Poissons marins de Wallis-et-Futuna
219 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
Référence | Total | Valides | Espèces | Taxons terminaux | ||||
---|---|---|---|---|---|---|---|---|
nb | % | nb | % | nb | % | nb | % | |
Fricke et al. (2011) | 684 | 14,66% | 663 | 84,78% | 662 | 84,87% | 662 | 84,76% |
Williams et al. (2006) | 589 | 12,63% | 559 | 71,48% | 559 | 71,67% | 558 | 71,45% |
Siu et al. (2017) | 522 | 11,19% | 504 | 64,45% | 504 | 64,62% | 503 | 64,4% |
Fricke et al. (2009) | 387 | 8,3% | 371 | 47,44% | 371 | 47,56% | 370 | 47,38% |
Wickel & Jamon (2010) | 348 | 7,46% | 333 | 42,58% | 333 | 42,69% | 332 | 42,51% |
Delrieu-Trottin et al. (2015) | 265 | 5,68% | 251 | 32,1% | 250 | 32,05% | 251 | 32,14% |
Kulbicki et al. (2000) | 245 | 5,25% | 214 | 27,37% | 214 | 27,44% | 213 | 27,27% |
Fricke et al. (2013) | 223 | 4,78% | 217 | 27,75% | 216 | 27,69% | 216 | 27,66% |
Chabanet & Durville (2005) | 188 | 4,03% | 170 | 21,74% | 170 | 21,79% | 170 | 21,77% |
Bacchet et al. (2007) | 168 | 3,6% | 155 | 19,82% | 155 | 19,87% | 155 | 19,85% |
Kulbicki (comm. pers., 2011) | 148 | 3,17% | 137 | 17,52% | 137 | 17,56% | 137 | 17,54% |
Richard et al. (1982) | 115 | 2,47% | 42 | 5,37% | 42 | 5,38% | 42 | 5,38% |
Allen (comm. pers., 2009) | 77 | 1,65% | 65 | 8,31% | 65 | 8,33% | 65 | 8,32% |
Béarez & Bouffandeau (2019) | 48 | 1,03% | 48 | 6,14% | 48 | 6,15% | 47 | 6,02% |
Legand (1950) | 40 | 0,86% | 20 | 2,56% | 20 | 2,56% | 20 | 2,56% |
Fourriére et al. (2014) | 36 | 0,77% | 35 | 4,48% | 35 | 4,49% | 35 | 4,48% |
Béarez & Séret (2009) | 30 | 0,64% | 29 | 3,71% | 29 | 3,72% | 29 | 3,71% |
Keith et al. (2013) | 28 | 0,6% | 22 | 2,81% | 22 | 2,82% | 22 | 2,82% |
Randall & Earle (2000) | 24 | 0,51% | 21 | 2,69% | 20 | 2,56% | 21 | 2,69% |
Questel (2020) | 21 | 0,45% | 21 | 2,69% | 21 | 2,69% | 20 | 2,56% |
Questel & Le Quellec (2012) | 20 | 0,43% | 19 | 2,43% | 19 | 2,44% | 18 | 2,3% |
Collette & Nauen (1983) | 19 | 0,41% | 19 | 2,43% | 19 | 2,44% | 19 | 2,43% |
Poey (1858-61) | 17 | 0,36% | 0 | 0% | 0 | 0% | 0 | 0% |
Bouchon-Navaro et al. (2005) | 16 | 0,34% | 11 | 1,41% | 11 | 1,41% | 10 | 1,28% |
Béarez et al. (2017) | 15 | 0,32% | 15 | 1,92% | 15 | 1,92% | 15 | 1,92% |
Séret (1997) | 15 | 0,32% | 15 | 1,92% | 15 | 1,92% | 15 | 1,92% |
Cuvier & Valenciennes (1833) | 14 | 0,3% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Kronen et al. (2008) | 14 | 0,3% | 14 | 1,79% | 14 | 1,79% | 14 | 1,79% |
Kronen et al. (2009) | 14 | 0,3% | 14 | 1,79% | 14 | 1,79% | 14 | 1,79% |
Keith et al. (2006) | 13 | 0,28% | 9 | 1,15% | 9 | 1,15% | 9 | 1,15% |
Eudeline (2022) | 12 | 0,26% | 12 | 1,53% | 12 | 1,54% | 12 | 1,54% |
Justine et al. (2010) | 11 | 0,24% | 11 | 1,41% | 11 | 1,41% | 11 | 1,41% |
Keith et al. (2002) | 11 | 0,24% | 8 | 1,02% | 8 | 1,03% | 8 | 1,02% |
Pearman et al. (2020) | 11 | 0,24% | 11 | 1,41% | 11 | 1,41% | 11 | 1,41% |
Causse et al. (2023) | 8 | 0,17% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Compagno (1984) | 8 | 0,17% | 8 | 1,02% | 8 | 1,03% | 8 | 1,02% |
Keith & Marquet (2011) | 8 | 0,17% | 8 | 1,02% | 8 | 1,03% | 8 | 1,02% |
Randall (1998) | 8 | 0,17% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Linnaeus (1758) | 7 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Rafinesque Schmaltz (1810) | 7 | 0,15% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Wantiez (comm. pers., 2008) | 7 | 0,15% | 6 | 0,77% | 6 | 0,77% | 6 | 0,77% |
Winterbottom & Hoese (2015) | 7 | 0,15% | 7 | 0,9% | 7 | 0,9% | 7 | 0,9% |
Compagno (1984) | 6 | 0,13% | 6 | 0,77% | 6 | 0,77% | 6 | 0,77% |
Goiran & Shine (2020) | 6 | 0,13% | 6 | 0,77% | 6 | 0,77% | 6 | 0,77% |
Keith et al. (2009) | 6 | 0,13% | 4 | 0,51% | 4 | 0,51% | 4 | 0,51% |
Motomura et al. (2011) | 6 | 0,13% | 6 | 0,77% | 6 | 0,77% | 6 | 0,77% |
Müller & Henle (1841) | 6 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Smith (1997) | 6 | 0,13% | 6 | 0,77% | 4 | 0,51% | 6 | 0,77% |
Borsa et al. (2013) | 5 | 0,11% | 3 | 0,38% | 2 | 0,26% | 3 | 0,38% |
Cuvier & Valenciennes ([1832]) | 5 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Soubeyran (2008) | 5 | 0,11% | 5 | 0,64% | 5 | 0,64% | 5 | 0,64% |
Berry & Smith-Vaniz (1978) | 4 | 0,09% | 4 | 0,51% | 4 | 0,51% | 4 | 0,51% |
Bouchon-Navaro & Louis (1986) | 4 | 0,09% | 3 | 0,38% | 3 | 0,38% | 3 | 0,38% |
Brugneaux & Pérès (2006) | 4 | 0,09% | 4 | 0,51% | 4 | 0,51% | 4 | 0,51% |
Charbonnel (1990) | 4 | 0,09% | 4 | 0,51% | 4 | 0,51% | 4 | 0,51% |
Fricke et al. (2024) | 4 | 0,09% | 4 | 0,51% | 4 | 0,51% | 4 | 0,51% |
Hadley & Hansen (1986) | 4 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Transactions of the Zoological Society of London, 1839: 1-20.">Lowe (1839) | 4 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Rousseau (2010) | 4 | 0,09% | 4 | 0,51% | 4 | 0,51% | 4 | 0,51% |
Snodgrass & Heller (1905) | 4 | 0,09% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Vaslet & Agrnsm (2018) | 4 | 0,09% | 4 | 0,51% | 4 | 0,51% | 4 | 0,51% |
Allen et al. (2017) | 3 | 0,06% | 3 | 0,38% | 3 | 0,38% | 3 | 0,38% |
Andrews et al. (2021) | 3 | 0,06% | 3 | 0,38% | 3 | 0,38% | 3 | 0,38% |
Borsa et al. (2014) | 3 | 0,06% | 3 | 0,38% | 3 | 0,38% | 3 | 0,38% |
Cohen et al. (1990) | 3 | 0,06% | 3 | 0,38% | 3 | 0,38% | 3 | 0,38% |
Endo & Chu (2020) | 3 | 0,06% | 3 | 0,38% | 3 | 0,38% | 3 | 0,38% |
Firmat et al. (2012) | 3 | 0,06% | 3 | 0,38% | 3 | 0,38% | 3 | 0,38% |
Goren (1981) | 3 | 0,06% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Greenfield & Randall (2011) | 3 | 0,06% | 3 | 0,38% | 3 | 0,38% | 3 | 0,38% |
Greenfield & Suzuki (2012) | 3 | 0,06% | 3 | 0,38% | 3 | 0,38% | 3 | 0,38% |
Gronow (1854) | 3 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Hutchinson et al. (2019) | 3 | 0,06% | 3 | 0,38% | 3 | 0,38% | 3 | 0,38% |
Klunzinger (1871) | 3 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Letourneur et al. (2004) | 3 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Lorvelec & Pascal (2009) | 3 | 0,06% | 3 | 0,38% | 3 | 0,38% | 3 | 0,38% |
Motomura & Kanade (2015) | 3 | 0,06% | 3 | 0,38% | 3 | 0,38% | 3 | 0,38% |
Mulochau et al. (2019) | 3 | 0,06% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Pinault et al. (2018) | 3 | 0,06% | 3 | 0,38% | 3 | 0,38% | 3 | 0,38% |
Schwarzhans et al. (2005) | 3 | 0,06% | 3 | 0,38% | 3 | 0,38% | 3 | 0,38% |
Simian et al. (2022) | 3 | 0,06% | 3 | 0,38% | 3 | 0,38% | 3 | 0,38% |
Wickel et al. (2014) | 3 | 0,06% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Allen et al. (2010) | 2 | 0,04% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Bennett (1834) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Cuvier & Valenciennes (1830) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Cuvier & Valenciennes (1830-1832) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Diaz & Cuzange (2009) | 2 | 0,04% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Downie et al. (2011) | 2 | 0,04% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Evermann & Clark (1928) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Fourmanoir & Rivaton (1979) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Fourmanoir (1988) | 2 | 0,04% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Fourt et al. (2017) | 2 | 0,04% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Fricke (1998) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Geange (2010) | 2 | 0,04% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Gill (2022) | 2 | 0,04% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Goode & Bean (1896) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Goulletquer (2016) | 2 | 0,04% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Guichenot (1848) | 2 | 0,04% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Günther (1880) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Ifremer (2024) | 2 | 0,04% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Johnson (1863) | 2 | 0,04% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Jordan & Starks (1904) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Karnella & Lachner (1981) | 2 | 0,04% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Keith & Marquet (2005) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Keith & Marquet (2006) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Keith et al. (2014) | 2 | 0,04% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Kiszka et al. (2009) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Lacepède (1801) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Macdonald & Barron (1868) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Marshall et al. (2009) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Matsumoto & Motomura (2024) | 2 | 0,04% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Matsunuma et al. (2017) | 2 | 0,04% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Mennesson et al. (2019) | 2 | 0,04% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Motomura & Causse (2011) | 2 | 0,04% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Myers (1991) | 2 | 0,04% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Pinault et al. (2013) | 2 | 0,04% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Rafinesque (1810) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Randall & Pyle (1989) | 2 | 0,04% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Randall & Steene (1983) | 2 | 0,04% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Richer de Forges et al. (2005) | 2 | 0,04% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Rignault & Chevallier (2017) | 2 | 0,04% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Risso (1810) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Rüppell (1835) | 2 | 0,04% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Schwarzhans & Prokofiev (2017) | 2 | 0,04% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Séret (2014) | 2 | 0,04% | 1 | 0,13% | 0 | 0% | 1 | 0,13% |
Swainson (1839) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Teichert et al. (2013) | 2 | 0,04% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Whitley (1931) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Whitley (1933) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Agassiz (1833-1843) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Allen (1995) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Atwood (1869) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Bertin (1928) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Bleeker (1847) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Bleeker (1852) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Bleeker (1854) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Bleeker (1856) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Bloch (1792) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Bodilis et al. (2011) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Bonnaterre (1788) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Bouchon-Navaro et al. (1992) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 0 | 0% |
Bourjon & Fricke (2019) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Bourjon & Fricke (2020) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Bray & Cribb (2002) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Brosse et al. (2021) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Causse & Hautecoeur (2006) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Clua & Planes (2019) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Clua et al. (2016) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Collet et al. (2017) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Cuvier & Valenciennes (1829) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Cuvier & Valenciennes (1829) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Cuvier (1829) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Faber (1829) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Foata et al. (2012) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Forsskål (1775) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Fourmanoir (1966) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Fritzsche (1980) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Gargominy et al. (1996) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Gill (1862) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Gill (2004) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Girondot et al. (2015) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Gmelin (1789) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Guichenot (1847) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Günther (1860) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Günther (1864) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Hibino et al. (2016) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Hoshino & Motomura (2022) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Ifremer (2009) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Inoue & Nakabo (2006) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
IUCN (2013) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Jordan et al. (1927) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Kawai (2016) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Keith et al. (2011) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Keith (2002) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Klausewitz & von Hentig (1975) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Lacepède (1800) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Last et al. (2016) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Legendre (1937) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Lesson (1830-1831) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Lesueur (1822) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Letourneur & Maggiorani (1995) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Louis et al. (1992) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 0 | 0% |
Lowe et al. (2007) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Lowe (1838) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Lowe (1843) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Maeda et al. (2011) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Marquet et al. (2003) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Matsunuma & Motomura (2018) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Monti et al. (2010) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Moravec & Justine (2014) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Mourier (2012) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Murray (1884) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Nelson-Smith et al. (2014) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Noël, Meunier (2010) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Okamoto & Motomura (2017) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Owen (1853) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Pallas (1770) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Parmentier (1999) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Philippi (1887) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
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 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Annales de la Société de Sciences naturelles de la Charente-Maritime, 10(2): 225-236.">Quéro et al. (2011) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Quero et al. (2013) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Ranzani (1839) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Rigby & Adamson (1997) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Schultz et al. (1953) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Sherborn (1925) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Smales et al. (2007) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Taquet (1994) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Tea & Larson (2023) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Tsadok et al. (2015) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Van & Kampen (1907) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Walbaum (1792) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Wantiez (2000) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Whitley (1929) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Whitley (1948) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Wickel & Fricke (2022) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Wickel et al. (2016) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Williams (2018) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Winterbottom & Burridge (1993) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Yang et al. (2019) | 1 | 0,02% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |