Vertébrés de Martinique
1156 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) | 429 | 9,72% | 421 | 45,27% | 407 | 46,62% | 407 | 46,41% |
Questel & Le Quellec (2012) | 379 | 8,59% | 362 | 38,92% | 356 | 40,78% | 345 | 39,34% |
Smith (1997) | 252 | 5,71% | 232 | 24,95% | 226 | 25,89% | 232 | 26,45% |
Bouchon-Navaro et al. (2005) | 224 | 5,08% | 184 | 19,78% | 184 | 21,08% | 183 | 20,87% |
Levesque & Delcroix (2018) | 192 | 4,35% | 186 | 20% | 164 | 18,79% | 180 | 20,52% |
Uicn et al. (2017) | 181 | 4,1% | 172 | 18,49% | 166 | 19,01% | 145 | 16,53% |
UICN Comité français, OFB & MNHN (2021) | 170 | 3,85% | 170 | 18,28% | 170 | 19,47% | 140 | 15,96% |
Yokoyama (2013) | 133 | 3,01% | 118 | 12,69% | 114 | 13,06% | 106 | 12,09% |
Belfan & Conde (2016) | 132 | 2,99% | 127 | 13,66% | 93 | 10,65% | 124 | 14,14% |
Linnaeus (1758) | 121 | 2,74% | 36 | 3,87% | 36 | 4,12% | 30 | 3,42% |
Bouchon-Navaro & Louis (1986) | 119 | 2,7% | 102 | 10,97% | 102 | 11,68% | 102 | 11,63% |
Diaz & Cuzange (2009) | 106 | 2,4% | 98 | 10,54% | 98 | 11,23% | 95 | 10,83% |
Remsen et al. (2013) | 104 | 2,36% | 98 | 10,54% | 98 | 11,23% | 79 | 9,01% |
Rinaldi (2016) | 92 | 2,08% | 92 | 9,89% | 92 | 10,54% | 68 | 7,75% |
Uicn et al. (2015) | 87 | 1,97% | 85 | 9,14% | 85 | 9,74% | 69 | 7,87% |
Brugneaux & Pérès (2006) | 85 | 1,93% | 76 | 8,17% | 76 | 8,71% | 76 | 8,67% |
Henderson & Breuil (2012) | 85 | 1,93% | 65 | 6,99% | 57 | 6,53% | 63 | 7,18% |
Carzon et al. (2016) | 69 | 1,56% | 69 | 7,42% | 69 | 7,9% | 51 | 5,82% |
Estrade et al. (2016) | 69 | 1,56% | 69 | 7,42% | 69 | 7,9% | 51 | 5,82% |
Louis et al. (1992) | 60 | 1,36% | 49 | 5,27% | 49 | 5,61% | 47 | 5,36% |
Fricke et al. (2011) | 56 | 1,27% | 54 | 5,81% | 54 | 6,19% | 52 | 5,93% |
Etcheberry & Abraham (2009) | 52 | 1,18% | 44 | 4,73% | 44 | 5,04% | 41 | 4,68% |
Fricke et al. (2009) | 52 | 1,18% | 50 | 5,38% | 50 | 5,73% | 47 | 5,36% |
Uicn et al. (2020) | 51 | 1,16% | 51 | 5,48% | 51 | 5,84% | 44 | 5,02% |
Rousseau (2010) | 48 | 1,09% | 46 | 4,95% | 46 | 5,27% | 46 | 5,25% |
Siu et al. (2017) | 46 | 1,04% | 43 | 4,62% | 43 | 4,93% | 41 | 4,68% |
Béarez et al. (2017) | 40 | 0,91% | 40 | 4,3% | 40 | 4,58% | 38 | 4,33% |
Wickel & Jamon (2010) | 36 | 0,82% | 35 | 3,76% | 35 | 4,01% | 34 | 3,88% |
Poey (1858-61) | 35 | 0,79% | 0 | 0% | 0 | 0% | 0 | 0% |
Dewynter et al. (2019) | 34 | 0,77% | 34 | 3,66% | 30 | 3,44% | 31 | 3,53% |
Mertens & Wermuth (1960) | 31 | 0,7% | 0 | 0% | 0 | 0% | 0 | 0% |
Collette & Nauen (1983) | 30 | 0,68% | 30 | 3,23% | 26 | 2,98% | 30 | 3,42% |
Dewynter et al. (2023) | 29 | 0,66% | 29 | 3,12% | 29 | 3,32% | 26 | 2,96% |
Dewynter (2021) | 27 | 0,61% | 27 | 2,9% | 26 | 2,98% | 27 | 3,08% |
Lorvelec et al. (2007) | 27 | 0,61% | 22 | 2,37% | 22 | 2,52% | 20 | 2,28% |
Bouchon-Navaro et al. (1992) | 25 | 0,57% | 22 | 2,37% | 22 | 2,52% | 21 | 2,39% |
Weimerskirch et al. (2009) | 25 | 0,57% | 19 | 2,04% | 19 | 2,18% | 16 | 1,82% |
Catzeflis (2012) | 24 | 0,54% | 24 | 2,58% | 24 | 2,75% | 18 | 2,05% |
Gmelin (1789) | 24 | 0,54% | 4 | 0,43% | 4 | 0,46% | 3 | 0,34% |
Tostain et al. (2013) | 24 | 0,54% | 19 | 2,04% | 18 | 2,06% | 18 | 2,05% |
Bordin et al. (2021) | 23 | 0,52% | 23 | 2,47% | 23 | 2,63% | 17 | 1,94% |
Charrassin (2016) | 23 | 0,52% | 23 | 2,47% | 23 | 2,63% | 17 | 1,94% |
Charrassin (2016) | 23 | 0,52% | 23 | 2,47% | 23 | 2,63% | 17 | 1,94% |
Clements (2012) | 23 | 0,52% | 23 | 2,47% | 21 | 2,41% | 22 | 2,51% |
Jarrett & Shirihai (2014) | 23 | 0,52% | 23 | 2,47% | 23 | 2,63% | 17 | 1,94% |
Moutou (2016) | 23 | 0,52% | 23 | 2,47% | 23 | 2,63% | 17 | 1,94% |
Questel (2017) | 23 | 0,52% | 23 | 2,47% | 23 | 2,63% | 23 | 2,62% |
Spitz et al. (2016) | 23 | 0,52% | 23 | 2,47% | 23 | 2,63% | 17 | 1,94% |
Thoisy & Bordin (2016) | 23 | 0,52% | 23 | 2,47% | 23 | 2,63% | 17 | 1,94% |
Urtizberea (2016) | 23 | 0,52% | 23 | 2,47% | 23 | 2,63% | 17 | 1,94% |
Dewynter et al. (2021) | 22 | 0,5% | 22 | 2,37% | 22 | 2,52% | 17 | 1,94% |
Fourriére et al. (2014) | 22 | 0,5% | 22 | 2,37% | 22 | 2,52% | 22 | 2,51% |
Garrigue (2007) | 22 | 0,5% | 22 | 2,37% | 22 | 2,52% | 17 | 1,94% |
Breuil (2009) | 21 | 0,48% | 16 | 1,72% | 16 | 1,83% | 14 | 1,6% |
Compagno (1984) | 21 | 0,48% | 21 | 2,26% | 21 | 2,41% | 21 | 2,39% |
Delrieu-Trottin et al. (2015) | 20 | 0,45% | 20 | 2,15% | 19 | 2,18% | 20 | 2,28% |
Le Bail et al. (2012) | 20 | 0,45% | 20 | 2,15% | 20 | 2,29% | 20 | 2,28% |
Lim et al. (2002) | 20 | 0,45% | 16 | 1,72% | 16 | 1,83% | 16 | 1,82% |
Massary et al. (2021) | 20 | 0,45% | 19 | 2,04% | 19 | 2,18% | 17 | 1,94% |
Aulagnier (2009) | 19 | 0,43% | 19 | 2,04% | 19 | 2,18% | 16 | 1,82% |
Bacchet et al. (2007) | 19 | 0,43% | 18 | 1,94% | 18 | 2,06% | 18 | 2,05% |
Barau et al. (2005) | 19 | 0,43% | 16 | 1,72% | 16 | 1,83% | 13 | 1,48% |
Gannier (2001) | 19 | 0,43% | 19 | 2,04% | 19 | 2,18% | 14 | 1,6% |
G.E.M.M. (2012) | 19 | 0,43% | 19 | 2,04% | 19 | 2,18% | 14 | 1,6% |
Rafinesque Schmaltz (1810) | 18 | 0,41% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Gannier (2002) | 17 | 0,39% | 17 | 1,83% | 17 | 1,95% | 13 | 1,48% |
Gannier (2009) | 17 | 0,39% | 17 | 1,83% | 17 | 1,95% | 12 | 1,37% |
Hoff & Daszkiewicz (2001) | 17 | 0,39% | 14 | 1,51% | 14 | 1,6% | 13 | 1,48% |
Proceedings of the Zoological Society of London, 1907: 1035-1037.">Hopkinson (1907) | 17 | 0,39% | 3 | 0,32% | 3 | 0,34% | 3 | 0,34% |
Linnaeus (1766) | 17 | 0,39% | 2 | 0,22% | 1 | 0,11% | 1 | 0,11% |
Uicn et al. (2015) | 17 | 0,39% | 14 | 1,51% | 14 | 1,6% | 13 | 1,48% |
Van Dijk et al. (2012) | 17 | 0,39% | 12 | 1,29% | 12 | 1,37% | 12 | 1,37% |
Cuvier & Valenciennes (1833) | 16 | 0,36% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Dewynter et al. (2023) | 16 | 0,36% | 16 | 1,72% | 16 | 1,83% | 15 | 1,71% |
Gannier (2000) | 16 | 0,36% | 16 | 1,72% | 16 | 1,83% | 11 | 1,25% |
Monti et al. (2010) | 16 | 0,36% | 14 | 1,51% | 14 | 1,6% | 14 | 1,6% |
Questel et al. (2023) | 16 | 0,36% | 16 | 1,72% | 16 | 1,83% | 15 | 1,71% |
Questel et al. (2023) | 16 | 0,36% | 16 | 1,72% | 16 | 1,83% | 15 | 1,71% |
Whitehead et al. (1988) | 16 | 0,36% | 16 | 1,72% | 16 | 1,83% | 16 | 1,82% |
Breuil et al. (2010) | 15 | 0,34% | 12 | 1,29% | 11 | 1,26% | 11 | 1,25% |
Breuil (2002) | 15 | 0,34% | 11 | 1,18% | 11 | 1,26% | 9 | 1,03% |
Dewynter & Claessens (2020) | 15 | 0,34% | 15 | 1,61% | 15 | 1,72% | 10 | 1,14% |
Dewynter et al. (2022) | 15 | 0,34% | 15 | 1,61% | 15 | 1,72% | 14 | 1,6% |
Heemstra & Randall (1993) | 15 | 0,34% | 15 | 1,61% | 15 | 1,72% | 15 | 1,71% |
Kiszka et al.(2007) | 15 | 0,34% | 15 | 1,61% | 15 | 1,72% | 11 | 1,25% |
Massary et al. (2018) | 15 | 0,34% | 15 | 1,61% | 15 | 1,72% | 14 | 1,6% |
Clements et al. (2015) | 14 | 0,32% | 13 | 1,4% | 3 | 0,34% | 12 | 1,37% |
Massary et al. (2017) | 14 | 0,32% | 14 | 1,51% | 14 | 1,6% | 13 | 1,48% |
Allen (1985) | 13 | 0,29% | 13 | 1,4% | 13 | 1,49% | 13 | 1,48% |
Dickinson & Remsen (2013) | 13 | 0,29% | 12 | 1,29% | 8 | 0,92% | 11 | 1,25% |
Gargominy et al. (1996) | 13 | 0,29% | 13 | 1,4% | 13 | 1,49% | 13 | 1,48% |
Kiszka et al. (2010) | 13 | 0,29% | 13 | 1,4% | 13 | 1,49% | 10 | 1,14% |
Laran et al. (2011) | 13 | 0,29% | 13 | 1,4% | 13 | 1,49% | 10 | 1,14% |
Barré (2021) | 12 | 0,27% | 12 | 1,29% | 12 | 1,37% | 12 | 1,37% |
Berry & Smith-Vaniz (1978) | 12 | 0,27% | 12 | 1,29% | 12 | 1,37% | 12 | 1,37% |
Compagno (1984) | 12 | 0,27% | 12 | 1,29% | 12 | 1,37% | 12 | 1,37% |
Hedges & Conn (2012) | 12 | 0,27% | 8 | 0,86% | 8 | 0,92% | 8 | 0,91% |
Nakamura (1985) | 12 | 0,27% | 12 | 1,29% | 12 | 1,37% | 12 | 1,37% |
Rocamora (2004) | 12 | 0,27% | 10 | 1,08% | 9 | 1,03% | 8 | 0,91% |
Deblock et al. (1960) | 11 | 0,25% | 5 | 0,54% | 5 | 0,57% | 5 | 0,57% |
Del Hoyo & Collar (2014) | 11 | 0,25% | 7 | 0,75% | 7 | 0,8% | 7 | 0,8% |
Dulau-Drouot et al. (2008) | 11 | 0,25% | 11 | 1,18% | 11 | 1,26% | 7 | 0,8% |
Kulbicki (comm. pers., 2011) | 11 | 0,25% | 9 | 0,97% | 9 | 1,03% | 9 | 1,03% |
Soubeyran et al. (2011) | 11 | 0,25% | 11 | 1,18% | 11 | 1,26% | 11 | 1,25% |
Cohen et al. (1990) | 10 | 0,23% | 10 | 1,08% | 10 | 1,15% | 10 | 1,14% |
Cuvier & Valenciennes ([1832]) | 10 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Fricke et al. (2013) | 10 | 0,23% | 10 | 1,08% | 10 | 1,15% | 9 | 1,03% |
Kulbicki et al. (2000) | 10 | 0,23% | 9 | 0,97% | 9 | 1,03% | 8 | 0,91% |
Soubeyran (2008) | 10 | 0,23% | 10 | 1,08% | 10 | 1,15% | 10 | 1,14% |
Theuerkauf et al. (2010) | 10 | 0,23% | 10 | 1,08% | 10 | 1,15% | 10 | 1,14% |
Béarez & Séret (2009) | 9 | 0,2% | 9 | 0,97% | 9 | 1,03% | 9 | 1,03% |
Bochaton et al. (2021) | 9 | 0,2% | 8 | 0,86% | 8 | 0,92% | 8 | 0,91% |
Commission de l’Avifaune Française (2016) | 9 | 0,2% | 9 | 0,97% | 9 | 1,03% | 7 | 0,8% |
Girard (2007) | 9 | 0,2% | 7 | 0,75% | 6 | 0,69% | 7 | 0,8% |
Guth (1971) | 9 | 0,2% | 9 | 0,97% | 9 | 1,03% | 5 | 0,57% |
UICN Comité français, OFB, MNHN & GEPOMAY (2025) | 9 | 0,2% | 9 | 0,97% | 9 | 1,03% | 8 | 0,91% |
Aulagnier et al. (2017) | 8 | 0,18% | 8 | 0,86% | 8 | 0,92% | 8 | 0,91% |
Béarez & Bouffandeau (2019) | 8 | 0,18% | 8 | 0,86% | 8 | 0,92% | 7 | 0,8% |
Charbonnel (1990) | 8 | 0,18% | 6 | 0,65% | 6 | 0,69% | 4 | 0,46% |
Gronow (1854) | 8 | 0,18% | 0 | 0% | 0 | 0% | 0 | 0% |
Lescure et al. (2012) | 8 | 0,18% | 7 | 0,75% | 6 | 0,69% | 6 | 0,68% |
Lowe et al. (2007) | 8 | 0,18% | 7 | 0,75% | 6 | 0,69% | 7 | 0,8% |
Massary et al. (2019) | 8 | 0,18% | 8 | 0,86% | 8 | 0,92% | 7 | 0,8% |
Muratet (2015) | 8 | 0,18% | 8 | 0,86% | 7 | 0,8% | 7 | 0,8% |
Pedersen et al. (2013) | 8 | 0,18% | 7 | 0,75% | 7 | 0,8% | 3 | 0,34% |
Richard et al. (1982) | 8 | 0,18% | 4 | 0,43% | 4 | 0,46% | 4 | 0,46% |
Samaran & Guinet (2009) | 8 | 0,18% | 8 | 0,86% | 8 | 0,92% | 7 | 0,8% |
Whitehead (1985) | 8 | 0,18% | 8 | 0,86% | 8 | 0,92% | 8 | 0,91% |
Bloch & Schneider (1801) | 7 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Bour et al. (2008) | 7 | 0,16% | 6 | 0,65% | 6 | 0,69% | 5 | 0,57% |
Camiñas et al. (2021) | 7 | 0,16% | 7 | 0,75% | 7 | 0,8% | 7 | 0,8% |
Dewynter et al. (2019) | 7 | 0,16% | 7 | 0,75% | 7 | 0,8% | 6 | 0,68% |
Genoways et al. (2007) | 7 | 0,16% | 7 | 0,75% | 6 | 0,69% | 6 | 0,68% |
Gill (1995) | 7 | 0,16% | 7 | 0,75% | 7 | 0,8% | 5 | 0,57% |
González-sánchez et al. (2021) | 7 | 0,16% | 7 | 0,75% | 7 | 0,8% | 6 | 0,68% |
Müller & Henle (1841) | 7 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Nicholson et al. (2012) | 7 | 0,16% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Perrin et al. (2002) | 7 | 0,16% | 7 | 0,75% | 7 | 0,8% | 5 | 0,57% |
Powell & Henderson (2023) | 7 | 0,16% | 7 | 0,75% | 7 | 0,8% | 7 | 0,8% |
Probst et al. (2022) | 7 | 0,16% | 7 | 0,75% | 7 | 0,8% | 7 | 0,8% |
Questel (2023) | 7 | 0,16% | 7 | 0,75% | 7 | 0,8% | 7 | 0,8% |
Randall & Vergara (1978) | 7 | 0,16% | 7 | 0,75% | 5 | 0,57% | 7 | 0,8% |
Simian et al. (2022) | 7 | 0,16% | 7 | 0,75% | 7 | 0,8% | 7 | 0,8% |
Thibault et al. (2014) | 7 | 0,16% | 7 | 0,75% | 7 | 0,8% | 6 | 0,68% |
Uicn et al. (2019) | 7 | 0,16% | 7 | 0,75% | 7 | 0,8% | 7 | 0,8% |
Williams et al. (2006) | 7 | 0,16% | 6 | 0,65% | 6 | 0,69% | 5 | 0,57% |
Busala et al. (2024) | 6 | 0,14% | 5 | 0,54% | 5 | 0,57% | 4 | 0,46% |
Casale et al. (2021) | 6 | 0,14% | 6 | 0,65% | 6 | 0,69% | 6 | 0,68% |
Chabanaud (1927) | 6 | 0,14% | 5 | 0,54% | 5 | 0,57% | 5 | 0,57% |
Cuvier & Valenciennes (1846) | 6 | 0,14% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Fourt et al. (2017) | 6 | 0,14% | 6 | 0,65% | 6 | 0,69% | 6 | 0,68% |
Fraga & Carvalho (2021) | 6 | 0,14% | 5 | 0,54% | 5 | 0,57% | 5 | 0,57% |
Fretey & Triplet (2022) | 6 | 0,14% | 6 | 0,65% | 6 | 0,69% | 6 | 0,68% |
Gmelin (1788) | 6 | 0,14% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Jourdan (2020) | 6 | 0,14% | 6 | 0,65% | 5 | 0,57% | 5 | 0,57% |
Massary et al. (2020) | 6 | 0,14% | 6 | 0,65% | 6 | 0,69% | 6 | 0,68% |
Nardo (1827) | 6 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Prévost & Mougin (1970) | 6 | 0,14% | 6 | 0,65% | 6 | 0,69% | 5 | 0,57% |
Probst (2001) | 6 | 0,14% | 5 | 0,54% | 5 | 0,57% | 4 | 0,46% |
Risso (1810) | 6 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Risso (1827) | 6 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Routtier et al. (2023) | 6 | 0,14% | 4 | 0,43% | 4 | 0,46% | 4 | 0,46% |
Safford & Hawkins (2013) | 6 | 0,14% | 6 | 0,65% | 6 | 0,69% | 5 | 0,57% |
Shirihai (2003) | 6 | 0,14% | 6 | 0,65% | 6 | 0,69% | 4 | 0,46% |
Vaslet & Agrnsm (2018) | 6 | 0,14% | 6 | 0,65% | 6 | 0,69% | 6 | 0,68% |
Yokoyama (2012) | 6 | 0,14% | 5 | 0,54% | 5 | 0,57% | 5 | 0,57% |
Allen (comm. pers., 2009) | 5 | 0,11% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Arnold & Ovenden (2014) | 5 | 0,11% | 4 | 0,43% | 4 | 0,46% | 3 | 0,34% |
Barrioz & Morinière (2007) | 5 | 0,11% | 5 | 0,54% | 5 | 0,57% | 5 | 0,57% |
Bioinsight/diren & Guyane (2006) | 5 | 0,11% | 5 | 0,54% | 5 | 0,57% | 5 | 0,57% |
Boer et al. (1999) | 5 | 0,11% | 5 | 0,54% | 5 | 0,57% | 4 | 0,46% |
Chabanet & Durville (2005) | 5 | 0,11% | 5 | 0,54% | 5 | 0,57% | 5 | 0,57% |
Chevalier (2006) | 5 | 0,11% | 5 | 0,54% | 5 | 0,57% | 5 | 0,57% |
Ciccione et al. (2011) | 5 | 0,11% | 5 | 0,54% | 5 | 0,57% | 5 | 0,57% |
Crillon & Cuzange (2020) | 5 | 0,11% | 5 | 0,54% | 5 | 0,57% | 5 | 0,57% |
Cuvier & Valenciennes (1830) | 5 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Cuvier & Valenciennes (1830-1832) | 5 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Duffaut et al. (2011) | 5 | 0,11% | 5 | 0,54% | 5 | 0,57% | 5 | 0,57% |
Entraygues (2014) | 5 | 0,11% | 5 | 0,54% | 5 | 0,57% | 5 | 0,57% |
Étaix-bonnin et al. (2011) | 5 | 0,11% | 5 | 0,54% | 5 | 0,57% | 5 | 0,57% |
Gmelin (1789) | 5 | 0,11% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Gonzalez et al. (2009) | 5 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
IUCN (2012) | 5 | 0,11% | 5 | 0,54% | 5 | 0,57% | 3 | 0,34% |
Karadjian et al. (2022) | 5 | 0,11% | 5 | 0,54% | 5 | 0,57% | 5 | 0,57% |
Keith et al. (2013) | 5 | 0,11% | 5 | 0,54% | 5 | 0,57% | 5 | 0,57% |
Lacepède (1800) | 5 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Lacepède (1801) | 5 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Lazell (1972) | 5 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Le Scao et al. (2011) | 5 | 0,11% | 5 | 0,54% | 5 | 0,57% | 5 | 0,57% |
Lee & Walsh-McGehee (2000) | 5 | 0,11% | 5 | 0,54% | 0 | 0% | 5 | 0,57% |
Transactions of the Zoological Society of London, 1839: 1-20.">Lowe (1839) | 5 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Maran & Frétey (2023) | 5 | 0,11% | 5 | 0,54% | 5 | 0,57% | 5 | 0,57% |
Maréchal & Trégarot (2012) | 5 | 0,11% | 4 | 0,43% | 4 | 0,46% | 4 | 0,46% |
Polanco & Acero (2016) | 5 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Read & Farman (2018) | 5 | 0,11% | 5 | 0,54% | 5 | 0,57% | 5 | 0,57% |
Read et al. (2023) | 5 | 0,11% | 5 | 0,54% | 5 | 0,57% | 5 | 0,57% |
Rhodin et al. (2017) | 5 | 0,11% | 3 | 0,32% | 3 | 0,34% | 3 | 0,34% |
Ronot (2007) | 5 | 0,11% | 4 | 0,43% | 3 | 0,34% | 4 | 0,46% |
Sauvignet et al. (2000) | 5 | 0,11% | 5 | 0,54% | 5 | 0,57% | 5 | 0,57% |
Schwartz (1964) | 5 | 0,11% | 3 | 0,32% | 0 | 0% | 3 | 0,34% |
Séret (1997) | 5 | 0,11% | 5 | 0,54% | 5 | 0,57% | 5 | 0,57% |
Snodgrass & Heller (1905) | 5 | 0,11% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Swainson (1839) | 5 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Valenciennes (1836-1844) | 5 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Van Dijk et al. (2014) | 5 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Bauer & Sadlier (2000) | 4 | 0,09% | 3 | 0,32% | 3 | 0,34% | 3 | 0,34% |
Birdlife International (2016) | 4 | 0,09% | 4 | 0,43% | 4 | 0,46% | 0 | 0% |
Breuil & Ibéné (2008) | 4 | 0,09% | 4 | 0,43% | 4 | 0,46% | 4 | 0,46% |
Breuil (2013) | 4 | 0,09% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Burneleau (1983) | 4 | 0,09% | 3 | 0,32% | 3 | 0,34% | 3 | 0,34% |
Butaud (2021) | 4 | 0,09% | 4 | 0,43% | 4 | 0,46% | 4 | 0,46% |
Collier et al. (2002) | 4 | 0,09% | 4 | 0,43% | 3 | 0,34% | 2 | 0,23% |
Cuvier & Valenciennes (1847) | 4 | 0,09% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Desbrosses & Etcheberry (1987) | 4 | 0,09% | 3 | 0,32% | 3 | 0,34% | 1 | 0,11% |
Dewynter (2021) | 4 | 0,09% | 4 | 0,43% | 4 | 0,46% | 4 | 0,46% |
Dubois et al. (2008) | 4 | 0,09% | 4 | 0,43% | 4 | 0,46% | 4 | 0,46% |
Duguy (1988) | 4 | 0,09% | 4 | 0,43% | 4 | 0,46% | 4 | 0,46% |
Duguy (1994) | 4 | 0,09% | 4 | 0,43% | 4 | 0,46% | 4 | 0,46% |
Duguy (1997) | 4 | 0,09% | 4 | 0,43% | 4 | 0,46% | 4 | 0,46% |
Ehrhardt (1971) | 4 | 0,09% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Fort & Barrière (2021) | 4 | 0,09% | 4 | 0,43% | 4 | 0,46% | 4 | 0,46% |
Frenot et al. (2005) | 4 | 0,09% | 4 | 0,43% | 4 | 0,46% | 4 | 0,46% |
Fretey & Lescure (1999) | 4 | 0,09% | 4 | 0,43% | 4 | 0,46% | 4 | 0,46% |
Furminieux (2019) | 4 | 0,09% | 4 | 0,43% | 4 | 0,46% | 4 | 0,46% |
Gentry et al. (2004) | 4 | 0,09% | 3 | 0,32% | 3 | 0,34% | 3 | 0,34% |
Keith et al. (2002) | 4 | 0,09% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Keith et al. (2006) | 4 | 0,09% | 4 | 0,43% | 4 | 0,46% | 4 | 0,46% |
Klunzinger (1871) | 4 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Lambert (1988) | 4 | 0,09% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Laurenti (1768) | 4 | 0,09% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Lescure & Marty (2000) | 4 | 0,09% | 3 | 0,32% | 3 | 0,34% | 3 | 0,34% |
Lescure et al. (2022) | 4 | 0,09% | 4 | 0,43% | 4 | 0,46% | 4 | 0,46% |
Lescure (2018) | 4 | 0,09% | 4 | 0,43% | 4 | 0,46% | 4 | 0,46% |
Levesque & Delcroix (2016) | 4 | 0,09% | 3 | 0,32% | 1 | 0,11% | 3 | 0,34% |
Marceniuk et al. (2020) | 4 | 0,09% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Méheust et al. (2018) | 4 | 0,09% | 4 | 0,43% | 4 | 0,46% | 4 | 0,46% |
Mitchill (1815) | 4 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Møller et al. (2005) | 4 | 0,09% | 4 | 0,43% | 4 | 0,46% | 4 | 0,46% |
Morinière & Dell'amico (2011) | 4 | 0,09% | 4 | 0,43% | 4 | 0,46% | 4 | 0,46% |
Morris (2012) | 4 | 0,09% | 4 | 0,43% | 4 | 0,46% | 4 | 0,46% |
Pezold et al. (2015) | 4 | 0,09% | 4 | 0,43% | 4 | 0,46% | 4 | 0,46% |
Probst (1997) | 4 | 0,09% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Probst (1998) | 4 | 0,09% | 3 | 0,32% | 3 | 0,34% | 3 | 0,34% |
Robineau & Duhamel (2006) | 4 | 0,09% | 4 | 0,43% | 4 | 0,46% | 3 | 0,34% |
Swanepoel & Genoways (1983) | 4 | 0,09% | 4 | 0,43% | 4 | 0,46% | 4 | 0,46% |
Vieillot (1819) | 4 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Walbaum (1792) | 4 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
AAMP (2012) | 3 | 0,07% | 3 | 0,32% | 3 | 0,34% | 0 | 0% |
Aubouin et al. (2016) | 3 | 0,07% | 3 | 0,32% | 3 | 0,34% | 3 | 0,34% |
Ausilio & Zotier (1989) | 3 | 0,07% | 3 | 0,32% | 3 | 0,34% | 3 | 0,34% |
Bartoli (1972) | 3 | 0,07% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Birdlife International (2014) | 3 | 0,07% | 3 | 0,32% | 3 | 0,34% | 3 | 0,34% |
Blanc (1909) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Bloch & Schneider (1801) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Carstens et al. (2004) | 3 | 0,07% | 3 | 0,32% | 3 | 0,34% | 0 | 0% |
Catzeflis (2018) | 3 | 0,07% | 3 | 0,32% | 3 | 0,34% | 3 | 0,34% |
Catzeflis (2019) | 3 | 0,07% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Champagne et al. (1997) | 3 | 0,07% | 3 | 0,32% | 2 | 0,23% | 3 | 0,34% |
Cuvier & Valenciennes (1839) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Cuvier (1829) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Dekay (1842) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Dekay (1842) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Delcroix et al. (2011) | 3 | 0,07% | 3 | 0,32% | 3 | 0,34% | 3 | 0,34% |
Dewynter et al. (2020) | 3 | 0,07% | 3 | 0,32% | 3 | 0,34% | 3 | 0,34% |
Dubief & Gallais (2011) | 3 | 0,07% | 3 | 0,32% | 3 | 0,34% | 3 | 0,34% |
Duguy et al. (1998) | 3 | 0,07% | 3 | 0,32% | 3 | 0,34% | 3 | 0,34% |
Duguy et al. (1999) | 3 | 0,07% | 3 | 0,32% | 3 | 0,34% | 3 | 0,34% |
Duguy et al. (2000) | 3 | 0,07% | 3 | 0,32% | 3 | 0,34% | 3 | 0,34% |
Duguy et al. (2002) | 3 | 0,07% | 3 | 0,32% | 3 | 0,34% | 3 | 0,34% |
Duguy et al. (2006) | 3 | 0,07% | 3 | 0,32% | 3 | 0,34% | 3 | 0,34% |
Duguy et al. (2007) | 3 | 0,07% | 3 | 0,32% | 3 | 0,34% | 3 | 0,34% |
Duguy (1990) | 3 | 0,07% | 3 | 0,32% | 3 | 0,34% | 3 | 0,34% |
Duguy (1996) | 3 | 0,07% | 3 | 0,32% | 3 | 0,34% | 3 | 0,34% |
Easteal (1981) | 3 | 0,07% | 3 | 0,32% | 3 | 0,34% | 3 | 0,34% |
Firmat et al. (2012) | 3 | 0,07% | 3 | 0,32% | 3 | 0,34% | 3 | 0,34% |
Girondot (2011) | 3 | 0,07% | 3 | 0,32% | 3 | 0,34% | 3 | 0,34% |
Humphries et al. (2019) | 3 | 0,07% | 3 | 0,32% | 3 | 0,34% | 0 | 0% |
Hutchinson et al. (2019) | 3 | 0,07% | 3 | 0,32% | 3 | 0,34% | 3 | 0,34% |
Ingels et al. (2003) | 3 | 0,07% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Kemp (2023) | 3 | 0,07% | 3 | 0,32% | 3 | 0,34% | 3 | 0,34% |
Kottelat ( 2013) | 3 | 0,07% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
La Cepède (1789) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Laran et al. (2012) | 3 | 0,07% | 3 | 0,32% | 3 | 0,34% | 2 | 0,23% |
Legand (1950) | 3 | 0,07% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Levesque & Delcroix (2013) | 3 | 0,07% | 3 | 0,32% | 0 | 0% | 3 | 0,34% |
Linné (1766) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Maréchal et al. (2006) | 3 | 0,07% | 3 | 0,32% | 3 | 0,34% | 3 | 0,34% |
Momont (1998) | 3 | 0,07% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Pascal et al. 2006 | 3 | 0,07% | 3 | 0,32% | 2 | 0,23% | 3 | 0,34% |
Poisson (1999) | 3 | 0,07% | 3 | 0,32% | 3 | 0,34% | 3 | 0,34% |
Potin (2013) | 3 | 0,07% | 3 | 0,32% | 3 | 0,34% | 3 | 0,34% |
Probst et al. (2000) | 3 | 0,07% | 3 | 0,32% | 3 | 0,34% | 3 | 0,34% |
Probst (1997) | 3 | 0,07% | 3 | 0,32% | 3 | 0,34% | 3 | 0,34% |
Randall & Earle (2000) | 3 | 0,07% | 3 | 0,32% | 2 | 0,23% | 3 | 0,34% |
Read & Jean (2021) | 3 | 0,07% | 3 | 0,32% | 3 | 0,34% | 3 | 0,34% |
Reynolds & Henderson (2018) | 3 | 0,07% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Rignault & Chevallier (2017) | 3 | 0,07% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Roux (1913) | 3 | 0,07% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Sanchez (2020) | 3 | 0,07% | 3 | 0,32% | 3 | 0,34% | 2 | 0,23% |
Surget-Groba & Thorpe (2013) | 3 | 0,07% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Swainson (1838) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Tirvengadum & Bour (1985) | 3 | 0,07% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Tostain & Dujardin (1988) | 3 | 0,07% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Tostain (1980) | 3 | 0,07% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
van den Burg et al. (2021) | 3 | 0,07% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Velazco & Patterson (2013) | 3 | 0,07% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Vieillot (1807) | 3 | 0,07% | 3 | 0,32% | 3 | 0,34% | 3 | 0,34% |
Vieira (2022) | 3 | 0,07% | 3 | 0,32% | 3 | 0,34% | 3 | 0,34% |
Wallach (2020) | 3 | 0,07% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Whitley (1933) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Adams (1989) | 2 | 0,05% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Adler et al. (2012) | 2 | 0,05% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Altamirano-Benavides & Woolrich-Piña (2023) | 2 | 0,05% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Altamirano-benavides & Woolrich-piña (2023) | 2 | 0,05% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Aulagnier (2021) | 2 | 0,05% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Baldi et al. (2022) | 2 | 0,05% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Bance (2022) | 2 | 0,05% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Bauer & Powell (2024) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Bauer (1987) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Behm et al. (2019) | 2 | 0,05% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Bénito-espinal (1990) | 2 | 0,05% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Bertin (1928) | 2 | 0,05% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Birdlife International (2016) | 2 | 0,05% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Birdlife International (2016) | 2 | 0,05% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Birdlife International (2016) | 2 | 0,05% | 2 | 0,22% | 2 | 0,23% | 0 | 0% |
Birdlife International (2016) | 2 | 0,05% | 2 | 0,22% | 2 | 0,23% | 0 | 0% |
Bleeker (1852) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Bochaton et al. (2016) | 2 | 0,05% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Bochaton et al. (2018) | 2 | 0,05% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Boddaert & Daubenton (1783) | 2 | 0,05% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Boer & Simmonds (2000) | 2 | 0,05% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Boer (2000) | 2 | 0,05% | 2 | 0,22% | 2 | 0,23% | 1 | 0,11% |
Bonnaterre (1788) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Bonnaterre (1789) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Borsa (1997) | 2 | 0,05% | 2 | 0,22% | 2 | 0,23% | 1 | 0,11% |
Bourgade (2020) | 2 | 0,05% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Bourgade (2021) | 2 | 0,05% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Bowdich (1825) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Breuil (2013) | 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 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Brugneaux & Pérès (2005) | 2 | 0,05% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Caceres & Salamolard (2021) | 2 | 0,05% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
CEN Nouvelle-Calédonie (2021) | 2 | 0,05% | 2 | 0,22% | 1 | 0,11% | 2 | 0,23% |
Chapuis et al. (2004) | 2 | 0,05% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Chartier et al. (2007) | 2 | 0,05% | 2 | 0,22% | 2 | 0,23% | 0 | 0% |
Cheke (1987) | 2 | 0,05% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Cheon et al. (2023) | 2 | 0,05% | 2 | 0,22% | 0 | 0% | 2 | 0,23% |
Chevallier et al. (2023) | 2 | 0,05% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Cicero & Johnson (1998) | 2 | 0,05% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
">Claes (2024) | 2 | 0,05% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Costa (2011) | 2 | 0,05% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Dacosta et al. (2019) | 2 | 0,05% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
dal Molin (2009) | 2 | 0,05% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Daniel et al. (2020) | 2 | 0,05% | 2 | 0,22% | 2 | 0,23% | 0 | 0% |
Davant (1967) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
de Massary et al. (2015) | 2 | 0,05% | 1 | 0,11% | 1 | 0,11% | 0 | 0% |
Del Hoyo & Collar (2016) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Dewynter et al. (2017) | 2 | 0,05% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Dewynter (2018) | 2 | 0,05% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Dewynter (2020) | 2 | 0,05% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
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 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Duguy et al. (2003) | 2 | 0,05% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Duguy et al. (2004) | 2 | 0,05% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Duguy (1986) | 2 | 0,05% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Duguy (1987) | 2 | 0,05% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Duguy (1992) | 2 | 0,05% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Duguy (1993) | 2 | 0,05% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Duguy (1995) | 2 | 0,05% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Duméril et al. (1870-1909) | 2 | 0,05% | 1 | 0,11% | 1 | 0,11% | 0 | 0% |
Durand (2016) | 2 | 0,05% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Evermann & Clark (1928) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Fontan (2019) | 2 | 0,05% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Fowler (1919) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Gannier & Petiau (2006) | 2 | 0,05% | 2 | 0,22% | 2 | 0,23% | 0 | 0% |
Geoffroy Saint-Hilaire ([1817]) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Gibson & Baker (2012) | 2 | 0,05% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Gill & Thiele (1997) | 2 | 0,05% | 2 | 0,22% | 2 | 0,23% | 1 | 0,11% |
Gilot et al. (1992) | 2 | 0,05% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Girondo (2023) | 2 | 0,05% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Guermeur (1987) | 2 | 0,05% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Hamdan et al. (2023) | 2 | 0,05% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Harrison et al. (2007) | 2 | 0,05% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Hass (1991) | 2 | 0,05% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Hedges (2022) | 2 | 0,05% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Hildebrand (1948) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Humeau et al. (2020) | 2 | 0,05% | 2 | 0,22% | 2 | 0,23% | 0 | 0% |
Impact-mer (2011) | 2 | 0,05% | 2 | 0,22% | 2 | 0,23% | 1 | 0,11% |
Ineich (2016) | 2 | 0,05% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
IUCN (2014) | 2 | 0,05% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Jouan (1863) | 2 | 0,05% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Jowers et al. (2013) | 2 | 0,05% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Kaiser & Altig (1994) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Kaiser et al. (1994) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Kasamatsu & Joyce (1995) | 2 | 0,05% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Kasamatsu et al. (2000) | 2 | 0,05% | 2 | 0,22% | 2 | 0,23% | 0 | 0% |
Keith et al. (1999) | 2 | 0,05% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Keith (2002) | 2 | 0,05% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Kock et al. (2006) | 2 | 0,05% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Köhler & Vesely (2011) | 2 | 0,05% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Kojadinovic et al. (2007) | 2 | 0,05% | 2 | 0,22% | 2 | 0,23% | 0 | 0% |
La Cepède (1788) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Lacepède (1802) | 2 | 0,05% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Lacoste (de) (2020) | 2 | 0,05% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Lawrence (1879) | 2 | 0,05% | 2 | 0,22% | 1 | 0,11% | 1 | 0,11% |
Lawrence (1879) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Leaper et al. (2008) | 2 | 0,05% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Lepechin (1769) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Lorvelec & Pascal (2009) | 2 | 0,05% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Lorvelec et al. (2004) | 2 | 0,05% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Lorvelec et al. (2021) | 2 | 0,05% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Macdonald & Barron (1868) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Maréchal & Pérès (2007) | 2 | 0,05% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Marquet et al. (2003) | 2 | 0,05% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Mas-Coma et al. (1989) | 2 | 0,05% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Mathews (1914) | 2 | 0,05% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
McNair & Cramer-Burke (2006) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Merrem (1820) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Millot et al. (2023) | 2 | 0,05% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Monti et al. (2018) | 2 | 0,05% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Nichols & Breder (1928) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Oliver (2011) | 2 | 0,05% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Olson & Normand (2014) | 2 | 0,05% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Oustalet (1895) | 2 | 0,05% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Palko et al. (1982) | 2 | 0,05% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Pallas (1770) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Parenti (2021) | 2 | 0,05% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Patou et al. (2009) | 2 | 0,05% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Pearman et al. (2020) | 2 | 0,05% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Pennant (1776) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Peron (2014) | 2 | 0,05% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Pinto-coelho et al. (2021) | 2 | 0,05% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Pons et al. (2005) | 2 | 0,05% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Powell et al. (2008) | 2 | 0,05% | 2 | 0,22% | 2 | 0,23% | 0 | 0% |
Probst et al. (2001) | 2 | 0,05% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Purenne (2016) | 2 | 0,05% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Questel (2017) | 2 | 0,05% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Questel (2022) | 2 | 0,05% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Rafinesque (1810) | 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 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Robineau (1989) | 2 | 0,05% | 2 | 0,22% | 2 | 0,23% | 1 | 0,11% |
Robineau (2005) | 2 | 0,05% | 2 | 0,22% | 2 | 0,23% | 1 | 0,11% |
Rossi-santos et al. (2007) | 2 | 0,05% | 2 | 0,22% | 2 | 0,23% | 1 | 0,11% |
Saint et al. (1978) | 2 | 0,05% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Schweigger (1812) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Scopoli (1786) | 2 | 0,05% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Seegers & Huber (1981) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Seutin et al. (1993) | 2 | 0,05% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Shaw (1802) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
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 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Temminck & Schlegel (1850) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Temminck et al. (1838) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Thévenot (2014) | 2 | 0,05% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Thiele et al. (1999) | 2 | 0,05% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Thiele et al. (2004) | 2 | 0,05% | 2 | 0,22% | 2 | 0,23% | 1 | 0,11% |
Thorpe & Malhotra (2023) | 2 | 0,05% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Thorpe et al. (2010) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Thunberg (1787) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Tunstall (1880) | 2 | 0,05% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
UNEP-WCMC (2005) | 2 | 0,05% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Van Canneytet al. (2008) | 2 | 0,05% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
van den Burg et al. (2021) | 2 | 0,05% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Vanderwerf et al. (2006) | 2 | 0,05% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Victor (2020) | 2 | 0,05% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Vieillot (1816) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Vieillot (1817) | 2 | 0,05% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Vieillot (1819) | 2 | 0,05% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Viel (2021) | 2 | 0,05% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Villanueva et al. (2021) | 2 | 0,05% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Weimerskirch et al. (2009) | 2 | 0,05% | 2 | 0,22% | 2 | 0,23% | 0 | 0% |
Wilson (1813) | 2 | 0,05% | 2 | 0,22% | 2 | 0,23% | 2 | 0,23% |
Abhaya & Probst (2009) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Abhaya et al. (1998) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 0 | 0% |
Abril et al. (1986) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Adalsteinsson et al. (2009) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Agarwal et al. (2021) | 1 | 0,02% | 1 | 0,11% | 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 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Al-hasson & Ali (2020) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Alley et al. (2023) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Almeida & Vasconcelos (2023) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Almeida et al. (2019) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Alvarez-berríos et al. (2016) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Andrew et al. (2008) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Angel (1935) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Angin (2017) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Angin (2017) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Anonyme. (2004) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 0 | 0% |
Anonyme. (2004) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Anonyme (2008) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 0 | 0% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Anonyme. (2012) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Anonyme. (2012) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Anonyme. (2012) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 0 | 0% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Anonyme. (2012) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
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 | 0,11% | 1 | 0,11% | 0 | 0% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Anonyme. (2012) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Anonyme. (2012) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Anonyme. (2012) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 0 | 0% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Anonyme. (2012) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Aquarium de La Rochelle (2017) | 1 | 0,02% | 1 | 0,11% | 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 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Astudillo et al. (2021) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Asztalos et al. (2020) | 1 | 0,02% | 1 | 0,11% | 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 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Bailon et al. (2015) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Baird (1858) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Baker & Allain (2020) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Baker et al. (1978) | 1 | 0,02% | 1 | 0,11% | 0 | 0% | 1 | 0,11% |
Baldi et al. (2023) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Balle et al. (2021) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Bancroft (1832) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Barbancey & Probst (1998) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Barbancey (2001) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Barbancey (2001) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Barbour (1912) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Barbour (1914) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Barbrour (1915) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Barre et al. (1991) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 0 | 0% |
Bassin (2003) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Bauer & Sadlier (1994) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Bauer et al. (2010) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Bauer et al. (2024) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Bavay (1869) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Bavay (1873) | 1 | 0,02% | 1 | 0,11% | 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% |
Béarez & Dauba (1996) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Beaucournu (1968) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Beaufils (1999) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Beauvieux et al. (2024) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Becerra et al. (2024) | 1 | 0,02% | 1 | 0,11% | 0 | 0% | 1 | 0,11% |
Bell (1827) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Bennett (1831) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Bennett (1860) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Bernal & Rocha (2011) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Bertault (1988) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Bertrand & Drogou (2000) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Bertrand et al. (2001) | 1 | 0,02% | 1 | 0,11% | 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 | 0,11% | 1 | 0,11% | 0 | 0% |
Birdlife International (2016) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Birdlife International (2016) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Birdlife International (2016) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Birdlife International (2017) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Birdlife International (2017) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Blanc et al. (1993) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Bleeker (1865) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Bleeker (1865) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Bloch (1785-1795) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Bloch (1785-1795) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Bloch (1790) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Bloch (1793) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Bochaton & Hanot (2021) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Bochaton et al. (2016) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Bochaton et al. (2020) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Bonnaterre (1790) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Bonnet et al. (1999) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Borcyk et al. (2023) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Borroto-páez (2018) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Boschert & Dronneau (1998) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Bouchon & Lemoine (2003) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Boulenger (1883) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Boulenger (1891) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 0 | 0% |
Bourgade (2013) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Bourgade (2020) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Bourgade (2020) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Branch (2010) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 0 | 0% |
Brandt (1838) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Breder & Nichols (1930) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Breuil & Serre-collet (2012) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Breuil et al. (2022) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Brito Capello (1867) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Brugneaux & Pérès (2005) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Brun (1958) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Brunes et al. (2021) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Brünnich (1764) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Caceres (2002) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Calenge et al. (2010) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 0 | 0% |
Callou (2003) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Cantera (2007) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Capalleras & Carretero (2000) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 0 | 0% |
Capape et al. (2002) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Carrillo (2023) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Carvajal-ocampo et al. (2019) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Castro et al. (2018) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Catzeflis (2014) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Caut & Jowers (2015) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Caut et al. (2008) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Censky (1988) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Cerchio et al. (2009) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 0 | 0% |
Chambault et al. (2020) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Chastel et al. (1981) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Cheke & Hume (2008) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Cheke (2010) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Chesser et al. (2016) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Chevallier et al. (2024) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Chevreux & de Guerne (1893) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Cheylan et al. (2022) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Chibon (1961) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Chibon (1962) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
CHN (2017) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Chocobar et al. (2023) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Ciccione (2001) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Ciccione (2001) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Clark (1905) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Clark (1905) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Clements (1992) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Clergeau & Pascal (2003) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Clergeau & Pascal (2003) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Colin (1992) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Collazos-astudillo et al. (2022) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Collectif (2009) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 0 | 0% |
Collet & Duguy (1981) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Collette (2003) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 0 | 0% |
Commecy et al. (2013) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Conway et al. (2017) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Cornuaille et al. (2021) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Cory (1881) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Cottarel et al. (2013) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Coues (1861) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Coues (1862) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Counihan et al. (2012) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 0 | 0% |
Crochet et al. (2022) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Crouzier (2009) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Csabaï (2020) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Cummings et al. (2021) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Cuvier & Valenciennes (1828-1830) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Dal Zotto et al. (2024) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Dalebout et al. (2005) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Dalleau et al. (2014) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Daltry & Gray (1988) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
D´angiolella et al. (2021) | 1 | 0,02% | 1 | 0,11% | 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 | 0,11% | 1 | 0,11% | 0 | 0% |
Daudin (1802) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 0 | 0% |
Daudin (1803) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Dauvin (1990) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Dávalos (2007) | 1 | 0,02% | 1 | 0,11% | 0 | 0% | 1 | 0,11% |
David et al. (2002) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Deblock (1966) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Debout (2001) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Dechelle & Ingels (2007) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Dedet et al. (1985) | 1 | 0,02% | 1 | 0,11% | 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 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Delacour (1963) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Delafontaine et al. (2018) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Delcroix et al. (2008) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Deliveyne et al. (2023) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Deméré (2014) | 1 | 0,02% | 1 | 0,11% | 0 | 0% | 1 | 0,11% |
Deniau & Provost (2020) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Denys et al. (2022) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Des et al. (2021) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Desbrosses (1934) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Desbrosses (1935) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Dewynter & Rufray (2012) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Dewynter et al. (2011) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Dewynter et al. (2012) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Dieme et al. (2015) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Dollfus (1966) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Donini & Doody (2021) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Dória et al. (2015) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Dorleans (2022) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Dreff & Delliere (1994) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Dubois & Louvet (2014) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Ducatez & Devore (2023) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Duguy & Duron (1981) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Duguy & Duron (1982) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Duguy & Duron (1983) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Duguy & Duron (1984) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Duguy & Duron (1985) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Duguy et al. (1980) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Duguy et al. (2000) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Duguy (1983) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Duguy (1988) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Duguy (1989) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Duméril & Bibron (1836) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Duméril & Bibron (1837) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Duval et al. (2019) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Efe et al. (2009) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 0 | 0% |
Ersts & Rosenbaum (2003) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 0 | 0% |
Eschscholtz (1829) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
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 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Ficetola & Scali (2010) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 0 | 0% |
Fieldsend et al. (2021) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Flechas et al. (2018) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Fleming & Jackson (2011) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 0 | 0% |
Flitti & Rocha (2014) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Forest (1946) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Forskål (1775) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Fouquet et al. (2013) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Fowler (1900) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Francour & Mouine (2008) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Franzini et al. (2018) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Fremont (2002) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Fretey & Bour (1980) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Fretey et al. (2023) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Fretey (1980) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Fretey (2003) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Frétey (2022) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Frétey (2023) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Fritz & Havaš (2007) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Fritz et al. (2010) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Fritz et al. (2020) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Gallien (2011) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Garman (1880) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Garman (1887) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Garman (1899) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Geneva et al. (2013) | 1 | 0,02% | 1 | 0,11% | 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 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Gérigny et al. (2020) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Gernigon (2008) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Gerovasileiou et al. (2020) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Gibson (2001) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Gill (1862) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Gill (1863) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Gill (1995) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Gillespie (1997) | 1 | 0,02% | 1 | 0,11% | 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 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Godet et al. (2021) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Golvan (1956) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Golvan (1962) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
González et al. (2018) | 1 | 0,02% | 1 | 0,11% | 0 | 0% | 1 | 0,11% |
Goodall et al. (1997) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Goode & Bean (1882) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Gouillard (1973) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Goulletquer (2016) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Gourreau et al. (1998) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Graber & Euzeby (1976) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Graitson et al. (2012) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Granjon et al. (2002) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Grant (1958) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Gray (1831) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
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 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Grisales-martínez & Arias-alvarez (2018) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Gros-désormeaux et al. (2017) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Guiller & Vacher (2022) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Guinet (1991) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Guinet (2004) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Günther (1859) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Harcourt (1851) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Havery et al. (2018) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Hedges et al. (2014) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Hedges (2008) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Heimlich-boran (1993) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Hellebuyck et al. (2017) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Henao-osorio et al. (2021) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Henderson & Powell (2009) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Henderson et al. (1993) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Herzberg (2018) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Hodges et al. (2024) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Holbrook (1836) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Houttuyn (1782) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Hudson et al. (2018) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Hudson et al. (2021) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Hudson et al. (2021) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Ifremer (2009) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Iglésias et al. (2021) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Iković et al. (2023) | 1 | 0,02% | 1 | 0,11% | 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 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Ineich (1999) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Ineich (2015) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Isenmann et al. (1971) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Issartel & Leblanc (2004) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
IUCN (2015) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Jairam et al. (2016) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Jameson et al. (2019) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Jamonneau et al. (2025) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Jayson et al. (2018) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Jefferson & Barros (1997) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Jehl et al. (1980) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Jim et al. (2022) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Johansson et al. (2013) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Johnson & Wolman (1984) | 1 | 0,02% | 1 | 0,11% | 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 (1882) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Jordan & Gilbert (1884) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Jordan (1888) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Jourde et al. (2017) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Judson et al. (2018) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Kadafi et al. (2024) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Kaiser & Hardy (1994) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Karaa et al. (2016) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Karin et al. (2021) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Kasamatsu et al. (1995) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 0 | 0% |
Kasamatsu et al. (1998) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 0 | 0% |
Kaup (1856) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Kawamura (1994) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 0 | 0% |
Keith & Marquet (2011) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Kiszka et al. (2009) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 0 | 0% |
Kiszka et al. (2009) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Heron, 36(1): 31-34.">Kiszka (2003) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 0 | 0% |
Knox et al. (1973) | 1 | 0,02% | 1 | 0,11% | 0 | 0% | 1 | 0,11% |
Kock & Stephan (1986) | 1 | 0,02% | 1 | 0,11% | 0 | 0% | 1 | 0,11% |
Koleska & Jablonski (2018) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Kornilev et al. (2020) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 0 | 0% |
Kuhl (1820) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Kwet (2013) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Labach et al. (2021) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 0 | 0% |
Lacepède (1803) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Lacoste (2021) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Lacoste (2021) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Lafresnaye (1848) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Lancastre et al. (1976) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Larsen et al. (2006) | 1 | 0,02% | 1 | 0,11% | 0 | 0% | 1 | 0,11% |
Latham (1787) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Lawrence (1877) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 0 | 0% |
Lawrence (1885) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Lazell (1994) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Le Corre & Jouventin (1999) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 0 | 0% |
Leaper et al. (2008) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 0 | 0% |
Leatherwood et al. (1979) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Ledreff & Raynaud (1993) | 1 | 0,02% | 1 | 0,11% | 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 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Léger (2008) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Legouez (2010) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Legros & Puissauve (2015) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Leonhardt et al. (2019) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Leonhardt et al. (2022) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Lesage et al. (2024) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Lescure et al. (2016) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Lescure et al. (2020) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Lescure (1979) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Lesson (1830-1831) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Lesson (1831) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 0 | 0% |
Lesson (1839) | 1 | 0,02% | 1 | 0,11% | 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 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Levesque & Yesou (2018) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Levesque (2001) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Levesque (2013) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Liardet & d'Auzon (2004) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Liardet (2004) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Liebart et al. (2021) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Liebgold et al. (2019) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Lim (1997) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Lizé (2018) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Lock & Griffiths (2022) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Loisier et al. (2021) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Loison (1989) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Lorvelec & Clergeau (2003) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Lorvelec & Vigne (2003) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Lorvelec & Vigne (2003) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Lorvelec et al. (2003) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Lorvelec et al. (2003) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Lorvelec et al. (2009) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Lorvelec et al. (2011) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Lorvelec et al. (2016) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Lorvelec et al. (2017) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Lorvelec (2011) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Louette & Cousin (1999) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Louisin & Probst (1996) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Lourie et al. (2016) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Loury & Puissauve (2016) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Lowe (1838) | 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% |
Maciel et al. (2021) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Macleod et al. (2006) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Maël Dewynter, Catherine Godefroid, Beatriz Conde, Willy Raitière, Distribution, écologie & statut de conservation du Colibri à tête bleue (Cyanophaia bicolor), Septembre (2014) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Mageski et al. (2017) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Mahé et al. (2013) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Maillard & David (2014) | 1 | 0,02% | 1 | 0,11% | 0 | 0% | 1 | 0,11% |
Maksimova (1976) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Malm (1877) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Mancino et al. (2022) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Mannings et al. (2023) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Marchandeau & Letty (2021) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Marchandeau et al. (2003) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Marinho (2022) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Marion & Clergeau (2003) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 0 | 0% |
Marion & Clergeau (2003) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Marion & Marion (1982) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 0 | 0% |
Marion (2003) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Marion (2003) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 0 | 0% |
Martin et al. (2007) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Martin et al. (2021) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Martinet et al. (1765) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Massary (2012) | 1 | 0,02% | 1 | 0,11% | 0 | 0% | 1 | 0,11% |
Matsuoka et al. (2005) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 0 | 0% |
Mctavish (2002) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Medetian & Miaud (2024) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Meek & Hildebrand (1923) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Ménard et al. (2000) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Meneses et al. (2019) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Miller (1779) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Montagu (1813) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Moravec et al. (2020) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Moreau de Jonnès (1816) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Moreau de Jonnès (1818) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Moreau (1881) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Morel (1959) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Morrison (2006) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Mothes et al. (2019) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Müller (1926) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Murase et al. (2002) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 0 | 0% |
Murphy et al. (1978) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Murray (1884) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Nadal & Tariel (2008) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Antonelli, Venezia. 128 pp.">Nardo (1847) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Nassi et al. (1975) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Nelson-Smith et al. (2014) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Nicholson et al. (2020) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Nicol et al. (2000) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 0 | 0% |
Noël (2017) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Novaes (2019) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Ogilby (1911) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
O'reilly (1818) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Oremus (2009) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Owen (1853) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
pallas (1764) | 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% |
Parmentier et al. (2017) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Pascal & Melin (2003) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Pascal & Vigne (2003) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Pascal & Vigne (2003) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Pascal & Vigne (2003) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Pascal et al. (2003) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Pascal et al. (2003) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Pearman et al. (2016) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 0 | 0% |
Pellegrin (1912) | 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 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Peters (1930) | 1 | 0,02% | 1 | 0,11% | 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 | 0,11% | 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 | 0,11% | 0 | 0% | 1 | 0,11% |
Pierpoint et al. (1997) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 0 | 0% |
Pieters & Dickinson (2005) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Pinchon (1976) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Pitman & Ensor (2003) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Poey (1863) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Poey (1868) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Pons et al. (1999) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Pontoppidan (1763) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Pool (2013) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 0 | 0% |
Portilla & Lamus (2020) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Praderi et al. (1992) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Prado et al. (2023) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Prato et al. (2022) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Preynat (2013) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Probst et al. (2023) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Probst (1997) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Probst (1999) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Probst (2001) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Probst (2007) | 1 | 0,02% | 1 | 0,11% | 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 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Puissauve, Cohen & De Massary (2015) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Puissauve, Comolet-tirman & Whal (2015) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Annales de la Société de Sciences naturelles de la Charente-Maritime, 10(2): 225-236.">Quéro et al. (2011) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Quéro & Delmas (1982) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Quero & Laborde (1996) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Quero et al. (1998) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Quero et al. (2006) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Quero et al. (2013) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Quero (1998) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Questel & Boggio (2012) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Questel & Vitry (2012) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Questel et al. (2012) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Questel (2014) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Réjaud et al. (2020) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Randi et al. (2001) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Ranzani (1839) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Ranzani (1842) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Read et al. (2015) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Recoder et al. (2018) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Reeber (2015) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Reinert et al. (2021) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Reis et al. (2003) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Renaud et al. (2013) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Renner (2002) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Résière et al. (2018) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Revuelta et al. (2015) | 1 | 0,02% | 1 | 0,11% | 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 | 0,11% | 1 | 0,11% | 0 | 0% |
Riccialdelli et al. (2010) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Richardson (1846) | 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 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Ringler et al. (2021) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Robert et al. (2002) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Robins & Sylva (1963) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Roche & Guinet (2007) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Rodrigues et al. (2021) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Romero et al. (2010) | 1 | 0,02% | 1 | 0,11% | 0 | 0% | 1 | 0,11% |
Roos (2000) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Roques (1991) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Rosen (1911) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Rosenbaum & Collins (2006) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 0 | 0% |
Roux & Coll. (2017) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Roux & Martinez (1987) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Rufz (1859 | 1 | 0,02% | 1 | 0,11% | 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 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Ruys & Coord (2012) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Sadlier et al. (2012) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Sanchez & Probst (2016) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Sanchez et al. (2004) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 0 | 0% |
Sanchez et al. (2019) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Savouré-Soubelet et al. (in prep.) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Sawai et al. (2018) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Sayah et al. (2023) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Schinz (1822) | 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% |
Schoepff (1792) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Schuchmann (1981) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Schultze et al. (2020) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Sclater (1866) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Scopoli (1769) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Sellier et al. (2016) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Servan & Arvy (1997) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 0 | 0% |
Servan (1976) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Shaver et al. (2019) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Shine et al. (2021) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Shine (2010) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Sigalas (1931) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Simmons (2005) | 1 | 0,02% | 1 | 0,11% | 0 | 0% | 1 | 0,11% |
Siorat & Rocamora (1995) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Siorat et al. (2003) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Slater et al. (2014) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Smith et al. (2005) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Smith-Vaniz & Carpenter (2007) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Smith-vaniz & Jelks (2014) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Snyder et al. (2019) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Sonsino (1893) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Spiroux (1996) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Steadman & Bollt (2010) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 0 | 0% |
Steindachner (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 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Stoleson & Beissinger (2001) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Suckow (1798) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Sulton (2020) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Swainson (1838) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 0 | 0% |
Széles et al. (2018) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Tejedor (2006) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Terrasse & Terrasse (1969) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Teunissen & Peters (2022) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Thibault et al. (2023) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Thoisy et al. (2003) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 0 | 0% |
Thorpe & Stenson (2003) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Timm & Genoways (2003) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Tregarot et al. (2015) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Trochet et al. (2024) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Tschudi (1838) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Turpin & Probst (1998) | 1 | 0,02% | 1 | 0,11% | 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 | 0,11% | 1 | 0,11% | 1 | 0,11% |
UICN (2009) | 1 | 0,02% | 1 | 0,11% | 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 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Van den burg et al. (2022) | 1 | 0,02% | 1 | 0,11% | 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% |
Vera-pérez et al. (2021) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Vernoux (1988) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Verreaux & Des Murs (1860) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Veysset (2003) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 0 | 0% |
Viale & Frontier (1989) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
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 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Waayers et al. (2011) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Wahl & Barbraud (2005) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Wallach et al. (2014) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Wallach (2009) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Wang & Liu (2016) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 0 | 0% |
Wang & Qiu (2022) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Wasilewski et al. (2022) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Weerdt (2023) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 0 | 0% |
Werner (1980) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Weterings & Vetter (2017) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Whitley (1929) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Whitley (1937) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Whitley (1944) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Whitley (1948) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Wickel et al. (2014) | 1 | 0,02% | 1 | 0,11% | 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 | 0,11% | 1 | 0,11% | 0 | 0% |
Works & Olson (2018) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 0 | 0% |
Wursig & Wursig (1980) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Wüster et al. (2002) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Yasumiba et al. (2015) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Yengle (2021) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Yésou (2003) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Yésou (2003) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Yésou (2003) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Yuan et al. (2022) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Zdunek (2022) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Zelhuber (2009) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Zug & Zug (1979) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
(2022) | 1 | 0,02% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |