Vertébrés des îles Éparses
744 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
Référence | Total | Valides | Espèces | Taxons terminaux | ||||
---|---|---|---|---|---|---|---|---|
nb | % | nb | % | nb | % | nb | % | |
Wickel & Jamon (2010) | 403 | 9,35% | 386 | 59,94% | 385 | 61,4% | 385 | 61,11% |
Fricke et al. (2009) | 395 | 9,17% | 378 | 58,7% | 378 | 60,29% | 376 | 59,68% |
Fricke et al. (2011) | 392 | 9,1% | 378 | 58,7% | 377 | 60,13% | 377 | 59,84% |
Fricke et al. (2013) | 382 | 8,87% | 369 | 57,3% | 368 | 58,69% | 367 | 58,25% |
Siu et al. (2017) | 293 | 6,8% | 284 | 44,1% | 284 | 45,3% | 283 | 44,92% |
Chabanet & Durville (2005) | 279 | 6,47% | 250 | 38,82% | 250 | 39,87% | 250 | 39,68% |
Williams et al. (2006) | 240 | 5,57% | 229 | 35,56% | 229 | 36,52% | 228 | 36,19% |
Delrieu-Trottin et al. (2015) | 191 | 4,43% | 183 | 28,42% | 182 | 29,03% | 183 | 29,05% |
Kulbicki et al. (2000) | 177 | 4,11% | 156 | 24,22% | 156 | 24,88% | 155 | 24,6% |
Uicn et al. (2015) | 153 | 3,55% | 137 | 21,27% | 132 | 21,05% | 119 | 18,89% |
Bacchet et al. (2007) | 113 | 2,62% | 107 | 16,61% | 107 | 17,07% | 107 | 16,98% |
Béarez & Bouffandeau (2019) | 69 | 1,6% | 67 | 10,4% | 67 | 10,69% | 66 | 10,48% |
Richard et al. (1982) | 62 | 1,44% | 19 | 2,95% | 19 | 3,03% | 19 | 3,02% |
Rinaldi (2016) | 60 | 1,39% | 60 | 9,32% | 60 | 9,57% | 40 | 6,35% |
Kulbicki (comm. pers., 2011) | 54 | 1,25% | 48 | 7,45% | 48 | 7,66% | 48 | 7,62% |
Allen (comm. pers., 2009) | 49 | 1,14% | 48 | 7,45% | 48 | 7,66% | 47 | 7,46% |
Questel & Le Quellec (2012) | 47 | 1,09% | 45 | 6,99% | 45 | 7,18% | 38 | 6,03% |
Carzon et al. (2016) | 45 | 1,04% | 45 | 6,99% | 45 | 7,18% | 30 | 4,76% |
Estrade et al. (2016) | 45 | 1,04% | 45 | 6,99% | 45 | 7,18% | 30 | 4,76% |
Linnaeus (1758) | 43 | 1% | 12 | 1,86% | 12 | 1,91% | 12 | 1,9% |
Questel (2020) | 42 | 0,97% | 40 | 6,21% | 39 | 6,22% | 35 | 5,56% |
Uicn et al. (2017) | 36 | 0,84% | 36 | 5,59% | 36 | 5,74% | 29 | 4,6% |
Legand (1950) | 33 | 0,77% | 16 | 2,48% | 16 | 2,55% | 16 | 2,54% |
Béarez & Séret (2009) | 30 | 0,7% | 29 | 4,5% | 29 | 4,63% | 29 | 4,6% |
Rocamora (2004) | 26 | 0,6% | 23 | 3,57% | 22 | 3,51% | 22 | 3,49% |
Barau et al. (2005) | 25 | 0,58% | 22 | 3,42% | 22 | 3,51% | 20 | 3,17% |
Mertens & Wermuth (1960) | 21 | 0,49% | 0 | 0% | 0 | 0% | 0 | 0% |
Fourriére et al. (2014) | 20 | 0,46% | 19 | 2,95% | 19 | 3,03% | 19 | 3,02% |
Aulagnier (2009) | 17 | 0,39% | 17 | 2,64% | 17 | 2,71% | 14 | 2,22% |
UICN Comité français, OFB & MNHN (2021) | 17 | 0,39% | 17 | 2,64% | 17 | 2,71% | 14 | 2,22% |
Yokoyama (2013) | 17 | 0,39% | 17 | 2,64% | 17 | 2,71% | 14 | 2,22% |
Levesque & Delcroix (2018) | 16 | 0,37% | 16 | 2,48% | 15 | 2,39% | 16 | 2,54% |
Bordin et al. (2021) | 15 | 0,35% | 15 | 2,33% | 15 | 2,39% | 10 | 1,59% |
Bouchon-Navaro et al. (2005) | 15 | 0,35% | 10 | 1,55% | 10 | 1,59% | 9 | 1,43% |
Charrassin (2016) | 15 | 0,35% | 15 | 2,33% | 15 | 2,39% | 10 | 1,59% |
Charrassin (2016) | 15 | 0,35% | 15 | 2,33% | 15 | 2,39% | 10 | 1,59% |
G.E.M.M. (2012) | 15 | 0,35% | 15 | 2,33% | 15 | 2,39% | 10 | 1,59% |
Jarrett & Shirihai (2014) | 15 | 0,35% | 15 | 2,33% | 15 | 2,39% | 10 | 1,59% |
Moutou (2016) | 15 | 0,35% | 15 | 2,33% | 15 | 2,39% | 10 | 1,59% |
Sanchez et al. (2019) | 15 | 0,35% | 13 | 2,02% | 12 | 1,91% | 13 | 2,06% |
Spitz et al. (2016) | 15 | 0,35% | 15 | 2,33% | 15 | 2,39% | 10 | 1,59% |
Thoisy & Bordin (2016) | 15 | 0,35% | 15 | 2,33% | 15 | 2,39% | 10 | 1,59% |
Urtizberea (2016) | 15 | 0,35% | 15 | 2,33% | 15 | 2,39% | 10 | 1,59% |
Van Dijk et al. (2012) | 15 | 0,35% | 12 | 1,86% | 12 | 1,91% | 12 | 1,9% |
Catzeflis (2012) | 14 | 0,32% | 14 | 2,17% | 14 | 2,23% | 9 | 1,43% |
Gannier (2001) | 14 | 0,32% | 14 | 2,17% | 14 | 2,23% | 10 | 1,59% |
Gannier (2002) | 14 | 0,32% | 14 | 2,17% | 14 | 2,23% | 10 | 1,59% |
Garrigue (2007) | 14 | 0,32% | 14 | 2,17% | 14 | 2,23% | 10 | 1,59% |
Lorvelec et al. (2007) | 14 | 0,32% | 14 | 2,17% | 14 | 2,23% | 14 | 2,22% |
Weimerskirch et al. (2009) | 14 | 0,32% | 13 | 2,02% | 13 | 2,07% | 11 | 1,75% |
Dewynter et al. (2021) | 13 | 0,3% | 13 | 2,02% | 13 | 2,07% | 10 | 1,59% |
Gannier (2000) | 13 | 0,3% | 13 | 2,02% | 13 | 2,07% | 9 | 1,43% |
Gannier (2009) | 13 | 0,3% | 13 | 2,02% | 13 | 2,07% | 9 | 1,43% |
Gill (1995) | 13 | 0,3% | 12 | 1,86% | 12 | 1,91% | 11 | 1,75% |
Kiszka et al. (2009) | 13 | 0,3% | 10 | 1,55% | 10 | 1,59% | 10 | 1,59% |
Kiszka et al.(2007) | 13 | 0,3% | 13 | 2,02% | 13 | 2,07% | 9 | 1,43% |
Massary et al. (2020) | 12 | 0,28% | 12 | 1,86% | 12 | 1,91% | 11 | 1,75% |
Probst et al. (2022) | 12 | 0,28% | 12 | 1,86% | 12 | 1,91% | 11 | 1,75% |
UICN Comité français, OFB, MNHN & GEPOMAY (2025) | 12 | 0,28% | 12 | 1,86% | 12 | 1,91% | 12 | 1,9% |
Remsen et al. (2013) | 11 | 0,26% | 11 | 1,71% | 11 | 1,75% | 11 | 1,75% |
Béarez et al. (2017) | 10 | 0,23% | 10 | 1,55% | 10 | 1,59% | 10 | 1,59% |
Deblock et al. (1960) | 10 | 0,23% | 7 | 1,09% | 7 | 1,12% | 7 | 1,11% |
Kiszka et al. (2010) | 10 | 0,23% | 10 | 1,55% | 10 | 1,59% | 7 | 1,11% |
Laran et al. (2011) | 10 | 0,23% | 10 | 1,55% | 10 | 1,59% | 7 | 1,11% |
Randall & Earle (2000) | 10 | 0,23% | 9 | 1,4% | 8 | 1,28% | 9 | 1,43% |
Soubeyran et al. (2011) | 10 | 0,23% | 10 | 1,55% | 10 | 1,59% | 10 | 1,59% |
Thibault et al. (2014) | 10 | 0,23% | 10 | 1,55% | 10 | 1,59% | 8 | 1,27% |
Caceres (2002) | 9 | 0,21% | 4 | 0,62% | 2 | 0,32% | 4 | 0,63% |
Clements (2012) | 9 | 0,21% | 9 | 1,4% | 6 | 0,96% | 8 | 1,27% |
Dulau-Drouot et al. (2008) | 9 | 0,21% | 9 | 1,4% | 9 | 1,44% | 5 | 0,79% |
Gargominy et al. (1996) | 9 | 0,21% | 9 | 1,4% | 9 | 1,44% | 9 | 1,43% |
Probst (2001) | 9 | 0,21% | 7 | 1,09% | 7 | 1,12% | 6 | 0,95% |
Barré (2021) | 8 | 0,19% | 8 | 1,24% | 8 | 1,28% | 8 | 1,27% |
Dewynter et al. (2022) | 8 | 0,19% | 8 | 1,24% | 8 | 1,28% | 8 | 1,27% |
Dewynter et al. (2023) | 8 | 0,19% | 8 | 1,24% | 8 | 1,28% | 8 | 1,27% |
Etcheberry & Abraham (2009) | 8 | 0,19% | 7 | 1,09% | 7 | 1,12% | 7 | 1,11% |
Probst et al. (2001) | 8 | 0,19% | 3 | 0,47% | 3 | 0,48% | 3 | 0,48% |
Probst (1997) | 8 | 0,19% | 4 | 0,62% | 2 | 0,32% | 3 | 0,48% |
Probst (1998) | 8 | 0,19% | 4 | 0,62% | 4 | 0,64% | 4 | 0,63% |
Questel et al. (2023) | 8 | 0,19% | 8 | 1,24% | 8 | 1,28% | 8 | 1,27% |
Questel et al. (2023) | 8 | 0,19% | 8 | 1,24% | 8 | 1,28% | 8 | 1,27% |
Ronot (2007) | 8 | 0,19% | 7 | 1,09% | 7 | 1,12% | 6 | 0,95% |
Smith (1997) | 8 | 0,19% | 8 | 1,24% | 6 | 0,96% | 8 | 1,27% |
Ausilio & Zotier (1989) | 7 | 0,16% | 7 | 1,09% | 7 | 1,12% | 7 | 1,11% |
Dewynter et al. (2019) | 7 | 0,16% | 7 | 1,09% | 7 | 1,12% | 7 | 1,11% |
Dewynter et al. (2023) | 7 | 0,16% | 7 | 1,09% | 7 | 1,12% | 7 | 1,11% |
Henderson & Breuil (2012) | 7 | 0,16% | 4 | 0,62% | 4 | 0,64% | 4 | 0,63% |
Lambert (1988) | 7 | 0,16% | 4 | 0,62% | 4 | 0,64% | 3 | 0,48% |
Massary et al. (2018) | 7 | 0,16% | 7 | 1,09% | 7 | 1,12% | 7 | 1,11% |
Massary et al. (2021) | 7 | 0,16% | 7 | 1,09% | 7 | 1,12% | 7 | 1,11% |
Pearman et al. (2020) | 7 | 0,16% | 7 | 1,09% | 7 | 1,12% | 7 | 1,11% |
Safford & Hawkins (2013) | 7 | 0,16% | 7 | 1,09% | 7 | 1,12% | 6 | 0,95% |
Samaran & Guinet (2009) | 7 | 0,16% | 7 | 1,09% | 7 | 1,12% | 5 | 0,79% |
Sanchez (2020) | 7 | 0,16% | 7 | 1,09% | 7 | 1,12% | 6 | 0,95% |
Theuerkauf et al. (2010) | 7 | 0,16% | 7 | 1,09% | 7 | 1,12% | 7 | 1,11% |
Tirvengadum & Bour (1985) | 7 | 0,16% | 6 | 0,93% | 6 | 0,96% | 6 | 0,95% |
Turpin & Probst (1998) | 7 | 0,16% | 4 | 0,62% | 2 | 0,32% | 4 | 0,63% |
Aulagnier et al. (2017) | 6 | 0,14% | 6 | 0,93% | 6 | 0,96% | 6 | 0,95% |
Belfan & Conde (2016) | 6 | 0,14% | 6 | 0,93% | 6 | 0,96% | 6 | 0,95% |
Camiñas et al. (2021) | 6 | 0,14% | 6 | 0,93% | 6 | 0,96% | 6 | 0,95% |
Compagno (1984) | 6 | 0,14% | 6 | 0,93% | 6 | 0,96% | 6 | 0,95% |
Justine et al. (2010) | 6 | 0,14% | 6 | 0,93% | 6 | 0,96% | 6 | 0,95% |
Kronen et al. (2009) | 6 | 0,14% | 6 | 0,93% | 6 | 0,96% | 6 | 0,95% |
Massary et al. (2017) | 6 | 0,14% | 6 | 0,93% | 6 | 0,96% | 6 | 0,95% |
Pavan-Kumar et al. (2018) | 6 | 0,14% | 5 | 0,78% | 5 | 0,8% | 5 | 0,79% |
Pinault et al. (2013) | 6 | 0,14% | 6 | 0,93% | 6 | 0,96% | 6 | 0,95% |
Poey (1858-61) | 6 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Probst et al. (2000) | 6 | 0,14% | 5 | 0,78% | 3 | 0,48% | 5 | 0,79% |
Probst (1997) | 6 | 0,14% | 2 | 0,31% | 2 | 0,32% | 2 | 0,32% |
Séret (1997) | 6 | 0,14% | 6 | 0,93% | 6 | 0,96% | 6 | 0,95% |
Bauer & Sadlier (2000) | 5 | 0,12% | 3 | 0,47% | 3 | 0,48% | 3 | 0,48% |
Bioinsight/diren & Guyane (2006) | 5 | 0,12% | 5 | 0,78% | 5 | 0,8% | 5 | 0,79% |
Casale et al. (2021) | 5 | 0,12% | 5 | 0,78% | 5 | 0,8% | 5 | 0,79% |
Chevalier (2006) | 5 | 0,12% | 5 | 0,78% | 5 | 0,8% | 5 | 0,79% |
Ciccione et al. (2011) | 5 | 0,12% | 5 | 0,78% | 5 | 0,8% | 5 | 0,79% |
Collette & Nauen (1983) | 5 | 0,12% | 5 | 0,78% | 5 | 0,8% | 5 | 0,79% |
Crillon & Cuzange (2020) | 5 | 0,12% | 5 | 0,78% | 5 | 0,8% | 5 | 0,79% |
Dewynter et al. (2019) | 5 | 0,12% | 5 | 0,78% | 5 | 0,8% | 5 | 0,79% |
Duffaut et al. (2011) | 5 | 0,12% | 5 | 0,78% | 5 | 0,8% | 5 | 0,79% |
Entraygues (2014) | 5 | 0,12% | 5 | 0,78% | 5 | 0,8% | 5 | 0,79% |
Étaix-bonnin et al. (2011) | 5 | 0,12% | 5 | 0,78% | 5 | 0,8% | 5 | 0,79% |
Fretey & Triplet (2022) | 5 | 0,12% | 5 | 0,78% | 5 | 0,8% | 5 | 0,79% |
Kronen et al. (2008) | 5 | 0,12% | 5 | 0,78% | 5 | 0,8% | 5 | 0,79% |
Le Scao et al. (2011) | 5 | 0,12% | 5 | 0,78% | 5 | 0,8% | 5 | 0,79% |
Letourneur et al. (2004) | 5 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Lowe et al. (2007) | 5 | 0,12% | 5 | 0,78% | 5 | 0,8% | 5 | 0,79% |
Massary et al. (2019) | 5 | 0,12% | 5 | 0,78% | 5 | 0,8% | 5 | 0,79% |
Perrin et al. (2002) | 5 | 0,12% | 5 | 0,78% | 5 | 0,8% | 3 | 0,48% |
Prévost & Mougin (1970) | 5 | 0,12% | 5 | 0,78% | 5 | 0,8% | 4 | 0,63% |
Read & Farman (2018) | 5 | 0,12% | 5 | 0,78% | 5 | 0,8% | 5 | 0,79% |
Read et al. (2023) | 5 | 0,12% | 5 | 0,78% | 5 | 0,8% | 5 | 0,79% |
Rhodin et al. (2017) | 5 | 0,12% | 3 | 0,47% | 3 | 0,48% | 3 | 0,48% |
Sauvignet et al. (2000) | 5 | 0,12% | 5 | 0,78% | 5 | 0,8% | 5 | 0,79% |
Shirihai (2003) | 5 | 0,12% | 5 | 0,78% | 5 | 0,8% | 3 | 0,48% |
Snodgrass & Heller (1905) | 5 | 0,12% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Tostain et al. (2013) | 5 | 0,12% | 5 | 0,78% | 5 | 0,8% | 4 | 0,63% |
Uicn et al. (2015) | 5 | 0,12% | 5 | 0,78% | 5 | 0,8% | 4 | 0,63% |
Uicn et al. (2020) | 5 | 0,12% | 5 | 0,78% | 5 | 0,8% | 3 | 0,48% |
Wickel et al. (2014) | 5 | 0,12% | 4 | 0,62% | 4 | 0,64% | 4 | 0,63% |
Barrioz & Morinière (2007) | 4 | 0,09% | 4 | 0,62% | 4 | 0,64% | 4 | 0,63% |
Bochaton et al. (2021) | 4 | 0,09% | 4 | 0,62% | 4 | 0,64% | 4 | 0,63% |
Bouchon-Navaro & Louis (1986) | 4 | 0,09% | 3 | 0,47% | 3 | 0,48% | 3 | 0,48% |
Bour et al. (2008) | 4 | 0,09% | 4 | 0,62% | 4 | 0,64% | 4 | 0,63% |
Breuil (2002) | 4 | 0,09% | 2 | 0,31% | 2 | 0,32% | 2 | 0,32% |
Diaz & Cuzange (2009) | 4 | 0,09% | 4 | 0,62% | 4 | 0,64% | 2 | 0,32% |
Frenot et al. (2005) | 4 | 0,09% | 4 | 0,62% | 4 | 0,64% | 4 | 0,63% |
Fretey & Lescure (1999) | 4 | 0,09% | 4 | 0,62% | 4 | 0,64% | 4 | 0,63% |
Fricke et al. (2024) | 4 | 0,09% | 4 | 0,62% | 4 | 0,64% | 4 | 0,63% |
González-sánchez et al. (2021) | 4 | 0,09% | 4 | 0,62% | 4 | 0,64% | 4 | 0,63% |
Hoff & Daszkiewicz (2001) | 4 | 0,09% | 4 | 0,62% | 4 | 0,64% | 4 | 0,63% |
Horner (2007) | 4 | 0,09% | 2 | 0,31% | 2 | 0,32% | 2 | 0,32% |
Ineich (2016) | 4 | 0,09% | 4 | 0,62% | 4 | 0,64% | 4 | 0,63% |
Kojadinovic et al. (2007) | 4 | 0,09% | 2 | 0,31% | 2 | 0,32% | 0 | 0% |
Lescure et al. (2012) | 4 | 0,09% | 4 | 0,62% | 4 | 0,64% | 4 | 0,63% |
Letourneur & Maggiorani (1995) | 4 | 0,09% | 4 | 0,62% | 4 | 0,64% | 4 | 0,63% |
Lorvelec & Pascal (2009) | 4 | 0,09% | 4 | 0,62% | 4 | 0,64% | 4 | 0,63% |
Marshall et al. (2009) | 4 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Muratet (2015) | 4 | 0,09% | 4 | 0,62% | 4 | 0,64% | 4 | 0,63% |
Randall (1998) | 4 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Robineau & Duhamel (2006) | 4 | 0,09% | 4 | 0,62% | 4 | 0,64% | 2 | 0,32% |
Röll et al. (2023) | 4 | 0,09% | 4 | 0,62% | 4 | 0,64% | 4 | 0,63% |
Routtier et al. (2023) | 4 | 0,09% | 2 | 0,31% | 2 | 0,32% | 2 | 0,32% |
Rüppell (1835) | 4 | 0,09% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Sanchez & Probst (2016) | 4 | 0,09% | 4 | 0,62% | 4 | 0,64% | 4 | 0,63% |
AAMP (2012) | 3 | 0,07% | 3 | 0,47% | 3 | 0,48% | 0 | 0% |
Arnold & Ovenden (2014) | 3 | 0,07% | 3 | 0,47% | 3 | 0,48% | 3 | 0,48% |
Blanc (1909) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Boer et al. (1999) | 3 | 0,07% | 3 | 0,47% | 3 | 0,48% | 3 | 0,48% |
Borsa et al. (2014) | 3 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Brugneaux & Pérès (2006) | 3 | 0,07% | 3 | 0,47% | 3 | 0,48% | 3 | 0,48% |
Burneleau (1983) | 3 | 0,07% | 3 | 0,47% | 3 | 0,48% | 3 | 0,48% |
Busala et al. (2024) | 3 | 0,07% | 2 | 0,31% | 2 | 0,32% | 2 | 0,32% |
Catzeflis (2018) | 3 | 0,07% | 3 | 0,47% | 3 | 0,48% | 3 | 0,48% |
Champagne et al. (1997) | 3 | 0,07% | 3 | 0,47% | 3 | 0,48% | 3 | 0,48% |
Cheke (1987) | 3 | 0,07% | 3 | 0,47% | 3 | 0,48% | 3 | 0,48% |
Cuvier & Valenciennes (1830-1832) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Cuvier & Valenciennes ([1832]) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Delcroix et al. (2011) | 3 | 0,07% | 3 | 0,47% | 3 | 0,48% | 3 | 0,48% |
Desbrosses & Etcheberry (1987) | 3 | 0,07% | 2 | 0,31% | 2 | 0,32% | 0 | 0% |
Dewynter (2021) | 3 | 0,07% | 3 | 0,47% | 3 | 0,48% | 3 | 0,48% |
Dubief & Gallais (2011) | 3 | 0,07% | 3 | 0,47% | 3 | 0,48% | 3 | 0,48% |
Duguy et al. (1998) | 3 | 0,07% | 3 | 0,47% | 3 | 0,48% | 3 | 0,48% |
Duguy et al. (2007) | 3 | 0,07% | 3 | 0,47% | 3 | 0,48% | 3 | 0,48% |
Duguy (1988) | 3 | 0,07% | 3 | 0,47% | 3 | 0,48% | 3 | 0,48% |
Duguy (1994) | 3 | 0,07% | 3 | 0,47% | 3 | 0,48% | 3 | 0,48% |
Duguy (1997) | 3 | 0,07% | 3 | 0,47% | 3 | 0,48% | 3 | 0,48% |
Durant et al. (2013) | 3 | 0,07% | 3 | 0,47% | 3 | 0,48% | 3 | 0,48% |
Girondot (2011) | 3 | 0,07% | 3 | 0,47% | 3 | 0,48% | 3 | 0,48% |
Goiran & Shine (2020) | 3 | 0,07% | 3 | 0,47% | 3 | 0,48% | 3 | 0,48% |
Gronow (1854) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Guth (1971) | 3 | 0,07% | 3 | 0,47% | 3 | 0,48% | 2 | 0,32% |
Hutchinson et al. (2019) | 3 | 0,07% | 3 | 0,47% | 3 | 0,48% | 3 | 0,48% |
IUCN (2012) | 3 | 0,07% | 3 | 0,47% | 3 | 0,48% | 1 | 0,16% |
Jourdan (2020) | 3 | 0,07% | 3 | 0,47% | 3 | 0,48% | 3 | 0,48% |
Klunzinger (1871) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Laran et al. (2012) | 3 | 0,07% | 3 | 0,47% | 3 | 0,48% | 2 | 0,32% |
Linnaeus (1766) | 3 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Méheust et al. (2018) | 3 | 0,07% | 3 | 0,47% | 3 | 0,48% | 3 | 0,48% |
Morinière & Dell'amico (2011) | 3 | 0,07% | 3 | 0,47% | 3 | 0,48% | 3 | 0,48% |
Mourier et al. (2013) | 3 | 0,07% | 3 | 0,47% | 3 | 0,48% | 3 | 0,48% |
Müller & Henle (1841) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Poisson (1999) | 3 | 0,07% | 3 | 0,47% | 3 | 0,48% | 3 | 0,48% |
Postel (1965) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Probst (1997) | 3 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Probst (2001) | 3 | 0,07% | 2 | 0,31% | 2 | 0,32% | 1 | 0,16% |
Rafinesque (1810) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Read & Jean (2021) | 3 | 0,07% | 3 | 0,47% | 3 | 0,48% | 3 | 0,48% |
Rignault & Chevallier (2017) | 3 | 0,07% | 3 | 0,47% | 3 | 0,48% | 3 | 0,48% |
Rousseau (2010) | 3 | 0,07% | 3 | 0,47% | 3 | 0,48% | 3 | 0,48% |
Roux (1913) | 3 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Wallach (2020) | 3 | 0,07% | 2 | 0,31% | 2 | 0,32% | 2 | 0,32% |
Aulagnier (2021) | 2 | 0,05% | 2 | 0,31% | 2 | 0,32% | 2 | 0,32% |
Baldi et al. (2022) | 2 | 0,05% | 2 | 0,31% | 2 | 0,32% | 2 | 0,32% |
Bartoli (1972) | 2 | 0,05% | 2 | 0,31% | 2 | 0,32% | 2 | 0,32% |
Bauer et al. (2010) | 2 | 0,05% | 2 | 0,31% | 2 | 0,32% | 2 | 0,32% |
Bauer (1987) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Bennett (1834) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Bloch & Schneider (1801) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Boer & Simmonds (2000) | 2 | 0,05% | 2 | 0,31% | 2 | 0,32% | 2 | 0,32% |
Boer (2000) | 2 | 0,05% | 2 | 0,31% | 2 | 0,32% | 1 | 0,16% |
Boettger (1913) | 2 | 0,05% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Bonnaterre (1789) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Bourjon & Fricke (2016) | 2 | 0,05% | 2 | 0,31% | 2 | 0,32% | 2 | 0,32% |
Bourjon et al. (2018) | 2 | 0,05% | 2 | 0,31% | 2 | 0,32% | 2 | 0,32% |
Breuil et al. (2010) | 2 | 0,05% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Brygoo (1985) | 2 | 0,05% | 2 | 0,31% | 0 | 0% | 2 | 0,32% |
Butaud (2021) | 2 | 0,05% | 2 | 0,31% | 2 | 0,32% | 2 | 0,32% |
Chapuis et al. (2004) | 2 | 0,05% | 2 | 0,31% | 2 | 0,32% | 2 | 0,32% |
Chartier et al. (2007) | 2 | 0,05% | 2 | 0,31% | 2 | 0,32% | 0 | 0% |
Cheke (2010) | 2 | 0,05% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Chevallier et al. (2023) | 2 | 0,05% | 2 | 0,31% | 2 | 0,32% | 2 | 0,32% |
Cole et al. (2005) | 2 | 0,05% | 2 | 0,31% | 2 | 0,32% | 2 | 0,32% |
Collinson et al. (2017) | 2 | 0,05% | 2 | 0,31% | 2 | 0,32% | 2 | 0,32% |
Commission de l’Avifaune Française (2016) | 2 | 0,05% | 2 | 0,31% | 2 | 0,32% | 1 | 0,16% |
Cuvier (1829) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
D'Amico (2001) | 2 | 0,05% | 2 | 0,31% | 2 | 0,32% | 2 | 0,32% |
Daniel et al. (2020) | 2 | 0,05% | 2 | 0,31% | 2 | 0,32% | 0 | 0% |
Odontaspis ferox" Agassiz dans le Golf de Gascogne. Bulletin de la Société zoologique de France, 54: 233-235.">Desbrosses (1930) | 2 | 0,05% | 2 | 0,31% | 2 | 0,32% | 2 | 0,32% |
Dewynter et al. (2020) | 2 | 0,05% | 2 | 0,31% | 2 | 0,32% | 2 | 0,32% |
Duguy et al. (1997) | 2 | 0,05% | 2 | 0,31% | 2 | 0,32% | 2 | 0,32% |
Duguy et al. (1999) | 2 | 0,05% | 2 | 0,31% | 2 | 0,32% | 2 | 0,32% |
Duguy et al. (2000) | 2 | 0,05% | 2 | 0,31% | 2 | 0,32% | 2 | 0,32% |
Duguy et al. (2002) | 2 | 0,05% | 2 | 0,31% | 2 | 0,32% | 2 | 0,32% |
Duguy et al. (2003) | 2 | 0,05% | 2 | 0,31% | 2 | 0,32% | 2 | 0,32% |
Duguy et al. (2004) | 2 | 0,05% | 2 | 0,31% | 2 | 0,32% | 2 | 0,32% |
Duguy et al. (2006) | 2 | 0,05% | 2 | 0,31% | 2 | 0,32% | 2 | 0,32% |
Duguy (1987) | 2 | 0,05% | 2 | 0,31% | 2 | 0,32% | 2 | 0,32% |
Duguy (1990) | 2 | 0,05% | 2 | 0,31% | 2 | 0,32% | 2 | 0,32% |
Duguy (1992) | 2 | 0,05% | 2 | 0,31% | 2 | 0,32% | 2 | 0,32% |
Duguy (1993) | 2 | 0,05% | 2 | 0,31% | 2 | 0,32% | 2 | 0,32% |
Duguy (1995) | 2 | 0,05% | 2 | 0,31% | 2 | 0,32% | 2 | 0,32% |
Duguy (1996) | 2 | 0,05% | 2 | 0,31% | 2 | 0,32% | 2 | 0,32% |
Fort & Barrière (2021) | 2 | 0,05% | 2 | 0,31% | 2 | 0,32% | 2 | 0,32% |
Fourt et al. (2017) | 2 | 0,05% | 2 | 0,31% | 2 | 0,32% | 2 | 0,32% |
Gannier & Petiau (2006) | 2 | 0,05% | 2 | 0,31% | 2 | 0,32% | 0 | 0% |
Geange (2010) | 2 | 0,05% | 2 | 0,31% | 2 | 0,32% | 2 | 0,32% |
Gilot et al. (1992) | 2 | 0,05% | 2 | 0,31% | 2 | 0,32% | 2 | 0,32% |
Girard (2007) | 2 | 0,05% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Girondo (2023) | 2 | 0,05% | 2 | 0,31% | 2 | 0,32% | 2 | 0,32% |
Gmelin (1789) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Godet et al. (2021) | 2 | 0,05% | 2 | 0,31% | 2 | 0,32% | 2 | 0,32% |
Goulletquer (2016) | 2 | 0,05% | 2 | 0,31% | 2 | 0,32% | 2 | 0,32% |
Griffith & Smith (1834) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Günther (1880) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Henao-osorio et al. (2021) | 2 | 0,05% | 2 | 0,31% | 2 | 0,32% | 2 | 0,32% |
Proceedings of the Zoological Society of London, 1907: 1035-1037.">Hopkinson (1907) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Humeau et al. (2020) | 2 | 0,05% | 2 | 0,31% | 2 | 0,32% | 0 | 0% |
Ifremer (2024) | 2 | 0,05% | 2 | 0,31% | 2 | 0,32% | 2 | 0,32% |
Ineich et al. (2019) | 2 | 0,05% | 2 | 0,31% | 2 | 0,32% | 2 | 0,32% |
Jouan (1863) | 2 | 0,05% | 2 | 0,31% | 2 | 0,32% | 2 | 0,32% |
Karadjian et al. (2022) | 2 | 0,05% | 2 | 0,31% | 2 | 0,32% | 2 | 0,32% |
Keith et al. (2006) | 2 | 0,05% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Keith et al. (2013) | 2 | 0,05% | 2 | 0,31% | 2 | 0,32% | 2 | 0,32% |
Lacoste (de) (2020) | 2 | 0,05% | 2 | 0,31% | 2 | 0,32% | 2 | 0,32% |
Le Corre & Jouventin (1999) | 2 | 0,05% | 2 | 0,31% | 1 | 0,16% | 1 | 0,16% |
Lepechin (1769) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Linné (1766) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Transactions of the Zoological Society of London, 1839: 1-20.">Lowe (1839) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Macdonald & Barron (1868) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Mas-Coma et al. (1989) | 2 | 0,05% | 2 | 0,31% | 2 | 0,32% | 2 | 0,32% |
Mathews (1914) | 2 | 0,05% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Matsuoka et al. (2005) | 2 | 0,05% | 2 | 0,31% | 2 | 0,32% | 0 | 0% |
Merrem (1820) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Mooi & Randall (2014) | 2 | 0,05% | 2 | 0,31% | 2 | 0,32% | 2 | 0,32% |
Mulochau et al. (2019) | 2 | 0,05% | 2 | 0,31% | 2 | 0,32% | 2 | 0,32% |
pallas (1764) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Peron (2014) | 2 | 0,05% | 2 | 0,31% | 2 | 0,32% | 2 | 0,32% |
Potin (2013) | 2 | 0,05% | 2 | 0,31% | 2 | 0,32% | 2 | 0,32% |
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 | 0,05% | 2 | 0,31% | 2 | 0,32% | 2 | 0,32% |
Pyle (1990) | 2 | 0,05% | 2 | 0,31% | 2 | 0,32% | 2 | 0,32% |
Quero et al. (2013) | 2 | 0,05% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Randall & Dibattista (2013) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Revilliod (1914) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Rinaldi et al. (2011) | 2 | 0,05% | 2 | 0,31% | 2 | 0,32% | 2 | 0,32% |
Ringler et al. (2015) | 2 | 0,05% | 2 | 0,31% | 2 | 0,32% | 2 | 0,32% |
Risso (1810) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Robineau (2005) | 2 | 0,05% | 2 | 0,31% | 2 | 0,32% | 0 | 0% |
Rossi-santos et al. (2007) | 2 | 0,05% | 2 | 0,31% | 2 | 0,32% | 0 | 0% |
Saint et al. (1978) | 2 | 0,05% | 2 | 0,31% | 2 | 0,32% | 2 | 0,32% |
Sanders et al. (2013) | 2 | 0,05% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Séret (2014) | 2 | 0,05% | 1 | 0,16% | 0 | 0% | 1 | 0,16% |
Smith (1849) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Solórzano & Sasa (2024) | 2 | 0,05% | 2 | 0,31% | 2 | 0,32% | 2 | 0,32% |
Thiele et al. (2004) | 2 | 0,05% | 2 | 0,31% | 2 | 0,32% | 1 | 0,16% |
Thunberg (1787) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Valenciennes (1836-1844) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Van Canneytet al. (2008) | 2 | 0,05% | 2 | 0,31% | 2 | 0,32% | 2 | 0,32% |
Vanderwerf et al. (2006) | 2 | 0,05% | 2 | 0,31% | 2 | 0,32% | 2 | 0,32% |
Vences et al. (2004) | 2 | 0,05% | 2 | 0,31% | 2 | 0,32% | 2 | 0,32% |
Wantiez (comm. pers., 2008) | 2 | 0,05% | 2 | 0,31% | 2 | 0,32% | 2 | 0,32% |
Weimerskirch et al. (2009) | 2 | 0,05% | 2 | 0,31% | 2 | 0,32% | 0 | 0% |
Weterings & Vetter (2017) | 2 | 0,05% | 2 | 0,31% | 2 | 0,32% | 2 | 0,32% |
Wickel et al. (2020) | 2 | 0,05% | 2 | 0,31% | 2 | 0,32% | 2 | 0,32% |
Yokoyama (2012) | 2 | 0,05% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Abhaya & Probst (2003) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Abhaya & Probst (2009) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Abhaya & Probst (2013) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Abril et al. (1986) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Agarwal et al. (2021) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Agassiz (1857) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Ainley et al. (2007) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 0 | 0% |
Al-hasson & Ali (2020) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Allen (1995) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Almeida & Vasconcelos (2023) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Almeida et al. (2019) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Amirault et al. (2022) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Anonyme. (2004) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Anonyme. (2004) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 0 | 0% |
Anonyme (2008) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Anonyme. (2012) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 0 | 0% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Anonyme. (2012) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Aquarium de La Rochelle (2017) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Astrongatt (2019) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Aubouin et al. (2016) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Bailenger et al. (1965) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Bailey et al. (2023) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Baldi et al. (2023) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Balouet & Olson (1989) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Bance (2022) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Barbancey (2001) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Barbancey (2001) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
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. (2009) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Bauer & Sadlier (1994) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Beaucournu (1968) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Beauvieux et al. (2024) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Behm et al. (2019) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Behm et al. (2022) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Bénito-espinal (1990) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Benson et al. (1975) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Benson (1967) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Bertin (1928) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Bertrand & Drogou (2000) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Bertrand et al. (2001) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Bertrand (1982) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Best et al. (1995) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 0 | 0% |
Birdlife International (2013) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Blanc et al. (1993) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
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 (1785-1795) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
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% |
Bochaton et al. (2018) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Boddaert & Daubenton (1783) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Bodilis et al. (2011) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Bonaparte (1839[1838]) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Bonnaterre (1788) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Borsa et al. (2013) | 1 | 0,02% | 1 | 0,16% | 0 | 0% | 1 | 0,16% |
Bouchon-Navaro et al. (1992) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 0 | 0% |
Bougeard & Siblet (2000) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Boulenger (1909) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Bourgade (2021) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Bourjon & Fricke (2019) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Branch (2010) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 0 | 0% |
Bray & Cribb (2002) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Brehm (1824) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Bretagnolle et al. (2000) | 1 | 0,02% | 1 | 0,16% | 0 | 0% | 1 | 0,16% |
Breuil (2009) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Brisbane et al. (2021) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Brischoux et al. (2018) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Brooke (1971) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Brünnich (1768) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Buray et al. (2009) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Caceres & Salamolard (2021) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Callou (2003) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Catil (2013) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Caut et al. (2008) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Cerchio et al. (2009) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 0 | 0% |
Chambault et al. (2020) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Cheke & Hume (2008) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Chevreux & de Guerne (1893) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Cheylan et al. (2022) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Chocobar et al. (2023) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Ciccione (2000) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Ciccione (2001) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Ciccione (2001) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Clements et al. (2015) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 0 | 0% |
Clergeau & Pascal (2003) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Clergeau et al. (2003) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Clua & Imirizaldu (2017) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Clua & Planes (2019) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Clua et al. (2016) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Coatmeur (1999) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Collectif (2009) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 0 | 0% |
Collet & Duguy (1981) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Collier et al. (2002) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 0 | 0% |
Corre & Jouventin (1997) | 1 | 0,02% | 1 | 0,16% | 0 | 0% | 1 | 0,16% |
Cottarel et al. (2013) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Cotte et al. (2001) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 0 | 0% |
Counihan et al. (2012) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 0 | 0% |
Cummings et al. (2021) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Cuvier & Valenciennes (1829) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Cuvier & Valenciennes (1830) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Dalebout et al. (2005) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Dalleau et al. (2014) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Daudin (1802) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 0 | 0% |
Daudin (1803) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Dauvin (1990) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Day (1865) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Deblock & Rose (1964) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Deblock (1966) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Deblock (1966) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Deflandre (2007) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Del Hoyo & Collar (2014) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Delcroix et al. (2008) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Deniau & Provost (2020) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Des et al. (2021) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Desjardins (1831) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Dickinson & Remsen (2013) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Dieme et al. (2015) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Dollfus (1966) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Downie et al. (2011) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Dubois et al. (2008) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Ducatez & Devore (2023) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Duguy & Duron (1981) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Duguy & Duron (1982) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Duguy & Duron (1983) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Duguy & Duron (1984) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Duguy & Duron (1985) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Duguy et al. (1980) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Duguy et al. (2000) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Duguy (1983) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Duguy (1986) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Duguy (1988) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Duguy (1989) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Duméril & Bibron (1836) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Duval et al. (2019) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Erens et al. (2017) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Ersts & Rosenbaum (2003) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 0 | 0% |
Eschscholtz (1829) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Eudeline (2022) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Faber (1829) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Finnerty et al. (2021) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Fleming & Jackson (2011) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 0 | 0% |
Flitti & Rocha (2014) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Forsskål (1775) | 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 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Franzini et al. (2018) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Fraser-brunner (1950) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Fretey & Bour (1980) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Fretey et al. (2023) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Fretey (1980) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Fretey (2003) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Frétey (2022) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Fricke (2015) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Fritz & Havaš (2007) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Furminieux (2019) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Garman (1913) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Géné (1839) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Geneva et al. (2013) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Gentry et al. (2004) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Geoffroy Saint-Hilaire ([1817]) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Gérigny et al. (2020) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Gill (1995) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Gill (2022) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Gillespie (1997) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Girondot et al. (2015) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Glaw & Vences (2007) | 1 | 0,02% | 1 | 0,16% | 0 | 0% | 1 | 0,16% |
Glaw (2015) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Gmelin (1789) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Goiran et al. (2022) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Goodall et al. (1997) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Goren (1981) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Gray (1842) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
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 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Guérin-Méneville (1843) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Guichenot (1847) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Gunnerus (1767) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Hartert (1914) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Havery et al. (2018) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Hedges et al. (2014) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Heimlich-boran (1993) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Herzberg (2018) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Honsterette & Probst (1999) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 0 | 0% |
Ifremer (2023) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Impact-mer (2011) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Ineich & Bauer (1992) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Ineich & Massary (1997) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Ineich et al. (2017) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Ineich et al. (2017) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Ineich et al. (2018) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Ineich (2007) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Ineich (2018) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Ingels et al. (2003) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
IUCN (2015) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Jairam et al. (2016) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Jeanne et al. (2018) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Jefferson & Barros (1997) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Jim et al. (2022) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Johnson & Wolman (1984) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 0 | 0% |
Joyeux & Baer (1955) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Karaa et al. (2016) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Kasamatsu & Joyce (1995) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Kasamatsu et al. (2000) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 0 | 0% |
Kawamura (1994) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 0 | 0% |
Kayser & Wilhelm (1991) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Keith & Mennesson (2021) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Keith et al. (2002) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Kiszka et al. (2009) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 0 | 0% |
Heron, 36(1): 31-34.">Kiszka (2003) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 0 | 0% |
Klaver (2008) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Kock et al. (2006) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Kostmann et al. (2023) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 0 | 0% |
Labach et al. (2021) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 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% |
Lacepède (1803) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Lancastre et al. (1976) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Lanza & Boscherini (2000) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Lapwong et al. (2021) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Lassauce et al. (2020) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Last et al. (2016) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Le Corre & Probst (1997) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Le Corre (1996) | 1 | 0,02% | 1 | 0,16% | 0 | 0% | 1 | 0,16% |
Leaper et al. (2008) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 0 | 0% |
Leaper et al. (2008) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Leatherwood et al. (1979) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Legros & Puissauve (2015) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Lescure et al. (2016) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Lescure et al. (2020) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Lescure (2018) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Lesson (1831) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 0 | 0% |
Lesueur (1818) | 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% |
Levesque & Mathurin (2008) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Liardet & d'Auzon (2004) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Liardet (2004) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Lichtenstein (1823) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Liebart et al. (2021) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Lillywhite & Menon (2019) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Lizé (2018) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Loisier et al. (2021) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Lorvelec & Pascal (2009) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Lorvelec & Vigne (2003) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Lorvelec et al. (2009) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Lorvelec et al. (2016) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Louis et al. (1992) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 0 | 0% |
Louisin & Probst (1996) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Loury & Puissauve (2016) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Loury & Puissauve (2016) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Macleod et al. (2006) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Maddalena & Zuffa (2008) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Mageski et al. (2017) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Mancino et al. (2022) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Maran & Frétey (2023) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Marchandeau & Letty (2021) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Marchandeau et al. (2003) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Marinho (2022) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Marion & Clergeau (2003) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 0 | 0% |
Marion & Marion (1982) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 0 | 0% |
Marion (2003) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Marquet et al. (2003) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Martin et al. (2021) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Matsunuma & Motomura (2018) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Mckay & Milenkaya (2020) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Medetian & Miaud (2024) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Ménard et al. (2000) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Meyen (1834) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Mocquard (1895) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Momont (1998) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Moreau de Jonnès (1818) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Morel (1959) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Morelon (2015) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Mothes et al. (2019) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Mourier (2012) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Müller (1776) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Murase et al. (2002) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 0 | 0% |
Murray (1887) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Nassi et al. (1975) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Nicol et al. (2000) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 0 | 0% |
Noël, Meunier (2010) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Noël (2017) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Notarbartolo et al. (2020) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Oliver (2011) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Olson & Warheit (1988) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Oremus (2009) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
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 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Pascal & Vigne (2003) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Pascal & Vigne (2003) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Pascal et al. 2006 | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Pearman et al. (2016) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 0 | 0% |
Peters (1854) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Peters (1874) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Petit (1976) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Pinault et al. (2018) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Pontoppidan (1763) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Prato et al. (2022) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Probst & Deso (2001) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Probst & Deso (2001) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 0 | 0% |
Probst & Tézier (2000) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Probst (1997) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Probst (1997) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 0 | 0% |
Probst (1998) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 0 | 0% |
Probst (2000) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Probst (2003) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 0 | 0% |
Probst (2007) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Quah & Grismer (2024) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Ramsay & Ogilby (1887) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Randall & Earle (2004) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Randall (2013) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Randi et al. (2001) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Ranzani (1839) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Read et al. (2015) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Renaud et al. (2013) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Revuelta et al. (2015) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Riccialdelli et al. (2010) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Ridgway (1893) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Rigby & Adamson (1997) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Rimblot et al. (1985) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Ringler et al. (2021) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Rocha et al. (2006) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Rocha et al. (2022) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Roche & Guinet (2007) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Rode (1938) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
ROGEON & SORDELLO (2012) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Roos (2000) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Rosenbaum & Collins (2006) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 0 | 0% |
Roux & Martinez (1987) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Rüppell (1835) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Russell & Le Corre (2009) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Ruys & Coord (2012) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Sadlier et al. (2012) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Samaran (2008) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 0 | 0% |
Sanchez & Probst (2009) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 0 | 0% |
Sanchez & Probst (2014) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Sanchez et al. (2012) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Savouré-Soubelet et al. (in prep.) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Schneider (1783) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Schwartz & Henderson (1991) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Schweigger (1812) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Scopoli (1769) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Servan (1976) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Shaver et al. (2019) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Shaw (1802) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Simian et al. (2022) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Sirovic et al. (2009) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 0 | 0% |
Smith et al. (2005) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Smith (1957) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Smith (1967) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Snyder et al. (2019) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Sonsino (1893) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
SORDELLO (2012) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Soubeyran (2008) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Springer (1941) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Steadman & Bollt (2010) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 0 | 0% |
Stejneger (1893) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Stelfox et al. (2020) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Storer (1848) | 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 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Taquet (1994) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Tea & Larson (2023) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
The International Barcode of Life Consortium (2016) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Thévenot (2014) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Thibault et al. (2023) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Thiele et al. (1999) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Tsadok et al. (2015) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
UICN France et al. (2013) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 0 | 0% |
Uicn et al. (2019) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
UICN (2009) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Van & Kampen (1907) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
van den Burg et al. (2021) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Van Dijk et al. (2014) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Vandelli (1761) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Vaslet & Agrnsm (2018) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Vásquez-cruz & Kelly-hernández (2024) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Viale & Frontier (1989) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Viel (2021) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Viganò & Corso (2015) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Vigne & Pascal (2003) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Von May et al. (2021) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Waayers et al. (2011) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Wallach (2009) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Wang & Liu (2016) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 0 | 0% |
Wantiez (2000) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Weerdt et al. (2021) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Weerdt (2023) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 0 | 0% |
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 (1939) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Whitley (1944) | 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 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Wickel et al. (2016) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Williams et al. (2009) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 0 | 0% |
Williams (2018) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Wink et al. (1979) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Winterbottom & Hoese (2015) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Wursig & Wursig (1980) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Yang et al. (2019) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Zdunek (2022) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Zug et al. (2007) | 1 | 0,02% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |