Araignées de Guyane
213 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
| Référence | Total | Valides | Espèces | Taxons terminaux | ||||
|---|---|---|---|---|---|---|---|---|
| nb | % | nb | % | nb | % | nb | % | |
| Vedel et al. (2013) | 364 | 30,49% | 315 | 65,62% | 312 | 65,55% | 313 | 65,62% |
| Caporiacco (1954) | 173 | 14,49% | 102 | 21,25% | 102 | 21,43% | 102 | 21,38% |
| Courtial (2023) | 121 | 10,13% | 118 | 24,58% | 118 | 24,79% | 118 | 24,74% |
| Taczanowski (1874) | 57 | 4,77% | 4 | 0,83% | 4 | 0,84% | 4 | 0,84% |
| Taczanowski (1872) | 56 | 4,69% | 8 | 1,67% | 8 | 1,68% | 8 | 1,68% |
| Taczanowski (1873) | 49 | 4,1% | 4 | 0,83% | 4 | 0,84% | 4 | 0,84% |
| Taczanowski (1871) | 44 | 3,69% | 0 | 0% | 0 | 0% | 0 | 0% |
| Taczanowski (1874) | 22 | 1,84% | 7 | 1,46% | 7 | 1,47% | 7 | 1,47% |
| Berland (1933) | 18 | 1,51% | 9 | 1,88% | 9 | 1,89% | 9 | 1,89% |
| Dierkens (2014) | 18 | 1,51% | 18 | 3,75% | 15 | 3,15% | 17 | 3,56% |
| Courtial et al. (2014) | 17 | 1,42% | 13 | 2,71% | 13 | 2,73% | 13 | 2,73% |
| Dierkens (2011) | 16 | 1,34% | 13 | 2,71% | 13 | 2,73% | 13 | 2,73% |
| Dierkens (2012) | 15 | 1,26% | 15 | 3,12% | 15 | 3,15% | 15 | 3,14% |
| Berland (1934) | 13 | 1,09% | 8 | 1,67% | 8 | 1,68% | 8 | 1,68% |
| Courtial et al. (2022) | 13 | 1,09% | 11 | 2,29% | 11 | 2,31% | 11 | 2,31% |
| Cazanove (2022) | 12 | 1,01% | 12 | 2,5% | 12 | 2,52% | 12 | 2,52% |
| Logunov (2015) | 12 | 1,01% | 12 | 2,5% | 12 | 2,52% | 12 | 2,52% |
| Fukushima & Bertani (2017) | 11 | 0,92% | 2 | 0,42% | 2 | 0,42% | 0 | 0% |
| Questel (2020) | 11 | 0,92% | 11 | 2,29% | 11 | 2,31% | 11 | 2,31% |
| Ramage (2017) | 10 | 0,84% | 10 | 2,08% | 10 | 2,1% | 10 | 2,1% |
| Ruiz et al. (2019) | 10 | 0,84% | 5 | 1,04% | 5 | 1,05% | 5 | 1,05% |
| Simon (1900) | 10 | 0,84% | 7 | 1,46% | 7 | 1,47% | 7 | 1,47% |
| Benavides & Hormiga (2016) | 9 | 0,75% | 2 | 0,42% | 2 | 0,42% | 2 | 0,42% |
| Berland (1924) | 9 | 0,75% | 3 | 0,62% | 3 | 0,63% | 3 | 0,63% |
| Dierkens (2013) | 9 | 0,75% | 9 | 1,88% | 9 | 1,89% | 9 | 1,89% |
| Ledoux & Hallé (1995) | 9 | 0,75% | 7 | 1,46% | 7 | 1,47% | 7 | 1,47% |
| Yokoyama (2013) | 9 | 0,75% | 9 | 1,88% | 9 | 1,89% | 9 | 1,89% |
| Bayer et al. (2020) | 8 | 0,67% | 8 | 1,67% | 8 | 1,68% | 8 | 1,68% |
| Berland (1935) | 8 | 0,67% | 4 | 0,83% | 4 | 0,84% | 4 | 0,84% |
| Dierkens & Charlat (2011) | 8 | 0,67% | 8 | 1,67% | 8 | 1,68% | 8 | 1,68% |
| Platnick (1993) | 8 | 0,67% | 8 | 1,67% | 8 | 1,68% | 8 | 1,68% |
| Bonaldo & Brescovit (1992) | 7 | 0,59% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
| Courtial & Picard (2024) | 7 | 0,59% | 7 | 1,46% | 7 | 1,47% | 7 | 1,47% |
| Saturnino et al. (2015) | 7 | 0,59% | 7 | 1,46% | 7 | 1,47% | 7 | 1,47% |
| Walckenaer (1837) | 7 | 0,59% | 0 | 0% | 0 | 0% | 0 | 0% |
| Aharon et al. (2017) | 6 | 0,5% | 0 | 0% | 0 | 0% | 0 | 0% |
| Berland (1929) | 6 | 0,5% | 2 | 0,42% | 2 | 0,42% | 2 | 0,42% |
| Berland (1934) | 6 | 0,5% | 4 | 0,83% | 4 | 0,84% | 4 | 0,84% |
| Dierkens & Ramage (2016) | 6 | 0,5% | 6 | 1,25% | 6 | 1,26% | 6 | 1,26% |
| Jourdan & Mille (2006) | 6 | 0,5% | 6 | 1,25% | 6 | 1,26% | 6 | 1,26% |
| Pickard-Cambridge (1889) | 6 | 0,5% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
| Questel & Le Quellec (2012) | 6 | 0,5% | 6 | 1,25% | 6 | 1,26% | 6 | 1,26% |
| Rheims & Jäger (2022) | 6 | 0,5% | 6 | 1,25% | 6 | 1,26% | 6 | 1,26% |
| Berland (1942) | 5 | 0,42% | 3 | 0,62% | 3 | 0,63% | 3 | 0,63% |
| Cifuentes & Bertani (2022) | 5 | 0,42% | 3 | 0,62% | 3 | 0,63% | 3 | 0,63% |
| Levi (1986) | 5 | 0,42% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
| Levi (2007) | 5 | 0,42% | 4 | 0,83% | 4 | 0,84% | 4 | 0,84% |
| Marusik & Omelko (2015) | 5 | 0,42% | 3 | 0,62% | 3 | 0,63% | 3 | 0,63% |
| Simon (1896) | 5 | 0,42% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
| Bigot (1992) | 4 | 0,34% | 3 | 0,62% | 3 | 0,63% | 3 | 0,63% |
| Caporiacco & Denis (1954) | 4 | 0,34% | 0 | 0% | 0 | 0% | 0 | 0% |
| Chickering (1964) | 4 | 0,34% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dierkens (2010) | 4 | 0,34% | 2 | 0,42% | 2 | 0,42% | 2 | 0,42% |
| Dierkens (2013) | 4 | 0,34% | 4 | 0,83% | 4 | 0,84% | 4 | 0,84% |
| Dierkens (2021) | 4 | 0,34% | 4 | 0,83% | 4 | 0,84% | 4 | 0,84% |
| Dupérré (2023) | 4 | 0,34% | 2 | 0,42% | 2 | 0,42% | 2 | 0,42% |
| Glueck (1994) | 4 | 0,34% | 0 | 0% | 0 | 0% | 0 | 0% |
| Levi (1997) | 4 | 0,34% | 4 | 0,83% | 4 | 0,84% | 4 | 0,84% |
| Lopez & Lopez (1997) | 4 | 0,34% | 4 | 0,83% | 4 | 0,84% | 4 | 0,84% |
| Roewer (1942) | 4 | 0,34% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
| UICN Comité français, OFB, MNHN & AsFrA (2023) | 4 | 0,34% | 3 | 0,62% | 3 | 0,63% | 3 | 0,63% |
| West & Marshall (2000) | 4 | 0,34% | 4 | 0,83% | 4 | 0,84% | 4 | 0,84% |
| Berland (1927) | 3 | 0,25% | 3 | 0,62% | 3 | 0,63% | 3 | 0,63% |
| Bragio & Bonaldo (2000) | 3 | 0,25% | 2 | 0,42% | 2 | 0,42% | 2 | 0,42% |
| Brescovit (1996) | 3 | 0,25% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
| Costa & Ruiz (2014) | 3 | 0,25% | 3 | 0,62% | 3 | 0,63% | 3 | 0,63% |
| Drolshagen & Backstam (2011) | 3 | 0,25% | 3 | 0,62% | 3 | 0,63% | 3 | 0,63% |
| Edwards (2015) | 3 | 0,25% | 2 | 0,42% | 2 | 0,42% | 2 | 0,42% |
| Galiano (1979) | 3 | 0,25% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
| Galiano (1979) | 3 | 0,25% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
| Galiano (2000) | 3 | 0,25% | 3 | 0,62% | 3 | 0,63% | 3 | 0,63% |
| Hervé & Garrouste (2009) | 3 | 0,25% | 3 | 0,62% | 3 | 0,63% | 3 | 0,63% |
| Keyserling (1865) | 3 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
| Levi (1993) | 3 | 0,25% | 2 | 0,42% | 2 | 0,42% | 2 | 0,42% |
| Linnaeus (1758) | 3 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lopez (1987) | 3 | 0,25% | 2 | 0,42% | 2 | 0,42% | 2 | 0,42% |
| Marechal (1996) | 3 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
| Marshall & West (2008) | 3 | 0,25% | 3 | 0,62% | 3 | 0,63% | 3 | 0,63% |
| Matos & Ruiz (2023) | 3 | 0,25% | 3 | 0,62% | 3 | 0,63% | 3 | 0,63% |
| Mello-Leitão (1948) | 3 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
| Nentwig et al. (2019) | 3 | 0,25% | 3 | 0,62% | 3 | 0,63% | 3 | 0,63% |
| Pickard-cambridge (1901) | 3 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rheims (2020) | 3 | 0,25% | 3 | 0,62% | 3 | 0,63% | 3 | 0,63% |
| Schmidt (1995) | 3 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sherwood & Gabriel (2021) | 3 | 0,25% | 3 | 0,62% | 3 | 0,63% | 3 | 0,63% |
| Simon (1889) | 3 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
| Simon (1892) | 3 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
| Walckenaer ([1841]) | 3 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
| Abrahim et al. (2012) | 2 | 0,17% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
| Beatty et al. (2008) | 2 | 0,17% | 2 | 0,42% | 2 | 0,42% | 2 | 0,42% |
| Buckup et al. (2012) | 2 | 0,17% | 2 | 0,42% | 2 | 0,42% | 2 | 0,42% |
| Caporiacco (1947) | 2 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Caporiacco (1948) | 2 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cochereau (1966) | 2 | 0,17% | 2 | 0,42% | 2 | 0,42% | 2 | 0,42% |
| Crane (1943) | 2 | 0,17% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
| Crane (1949) | 2 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gabriel (2011) | 2 | 0,17% | 2 | 0,42% | 2 | 0,42% | 2 | 0,42% |
| Hentz (1847) | 2 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hofer et al. (1994) | 2 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Huber (2000) | 2 | 0,17% | 2 | 0,42% | 2 | 0,42% | 2 | 0,42% |
| Jäger (2020) | 2 | 0,17% | 2 | 0,42% | 2 | 0,42% | 2 | 0,42% |
| Jourdan (2020) | 2 | 0,17% | 2 | 0,42% | 2 | 0,42% | 2 | 0,42% |
| Keyserling (1883) | 2 | 0,17% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
| Koch (1838) | 2 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Koch (1842) | 2 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Latreille (1804) | 2 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Levi (1985) | 2 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Levi (2008) | 2 | 0,17% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
| Lopez (1996) | 2 | 0,17% | 2 | 0,42% | 2 | 0,42% | 2 | 0,42% |
| Machado et al. (2015) | 2 | 0,17% | 2 | 0,42% | 2 | 0,42% | 2 | 0,42% |
| Machado et al. (2021) | 2 | 0,17% | 2 | 0,42% | 2 | 0,42% | 2 | 0,42% |
| Marechal & Marty (1998) | 2 | 0,17% | 2 | 0,42% | 2 | 0,42% | 2 | 0,42% |
| Marples (1957) | 2 | 0,17% | 2 | 0,42% | 2 | 0,42% | 2 | 0,42% |
| Mello-Leitão (1929) | 2 | 0,17% | 2 | 0,42% | 2 | 0,42% | 2 | 0,42% |
| Mello-Leitão (1930) | 2 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mello-leitão (1932) | 2 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Moeller et al. (2023) | 2 | 0,17% | 2 | 0,42% | 2 | 0,42% | 2 | 0,42% |
| Mori & Bertani (2020) | 2 | 0,17% | 2 | 0,42% | 2 | 0,42% | 2 | 0,42% |
| Paula et al. (2014) | 2 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Poeta & Teixeira (2017) | 2 | 0,17% | 2 | 0,42% | 2 | 0,42% | 2 | 0,42% |
| Polotow & Brescovit (2009) | 2 | 0,17% | 2 | 0,42% | 2 | 0,42% | 2 | 0,42% |
| Rheims (2021) | 2 | 0,17% | 2 | 0,42% | 2 | 0,42% | 2 | 0,42% |
| Ruiz & Brescovit (2008) | 2 | 0,17% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
| Ruiz & Brescovit (2013) | 2 | 0,17% | 2 | 0,42% | 2 | 0,42% | 2 | 0,42% |
| Ruiz & Rego (2019) | 2 | 0,17% | 2 | 0,42% | 2 | 0,42% | 2 | 0,42% |
| Santos & Brescovit (2001) | 2 | 0,17% | 2 | 0,42% | 2 | 0,42% | 2 | 0,42% |
| Santos (2007) | 2 | 0,17% | 2 | 0,42% | 2 | 0,42% | 2 | 0,42% |
| Sherwood et al. (2023) | 2 | 0,17% | 2 | 0,42% | 2 | 0,42% | 2 | 0,42% |
| Simon (1897) | 2 | 0,17% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
| Souza et al. (2020) | 2 | 0,17% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
| Taczanowski (1878) | 2 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Tesmoingt & Schmidt (2002) | 2 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Touroult et al. (2020) | 2 | 0,17% | 2 | 0,42% | 2 | 0,42% | 2 | 0,42% |
| Vayssières et al. (2001) | 2 | 0,17% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
| Vol (2000) | 2 | 0,17% | 2 | 0,42% | 2 | 0,42% | 2 | 0,42% |
| Anonyme (2017) | 1 | 0,08% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
| Audouin (1826) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Banks (1909) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Berry et al. (1997) | 1 | 0,08% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
| Berry et al. (1998) | 1 | 0,08% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
| Cambridge (1896) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Casas & Rheims (2024) | 1 | 0,08% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
| Chamberlian & Ivie (1936) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Chickering (1940) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Chickering (1960) | 1 | 0,08% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
| Chickering (1960) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Chickering (1961) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Crane (1948) | 1 | 0,08% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
| Cruz et al. (2012) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dufour (1831) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dumitrescu & Georgescu (1987) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dupérré & Tapia (2021) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| European Nucleotide Archive (2019) | 1 | 0,08% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
| Exline & Levi (1962) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ferreira-sousa et al. (2023) | 1 | 0,08% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
| Figueiredo et al. (2020) | 1 | 0,08% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
| Gabriel (2020) | 1 | 0,08% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
| Hacala et al. (2024) | 1 | 0,08% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
| Huesser (2018) | 1 | 0,08% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
| Jäger (2002) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Keyserling & Marx (1892) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Keyserling & Marx (1893) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Keyserling (1879) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Keyserling (1881) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Keyserling (1885) | 1 | 0,08% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
| Koch (1836) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Koch (1841) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Koch (1846) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kuntner et al. (2018) | 1 | 0,08% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
| Ledoux (2004) | 1 | 0,08% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
| Ledoux (2007) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Levi (1963) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lise et al. (2015) | 1 | 0,08% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
| Lucas (1872) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Luo (2023) | 1 | 0,08% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
| Magalhaes & Santos (2011) | 1 | 0,08% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
| Maréchal & Iinuma (2013) | 1 | 0,08% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
| Mello-Leitão (1915) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mello-Leitão (1929) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mello-leitao (1939) | 1 | 0,08% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
| Mello-leitao (1942) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mello-leitão (1944) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mello-Leitão (1945) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Nobre & Ruiz (2024) | 1 | 0,08% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
| Odin (2014) | 1 | 0,08% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
| Petrunkevitch (1910) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ponel et al. (2017) | 1 | 0,08% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
| Reimoser (1917) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rheims & Jager (2008) | 1 | 0,08% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
| Rinaldi (1988) | 1 | 0,08% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
| Rivière (1979) | 1 | 0,08% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
| Roewer (1951) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Roger (2018) | 1 | 0,08% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
| Rossi & Godoy (2006) | 1 | 0,08% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
| Salgado & Ruiz (2020) | 1 | 0,08% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
| Sanchez-ruiz & Brescovit (2018) | 1 | 0,08% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
| Santos & Brescovit (2003) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Tarantulas of the World, 142: 28-29.">Schmidt (2010) | 1 | 0,08% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
| Seurat (1934) | 1 | 0,08% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
| Sherwood et al. (2023) | 1 | 0,08% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
| Simon (1864) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Simon (1873) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Simon (1880) | 1 | 0,08% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
| Simon (1891) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Simon (1892) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Simon (1893) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Strand (1916) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Taczanowski (1878) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Valerio (1981) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Walckenaer (1805) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Walckenaer (1837) | 1 | 0,08% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
| White (1841) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Zhang & Maddison (2015) | 1 | 0,08% | 1 | 0,21% | 1 | 0,21% | 1 | 0,21% |
