Echinodermes de Polynésie française
100 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
| Référence | Total | Valides | Espèces | Taxons terminaux | ||||
|---|---|---|---|---|---|---|---|---|
| nb | % | nb | % | nb | % | nb | % | |
| Ducarme (2023) | 216 | 13,17% | 215 | 57,95% | 215 | 58,42% | 215 | 58,42% |
| Clark & Rowe (1971) | 167 | 10,18% | 135 | 36,39% | 135 | 36,68% | 135 | 36,68% |
| Améziane (2007) | 166 | 10,12% | 135 | 36,39% | 135 | 36,68% | 135 | 36,68% |
| Guille et al. (1986) | 124 | 7,56% | 105 | 28,3% | 105 | 28,53% | 105 | 28,53% |
| Guille & Vadon (1985) | 35 | 2,13% | 27 | 7,28% | 27 | 7,34% | 27 | 7,34% |
| Conand & ARVAM (2005) | 33 | 2,01% | 26 | 7,01% | 26 | 7,07% | 26 | 7,07% |
| Bourmaud (2003) | 31 | 1,89% | 23 | 6,2% | 23 | 6,25% | 23 | 6,25% |
| Conand et al. (2016) | 28 | 1,71% | 21 | 5,66% | 21 | 5,71% | 21 | 5,71% |
| Ameziane et al. (2020) | 26 | 1,59% | 25 | 6,74% | 24 | 6,52% | 25 | 6,79% |
| Devaney (1974) | 25 | 1,52% | 17 | 4,58% | 15 | 4,08% | 17 | 4,62% |
| Conand et al. (2018) | 24 | 1,46% | 23 | 6,2% | 23 | 6,25% | 23 | 6,25% |
| Conand et al. (2010) | 22 | 1,34% | 22 | 5,93% | 22 | 5,98% | 22 | 5,98% |
| Conand et al. (2013) | 19 | 1,16% | 15 | 4,04% | 15 | 4,08% | 15 | 4,08% |
| Kronen et al. (2008) | 16 | 0,98% | 15 | 4,04% | 15 | 4,08% | 15 | 4,08% |
| Marsh (1974) | 16 | 0,98% | 16 | 4,31% | 16 | 4,35% | 16 | 4,35% |
| Mulochau & Conand (2008) | 15 | 0,91% | 13 | 3,5% | 13 | 3,53% | 13 | 3,53% |
| Solís-Marín & Laguarda Figueras (2009) | 15 | 0,91% | 14 | 3,77% | 14 | 3,8% | 14 | 3,8% |
| Eriksson et al. (2010) | 14 | 0,85% | 14 | 3,77% | 14 | 3,8% | 14 | 3,8% |
| Paulay & Brown (2019) | 13 | 0,79% | 12 | 3,23% | 12 | 3,26% | 12 | 3,26% |
| Linnaeus (1758) | 12 | 0,73% | 0 | 0% | 0 | 0% | 0 | 0% |
| Stöhr (2011) | 12 | 0,73% | 10 | 2,7% | 10 | 2,72% | 10 | 2,72% |
| Conand et al. (2014) | 10 | 0,61% | 10 | 2,7% | 10 | 2,72% | 10 | 2,72% |
| Stöhr et al. (2008) | 9 | 0,55% | 8 | 2,16% | 8 | 2,17% | 8 | 2,17% |
| Boissin et al. (2016) | 8 | 0,49% | 5 | 1,35% | 5 | 1,36% | 5 | 1,36% |
| Bollard et al. (2013) | 8 | 0,49% | 5 | 1,35% | 5 | 1,36% | 5 | 1,36% |
| Wantiez (2001) | 7 | 0,43% | 7 | 1,89% | 7 | 1,9% | 7 | 1,9% |
| Chabanet et al. (2007) | 6 | 0,37% | 5 | 1,35% | 5 | 1,36% | 5 | 1,36% |
| Uthicke et al. (2004) | 6 | 0,37% | 5 | 1,35% | 5 | 1,36% | 5 | 1,36% |
| Carpenter (1888) | 5 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
| Clark (1917) | 5 | 0,3% | 1 | 0,27% | 1 | 0,27% | 1 | 0,27% |
| Orrell (2019) | 5 | 0,3% | 5 | 1,35% | 5 | 1,36% | 5 | 1,36% |
| Vergonzanne (1977) | 5 | 0,3% | 4 | 1,08% | 4 | 1,09% | 4 | 1,09% |
| Conand et al. (2005) | 4 | 0,24% | 3 | 0,81% | 3 | 0,82% | 3 | 0,82% |
| Deichmann (1963) | 4 | 0,24% | 3 | 0,81% | 3 | 0,82% | 3 | 0,82% |
| Ludwig (1905) | 4 | 0,24% | 4 | 1,08% | 4 | 1,09% | 4 | 1,09% |
| Pyle et al. (2016) | 4 | 0,24% | 3 | 0,81% | 3 | 0,82% | 3 | 0,82% |
| Memoirs of the Museum of Comparative Zoology at Harvard College, 39: 115–154.">Clark (1920) | 3 | 0,18% | 2 | 0,54% | 2 | 0,54% | 2 | 0,54% |
| Hardouin Michelin (1844) | 3 | 0,18% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jangoux & Aziz (1988) | 3 | 0,18% | 2 | 0,54% | 2 | 0,54% | 2 | 0,54% |
| Mah (2017) | 3 | 0,18% | 3 | 0,81% | 3 | 0,82% | 3 | 0,82% |
| Nelson-Smith et al. (2014) | 3 | 0,18% | 2 | 0,54% | 2 | 0,54% | 1 | 0,27% |
| O'hara et al. (2019) | 3 | 0,18% | 3 | 0,81% | 3 | 0,82% | 3 | 0,82% |
| Perrier (1875) | 3 | 0,18% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rignault & Chevallier (2017) | 3 | 0,18% | 3 | 0,81% | 3 | 0,82% | 3 | 0,82% |
| Bedford (1899) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bigot et al. (2006) | 2 | 0,12% | 2 | 0,54% | 2 | 0,54% | 2 | 0,54% |
| Bigot et al. (2006) | 2 | 0,12% | 2 | 0,54% | 2 | 0,54% | 2 | 0,54% |
| Brugneaux & Pérès (2006) | 2 | 0,12% | 2 | 0,54% | 2 | 0,54% | 2 | 0,54% |
| Cherbonnier (1980) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cherbonnier (1986) | 2 | 0,12% | 2 | 0,54% | 2 | 0,54% | 2 | 0,54% |
| Clark (1915) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Haszprunar & Spies (2014) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hendler & Brugneaux (2013) | 2 | 0,12% | 2 | 0,54% | 2 | 0,54% | 2 | 0,54% |
| Hertlein & Emerson (1957) | 2 | 0,12% | 1 | 0,27% | 1 | 0,27% | 1 | 0,27% |
| Koehler (1921) | 2 | 0,12% | 2 | 0,54% | 2 | 0,54% | 2 | 0,54% |
| Mah (2015) | 2 | 0,12% | 2 | 0,54% | 2 | 0,54% | 2 | 0,54% |
| Martin (2011) | 2 | 0,12% | 2 | 0,54% | 2 | 0,54% | 2 | 0,54% |
| Natural History Museum of London (2020) | 2 | 0,12% | 2 | 0,54% | 2 | 0,54% | 2 | 0,54% |
| Pearman et al. (2020) | 2 | 0,12% | 2 | 0,54% | 2 | 0,54% | 2 | 0,54% |
| Perrier (1875) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Perrier (1881) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Questel (2020) | 2 | 0,12% | 1 | 0,27% | 1 | 0,27% | 1 | 0,27% |
| Verrill (1867) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bartsch (2008) | 1 | 0,06% | 1 | 0,27% | 1 | 0,27% | 1 | 0,27% |
| Bocquet (1953) | 1 | 0,06% | 1 | 0,27% | 1 | 0,27% | 1 | 0,27% |
| Bourcier (1988) | 1 | 0,06% | 1 | 0,27% | 1 | 0,27% | 1 | 0,27% |
| Breton (2014) | 1 | 0,06% | 1 | 0,27% | 1 | 0,27% | 1 | 0,27% |
| Brugneaux & Pibot (2012) | 1 | 0,06% | 1 | 0,27% | 1 | 0,27% | 1 | 0,27% |
| Byrne & O'Hara (2017) | 1 | 0,06% | 1 | 0,27% | 1 | 0,27% | 1 | 0,27% |
| Canu (1891) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Conand & Mangion (2002) | 1 | 0,06% | 1 | 0,27% | 1 | 0,27% | 1 | 0,27% |
| Cook et al. (2023) | 1 | 0,06% | 1 | 0,27% | 1 | 0,27% | 1 | 0,27% |
| Delle & Chiaje (1823-1831) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ducarme (2023) | 1 | 0,06% | 1 | 0,27% | 1 | 0,27% | 1 | 0,27% |
| Ferry et al. (2020) | 1 | 0,06% | 1 | 0,27% | 1 | 0,27% | 1 | 0,27% |
| Godet et al. (2010) | 1 | 0,06% | 1 | 0,27% | 1 | 0,27% | 1 | 0,27% |
| Humes (1976) | 1 | 0,06% | 1 | 0,27% | 1 | 0,27% | 1 | 0,27% |
| Ifremer (2009) | 1 | 0,06% | 1 | 0,27% | 1 | 0,27% | 1 | 0,27% |
| Ifremer (2022) | 1 | 0,06% | 1 | 0,27% | 1 | 0,27% | 1 | 0,27% |
| Kogo et al. (2019) | 1 | 0,06% | 1 | 0,27% | 1 | 0,27% | 1 | 0,27% |
| Lessios et al. (1996) | 1 | 0,06% | 1 | 0,27% | 1 | 0,27% | 1 | 0,27% |
| Mah (2015) | 1 | 0,06% | 1 | 0,27% | 1 | 0,27% | 1 | 0,27% |
| Mah (2015) | 1 | 0,06% | 1 | 0,27% | 1 | 0,27% | 1 | 0,27% |
| Mah (2015) | 1 | 0,06% | 1 | 0,27% | 1 | 0,27% | 1 | 0,27% |
| Mah (2021) | 1 | 0,06% | 1 | 0,27% | 1 | 0,27% | 1 | 0,27% |
| Mah (2023) | 1 | 0,06% | 1 | 0,27% | 1 | 0,27% | 1 | 0,27% |
| Mills et al. (2018) | 1 | 0,06% | 1 | 0,27% | 1 | 0,27% | 1 | 0,27% |
| Murakami (1943) | 1 | 0,06% | 1 | 0,27% | 1 | 0,27% | 1 | 0,27% |
| O’Hara & Thuy (2022) | 1 | 0,06% | 1 | 0,27% | 1 | 0,27% | 1 | 0,27% |
| O'hara (2015) | 1 | 0,06% | 1 | 0,27% | 1 | 0,27% | 1 | 0,27% |
| O'hara (2015) | 1 | 0,06% | 1 | 0,27% | 1 | 0,27% | 1 | 0,27% |
| Purcell et al. (2012) | 1 | 0,06% | 1 | 0,27% | 1 | 0,27% | 1 | 0,27% |
| Questel & Le Quellec (2012) | 1 | 0,06% | 1 | 0,27% | 1 | 0,27% | 1 | 0,27% |
| Sladen (1882) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sladen (1889) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Smirnov et al. (2018) | 1 | 0,06% | 1 | 0,27% | 1 | 0,27% | 1 | 0,27% |
| Telenius & Shah (2019) | 1 | 0,06% | 1 | 0,27% | 1 | 0,27% | 1 | 0,27% |
| Uicn et al. (2019) | 1 | 0,06% | 1 | 0,27% | 1 | 0,27% | 1 | 0,27% |
| Walenkamp (1979) | 1 | 0,06% | 1 | 0,27% | 1 | 0,27% | 1 | 0,27% |
| Wickel et al. (2016) | 1 | 0,06% | 1 | 0,27% | 1 | 0,27% | 1 | 0,27% |
