Vertébrés de Guadeloupe
1195 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
Référence | Total | Valides | Espèces | Taxons terminaux | ||||
---|---|---|---|---|---|---|---|---|
nb | % | nb | % | nb | % | nb | % | |
Questel (2020) | 440 | 10,3% | 431 | 42,55% | 404 | 44,89% | 416 | 44,3% |
Questel & Le Quellec (2012) | 382 | 8,94% | 364 | 35,93% | 348 | 38,67% | 343 | 36,53% |
Levesque & Delcroix (2018) | 305 | 7,14% | 294 | 29,02% | 249 | 27,67% | 290 | 30,88% |
Smith (1997) | 251 | 5,87% | 231 | 22,8% | 225 | 25% | 231 | 24,6% |
Bouchon-Navaro et al. (2005) | 224 | 5,24% | 184 | 18,16% | 184 | 20,44% | 183 | 19,49% |
Uicn et al. (2017) | 209 | 4,89% | 202 | 19,94% | 185 | 20,56% | 162 | 17,25% |
UICN Comité français, OFB & MNHN (2021) | 192 | 4,49% | 192 | 18,95% | 192 | 21,33% | 150 | 15,97% |
Yokoyama (2013) | 150 | 3,51% | 131 | 12,93% | 123 | 13,67% | 107 | 11,4% |
Linnaeus (1758) | 138 | 3,23% | 37 | 3,65% | 37 | 4,11% | 30 | 3,19% |
Bouchon-Navaro & Louis (1986) | 115 | 2,69% | 98 | 9,67% | 98 | 10,89% | 98 | 10,44% |
Remsen et al. (2013) | 110 | 2,57% | 105 | 10,37% | 105 | 11,67% | 75 | 7,99% |
Belfan & Conde (2016) | 105 | 2,46% | 102 | 10,07% | 75 | 8,33% | 98 | 10,44% |
Diaz & Cuzange (2009) | 104 | 2,43% | 96 | 9,48% | 96 | 10,67% | 94 | 10,01% |
Rinaldi (2016) | 100 | 2,34% | 100 | 9,87% | 100 | 11,11% | 72 | 7,67% |
Uicn et al. (2015) | 94 | 2,2% | 92 | 9,08% | 92 | 10,22% | 69 | 7,35% |
Henderson & Breuil (2012) | 86 | 2,01% | 57 | 5,63% | 44 | 4,89% | 56 | 5,96% |
Brugneaux & Pérès (2006) | 83 | 1,94% | 75 | 7,4% | 75 | 8,33% | 75 | 7,99% |
Carzon et al. (2016) | 75 | 1,76% | 75 | 7,4% | 75 | 8,33% | 54 | 5,75% |
Estrade et al. (2016) | 75 | 1,76% | 75 | 7,4% | 75 | 8,33% | 54 | 5,75% |
Etcheberry & Abraham (2009) | 64 | 1,5% | 56 | 5,53% | 56 | 6,22% | 46 | 4,9% |
Massary et al. (2021) | 64 | 1,5% | 63 | 6,22% | 37 | 4,11% | 55 | 5,86% |
Fricke et al. (2011) | 49 | 1,15% | 47 | 4,64% | 47 | 5,22% | 45 | 4,79% |
Rousseau (2010) | 47 | 1,1% | 45 | 4,44% | 45 | 5% | 45 | 4,79% |
Fricke et al. (2009) | 46 | 1,08% | 42 | 4,15% | 42 | 4,67% | 39 | 4,15% |
Uicn et al. (2020) | 45 | 1,05% | 45 | 4,44% | 45 | 5% | 36 | 3,83% |
Siu et al. (2017) | 41 | 0,96% | 37 | 3,65% | 37 | 4,11% | 36 | 3,83% |
Breuil (2002) | 39 | 0,91% | 23 | 2,27% | 13 | 1,44% | 19 | 2,02% |
Béarez et al. (2017) | 35 | 0,82% | 35 | 3,46% | 35 | 3,89% | 33 | 3,51% |
Tostain et al. (2013) | 35 | 0,82% | 29 | 2,86% | 28 | 3,11% | 28 | 2,98% |
Louis et al. (1992) | 33 | 0,77% | 25 | 2,47% | 25 | 2,78% | 24 | 2,56% |
Wickel & Jamon (2010) | 32 | 0,75% | 30 | 2,96% | 30 | 3,33% | 29 | 3,09% |
Poey (1858-61) | 31 | 0,73% | 0 | 0% | 0 | 0% | 0 | 0% |
Clements (2012) | 30 | 0,7% | 30 | 2,96% | 25 | 2,78% | 22 | 2,34% |
Weimerskirch et al. (2009) | 29 | 0,68% | 23 | 2,27% | 23 | 2,56% | 16 | 1,7% |
Gmelin (1789) | 28 | 0,66% | 5 | 0,49% | 5 | 0,56% | 4 | 0,43% |
Collette & Nauen (1983) | 27 | 0,63% | 27 | 2,67% | 23 | 2,56% | 27 | 2,88% |
Dewynter (2021) | 27 | 0,63% | 27 | 2,67% | 26 | 2,89% | 24 | 2,56% |
Linnaeus (1766) | 27 | 0,63% | 2 | 0,2% | 1 | 0,11% | 1 | 0,11% |
Lorvelec et al. (2007) | 26 | 0,61% | 21 | 2,07% | 21 | 2,33% | 19 | 2,02% |
Charrassin (2016) | 25 | 0,59% | 25 | 2,47% | 25 | 2,78% | 18 | 1,92% |
Charrassin (2016) | 25 | 0,59% | 25 | 2,47% | 25 | 2,78% | 18 | 1,92% |
Jarrett & Shirihai (2014) | 25 | 0,59% | 25 | 2,47% | 25 | 2,78% | 18 | 1,92% |
Moutou (2016) | 25 | 0,59% | 25 | 2,47% | 25 | 2,78% | 18 | 1,92% |
Spitz et al. (2016) | 25 | 0,59% | 25 | 2,47% | 25 | 2,78% | 18 | 1,92% |
Thoisy & Bordin (2016) | 25 | 0,59% | 25 | 2,47% | 25 | 2,78% | 18 | 1,92% |
Urtizberea (2016) | 25 | 0,59% | 25 | 2,47% | 25 | 2,78% | 18 | 1,92% |
Bordin et al. (2021) | 24 | 0,56% | 24 | 2,37% | 24 | 2,67% | 17 | 1,81% |
Nicholson et al. (2012) | 24 | 0,56% | 19 | 1,88% | 4 | 0,44% | 17 | 1,81% |
Barau et al. (2005) | 23 | 0,54% | 19 | 1,88% | 19 | 2,11% | 15 | 1,6% |
Catzeflis (2012) | 23 | 0,54% | 23 | 2,27% | 23 | 2,56% | 14 | 1,49% |
Dewynter et al. (2021) | 23 | 0,54% | 23 | 2,27% | 23 | 2,56% | 18 | 1,92% |
Garrigue (2007) | 23 | 0,54% | 23 | 2,27% | 23 | 2,56% | 17 | 1,81% |
Compagno (1984) | 21 | 0,49% | 21 | 2,07% | 21 | 2,33% | 21 | 2,24% |
Fourriére et al. (2014) | 21 | 0,49% | 21 | 2,07% | 21 | 2,33% | 21 | 2,24% |
Mertens & Wermuth (1960) | 21 | 0,49% | 0 | 0% | 0 | 0% | 0 | 0% |
Questel (2017) | 21 | 0,49% | 21 | 2,07% | 21 | 2,33% | 21 | 2,24% |
Aulagnier (2009) | 20 | 0,47% | 20 | 1,97% | 20 | 2,22% | 16 | 1,7% |
Bouchon-Navaro et al. (1992) | 20 | 0,47% | 17 | 1,68% | 17 | 1,89% | 16 | 1,7% |
Hedges & Conn (2012) | 20 | 0,47% | 8 | 0,79% | 8 | 0,89% | 4 | 0,43% |
Delrieu-Trottin et al. (2015) | 19 | 0,44% | 19 | 1,88% | 18 | 2% | 19 | 2,02% |
Dewynter et al. (2023) | 19 | 0,44% | 19 | 1,88% | 19 | 2,11% | 18 | 1,92% |
Gannier (2001) | 19 | 0,44% | 19 | 1,88% | 19 | 2,11% | 13 | 1,38% |
G.E.M.M. (2012) | 19 | 0,44% | 19 | 1,88% | 19 | 2,11% | 14 | 1,49% |
Proceedings of the Zoological Society of London, 1907: 1035-1037.">Hopkinson (1907) | 19 | 0,44% | 2 | 0,2% | 2 | 0,22% | 2 | 0,21% |
Van Dijk et al. (2012) | 19 | 0,44% | 12 | 1,18% | 12 | 1,33% | 12 | 1,28% |
Hoff & Daszkiewicz (2001) | 18 | 0,42% | 14 | 1,38% | 14 | 1,56% | 11 | 1,17% |
Bacchet et al. (2007) | 17 | 0,4% | 16 | 1,58% | 16 | 1,78% | 16 | 1,7% |
Dewynter et al. (2023) | 17 | 0,4% | 17 | 1,68% | 17 | 1,89% | 16 | 1,7% |
Gannier (2002) | 17 | 0,4% | 17 | 1,68% | 17 | 1,89% | 13 | 1,38% |
Gannier (2009) | 17 | 0,4% | 17 | 1,68% | 17 | 1,89% | 12 | 1,28% |
Le Bail et al. (2012) | 17 | 0,4% | 17 | 1,68% | 17 | 1,89% | 17 | 1,81% |
Monti et al. (2010) | 17 | 0,4% | 15 | 1,48% | 15 | 1,67% | 15 | 1,6% |
Rafinesque Schmaltz (1810) | 17 | 0,4% | 2 | 0,2% | 2 | 0,22% | 2 | 0,21% |
Uicn et al. (2015) | 17 | 0,4% | 14 | 1,38% | 14 | 1,56% | 12 | 1,28% |
Barré (2021) | 16 | 0,37% | 16 | 1,58% | 16 | 1,78% | 16 | 1,7% |
Bochaton et al. (2021) | 16 | 0,37% | 15 | 1,48% | 15 | 1,67% | 12 | 1,28% |
Cuvier & Valenciennes (1833) | 16 | 0,37% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Dewynter et al. (2019) | 16 | 0,37% | 16 | 1,58% | 16 | 1,78% | 15 | 1,6% |
Dewynter et al. (2022) | 16 | 0,37% | 16 | 1,58% | 16 | 1,78% | 15 | 1,6% |
Dickinson & Remsen (2013) | 16 | 0,37% | 15 | 1,48% | 8 | 0,89% | 13 | 1,38% |
Massary et al. (2018) | 16 | 0,37% | 15 | 1,48% | 15 | 1,67% | 14 | 1,49% |
Questel et al. (2023) | 16 | 0,37% | 16 | 1,58% | 16 | 1,78% | 15 | 1,6% |
Questel et al. (2023) | 16 | 0,37% | 16 | 1,58% | 16 | 1,78% | 15 | 1,6% |
Whitehead et al. (1988) | 16 | 0,37% | 16 | 1,58% | 16 | 1,78% | 16 | 1,7% |
Gannier (2000) | 15 | 0,35% | 15 | 1,48% | 15 | 1,67% | 10 | 1,06% |
Heemstra & Randall (1993) | 15 | 0,35% | 15 | 1,48% | 15 | 1,67% | 15 | 1,6% |
Lim et al. (2002) | 15 | 0,35% | 13 | 1,28% | 13 | 1,44% | 13 | 1,38% |
Rocamora (2004) | 15 | 0,35% | 14 | 1,38% | 13 | 1,44% | 11 | 1,17% |
Deblock et al. (1960) | 14 | 0,33% | 8 | 0,79% | 8 | 0,89% | 7 | 0,75% |
Gargominy et al. (1996) | 14 | 0,33% | 14 | 1,38% | 14 | 1,56% | 14 | 1,49% |
Kiszka et al.(2007) | 14 | 0,33% | 14 | 1,38% | 14 | 1,56% | 10 | 1,06% |
Massary et al. (2017) | 14 | 0,33% | 13 | 1,28% | 13 | 1,44% | 12 | 1,28% |
Allen (1985) | 13 | 0,3% | 13 | 1,28% | 13 | 1,44% | 13 | 1,38% |
Clements et al. (2015) | 13 | 0,3% | 13 | 1,28% | 3 | 0,33% | 12 | 1,28% |
Del Hoyo & Collar (2014) | 13 | 0,3% | 9 | 0,89% | 8 | 0,89% | 9 | 0,96% |
Dewynter & Claessens (2020) | 13 | 0,3% | 13 | 1,28% | 13 | 1,44% | 6 | 0,64% |
Guth (1971) | 13 | 0,3% | 12 | 1,18% | 12 | 1,33% | 7 | 0,75% |
Berry & Smith-Vaniz (1978) | 12 | 0,28% | 12 | 1,18% | 12 | 1,33% | 12 | 1,28% |
Compagno (1984) | 12 | 0,28% | 12 | 1,18% | 12 | 1,33% | 12 | 1,28% |
Kiszka et al. (2010) | 12 | 0,28% | 12 | 1,18% | 12 | 1,33% | 9 | 0,96% |
Laran et al. (2011) | 12 | 0,28% | 12 | 1,18% | 12 | 1,33% | 9 | 0,96% |
Soubeyran et al. (2011) | 12 | 0,28% | 12 | 1,18% | 12 | 1,33% | 12 | 1,28% |
Breuil (2009) | 11 | 0,26% | 8 | 0,79% | 8 | 0,89% | 8 | 0,85% |
Dulau-Drouot et al. (2008) | 11 | 0,26% | 11 | 1,09% | 11 | 1,22% | 7 | 0,75% |
Kulbicki et al. (2000) | 11 | 0,26% | 9 | 0,89% | 9 | 1% | 8 | 0,85% |
Soubeyran (2008) | 11 | 0,26% | 11 | 1,09% | 11 | 1,22% | 11 | 1,17% |
UICN Comité français, OFB, MNHN & GEPOMAY (2025) | 11 | 0,26% | 11 | 1,09% | 11 | 1,22% | 10 | 1,06% |
Aulagnier et al. (2017) | 10 | 0,23% | 9 | 0,89% | 9 | 1% | 9 | 0,96% |
Breuil et al. (2010) | 10 | 0,23% | 8 | 0,79% | 7 | 0,78% | 7 | 0,75% |
Cohen et al. (1990) | 10 | 0,23% | 10 | 0,99% | 10 | 1,11% | 10 | 1,06% |
Cuvier & Valenciennes ([1832]) | 10 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Fricke et al. (2013) | 10 | 0,23% | 10 | 0,99% | 10 | 1,11% | 9 | 0,96% |
Genoways et al. (2007) | 10 | 0,23% | 10 | 0,99% | 6 | 0,67% | 7 | 0,75% |
Kulbicki (comm. pers., 2011) | 10 | 0,23% | 8 | 0,79% | 8 | 0,89% | 8 | 0,85% |
Nakamura (1985) | 10 | 0,23% | 10 | 0,99% | 10 | 1,11% | 10 | 1,06% |
Pedersen et al. (2013) | 10 | 0,23% | 9 | 0,89% | 9 | 1% | 5 | 0,53% |
Routtier et al. (2023) | 10 | 0,23% | 8 | 0,79% | 8 | 0,89% | 5 | 0,53% |
Theuerkauf et al. (2010) | 10 | 0,23% | 10 | 0,99% | 10 | 1,11% | 10 | 1,06% |
Béarez & Séret (2009) | 9 | 0,21% | 8 | 0,79% | 8 | 0,89% | 8 | 0,85% |
Commission de l’Avifaune Française (2016) | 9 | 0,21% | 9 | 0,89% | 9 | 1% | 7 | 0,75% |
Gill (1995) | 9 | 0,21% | 9 | 0,89% | 9 | 1% | 5 | 0,53% |
Girard (2007) | 9 | 0,21% | 7 | 0,69% | 6 | 0,67% | 7 | 0,75% |
Richard et al. (1982) | 9 | 0,21% | 4 | 0,39% | 4 | 0,44% | 4 | 0,43% |
Béarez & Bouffandeau (2019) | 8 | 0,19% | 8 | 0,79% | 8 | 0,89% | 7 | 0,75% |
Charbonnel (1990) | 8 | 0,19% | 6 | 0,59% | 6 | 0,67% | 4 | 0,43% |
Dewynter et al. (2019) | 8 | 0,19% | 8 | 0,79% | 8 | 0,89% | 7 | 0,75% |
Gmelin (1788) | 8 | 0,19% | 1 | 0,1% | 1 | 0,11% | 0 | 0% |
González-sánchez et al. (2021) | 8 | 0,19% | 8 | 0,79% | 8 | 0,89% | 7 | 0,75% |
Karadjian et al. (2022) | 8 | 0,19% | 8 | 0,79% | 8 | 0,89% | 8 | 0,85% |
Lowe et al. (2007) | 8 | 0,19% | 7 | 0,69% | 6 | 0,67% | 7 | 0,75% |
Questel (2023) | 8 | 0,19% | 8 | 0,79% | 8 | 0,89% | 8 | 0,85% |
Samaran & Guinet (2009) | 8 | 0,19% | 8 | 0,79% | 8 | 0,89% | 6 | 0,64% |
Thibault et al. (2014) | 8 | 0,19% | 8 | 0,79% | 8 | 0,89% | 5 | 0,53% |
Whitehead (1985) | 8 | 0,19% | 8 | 0,79% | 8 | 0,89% | 8 | 0,85% |
Jourdan (2020) | 7 | 0,16% | 7 | 0,69% | 6 | 0,67% | 6 | 0,64% |
Lazell (1964) | 7 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Muñoz et al. (2013) | 7 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Perrin et al. (2002) | 7 | 0,16% | 7 | 0,69% | 7 | 0,78% | 4 | 0,43% |
Pezold et al. (2015) | 7 | 0,16% | 7 | 0,69% | 7 | 0,78% | 7 | 0,75% |
Prévost & Mougin (1970) | 7 | 0,16% | 7 | 0,69% | 7 | 0,78% | 6 | 0,64% |
Probst et al. (2022) | 7 | 0,16% | 7 | 0,69% | 7 | 0,78% | 7 | 0,75% |
Randall & Vergara (1978) | 7 | 0,16% | 7 | 0,69% | 5 | 0,56% | 7 | 0,75% |
Vaslet & Agrnsm (2018) | 7 | 0,16% | 7 | 0,69% | 7 | 0,78% | 7 | 0,75% |
Williams et al. (2006) | 7 | 0,16% | 6 | 0,59% | 6 | 0,67% | 5 | 0,53% |
Yokoyama (2012) | 7 | 0,16% | 6 | 0,59% | 6 | 0,67% | 6 | 0,64% |
Boer et al. (1999) | 6 | 0,14% | 6 | 0,59% | 6 | 0,67% | 4 | 0,43% |
Busala et al. (2024) | 6 | 0,14% | 4 | 0,39% | 4 | 0,44% | 3 | 0,32% |
Camiñas et al. (2021) | 6 | 0,14% | 6 | 0,59% | 6 | 0,67% | 6 | 0,64% |
Chabanet & Durville (2005) | 6 | 0,14% | 5 | 0,49% | 5 | 0,56% | 5 | 0,53% |
Cuvier & Valenciennes (1830-1832) | 6 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Fourt et al. (2017) | 6 | 0,14% | 6 | 0,59% | 6 | 0,67% | 6 | 0,64% |
Furminieux (2019) | 6 | 0,14% | 6 | 0,59% | 6 | 0,67% | 6 | 0,64% |
Gonzalez et al. (2009) | 6 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Gronow (1854) | 6 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Lescure et al. (2012) | 6 | 0,14% | 6 | 0,59% | 5 | 0,56% | 5 | 0,53% |
Levesque & Delcroix (2016) | 6 | 0,14% | 5 | 0,49% | 2 | 0,22% | 5 | 0,53% |
Massary et al. (2019) | 6 | 0,14% | 6 | 0,59% | 6 | 0,67% | 5 | 0,53% |
Massary et al. (2020) | 6 | 0,14% | 6 | 0,59% | 6 | 0,67% | 6 | 0,64% |
Müller & Henle (1841) | 6 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Muratet (2015) | 6 | 0,14% | 6 | 0,59% | 5 | 0,56% | 5 | 0,53% |
Powell & Henderson (2023) | 6 | 0,14% | 6 | 0,59% | 6 | 0,67% | 6 | 0,64% |
Probst (2001) | 6 | 0,14% | 5 | 0,49% | 5 | 0,56% | 4 | 0,43% |
Risso (1810) | 6 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Safford & Hawkins (2013) | 6 | 0,14% | 6 | 0,59% | 6 | 0,67% | 5 | 0,53% |
Sayah et al. (2023) | 6 | 0,14% | 5 | 0,49% | 5 | 0,56% | 5 | 0,53% |
Shirihai (2003) | 6 | 0,14% | 6 | 0,59% | 6 | 0,67% | 3 | 0,32% |
Simian et al. (2022) | 6 | 0,14% | 6 | 0,59% | 6 | 0,67% | 6 | 0,64% |
Thomas (1964) | 6 | 0,14% | 5 | 0,49% | 0 | 0% | 5 | 0,53% |
Vieillot (1819) | 6 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Bioinsight/diren & Guyane (2006) | 5 | 0,12% | 5 | 0,49% | 5 | 0,56% | 5 | 0,53% |
Bloch & Schneider (1801) | 5 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Bour et al. (2008) | 5 | 0,12% | 5 | 0,49% | 5 | 0,56% | 4 | 0,43% |
Butaud (2021) | 5 | 0,12% | 5 | 0,49% | 5 | 0,56% | 5 | 0,53% |
Casale et al. (2021) | 5 | 0,12% | 5 | 0,49% | 5 | 0,56% | 5 | 0,53% |
Chevalier (2006) | 5 | 0,12% | 5 | 0,49% | 5 | 0,56% | 5 | 0,53% |
Ciccione et al. (2011) | 5 | 0,12% | 5 | 0,49% | 5 | 0,56% | 5 | 0,53% |
Crillon & Cuzange (2020) | 5 | 0,12% | 5 | 0,49% | 5 | 0,56% | 5 | 0,53% |
Desbrosses & Etcheberry (1987) | 5 | 0,12% | 4 | 0,39% | 4 | 0,44% | 2 | 0,21% |
Duffaut et al. (2011) | 5 | 0,12% | 5 | 0,49% | 5 | 0,56% | 5 | 0,53% |
Ehrhardt (1971) | 5 | 0,12% | 2 | 0,2% | 2 | 0,22% | 2 | 0,21% |
Entraygues (2014) | 5 | 0,12% | 5 | 0,49% | 5 | 0,56% | 5 | 0,53% |
Étaix-bonnin et al. (2011) | 5 | 0,12% | 5 | 0,49% | 5 | 0,56% | 5 | 0,53% |
Frenot et al. (2005) | 5 | 0,12% | 5 | 0,49% | 5 | 0,56% | 5 | 0,53% |
Fretey & Triplet (2022) | 5 | 0,12% | 5 | 0,49% | 5 | 0,56% | 5 | 0,53% |
Gentry et al. (2004) | 5 | 0,12% | 4 | 0,39% | 4 | 0,44% | 4 | 0,43% |
IUCN (2012) | 5 | 0,12% | 5 | 0,49% | 5 | 0,56% | 3 | 0,32% |
Keith et al. (2006) | 5 | 0,12% | 5 | 0,49% | 5 | 0,56% | 5 | 0,53% |
Keith et al. (2013) | 5 | 0,12% | 5 | 0,49% | 5 | 0,56% | 5 | 0,53% |
Le Scao et al. (2011) | 5 | 0,12% | 5 | 0,49% | 5 | 0,56% | 5 | 0,53% |
Lee & Walsh-McGehee (2000) | 5 | 0,12% | 5 | 0,49% | 0 | 0% | 5 | 0,53% |
Transactions of the Zoological Society of London, 1839: 1-20.">Lowe (1839) | 5 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Polanco & Acero (2016) | 5 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Read & Farman (2018) | 5 | 0,12% | 5 | 0,49% | 5 | 0,56% | 5 | 0,53% |
Read et al. (2023) | 5 | 0,12% | 5 | 0,49% | 5 | 0,56% | 5 | 0,53% |
Rhodin et al. (2017) | 5 | 0,12% | 3 | 0,3% | 3 | 0,33% | 3 | 0,32% |
Risso (1827) | 5 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Robineau & Duhamel (2006) | 5 | 0,12% | 5 | 0,49% | 5 | 0,56% | 3 | 0,32% |
Ronot (2007) | 5 | 0,12% | 4 | 0,39% | 3 | 0,33% | 4 | 0,43% |
Sauvignet et al. (2000) | 5 | 0,12% | 5 | 0,49% | 5 | 0,56% | 5 | 0,53% |
Scopoli (1769) | 5 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Séret (1997) | 5 | 0,12% | 5 | 0,49% | 5 | 0,56% | 5 | 0,53% |
Snodgrass & Heller (1905) | 5 | 0,12% | 2 | 0,2% | 2 | 0,22% | 2 | 0,21% |
Swainson (1839) | 5 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Allen (comm. pers., 2009) | 4 | 0,09% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Arnold & Ovenden (2014) | 4 | 0,09% | 4 | 0,39% | 4 | 0,44% | 3 | 0,32% |
Baker et al. (1978) | 4 | 0,09% | 4 | 0,39% | 0 | 0% | 4 | 0,43% |
Barbrour (1915) | 4 | 0,09% | 2 | 0,2% | 1 | 0,11% | 1 | 0,11% |
Barrioz & Morinière (2007) | 4 | 0,09% | 4 | 0,39% | 4 | 0,44% | 4 | 0,43% |
Bartoli (1972) | 4 | 0,09% | 3 | 0,3% | 3 | 0,33% | 3 | 0,32% |
Bauer & Sadlier (2000) | 4 | 0,09% | 3 | 0,3% | 3 | 0,33% | 3 | 0,32% |
Birdlife International (2016) | 4 | 0,09% | 4 | 0,39% | 4 | 0,44% | 0 | 0% |
Boddaert & Daubenton (1783) | 4 | 0,09% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Breuil (2013) | 4 | 0,09% | 2 | 0,2% | 2 | 0,22% | 2 | 0,21% |
Collier et al. (2002) | 4 | 0,09% | 4 | 0,39% | 3 | 0,33% | 2 | 0,21% |
Cuvier & Valenciennes (1847) | 4 | 0,09% | 2 | 0,2% | 2 | 0,22% | 2 | 0,21% |
Dubois et al. (2008) | 4 | 0,09% | 4 | 0,39% | 4 | 0,44% | 4 | 0,43% |
Fort & Barrière (2021) | 4 | 0,09% | 4 | 0,39% | 4 | 0,44% | 4 | 0,43% |
Fraga & Carvalho (2021) | 4 | 0,09% | 4 | 0,39% | 4 | 0,44% | 4 | 0,43% |
Fretey & Lescure (1999) | 4 | 0,09% | 4 | 0,39% | 4 | 0,44% | 4 | 0,43% |
Goicoechea et al. (2016) | 4 | 0,09% | 2 | 0,2% | 2 | 0,22% | 2 | 0,21% |
Keith et al. (2002) | 4 | 0,09% | 2 | 0,2% | 2 | 0,22% | 2 | 0,21% |
Klunzinger (1871) | 4 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Lacepède (1800) | 4 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Lacepède (1801) | 4 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Lambert (1988) | 4 | 0,09% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Lescure et al. (2020) | 4 | 0,09% | 4 | 0,39% | 3 | 0,33% | 4 | 0,43% |
Linné (1766) | 4 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Morris (2012) | 4 | 0,09% | 4 | 0,39% | 4 | 0,44% | 4 | 0,43% |
Olson & Normand (2014) | 4 | 0,09% | 2 | 0,2% | 2 | 0,22% | 2 | 0,21% |
Pascal et al. 2006 | 4 | 0,09% | 4 | 0,39% | 3 | 0,33% | 4 | 0,43% |
Probst (1997) | 4 | 0,09% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Probst (1998) | 4 | 0,09% | 3 | 0,3% | 3 | 0,33% | 3 | 0,32% |
Randall & Earle (2000) | 4 | 0,09% | 4 | 0,39% | 3 | 0,33% | 4 | 0,43% |
Swanepoel & Genoways (1983) | 4 | 0,09% | 4 | 0,39% | 4 | 0,44% | 0 | 0% |
Tostain & Dujardin (1988) | 4 | 0,09% | 2 | 0,2% | 2 | 0,22% | 2 | 0,21% |
Uicn et al. (2019) | 4 | 0,09% | 4 | 0,39% | 4 | 0,44% | 4 | 0,43% |
AAMP (2012) | 3 | 0,07% | 3 | 0,3% | 3 | 0,33% | 0 | 0% |
Aubouin et al. (2016) | 3 | 0,07% | 3 | 0,3% | 3 | 0,33% | 3 | 0,32% |
Ausilio & Zotier (1989) | 3 | 0,07% | 3 | 0,3% | 3 | 0,33% | 2 | 0,21% |
Bailon et al. (2015) | 3 | 0,07% | 2 | 0,2% | 2 | 0,22% | 2 | 0,21% |
Bénito-espinal (1990) | 3 | 0,07% | 3 | 0,3% | 2 | 0,22% | 3 | 0,32% |
Birdlife International (2014) | 3 | 0,07% | 3 | 0,3% | 3 | 0,33% | 3 | 0,32% |
Blanc (1909) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Bochaton et al. (2016) | 3 | 0,07% | 3 | 0,3% | 3 | 0,33% | 3 | 0,32% |
Bochaton et al. (2017) | 3 | 0,07% | 3 | 0,3% | 3 | 0,33% | 3 | 0,32% |
Boer (2000) | 3 | 0,07% | 3 | 0,3% | 3 | 0,33% | 1 | 0,11% |
Borsa (1997) | 3 | 0,07% | 3 | 0,3% | 3 | 0,33% | 1 | 0,11% |
Breuil & Ibéné (2008) | 3 | 0,07% | 3 | 0,3% | 3 | 0,33% | 3 | 0,32% |
Burneleau (1983) | 3 | 0,07% | 3 | 0,3% | 3 | 0,33% | 3 | 0,32% |
Carstens et al. (2004) | 3 | 0,07% | 3 | 0,3% | 3 | 0,33% | 0 | 0% |
Catzeflis (2018) | 3 | 0,07% | 3 | 0,3% | 3 | 0,33% | 3 | 0,32% |
Catzeflis (2019) | 3 | 0,07% | 2 | 0,2% | 2 | 0,22% | 2 | 0,21% |
Chabanaud (1927) | 3 | 0,07% | 3 | 0,3% | 3 | 0,33% | 3 | 0,32% |
Champagne et al. (1997) | 3 | 0,07% | 3 | 0,3% | 2 | 0,22% | 3 | 0,32% |
Cochard et al. (2019) | 3 | 0,07% | 3 | 0,3% | 3 | 0,33% | 3 | 0,32% |
Cuvier & Valenciennes (1839) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Cuvier & Valenciennes (1846) | 3 | 0,07% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Cuvier (1829) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Delcroix et al. (2011) | 3 | 0,07% | 3 | 0,3% | 3 | 0,33% | 3 | 0,32% |
Dewynter et al. (2020) | 3 | 0,07% | 3 | 0,3% | 3 | 0,33% | 3 | 0,32% |
Dewynter (2021) | 3 | 0,07% | 3 | 0,3% | 3 | 0,33% | 3 | 0,32% |
Dubief & Gallais (2011) | 3 | 0,07% | 3 | 0,3% | 3 | 0,33% | 3 | 0,32% |
Duguy et al. (1998) | 3 | 0,07% | 3 | 0,3% | 3 | 0,33% | 3 | 0,32% |
Duguy et al. (2007) | 3 | 0,07% | 3 | 0,3% | 3 | 0,33% | 3 | 0,32% |
Duguy (1988) | 3 | 0,07% | 3 | 0,3% | 3 | 0,33% | 3 | 0,32% |
Duguy (1994) | 3 | 0,07% | 3 | 0,3% | 3 | 0,33% | 3 | 0,32% |
Duguy (1997) | 3 | 0,07% | 3 | 0,3% | 3 | 0,33% | 3 | 0,32% |
Duméril & Bibron (1836) | 3 | 0,07% | 2 | 0,2% | 1 | 0,11% | 1 | 0,11% |
Duméril & Bibron (1837) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Durant et al. (2013) | 3 | 0,07% | 3 | 0,3% | 3 | 0,33% | 3 | 0,32% |
Easteal (1981) | 3 | 0,07% | 3 | 0,3% | 3 | 0,33% | 3 | 0,32% |
Firmat et al. (2012) | 3 | 0,07% | 3 | 0,3% | 3 | 0,33% | 3 | 0,32% |
Girondot (2011) | 3 | 0,07% | 3 | 0,3% | 3 | 0,33% | 3 | 0,32% |
Hass (1991) | 3 | 0,07% | 3 | 0,3% | 3 | 0,33% | 2 | 0,21% |
Hedges et al. (2014) | 3 | 0,07% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Humphries et al. (2019) | 3 | 0,07% | 3 | 0,3% | 3 | 0,33% | 0 | 0% |
Hutchinson et al. (2019) | 3 | 0,07% | 3 | 0,3% | 3 | 0,33% | 3 | 0,32% |
Ingels et al. (2003) | 3 | 0,07% | 2 | 0,2% | 2 | 0,22% | 2 | 0,21% |
Kemp (2023) | 3 | 0,07% | 3 | 0,3% | 3 | 0,33% | 3 | 0,32% |
Kottelat ( 2013) | 3 | 0,07% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Laran et al. (2012) | 3 | 0,07% | 3 | 0,3% | 3 | 0,33% | 2 | 0,21% |
Larsen et al. (2006) | 3 | 0,07% | 3 | 0,3% | 0 | 0% | 3 | 0,32% |
Lawrence (1879) | 3 | 0,07% | 3 | 0,3% | 2 | 0,22% | 2 | 0,21% |
Legand (1950) | 3 | 0,07% | 2 | 0,2% | 2 | 0,22% | 2 | 0,21% |
Lescure & Marty (2000) | 3 | 0,07% | 2 | 0,2% | 2 | 0,22% | 2 | 0,21% |
Lescure et al. (2022) | 3 | 0,07% | 3 | 0,3% | 3 | 0,33% | 3 | 0,32% |
Levesque & Delcroix (2013) | 3 | 0,07% | 3 | 0,3% | 0 | 0% | 3 | 0,32% |
Maréchal & Trégarot (2012) | 3 | 0,07% | 2 | 0,2% | 2 | 0,22% | 2 | 0,21% |
Maréchal et al. (2006) | 3 | 0,07% | 3 | 0,3% | 3 | 0,33% | 3 | 0,32% |
Méheust et al. (2018) | 3 | 0,07% | 3 | 0,3% | 3 | 0,33% | 3 | 0,32% |
Miralles et al. (2017) | 3 | 0,07% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Møller et al. (2005) | 3 | 0,07% | 3 | 0,3% | 3 | 0,33% | 3 | 0,32% |
Morinière & Dell'amico (2011) | 3 | 0,07% | 3 | 0,3% | 3 | 0,33% | 3 | 0,32% |
Poisson (1999) | 3 | 0,07% | 3 | 0,3% | 3 | 0,33% | 3 | 0,32% |
Pontoppidan (1763) | 3 | 0,07% | 2 | 0,2% | 2 | 0,22% | 2 | 0,21% |
Potin (2013) | 3 | 0,07% | 3 | 0,3% | 3 | 0,33% | 3 | 0,32% |
Probst et al. (2000) | 3 | 0,07% | 3 | 0,3% | 3 | 0,33% | 3 | 0,32% |
Probst (1997) | 3 | 0,07% | 3 | 0,3% | 3 | 0,33% | 3 | 0,32% |
Questel (2017) | 3 | 0,07% | 3 | 0,3% | 3 | 0,33% | 3 | 0,32% |
Questel (2022) | 3 | 0,07% | 3 | 0,3% | 3 | 0,33% | 3 | 0,32% |
Read & Jean (2021) | 3 | 0,07% | 3 | 0,3% | 3 | 0,33% | 3 | 0,32% |
Rignault & Chevallier (2017) | 3 | 0,07% | 2 | 0,2% | 2 | 0,22% | 2 | 0,21% |
Roughgarden (1995) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Roux (1913) | 3 | 0,07% | 2 | 0,2% | 2 | 0,22% | 2 | 0,21% |
Sanchez (2020) | 3 | 0,07% | 3 | 0,3% | 3 | 0,33% | 2 | 0,21% |
Stoetzel et al. (2016) | 3 | 0,07% | 3 | 0,3% | 3 | 0,33% | 3 | 0,32% |
Swainson (1838) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Thorpe et al. (2008) | 3 | 0,07% | 2 | 0,2% | 2 | 0,22% | 1 | 0,11% |
Tirvengadum & Bour (1985) | 3 | 0,07% | 2 | 0,2% | 2 | 0,22% | 2 | 0,21% |
Tostain (1980) | 3 | 0,07% | 2 | 0,2% | 2 | 0,22% | 2 | 0,21% |
Valenciennes (1836-1844) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
van den Burg et al. (2021) | 3 | 0,07% | 2 | 0,2% | 2 | 0,22% | 2 | 0,21% |
Velazco & Patterson (2013) | 3 | 0,07% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Vieillot (1807) | 3 | 0,07% | 3 | 0,3% | 3 | 0,33% | 3 | 0,32% |
Vieira (2022) | 3 | 0,07% | 3 | 0,3% | 3 | 0,33% | 3 | 0,32% |
Wallach (2020) | 3 | 0,07% | 2 | 0,2% | 2 | 0,22% | 2 | 0,21% |
Adams (1989) | 2 | 0,05% | 2 | 0,2% | 2 | 0,22% | 2 | 0,21% |
Alley et al. (2023) | 2 | 0,05% | 2 | 0,2% | 2 | 0,22% | 2 | 0,21% |
Anonyme (2016) | 2 | 0,05% | 2 | 0,2% | 2 | 0,22% | 2 | 0,21% |
Aulagnier (2021) | 2 | 0,05% | 2 | 0,2% | 2 | 0,22% | 2 | 0,21% |
Baldi et al. (2022) | 2 | 0,05% | 2 | 0,2% | 2 | 0,22% | 2 | 0,21% |
Balle et al. (2021) | 2 | 0,05% | 2 | 0,2% | 2 | 0,22% | 2 | 0,21% |
Bance (2022) | 2 | 0,05% | 2 | 0,2% | 2 | 0,22% | 2 | 0,21% |
Barbour & Noble (1915) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Barbour (1914) | 2 | 0,05% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Barre et al. (2009) | 2 | 0,05% | 2 | 0,2% | 2 | 0,22% | 2 | 0,21% |
Barré et al. (2016) | 2 | 0,05% | 1 | 0,1% | 1 | 0,11% | 0 | 0% |
Bauer (1987) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Behm et al. (2019) | 2 | 0,05% | 2 | 0,2% | 2 | 0,22% | 2 | 0,21% |
Birdlife International (2016) | 2 | 0,05% | 2 | 0,2% | 2 | 0,22% | 0 | 0% |
Birdlife International (2016) | 2 | 0,05% | 2 | 0,2% | 2 | 0,22% | 2 | 0,21% |
Birdlife International (2016) | 2 | 0,05% | 2 | 0,2% | 2 | 0,22% | 2 | 0,21% |
Birdlife International (2016) | 2 | 0,05% | 2 | 0,2% | 2 | 0,22% | 0 | 0% |
Bleeker (1852) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Bochaton & Bailon (2018) | 2 | 0,05% | 2 | 0,2% | 2 | 0,22% | 2 | 0,21% |
Bochaton & Hanot (2021) | 2 | 0,05% | 2 | 0,2% | 2 | 0,22% | 1 | 0,11% |
Bochaton et al. (2018) | 2 | 0,05% | 2 | 0,2% | 2 | 0,22% | 2 | 0,21% |
Bochaton et al. (2021) | 2 | 0,05% | 2 | 0,2% | 2 | 0,22% | 2 | 0,21% |
Boer & Simmonds (2000) | 2 | 0,05% | 2 | 0,2% | 2 | 0,22% | 2 | 0,21% |
Bosc (1792) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Bourgade (2020) | 2 | 0,05% | 2 | 0,2% | 2 | 0,22% | 2 | 0,21% |
Bowdich (1825) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Breuil (2021) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Brosse et al. (2021) | 2 | 0,05% | 2 | 0,2% | 2 | 0,22% | 2 | 0,21% |
Brugneaux & Pérès (2005) | 2 | 0,05% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Caceres & Salamolard (2021) | 2 | 0,05% | 2 | 0,2% | 2 | 0,22% | 2 | 0,21% |
CEN Nouvelle-Calédonie (2021) | 2 | 0,05% | 2 | 0,2% | 1 | 0,11% | 2 | 0,21% |
Chapuis et al. (2004) | 2 | 0,05% | 2 | 0,2% | 2 | 0,22% | 2 | 0,21% |
Chartier et al. (2007) | 2 | 0,05% | 2 | 0,2% | 2 | 0,22% | 0 | 0% |
Cheke (1987) | 2 | 0,05% | 2 | 0,2% | 2 | 0,22% | 2 | 0,21% |
Cheon et al. (2023) | 2 | 0,05% | 2 | 0,2% | 0 | 0% | 2 | 0,21% |
Chevallier et al. (2023) | 2 | 0,05% | 2 | 0,2% | 2 | 0,22% | 2 | 0,21% |
CHN (2017) | 2 | 0,05% | 2 | 0,2% | 2 | 0,22% | 1 | 0,11% |
Cicero & Johnson (1998) | 2 | 0,05% | 2 | 0,2% | 2 | 0,22% | 2 | 0,21% |
Clements et al. (2017) | 2 | 0,05% | 2 | 0,2% | 0 | 0% | 2 | 0,21% |
Cope (1864) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
dal Molin (2009) | 2 | 0,05% | 2 | 0,2% | 2 | 0,22% | 2 | 0,21% |
Danforth (1937) | 2 | 0,05% | 2 | 0,2% | 0 | 0% | 2 | 0,21% |
Daniel et al. (2020) | 2 | 0,05% | 2 | 0,2% | 2 | 0,22% | 0 | 0% |
Davant (1967) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Del Hoyo & Collar (2016) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Deméré (2014) | 2 | 0,05% | 2 | 0,2% | 0 | 0% | 2 | 0,21% |
Des et al. (2021) | 2 | 0,05% | 2 | 0,2% | 2 | 0,22% | 2 | 0,21% |
Dickinson & Christidis (2014) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Donovan (1816) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Duguy et al. (1997) | 2 | 0,05% | 2 | 0,2% | 2 | 0,22% | 2 | 0,21% |
Duguy et al. (1999) | 2 | 0,05% | 2 | 0,2% | 2 | 0,22% | 2 | 0,21% |
Duguy et al. (2000) | 2 | 0,05% | 2 | 0,2% | 2 | 0,22% | 2 | 0,21% |
Duguy et al. (2002) | 2 | 0,05% | 2 | 0,2% | 2 | 0,22% | 2 | 0,21% |
Duguy et al. (2003) | 2 | 0,05% | 2 | 0,2% | 2 | 0,22% | 2 | 0,21% |
Duguy et al. (2004) | 2 | 0,05% | 2 | 0,2% | 2 | 0,22% | 2 | 0,21% |
Duguy et al. (2006) | 2 | 0,05% | 2 | 0,2% | 2 | 0,22% | 2 | 0,21% |
Duguy (1987) | 2 | 0,05% | 2 | 0,2% | 2 | 0,22% | 2 | 0,21% |
Duguy (1990) | 2 | 0,05% | 2 | 0,2% | 2 | 0,22% | 2 | 0,21% |
Duguy (1992) | 2 | 0,05% | 2 | 0,2% | 2 | 0,22% | 2 | 0,21% |
Duguy (1993) | 2 | 0,05% | 2 | 0,2% | 2 | 0,22% | 2 | 0,21% |
Duguy (1995) | 2 | 0,05% | 2 | 0,2% | 2 | 0,22% | 2 | 0,21% |
Duguy (1996) | 2 | 0,05% | 2 | 0,2% | 2 | 0,22% | 2 | 0,21% |
Durand (2016) | 2 | 0,05% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Evermann & Clark (1928) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Fontan (2019) | 2 | 0,05% | 2 | 0,2% | 2 | 0,22% | 2 | 0,21% |
Fowler (1919) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Fritz & Havaš (2007) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Gannier & Petiau (2006) | 2 | 0,05% | 2 | 0,2% | 2 | 0,22% | 0 | 0% |
Geoffroy Saint-Hilaire ([1817]) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Gibson & Baker (2012) | 2 | 0,05% | 2 | 0,2% | 2 | 0,22% | 2 | 0,21% |
Gill & Thiele (1997) | 2 | 0,05% | 2 | 0,2% | 2 | 0,22% | 1 | 0,11% |
Gilot et al. (1992) | 2 | 0,05% | 2 | 0,2% | 2 | 0,22% | 2 | 0,21% |
Girondo (2023) | 2 | 0,05% | 2 | 0,2% | 2 | 0,22% | 2 | 0,21% |
Gomés et al. (2018) | 2 | 0,05% | 2 | 0,2% | 1 | 0,11% | 2 | 0,21% |
Goode & Bean (1896) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Gourreau et al. (1998) | 2 | 0,05% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Guermeur (1987) | 2 | 0,05% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Harrison et al. (2007) | 2 | 0,05% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Hedges et al. (2016) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Hedges (2022) | 2 | 0,05% | 2 | 0,2% | 2 | 0,22% | 2 | 0,21% |
Henderson & Powell (2009) | 2 | 0,05% | 1 | 0,1% | 1 | 0,11% | 0 | 0% |
Hildebrand (1948) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Humeau et al. (2020) | 2 | 0,05% | 2 | 0,2% | 2 | 0,22% | 0 | 0% |
Impact-mer (2011) | 2 | 0,05% | 2 | 0,2% | 2 | 0,22% | 1 | 0,11% |
Ineich (2016) | 2 | 0,05% | 2 | 0,2% | 2 | 0,22% | 2 | 0,21% |
IUCN (2014) | 2 | 0,05% | 2 | 0,2% | 2 | 0,22% | 2 | 0,21% |
Jardine & Selby (1826-1835) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Jouan (1863) | 2 | 0,05% | 2 | 0,2% | 2 | 0,22% | 2 | 0,21% |
Kasamatsu & Joyce (1995) | 2 | 0,05% | 2 | 0,2% | 2 | 0,22% | 2 | 0,21% |
Kasamatsu et al. (2000) | 2 | 0,05% | 2 | 0,2% | 2 | 0,22% | 0 | 0% |
Kawamura (1994) | 2 | 0,05% | 2 | 0,2% | 2 | 0,22% | 0 | 0% |
Keith et al. (1999) | 2 | 0,05% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Keith (2002) | 2 | 0,05% | 2 | 0,2% | 2 | 0,22% | 2 | 0,21% |
Kock et al. (2006) | 2 | 0,05% | 2 | 0,2% | 2 | 0,22% | 2 | 0,21% |
Köhler & Vesely (2011) | 2 | 0,05% | 2 | 0,2% | 2 | 0,22% | 2 | 0,21% |
Kojadinovic et al. (2007) | 2 | 0,05% | 2 | 0,2% | 2 | 0,22% | 0 | 0% |
Lacepède (1802) | 2 | 0,05% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Lacoste (de) (2020) | 2 | 0,05% | 2 | 0,2% | 2 | 0,22% | 2 | 0,21% |
Lafresnaye (1844) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Laurenti (1768) | 2 | 0,05% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Leaper et al. (2008) | 2 | 0,05% | 2 | 0,2% | 2 | 0,22% | 2 | 0,21% |
Lepechin (1769) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Lesson (1831) | 2 | 0,05% | 1 | 0,1% | 1 | 0,11% | 0 | 0% |
Levesque & Clergeau (2002) | 2 | 0,05% | 2 | 0,2% | 2 | 0,22% | 2 | 0,21% |
Lorvelec & Pascal (2009) | 2 | 0,05% | 2 | 0,2% | 2 | 0,22% | 2 | 0,21% |
Lorvelec et al. (2004) | 2 | 0,05% | 2 | 0,2% | 2 | 0,22% | 2 | 0,21% |
Lorvelec et al. (2021) | 2 | 0,05% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Lowe (1838) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Macdonald & Barron (1868) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Maran & Frétey (2023) | 2 | 0,05% | 2 | 0,2% | 2 | 0,22% | 2 | 0,21% |
Maréchal & Pérès (2007) | 2 | 0,05% | 2 | 0,2% | 2 | 0,22% | 2 | 0,21% |
Marquet et al. (2003) | 2 | 0,05% | 2 | 0,2% | 2 | 0,22% | 2 | 0,21% |
Marshall et al. (2009) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Mas-Coma et al. (1989) | 2 | 0,05% | 2 | 0,2% | 2 | 0,22% | 2 | 0,21% |
Mathews (1914) | 2 | 0,05% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Mays et al. (2006) | 2 | 0,05% | 2 | 0,2% | 2 | 0,22% | 2 | 0,21% |
McNair & Cramer-Burke (2006) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Merrem (1820) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Mitchill (1815) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Momont (1998) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Monti et al. (2018) | 2 | 0,05% | 2 | 0,2% | 2 | 0,22% | 2 | 0,21% |
Mothes et al. (2019) | 2 | 0,05% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Nardo (1827) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Oustalet (1895) | 2 | 0,05% | 2 | 0,2% | 2 | 0,22% | 0 | 0% |
Palko et al. (1982) | 2 | 0,05% | 2 | 0,2% | 2 | 0,22% | 2 | 0,21% |
pallas (1764) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Pallas (1770) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Parenti (2021) | 2 | 0,05% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Patou et al. (2009) | 2 | 0,05% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Peron (2014) | 2 | 0,05% | 2 | 0,2% | 2 | 0,22% | 2 | 0,21% |
Pezy et al. (2022) | 2 | 0,05% | 2 | 0,2% | 2 | 0,22% | 2 | 0,21% |
Poey (1851-1854) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Pons et al. (2005) | 2 | 0,05% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Powell et al. (2008) | 2 | 0,05% | 2 | 0,2% | 2 | 0,22% | 0 | 0% |
Probst et al. (2001) | 2 | 0,05% | 2 | 0,2% | 2 | 0,22% | 2 | 0,21% |
Questel (2011) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Rafinesque (1810) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Reilly et al. (2014) | 2 | 0,05% | 2 | 0,2% | 2 | 0,22% | 2 | 0,21% |
Reis et al. (2003) | 2 | 0,05% | 2 | 0,2% | 2 | 0,22% | 2 | 0,21% |
Revilliod (1914) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Reynolds & Henderson (2018) | 2 | 0,05% | 2 | 0,2% | 2 | 0,22% | 2 | 0,21% |
Rinaldi et al. (2011) | 2 | 0,05% | 2 | 0,2% | 2 | 0,22% | 2 | 0,21% |
Robineau (1989) | 2 | 0,05% | 2 | 0,2% | 2 | 0,22% | 1 | 0,11% |
Robineau (2005) | 2 | 0,05% | 2 | 0,2% | 2 | 0,22% | 1 | 0,11% |
Rossi-santos et al. (2007) | 2 | 0,05% | 2 | 0,2% | 2 | 0,22% | 1 | 0,11% |
Saint et al. (1978) | 2 | 0,05% | 2 | 0,2% | 2 | 0,22% | 2 | 0,21% |
Schwartz & Thomas (1975) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Schweigger (1812) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Seutin et al. (1993) | 2 | 0,05% | 2 | 0,2% | 2 | 0,22% | 0 | 0% |
Simmons (2005) | 2 | 0,05% | 2 | 0,2% | 0 | 0% | 2 | 0,21% |
Speare (1990) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Spix & Agassiz (1829-31) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Spix (1824) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Tavera et al. (2018) | 2 | 0,05% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Thévenot (2014) | 2 | 0,05% | 2 | 0,2% | 2 | 0,22% | 2 | 0,21% |
Thiele et al. (1999) | 2 | 0,05% | 2 | 0,2% | 2 | 0,22% | 2 | 0,21% |
Thiele et al. (2004) | 2 | 0,05% | 2 | 0,2% | 2 | 0,22% | 1 | 0,11% |
Thorpe & Malhotra (2023) | 2 | 0,05% | 2 | 0,2% | 2 | 0,22% | 2 | 0,21% |
Thunberg (1787) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Timm & Genoways (2003) | 2 | 0,05% | 2 | 0,2% | 1 | 0,11% | 2 | 0,21% |
Tunstall (1880) | 2 | 0,05% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
UNEP-WCMC (2005) | 2 | 0,05% | 2 | 0,2% | 2 | 0,22% | 2 | 0,21% |
Van Canneytet al. (2008) | 2 | 0,05% | 2 | 0,2% | 2 | 0,22% | 2 | 0,21% |
van den Burg et al. (2021) | 2 | 0,05% | 2 | 0,2% | 2 | 0,22% | 2 | 0,21% |
Van Dijk et al. (2014) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Vanderwerf et al. (2006) | 2 | 0,05% | 2 | 0,2% | 2 | 0,22% | 2 | 0,21% |
Vieillot (1817) | 2 | 0,05% | 1 | 0,1% | 1 | 0,11% | 0 | 0% |
Vieillot (1819) | 2 | 0,05% | 2 | 0,2% | 2 | 0,22% | 2 | 0,21% |
Viel (2021) | 2 | 0,05% | 2 | 0,2% | 2 | 0,22% | 2 | 0,21% |
Villanueva et al. (2021) | 2 | 0,05% | 2 | 0,2% | 2 | 0,22% | 2 | 0,21% |
Vuillaume et al. (2015) | 2 | 0,05% | 2 | 0,2% | 2 | 0,22% | 2 | 0,21% |
Weber (1913) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Weimerskirch et al. (2009) | 2 | 0,05% | 2 | 0,2% | 2 | 0,22% | 0 | 0% |
Wilson (1813) | 2 | 0,05% | 2 | 0,2% | 2 | 0,22% | 2 | 0,21% |
Abhaya & Probst (2009) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Abhaya et al. (1998) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 0 | 0% |
Abril et al. (1986) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Agarwal et al. (2021) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Agassiz (1833-1843) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Agassiz (1857) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Ainley et al. (2007) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Al-hasson & Ali (2020) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Almeida & Vasconcelos (2023) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Almeida et al. (2019) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Altamirano-Benavides & Woolrich-Piña (2023) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Altamirano-benavides & Woolrich-piña (2023) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Alvarez-berríos et al. (2016) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Andrew et al. (2008) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Angel (1935) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Angin (2017) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Angin (2017) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Anonyme. (2004) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Anonyme. (2004) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 0 | 0% |
Anonyme (2008) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 0 | 0% |
Anonyme. (2012) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2012) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 0 | 0% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 0 | 0% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Anonyme. (2012) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 0 | 0% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 0 | 0% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Anonyme. (2012) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Anonyme. (2012) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 0 | 0% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 0 | 0% |
Anonyme. (2012) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 0 | 0% |
Anonyme. (2012) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Anonyme. (2012) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 0 | 0% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Anonyme. (2012) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 0 | 0% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Anonyme. (2012) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 0 | 0% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Anonyme. (2012) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Anthony (1917) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Aquarium de La Rochelle (2017) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Araujo-vieira et al. (2020) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Armand & Ferlay (2023) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Astudillo et al. (2021) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Attié et al. (1997) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Atwood (1869) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Bailenger et al. (1965) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Baird (1858) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Baird (1865) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Baldi et al. (2023) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Balouet & Olson (1989) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Bancroft (1832) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Bangs (1913) | 1 | 0,02% | 1 | 0,1% | 0 | 0% | 1 | 0,11% |
Barbancey & Probst (1998) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Barbancey (2001) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Barbancey (2001) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Barbour (1912) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Barbraud (2012) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Barlow (1978) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Barre et al. (1991) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 0 | 0% |
Bassett (2022) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Bauer & Sadlier (1994) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Bauer et al. (2010) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Bavay (1869) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Bavay (1873) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Bavay (1899) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Bean (1912) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Beaucournu (1968) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Beaufils (1999) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Beauvieux et al. (2024) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Becerra et al. (2024) | 1 | 0,02% | 1 | 0,1% | 0 | 0% | 1 | 0,11% |
Bell (1827) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Bennett (1831) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Bernal & Rocha (2011) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Bertault (1988) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Bertin (1928) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Bertrand & Drogou (2000) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Bertrand et al. (2001) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Bertrand (1982) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Best et al. (1995) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 0 | 0% |
Birdlife International (2012) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Birdlife International (2012) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Birdlife International (2016) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Birdlife International (2016) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Birdlife International (2017) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Birdlife International (2017) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Blanc et al. (1993) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Bleeker (1865) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Bloch & Schneider (1801) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Bloch (1785-1795) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Bloch (1793) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Bochaton et al. (2016) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Bochaton et al. (2017) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Bochaton et al. (2020) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Boie (1835) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Bonnaterre (1788) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Bonnaterre (1789) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Borcyk et al. (2023) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Borroto-páez (2018) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Boschert & Dronneau (1998) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Bouchon & Lemoine (2003) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Bougeard & Siblet (2000) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Boulenger (1883) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Bourgade (2021) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Brace et al. (2015) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Brace et al. (2023) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Branch (2010) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 0 | 0% |
Brandt (1838) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Brehm (1831) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Breuil & Serre-collet (2012) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Breuil et al. (2022) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Brewster (1895) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Brewster (1902) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Brito Capello (1867) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Brown (2008) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Brugneaux & Pérès (2005) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Brun (1958) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Brunes et al. (2021) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Brünnich (1764) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Budylenko (1977) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 0 | 0% |
Bush et al. (2021) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Caceres (2002) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Calenge et al. (2010) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 0 | 0% |
Callou (2003) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Capalleras & Carretero (2000) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 0 | 0% |
Capape et al. (2002) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Carte (1866) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Castro et al. (2018) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Catil (2013) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Causse & Hautecoeur (2006) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Caut et al. (2008) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Censky (1988) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Cerchio et al. (2009) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 0 | 0% |
Chambault et al. (2020) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Champion (2017) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Chastel et al. (1981) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Chastel et al. (1987) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Chastel et al. (2003) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Cheke & Hume (2008) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Cheke (2010) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Chesser et al. (2016) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Chevreux & de Guerne (1893) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Cheylan et al. (2022) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Chibon (1961) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Chibon (1962) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Chocobar et al. (2023) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Ciccione (2001) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Ciccione (2001) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Clark (1905) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Clements (1992) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Clergeau & Pascal (2003) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Clergeau & Pascal (2003) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 0 | 0% |
Clergeau & Pascal (2003) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Clergeau et al. (2003) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Coatmeur (1999) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Cochran (1938) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Colin (1992) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Collazos-astudillo et al. (2022) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Collectif (2009) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 0 | 0% |
Collet & Duguy (1981) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Commecy et al. (2013) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Cope (1879) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Cornuaille et al. (2021) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Cory (1886) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Cottarel et al. (2013) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Coues (1861) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Coues (1862) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Counihan et al. (2012) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 0 | 0% |
Crochet et al. (2022) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Crouzier (2009) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Csabaï (2020) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 0 | 0% |
Dal Zotto et al. (2024) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Dalebout et al. (2005) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Dalleau et al. (2014) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Danforth (1935) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
D´angiolella et al. (2021) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Daszkiewicz, P. & Massary, J.-C. de 2006. Overlooked historical testimony as to the presence of Red-billed Tropicbird Phaeton aethereus in French Guiana. Bulletin of the British Ornithologists'Club, 126(1): 71-73.">Daszkiewicz & Massary (2006) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 0 | 0% |
Daudin (1802) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 0 | 0% |
Daudin (1803) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Dauvin (1990) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Davis (1973) | 1 | 0,02% | 1 | 0,1% | 0 | 0% | 1 | 0,11% |
de Massary et al. (2015) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 0 | 0% |
Deblock & Rose (1964) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Deblock (1966) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Debout (2001) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Dechelle & Ingels (2007) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Deflandre (2007) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Deflorenne et al. (2012) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Delacour (1963) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Delaney & Warner (2017) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Delcroix et al. (2008) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Deliveyne et al. (2023) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Deniau & Provost (2020) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Denys et al. (2022) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Deutsche & Ornithologen-gesellschaft (1887) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Dewynter et al. (2017) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Dewynter (2018) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Dewynter (2020) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Dieme et al. (2015) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Dollfus (1934) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Dollfus (1966) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Donini & Doody (2021) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Dore (2017) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Dória et al. (2015) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Dorleans (2022) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Dreff & Delliere (1994) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Dubois & Cugnasse (2015) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Dubois & Louvet (2014) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Ducatez & Devore (2023) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Duguy & Duron (1981) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Duguy & Duron (1982) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Duguy & Duron (1983) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Duguy & Duron (1984) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Duguy & Duron (1985) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Duguy et al. (1980) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Duguy et al. (2000) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Duguy (1983) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Duguy (1986) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Duguy (1988) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Duguy (1989) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Duméril & Bibron (1839) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Duval et al. (2019) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Efe et al. (2009) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 0 | 0% |
Ersts & Rosenbaum (2003) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 0 | 0% |
Eschscholtz (1829) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Etheridge (1964) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Eyton (1838) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Faber (1829) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabre & Orsini (2016) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Ficetola & Scali (2010) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 0 | 0% |
Fieldsend et al. (2021) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Flechas et al. (2018) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Fleming & Jackson (2011) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 0 | 0% |
Flitti & Rocha (2014) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Forest (1946) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Forskål (1775) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Fowler (1900) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Francour & Mouine (2008) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Franzini et al. (2018) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Fremont (2002) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Fretey & Bour (1980) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Fretey et al. (2023) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Fretey (1980) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Fretey (2003) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Frétey (2022) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Frétey (2023) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Fritz et al. (2010) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Gallien (2011) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Garbino et al. (2020) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Garman (1887) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Garman (1899) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Garrigue & Poupon (2013) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Gauthier-clerc & Lambert (2002) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Geneva et al. (2013) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Genoways & Jones (1975) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Gérard et al. (2016) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Gérigny et al. (2020) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Gernigon (2008) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Giglioli & Salvadori (1868) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Gill (1862) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Gill (1995) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Gillespie (1997) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Giovannotti et al. (2017) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Girard (1859) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Giraud-Audine et al. (2007) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 0 | 0% |
Girondot et al. (2015) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Gmelin (1770) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Gmelin (1789) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Godet et al. (2021) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Goedert et al. (2020) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Golvan (1956) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Gomès & Ibéné (2013) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 0 | 0% |
González et al. (2018) | 1 | 0,02% | 1 | 0,1% | 0 | 0% | 1 | 0,11% |
Goode & Bean (1882) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Goulletquer (2016) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Graber & Euzeby (1976) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Grant (1958) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Gray (1846) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Gray (1850) | 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% |
Grazziotin et al. (2012) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 0 | 0% |
Guiguen et al. (1984) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Guinet (1991) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Guinet (2004) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Gunderson et al. (2020) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Günther (1860) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Hamdan et al. (2023) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Havery et al. (2018) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Hedges et al. (2009) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Heimlich-boran (1993) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Hellebuyck et al. (2017) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Henao-osorio et al. (2021) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Henderson et al. (1993) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Hennique et al. (2013) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Herzberg (2018) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Houttuyn (1782) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Howell & Clements (2019) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Hudson et al. (2018) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Hudson et al. (2021) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Hudson et al. (2021) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Huey (1927) | 1 | 0,02% | 1 | 0,1% | 0 | 0% | 1 | 0,11% |
Ibéné et al. (2007) | 1 | 0,02% | 1 | 0,1% | 0 | 0% | 1 | 0,11% |
Ifremer (2009) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Iglésias et al. (2021) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Iković et al. (2023) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 0 | 0% |
Ineich & Bauer (1992) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Ineich et al. (2017) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Ineich (1999) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Ineich (2015) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Isaac (2020) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Isbell & Enstam Jaffe (2013) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Isenmann et al. (1971) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Issartel & Leblanc (2004) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Jairam et al. (2016) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Jamonneau et al. (2025) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Jefferson & Barros (1997) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Jehl et al. (1980) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Jim et al. (2022) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Johnson & Wolman (1984) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 0 | 0% |
Johnson (1973) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Jordan & Evermann (1903) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Jordan & Gilbert (1882) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Jordan & Gilbert (1884) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Jordan & Jordan (1922) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Jordan et al. (1927) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Jordan (1888) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Jouventin (1994) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Joyeux & Baer (1955) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Judson et al. (2018) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Kadafi et al. (2024) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Kaiser & Hardy (1994) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Kaiser et al. (2003) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Karaa et al. (2016) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Karin et al. (2021) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Kasamatsu et al. (1995) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 0 | 0% |
Kasamatsu et al. (1998) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 0 | 0% |
Kaup (1856) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Kayser & Wilhelm (1991) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Keith & Marquet (2011) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Keith et al. (2014) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Kiszka et al. (2009) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Kiszka et al. (2009) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 0 | 0% |
Heron, 36(1): 31-34.">Kiszka (2003) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 0 | 0% |
Kock & Stephan (1986) | 1 | 0,02% | 1 | 0,1% | 0 | 0% | 1 | 0,11% |
Koleska & Jablonski (2018) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Kornilev et al. (2020) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 0 | 0% |
Kuhl (1820) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Labach et al. (2021) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 0 | 0% |
Lacoste (2021) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Lacoste (2021) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Lafresnaye (1848) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Lancastre et al. (1976) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Latham (1787) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Lawrence (1877) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Lawrence (1885) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Lazell (1964) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Le Corre & Jouventin (1999) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 0 | 0% |
Leaper et al. (2008) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 0 | 0% |
Ledreff & Raynaud (1993) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Legendre (1937) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Léger & Mouzels (1917) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Léger (2003) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Léger (2008) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Legouez (2010) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Legros & Puissauve (2015) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Leimroth et al. (2022) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Lenoble et al. (2020) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Lenoble (2015) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Lenoble (2019) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Leonhardt et al. (2019) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Leonhardt et al. (2022) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Lesage et al. (2024) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Lescure et al. (2016) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Lescure (2018) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Lesson (1828) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 0 | 0% |
Lesson (1830-1831) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Lesson (1839) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Lesueur (1822) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Letacq (1924) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Letourneur et al. (2004) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Levesque & Mathurin (2008) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Levesque & Yesou (2018) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Levesque (2001) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Levesque (2013) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Liardet & d'Auzon (2004) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Liardet (2004) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Liebart et al. (2021) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Liebgold et al. (2019) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Lim (1997) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Lizé (2018) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Loisier et al. (2021) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Loison (1989) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 0 | 0% |
Lorvelec & Clergeau (2003) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Lorvelec & Vigne (2003) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Lorvelec & Vigne (2003) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Lorvelec et al. (2003) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Lorvelec et al. (2003) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Lorvelec et al. (2009) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Lorvelec et al. (2011) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Lorvelec et al. (2016) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Lorvelec et al. (2017) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Louette & Cousin (1999) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Louisin & Probst (1996) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Loury & Puissauve (2016) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Lowe (1834) | 1 | 0,02% | 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) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Lowe (1841) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Lowe (1843) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Lynch (1965) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Maciel et al. (2021) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Macleod et al. (2006) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Mageski et al. (2017) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Mahé et al. (2013) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Maillard & David (2014) | 1 | 0,02% | 1 | 0,1% | 0 | 0% | 1 | 0,11% |
Malm (1877) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Mancino et al. (2022) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Marchandeau & Letty (2021) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Marchandeau et al. (2003) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Marinho (2022) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Marion & Clergeau (2003) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 0 | 0% |
Marion & Marion (1982) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 0 | 0% |
Marion (2003) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 0 | 0% |
Marion (2003) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Martin et al. (2021) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Martinet et al. (1765) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Martinet et al. (1765) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Martinet et al. (1765) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Massary (2012) | 1 | 0,02% | 1 | 0,1% | 0 | 0% | 1 | 0,11% |
Matsuoka et al. (2005) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 0 | 0% |
Mckenzie (2016) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Mctavish (2002) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Medetian & Miaud (2024) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Meek & Hildebrand (1923) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Melin et al. (2003) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Ménard et al. (2000) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Meneses et al. (2019) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Montagu (1813) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Moon & Kamath (2019) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Moravec et al. (2020) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Moreau de Jonnès (1818) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Morel (1959) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Morrison (2006) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 0 | 0% |
Mourier (2012) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Murase et al. (2002) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 0 | 0% |
Murray (1884) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Nadal & Tariel (2008) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 0 | 0% |
Nassi et al. (1975) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Naumann (1819) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Nelson-Smith et al. (2014) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Nicol et al. (2000) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 0 | 0% |
Noel et al. (2004) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Noël (2017) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Nuttall (1834) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Oliveira et al. (2018) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Oliver (2011) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
O'reilly (1818) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Oremus (2009) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
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% |
Paré & Lorvelec (2012) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 0 | 0% |
Parker (1936) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Parmentier et al. (2017) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Pascal & Vigne (2003) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Pascal & Vigne (2003) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Pascal & Vigne (2003) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Pascal et al. (2003) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Pascal et al. (2003) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Pascal et al. (2003) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Pearman et al. (2016) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 0 | 0% |
Pearman et al. (2020) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Pearson & Prévot (1971) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Pérez-delgadillo & Lara-reséndiz (2024) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Perkins (1928) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Perrin et al. (1994) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Perry et al. (1999) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 0 | 0% |
Peters (1864) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Peters (1930) | 1 | 0,02% | 1 | 0,1% | 0 | 0% | 1 | 0,11% |
Petit et al. (2021) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Pettit et al. (2021) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Philippi (1887) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Philippot et al. (2019) | 1 | 0,02% | 1 | 0,1% | 0 | 0% | 1 | 0,11% |
Pierpoint et al. (1997) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 0 | 0% |
Pinaud et al. (2005) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Pinchon (1976) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Pinto-coelho et al. (2021) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Pitman & Ensor (2003) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Poey (1863) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Pons et al. (1999) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Pool (2013) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 0 | 0% |
Praderi et al. (1992) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Prado et al. (2023) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Prato et al. (2022) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Prevot (1971) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Preynat (2013) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Probst et al. (2023) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Probst (1997) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Probst (1999) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Probst (2001) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Probst (2007) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
protection du biotope des eaux territoriales de l'île de Clipperton dénommée « aire marine protégée dans les eaux territoriales de l'île de Clipperton » | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Puissauve & Legros (2015) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Puissauve, Comolet-tirman & Whal (2015) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 0 | 0% |
Purenne (2016) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Annales de la Société de Sciences naturelles de la Charente-Maritime, 10(2): 225-236.">Quéro et al. (2011) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Quéro & Delmas (1982) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Quero & Laborde (1996) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Quero et al. (1998) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Quero et al. (2013) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Quero (1998) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Questel & Boggio (2012) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Questel et al. (2012) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Questel (2014) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Randi et al. (2001) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Ranzani (1839) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Read et al. (2015) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Recoder et al. (2018) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Reeber (2015) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Reinert et al. (2021) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Remsen et al. (2013) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Renaud et al. (2013) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Revuelta et al. (2015) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Rhodin & Carr (2009) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Ribic et al. (1991) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 0 | 0% |
Richardson (1846) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Richmond (1966) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Ridgway (1880) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Rimblot et al. (1985) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Ringler et al. (2021) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Robert et al. (2002) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Robins & Sylva (1963) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Roche & Guinet (2007) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Rodrigues et al. (2021) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Romero et al. (2010) | 1 | 0,02% | 1 | 0,1% | 0 | 0% | 1 | 0,11% |
Roos (2000) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Roques (1991) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Rosen (1911) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Rosenbaum & Collins (2006) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 0 | 0% |
Roughgarden (1974) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Roux & Coll. (2017) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Runde (2016) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Cormoran, 15(4): 218.">Rundle & Rundle (2007) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Rüppell (1835) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Rüppell (1835) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Russell & Bauer (2002) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Ruys & Coord (2012) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Sadlier et al. (2012) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Sanchez & Probst (2016) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Sanchez et al. (2004) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Sanchez et al. (2019) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Savouré-Soubelet et al. (in prep.) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Sawai et al. (2018) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Schiebel (1910) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Schinz (1822) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Schlegel (1837) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Schmidt (1928) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Schneider (1783) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Schneider (1801) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Schoepff (1792) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Schuchmann (1981) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Schwartz & Henderson (1991) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Schwartz (1967) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Sclater (1866) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Scopoli (1786) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Sellier et al. (2016) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Séret (1993) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Séret (2014) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Seriot et al. (1988) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Servan & Arvy (1997) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 0 | 0% |
Servan (1976) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Shaver et al. (2019) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Ibis, 6 6: 326">Sherborn (1894) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Shine et al. (2021) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Shine (2010) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Shukla et al. (2024) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Siorat & Rocamora (1995) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Siorat et al. (2003) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Slater et al. (2014) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Smith et al. (2005) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Smith-Vaniz & Carpenter (2007) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Smith-vaniz & Jelks (2014) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Snyder et al. (2019) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Socolovschi et al. (2012) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Sonsino (1893) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Spiroux (1996) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Steadman & Bollt (2010) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 0 | 0% |
Steindachner (1861) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Steindachner (1867) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Stelfox et al. (2020) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Stephan (2011) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Sundevall (1857) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Swainson (1838) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 0 | 0% |
Széles et al. (2018) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Taberlet (1983) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Tejedor (2006) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Terrasse & Terrasse (1969) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Teunissen & Peters (2022) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Thawley & Kolbe (2020) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Thawley et al. (2019) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Thibault et al. (2023) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Thoisy et al. (2003) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 0 | 0% |
Toohey et al. (2022) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Tregarot et al. (2015) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Trevoux & Trevoux (2007) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Tschudi (1838) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Turpin & Probst (1998) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 0 | 0% |
Turpin et al. (2001) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Uicn et al. (2016) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
UICN (2009) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Valencia-zuleta et al. (2024) | 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. (2018) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Van den burg et al. (2022) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Vandelli (1761) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Vanderwerf et al. (2004) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Vaslet et al. (2010) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Vera-pérez et al. (2021) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Vernoux (1988) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Verreaux & Des Murs (1860) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 0 | 0% |
Veysset (2003) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 0 | 0% |
Viale & Frontier (1989) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Vieillot (1816) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Vieillot (1817) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Vieillot (1817) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Von May et al. (2021) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Waayers et al. (2011) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Wahl & Barbraud (2005) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 0 | 0% |
Walbaum (1792) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Wallach (2009) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Wang & Liu (2016) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 0 | 0% |
Wang & Qiu (2022) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Wasilewski et al. (2022) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Weerdt (2023) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 0 | 0% |
Weimerskirch & Jouventin (1998) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Werner (1980) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Weterings & Vetter (2017) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Whitley (1929) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Whitley (1933) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Whitley (1937) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Whitley (1948) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Wickel et al. (2014) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Wied (1839) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Wiegmann (1834) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Williams et al. (2009) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 0 | 0% |
Williams et al. (2019) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Works & Olson (2018) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 0 | 0% |
Yasumiba et al. (2015) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Yengle (2021) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Yésou (2003) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Yésou (2003) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Yésou (2003) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Yésou (2003) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Yuan et al. (2022) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Zdunek (2022) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Zelhuber (2009) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
Zug & Zug (1979) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
(2022) | 1 | 0,02% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |