Ctenuchina de Guyane et des petites Antilles
41 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
| Référence | Total | Valides | Espèces | Taxons terminaux | ||||
|---|---|---|---|---|---|---|---|---|
| nb | % | nb | % | nb | % | nb | % | |
| Betz (1980) | 23 | 9,83% | 20 | 10,53% | 20 | 10,58% | 20 | 10,58% |
| Cerda (2014) | 15 | 6,41% | 10 | 5,26% | 10 | 5,29% | 10 | 5,29% |
| Cerda (2017) | 14 | 5,98% | 14 | 7,37% | 14 | 7,41% | 14 | 7,41% |
| Schaus (1905) | 13 | 5,56% | 8 | 4,21% | 8 | 4,23% | 8 | 4,23% |
| Pinheiro et al. (2016) | 7 | 2,99% | 7 | 3,68% | 7 | 3,7% | 7 | 3,7% |
| Meurgey & Ramage (2020) | 6 | 2,56% | 6 | 3,16% | 5 | 2,65% | 6 | 3,17% |
| Deknuydt et al. (2016) | 5 | 2,14% | 5 | 2,63% | 4 | 2,12% | 4 | 2,12% |
| Laguerre et al. (2014) | 5 | 2,14% | 4 | 2,11% | 4 | 2,12% | 4 | 2,12% |
| Meurgey (2011) | 5 | 2,14% | 3 | 1,58% | 2 | 1,06% | 3 | 1,59% |
| Möschler (1872) | 5 | 2,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rothschild (1912) | 5 | 2,14% | 3 | 1,58% | 3 | 1,59% | 3 | 1,59% |
| Dognin (1909) | 4 | 1,71% | 4 | 2,11% | 4 | 2,12% | 4 | 2,12% |
| Dognin (1910) | 4 | 1,71% | 0 | 0% | 0 | 0% | 0 | 0% |
| Felder & Rogenhofer (1864-1875) | 3 | 1,28% | 0 | 0% | 0 | 0% | 0 | 0% |
| Toulgoët (1987) | 3 | 1,28% | 3 | 1,58% | 3 | 1,59% | 3 | 1,59% |
| Walker (1854) | 3 | 1,28% | 0 | 0% | 0 | 0% | 0 | 0% |
| Butler (1878) | 2 | 0,85% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cramer ([1775-1776]) | 2 | 0,85% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cramer ([1779]) | 2 | 0,85% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dognin (1911) | 2 | 0,85% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hampson (1914) | 2 | 0,85% | 1 | 0,53% | 1 | 0,53% | 1 | 0,53% |
| Haus der Natur Salzburg, Museum für Natur und Technik (2014) | 2 | 0,85% | 1 | 0,53% | 1 | 0,53% | 1 | 0,53% |
| Laguerre (2022) | 2 | 0,85% | 2 | 1,05% | 2 | 1,06% | 2 | 1,06% |
| Mantilla & Grados (2021) | 2 | 0,85% | 2 | 1,05% | 2 | 1,06% | 2 | 1,06% |
| UICN Comité français, OFB & MNHN (2021) | 2 | 0,85% | 0 | 0% | 0 | 0% | 0 | 0% |
| Becker (2013) | 1 | 0,43% | 0 | 0% | 0 | 0% | 0 | 0% |
| Butler (1876) | 1 | 0,43% | 0 | 0% | 0 | 0% | 0 | 0% |
| Butler (1877) | 1 | 0,43% | 1 | 0,53% | 1 | 0,53% | 1 | 0,53% |
| Butler (1878) | 1 | 0,43% | 0 | 0% | 0 | 0% | 0 | 0% |
| Chainey (2005) | 1 | 0,43% | 0 | 0% | 0 | 0% | 0 | 0% |
| Druce (1895) | 1 | 0,43% | 0 | 0% | 0 | 0% | 0 | 0% |
| Druce (1905) | 1 | 0,43% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fabricius ([1777]) | 1 | 0,43% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hampson (1898) | 1 | 0,43% | 1 | 0,53% | 1 | 0,53% | 1 | 0,53% |
| Hampson (1905) | 1 | 0,43% | 1 | 0,53% | 1 | 0,53% | 1 | 0,53% |
| Hampson (1915) | 1 | 0,43% | 0 | 0% | 0 | 0% | 0 | 0% |
| Heppner (1982) | 1 | 0,43% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lathy (1899) | 1 | 0,43% | 0 | 0% | 0 | 0% | 0 | 0% |
| Walker (1856) | 1 | 0,43% | 0 | 0% | 0 | 0% | 0 | 0% |
| Walker ([1865]) | 1 | 0,43% | 0 | 0% | 0 | 0% | 0 | 0% |
| Zagatti et al. (2006) | 1 | 0,43% | 1 | 0,53% | 0 | 0% | 1 | 0,53% |
