Vertébrés de Wallis-et-Futuna
673 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) | 686 | 12,86% | 665 | 74,3% | 664 | 75,28% | 664 | 75,2% |
Williams et al. (2006) | 589 | 11,04% | 559 | 62,46% | 559 | 63,38% | 558 | 63,19% |
Siu et al. (2017) | 523 | 9,8% | 505 | 56,42% | 505 | 57,26% | 504 | 57,08% |
Fricke et al. (2009) | 389 | 7,29% | 373 | 41,68% | 373 | 42,29% | 371 | 42,02% |
Wickel & Jamon (2010) | 348 | 6,52% | 333 | 37,21% | 333 | 37,76% | 332 | 37,6% |
Delrieu-Trottin et al. (2015) | 265 | 4,97% | 251 | 28,04% | 250 | 28,34% | 251 | 28,43% |
Kulbicki et al. (2000) | 245 | 4,59% | 214 | 23,91% | 214 | 24,26% | 213 | 24,12% |
Fricke et al. (2013) | 223 | 4,18% | 217 | 24,25% | 216 | 24,49% | 216 | 24,46% |
Chabanet & Durville (2005) | 188 | 3,52% | 170 | 18,99% | 170 | 19,27% | 170 | 19,25% |
Bacchet et al. (2007) | 168 | 3,15% | 155 | 17,32% | 155 | 17,57% | 155 | 17,55% |
Kulbicki (comm. pers., 2011) | 148 | 2,77% | 137 | 15,31% | 137 | 15,53% | 137 | 15,52% |
Richard et al. (1982) | 115 | 2,16% | 42 | 4,69% | 42 | 4,76% | 42 | 4,76% |
Allen (comm. pers., 2009) | 77 | 1,44% | 65 | 7,26% | 65 | 7,37% | 65 | 7,36% |
Rinaldi (2016) | 64 | 1,2% | 64 | 7,15% | 64 | 7,26% | 48 | 5,44% |
Uicn et al. (2015) | 50 | 0,94% | 50 | 5,59% | 50 | 5,67% | 42 | 4,76% |
Béarez & Bouffandeau (2019) | 48 | 0,9% | 48 | 5,36% | 48 | 5,44% | 47 | 5,32% |
Carzon et al. (2016) | 48 | 0,9% | 48 | 5,36% | 48 | 5,44% | 36 | 4,08% |
Estrade et al. (2016) | 48 | 0,9% | 48 | 5,36% | 48 | 5,44% | 36 | 4,08% |
Questel & Le Quellec (2012) | 43 | 0,81% | 40 | 4,47% | 40 | 4,54% | 35 | 3,96% |
Questel (2020) | 43 | 0,81% | 40 | 4,47% | 40 | 4,54% | 35 | 3,96% |
Thibault et al. (2014) | 42 | 0,79% | 37 | 4,13% | 33 | 3,74% | 33 | 3,74% |
Legand (1950) | 40 | 0,75% | 20 | 2,23% | 20 | 2,27% | 20 | 2,27% |
Fourriére et al. (2014) | 36 | 0,67% | 35 | 3,91% | 35 | 3,97% | 35 | 3,96% |
Gill (1995) | 34 | 0,64% | 29 | 3,24% | 29 | 3,29% | 24 | 2,72% |
Keith et al. (2013) | 34 | 0,64% | 28 | 3,13% | 28 | 3,17% | 28 | 3,17% |
Béarez & Séret (2009) | 30 | 0,56% | 29 | 3,24% | 29 | 3,29% | 29 | 3,28% |
Linnaeus (1758) | 27 | 0,51% | 6 | 0,67% | 6 | 0,68% | 6 | 0,68% |
Randall & Earle (2000) | 24 | 0,45% | 21 | 2,35% | 20 | 2,27% | 21 | 2,38% |
Uicn et al. (2017) | 24 | 0,45% | 24 | 2,68% | 24 | 2,72% | 20 | 2,27% |
Collette & Nauen (1983) | 19 | 0,36% | 19 | 2,12% | 19 | 2,15% | 19 | 2,15% |
G.E.M.M. (2012) | 17 | 0,32% | 17 | 1,9% | 17 | 1,93% | 13 | 1,47% |
Poey (1858-61) | 17 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
Yokoyama (2013) | 17 | 0,32% | 16 | 1,79% | 16 | 1,81% | 15 | 1,7% |
Aulagnier (2009) | 16 | 0,3% | 16 | 1,79% | 16 | 1,81% | 14 | 1,59% |
Bouchon-Navaro et al. (2005) | 16 | 0,3% | 11 | 1,23% | 11 | 1,25% | 10 | 1,13% |
Charrassin (2016) | 16 | 0,3% | 16 | 1,79% | 16 | 1,81% | 12 | 1,36% |
Charrassin (2016) | 16 | 0,3% | 16 | 1,79% | 16 | 1,81% | 12 | 1,36% |
Jarrett & Shirihai (2014) | 16 | 0,3% | 16 | 1,79% | 16 | 1,81% | 12 | 1,36% |
Moutou (2016) | 16 | 0,3% | 16 | 1,79% | 16 | 1,81% | 12 | 1,36% |
Séret (1997) | 16 | 0,3% | 16 | 1,79% | 16 | 1,81% | 16 | 1,81% |
Spitz et al. (2016) | 16 | 0,3% | 16 | 1,79% | 16 | 1,81% | 12 | 1,36% |
Thoisy & Bordin (2016) | 16 | 0,3% | 16 | 1,79% | 16 | 1,81% | 12 | 1,36% |
Urtizberea (2016) | 16 | 0,3% | 16 | 1,79% | 16 | 1,81% | 12 | 1,36% |
Béarez et al. (2017) | 15 | 0,28% | 15 | 1,68% | 15 | 1,7% | 15 | 1,7% |
Bordin et al. (2021) | 15 | 0,28% | 15 | 1,68% | 15 | 1,7% | 11 | 1,25% |
Gannier (2001) | 15 | 0,28% | 15 | 1,68% | 15 | 1,7% | 11 | 1,25% |
Garrigue (2007) | 15 | 0,28% | 15 | 1,68% | 15 | 1,7% | 11 | 1,25% |
Keith et al. (2006) | 15 | 0,28% | 11 | 1,23% | 11 | 1,25% | 11 | 1,25% |
Catzeflis (2012) | 14 | 0,26% | 14 | 1,56% | 14 | 1,59% | 10 | 1,13% |
Cuvier & Valenciennes (1833) | 14 | 0,26% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Dewynter et al. (2021) | 14 | 0,26% | 14 | 1,56% | 14 | 1,59% | 11 | 1,25% |
Gannier (2009) | 14 | 0,26% | 14 | 1,56% | 14 | 1,59% | 10 | 1,13% |
Gargominy et al. (1996) | 14 | 0,26% | 13 | 1,45% | 13 | 1,47% | 13 | 1,47% |
Kronen et al. (2008) | 14 | 0,26% | 14 | 1,56% | 14 | 1,59% | 14 | 1,59% |
Kronen et al. (2009) | 14 | 0,26% | 14 | 1,56% | 14 | 1,59% | 14 | 1,59% |
Lorvelec et al. (2007) | 14 | 0,26% | 14 | 1,56% | 14 | 1,59% | 14 | 1,59% |
Gannier (2000) | 13 | 0,24% | 13 | 1,45% | 13 | 1,47% | 9 | 1,02% |
Gannier (2002) | 13 | 0,24% | 13 | 1,45% | 13 | 1,47% | 9 | 1,02% |
Gill (1995) | 13 | 0,24% | 11 | 1,23% | 11 | 1,25% | 11 | 1,25% |
Kiszka et al.(2007) | 13 | 0,24% | 12 | 1,34% | 12 | 1,36% | 8 | 0,91% |
Rocamora (2004) | 13 | 0,24% | 12 | 1,34% | 12 | 1,36% | 11 | 1,25% |
Theuerkauf et al. (2010) | 13 | 0,24% | 13 | 1,45% | 13 | 1,47% | 13 | 1,47% |
Eudeline (2022) | 12 | 0,22% | 12 | 1,34% | 12 | 1,36% | 12 | 1,36% |
Keith et al. (2002) | 12 | 0,22% | 9 | 1,01% | 9 | 1,02% | 9 | 1,02% |
Barau et al. (2005) | 11 | 0,21% | 10 | 1,12% | 10 | 1,13% | 9 | 1,02% |
Gmelin (1789) | 11 | 0,21% | 3 | 0,34% | 3 | 0,34% | 3 | 0,34% |
Justine et al. (2010) | 11 | 0,21% | 11 | 1,23% | 11 | 1,25% | 11 | 1,25% |
Keith & Marquet (2011) | 11 | 0,21% | 11 | 1,23% | 11 | 1,25% | 11 | 1,25% |
Kiszka et al. (2010) | 11 | 0,21% | 11 | 1,23% | 11 | 1,25% | 8 | 0,91% |
Laran et al. (2011) | 11 | 0,21% | 11 | 1,23% | 11 | 1,25% | 8 | 0,91% |
Pearman et al. (2020) | 11 | 0,21% | 11 | 1,23% | 11 | 1,25% | 11 | 1,25% |
UICN Comité français, OFB & MNHN (2021) | 10 | 0,19% | 10 | 1,12% | 10 | 1,13% | 9 | 1,02% |
Remsen et al. (2013) | 9 | 0,17% | 9 | 1,01% | 9 | 1,02% | 9 | 1,02% |
Weimerskirch et al. (2009) | 9 | 0,17% | 9 | 1,01% | 9 | 1,02% | 9 | 1,02% |
Barré (2021) | 8 | 0,15% | 8 | 0,89% | 8 | 0,91% | 8 | 0,91% |
Causse et al. (2023) | 8 | 0,15% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Compagno (1984) | 8 | 0,15% | 8 | 0,89% | 8 | 0,91% | 8 | 0,91% |
Dulau-Drouot et al. (2008) | 8 | 0,15% | 8 | 0,89% | 8 | 0,91% | 4 | 0,45% |
Levesque & Delcroix (2018) | 8 | 0,15% | 8 | 0,89% | 8 | 0,91% | 8 | 0,91% |
Randall (1998) | 8 | 0,15% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Aulagnier et al. (2017) | 7 | 0,13% | 7 | 0,78% | 7 | 0,79% | 7 | 0,79% |
Bauer & Sadlier (2000) | 7 | 0,13% | 5 | 0,56% | 5 | 0,57% | 5 | 0,57% |
Proceedings of the Zoological Society of London, 1907: 1035-1037.">Hopkinson (1907) | 7 | 0,13% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Ineich (2016) | 7 | 0,13% | 6 | 0,67% | 6 | 0,68% | 6 | 0,68% |
Keith et al. (2009) | 7 | 0,13% | 5 | 0,56% | 5 | 0,57% | 5 | 0,57% |
Rafinesque Schmaltz (1810) | 7 | 0,13% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Samaran & Guinet (2009) | 7 | 0,13% | 7 | 0,78% | 7 | 0,79% | 6 | 0,68% |
Soubeyran et al. (2011) | 7 | 0,13% | 7 | 0,78% | 7 | 0,79% | 7 | 0,79% |
Wantiez (comm. pers., 2008) | 7 | 0,13% | 6 | 0,67% | 6 | 0,68% | 6 | 0,68% |
Winterbottom & Hoese (2015) | 7 | 0,13% | 7 | 0,78% | 7 | 0,79% | 7 | 0,79% |
Compagno (1984) | 6 | 0,11% | 6 | 0,67% | 6 | 0,68% | 6 | 0,68% |
Goiran & Shine (2020) | 6 | 0,11% | 6 | 0,67% | 6 | 0,68% | 6 | 0,68% |
Jourdan (2020) | 6 | 0,11% | 6 | 0,67% | 6 | 0,68% | 6 | 0,68% |
Lowe et al. (2007) | 6 | 0,11% | 6 | 0,67% | 6 | 0,68% | 6 | 0,68% |
Motomura et al. (2011) | 6 | 0,11% | 6 | 0,67% | 6 | 0,68% | 6 | 0,68% |
Müller & Henle (1841) | 6 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Perrin et al. (2002) | 6 | 0,11% | 6 | 0,67% | 6 | 0,68% | 5 | 0,57% |
Prévost & Mougin (1970) | 6 | 0,11% | 6 | 0,67% | 6 | 0,68% | 5 | 0,57% |
Roux (1913) | 6 | 0,11% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Shirihai (2003) | 6 | 0,11% | 6 | 0,67% | 6 | 0,68% | 5 | 0,57% |
Smith (1997) | 6 | 0,11% | 6 | 0,67% | 4 | 0,45% | 6 | 0,68% |
Soubeyran (2008) | 6 | 0,11% | 6 | 0,67% | 6 | 0,68% | 6 | 0,68% |
Zdunek (2022) | 6 | 0,11% | 5 | 0,56% | 5 | 0,57% | 5 | 0,57% |
Blanc et al. (1993) | 5 | 0,09% | 4 | 0,45% | 4 | 0,45% | 4 | 0,45% |
Boer et al. (1999) | 5 | 0,09% | 5 | 0,56% | 5 | 0,57% | 5 | 0,57% |
Borsa et al. (2013) | 5 | 0,09% | 3 | 0,34% | 2 | 0,23% | 3 | 0,34% |
Cuvier & Valenciennes ([1832]) | 5 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Dewynter et al. (2023) | 5 | 0,09% | 5 | 0,56% | 5 | 0,57% | 5 | 0,57% |
Mertens & Wermuth (1960) | 5 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Angel (1935) | 4 | 0,07% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Belfan & Conde (2016) | 4 | 0,07% | 4 | 0,45% | 4 | 0,45% | 4 | 0,45% |
Berry & Smith-Vaniz (1978) | 4 | 0,07% | 4 | 0,45% | 4 | 0,45% | 4 | 0,45% |
Bochaton et al. (2021) | 4 | 0,07% | 4 | 0,45% | 4 | 0,45% | 4 | 0,45% |
Bouchon-Navaro & Louis (1986) | 4 | 0,07% | 3 | 0,34% | 3 | 0,34% | 3 | 0,34% |
Brugneaux & Pérès (2006) | 4 | 0,07% | 4 | 0,45% | 4 | 0,45% | 4 | 0,45% |
Charbonnel (1990) | 4 | 0,07% | 4 | 0,45% | 4 | 0,45% | 4 | 0,45% |
Clements (2012) | 4 | 0,07% | 4 | 0,45% | 4 | 0,45% | 4 | 0,45% |
Desbrosses & Etcheberry (1987) | 4 | 0,07% | 3 | 0,34% | 3 | 0,34% | 2 | 0,23% |
Dewynter et al. (2022) | 4 | 0,07% | 4 | 0,45% | 4 | 0,45% | 4 | 0,45% |
Diaz & Cuzange (2009) | 4 | 0,07% | 4 | 0,45% | 4 | 0,45% | 2 | 0,23% |
Fourt et al. (2017) | 4 | 0,07% | 4 | 0,45% | 4 | 0,45% | 4 | 0,45% |
Frenot et al. (2005) | 4 | 0,07% | 4 | 0,45% | 4 | 0,45% | 4 | 0,45% |
Fricke et al. (2024) | 4 | 0,07% | 4 | 0,45% | 4 | 0,45% | 4 | 0,45% |
Gentry et al. (2004) | 4 | 0,07% | 3 | 0,34% | 3 | 0,34% | 3 | 0,34% |
Hadley & Hansen (1986) | 4 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Henderson & Breuil (2012) | 4 | 0,07% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Hoser (2016) | 4 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Humeau et al. (2020) | 4 | 0,07% | 4 | 0,45% | 2 | 0,23% | 2 | 0,23% |
Ineich et al. (2007) | 4 | 0,07% | 4 | 0,45% | 4 | 0,45% | 4 | 0,45% |
IUCN (2012) | 4 | 0,07% | 4 | 0,45% | 4 | 0,45% | 2 | 0,23% |
Lorvelec & Pascal (2009) | 4 | 0,07% | 4 | 0,45% | 4 | 0,45% | 4 | 0,45% |
Transactions of the Zoological Society of London, 1839: 1-20.">Lowe (1839) | 4 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Revilliod (1914) | 4 | 0,07% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Robineau & Duhamel (2006) | 4 | 0,07% | 4 | 0,45% | 4 | 0,45% | 3 | 0,34% |
Rousseau (2010) | 4 | 0,07% | 4 | 0,45% | 4 | 0,45% | 4 | 0,45% |
Routtier et al. (2023) | 4 | 0,07% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Snodgrass & Heller (1905) | 4 | 0,07% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Uicn et al. (2020) | 4 | 0,07% | 4 | 0,45% | 4 | 0,45% | 3 | 0,34% |
Vaslet & Agrnsm (2018) | 4 | 0,07% | 4 | 0,45% | 4 | 0,45% | 4 | 0,45% |
AAMP (2012) | 3 | 0,06% | 3 | 0,34% | 3 | 0,34% | 0 | 0% |
Allen et al. (2017) | 3 | 0,06% | 3 | 0,34% | 3 | 0,34% | 3 | 0,34% |
Andrews et al. (2021) | 3 | 0,06% | 3 | 0,34% | 3 | 0,34% | 3 | 0,34% |
Balouet & Olson (1989) | 3 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Bauer & Sadlier (1994) | 3 | 0,06% | 3 | 0,34% | 3 | 0,34% | 3 | 0,34% |
Borsa et al. (2014) | 3 | 0,06% | 3 | 0,34% | 3 | 0,34% | 3 | 0,34% |
Burneleau (1983) | 3 | 0,06% | 3 | 0,34% | 3 | 0,34% | 3 | 0,34% |
Butaud (2021) | 3 | 0,06% | 3 | 0,34% | 3 | 0,34% | 3 | 0,34% |
Catzeflis (2018) | 3 | 0,06% | 3 | 0,34% | 3 | 0,34% | 3 | 0,34% |
Cohen et al. (1990) | 3 | 0,06% | 3 | 0,34% | 3 | 0,34% | 3 | 0,34% |
Deblock et al. (1960) | 3 | 0,06% | 3 | 0,34% | 3 | 0,34% | 3 | 0,34% |
Dewynter et al. (2023) | 3 | 0,06% | 3 | 0,34% | 3 | 0,34% | 3 | 0,34% |
Durant et al. (2013) | 3 | 0,06% | 3 | 0,34% | 3 | 0,34% | 3 | 0,34% |
Endo & Chu (2020) | 3 | 0,06% | 3 | 0,34% | 3 | 0,34% | 3 | 0,34% |
Etcheberry & Abraham (2009) | 3 | 0,06% | 3 | 0,34% | 3 | 0,34% | 3 | 0,34% |
Firmat et al. (2012) | 3 | 0,06% | 3 | 0,34% | 3 | 0,34% | 3 | 0,34% |
Fort & Barrière (2021) | 3 | 0,06% | 3 | 0,34% | 3 | 0,34% | 3 | 0,34% |
Geneva et al. (2013) | 3 | 0,06% | 3 | 0,34% | 3 | 0,34% | 3 | 0,34% |
González-sánchez et al. (2021) | 3 | 0,06% | 3 | 0,34% | 3 | 0,34% | 3 | 0,34% |
Goren (1981) | 3 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Greenfield & Randall (2011) | 3 | 0,06% | 3 | 0,34% | 3 | 0,34% | 3 | 0,34% |
Greenfield & Suzuki (2012) | 3 | 0,06% | 3 | 0,34% | 3 | 0,34% | 3 | 0,34% |
Gronow (1854) | 3 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Havery et al. (2018) | 3 | 0,06% | 3 | 0,34% | 3 | 0,34% | 3 | 0,34% |
Hutchinson et al. (2019) | 3 | 0,06% | 3 | 0,34% | 3 | 0,34% | 3 | 0,34% |
Jourdan et al. (2014) | 3 | 0,06% | 3 | 0,34% | 3 | 0,34% | 3 | 0,34% |
Klunzinger (1871) | 3 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Lambert (1988) | 3 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Laran et al. (2012) | 3 | 0,06% | 3 | 0,34% | 3 | 0,34% | 2 | 0,23% |
Letourneur et al. (2004) | 3 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Marquet et al. (2003) | 3 | 0,06% | 3 | 0,34% | 3 | 0,34% | 3 | 0,34% |
Massary et al. (2020) | 3 | 0,06% | 3 | 0,34% | 3 | 0,34% | 3 | 0,34% |
Massary et al. (2021) | 3 | 0,06% | 3 | 0,34% | 3 | 0,34% | 3 | 0,34% |
Motomura & Kanade (2015) | 3 | 0,06% | 3 | 0,34% | 3 | 0,34% | 3 | 0,34% |
Mulochau et al. (2019) | 3 | 0,06% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Ohler et al. (2021) | 3 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Pinault et al. (2018) | 3 | 0,06% | 3 | 0,34% | 3 | 0,34% | 3 | 0,34% |
Probst et al. (2022) | 3 | 0,06% | 3 | 0,34% | 3 | 0,34% | 3 | 0,34% |
Probst (2001) | 3 | 0,06% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Questel et al. (2023) | 3 | 0,06% | 3 | 0,34% | 3 | 0,34% | 3 | 0,34% |
Questel et al. (2023) | 3 | 0,06% | 3 | 0,34% | 3 | 0,34% | 3 | 0,34% |
Ronot (2007) | 3 | 0,06% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Sadlier et al. (2012) | 3 | 0,06% | 3 | 0,34% | 3 | 0,34% | 3 | 0,34% |
Safford & Hawkins (2013) | 3 | 0,06% | 3 | 0,34% | 3 | 0,34% | 3 | 0,34% |
Schwarzhans et al. (2005) | 3 | 0,06% | 3 | 0,34% | 3 | 0,34% | 3 | 0,34% |
Simian et al. (2022) | 3 | 0,06% | 3 | 0,34% | 3 | 0,34% | 3 | 0,34% |
Tirvengadum & Bour (1985) | 3 | 0,06% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Vanderwerf et al. (2006) | 3 | 0,06% | 3 | 0,34% | 3 | 0,34% | 3 | 0,34% |
Wallach (2020) | 3 | 0,06% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Wickel et al. (2014) | 3 | 0,06% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Allen et al. (2010) | 2 | 0,04% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Alvarez et al. (2023) | 2 | 0,04% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Aubouin et al. (2016) | 2 | 0,04% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Bauer (1987) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Behm et al. (2019) | 2 | 0,04% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Bennett (1834) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Blanvillain et al. (2002) | 2 | 0,04% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Boer & Simmonds (2000) | 2 | 0,04% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Boer (2000) | 2 | 0,04% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Borsa (1997) | 2 | 0,04% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Boulenger (1883) | 2 | 0,04% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Breuil (2002) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Brosse et al. (2021) | 2 | 0,04% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Busala et al. (2024) | 2 | 0,04% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Carille (2012) | 2 | 0,04% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Chapuis et al. (2004) | 2 | 0,04% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Cheke (1987) | 2 | 0,04% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Cole et al. (2005) | 2 | 0,04% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Collinson et al. (2017) | 2 | 0,04% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Cottarel et al. (2013) | 2 | 0,04% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Crouzier (2017) | 2 | 0,04% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
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% |
Cuvier (1829) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Dewynter et al. (2019) | 2 | 0,04% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Dewynter (2021) | 2 | 0,04% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Downie et al. (2011) | 2 | 0,04% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Duméril & Bibron (1836) | 2 | 0,04% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Duval et al. (2019) | 2 | 0,04% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
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 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Fricke (1998) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Gannier & Petiau (2006) | 2 | 0,04% | 2 | 0,22% | 2 | 0,23% | 0 | 0% |
Geange (2010) | 2 | 0,04% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Gill & Thiele (1997) | 2 | 0,04% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Gill (2022) | 2 | 0,04% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Gilot et al. (1992) | 2 | 0,04% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Girard (1858) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Gmelin (1788) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Goode & Bean (1896) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Goulletquer (2016) | 2 | 0,04% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Guichenot (1848) | 2 | 0,04% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Günther (1880) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Ifremer (2024) | 2 | 0,04% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Ineich et al. (2015) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Johnson (1863) | 2 | 0,04% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Jordan & Starks (1904) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Karnella & Lachner (1981) | 2 | 0,04% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Kasamatsu & Joyce (1995) | 2 | 0,04% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Kasamatsu et al. (2000) | 2 | 0,04% | 2 | 0,22% | 2 | 0,23% | 1 | 0,11% |
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 & Marquet (2007) | 2 | 0,04% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Keith et al. (2007) | 2 | 0,04% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Keith et al. (2014) | 2 | 0,04% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Keith (2002) | 2 | 0,04% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Kiszka et al. (2009) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Klein et al. (2016) | 2 | 0,04% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Kock et al. (2006) | 2 | 0,04% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Kojadinovic et al. (2007) | 2 | 0,04% | 2 | 0,22% | 2 | 0,23% | 0 | 0% |
Lacepède (1801) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Lacoste (de) (2020) | 2 | 0,04% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Le Corre & Jouventin (1999) | 2 | 0,04% | 2 | 0,22% | 1 | 0,11% | 1 | 0,11% |
Leaper et al. (2008) | 2 | 0,04% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Leopold (1965) | 2 | 0,04% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Lesson (1830) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Linnaeus (1766) | 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% |
Mas-Coma et al. (1989) | 2 | 0,04% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Massary et al. (2017) | 2 | 0,04% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Massary et al. (2018) | 2 | 0,04% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Matsumoto & Motomura (2024) | 2 | 0,04% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Matsunuma et al. (2017) | 2 | 0,04% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Mennesson et al. (2019) | 2 | 0,04% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Miller & Wilson (1997) | 2 | 0,04% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Monti et al. (2010) | 2 | 0,04% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Motomura & Causse (2011) | 2 | 0,04% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Myers (1991) | 2 | 0,04% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Nicolas et al. (2015) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Oatleya et al. (2015) | 2 | 0,04% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Pascal et al. 2006 | 2 | 0,04% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Peale (1848) | 2 | 0,04% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Pinault et al. (2013) | 2 | 0,04% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Probst (1997) | 2 | 0,04% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Probst (1998) | 2 | 0,04% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Rafinesque (1810) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Randall & Pyle (1989) | 2 | 0,04% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Randall & Steene (1983) | 2 | 0,04% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Rhodin et al. (2017) | 2 | 0,04% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Richer de Forges et al. (2005) | 2 | 0,04% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Rignault & Chevallier (2017) | 2 | 0,04% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Ringler et al. (2015) | 2 | 0,04% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Risso (1810) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Robineau (1989) | 2 | 0,04% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Robineau (2005) | 2 | 0,04% | 2 | 0,22% | 2 | 0,23% | 1 | 0,11% |
Rossi-santos et al. (2007) | 2 | 0,04% | 2 | 0,22% | 2 | 0,23% | 1 | 0,11% |
Rüppell (1835) | 2 | 0,04% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Saint et al. (1978) | 2 | 0,04% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Sanchez & Probst (2016) | 2 | 0,04% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Sanchez et al. (2019) | 2 | 0,04% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Sanchez (2020) | 2 | 0,04% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Schwarzhans & Prokofiev (2017) | 2 | 0,04% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Séret (2014) | 2 | 0,04% | 1 | 0,11% | 0 | 0% | 1 | 0,11% |
Swainson (1839) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Teichert et al. (2013) | 2 | 0,04% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Thiele et al. (1999) | 2 | 0,04% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Thiele et al. (2004) | 2 | 0,04% | 2 | 0,22% | 2 | 0,23% | 1 | 0,11% |
Thunberg (1787) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Tostain et al. (2013) | 2 | 0,04% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Uicn et al. (2015) | 2 | 0,04% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Van Canneytet al. (2008) | 2 | 0,04% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Van Dijk et al. (2012) | 2 | 0,04% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Verreaux & Des Murs (1860) | 2 | 0,04% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Whitley (1931) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Whitley (1933) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Wilcox & Spotswood (2011) | 2 | 0,04% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Agassiz (1833-1843) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Ainley et al. (2007) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Allen (1995) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Alley et al. (2023) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Alston (1877) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Andrew et al. (2008) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Anonyme. (2004) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 0 | 0% |
Anonyme (2008) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Armand & Ferlay (2023) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Arnold & Ovenden (2014) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Astrongatt (2019) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Atwood (1869) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Aulagnier (2021) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Ausilio & Zotier (1989) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Austin & Zug (1999) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Bailenger et al. (1965) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Baker-gabb (1979) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Bance (2022) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Barbancey (2001) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Barbancey (2001) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Barbour (1912) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Barré et al. (2006) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Barre et al. (2009) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 0 | 0% |
Barre (2002) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 0 | 0% |
Barrioz & Morinière (2007) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Bassett et al. (2021) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Bauer & DeVaney (1987) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Bauer et al. (1997) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Bauer et al. (2010) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Bavay (1869) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Beaucournu (1968) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Beauvieux et al. (2024) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Behm et al. (2022) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Bénito-espinal (1990) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Bertin (1928) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Best et al. (1995) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 0 | 0% |
Bioinsight/diren & Guyane (2006) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Birdlife International (2013) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Blanc (1909) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
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% |
Blom et al. (2019) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Blom (2015) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Boddaert & Daubenton (1783) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Bodilis et al. (2011) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Bonnaterre (1788) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Borroto-páez (2018) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Bouchon-Navaro et al. (1992) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 0 | 0% |
Bougeard & Siblet (2000) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Boulenger (1912) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Bour et al. (2008) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Bourjon & Fricke (2019) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Bourjon & Fricke (2020) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Branch (2010) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 0 | 0% |
Bray & Cribb (2002) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Breuil et al. (2010) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Brisbane et al. (2021) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Brown & Gibbons (1986) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Caceres & Salamolard (2021) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Callou (2003) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Camiñas et al. (2021) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Casale et al. (2021) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Causse & Hautecoeur (2006) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Caut et al. (2008) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Cerchio et al. (2009) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 0 | 0% |
Chambault et al. (2020) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Champagne et al. (1997) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Cheke & Hume (2008) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Cheke (2010) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Chevalier (2006) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Chevallier et al. (2023) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Cheylan et al. (2022) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Ciccione et al. (2011) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Ciccione (2001) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Ciccione (2001) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Clause et al. (2017) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Clua & Planes (2019) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Clua et al. (2016) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Collazos-astudillo et al. (2022) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Collectif (2009) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 0 | 0% |
Collet & Duguy (1981) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Collet et al. (2017) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Collier et al. (2002) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 0 | 0% |
Commission de l’Avifaune Française (2016) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Counihan et al. (2012) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 0 | 0% |
Cox (1970) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Crillon & Cuzange (2020) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Crouzier (2009) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Cummings et al. (2021) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Cuvier & Valenciennes (1829) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Cuvier & Valenciennes (1829) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Dal Zotto et al. (2024) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Dalebout et al. (2005) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Dalebout et al. (2012) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Daly et al. (2023) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
D´angiolella et al. (2021) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Daudin (1802) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 0 | 0% |
Daudin (1803) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Delcroix et al. (2008) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Delcroix et al. (2011) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Deniau & Provost (2020) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Des et al. (2021) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Deuss & Jourdan (2022) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Dewynter & Claessens (2020) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Dewynter et al. (2019) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Dewynter et al. (2020) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Dickinson & Remsen (2013) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Dieme et al. (2015) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Dollfus (1966) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Dubief & Gallais (2011) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Dubois & Frétey (2016) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Dubois et al. (2008) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 0 | 0% |
Ducatez & Devore (2023) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Duffaut et al. (2011) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Duguy et al. (1998) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Duguy et al. (2007) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Duguy (1987) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Duguy (1988) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Duguy (1994) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Duguy (1997) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Duméril & Bibron (1844) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Duméril & Duméril (1851) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Entraygues (2014) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Ersts & Rosenbaum (2003) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 0 | 0% |
Étaix-bonnin et al. (2011) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Faber (1829) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabre & Orsini (2016) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Finnerty et al. (2021) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Fleming & Jackson (2011) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 0 | 0% |
Flitti & Rocha (2014) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Foata et al. (2012) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Forsskål (1775) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Fourmanoir (1966) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Fretey & Triplet (2022) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Fretey et al. (2023) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Fritzsche (1980) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Garrigue & Poupon (2013) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Gherghel et al. (2016) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Gill (1862) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Gill (2004) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Gillespie (1997) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Girard (2007) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Girondo (2023) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Girondot et al. (2015) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Girondot (2011) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Gmelin (1789) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Godet et al. (2021) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Goldberg et al. (2011) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Goodall et al. (1997) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Gould et al. (2023) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Grant-mackie et al. (2003) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Gray (1846) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Gray (1864) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Gray (1865) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Griffing et al. (2022) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Guichenot (1847) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Guinet (1991) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Guinet (2004) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Günther (1860) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Günther (1864) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Hedges et al. (2014) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Heimlich-boran (1993) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Heinicke et al. (2010) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Henao-osorio et al. (2021) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Hibino et al. (2016) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Hoshino & Motomura (2022) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Ifremer (2009) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Ineich & Bauer (1992) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Ineich & Blanc (1988) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Ineich et al. (2017) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Ineich et al. (2019) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Ineich (1987) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Ineich (1999) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Ineich (2015) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Inoue & Nakabo (2006) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
IUCN (2013) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Jacquinot & Guichenot (1853) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Jamonneau et al. (2025) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Jefferson & Barros (1997) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Jehl et al. (1980) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Jiguet (2023) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Johnson & Wolman (1984) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 0 | 0% |
Jordan et al. (1927) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Jouan (1863) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Karadjian et al. (2022) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Karin et al. (2021) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Kasamatsu et al. (1995) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Kasamatsu et al. (1998) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Kawai (2016) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Kawamura (1994) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Kayser & Wilhelm (1991) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Keith et al. (1999) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Keith et al. (2011) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Kiszka et al. (2009) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 0 | 0% |
Heron, 36(1): 31-34.">Kiszka (2003) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 0 | 0% |
Klausewitz & von Hentig (1975) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Labach et al. (2021) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 0 | 0% |
Lacepède (1800) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Lacoste (2021) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Lacoste (2021) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Lancastre et al. (1976) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Lapwong et al. (2021) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Last et al. (2016) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Le Bail et al. (2012) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Le Scao et al. (2011) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Leaper et al. (2008) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 0 | 0% |
Leatherwood et al. (1979) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Legendre (1937) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Lescure et al. (2012) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Lescure et al. (2016) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Lescure et al. (2020) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Lesson (1826-1830) | 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% |
Letacq (1924) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Letourneur & Maggiorani (1995) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Levesque & Mathurin (2008) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Liardet & d'Auzon (2004) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Liardet (2004) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Lichtenstein (1823) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Liebart et al. (2021) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Liebgold et al. (2019) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Lim et al. (2002) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Lorvelec & Pascal (2009) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Lorvelec et al. (2003) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Lorvelec et al. (2011) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Lorvelec et al. (2016) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Lorvelec et al. (2017) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Louis et al. (1992) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 0 | 0% |
Louisin & Probst (1996) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Lowe (1838) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Lowe (1843) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Macleod et al. (2006) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Maeda et al. (2011) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Marchandeau & Letty (2021) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Marchandeau et al. (2003) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Massary et al. (2019) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Mathews (1913) | 1 | 0,02% | 1 | 0,11% | 0 | 0% | 1 | 0,11% |
Matsunuma & Motomura (2018) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Matsuoka et al. (2005) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 0 | 0% |
Mckay & Milenkaya (2020) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Ménard et al. (2000) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Merrem (1820) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Meyen (1834) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Montrousier (1860) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Moravec & Justine (2014) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Morelon (2015) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Morinière & Dell'amico (2011) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Mourier (2012) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Murase et al. (2002) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 0 | 0% |
Muratet (2015) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Murphy et al. (1978) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Murray (1884) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Nassi et al. (1975) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Nelson-Smith et al. (2014) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Nicol et al. (2000) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 0 | 0% |
Noël, Meunier (2010) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Noël (2017) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Okamoto & Motomura (2017) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Oremus (2009) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Owen (1853) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Pallas (1770) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Parmentier et al. (2017) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Parmentier (1999) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Pascal & Vigne (2003) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Pascal & Vigne (2003) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Pascal & Vigne (2003) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Peron (2014) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Philippi (1887) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Pierpoint et al. (1997) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Pitman & Ensor (2003) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Poisson (1999) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Potin (2013) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Probst et al. (2000) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Probst et al. (2001) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Probst (1997) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Probst (1997) | 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 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Annales de la Société de Sciences naturelles de la Charente-Maritime, 10(2): 225-236.">Quéro et al. (2011) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Quero et al. (2013) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Questel (2023) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Randi et al. (2001) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Ranzani (1839) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Read & Farman (2018) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Read & Jean (2021) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Read et al. (2015) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Read et al. (2023) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Renaud et al. (2013) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Reynolds & Henderson (2018) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Ribic et al. (1991) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Riccialdelli et al. (2010) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Rigby & Adamson (1997) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Rinaldi et al. (2011) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Rocha et al. (2022) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Roche & Guinet (2007) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Roos (2000) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Roques (1991) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Rosenbaum & Collins (2006) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 0 | 0% |
Samaniego et al. (2020) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Sauvignet et al. (2000) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Savouré-Soubelet et al. (in prep.) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Savouré-Soubelet et al. (2016) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Schneider (1783) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Schneider (1799) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Schultz et al. (1953) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Schwaner & Brown (1984) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Schweigger (1812) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Scopoli (1769) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Scopoli (1786) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Servan (1976) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Shaver et al. (2019) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Shea et al. (2021) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Sherborn (1925) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Shine et al. (2002) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Smales et al. (2007) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Smith et al. (2005) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Snyder et al. (2019) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Steadman & Bollt (2010) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 0 | 0% |
Steindachner (1870) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Széles et al. (2018) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Taberlet (1983) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Taquet (1994) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Tea & Larson (2023) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Thévenot (2014) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Thibault (1989) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Tsadok et al. (2015) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Van & Kampen (1907) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
van den Burg et al. (2021) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Vieillot (1819) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Viel (2021) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Waayers et al. (2011) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Walbaum (1792) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Wallach (2009) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Wang & Liu (2016) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 0 | 0% |
Wang & Qiu (2022) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Wantiez (2000) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Watson (1999) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Webb & Waddle (2022) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Weerdt (2023) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 0 | 0% |
Weisler et al. (2006) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Werner (1898) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Werner (1899) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Werner (1980) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Weterings & Vetter (2017) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
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 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Wickel et al. (2016) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Williams et al. (2009) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 0 | 0% |
Williams (2018) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Winterbottom & Burridge (1993) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Wursig & Wursig (1980) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Yang et al. (2019) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Yokoyama (2012) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Zelhuber (2009) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Zug et al. (2007) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
(2021) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |