Poissons marins de Saint-Martin
120 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
| Référence | Total | Valides | Espèces | Taxons terminaux | ||||
|---|---|---|---|---|---|---|---|---|
| nb | % | nb | % | nb | % | nb | % | |
| Bouchon-Navaro et al. (2005) | 176 | 17,37% | 148 | 87,06% | 148 | 87,06% | 148 | 87,06% |
| Questel (2020) | 145 | 14,31% | 144 | 84,71% | 144 | 84,71% | 144 | 84,71% |
| Questel & Le Quellec (2012) | 137 | 13,52% | 131 | 77,06% | 131 | 77,06% | 131 | 77,06% |
| Diaz & Cuzange (2009) | 104 | 10,27% | 96 | 56,47% | 96 | 56,47% | 96 | 56,47% |
| Bouchon-Navaro & Louis (1986) | 96 | 9,48% | 81 | 47,65% | 81 | 47,65% | 81 | 47,65% |
| Brugneaux & Pérès (2006) | 67 | 6,61% | 61 | 35,88% | 61 | 35,88% | 61 | 35,88% |
| Rousseau (2010) | 30 | 2,96% | 28 | 16,47% | 28 | 16,47% | 28 | 16,47% |
| Louis et al. (1992) | 18 | 1,78% | 11 | 6,47% | 11 | 6,47% | 11 | 6,47% |
| Fricke et al. (2009) | 16 | 1,58% | 15 | 8,82% | 15 | 8,82% | 15 | 8,82% |
| Fricke et al. (2011) | 15 | 1,48% | 15 | 8,82% | 15 | 8,82% | 15 | 8,82% |
| Siu et al. (2017) | 14 | 1,38% | 13 | 7,65% | 13 | 7,65% | 13 | 7,65% |
| Wickel & Jamon (2010) | 14 | 1,38% | 13 | 7,65% | 13 | 7,65% | 13 | 7,65% |
| Smith (1997) | 13 | 1,28% | 13 | 7,65% | 13 | 7,65% | 13 | 7,65% |
| Compagno (1984) | 12 | 1,18% | 12 | 7,06% | 12 | 7,06% | 12 | 7,06% |
| Bouchon-Navaro et al. (1992) | 11 | 1,09% | 9 | 5,29% | 9 | 5,29% | 9 | 5,29% |
| Béarez et al. (2017) | 9 | 0,89% | 9 | 5,29% | 9 | 5,29% | 9 | 5,29% |
| Collette & Nauen (1983) | 8 | 0,79% | 8 | 4,71% | 8 | 4,71% | 8 | 4,71% |
| Poey (1858-61) | 8 | 0,79% | 0 | 0% | 0 | 0% | 0 | 0% |
| Delrieu-Trottin et al. (2015) | 7 | 0,69% | 7 | 4,12% | 7 | 4,12% | 7 | 4,12% |
| Fourriére et al. (2014) | 7 | 0,69% | 7 | 4,12% | 7 | 4,12% | 7 | 4,12% |
| Pezold et al. (2015) | 7 | 0,69% | 7 | 4,12% | 7 | 4,12% | 7 | 4,12% |
| Vaslet & Agrnsm (2018) | 7 | 0,69% | 7 | 4,12% | 7 | 4,12% | 7 | 4,12% |
| Bacchet et al. (2007) | 6 | 0,59% | 5 | 2,94% | 5 | 2,94% | 5 | 2,94% |
| Heemstra & Randall (1993) | 6 | 0,59% | 6 | 3,53% | 6 | 3,53% | 6 | 3,53% |
| Kulbicki et al. (2000) | 6 | 0,59% | 5 | 2,94% | 5 | 2,94% | 5 | 2,94% |
| Richard et al. (1982) | 6 | 0,59% | 3 | 1,76% | 3 | 1,76% | 3 | 1,76% |
| Béarez & Bouffandeau (2019) | 5 | 0,49% | 5 | 2,94% | 5 | 2,94% | 5 | 2,94% |
| Chabanet & Durville (2005) | 5 | 0,49% | 4 | 2,35% | 4 | 2,35% | 4 | 2,35% |
| Fricke et al. (2013) | 5 | 0,49% | 5 | 2,94% | 5 | 2,94% | 5 | 2,94% |
| Linnaeus (1758) | 5 | 0,49% | 0 | 0% | 0 | 0% | 0 | 0% |
| Nakamura (1985) | 5 | 0,49% | 5 | 2,94% | 5 | 2,94% | 5 | 2,94% |
| Questel (2017) | 5 | 0,49% | 5 | 2,94% | 5 | 2,94% | 5 | 2,94% |
| Swainson (1839) | 5 | 0,49% | 0 | 0% | 0 | 0% | 0 | 0% |
| Uicn et al. (2019) | 5 | 0,49% | 5 | 2,94% | 5 | 2,94% | 5 | 2,94% |
| Allen (1985) | 4 | 0,39% | 4 | 2,35% | 4 | 2,35% | 4 | 2,35% |
| Béarez & Séret (2009) | 4 | 0,39% | 3 | 1,76% | 3 | 1,76% | 3 | 1,76% |
| Berry & Smith-Vaniz (1978) | 4 | 0,39% | 4 | 2,35% | 4 | 2,35% | 4 | 2,35% |
| Bloch & Schneider (1801) | 4 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
| Charbonnel (1990) | 4 | 0,39% | 2 | 1,18% | 2 | 1,18% | 2 | 1,18% |
| Le Bail et al. (2012) | 4 | 0,39% | 4 | 2,35% | 4 | 2,35% | 4 | 2,35% |
| Morris (2012) | 4 | 0,39% | 4 | 2,35% | 4 | 2,35% | 4 | 2,35% |
| Müller & Henle (1841) | 4 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rafinesque Schmaltz (1810) | 4 | 0,39% | 2 | 1,18% | 2 | 1,18% | 2 | 1,18% |
| Williams et al. (2006) | 4 | 0,39% | 3 | 1,76% | 3 | 1,76% | 3 | 1,76% |
| Lim et al. (2002) | 3 | 0,3% | 1 | 0,59% | 1 | 0,59% | 1 | 0,59% |
| Maréchal et al. (2006) | 3 | 0,3% | 3 | 1,76% | 3 | 1,76% | 3 | 1,76% |
| Monti et al. (2010) | 3 | 0,3% | 1 | 0,59% | 1 | 0,59% | 1 | 0,59% |
| Randall & Vergara (1978) | 3 | 0,3% | 3 | 1,76% | 3 | 1,76% | 3 | 1,76% |
| Simian et al. (2022) | 3 | 0,3% | 3 | 1,76% | 3 | 1,76% | 3 | 1,76% |
| UICN Comité français, OFB & MNHN (2021) | 3 | 0,3% | 3 | 1,76% | 3 | 1,76% | 3 | 1,76% |
| Brugneaux & Pérès (2005) | 2 | 0,2% | 1 | 0,59% | 1 | 0,59% | 1 | 0,59% |
| Compagno (1984) | 2 | 0,2% | 2 | 1,18% | 2 | 1,18% | 2 | 1,18% |
| Durand (2016) | 2 | 0,2% | 1 | 0,59% | 1 | 0,59% | 1 | 0,59% |
| Fontan (2019) | 2 | 0,2% | 2 | 1,18% | 2 | 1,18% | 2 | 1,18% |
| Fourt et al. (2017) | 2 | 0,2% | 2 | 1,18% | 2 | 1,18% | 2 | 1,18% |
| Gronow (1854) | 2 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Holbrook (1855) | 2 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kulbicki (comm. pers., 2011) | 2 | 0,2% | 2 | 1,18% | 2 | 1,18% | 2 | 1,18% |
| Lacepède (1800) | 2 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lacepède (1802) | 2 | 0,2% | 1 | 0,59% | 1 | 0,59% | 1 | 0,59% |
| Maréchal & Trégarot (2012) | 2 | 0,2% | 1 | 0,59% | 1 | 0,59% | 1 | 0,59% |
| Marshall et al. (2009) | 2 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Nardo (1827) | 2 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rafinesque (1810) | 2 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Risso (1827) | 2 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Snodgrass & Heller (1905) | 2 | 0,2% | 1 | 0,59% | 1 | 0,59% | 1 | 0,59% |
| Yokoyama (2013) | 2 | 0,2% | 1 | 0,59% | 1 | 0,59% | 1 | 0,59% |
| Agassiz (1833-1843) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Allen (comm. pers., 2009) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Atwood (1869) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bancroft (1832) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bernal & Rocha (2011) | 1 | 0,1% | 1 | 0,59% | 1 | 0,59% | 1 | 0,59% |
| Bloch & Schneider (1801) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bonnaterre (1788) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Brito Capello (1867) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Capape et al. (2002) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Chabanaud (1927) | 1 | 0,1% | 1 | 0,59% | 1 | 0,59% | 1 | 0,59% |
| Collette (2003) | 1 | 0,1% | 1 | 0,59% | 1 | 0,59% | 1 | 0,59% |
| Cuvier & Valenciennes (1830-1832) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cuvier & Valenciennes ([1832]) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cuvier & Valenciennes (1846) | 1 | 0,1% | 1 | 0,59% | 1 | 0,59% | 1 | 0,59% |
| Denys et al. (2022) | 1 | 0,1% | 1 | 0,59% | 1 | 0,59% | 1 | 0,59% |
| Etcheberry & Abraham (2009) | 1 | 0,1% | 1 | 0,59% | 1 | 0,59% | 1 | 0,59% |
| Francour & Mouine (2008) | 1 | 0,1% | 1 | 0,59% | 1 | 0,59% | 1 | 0,59% |
| Gill (1862) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Girard (1859) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Girondot et al. (2015) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Goulletquer (2016) | 1 | 0,1% | 1 | 0,59% | 1 | 0,59% | 1 | 0,59% |
| Hein et al. (2010) | 1 | 0,1% | 1 | 0,59% | 1 | 0,59% | 1 | 0,59% |
| Iglésias et al. (2021) | 1 | 0,1% | 1 | 0,59% | 1 | 0,59% | 1 | 0,59% |
| IUCN (2014) | 1 | 0,1% | 1 | 0,59% | 1 | 0,59% | 1 | 0,59% |
| Legendre (1937) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lesson (1830-1831) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lizé (2018) | 1 | 0,1% | 1 | 0,59% | 1 | 0,59% | 1 | 0,59% |
| Lorvelec & Pascal (2009) | 1 | 0,1% | 1 | 0,59% | 1 | 0,59% | 1 | 0,59% |
| Transactions of the Zoological Society of London, 1839: 1-20.">Lowe (1839) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mahé et al. (2013) | 1 | 0,1% | 1 | 0,59% | 1 | 0,59% | 1 | 0,59% |
| Malm (1877) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mourier (2012) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Murray (1884) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Nelson-Smith et al. (2014) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Owen (1853) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pallas (1770) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pearman et al. (2020) | 1 | 0,1% | 1 | 0,59% | 1 | 0,59% | 1 | 0,59% |
| Philippi (1887) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Preynat (2013) | 1 | 0,1% | 1 | 0,59% | 1 | 0,59% | 1 | 0,59% |
| protection du biotope des eaux territoriales de l'île de Clipperton dénommée « aire marine protégée dans les eaux territoriales de l'île de Clipperton » | 1 | 0,1% | 1 | 0,59% | 1 | 0,59% | 1 | 0,59% |
| Quéro & Delmas (1982) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Questel (2017) | 1 | 0,1% | 1 | 0,59% | 1 | 0,59% | 1 | 0,59% |
| Questel (2022) | 1 | 0,1% | 1 | 0,59% | 1 | 0,59% | 1 | 0,59% |
| Questel (2023) | 1 | 0,1% | 1 | 0,59% | 1 | 0,59% | 1 | 0,59% |
| Reis et al. (2003) | 1 | 0,1% | 1 | 0,59% | 1 | 0,59% | 1 | 0,59% |
| Rignault & Chevallier (2017) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sawai et al. (2018) | 1 | 0,1% | 1 | 0,59% | 1 | 0,59% | 1 | 0,59% |
| Sellier et al. (2016) | 1 | 0,1% | 1 | 0,59% | 1 | 0,59% | 1 | 0,59% |
| Séret (2014) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Smith-vaniz & Jelks (2014) | 1 | 0,1% | 1 | 0,59% | 1 | 0,59% | 1 | 0,59% |
| Tregarot et al. (2015) | 1 | 0,1% | 1 | 0,59% | 1 | 0,59% | 1 | 0,59% |
| Walbaum (1792) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Whitley (1929) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
