Poissons de Saint-Martin
127 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 | 17,15% | 148 | 86,55% | 148 | 86,55% | 148 | 86,55% |
Questel (2020) | 146 | 14,23% | 145 | 84,8% | 145 | 84,8% | 145 | 84,8% |
Questel & Le Quellec (2012) | 138 | 13,45% | 132 | 77,19% | 132 | 77,19% | 132 | 77,19% |
Diaz & Cuzange (2009) | 104 | 10,14% | 96 | 56,14% | 96 | 56,14% | 96 | 56,14% |
Bouchon-Navaro & Louis (1986) | 96 | 9,36% | 81 | 47,37% | 81 | 47,37% | 81 | 47,37% |
Brugneaux & Pérès (2006) | 67 | 6,53% | 61 | 35,67% | 61 | 35,67% | 61 | 35,67% |
Rousseau (2010) | 30 | 2,92% | 28 | 16,37% | 28 | 16,37% | 28 | 16,37% |
Louis et al. (1992) | 18 | 1,75% | 11 | 6,43% | 11 | 6,43% | 11 | 6,43% |
Fricke et al. (2009) | 17 | 1,66% | 16 | 9,36% | 16 | 9,36% | 16 | 9,36% |
Fricke et al. (2011) | 16 | 1,56% | 16 | 9,36% | 16 | 9,36% | 16 | 9,36% |
Siu et al. (2017) | 15 | 1,46% | 14 | 8,19% | 14 | 8,19% | 14 | 8,19% |
Wickel & Jamon (2010) | 14 | 1,36% | 13 | 7,6% | 13 | 7,6% | 13 | 7,6% |
Smith (1997) | 13 | 1,27% | 13 | 7,6% | 13 | 7,6% | 13 | 7,6% |
Compagno (1984) | 12 | 1,17% | 12 | 7,02% | 12 | 7,02% | 12 | 7,02% |
Bouchon-Navaro et al. (1992) | 11 | 1,07% | 9 | 5,26% | 9 | 5,26% | 9 | 5,26% |
Béarez et al. (2017) | 9 | 0,88% | 9 | 5,26% | 9 | 5,26% | 9 | 5,26% |
Collette & Nauen (1983) | 8 | 0,78% | 8 | 4,68% | 8 | 4,68% | 8 | 4,68% |
Poey (1858-61) | 8 | 0,78% | 0 | 0% | 0 | 0% | 0 | 0% |
Delrieu-Trottin et al. (2015) | 7 | 0,68% | 7 | 4,09% | 7 | 4,09% | 7 | 4,09% |
Fourriére et al. (2014) | 7 | 0,68% | 7 | 4,09% | 7 | 4,09% | 7 | 4,09% |
Pezold et al. (2015) | 7 | 0,68% | 7 | 4,09% | 7 | 4,09% | 7 | 4,09% |
Vaslet & Agrnsm (2018) | 7 | 0,68% | 7 | 4,09% | 7 | 4,09% | 7 | 4,09% |
Bacchet et al. (2007) | 6 | 0,58% | 5 | 2,92% | 5 | 2,92% | 5 | 2,92% |
Heemstra & Randall (1993) | 6 | 0,58% | 6 | 3,51% | 6 | 3,51% | 6 | 3,51% |
Kulbicki et al. (2000) | 6 | 0,58% | 5 | 2,92% | 5 | 2,92% | 5 | 2,92% |
Richard et al. (1982) | 6 | 0,58% | 3 | 1,75% | 3 | 1,75% | 3 | 1,75% |
Béarez & Bouffandeau (2019) | 5 | 0,49% | 5 | 2,92% | 5 | 2,92% | 5 | 2,92% |
Chabanet & Durville (2005) | 5 | 0,49% | 4 | 2,34% | 4 | 2,34% | 4 | 2,34% |
Fricke et al. (2013) | 5 | 0,49% | 5 | 2,92% | 5 | 2,92% | 5 | 2,92% |
Le Bail et al. (2012) | 5 | 0,49% | 5 | 2,92% | 5 | 2,92% | 5 | 2,92% |
Nakamura (1985) | 5 | 0,49% | 5 | 2,92% | 5 | 2,92% | 5 | 2,92% |
Questel (2017) | 5 | 0,49% | 5 | 2,92% | 5 | 2,92% | 5 | 2,92% |
Swainson (1839) | 5 | 0,49% | 0 | 0% | 0 | 0% | 0 | 0% |
Uicn et al. (2019) | 5 | 0,49% | 5 | 2,92% | 5 | 2,92% | 5 | 2,92% |
Allen (1985) | 4 | 0,39% | 4 | 2,34% | 4 | 2,34% | 4 | 2,34% |
Béarez & Séret (2009) | 4 | 0,39% | 3 | 1,75% | 3 | 1,75% | 3 | 1,75% |
Berry & Smith-Vaniz (1978) | 4 | 0,39% | 4 | 2,34% | 4 | 2,34% | 4 | 2,34% |
Bloch & Schneider (1801) | 4 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
Lim et al. (2002) | 4 | 0,39% | 2 | 1,17% | 2 | 1,17% | 2 | 1,17% |
Linnaeus (1758) | 4 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
Monti et al. (2010) | 4 | 0,39% | 2 | 1,17% | 2 | 1,17% | 2 | 1,17% |
Morris (2012) | 4 | 0,39% | 4 | 2,34% | 4 | 2,34% | 4 | 2,34% |
Müller & Henle (1841) | 4 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
Rafinesque Schmaltz (1810) | 4 | 0,39% | 2 | 1,17% | 2 | 1,17% | 2 | 1,17% |
Williams et al. (2006) | 4 | 0,39% | 3 | 1,75% | 3 | 1,75% | 3 | 1,75% |
Maréchal et al. (2006) | 3 | 0,29% | 3 | 1,75% | 3 | 1,75% | 3 | 1,75% |
Randall & Vergara (1978) | 3 | 0,29% | 3 | 1,75% | 3 | 1,75% | 3 | 1,75% |
Simian et al. (2022) | 3 | 0,29% | 3 | 1,75% | 3 | 1,75% | 3 | 1,75% |
UICN Comité français, OFB & MNHN (2021) | 3 | 0,29% | 3 | 1,75% | 3 | 1,75% | 3 | 1,75% |
Yokoyama (2013) | 3 | 0,29% | 2 | 1,17% | 2 | 1,17% | 2 | 1,17% |
Brugneaux & Pérès (2005) | 2 | 0,19% | 1 | 0,58% | 1 | 0,58% | 1 | 0,58% |
Compagno (1984) | 2 | 0,19% | 2 | 1,17% | 2 | 1,17% | 2 | 1,17% |
Durand (2016) | 2 | 0,19% | 1 | 0,58% | 1 | 0,58% | 1 | 0,58% |
Fontan (2019) | 2 | 0,19% | 2 | 1,17% | 2 | 1,17% | 2 | 1,17% |
Fourt et al. (2017) | 2 | 0,19% | 2 | 1,17% | 2 | 1,17% | 2 | 1,17% |
Gronow (1854) | 2 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Holbrook (1855) | 2 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Keith et al. (2006) | 2 | 0,19% | 2 | 1,17% | 2 | 1,17% | 2 | 1,17% |
Keith et al. (2013) | 2 | 0,19% | 2 | 1,17% | 2 | 1,17% | 2 | 1,17% |
Kulbicki (comm. pers., 2011) | 2 | 0,19% | 2 | 1,17% | 2 | 1,17% | 2 | 1,17% |
Lacepède (1800) | 2 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Lacepède (1802) | 2 | 0,19% | 1 | 0,58% | 1 | 0,58% | 1 | 0,58% |
Maréchal & Trégarot (2012) | 2 | 0,19% | 1 | 0,58% | 1 | 0,58% | 1 | 0,58% |
Marquet et al. (2003) | 2 | 0,19% | 2 | 1,17% | 2 | 1,17% | 2 | 1,17% |
Marshall et al. (2009) | 2 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Nardo (1827) | 2 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Rafinesque (1810) | 2 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Risso (1827) | 2 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Snodgrass & Heller (1905) | 2 | 0,19% | 1 | 0,58% | 1 | 0,58% | 1 | 0,58% |
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% |
Alley et al. (2023) | 1 | 0,1% | 1 | 0,58% | 1 | 0,58% | 1 | 0,58% |
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 | 0,58% | 1 | 0,58% | 1 | 0,58% |
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% |
Brosse et al. (2021) | 1 | 0,1% | 1 | 0,58% | 1 | 0,58% | 1 | 0,58% |
Capape et al. (2002) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Chabanaud (1927) | 1 | 0,1% | 1 | 0,58% | 1 | 0,58% | 1 | 0,58% |
Collette (2003) | 1 | 0,1% | 1 | 0,58% | 1 | 0,58% | 1 | 0,58% |
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 | 0,58% | 1 | 0,58% | 1 | 0,58% |
Denys et al. (2022) | 1 | 0,1% | 1 | 0,58% | 1 | 0,58% | 1 | 0,58% |
Etcheberry & Abraham (2009) | 1 | 0,1% | 1 | 0,58% | 1 | 0,58% | 1 | 0,58% |
Francour & Mouine (2008) | 1 | 0,1% | 1 | 0,58% | 1 | 0,58% | 1 | 0,58% |
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 | 0,58% | 1 | 0,58% | 1 | 0,58% |
Hein et al. (2010) | 1 | 0,1% | 1 | 0,58% | 1 | 0,58% | 1 | 0,58% |
Iglésias et al. (2021) | 1 | 0,1% | 1 | 0,58% | 1 | 0,58% | 1 | 0,58% |
IUCN (2014) | 1 | 0,1% | 1 | 0,58% | 1 | 0,58% | 1 | 0,58% |
Keith & Marquet (2011) | 1 | 0,1% | 1 | 0,58% | 1 | 0,58% | 1 | 0,58% |
Keith et al. (2002) | 1 | 0,1% | 1 | 0,58% | 1 | 0,58% | 1 | 0,58% |
Keith et al. (1999) | 1 | 0,1% | 1 | 0,58% | 1 | 0,58% | 1 | 0,58% |
Keith (2002) | 1 | 0,1% | 1 | 0,58% | 1 | 0,58% | 1 | 0,58% |
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 | 0,58% | 1 | 0,58% | 1 | 0,58% |
Lorvelec & Pascal (2009) | 1 | 0,1% | 1 | 0,58% | 1 | 0,58% | 1 | 0,58% |
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 | 0,58% | 1 | 0,58% | 1 | 0,58% |
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% |
Philippi (1887) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Preynat (2013) | 1 | 0,1% | 1 | 0,58% | 1 | 0,58% | 1 | 0,58% |
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 | 0,58% | 1 | 0,58% | 1 | 0,58% |
Quéro & Delmas (1982) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Questel (2017) | 1 | 0,1% | 1 | 0,58% | 1 | 0,58% | 1 | 0,58% |
Questel (2022) | 1 | 0,1% | 1 | 0,58% | 1 | 0,58% | 1 | 0,58% |
Reis et al. (2003) | 1 | 0,1% | 1 | 0,58% | 1 | 0,58% | 1 | 0,58% |
Rignault & Chevallier (2017) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Sawai et al. (2018) | 1 | 0,1% | 1 | 0,58% | 1 | 0,58% | 1 | 0,58% |
Sellier et al. (2016) | 1 | 0,1% | 1 | 0,58% | 1 | 0,58% | 1 | 0,58% |
Séret (1997) | 1 | 0,1% | 1 | 0,58% | 1 | 0,58% | 1 | 0,58% |
Séret (2014) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Smith-vaniz & Jelks (2014) | 1 | 0,1% | 1 | 0,58% | 1 | 0,58% | 1 | 0,58% |
Tregarot et al. (2015) | 1 | 0,1% | 1 | 0,58% | 1 | 0,58% | 1 | 0,58% |
Walbaum (1792) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Whitley (1929) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |