Vertébrés des TAAF
1116 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) | 412 | 7,03% | 398 | 36,38% | 397 | 37,74% | 396 | 37,39% |
Wickel & Jamon (2010) | 403 | 6,88% | 386 | 35,28% | 385 | 36,6% | 385 | 36,36% |
Fricke et al. (2009) | 400 | 6,82% | 383 | 35,01% | 383 | 36,41% | 381 | 35,98% |
Fricke et al. (2013) | 382 | 6,52% | 369 | 33,73% | 368 | 34,98% | 367 | 34,66% |
Siu et al. (2017) | 301 | 5,14% | 291 | 26,6% | 291 | 27,66% | 290 | 27,38% |
Uicn et al. (2015) | 294 | 5,02% | 267 | 24,41% | 256 | 24,33% | 228 | 21,53% |
Chabanet & Durville (2005) | 279 | 4,76% | 250 | 22,85% | 250 | 23,76% | 250 | 23,61% |
Williams et al. (2006) | 241 | 4,11% | 230 | 21,02% | 230 | 21,86% | 229 | 21,62% |
Delrieu-Trottin et al. (2015) | 192 | 3,28% | 184 | 16,82% | 183 | 17,4% | 184 | 17,37% |
Kulbicki et al. (2000) | 177 | 3,02% | 156 | 14,26% | 156 | 14,83% | 155 | 14,64% |
Rinaldi (2016) | 152 | 2,59% | 140 | 12,8% | 140 | 13,31% | 104 | 9,82% |
Duhamel et al. (2005) | 130 | 2,22% | 125 | 11,43% | 122 | 11,6% | 125 | 11,8% |
Bacchet et al. (2007) | 114 | 1,95% | 108 | 9,87% | 108 | 10,27% | 108 | 10,2% |
Carzon et al. (2016) | 114 | 1,95% | 105 | 9,6% | 105 | 9,98% | 78 | 7,37% |
Estrade et al. (2016) | 114 | 1,95% | 105 | 9,6% | 105 | 9,98% | 78 | 7,37% |
Béarez & Bouffandeau (2019) | 69 | 1,18% | 67 | 6,12% | 67 | 6,37% | 66 | 6,23% |
Dettaï et al. (2011) | 64 | 1,09% | 61 | 5,58% | 61 | 5,8% | 61 | 5,76% |
Linnaeus (1758) | 63 | 1,07% | 21 | 1,92% | 21 | 2% | 20 | 1,89% |
Richard et al. (1982) | 62 | 1,06% | 19 | 1,74% | 19 | 1,81% | 19 | 1,79% |
Kulbicki (comm. pers., 2011) | 54 | 0,92% | 48 | 4,39% | 48 | 4,56% | 48 | 4,53% |
Uicn et al. (2017) | 51 | 0,87% | 51 | 4,66% | 51 | 4,85% | 42 | 3,97% |
Questel & Le Quellec (2012) | 50 | 0,85% | 47 | 4,3% | 47 | 4,47% | 40 | 3,78% |
Questel (2020) | 50 | 0,85% | 48 | 4,39% | 47 | 4,47% | 43 | 4,06% |
Allen (comm. pers., 2009) | 49 | 0,84% | 48 | 4,39% | 48 | 4,56% | 47 | 4,44% |
Béarez et al. (2017) | 41 | 0,7% | 40 | 3,66% | 40 | 3,8% | 38 | 3,59% |
Jarrett & Shirihai (2014) | 39 | 0,67% | 36 | 3,29% | 36 | 3,42% | 27 | 2,55% |
Charrassin (2016) | 38 | 0,65% | 35 | 3,2% | 35 | 3,33% | 26 | 2,46% |
Charrassin (2016) | 38 | 0,65% | 35 | 3,2% | 35 | 3,33% | 26 | 2,46% |
Moutou (2016) | 38 | 0,65% | 35 | 3,2% | 35 | 3,33% | 26 | 2,46% |
Spitz et al. (2016) | 38 | 0,65% | 35 | 3,2% | 35 | 3,33% | 26 | 2,46% |
Thoisy & Bordin (2016) | 38 | 0,65% | 35 | 3,2% | 35 | 3,33% | 26 | 2,46% |
Urtizberea (2016) | 38 | 0,65% | 35 | 3,2% | 35 | 3,33% | 26 | 2,46% |
Legand (1950) | 33 | 0,56% | 16 | 1,46% | 16 | 1,52% | 16 | 1,51% |
Barau et al. (2005) | 31 | 0,53% | 26 | 2,38% | 26 | 2,47% | 24 | 2,27% |
Béarez & Séret (2009) | 30 | 0,51% | 29 | 2,65% | 29 | 2,76% | 29 | 2,74% |
UICN Comité français, OFB & MNHN (2021) | 28 | 0,48% | 28 | 2,56% | 28 | 2,66% | 25 | 2,36% |
Levesque & Delcroix (2018) | 26 | 0,44% | 26 | 2,38% | 25 | 2,38% | 26 | 2,46% |
Rocamora (2004) | 26 | 0,44% | 23 | 2,1% | 22 | 2,09% | 22 | 2,08% |
Aulagnier (2009) | 25 | 0,43% | 23 | 2,1% | 23 | 2,19% | 16 | 1,51% |
Mertens & Wermuth (1960) | 21 | 0,36% | 0 | 0% | 0 | 0% | 0 | 0% |
Uicn et al. (2015) | 21 | 0,36% | 19 | 1,74% | 19 | 1,81% | 17 | 1,61% |
Yokoyama (2013) | 21 | 0,36% | 21 | 1,92% | 21 | 2% | 18 | 1,7% |
Fourriére et al. (2014) | 20 | 0,34% | 19 | 1,74% | 19 | 1,81% | 19 | 1,79% |
Shirihai (2003) | 20 | 0,34% | 16 | 1,46% | 15 | 1,43% | 12 | 1,13% |
Bordin et al. (2021) | 19 | 0,32% | 19 | 1,74% | 19 | 1,81% | 12 | 1,13% |
Gannier (2001) | 19 | 0,32% | 19 | 1,74% | 19 | 1,81% | 13 | 1,23% |
Garrigue (2007) | 19 | 0,32% | 19 | 1,74% | 19 | 1,81% | 13 | 1,23% |
G.E.M.M. (2012) | 19 | 0,32% | 19 | 1,74% | 19 | 1,81% | 13 | 1,23% |
Perrin et al. (2002) | 19 | 0,32% | 16 | 1,46% | 15 | 1,43% | 12 | 1,13% |
Ausilio & Zotier (1989) | 17 | 0,29% | 16 | 1,46% | 16 | 1,52% | 15 | 1,42% |
Catzeflis (2012) | 17 | 0,29% | 17 | 1,55% | 17 | 1,62% | 10 | 0,94% |
Prévost & Mougin (1970) | 17 | 0,29% | 15 | 1,37% | 14 | 1,33% | 13 | 1,23% |
Remsen et al. (2013) | 17 | 0,29% | 16 | 1,46% | 16 | 1,52% | 16 | 1,51% |
UICN Comité français, OFB, MNHN & GEPOMAY (2025) | 16 | 0,27% | 16 | 1,46% | 16 | 1,52% | 15 | 1,42% |
Bouchon-Navaro et al. (2005) | 15 | 0,26% | 10 | 0,91% | 10 | 0,95% | 9 | 0,85% |
Dewynter et al. (2021) | 15 | 0,26% | 15 | 1,37% | 15 | 1,43% | 12 | 1,13% |
Gannier (2002) | 15 | 0,26% | 15 | 1,37% | 15 | 1,43% | 11 | 1,04% |
Gannier (2009) | 15 | 0,26% | 15 | 1,37% | 15 | 1,43% | 11 | 1,04% |
Samaran & Guinet (2009) | 15 | 0,26% | 13 | 1,19% | 11 | 1,05% | 9 | 0,85% |
Sanchez et al. (2019) | 15 | 0,26% | 13 | 1,19% | 12 | 1,14% | 13 | 1,23% |
Van Dijk et al. (2012) | 15 | 0,26% | 12 | 1,1% | 12 | 1,14% | 12 | 1,13% |
Arnaud (1974) | 14 | 0,24% | 9 | 0,82% | 9 | 0,86% | 9 | 0,85% |
Gannier (2000) | 14 | 0,24% | 14 | 1,28% | 14 | 1,33% | 10 | 0,94% |
Lorvelec et al. (2007) | 14 | 0,24% | 14 | 1,28% | 14 | 1,33% | 14 | 1,32% |
Weimerskirch et al. (2009) | 14 | 0,24% | 13 | 1,19% | 13 | 1,24% | 11 | 1,04% |
Gill (1995) | 13 | 0,22% | 12 | 1,1% | 12 | 1,14% | 11 | 1,04% |
Kiszka et al. (2009) | 13 | 0,22% | 10 | 0,91% | 10 | 0,95% | 10 | 0,94% |
Kiszka et al.(2007) | 13 | 0,22% | 13 | 1,19% | 13 | 1,24% | 9 | 0,85% |
Soubeyran et al. (2011) | 13 | 0,22% | 13 | 1,19% | 13 | 1,24% | 13 | 1,23% |
Barré (2021) | 12 | 0,2% | 12 | 1,1% | 12 | 1,14% | 12 | 1,13% |
Frenot et al. (2005) | 12 | 0,2% | 11 | 1,01% | 11 | 1,05% | 10 | 0,94% |
Massary et al. (2020) | 12 | 0,2% | 12 | 1,1% | 12 | 1,14% | 11 | 1,04% |
Probst et al. (2022) | 12 | 0,2% | 12 | 1,1% | 12 | 1,14% | 11 | 1,04% |
Tostain et al. (2013) | 12 | 0,2% | 12 | 1,1% | 12 | 1,14% | 10 | 0,94% |
Walbaum (1792) | 12 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Aulagnier et al. (2017) | 11 | 0,19% | 10 | 0,91% | 10 | 0,95% | 9 | 0,85% |
Boer et al. (1999) | 11 | 0,19% | 10 | 0,91% | 9 | 0,86% | 9 | 0,85% |
Clements (2012) | 11 | 0,19% | 11 | 1,01% | 8 | 0,76% | 9 | 0,85% |
Cuvier & Valenciennes (1848) | 11 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Etcheberry & Abraham (2009) | 11 | 0,19% | 10 | 0,91% | 10 | 0,95% | 10 | 0,94% |
Gargominy et al. (1996) | 11 | 0,19% | 11 | 1,01% | 11 | 1,05% | 11 | 1,04% |
Laran et al. (2011) | 11 | 0,19% | 11 | 1,01% | 11 | 1,05% | 8 | 0,76% |
Robineau & Duhamel (2006) | 11 | 0,19% | 9 | 0,82% | 8 | 0,76% | 5 | 0,47% |
Safford & Hawkins (2013) | 11 | 0,19% | 11 | 1,01% | 10 | 0,95% | 10 | 0,94% |
Boer (2000) | 10 | 0,17% | 8 | 0,73% | 7 | 0,67% | 5 | 0,47% |
Chastel & Beaucournu (1992) | 10 | 0,17% | 10 | 0,91% | 10 | 0,95% | 8 | 0,76% |
Deblock et al. (1960) | 10 | 0,17% | 7 | 0,64% | 7 | 0,67% | 7 | 0,66% |
Dulau-Drouot et al. (2008) | 10 | 0,17% | 10 | 0,91% | 10 | 0,95% | 6 | 0,57% |
Fourt et al. (2017) | 10 | 0,17% | 10 | 0,91% | 10 | 0,95% | 8 | 0,76% |
Kiszka et al. (2010) | 10 | 0,17% | 10 | 0,91% | 10 | 0,95% | 7 | 0,66% |
Lacepède (1803) | 10 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Randall & Earle (2000) | 10 | 0,17% | 9 | 0,82% | 8 | 0,76% | 9 | 0,85% |
Shandikov (2011) | 10 | 0,17% | 10 | 0,91% | 10 | 0,95% | 10 | 0,94% |
Thibault et al. (2014) | 10 | 0,17% | 10 | 0,91% | 10 | 0,95% | 8 | 0,76% |
Belfan & Conde (2016) | 9 | 0,15% | 9 | 0,82% | 9 | 0,86% | 9 | 0,85% |
Caceres (2002) | 9 | 0,15% | 4 | 0,37% | 2 | 0,19% | 4 | 0,38% |
Chernova & Duhamel (2003) | 9 | 0,15% | 9 | 0,82% | 7 | 0,67% | 9 | 0,85% |
Duhamel & King (2007) | 9 | 0,15% | 9 | 0,82% | 9 | 0,86% | 9 | 0,85% |
Ifremer (2009) | 9 | 0,15% | 7 | 0,64% | 7 | 0,67% | 6 | 0,57% |
Probst (2001) | 9 | 0,15% | 7 | 0,64% | 7 | 0,67% | 6 | 0,57% |
Robineau (1989) | 9 | 0,15% | 5 | 0,46% | 4 | 0,38% | 4 | 0,38% |
Dewynter et al. (2022) | 8 | 0,14% | 8 | 0,73% | 8 | 0,76% | 8 | 0,76% |
Dewynter et al. (2023) | 8 | 0,14% | 8 | 0,73% | 8 | 0,76% | 8 | 0,76% |
Moreau & Duhamel (1997) | 8 | 0,14% | 8 | 0,73% | 8 | 0,76% | 8 | 0,76% |
Probst et al. (2001) | 8 | 0,14% | 3 | 0,27% | 3 | 0,29% | 3 | 0,28% |
Probst (1997) | 8 | 0,14% | 4 | 0,37% | 2 | 0,19% | 3 | 0,28% |
Probst (1998) | 8 | 0,14% | 4 | 0,37% | 4 | 0,38% | 4 | 0,38% |
Questel et al. (2023) | 8 | 0,14% | 8 | 0,73% | 8 | 0,76% | 8 | 0,76% |
Questel et al. (2023) | 8 | 0,14% | 8 | 0,73% | 8 | 0,76% | 8 | 0,76% |
Ronot (2007) | 8 | 0,14% | 7 | 0,64% | 7 | 0,67% | 6 | 0,57% |
Smith (1997) | 8 | 0,14% | 8 | 0,73% | 6 | 0,57% | 8 | 0,76% |
Theuerkauf et al. (2010) | 8 | 0,14% | 8 | 0,73% | 8 | 0,76% | 8 | 0,76% |
Dewynter et al. (2019) | 7 | 0,12% | 7 | 0,64% | 7 | 0,67% | 7 | 0,66% |
Dewynter et al. (2023) | 7 | 0,12% | 7 | 0,64% | 7 | 0,67% | 7 | 0,66% |
Gmelin (1789) | 7 | 0,12% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Henderson & Breuil (2012) | 7 | 0,12% | 4 | 0,37% | 4 | 0,38% | 4 | 0,38% |
Jourdan (2020) | 7 | 0,12% | 6 | 0,55% | 6 | 0,57% | 6 | 0,57% |
Lambert (1988) | 7 | 0,12% | 4 | 0,37% | 4 | 0,38% | 3 | 0,28% |
Lowe et al. (2007) | 7 | 0,12% | 7 | 0,64% | 7 | 0,67% | 7 | 0,66% |
Massary et al. (2018) | 7 | 0,12% | 7 | 0,64% | 7 | 0,67% | 7 | 0,66% |
Massary et al. (2021) | 7 | 0,12% | 7 | 0,64% | 7 | 0,67% | 7 | 0,66% |
Moller & King (2007) | 7 | 0,12% | 7 | 0,64% | 7 | 0,67% | 7 | 0,66% |
Pearman et al. (2020) | 7 | 0,12% | 7 | 0,64% | 7 | 0,67% | 7 | 0,66% |
Potin (2013) | 7 | 0,12% | 7 | 0,64% | 7 | 0,67% | 7 | 0,66% |
Probst (1997) | 7 | 0,12% | 5 | 0,46% | 5 | 0,48% | 4 | 0,38% |
Sanchez (2020) | 7 | 0,12% | 7 | 0,64% | 7 | 0,67% | 6 | 0,57% |
Soubeyran (2008) | 7 | 0,12% | 6 | 0,55% | 6 | 0,57% | 6 | 0,57% |
Tirvengadum & Bour (1985) | 7 | 0,12% | 6 | 0,55% | 6 | 0,57% | 6 | 0,57% |
Turpin & Probst (1998) | 7 | 0,12% | 4 | 0,37% | 2 | 0,19% | 4 | 0,38% |
Uicn et al. (2020) | 7 | 0,12% | 7 | 0,64% | 7 | 0,67% | 5 | 0,47% |
Blanc (1954) | 6 | 0,1% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Camiñas et al. (2021) | 6 | 0,1% | 6 | 0,55% | 6 | 0,57% | 6 | 0,57% |
Compagno (1984) | 6 | 0,1% | 6 | 0,55% | 6 | 0,57% | 6 | 0,57% |
Desbrosses & Etcheberry (1987) | 6 | 0,1% | 5 | 0,46% | 5 | 0,48% | 2 | 0,19% |
Gmelin (1789) | 6 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Günther (1866) | 6 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Proceedings of the Zoological Society of London, 1907: 1035-1037.">Hopkinson (1907) | 6 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Justine et al. (2010) | 6 | 0,1% | 6 | 0,55% | 6 | 0,57% | 6 | 0,57% |
Kojadinovic et al. (2007) | 6 | 0,1% | 4 | 0,37% | 4 | 0,38% | 2 | 0,19% |
Kronen et al. (2009) | 6 | 0,1% | 6 | 0,55% | 6 | 0,57% | 6 | 0,57% |
Letourneur et al. (2004) | 6 | 0,1% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Massary et al. (2017) | 6 | 0,1% | 6 | 0,55% | 6 | 0,57% | 6 | 0,57% |
Pallas [1814] | 6 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Pavan-Kumar et al. (2018) | 6 | 0,1% | 5 | 0,46% | 5 | 0,48% | 5 | 0,47% |
Pinault et al. (2013) | 6 | 0,1% | 6 | 0,55% | 6 | 0,57% | 6 | 0,57% |
Poey (1858-61) | 6 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Probst et al. (2000) | 6 | 0,1% | 5 | 0,46% | 3 | 0,29% | 5 | 0,47% |
Probst (1997) | 6 | 0,1% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Rafinesque Schmaltz (1810) | 6 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Rossi-santos et al. (2007) | 6 | 0,1% | 4 | 0,37% | 4 | 0,38% | 2 | 0,19% |
Séret (1997) | 6 | 0,1% | 6 | 0,55% | 6 | 0,57% | 6 | 0,57% |
Shandikov (1995) | 6 | 0,1% | 6 | 0,55% | 6 | 0,57% | 6 | 0,57% |
Banks et al. (2006) | 5 | 0,09% | 4 | 0,37% | 4 | 0,38% | 1 | 0,09% |
Bauer & Sadlier (2000) | 5 | 0,09% | 3 | 0,27% | 3 | 0,29% | 3 | 0,28% |
Bioinsight/diren & Guyane (2006) | 5 | 0,09% | 5 | 0,46% | 5 | 0,48% | 5 | 0,47% |
Bloch & Schneider (1801) | 5 | 0,09% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Boer & Simmonds (2000) | 5 | 0,09% | 4 | 0,37% | 4 | 0,38% | 4 | 0,38% |
Borsa (1997) | 5 | 0,09% | 4 | 0,37% | 3 | 0,29% | 3 | 0,28% |
Casale et al. (2021) | 5 | 0,09% | 5 | 0,46% | 5 | 0,48% | 5 | 0,47% |
Chevalier (2006) | 5 | 0,09% | 5 | 0,46% | 5 | 0,48% | 5 | 0,47% |
Ciccione et al. (2011) | 5 | 0,09% | 5 | 0,46% | 5 | 0,48% | 5 | 0,47% |
Collette & Nauen (1983) | 5 | 0,09% | 5 | 0,46% | 5 | 0,48% | 5 | 0,47% |
Crillon & Cuzange (2020) | 5 | 0,09% | 5 | 0,46% | 5 | 0,48% | 5 | 0,47% |
Cuvier (1829) | 5 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Del Hoyo & Collar (2014) | 5 | 0,09% | 2 | 0,18% | 1 | 0,1% | 2 | 0,19% |
Dewynter et al. (2019) | 5 | 0,09% | 5 | 0,46% | 5 | 0,48% | 5 | 0,47% |
Duffaut et al. (2011) | 5 | 0,09% | 5 | 0,46% | 5 | 0,48% | 5 | 0,47% |
Entraygues (2014) | 5 | 0,09% | 5 | 0,46% | 5 | 0,48% | 5 | 0,47% |
Étaix-bonnin et al. (2011) | 5 | 0,09% | 5 | 0,46% | 5 | 0,48% | 5 | 0,47% |
Fretey & Triplet (2022) | 5 | 0,09% | 5 | 0,46% | 5 | 0,48% | 5 | 0,47% |
Günther (1878) | 5 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Kasamatsu & Joyce (1995) | 5 | 0,09% | 4 | 0,37% | 3 | 0,29% | 4 | 0,38% |
Kronen et al. (2008) | 5 | 0,09% | 5 | 0,46% | 5 | 0,48% | 5 | 0,47% |
Le Scao et al. (2011) | 5 | 0,09% | 5 | 0,46% | 5 | 0,48% | 5 | 0,47% |
Massary et al. (2019) | 5 | 0,09% | 5 | 0,46% | 5 | 0,48% | 5 | 0,47% |
Read & Farman (2018) | 5 | 0,09% | 5 | 0,46% | 5 | 0,48% | 5 | 0,47% |
Read et al. (2023) | 5 | 0,09% | 5 | 0,46% | 5 | 0,48% | 5 | 0,47% |
Rhodin et al. (2017) | 5 | 0,09% | 3 | 0,27% | 3 | 0,29% | 3 | 0,28% |
Riccialdelli et al. (2010) | 5 | 0,09% | 3 | 0,27% | 3 | 0,29% | 2 | 0,19% |
Sauvignet et al. (2000) | 5 | 0,09% | 5 | 0,46% | 5 | 0,48% | 5 | 0,47% |
Snodgrass & Heller (1905) | 5 | 0,09% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Wickel et al. (2014) | 5 | 0,09% | 4 | 0,37% | 4 | 0,38% | 4 | 0,38% |
Aulagnier (2021) | 4 | 0,07% | 4 | 0,37% | 4 | 0,38% | 3 | 0,28% |
Barbraud et al. (2009) | 4 | 0,07% | 4 | 0,37% | 4 | 0,38% | 4 | 0,38% |
Barre et al. (2009) | 4 | 0,07% | 4 | 0,37% | 4 | 0,38% | 3 | 0,28% |
Barrioz & Morinière (2007) | 4 | 0,07% | 4 | 0,37% | 4 | 0,38% | 4 | 0,38% |
Bochaton et al. (2021) | 4 | 0,07% | 4 | 0,37% | 4 | 0,38% | 4 | 0,38% |
Bost et al. (2022) | 4 | 0,07% | 4 | 0,37% | 4 | 0,38% | 2 | 0,19% |
Bouchon-Navaro & Louis (1986) | 4 | 0,07% | 3 | 0,27% | 3 | 0,29% | 3 | 0,28% |
Bour et al. (2008) | 4 | 0,07% | 4 | 0,37% | 4 | 0,38% | 4 | 0,38% |
Breuil (2002) | 4 | 0,07% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Butaud (2021) | 4 | 0,07% | 4 | 0,37% | 4 | 0,38% | 4 | 0,38% |
Clements et al. (2015) | 4 | 0,07% | 4 | 0,37% | 4 | 0,38% | 2 | 0,19% |
Delord et al. (2005) | 4 | 0,07% | 4 | 0,37% | 4 | 0,38% | 4 | 0,38% |
Delord et al. (2008) | 4 | 0,07% | 4 | 0,37% | 4 | 0,38% | 4 | 0,38% |
Des et al. (2021) | 4 | 0,07% | 4 | 0,37% | 4 | 0,38% | 4 | 0,38% |
Dewynter (2021) | 4 | 0,07% | 4 | 0,37% | 4 | 0,38% | 4 | 0,38% |
Diaz & Cuzange (2009) | 4 | 0,07% | 4 | 0,37% | 4 | 0,38% | 2 | 0,19% |
Forster (1781) | 4 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Fretey & Lescure (1999) | 4 | 0,07% | 4 | 0,37% | 4 | 0,38% | 4 | 0,38% |
Fricke et al. (2024) | 4 | 0,07% | 4 | 0,37% | 4 | 0,38% | 4 | 0,38% |
Gentry et al. (2004) | 4 | 0,07% | 3 | 0,27% | 3 | 0,29% | 3 | 0,28% |
Gilchrist (1906) | 4 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
González-sánchez et al. (2021) | 4 | 0,07% | 4 | 0,37% | 4 | 0,38% | 4 | 0,38% |
Hoff & Daszkiewicz (2001) | 4 | 0,07% | 4 | 0,37% | 4 | 0,38% | 4 | 0,38% |
Horner (2007) | 4 | 0,07% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Ineich (2016) | 4 | 0,07% | 4 | 0,37% | 4 | 0,38% | 4 | 0,38% |
Isenmann et al. (1971) | 4 | 0,07% | 4 | 0,37% | 4 | 0,38% | 4 | 0,38% |
Jaeger et al. (2020) | 4 | 0,07% | 4 | 0,37% | 4 | 0,38% | 4 | 0,38% |
Jordan (1894) | 4 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Karadjian et al. (2022) | 4 | 0,07% | 4 | 0,37% | 4 | 0,38% | 4 | 0,38% |
Kenaley (2007) | 4 | 0,07% | 4 | 0,37% | 4 | 0,38% | 4 | 0,38% |
Lescure et al. (2012) | 4 | 0,07% | 4 | 0,37% | 4 | 0,38% | 4 | 0,38% |
Letourneur & Maggiorani (1995) | 4 | 0,07% | 4 | 0,37% | 4 | 0,38% | 4 | 0,38% |
Linnaeus (1766) | 4 | 0,07% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Lorvelec & Pascal (2009) | 4 | 0,07% | 4 | 0,37% | 4 | 0,38% | 4 | 0,38% |
Macleod et al. (2006) | 4 | 0,07% | 3 | 0,27% | 3 | 0,29% | 3 | 0,28% |
Marshall et al. (2009) | 4 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Matsuoka et al. (2005) | 4 | 0,07% | 4 | 0,37% | 3 | 0,29% | 2 | 0,19% |
Muratet (2015) | 4 | 0,07% | 4 | 0,37% | 4 | 0,38% | 4 | 0,38% |
Nielsen et al. (2008) | 4 | 0,07% | 4 | 0,37% | 4 | 0,38% | 4 | 0,38% |
Nilsson (1832) | 4 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Rafinesque (1810) | 4 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Randall (1998) | 4 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Rignault & Chevallier (2017) | 4 | 0,07% | 4 | 0,37% | 4 | 0,38% | 4 | 0,38% |
Risso (1810) | 4 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Risso (1827) | 4 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Röll et al. (2023) | 4 | 0,07% | 4 | 0,37% | 4 | 0,38% | 4 | 0,38% |
Routtier et al. (2023) | 4 | 0,07% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Rüppell (1835) | 4 | 0,07% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Sanchez & Probst (2016) | 4 | 0,07% | 4 | 0,37% | 4 | 0,38% | 4 | 0,38% |
Thiele et al. (1999) | 4 | 0,07% | 3 | 0,27% | 2 | 0,19% | 3 | 0,28% |
Vaillant (1888) | 4 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
AAMP (2012) | 3 | 0,05% | 3 | 0,27% | 3 | 0,29% | 0 | 0% |
Abeyrama et al. (2021) | 3 | 0,05% | 3 | 0,27% | 3 | 0,29% | 3 | 0,28% |
Ainley et al. (2007) | 3 | 0,05% | 3 | 0,27% | 3 | 0,29% | 2 | 0,19% |
Andriashev (1982) | 3 | 0,05% | 3 | 0,27% | 2 | 0,19% | 3 | 0,28% |
Arnold & Ovenden (2014) | 3 | 0,05% | 3 | 0,27% | 3 | 0,29% | 3 | 0,28% |
Barbosa du Bocage & Brito Capello (1864) | 3 | 0,05% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Barbraud et al. (2021) | 3 | 0,05% | 3 | 0,27% | 3 | 0,29% | 3 | 0,28% |
Blanc (1909) | 3 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Bonnaterre (1788) | 3 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Borsa et al. (2014) | 3 | 0,05% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Brugneaux & Pérès (2006) | 3 | 0,05% | 3 | 0,27% | 3 | 0,29% | 3 | 0,28% |
Burneleau (1983) | 3 | 0,05% | 3 | 0,27% | 3 | 0,29% | 3 | 0,28% |
Busala et al. (2024) | 3 | 0,05% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Carravieri et al. (2016) | 3 | 0,05% | 3 | 0,27% | 3 | 0,29% | 3 | 0,28% |
Catzeflis (2018) | 3 | 0,05% | 3 | 0,27% | 3 | 0,29% | 3 | 0,28% |
Champagne et al. (1997) | 3 | 0,05% | 3 | 0,27% | 3 | 0,29% | 3 | 0,28% |
Cheke (1987) | 3 | 0,05% | 3 | 0,27% | 3 | 0,29% | 3 | 0,28% |
Cohen et al. (1990) | 3 | 0,05% | 3 | 0,27% | 3 | 0,29% | 3 | 0,28% |
Commission de l’Avifaune Française (2016) | 3 | 0,05% | 3 | 0,27% | 3 | 0,29% | 1 | 0,09% |
Cousins et al. (2013) | 3 | 0,05% | 3 | 0,27% | 3 | 0,29% | 3 | 0,28% |
Cuvier & Valenciennes (1830-1832) | 3 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Cuvier & Valenciennes ([1832]) | 3 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Delcroix et al. (2011) | 3 | 0,05% | 3 | 0,27% | 3 | 0,29% | 3 | 0,28% |
Dickinson & Remsen (2013) | 3 | 0,05% | 3 | 0,27% | 2 | 0,19% | 3 | 0,28% |
Dubief & Gallais (2011) | 3 | 0,05% | 3 | 0,27% | 3 | 0,29% | 3 | 0,28% |
Duguy et al. (1998) | 3 | 0,05% | 3 | 0,27% | 3 | 0,29% | 3 | 0,28% |
Duguy et al. (2007) | 3 | 0,05% | 3 | 0,27% | 3 | 0,29% | 3 | 0,28% |
Duguy (1988) | 3 | 0,05% | 3 | 0,27% | 3 | 0,29% | 3 | 0,28% |
Duguy (1994) | 3 | 0,05% | 3 | 0,27% | 3 | 0,29% | 3 | 0,28% |
Duguy (1997) | 3 | 0,05% | 3 | 0,27% | 3 | 0,29% | 3 | 0,28% |
Duhamel (1986) | 3 | 0,05% | 3 | 0,27% | 3 | 0,29% | 3 | 0,28% |
Durant et al. (2013) | 3 | 0,05% | 3 | 0,27% | 3 | 0,29% | 3 | 0,28% |
Fort & Barrière (2021) | 3 | 0,05% | 3 | 0,27% | 3 | 0,29% | 3 | 0,28% |
Gill & Townsend (1897) | 3 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Girondot (2011) | 3 | 0,05% | 3 | 0,27% | 3 | 0,29% | 3 | 0,28% |
Goiran & Shine (2020) | 3 | 0,05% | 3 | 0,27% | 3 | 0,29% | 3 | 0,28% |
Goren & Galil (2015) | 3 | 0,05% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Gronow (1854) | 3 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Guth (1971) | 3 | 0,05% | 3 | 0,27% | 3 | 0,29% | 2 | 0,19% |
Hureau (1966) | 3 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Hutchinson et al. (2019) | 3 | 0,05% | 3 | 0,27% | 3 | 0,29% | 3 | 0,28% |
Iglesias et al. (2012) | 3 | 0,05% | 3 | 0,27% | 3 | 0,29% | 3 | 0,28% |
IUCN (2012) | 3 | 0,05% | 3 | 0,27% | 3 | 0,29% | 1 | 0,09% |
IUCN (2013) | 3 | 0,05% | 2 | 0,18% | 2 | 0,19% | 1 | 0,09% |
Jouventin et al. (1989) | 3 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Kawamura (1994) | 3 | 0,05% | 3 | 0,27% | 3 | 0,29% | 1 | 0,09% |
Keith et al. (2006) | 3 | 0,05% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Keith et al. (2011) | 3 | 0,05% | 3 | 0,27% | 3 | 0,29% | 3 | 0,28% |
Klunzinger (1871) | 3 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Kock et al. (2006) | 3 | 0,05% | 3 | 0,27% | 2 | 0,19% | 3 | 0,28% |
Laran et al. (2012) | 3 | 0,05% | 3 | 0,27% | 3 | 0,29% | 2 | 0,19% |
Leach (1818) | 3 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Leaper et al. (2008) | 3 | 0,05% | 3 | 0,27% | 2 | 0,19% | 3 | 0,28% |
Lescroel et al. (2009) | 3 | 0,05% | 3 | 0,27% | 3 | 0,29% | 3 | 0,28% |
Méheust et al. (2018) | 3 | 0,05% | 3 | 0,27% | 3 | 0,29% | 3 | 0,28% |
Morinière & Dell'amico (2011) | 3 | 0,05% | 3 | 0,27% | 3 | 0,29% | 3 | 0,28% |
Mourier et al. (2013) | 3 | 0,05% | 3 | 0,27% | 3 | 0,29% | 3 | 0,28% |
Müller & Henle (1841) | 3 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Pascal et al. (2006) | 3 | 0,05% | 3 | 0,27% | 3 | 0,29% | 3 | 0,28% |
Poisson (1999) | 3 | 0,05% | 3 | 0,27% | 3 | 0,29% | 3 | 0,28% |
Ponchon et al. (2021) | 3 | 0,05% | 3 | 0,27% | 3 | 0,29% | 3 | 0,28% |
Postel (1965) | 3 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Probst (2001) | 3 | 0,05% | 2 | 0,18% | 2 | 0,19% | 1 | 0,09% |
Annales de la Société de Sciences naturelles de la Charente-Maritime, 10(2): 225-236.">Quéro et al. (2011) | 3 | 0,05% | 3 | 0,27% | 3 | 0,29% | 3 | 0,28% |
Read & Jean (2021) | 3 | 0,05% | 3 | 0,27% | 3 | 0,29% | 3 | 0,28% |
Robineau (2005) | 3 | 0,05% | 3 | 0,27% | 3 | 0,29% | 1 | 0,09% |
Rousseau (2010) | 3 | 0,05% | 3 | 0,27% | 3 | 0,29% | 3 | 0,28% |
Roux (1913) | 3 | 0,05% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Sagar (1991) | 3 | 0,05% | 3 | 0,27% | 3 | 0,29% | 0 | 0% |
Séret (2014) | 3 | 0,05% | 1 | 0,09% | 0 | 0% | 1 | 0,09% |
Simian et al. (2022) | 3 | 0,05% | 3 | 0,27% | 3 | 0,29% | 2 | 0,19% |
Smith (1849) | 3 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Thiebot et al. (2011) | 3 | 0,05% | 3 | 0,27% | 3 | 0,29% | 3 | 0,28% |
Thiele et al. (2004) | 3 | 0,05% | 3 | 0,27% | 2 | 0,19% | 2 | 0,19% |
Tremblay & Cherel (2005) | 3 | 0,05% | 3 | 0,27% | 0 | 0% | 3 | 0,28% |
Valenciennes (1836-1844) | 3 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Wallach (2020) | 3 | 0,05% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Baldi et al. (2022) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Balushkin (1996) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Barthélémy (1926) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Bartoli (1972) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Bauer et al. (2010) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Bauer (1987) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Benedetti et al. (2021) | 2 | 0,03% | 2 | 0,18% | 1 | 0,1% | 1 | 0,09% |
Bennett (1834) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Berrebi et al. (2018) | 2 | 0,03% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Berta & Churchill (2012) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Bertin (1928) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 1 | 0,09% |
Birdlife International (2013) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Bloch (1795) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Boettger (1913) | 2 | 0,03% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Bonnaterre (1789) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Bourjon & Fricke (2016) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Bourjon et al. (2018) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Bretagnolle & Attie (1991) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Breuil et al. (2010) | 2 | 0,03% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Brodier et al. (2011) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Brygoo (1985) | 2 | 0,03% | 2 | 0,18% | 0 | 0% | 2 | 0,19% |
Cabanis (1875) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 0 | 0% |
Caceres & Salamolard (2021) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Chapuis et al. (2004) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Chartier et al. (2007) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 0 | 0% |
Cheke (2010) | 2 | 0,03% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Cherel et al. (2014) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 0 | 0% |
Cherel et al. (2022) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Chevallier et al. (2023) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Cole et al. (2005) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Collinson et al. (2017) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Cottarel et al. (2013) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Couch (1877) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
D'Amico (2001) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Daniel et al. (2020) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 0 | 0% |
Denys et al. (2022) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Odontaspis ferox" Agassiz dans le Golf de Gascogne. Bulletin de la Société zoologique de France, 54: 233-235.">Desbrosses (1930) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Dewynter et al. (2020) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Dronneau & Wassmer (2008) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Dubois et al. (2008) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Duguy et al. (1997) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Duguy et al. (1999) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Duguy et al. (2000) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Duguy et al. (2002) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Duguy et al. (2003) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Duguy et al. (2004) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Duguy et al. (2006) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Duguy (1987) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Duguy (1990) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Duguy (1992) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Duguy (1993) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Duguy (1995) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Duguy (1996) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Duhamel (2019) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Faber (1829) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Frugone et al. (2021) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 0 | 0% |
Gannier & Petiau (2006) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 0 | 0% |
Garman (1896) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Garman (1906) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Geange (2010) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Gilbert (1915) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Gill & Thiele (1997) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Gill (1883) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Gilot et al. (1992) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Girard (2007) | 2 | 0,03% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Girondo (2023) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Godet et al. (2021) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Gomez & Voisin (2002) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 0 | 0% |
Goodall et al. (1997) | 2 | 0,03% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Goode & Bean (1895) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Goode & Bean (1896) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Gould (1844) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Goulletquer (2016) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Green (1996) | 2 | 0,03% | 2 | 0,18% | 0 | 0% | 2 | 0,19% |
Griffith & Smith (1834) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Grosser et al. (2021) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 0 | 0% |
Günther (1876) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Günther (1880) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Hall (1900) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 0 | 0% |
Heckel & Kner (1858) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Henao-osorio et al. (2021) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Howell Rivero (1936) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Humeau et al. (2020) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 0 | 0% |
Hureau (1966) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Ifremer (2024) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Iglésias et al. (2020) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Iglesias et al. (2022) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Impact-mer (2011) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Ineich et al. (2019) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Proceedings of the California Academy of Sciences, 55(10): 190-207.">Iwamoto et al. (2004) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Jiguet (2002) | 2 | 0,03% | 2 | 0,18% | 0 | 0% | 2 | 0,19% |
Jordan & Thompson (1914) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Jordan (1896) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Jouan (1863) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Jung et al. (2024) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Kasamatsu et al. (2000) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 1 | 0,09% |
Keith et al. (2002) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Keith et al. (2013) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Kuhl (1820) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Lacoste (de) (2020) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Le Corre & Jouventin (1999) | 2 | 0,03% | 2 | 0,18% | 1 | 0,1% | 1 | 0,09% |
Leaper et al. (2008) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 1 | 0,09% |
Lepechin (1769) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Lesage et al. (2024) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Lescroel et al. (2004) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Lesueur (1818) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Lesueur (1821) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Linné (1766) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Transactions of the Zoological Society of London, 1839: 1-20.">Lowe (1839) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Proceedings of the general meetings for scientific business of the Zoological Society of London, 1839: 76-92.">Lowe (1839) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Macdonald & Barron (1868) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Mahé et al. (2016) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Mas-Coma et al. (1989) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Mathews (1912) | 2 | 0,03% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Mathews (1914) | 2 | 0,03% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Mays et al. (2006) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Merrem (1820) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Mooi & Randall (2014) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Mulochau et al. (2019) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Olson & Jouventin (1996) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Oremus (2009) | 2 | 0,03% | 2 | 0,18% | 1 | 0,1% | 2 | 0,19% |
Osório (1909) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
pallas (1764) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Pallas (1831) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Pascal et al. 2006 | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Peron (2014) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Pontoppidan (1763) | 2 | 0,03% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Poss & Duhamel (1991) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Preynat (2013) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Prirodina (2004) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
protection du biotope des eaux territoriales de l'île de Clipperton dénommée « aire marine protégée dans les eaux territoriales de l'île de Clipperton » | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Pyle (1990) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Quero et al. (2013) | 2 | 0,03% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Randall & Dibattista (2013) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Raust & Sanford (2007) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Reichenow (1904) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Reinhardt (1837) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Revilliod (1914) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Richardson (1844-48) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Richer de Forges et al. (2005) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Ridoux (1989) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Rinaldi et al. (2011) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Ringler et al. (2015) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Robineau et al. (2007) | 2 | 0,03% | 2 | 0,18% | 0 | 0% | 2 | 0,19% |
Roux & Martinez (1987) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Roux et al. (1983) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Ruys & Coord (2012) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Sabine (1819) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Saint et al. (1978) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Salvin (1896) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Samaran (2008) | 2 | 0,03% | 2 | 0,18% | 1 | 0,1% | 1 | 0,09% |
Sanders et al. (2013) | 2 | 0,03% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Savouré-Soubelet et al. (in prep.) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Scopoli (1769) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Searby & Jouventin (2005) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 0 | 0% |
Shandikov (2008) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Solórzano & Sasa (2024) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Stahl et al. (1985) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Storer (1839) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Straube et al. (2011) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Temminck et al. (1838) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Tennyson et al. (2022) | 2 | 0,03% | 2 | 0,18% | 0 | 0% | 2 | 0,19% |
Thunberg (1787) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Tostain & Dujardin (1988) | 2 | 0,03% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Tremblay & Cherel (2003) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 0 | 0% |
Van Canneytet al. (2008) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Vanderwerf et al. (2006) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Vences et al. (2004) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Voisin (1971) | 2 | 0,03% | 2 | 0,18% | 0 | 0% | 2 | 0,19% |
Vollmer et al. (2019) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 1 | 0,09% |
Wantiez (comm. pers., 2008) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Waugh & Weimerskirch (2003) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Weimerskirch et al. (2009) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 0 | 0% |
Weterings & Vetter (2017) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Whitley (1939) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Wickel et al. (2020) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Wursig & Wursig (1980) | 2 | 0,03% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Yokoyama (2012) | 2 | 0,03% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Abhaya & Probst (2003) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Abhaya & Probst (2009) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Abhaya & Probst (2013) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Aboussouan & Rasonarivo (1986) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Abril et al. (1986) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Agarwal et al. (2021) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Agassiz (1857) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Al-hasson & Ali (2020) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Allen (1995) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Almeida & Vasconcelos (2023) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Almeida et al. (2019) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Amirault et al. (2022) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Andrew et al. (2008) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Anonyme (1996) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2004) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2004) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 0 | 0% |
Anonyme. (2004) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Anonyme. (2004) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 0 | 0% |
Anonyme. (2004) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Anonyme (2008) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 0 | 0% |
Anonyme. (2012) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Anonyme. (2012) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Aquarium de La Rochelle (2017) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Astrongatt (2019) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Aubouin et al. (2016) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Audige (1927) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Bailenger et al. (1965) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Bailey et al. (2023) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Baker (1977) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Baker (1985) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Baldi et al. (2023) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Balouet & Olson (1989) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Bance (2022) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Barbancey (2001) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Barbancey (2001) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Journal of the Society for the Bibliography of Natural History, 2(6): 187-189.">Barnard (1950) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Barre et al. (1977) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Bauer & Sadlier (1994) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Beaucournu (1968) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Beauvieux et al. (2024) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Behm et al. (2019) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Behm et al. (2022) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Bénito-espinal (1990) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Bennett (1831) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Benson et al. (1975) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Benson (1967) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Bertrand & Drogou (2000) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Bertrand et al. (2001) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Bertrand (1982) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Beslagic et al. (2013) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Best & Scott (1993) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Best et al. (1995) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 0 | 0% |
Bester & Roux (1986) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Bigelow et al. (1953) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Birdlife International (2013) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Blanc et al. (1993) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Bleeker (1847) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Bleeker (1852) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Bleeker (1856) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Bloch & Schneider (1801) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Bloch (1782-1784) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Bloch (1784) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Bloch (1785-1795) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Bloch (1788) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Bloch (1791) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Bloch (1792) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Bloch (1793) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Blyth (1841) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 0 | 0% |
Blyth (1860) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Bochaton et al. (2018) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Boddaert & Daubenton (1783) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Bodilis et al. (2011) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Body (2021) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Boie (1835) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Bonaparte (1837) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Bonaparte (1839[1838]) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Borsa et al. (2013) | 1 | 0,02% | 1 | 0,09% | 0 | 0% | 1 | 0,09% |
Bouchon-Navaro et al. (1992) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 0 | 0% |
Bougeard & Siblet (2000) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Boulenger (1909) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Bourgade (2021) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Bourjon & Fricke (2019) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Bouteiller & Borsa (2022) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Branch et al. (2007) | 1 | 0,02% | 1 | 0,09% | 0 | 0% | 1 | 0,09% |
Branch (2010) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 0 | 0% |
Brandt (1837) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Bray & Cribb (2002) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Brehm (1824) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Bretagnolle et al. (2000) | 1 | 0,02% | 1 | 0,09% | 0 | 0% | 1 | 0,09% |
Breuil (2009) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Brisbane et al. (2021) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Brischoux et al. (2018) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Brooke (1971) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Brownell & Cipriano (1999) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Brownell et al. (1999) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Brünnich (1768) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Bruyn et al. (2006) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 0 | 0% |
Budylenko (1977) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 0 | 0% |
Buffrenil et al. (1989) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 0 | 0% |
Buray et al. (2009) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Callou (2003) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Carzon (2012) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Catil (2013) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Causse et al. (2011) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Caut et al. (2008) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Cerchio et al. (2009) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 0 | 0% |
Chambault et al. (2020) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Chapuis et al. (2001) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Cheke & Hume (2008) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Cherel & Boxshall (2004) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 0 | 0% |
Cherel et al. (2004) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Chevreux & de Guerne (1893) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Cheylan et al. (2022) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Chocobar et al. (2023) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Cibois et al. (2015) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Ciccione (2000) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Ciccione (2001) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Ciccione (2001) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Clapham et al. (1999) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Clergeau & Pascal (2003) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Clergeau et al. (2003) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Clua & Imirizaldu (2017) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Clua & Planes (2019) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Clua et al. (2016) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Coatmeur (1999) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Collectif (2009) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 0 | 0% |
Collet & Duguy (1981) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Collett (1889) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Collett (1904) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Collier et al. (2002) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 0 | 0% |
Condamin (1979) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Corre & Jouventin (1997) | 1 | 0,02% | 1 | 0,09% | 0 | 0% | 1 | 0,09% |
Costa (1862) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Cotte et al. (2001) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 0 | 0% |
Counihan et al. (2012) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 0 | 0% |
Couteyen (2006) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Crespo et al. (1997) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Cummings et al. (2021) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Cuvier & Valenciennes (1829) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Cuvier & Valenciennes (1829) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Cuvier & Valenciennes (1830) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Cuvier & Valenciennes (1846) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Cuvier & Valenciennes (1849) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Dalebout et al. (2005) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Dalleau et al. (2014) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Danel et al. (2023) | 1 | 0,02% | 1 | 0,09% | 0 | 0% | 1 | 0,09% |
Daudin (1802) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 0 | 0% |
Daudin (1803) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Dauvin (1990) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Day (1865) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Deblock & Rose (1964) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Deblock (1966) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Deblock (1966) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Debout (2001) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Deflandre (2007) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Dekay (1842) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Dekay (1842) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Delcroix et al. (2008) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Delord et al. (2011) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Demay et al. (2014) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Deméré (2014) | 1 | 0,02% | 1 | 0,09% | 0 | 0% | 1 | 0,09% |
Deniau & Provost (2020) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Desjardins (1831) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Dieme et al. (2015) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Dollfus (1966) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Dorleans (2022) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Downie et al. (2011) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Ducatez & Devore (2023) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Duguy & Duron (1981) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Duguy & Duron (1982) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Duguy & Duron (1983) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Duguy & Duron (1984) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Duguy & Duron (1985) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Duguy et al. (1980) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Duguy et al. (2000) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Duguy (1983) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Duguy (1986) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Duguy (1988) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Duguy (1989) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Duhamel & Pruvost (2001) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Duhamel & Pruvost (2001) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Duhamel & Pruvost (2001) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Duhamel & Pruvost (2001) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Duhamel & Pruvost (2001) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Duhamel & Pruvost (2001) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Duhamel & Pruvost (2001) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Duhamel (1989) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Duhamel (1996) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Duhamel (1996) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Duhamel (1997) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Duhamel (1998) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Duhamel (1998) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Duhamel (1998) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Duhamel (1998) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Duhamel (1998) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Duhamel (1998) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Duhamel (1998) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Duhamel (1998) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Duhamel (1998) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Duhamel (1998) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Duhamel (1998) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Duhamel (1998) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Duhamel (1998) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Duhamel (2004) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Duhamel (2005) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Duméril & Bibron (1836) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Duval et al. (2019) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Ebels (2001) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Elkins & Yesou (1998) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Erens et al. (2017) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Ersts & Rosenbaum (2003) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 0 | 0% |
Eschscholtz (1829) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Eudeline (2022) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Fabricius (1780) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Fain & Beaucournu (1984) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Falla (1933) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Finnerty et al. (2021) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Finsch (1876) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Fleming & Jackson (2011) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 0 | 0% |
Fleming (1828) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Flitti & Rocha (2014) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Flood et al. (2021) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Fordyce & Marx (2012) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Forsskål (1775) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Forster (1844) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Fourmanoir (1966) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Fraga & Carvalho (2021) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Franzini et al. (2018) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Fraser-brunner (1949) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Fraser-brunner (1950) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Fretey & Bour (1980) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Fretey et al. (2023) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Fretey (1980) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Fretey (2003) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Frétey (2022) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Fricke (2015) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Friedlaender et al. (2010) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Fritz & Havaš (2007) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Furminieux (2019) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Garman (1899) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Garman (1913) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
GARNOT (1826) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Gauthier-clerc & Lambert (2002) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Géné (1839) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Geneva et al. (2013) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Genevois (1991) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Geoffroy Saint-Hilaire ([1817]) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Gérigny et al. (2020) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Gill et al. (2000) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Gill (1861) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Gill (1995) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Gill (2022) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Gillespie (1997) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Girard (1855) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Girard (1859) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Girondot et al. (2015) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Gistel (1848) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Glaw & Vences (2007) | 1 | 0,02% | 1 | 0,09% | 0 | 0% | 1 | 0,09% |
Glaw (2015) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Goiran et al. (2022) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Goode & Bean (1878-1879) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Goode & Bean (1883) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Goode (1881) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Goren (1981) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Gould (1838) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 0 | 0% |
Gray (1842) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
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% |
Gray (1872) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Griffing et al. (2022) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Groves & Grubb (2011) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Guérin-Méneville (1843) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Guichenot (1847) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Guiguen et al. (1984) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Guinet (1991) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Guinet (2004) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Gunnerus (1767) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Günther (1862) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Günther (1864) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Günther (1877) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Günther (1887) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Harrison (1981) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Hartert (1914) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Havery et al. (2018) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Hector (1875) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Hedges et al. (2014) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Hedley et al. (2007) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Heimlich-boran (1993) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Herzberg (2018) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Hombron & Jacquinot (1841) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Honsterette & Probst (1999) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 0 | 0% |
Hulley (1988) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Hureau & Ozouf-Costaz (1980) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Ifremer (2023) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Ineich & Bauer (1992) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Ineich & Massary (1997) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Ineich et al. (2017) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Ineich et al. (2017) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Ineich et al. (2018) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Ineich (2007) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Ineich (2018) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Ingels et al. (2003) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
IUCN (2015) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Jaeger et al. (2018) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Jairam et al. (2016) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Jeanne et al. (2018) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Jefferson & Barros (1997) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Jefferson et al. (1993) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Jehl et al. (1980) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Jim et al. (2022) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Johnson & Wolman (1984) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 0 | 0% |
Jordan & Gilbert (1881) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Jordan & Snyder (1902) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Jordan (1892) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Jordan (1894) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Bulweria baraui. Bulletin du Muséum National d'Histoire Naturelle, 35(6): 593-597.">Jouanin (1964) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Jouventin & Roux (1984) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Jouventin (1994) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Joyeux & Baer (1955) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Karaa et al. (2016) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Kasamatsu et al. (1995) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Kasamatsu et al. (1998) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Kayser & Wilhelm (1991) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Keith & Dorson (2003) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Keith & Machino (2003) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Keith & Mennesson (2021) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Keith (2002) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Keith (2003) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Kiszka et al. (2009) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 0 | 0% |
Heron, 36(1): 31-34.">Kiszka (2003) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 0 | 0% |
Klaver (2008) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Kostmann et al. (2023) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 0 | 0% |
Labach et al. (2021) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 0 | 0% |
Lacepède (1798) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Lacepède (1800) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Lacepède (1801) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Lancastre et al. (1976) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Lanza & Boscherini (2000) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Lapwong et al. (2021) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Lassauce et al. (2020) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Last et al. (2016) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Le Corre & Probst (1997) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Le Corre (1996) | 1 | 0,02% | 1 | 0,09% | 0 | 0% | 1 | 0,09% |
Leatherwood et al. (1979) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Legendre (1942) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Legros & Puissauve (2015) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Lescroel & Bost (2006) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Lescure et al. (2016) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Lescure et al. (2020) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Lescure (2018) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Lesson (1825) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Lesson (1828) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 0 | 0% |
Lesson (1831) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 0 | 0% |
Lesueur (1822) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Letacq (1924) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Levesque & Mathurin (2008) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Liardet & d'Auzon (2004) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Liardet (2004) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Lichtenstein (1823) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Liebart et al. (2021) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Lillywhite & Menon (2019) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Lizé (2018) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Loisier et al. (2021) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Lönnberg (1905) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Lorance et al. (2002) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Lorvelec & Pascal (2009) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Lorvelec & Vigne (2003) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Lorvelec et al. (2009) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Lorvelec et al. (2016) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Louis et al. (1992) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 0 | 0% |
Louisin & Probst (1996) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Loury & Puissauve (2016) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Loury & Puissauve (2016) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Lowe (1834) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Lowe (1843) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Lowe (1846) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Lütken (1892) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Machino (2003) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Maddalena & Zuffa (2008) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Mageski et al. (2017) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Malm (1877) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Mancino et al. (2022) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Maran & Frétey (2023) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Marchandeau & Letty (2021) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Marchandeau et al. (2003) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Marinho (2022) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Marion & Clergeau (2003) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 0 | 0% |
Marion & Marion (1982) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 0 | 0% |
Marion (2003) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Marquet et al. (2003) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Martin et al. (2021) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Mathews & Iredale (1921) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Mathews (1912) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Matsunuma & Motomura (2018) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Matsuoka et al. (1996) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Matsuoka et al. (2005) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Mckay & Milenkaya (2020) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Medetian & Miaud (2024) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Medway (2009) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Ménard et al. (2000) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Mey (2010) | 1 | 0,02% | 1 | 0,09% | 0 | 0% | 1 | 0,09% |
Meyen (1834) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Miskelly (2012) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Mocquard (1895) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Momont (1998) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Monod & Dollfus (1932) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Moreau de Jonnès (1818) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Moreau (1881) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Morel (1959) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Morelon (2015) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Morrison (2006) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Mothes et al. (2019) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Mougin (1984) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Mourier (2012) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Müller (1776) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Murase et al. (2002) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 0 | 0% |
Murphy & Harper (1916) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Murphy (1929) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Murray (1887) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Nassi et al. (1975) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Naumann (1819) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Naurois (1978) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Nelson-Smith et al. (2014) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Nicol et al. (2000) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 0 | 0% |
Noël, Meunier (2010) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Noël (2017) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Notarbartolo et al. (2020) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Okamura & Kitakado (2008) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Oliver (2011) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Olson & Warheit (1988) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
O'reilly (1818) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Owen (1853) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Pallas (1769) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Paperna & Landsberg (1989) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Pascal & Vigne (2003) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Pascal & Vigne (2003) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Pascal & Vigne (2003) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Pascal et al. (2003) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Pascal et al. (2003) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Pearman et al. (2016) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 0 | 0% |
Pennant (1787) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Pennant (1812) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Perez Canto (1886) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Perry et al. (1999) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 0 | 0% |
Peters (1854) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Peters (1874) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Peters (1875) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Petit (1976) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Pierpoint et al. (1997) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Pinaud et al. (2005) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Pinault et al. (2018) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Pitman & Ensor (2003) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Prato et al. (2022) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Prevost (1970) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Probst & Deso (2001) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Probst & Deso (2001) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 0 | 0% |
Probst & Tézier (2000) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Probst (1997) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Probst (1997) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 0 | 0% |
Probst (1998) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 0 | 0% |
Probst (2000) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Probst (2003) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 0 | 0% |
Probst (2007) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Puissauve, Legros & Poulet (2015) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Quah & Grismer (2024) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Ramsay & Ogilby (1887) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Randall & Earle (2004) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Randall (2013) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Randi et al. (2001) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Ranzani (1839) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Read et al. (2015) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Renaud et al. (2013) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Revuelta et al. (2015) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Ribic et al. (1991) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Richards (2009) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Richardson (1843) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Richardson (1844) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Ridgway (1893) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Rigby & Adamson (1997) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Rimblot et al. (1985) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Ringler et al. (2021) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Robert et al. (2002) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Robertson (2002) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Rocha et al. (2006) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Rocha et al. (2022) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Roche & Guinet (2007) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Rode (1938) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
ROGEON & SORDELLO (2012) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Rogers & Brown (1999) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Roos (2000) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Rosenbaum & Collins (2006) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 0 | 0% |
Rotschikd (1903) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Rotschild (1893) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Roule (1916) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Rüppell (1835) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Russell & Le Corre (2009) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Russell et al. (2015) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Sadlier et al. (2012) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Samaran & Guinet (2010) | 1 | 0,02% | 1 | 0,09% | 0 | 0% | 1 | 0,09% |
Samaran et al. (2010) | 1 | 0,02% | 1 | 0,09% | 0 | 0% | 1 | 0,09% |
Sanchez & Probst (2009) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 0 | 0% |
Sanchez & Probst (2014) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Sanchez et al. (2012) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Sardou (1980) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Schiebel (1910) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Schneider (1783) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Schramm et al. (2014) | 1 | 0,02% | 1 | 0,09% | 0 | 0% | 1 | 0,09% |
Schwartz & Henderson (1991) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Schweigger (1812) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Scoresby (1820) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Scoresby (1820) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Sekiguchi et al. (1992) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Sekiguchi et al. (1993) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Sekiguchi et al. (2006) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Servan (1976) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Shaver et al. (2019) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Shaw (1802) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Shaw (1804) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Siciliano & Santos (2003) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Sirovic et al. (2009) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 0 | 0% |
Smith et al. (2005) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Smith (1957) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Smith (1967) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Snyder et al. (2019) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Sonsino (1893) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
SORDELLO (2012) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Spitz et al. (2007) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Springer (1941) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Stahl & Weimerskirch (1982) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 0 | 0% |
Stahl et al. (1984) | 1 | 0,02% | 1 | 0,09% | 0 | 0% | 1 | 0,09% |
Steadman & Bollt (2010) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 0 | 0% |
Stejneger (1893) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Stelfox et al. (2020) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Storer (1846) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Storer (1848) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Sueur (2018) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Széles et al. (2018) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Taberlet (1983) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Taquet (1994) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Tea & Larson (2023) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Terrasse & Terrasse (1969) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
The International Barcode of Life Consortium (2016) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Thévenot (2014) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Thibault et al. (2023) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Thiebot et al. (2011) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Thiebot et al. (2015) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Tougaard (2010) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Tsadok et al. (2015) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Tunstall (1880) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
UICN France et al. (2013) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 0 | 0% |
Uicn et al. (2019) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
UICN (2009) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Vaillant (1888) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Van & Kampen (1907) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
van den Burg et al. (2021) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Van Dijk et al. (2014) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Van Guelpen (2016) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Vandelli (1761) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Vanwaerebeek et al. (1995) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Vaslet & Agrnsm (2018) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Vásquez-cruz & Kelly-hernández (2024) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Viale & Frontier (1989) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Vieillot (1819) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Viel (2021) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Viganò & Corso (2015) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Vigne & Pascal (2003) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Von May et al. (2021) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Waayers et al. (2011) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Waite (1914) | 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 | 0,09% | 1 | 0,1% | 0 | 0% |
Wantiez (2000) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Warham et al. (1977) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Watson et al. (1975) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Weerdt et al. (2021) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Weerdt (2023) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 0 | 0% |
Weimerskirch & Jouventin (1998) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Weimerskirch et al. (2018) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Weinell et al. (2019) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Whitley (1933) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Whitley (1934) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Whitley (1944) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Whitley (1948) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Whitley (1950) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Wickel & Fricke (2022) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Wickel et al. (2016) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Williams et al. (2009) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 0 | 0% |
Williams (2018) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Wink et al. (1979) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Winterbottom & Hoese (2015) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Wood (1848) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Wursig et al. (2007) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Yang et al. (2019) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Yarrell (1839) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Zdunek (2022) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Zhukov (2020) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Zug et al. (2007) | 1 | 0,02% | 1 | 0,09% | 1 | 0,1% | 1 | 0,09% |
Zugmayer (1914) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |