,59% | 1 | 1,59% | 1 | 1,59% |
Rheims (2020) | 1 | 0,7% | 1 | 1,59% | 1 | 1,59% | 1 | 1,59% |
Roger (2018) | 1 | 0,7% | 1 | 1,59% | 1 | 1,59% | 1 | 1,59% |
Seurat (1934) | 1 | 0,7% | 1 | 1,59% | 1 | 1,59% | 1 | 1,59% |
Simon (1864) | 1 | 0,7% | 0 | 0% | 0 | 0% | 0 | 0% |
Simon (1892) | 1 | 0,7% | 1 | 1,59% | 1 | 1,59% | 1 | 1,59% |
Simon (1893) | 1 | 0,7% | 1 | 1,59% | 1 | 1,59% | 1 | 1,59% |
Simon (1897) | 1 | 0,7% | 0 | 0% | 0 | 0% | 0 | 0% |
Vayssières et al. (2001) | 1 | 0,7% | 1 | 1,59% | 1 | 1,59% | 1 | 1,59% |
Vinson (1863) | 1 | 0,7% | 0 | 0% | 0 | 0% | 0 | 0% |
Walckenaer (1837) | 1 | 0,7% | 0 | 0% | 0 | 0% | 0 | 0% |