Echinodermes des Antilles françaises
91 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
| Référence | Total | Valides | Espèces | Taxons terminaux | ||||
|---|---|---|---|---|---|---|---|---|
| nb | % | nb | % | nb | % | nb | % | |
| Ameziane et al. (2020) | 32 | 4,82% | 31 | 13,96% | 31 | 14,09% | 31 | 14,09% |
| Questel (2020) | 32 | 4,82% | 27 | 12,16% | 27 | 12,27% | 27 | 12,27% |
| Harvard University Museum & Morris P.J. (2020) | 30 | 4,52% | 28 | 12,61% | 28 | 12,73% | 28 | 12,73% |
| Lyman (1883) | 29 | 4,37% | 12 | 5,41% | 12 | 5,45% | 12 | 5,45% |
| Brugneaux & Pérès (2006) | 26 | 3,92% | 22 | 9,91% | 22 | 10% | 22 | 10% |
| Orrell (2019) | 25 | 3,77% | 25 | 11,26% | 24 | 10,91% | 25 | 11,36% |
| Paulay & Brown (2019) | 23 | 3,46% | 22 | 9,91% | 22 | 10% | 22 | 10% |
| Questel & Le Quellec (2012) | 21 | 3,16% | 20 | 9,01% | 20 | 9,09% | 20 | 9,09% |
| Ducarme (2023) | 17 | 2,56% | 17 | 7,66% | 17 | 7,73% | 17 | 7,73% |
| Brugneaux & Pibot (2012) | 12 | 1,81% | 10 | 4,5% | 9 | 4,09% | 10 | 4,55% |
| IUCN (2013) | 10 | 1,51% | 9 | 4,05% | 9 | 4,09% | 9 | 4,09% |
| Clark (1915) | 9 | 1,36% | 7 | 3,15% | 7 | 3,18% | 7 | 3,18% |
| Diaz & Cuzange (2009) | 8 | 1,2% | 7 | 3,15% | 7 | 3,18% | 7 | 3,18% |
| Walenkamp (1979) | 6 | 0,9% | 6 | 2,7% | 6 | 2,73% | 6 | 2,73% |
| Conand et al. (2013) | 5 | 0,75% | 4 | 1,8% | 4 | 1,82% | 4 | 1,82% |
| Koehler (1921) | 5 | 0,75% | 4 | 1,8% | 4 | 1,82% | 4 | 1,82% |
| Pawson et al. (2009) | 5 | 0,75% | 3 | 1,35% | 3 | 1,36% | 3 | 1,36% |
| Clark & Rowe (1971) | 4 | 0,6% | 3 | 1,35% | 3 | 1,36% | 3 | 1,36% |
| Grolière et al. (1980) | 4 | 0,6% | 3 | 1,35% | 3 | 1,36% | 3 | 1,36% |
| Guille et al. (1986) | 4 | 0,6% | 3 | 1,35% | 3 | 1,36% | 3 | 1,36% |
| Martin (2011) | 4 | 0,6% | 4 | 1,8% | 4 | 1,82% | 4 | 1,82% |
| Miloslavich, P., Díaz, J. M., Klein, E., Alvarado, J. J., Díaz, C., Gobin, J., ... & Ortiz, M. (2010). Marine biodiversity in the Caribbean: regional estimates and distribution patterns. PloS one, 5(8), e11916">Miloslavich et al. (2010) | 4 | 0,6% | 4 | 1,8% | 4 | 1,82% | 4 | 1,82% |
| Améziane (2007) | 3 | 0,45% | 2 | 0,9% | 2 | 0,91% | 2 | 0,91% |
| Gebruk et al. (2012) | 3 | 0,45% | 3 | 1,35% | 3 | 1,36% | 3 | 1,36% |
| Hernández-herrejón et al. (2008) | 3 | 0,45% | 3 | 1,35% | 3 | 1,36% | 3 | 1,36% |
| Ifremer (2009) | 3 | 0,45% | 3 | 1,35% | 3 | 1,36% | 2 | 0,91% |
| Linnaeus (1758) | 3 | 0,45% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mah (2020) | 3 | 0,45% | 3 | 1,35% | 3 | 1,36% | 3 | 1,36% |
| Bulletin of the Museum of Comparative Zoölogy at Harvard College. 5: 181-195.">Agassiz (1878) | 2 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bulletin of the Museum of Comparative Zoology at Harvard College. 8(2): 69-84.">Agassiz (1880) | 2 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anker & Corbari (2020) | 2 | 0,3% | 2 | 0,9% | 2 | 0,91% | 2 | 0,91% |
| Bourmaud (2003) | 2 | 0,3% | 2 | 0,9% | 2 | 0,91% | 2 | 0,91% |
| Carpenter (1884) | 2 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
| Conand & ARVAM (2005) | 2 | 0,3% | 2 | 0,9% | 2 | 0,91% | 2 | 0,91% |
| Conand et al. (2010) | 2 | 0,3% | 2 | 0,9% | 2 | 0,91% | 2 | 0,91% |
| Conand et al. (2018) | 2 | 0,3% | 2 | 0,9% | 2 | 0,91% | 2 | 0,91% |
| Fourt et al. (2017) | 2 | 0,3% | 2 | 0,9% | 2 | 0,91% | 2 | 0,91% |
| Hendler & Brugneaux (2013) | 2 | 0,3% | 2 | 0,9% | 2 | 0,91% | 2 | 0,91% |
| Mironov et al. (2014) | 2 | 0,3% | 2 | 0,9% | 2 | 0,91% | 2 | 0,91% |
| Natural History Museum of London (2020) | 2 | 0,3% | 2 | 0,9% | 2 | 0,91% | 2 | 0,91% |
| Nelson-Smith et al. (2014) | 2 | 0,3% | 2 | 0,9% | 2 | 0,91% | 2 | 0,91% |
| Stöhr et al. (2008) | 2 | 0,3% | 2 | 0,9% | 2 | 0,91% | 2 | 0,91% |
| Verrill (1867) | 2 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
| Barreras & Messing (2013) | 1 | 0,15% | 1 | 0,45% | 1 | 0,45% | 1 | 0,45% |
| Bartsch (2008) | 1 | 0,15% | 1 | 0,45% | 1 | 0,45% | 1 | 0,45% |
| Bocquet (1953) | 1 | 0,15% | 1 | 0,45% | 1 | 0,45% | 1 | 0,45% |
| Bollard et al. (2013) | 1 | 0,15% | 1 | 0,45% | 1 | 0,45% | 1 | 0,45% |
| Borrero-Pérez et al. (2008) | 1 | 0,15% | 1 | 0,45% | 1 | 0,45% | 1 | 0,45% |
| Bourcier (1988) | 1 | 0,15% | 1 | 0,45% | 1 | 0,45% | 1 | 0,45% |
| Breton (2014) | 1 | 0,15% | 1 | 0,45% | 1 | 0,45% | 1 | 0,45% |
| Canu (1891) | 1 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
| Carpenter (1881) | 1 | 0,15% | 1 | 0,45% | 1 | 0,45% | 1 | 0,45% |
| Clark et al. (493-507) | 1 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
| Clark (1907) | 1 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
| Conand et al. (2014) | 1 | 0,15% | 1 | 0,45% | 1 | 0,45% | 1 | 0,45% |
| Delle & Chiaje (1823-1831) | 1 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
| Devaney (1974) | 1 | 0,15% | 1 | 0,45% | 1 | 0,45% | 1 | 0,45% |
| Downey (1973) | 1 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
| Eriksson et al. (2010) | 1 | 0,15% | 1 | 0,45% | 1 | 0,45% | 1 | 0,45% |
| European Nucleotide Archive (2019) | 1 | 0,15% | 1 | 0,45% | 1 | 0,45% | 1 | 0,45% |
| Ferry et al. (2020) | 1 | 0,15% | 1 | 0,45% | 1 | 0,45% | 1 | 0,45% |
| Gebruk et al. (2014) | 1 | 0,15% | 1 | 0,45% | 1 | 0,45% | 1 | 0,45% |
| Géry Parent | 1 | 0,15% | 1 | 0,45% | 1 | 0,45% | 1 | 0,45% |
| Godet et al. (2010) | 1 | 0,15% | 1 | 0,45% | 1 | 0,45% | 1 | 0,45% |
| Guille & Vadon (1985) | 1 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ifremer (2022) | 1 | 0,15% | 1 | 0,45% | 1 | 0,45% | 1 | 0,45% |
| Impact-Mer et al. (2011) | 1 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
| Laguarda-Figueras et al. (2013) | 1 | 0,15% | 1 | 0,45% | 1 | 0,45% | 1 | 0,45% |
| Lyman (1869) | 1 | 0,15% | 1 | 0,45% | 1 | 0,45% | 1 | 0,45% |
| Lyman (1875) | 1 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
| Maréchal & Trégarot (2012) | 1 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
| Marenzeller & Von (1892) | 1 | 0,15% | 1 | 0,45% | 1 | 0,45% | 1 | 0,45% |
| Marsh (1974) | 1 | 0,15% | 1 | 0,45% | 1 | 0,45% | 1 | 0,45% |
| Messing (2013) | 1 | 0,15% | 1 | 0,45% | 1 | 0,45% | 1 | 0,45% |
| Messing (2016) | 1 | 0,15% | 1 | 0,45% | 1 | 0,45% | 1 | 0,45% |
| Mironov (2006) | 1 | 0,15% | 1 | 0,45% | 1 | 0,45% | 1 | 0,45% |
| Mironov (2014) | 1 | 0,15% | 1 | 0,45% | 1 | 0,45% | 0 | 0% |
| Müller & Troschel (1842) | 1 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
| O’Hara & Thuy (2022) | 1 | 0,15% | 1 | 0,45% | 1 | 0,45% | 1 | 0,45% |
| O'hara (2015) | 1 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
| Perrier (1881) | 1 | 0,15% | 1 | 0,45% | 1 | 0,45% | 1 | 0,45% |
| Philippi (1845) | 1 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rignault & Chevallier (2017) | 1 | 0,15% | 1 | 0,45% | 1 | 0,45% | 1 | 0,45% |
| Rogacheva et al. (2013) | 1 | 0,15% | 1 | 0,45% | 1 | 0,45% | 1 | 0,45% |
| Serafy (1979) | 1 | 0,15% | 1 | 0,45% | 1 | 0,45% | 1 | 0,45% |
| Solís-Marín & Laguarda Figueras (2009) | 1 | 0,15% | 1 | 0,45% | 1 | 0,45% | 1 | 0,45% |
| Stöhr (2011) | 1 | 0,15% | 1 | 0,45% | 1 | 0,45% | 1 | 0,45% |
| Uicn et al. (2019) | 1 | 0,15% | 1 | 0,45% | 1 | 0,45% | 1 | 0,45% |
| Vázquez Bader & Gracia G. (1994) | 1 | 0,15% | 1 | 0,45% | 1 | 0,45% | 1 | 0,45% |
| Vergonzanne (1977) | 1 | 0,15% | 1 | 0,45% | 1 | 0,45% | 1 | 0,45% |
| Verrill (1915) | 1 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
