Vertébrés de Saint-Barthélemy
947 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) | 528 | 16,77% | 519 | 76,66% | 485 | 77,85% | 509 | 81,57% |
Questel & Le Quellec (2012) | 455 | 14,45% | 430 | 63,52% | 408 | 65,49% | 407 | 65,22% |
Bouchon-Navaro et al. (2005) | 217 | 6,89% | 179 | 26,44% | 179 | 28,73% | 178 | 28,53% |
Yokoyama (2013) | 146 | 4,64% | 131 | 19,35% | 121 | 19,42% | 101 | 16,19% |
Levesque & Delcroix (2018) | 143 | 4,54% | 137 | 20,24% | 115 | 18,46% | 127 | 20,35% |
UICN Comité français, OFB & MNHN (2021) | 135 | 4,29% | 135 | 19,94% | 135 | 21,67% | 99 | 15,87% |
Uicn et al. (2017) | 130 | 4,13% | 126 | 18,61% | 119 | 19,1% | 93 | 14,9% |
Bouchon-Navaro & Louis (1986) | 110 | 3,49% | 93 | 13,74% | 93 | 14,93% | 93 | 14,9% |
Smith (1997) | 107 | 3,4% | 99 | 14,62% | 95 | 15,25% | 99 | 15,87% |
Diaz & Cuzange (2009) | 105 | 3,33% | 97 | 14,33% | 97 | 15,57% | 95 | 15,22% |
Linnaeus (1758) | 94 | 2,99% | 27 | 3,99% | 27 | 4,33% | 18 | 2,88% |
Brugneaux & Pérès (2006) | 79 | 2,51% | 72 | 10,64% | 72 | 11,56% | 72 | 11,54% |
Remsen et al. (2013) | 75 | 2,38% | 72 | 10,64% | 72 | 11,56% | 51 | 8,17% |
Uicn et al. (2015) | 65 | 2,06% | 64 | 9,45% | 64 | 10,27% | 45 | 7,21% |
Henderson & Breuil (2012) | 56 | 1,78% | 43 | 6,35% | 39 | 6,26% | 43 | 6,89% |
Belfan & Conde (2016) | 54 | 1,71% | 52 | 7,68% | 37 | 5,94% | 50 | 8,01% |
Rinaldi (2016) | 44 | 1,4% | 44 | 6,5% | 44 | 7,06% | 28 | 4,49% |
Rousseau (2010) | 43 | 1,37% | 41 | 6,06% | 41 | 6,58% | 41 | 6,57% |
Etcheberry & Abraham (2009) | 41 | 1,3% | 36 | 5,32% | 36 | 5,78% | 30 | 4,81% |
Fricke et al. (2011) | 41 | 1,3% | 41 | 6,06% | 41 | 6,58% | 40 | 6,41% |
Fricke et al. (2009) | 36 | 1,14% | 35 | 5,17% | 35 | 5,62% | 34 | 5,45% |
Siu et al. (2017) | 35 | 1,11% | 34 | 5,02% | 34 | 5,46% | 33 | 5,29% |
Carzon et al. (2016) | 33 | 1,05% | 33 | 4,87% | 33 | 5,3% | 21 | 3,37% |
Estrade et al. (2016) | 33 | 1,05% | 33 | 4,87% | 33 | 5,3% | 21 | 3,37% |
Louis et al. (1992) | 31 | 0,98% | 23 | 3,4% | 23 | 3,69% | 22 | 3,53% |
Questel (2017) | 30 | 0,95% | 30 | 4,43% | 30 | 4,82% | 30 | 4,81% |
Wickel & Jamon (2010) | 30 | 0,95% | 28 | 4,14% | 28 | 4,49% | 27 | 4,33% |
Questel et al. (2023) | 29 | 0,92% | 28 | 4,14% | 28 | 4,49% | 26 | 4,17% |
Béarez et al. (2017) | 28 | 0,89% | 28 | 4,14% | 28 | 4,49% | 28 | 4,49% |
Dewynter et al. (2022) | 28 | 0,89% | 26 | 3,84% | 26 | 4,17% | 24 | 3,85% |
Questel et al. (2023) | 28 | 0,89% | 28 | 4,14% | 28 | 4,49% | 26 | 4,17% |
Uicn et al. (2020) | 26 | 0,83% | 26 | 3,84% | 26 | 4,17% | 22 | 3,53% |
Dewynter et al. (2023) | 25 | 0,79% | 25 | 3,69% | 25 | 4,01% | 23 | 3,69% |
Dewynter (2021) | 25 | 0,79% | 25 | 3,69% | 25 | 4,01% | 24 | 3,85% |
Mertens & Wermuth (1960) | 25 | 0,79% | 0 | 0% | 0 | 0% | 0 | 0% |
Poey (1858-61) | 25 | 0,79% | 0 | 0% | 0 | 0% | 0 | 0% |
Weimerskirch et al. (2009) | 25 | 0,79% | 19 | 2,81% | 19 | 3,05% | 9 | 1,44% |
Breuil (2002) | 24 | 0,76% | 12 | 1,77% | 12 | 1,93% | 12 | 1,92% |
Massary et al. (2017) | 24 | 0,76% | 21 | 3,1% | 20 | 3,21% | 19 | 3,04% |
Massary et al. (2018) | 24 | 0,76% | 22 | 3,25% | 21 | 3,37% | 20 | 3,21% |
Delrieu-Trottin et al. (2015) | 22 | 0,7% | 22 | 3,25% | 21 | 3,37% | 22 | 3,53% |
Bouchon-Navaro et al. (1992) | 20 | 0,64% | 18 | 2,66% | 18 | 2,89% | 17 | 2,72% |
Genevois & Barbraud (2020) | 19 | 0,6% | 18 | 2,66% | 18 | 2,89% | 11 | 1,76% |
Tostain et al. (2013) | 19 | 0,6% | 15 | 2,22% | 14 | 2,25% | 12 | 1,92% |
Bacchet et al. (2007) | 18 | 0,57% | 17 | 2,51% | 17 | 2,73% | 17 | 2,72% |
Clements (2012) | 18 | 0,57% | 18 | 2,66% | 17 | 2,73% | 14 | 2,24% |
Fourriére et al. (2014) | 18 | 0,57% | 18 | 2,66% | 18 | 2,89% | 18 | 2,88% |
Gmelin (1789) | 17 | 0,54% | 3 | 0,44% | 3 | 0,48% | 3 | 0,48% |
Lorvelec et al. (2007) | 17 | 0,54% | 16 | 2,36% | 16 | 2,57% | 14 | 2,24% |
Van Dijk et al. (2012) | 17 | 0,54% | 12 | 1,77% | 12 | 1,93% | 12 | 1,92% |
Girard (2007) | 16 | 0,51% | 9 | 1,33% | 8 | 1,28% | 9 | 1,44% |
Collette & Nauen (1983) | 15 | 0,48% | 15 | 2,22% | 15 | 2,41% | 15 | 2,4% |
Cuvier & Valenciennes (1833) | 15 | 0,48% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Dewynter et al. (2023) | 15 | 0,48% | 15 | 2,22% | 15 | 2,41% | 14 | 2,24% |
Linnaeus (1766) | 15 | 0,48% | 2 | 0,3% | 1 | 0,16% | 1 | 0,16% |
Massary et al. (2021) | 15 | 0,48% | 14 | 2,07% | 14 | 2,25% | 13 | 2,08% |
Dewynter et al. (2019) | 14 | 0,44% | 14 | 2,07% | 14 | 2,25% | 13 | 2,08% |
Deynat (2011) | 14 | 0,44% | 13 | 1,92% | 13 | 2,09% | 13 | 2,08% |
Soubeyran et al. (2011) | 14 | 0,44% | 14 | 2,07% | 14 | 2,25% | 14 | 2,24% |
Barau et al. (2005) | 13 | 0,41% | 11 | 1,62% | 11 | 1,77% | 8 | 1,28% |
Compagno (1984) | 13 | 0,41% | 13 | 1,92% | 13 | 2,09% | 13 | 2,08% |
Proceedings of the Zoological Society of London, 1907: 1035-1037.">Hopkinson (1907) | 13 | 0,41% | 3 | 0,44% | 3 | 0,48% | 3 | 0,48% |
Uicn et al. (2015) | 13 | 0,41% | 12 | 1,77% | 12 | 1,93% | 11 | 1,76% |
Barré (2021) | 12 | 0,38% | 12 | 1,77% | 12 | 1,93% | 12 | 1,92% |
Catzeflis (2012) | 12 | 0,38% | 12 | 1,77% | 12 | 1,93% | 5 | 0,8% |
Fricke et al. (2013) | 12 | 0,38% | 12 | 1,77% | 12 | 1,93% | 11 | 1,76% |
Gargominy et al. (1996) | 12 | 0,38% | 12 | 1,77% | 12 | 1,93% | 12 | 1,92% |
Hoff & Daszkiewicz (2001) | 12 | 0,38% | 11 | 1,62% | 11 | 1,77% | 6 | 0,96% |
Kulbicki et al. (2000) | 12 | 0,38% | 10 | 1,48% | 10 | 1,61% | 8 | 1,28% |
Aulagnier (2009) | 11 | 0,35% | 11 | 1,62% | 11 | 1,77% | 9 | 1,44% |
Charrassin (2016) | 11 | 0,35% | 11 | 1,62% | 11 | 1,77% | 7 | 1,12% |
Charrassin (2016) | 11 | 0,35% | 11 | 1,62% | 11 | 1,77% | 7 | 1,12% |
Clements et al. (2015) | 11 | 0,35% | 11 | 1,62% | 1 | 0,16% | 10 | 1,6% |
Dewynter et al. (2021) | 11 | 0,35% | 11 | 1,62% | 11 | 1,77% | 7 | 1,12% |
Genoways et al. (2007) | 11 | 0,35% | 11 | 1,62% | 5 | 0,8% | 6 | 0,96% |
Jarrett & Shirihai (2014) | 11 | 0,35% | 11 | 1,62% | 11 | 1,77% | 7 | 1,12% |
Le Bail et al. (2012) | 11 | 0,35% | 11 | 1,62% | 11 | 1,77% | 11 | 1,76% |
Moutou (2016) | 11 | 0,35% | 11 | 1,62% | 11 | 1,77% | 7 | 1,12% |
Rafinesque Schmaltz (1810) | 11 | 0,35% | 2 | 0,3% | 2 | 0,32% | 2 | 0,32% |
Spitz et al. (2016) | 11 | 0,35% | 11 | 1,62% | 11 | 1,77% | 7 | 1,12% |
Theuerkauf et al. (2010) | 11 | 0,35% | 11 | 1,62% | 11 | 1,77% | 11 | 1,76% |
Thoisy & Bordin (2016) | 11 | 0,35% | 11 | 1,62% | 11 | 1,77% | 7 | 1,12% |
Urtizberea (2016) | 11 | 0,35% | 11 | 1,62% | 11 | 1,77% | 7 | 1,12% |
Aulagnier et al. (2017) | 10 | 0,32% | 9 | 1,33% | 9 | 1,44% | 9 | 1,44% |
Berry & Smith-Vaniz (1978) | 10 | 0,32% | 10 | 1,48% | 10 | 1,61% | 10 | 1,6% |
Bordin et al. (2021) | 10 | 0,32% | 10 | 1,48% | 10 | 1,61% | 6 | 0,96% |
Dickinson & Remsen (2013) | 10 | 0,32% | 9 | 1,33% | 6 | 0,96% | 8 | 1,28% |
Richard et al. (1982) | 10 | 0,32% | 5 | 0,74% | 5 | 0,8% | 4 | 0,64% |
Béarez & Séret (2009) | 9 | 0,29% | 8 | 1,18% | 8 | 1,28% | 8 | 1,28% |
Breuil et al. (2010) | 9 | 0,29% | 8 | 1,18% | 7 | 1,12% | 8 | 1,28% |
Garrigue (2007) | 9 | 0,29% | 9 | 1,33% | 9 | 1,44% | 6 | 0,96% |
Heemstra & Randall (1993) | 9 | 0,29% | 9 | 1,33% | 9 | 1,44% | 9 | 1,44% |
Müller & Henle (1841) | 9 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
Arnold & Ovenden (2014) | 8 | 0,25% | 6 | 0,89% | 6 | 0,96% | 5 | 0,8% |
Béarez & Bouffandeau (2019) | 8 | 0,25% | 8 | 1,18% | 8 | 1,28% | 7 | 1,12% |
Bénito-espinal (1990) | 8 | 0,25% | 7 | 1,03% | 2 | 0,32% | 7 | 1,12% |
Commission de l’Avifaune Française (2016) | 8 | 0,25% | 8 | 1,18% | 8 | 1,28% | 4 | 0,64% |
Compagno (1984) | 8 | 0,25% | 8 | 1,18% | 8 | 1,28% | 8 | 1,28% |
Gannier (2001) | 8 | 0,25% | 8 | 1,18% | 8 | 1,28% | 5 | 0,8% |
Gannier (2002) | 8 | 0,25% | 8 | 1,18% | 8 | 1,28% | 5 | 0,8% |
Gannier (2009) | 8 | 0,25% | 8 | 1,18% | 8 | 1,28% | 5 | 0,8% |
G.E.M.M. (2012) | 8 | 0,25% | 8 | 1,18% | 8 | 1,28% | 5 | 0,8% |
Guth (1971) | 8 | 0,25% | 7 | 1,03% | 7 | 1,12% | 4 | 0,64% |
Jourdan (2020) | 8 | 0,25% | 8 | 1,18% | 7 | 1,12% | 7 | 1,12% |
Lescure et al. (2012) | 8 | 0,25% | 8 | 1,18% | 7 | 1,12% | 7 | 1,12% |
Massary et al. (2019) | 8 | 0,25% | 8 | 1,18% | 8 | 1,28% | 7 | 1,12% |
Prévost & Mougin (1970) | 8 | 0,25% | 8 | 1,18% | 8 | 1,28% | 7 | 1,12% |
Rocamora (2004) | 8 | 0,25% | 8 | 1,18% | 7 | 1,12% | 5 | 0,8% |
Bochaton et al. (2021) | 7 | 0,22% | 7 | 1,03% | 7 | 1,12% | 7 | 1,12% |
Bour et al. (2008) | 7 | 0,22% | 7 | 1,03% | 7 | 1,12% | 6 | 0,96% |
Breuil (2009) | 7 | 0,22% | 6 | 0,89% | 6 | 0,96% | 6 | 0,96% |
Chaezl & Chazel (2011) | 7 | 0,22% | 7 | 1,03% | 7 | 1,12% | 7 | 1,12% |
Dewynter et al. (2019) | 7 | 0,22% | 7 | 1,03% | 7 | 1,12% | 6 | 0,96% |
Dulau-Drouot et al. (2008) | 7 | 0,22% | 7 | 1,03% | 7 | 1,12% | 4 | 0,64% |
Gannier (2000) | 7 | 0,22% | 7 | 1,03% | 7 | 1,12% | 4 | 0,64% |
Gill (1995) | 7 | 0,22% | 7 | 1,03% | 7 | 1,12% | 2 | 0,32% |
González-sánchez et al. (2021) | 7 | 0,22% | 7 | 1,03% | 7 | 1,12% | 6 | 0,96% |
Gronow (1854) | 7 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Kiszka et al.(2007) | 7 | 0,22% | 7 | 1,03% | 7 | 1,12% | 4 | 0,64% |
Laran et al. (2011) | 7 | 0,22% | 7 | 1,03% | 7 | 1,12% | 5 | 0,8% |
Lowe et al. (2007) | 7 | 0,22% | 7 | 1,03% | 6 | 0,96% | 7 | 1,12% |
Pezold et al. (2015) | 7 | 0,22% | 7 | 1,03% | 7 | 1,12% | 7 | 1,12% |
Probst et al. (2022) | 7 | 0,22% | 7 | 1,03% | 7 | 1,12% | 7 | 1,12% |
Questel (2023) | 7 | 0,22% | 7 | 1,03% | 7 | 1,12% | 7 | 1,12% |
Thibault et al. (2014) | 7 | 0,22% | 7 | 1,03% | 7 | 1,12% | 2 | 0,32% |
Williams et al. (2006) | 7 | 0,22% | 6 | 0,89% | 6 | 0,96% | 5 | 0,8% |
Yokoyama (2012) | 7 | 0,22% | 6 | 0,89% | 6 | 0,96% | 6 | 0,96% |
Bloch & Schneider (1801) | 6 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Camiñas et al. (2021) | 6 | 0,19% | 6 | 0,89% | 6 | 0,96% | 6 | 0,96% |
Chabanet & Durville (2005) | 6 | 0,19% | 5 | 0,74% | 5 | 0,8% | 5 | 0,8% |
Cuvier & Valenciennes ([1832]) | 6 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Deblock et al. (1960) | 6 | 0,19% | 4 | 0,59% | 4 | 0,64% | 3 | 0,48% |
Del Hoyo & Collar (2014) | 6 | 0,19% | 3 | 0,44% | 3 | 0,48% | 3 | 0,48% |
Gmelin (1788) | 6 | 0,19% | 1 | 0,15% | 1 | 0,16% | 0 | 0% |
Kiszka et al. (2010) | 6 | 0,19% | 6 | 0,89% | 6 | 0,96% | 4 | 0,64% |
Lim et al. (2002) | 6 | 0,19% | 5 | 0,74% | 5 | 0,8% | 5 | 0,8% |
Massary et al. (2020) | 6 | 0,19% | 6 | 0,89% | 6 | 0,96% | 6 | 0,96% |
Monti et al. (2010) | 6 | 0,19% | 5 | 0,74% | 5 | 0,8% | 5 | 0,8% |
Muratet (2015) | 6 | 0,19% | 6 | 0,89% | 5 | 0,8% | 5 | 0,8% |
Probst (2001) | 6 | 0,19% | 5 | 0,74% | 5 | 0,8% | 4 | 0,64% |
Questel (2022) | 6 | 0,19% | 6 | 0,89% | 6 | 0,96% | 6 | 0,96% |
Rhodin et al. (2017) | 6 | 0,19% | 4 | 0,59% | 4 | 0,64% | 4 | 0,64% |
Routtier et al. (2023) | 6 | 0,19% | 4 | 0,59% | 4 | 0,64% | 4 | 0,64% |
Soubeyran (2008) | 6 | 0,19% | 6 | 0,89% | 6 | 0,96% | 6 | 0,96% |
Vieillot (1819) | 6 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Allen (1985) | 5 | 0,16% | 5 | 0,74% | 5 | 0,8% | 5 | 0,8% |
Bioinsight/diren & Guyane (2006) | 5 | 0,16% | 5 | 0,74% | 5 | 0,8% | 5 | 0,8% |
Busala et al. (2024) | 5 | 0,16% | 2 | 0,3% | 2 | 0,32% | 1 | 0,16% |
Butaud (2021) | 5 | 0,16% | 5 | 0,74% | 5 | 0,8% | 5 | 0,8% |
Casale et al. (2021) | 5 | 0,16% | 5 | 0,74% | 5 | 0,8% | 5 | 0,8% |
Chevalier (2006) | 5 | 0,16% | 5 | 0,74% | 5 | 0,8% | 5 | 0,8% |
Ciccione et al. (2011) | 5 | 0,16% | 5 | 0,74% | 5 | 0,8% | 5 | 0,8% |
Crillon & Cuzange (2020) | 5 | 0,16% | 5 | 0,74% | 5 | 0,8% | 5 | 0,8% |
Duffaut et al. (2011) | 5 | 0,16% | 5 | 0,74% | 5 | 0,8% | 5 | 0,8% |
Entraygues (2014) | 5 | 0,16% | 5 | 0,74% | 5 | 0,8% | 5 | 0,8% |
Étaix-bonnin et al. (2011) | 5 | 0,16% | 5 | 0,74% | 5 | 0,8% | 5 | 0,8% |
Frenot et al. (2005) | 5 | 0,16% | 5 | 0,74% | 5 | 0,8% | 5 | 0,8% |
Fretey & Triplet (2022) | 5 | 0,16% | 5 | 0,74% | 5 | 0,8% | 5 | 0,8% |
Hedges & Conn (2012) | 5 | 0,16% | 4 | 0,59% | 4 | 0,64% | 4 | 0,64% |
Klunzinger (1871) | 5 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Larsen et al. (2006) | 5 | 0,16% | 5 | 0,74% | 0 | 0% | 5 | 0,8% |
Le Scao et al. (2011) | 5 | 0,16% | 5 | 0,74% | 5 | 0,8% | 5 | 0,8% |
Lee & Walsh-McGehee (2000) | 5 | 0,16% | 5 | 0,74% | 0 | 0% | 5 | 0,8% |
Nicholson et al. (2012) | 5 | 0,16% | 4 | 0,59% | 4 | 0,64% | 4 | 0,64% |
Questel (2017) | 5 | 0,16% | 4 | 0,59% | 4 | 0,64% | 4 | 0,64% |
Read & Farman (2018) | 5 | 0,16% | 5 | 0,74% | 5 | 0,8% | 5 | 0,8% |
Read et al. (2023) | 5 | 0,16% | 5 | 0,74% | 5 | 0,8% | 5 | 0,8% |
Ronot (2007) | 5 | 0,16% | 4 | 0,59% | 3 | 0,48% | 4 | 0,64% |
Safford & Hawkins (2013) | 5 | 0,16% | 5 | 0,74% | 5 | 0,8% | 3 | 0,48% |
Samaran & Guinet (2009) | 5 | 0,16% | 5 | 0,74% | 5 | 0,8% | 4 | 0,64% |
Sauvignet et al. (2000) | 5 | 0,16% | 5 | 0,74% | 5 | 0,8% | 5 | 0,8% |
Swainson (1839) | 5 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Valenciennes (1836-1844) | 5 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Allen (comm. pers., 2009) | 4 | 0,13% | 3 | 0,44% | 3 | 0,48% | 2 | 0,32% |
Barrioz & Morinière (2007) | 4 | 0,13% | 4 | 0,59% | 4 | 0,64% | 4 | 0,64% |
Bauer & Sadlier (2000) | 4 | 0,13% | 3 | 0,44% | 3 | 0,48% | 3 | 0,48% |
Birdlife International (2016) | 4 | 0,13% | 4 | 0,59% | 4 | 0,64% | 0 | 0% |
Burneleau (1983) | 4 | 0,13% | 3 | 0,44% | 3 | 0,48% | 3 | 0,48% |
Charbonnel (1990) | 4 | 0,13% | 2 | 0,3% | 2 | 0,32% | 2 | 0,32% |
Collier et al. (2002) | 4 | 0,13% | 4 | 0,59% | 3 | 0,48% | 2 | 0,32% |
Desbrosses & Etcheberry (1987) | 4 | 0,13% | 3 | 0,44% | 3 | 0,48% | 2 | 0,32% |
Dewynter & Claessens (2020) | 4 | 0,13% | 4 | 0,59% | 4 | 0,64% | 1 | 0,16% |
Dubois & Ohler (1994) | 4 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Ehrhardt (1971) | 4 | 0,13% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Fort & Barrière (2021) | 4 | 0,13% | 4 | 0,59% | 4 | 0,64% | 4 | 0,64% |
Fourt et al. (2017) | 4 | 0,13% | 4 | 0,59% | 4 | 0,64% | 4 | 0,64% |
Fretey & Lescure (1999) | 4 | 0,13% | 4 | 0,59% | 4 | 0,64% | 4 | 0,64% |
Furminieux (2019) | 4 | 0,13% | 4 | 0,59% | 4 | 0,64% | 4 | 0,64% |
Gentry et al. (2004) | 4 | 0,13% | 4 | 0,59% | 4 | 0,64% | 4 | 0,64% |
Gmelin (1789) | 4 | 0,13% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
IUCN (2012) | 4 | 0,13% | 4 | 0,59% | 4 | 0,64% | 3 | 0,48% |
Keith et al. (2013) | 4 | 0,13% | 4 | 0,59% | 4 | 0,64% | 4 | 0,64% |
Köhler & Vesely (2011) | 4 | 0,13% | 4 | 0,59% | 4 | 0,64% | 4 | 0,64% |
Kulbicki (comm. pers., 2011) | 4 | 0,13% | 4 | 0,59% | 4 | 0,64% | 4 | 0,64% |
Lambert (1988) | 4 | 0,13% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Levesque & Delcroix (2016) | 4 | 0,13% | 3 | 0,44% | 1 | 0,16% | 3 | 0,48% |
Transactions of the Zoological Society of London, 1839: 1-20.">Lowe (1839) | 4 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Mitchill (1815) | 4 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Morris (2012) | 4 | 0,13% | 4 | 0,59% | 4 | 0,64% | 4 | 0,64% |
Pascal et al. 2006 | 4 | 0,13% | 4 | 0,59% | 3 | 0,48% | 4 | 0,64% |
Pedersen et al. (2013) | 4 | 0,13% | 4 | 0,59% | 4 | 0,64% | 0 | 0% |
Perrin et al. (2002) | 4 | 0,13% | 4 | 0,59% | 4 | 0,64% | 3 | 0,48% |
Powell & Henderson (2023) | 4 | 0,13% | 3 | 0,44% | 3 | 0,48% | 3 | 0,48% |
Probst (1997) | 4 | 0,13% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Probst (1998) | 4 | 0,13% | 3 | 0,44% | 3 | 0,48% | 3 | 0,48% |
Randall & Earle (2000) | 4 | 0,13% | 4 | 0,59% | 3 | 0,48% | 4 | 0,64% |
Rignault & Chevallier (2017) | 4 | 0,13% | 3 | 0,44% | 3 | 0,48% | 3 | 0,48% |
Risso (1810) | 4 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Swanepoel & Genoways (1983) | 4 | 0,13% | 4 | 0,59% | 4 | 0,64% | 0 | 0% |
Uicn et al. (2019) | 4 | 0,13% | 4 | 0,59% | 4 | 0,64% | 4 | 0,64% |
Whitehead (1985) | 4 | 0,13% | 4 | 0,59% | 4 | 0,64% | 4 | 0,64% |
AAMP (2012) | 3 | 0,1% | 3 | 0,44% | 3 | 0,48% | 1 | 0,16% |
Angin et al. (2024) | 3 | 0,1% | 3 | 0,44% | 3 | 0,48% | 3 | 0,48% |
Aulagnier (2021) | 3 | 0,1% | 3 | 0,44% | 3 | 0,48% | 3 | 0,48% |
Baker et al. (1978) | 3 | 0,1% | 3 | 0,44% | 0 | 0% | 3 | 0,48% |
Blanc (1909) | 3 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Bochaton et al. (2016) | 3 | 0,1% | 3 | 0,44% | 3 | 0,48% | 3 | 0,48% |
Catzeflis (2018) | 3 | 0,1% | 3 | 0,44% | 3 | 0,48% | 3 | 0,48% |
Champagne et al. (1997) | 3 | 0,1% | 3 | 0,44% | 2 | 0,32% | 3 | 0,48% |
Cuvier & Valenciennes (1830) | 3 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Cuvier & Valenciennes (1830-1832) | 3 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Cuvier & Valenciennes (1839) | 3 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Cuvier & Valenciennes (1846) | 3 | 0,1% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Cuvier (1829) | 3 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Delcroix et al. (2011) | 3 | 0,1% | 3 | 0,44% | 3 | 0,48% | 3 | 0,48% |
Des et al. (2021) | 3 | 0,1% | 3 | 0,44% | 3 | 0,48% | 3 | 0,48% |
Dubief & Gallais (2011) | 3 | 0,1% | 3 | 0,44% | 3 | 0,48% | 3 | 0,48% |
Dubois et al. (2008) | 3 | 0,1% | 3 | 0,44% | 3 | 0,48% | 3 | 0,48% |
Duguy et al. (1998) | 3 | 0,1% | 3 | 0,44% | 3 | 0,48% | 3 | 0,48% |
Duguy et al. (2007) | 3 | 0,1% | 3 | 0,44% | 3 | 0,48% | 3 | 0,48% |
Duguy (1988) | 3 | 0,1% | 3 | 0,44% | 3 | 0,48% | 3 | 0,48% |
Duguy (1994) | 3 | 0,1% | 3 | 0,44% | 3 | 0,48% | 3 | 0,48% |
Duguy (1997) | 3 | 0,1% | 3 | 0,44% | 3 | 0,48% | 3 | 0,48% |
Firmat et al. (2012) | 3 | 0,1% | 3 | 0,44% | 3 | 0,48% | 3 | 0,48% |
Fraga & Carvalho (2021) | 3 | 0,1% | 3 | 0,44% | 3 | 0,48% | 3 | 0,48% |
Gill (1862) | 3 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Giovannotti et al. (2017) | 3 | 0,1% | 2 | 0,3% | 2 | 0,32% | 2 | 0,32% |
Girondot (2011) | 3 | 0,1% | 3 | 0,44% | 3 | 0,48% | 3 | 0,48% |
Goicoechea et al. (2016) | 3 | 0,1% | 2 | 0,3% | 2 | 0,32% | 0 | 0% |
Gonzalez et al. (2009) | 3 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Hedges et al. (2014) | 3 | 0,1% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Hedges (2022) | 3 | 0,1% | 3 | 0,44% | 3 | 0,48% | 3 | 0,48% |
Humphries et al. (2019) | 3 | 0,1% | 3 | 0,44% | 3 | 0,48% | 0 | 0% |
Hutchinson et al. (2019) | 3 | 0,1% | 3 | 0,44% | 3 | 0,48% | 3 | 0,48% |
Karadjian et al. (2022) | 3 | 0,1% | 3 | 0,44% | 3 | 0,48% | 3 | 0,48% |
Lacepède (1801) | 3 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Laurenti (1768) | 3 | 0,1% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Legand (1950) | 3 | 0,1% | 2 | 0,3% | 2 | 0,32% | 2 | 0,32% |
Levesque & Delcroix (2013) | 3 | 0,1% | 3 | 0,44% | 0 | 0% | 3 | 0,48% |
Linné (1766) | 3 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Maréchal & Trégarot (2012) | 3 | 0,1% | 2 | 0,3% | 2 | 0,32% | 2 | 0,32% |
Maréchal et al. (2006) | 3 | 0,1% | 3 | 0,44% | 3 | 0,48% | 3 | 0,48% |
Méheust et al. (2018) | 3 | 0,1% | 3 | 0,44% | 3 | 0,48% | 3 | 0,48% |
Merrem (1820) | 3 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Møller et al. (2005) | 3 | 0,1% | 3 | 0,44% | 3 | 0,48% | 3 | 0,48% |
Morinière & Dell'amico (2011) | 3 | 0,1% | 3 | 0,44% | 3 | 0,48% | 3 | 0,48% |
Oustalet (1895) | 3 | 0,1% | 2 | 0,3% | 2 | 0,32% | 0 | 0% |
Philippi (1887) | 3 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Poisson (1999) | 3 | 0,1% | 3 | 0,44% | 3 | 0,48% | 3 | 0,48% |
Potin (2013) | 3 | 0,1% | 3 | 0,44% | 3 | 0,48% | 3 | 0,48% |
Probst et al. (2000) | 3 | 0,1% | 3 | 0,44% | 3 | 0,48% | 3 | 0,48% |
Randall & Vergara (1978) | 3 | 0,1% | 3 | 0,44% | 3 | 0,48% | 3 | 0,48% |
Read & Jean (2021) | 3 | 0,1% | 3 | 0,44% | 3 | 0,48% | 3 | 0,48% |
Risso (1827) | 3 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Robineau & Duhamel (2006) | 3 | 0,1% | 3 | 0,44% | 3 | 0,48% | 2 | 0,32% |
Rüppell (1835) | 3 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Sanchez (2020) | 3 | 0,1% | 3 | 0,44% | 3 | 0,48% | 2 | 0,32% |
Shirihai (2003) | 3 | 0,1% | 3 | 0,44% | 3 | 0,48% | 2 | 0,32% |
Simian et al. (2022) | 3 | 0,1% | 3 | 0,44% | 3 | 0,48% | 3 | 0,48% |
Tirvengadum & Bour (1985) | 3 | 0,1% | 2 | 0,3% | 2 | 0,32% | 2 | 0,32% |
Tostain (1980) | 3 | 0,1% | 2 | 0,3% | 2 | 0,32% | 2 | 0,32% |
UICN Comité français, OFB, MNHN & GEPOMAY (2025) | 3 | 0,1% | 3 | 0,44% | 3 | 0,48% | 2 | 0,32% |
Vaslet & Agrnsm (2018) | 3 | 0,1% | 3 | 0,44% | 3 | 0,48% | 3 | 0,48% |
Wallach (2020) | 3 | 0,1% | 2 | 0,3% | 2 | 0,32% | 2 | 0,32% |
Aubouin et al. (2016) | 2 | 0,06% | 2 | 0,3% | 2 | 0,32% | 2 | 0,32% |
Ausilio & Zotier (1989) | 2 | 0,06% | 2 | 0,3% | 2 | 0,32% | 1 | 0,16% |
Baldi et al. (2022) | 2 | 0,06% | 2 | 0,3% | 2 | 0,32% | 2 | 0,32% |
Bartoli (1972) | 2 | 0,06% | 2 | 0,3% | 2 | 0,32% | 2 | 0,32% |
Bauer (1987) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Bertin (1928) | 2 | 0,06% | 2 | 0,3% | 2 | 0,32% | 2 | 0,32% |
Bleeker (1852) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Bochaton et al. (2018) | 2 | 0,06% | 2 | 0,3% | 2 | 0,32% | 2 | 0,32% |
Boddaert & Daubenton (1783) | 2 | 0,06% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Boer et al. (1999) | 2 | 0,06% | 2 | 0,3% | 2 | 0,32% | 2 | 0,32% |
Bowdich (1825) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Breuil & Ibéné (2008) | 2 | 0,06% | 2 | 0,3% | 2 | 0,32% | 2 | 0,32% |
Breuil (2013) | 2 | 0,06% | 2 | 0,3% | 2 | 0,32% | 2 | 0,32% |
Brosse et al. (2021) | 2 | 0,06% | 2 | 0,3% | 2 | 0,32% | 2 | 0,32% |
Brugneaux & Pérès (2005) | 2 | 0,06% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Caceres & Salamolard (2021) | 2 | 0,06% | 2 | 0,3% | 2 | 0,32% | 2 | 0,32% |
Chabanaud (1927) | 2 | 0,06% | 2 | 0,3% | 2 | 0,32% | 2 | 0,32% |
Chapuis et al. (2004) | 2 | 0,06% | 2 | 0,3% | 2 | 0,32% | 2 | 0,32% |
Chartier et al. (2007) | 2 | 0,06% | 2 | 0,3% | 2 | 0,32% | 0 | 0% |
Cheke (1987) | 2 | 0,06% | 2 | 0,3% | 2 | 0,32% | 2 | 0,32% |
Cheon et al. (2023) | 2 | 0,06% | 2 | 0,3% | 0 | 0% | 2 | 0,32% |
Chevallier et al. (2023) | 2 | 0,06% | 2 | 0,3% | 2 | 0,32% | 2 | 0,32% |
Colin (1994) | 2 | 0,06% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Curado et al. (2011) | 2 | 0,06% | 2 | 0,3% | 2 | 0,32% | 2 | 0,32% |
dal Molin (2009) | 2 | 0,06% | 2 | 0,3% | 2 | 0,32% | 2 | 0,32% |
Daniel et al. (2020) | 2 | 0,06% | 2 | 0,3% | 2 | 0,32% | 0 | 0% |
Davant (1967) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Dewynter et al. (2020) | 2 | 0,06% | 2 | 0,3% | 2 | 0,32% | 2 | 0,32% |
Donovan (1816) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Duguet & Melki (2003) | 2 | 0,06% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Duguy et al. (1997) | 2 | 0,06% | 2 | 0,3% | 2 | 0,32% | 2 | 0,32% |
Duguy et al. (1999) | 2 | 0,06% | 2 | 0,3% | 2 | 0,32% | 2 | 0,32% |
Duguy et al. (2000) | 2 | 0,06% | 2 | 0,3% | 2 | 0,32% | 2 | 0,32% |
Duguy et al. (2002) | 2 | 0,06% | 2 | 0,3% | 2 | 0,32% | 2 | 0,32% |
Duguy et al. (2003) | 2 | 0,06% | 2 | 0,3% | 2 | 0,32% | 2 | 0,32% |
Duguy et al. (2004) | 2 | 0,06% | 2 | 0,3% | 2 | 0,32% | 2 | 0,32% |
Duguy et al. (2006) | 2 | 0,06% | 2 | 0,3% | 2 | 0,32% | 2 | 0,32% |
Duguy (1987) | 2 | 0,06% | 2 | 0,3% | 2 | 0,32% | 2 | 0,32% |
Duguy (1990) | 2 | 0,06% | 2 | 0,3% | 2 | 0,32% | 2 | 0,32% |
Duguy (1992) | 2 | 0,06% | 2 | 0,3% | 2 | 0,32% | 2 | 0,32% |
Duguy (1993) | 2 | 0,06% | 2 | 0,3% | 2 | 0,32% | 2 | 0,32% |
Duguy (1995) | 2 | 0,06% | 2 | 0,3% | 2 | 0,32% | 2 | 0,32% |
Duguy (1996) | 2 | 0,06% | 2 | 0,3% | 2 | 0,32% | 2 | 0,32% |
Evermann & Clark (1928) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Fontan (2019) | 2 | 0,06% | 2 | 0,3% | 2 | 0,32% | 2 | 0,32% |
Fowler (1919) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Gannier & Petiau (2006) | 2 | 0,06% | 2 | 0,3% | 2 | 0,32% | 2 | 0,32% |
Geoffroy Saint-Hilaire ([1817]) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Gilot et al. (1992) | 2 | 0,06% | 2 | 0,3% | 2 | 0,32% | 2 | 0,32% |
Girondo (2023) | 2 | 0,06% | 2 | 0,3% | 2 | 0,32% | 2 | 0,32% |
Griffith & Smith (1834) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Hass (1991) | 2 | 0,06% | 2 | 0,3% | 2 | 0,32% | 2 | 0,32% |
Hildebrand (1948) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Holenweg Peter (2001) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Humeau et al. (2020) | 2 | 0,06% | 2 | 0,3% | 2 | 0,32% | 0 | 0% |
Impact-mer (2011) | 2 | 0,06% | 2 | 0,3% | 2 | 0,32% | 2 | 0,32% |
Ingels et al. (2003) | 2 | 0,06% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Jouan (1863) | 2 | 0,06% | 2 | 0,3% | 2 | 0,32% | 2 | 0,32% |
Kasamatsu & Joyce (1995) | 2 | 0,06% | 2 | 0,3% | 2 | 0,32% | 2 | 0,32% |
Keith et al. (2002) | 2 | 0,06% | 2 | 0,3% | 2 | 0,32% | 2 | 0,32% |
Keith et al. (2006) | 2 | 0,06% | 2 | 0,3% | 2 | 0,32% | 2 | 0,32% |
Keith (2002) | 2 | 0,06% | 2 | 0,3% | 2 | 0,32% | 2 | 0,32% |
Kemp (2023) | 2 | 0,06% | 2 | 0,3% | 2 | 0,32% | 2 | 0,32% |
Kiszka et al. (2009) | 2 | 0,06% | 2 | 0,3% | 2 | 0,32% | 2 | 0,32% |
Kock et al. (2006) | 2 | 0,06% | 2 | 0,3% | 2 | 0,32% | 2 | 0,32% |
Kojadinovic et al. (2007) | 2 | 0,06% | 2 | 0,3% | 2 | 0,32% | 0 | 0% |
Kuhl (1820) | 2 | 0,06% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Kwet (2009) | 2 | 0,06% | 2 | 0,3% | 2 | 0,32% | 2 | 0,32% |
Lacepède (1800) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Lacoste (de) (2020) | 2 | 0,06% | 2 | 0,3% | 2 | 0,32% | 2 | 0,32% |
Laran et al. (2012) | 2 | 0,06% | 2 | 0,3% | 2 | 0,32% | 2 | 0,32% |
Leaper et al. (2008) | 2 | 0,06% | 2 | 0,3% | 2 | 0,32% | 2 | 0,32% |
Levesque & Clergeau (2002) | 2 | 0,06% | 2 | 0,3% | 2 | 0,32% | 2 | 0,32% |
Lorvelec & Pascal (2009) | 2 | 0,06% | 2 | 0,3% | 2 | 0,32% | 2 | 0,32% |
Lorvelec et al. (2004) | 2 | 0,06% | 2 | 0,3% | 2 | 0,32% | 2 | 0,32% |
Louette & Cousin (1999) | 2 | 0,06% | 2 | 0,3% | 2 | 0,32% | 2 | 0,32% |
Macdonald & Barron (1868) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Maréchal & Pérès (2007) | 2 | 0,06% | 2 | 0,3% | 2 | 0,32% | 2 | 0,32% |
Marquet et al. (2003) | 2 | 0,06% | 2 | 0,3% | 2 | 0,32% | 2 | 0,32% |
Marshall et al. (2009) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Mas-Coma et al. (1989) | 2 | 0,06% | 2 | 0,3% | 2 | 0,32% | 2 | 0,32% |
Mathews (1914) | 2 | 0,06% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
McNair & Cramer-Burke (2006) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Miaud & Muratet (2018) | 2 | 0,06% | 2 | 0,3% | 2 | 0,32% | 2 | 0,32% |
Mothes et al. (2019) | 2 | 0,06% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Nardo (1827) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Olson & Normand (2014) | 2 | 0,06% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Palko et al. (1982) | 2 | 0,06% | 2 | 0,3% | 2 | 0,32% | 2 | 0,32% |
Pallas (1770) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Peron (2014) | 2 | 0,06% | 2 | 0,3% | 2 | 0,32% | 2 | 0,32% |
Powell et al. (2008) | 2 | 0,06% | 2 | 0,3% | 2 | 0,32% | 0 | 0% |
Probst et al. (2001) | 2 | 0,06% | 2 | 0,3% | 2 | 0,32% | 2 | 0,32% |
protection du biotope des eaux territoriales de l'île de Clipperton dénommée « aire marine protégée dans les eaux territoriales de l'île de Clipperton » | 2 | 0,06% | 2 | 0,3% | 2 | 0,32% | 2 | 0,32% |
Quero et al. (2013) | 2 | 0,06% | 2 | 0,3% | 2 | 0,32% | 2 | 0,32% |
Rafinesque (1810) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Revilliod (1914) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
. SFEPM, Bourges. 56 pp. ">Rigaux & Dupasquier (2012) | 2 | 0,06% | 2 | 0,3% | 2 | 0,32% | 2 | 0,32% |
Rinaldi et al. (2011) | 2 | 0,06% | 2 | 0,3% | 2 | 0,32% | 2 | 0,32% |
Robineau (2005) | 2 | 0,06% | 2 | 0,3% | 2 | 0,32% | 1 | 0,16% |
Rossi-santos et al. (2007) | 2 | 0,06% | 2 | 0,3% | 2 | 0,32% | 1 | 0,16% |
Roux (1913) | 2 | 0,06% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Ruys & Coord (2012) | 2 | 0,06% | 2 | 0,3% | 2 | 0,32% | 2 | 0,32% |
Saint et al. (1978) | 2 | 0,06% | 2 | 0,3% | 2 | 0,32% | 2 | 0,32% |
Savouré-Soubelet et al. (in prep.) | 2 | 0,06% | 2 | 0,3% | 2 | 0,32% | 2 | 0,32% |
Séret (1997) | 2 | 0,06% | 2 | 0,3% | 2 | 0,32% | 2 | 0,32% |
Serre-collet (2013) | 2 | 0,06% | 2 | 0,3% | 2 | 0,32% | 2 | 0,32% |
Simmons (2005) | 2 | 0,06% | 2 | 0,3% | 0 | 0% | 2 | 0,32% |
Snodgrass & Heller (1905) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Spix & Agassiz (1829-31) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Swainson (1838) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Thawley & Kolbe (2020) | 2 | 0,06% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Thiele et al. (1999) | 2 | 0,06% | 2 | 0,3% | 2 | 0,32% | 2 | 0,32% |
Thiele et al. (2004) | 2 | 0,06% | 2 | 0,3% | 2 | 0,32% | 1 | 0,16% |
Thirion & Evrard (2012) | 2 | 0,06% | 2 | 0,3% | 2 | 0,32% | 2 | 0,32% |
Thomas (1855) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Thunberg (1787) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Timm & Genoways (2003) | 2 | 0,06% | 2 | 0,3% | 1 | 0,16% | 1 | 0,16% |
Tunstall (1880) | 2 | 0,06% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Van Canneytet al. (2008) | 2 | 0,06% | 2 | 0,3% | 2 | 0,32% | 2 | 0,32% |
van den Burg et al. (2021) | 2 | 0,06% | 2 | 0,3% | 2 | 0,32% | 2 | 0,32% |
van den Burg et al. (2021) | 2 | 0,06% | 2 | 0,3% | 2 | 0,32% | 2 | 0,32% |
Vanderwerf et al. (2006) | 2 | 0,06% | 2 | 0,3% | 2 | 0,32% | 1 | 0,16% |
Villanueva et al. (2021) | 2 | 0,06% | 2 | 0,3% | 2 | 0,32% | 2 | 0,32% |
Vuillaume et al. (2015) | 2 | 0,06% | 2 | 0,3% | 2 | 0,32% | 2 | 0,32% |
Walbaum (1792) | 2 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Weimerskirch et al. (2009) | 2 | 0,06% | 2 | 0,3% | 2 | 0,32% | 0 | 0% |
Wickel et al. (2014) | 2 | 0,06% | 2 | 0,3% | 2 | 0,32% | 2 | 0,32% |
Wilson (1813) | 2 | 0,06% | 2 | 0,3% | 2 | 0,32% | 2 | 0,32% |
Abhaya & Probst (2009) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Abhaya et al. (1998) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 0 | 0% |
Agarwal et al. (2021) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Agassiz (1833-1843) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Agassiz (1857) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Ainley et al. (2007) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Al-hasson & Ali (2020) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Alley et al. (2023) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Almeida & Vasconcelos (2023) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Almeida et al. (2019) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Almeida et al. (2024) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Amoureux (1959) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Andrew et al. (2008) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Angin (2017) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Angin (2017) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Anonyme. (2004) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Anonyme. (2004) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 0 | 0% |
Anonyme (2008) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 0 | 0% |
Anonyme. (2012) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2012) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Anonyme. (2012) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Anonyme. (2012) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Anonyme. (2012) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Anonyme. (2012) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Anonyme. (2012) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Anonyme. (2012) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Anonyme. (2012) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2012) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Anonyme. (2012) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Anonyme. (2012) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Anonyme. (2012) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 0 | 0% |
Anonyme. (2012) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 0 | 0% |
Anonyme. (2012) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Anonyme. (2012) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Anonyme. (2012) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 0 | 0% |
Anonyme. (2012) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2012) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 0 | 0% |
Anonyme. (2012) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Anonyme. (2012) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2012) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Anonyme. (2012) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Anonyme. (2012) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 0 | 0% |
Anonyme. (2012) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Anonyme. (2012) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Anonyme. (2012) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Aquarium de La Rochelle (2017) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Astudillo et al. (2021) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Atkinson (2023) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Atwood (1869) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Bailenger et al. (1965) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Bailon et al. (2015) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Baldi et al. (2023) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Balle et al. (2021) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Bance (2022) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Bancroft (1832) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Bangs (1913) | 1 | 0,03% | 1 | 0,15% | 0 | 0% | 1 | 0,16% |
Barbancey & Probst (1998) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Barbancey (2001) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Barbancey (2001) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Barbour (1912) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Barre et al. (1991) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 0 | 0% |
Bassett (2022) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Bauer et al. (2010) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Bavay (1873) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Bavay (1899) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Beaucournu (1968) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Beauvieux et al. (2024) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Becerra et al. (2024) | 1 | 0,03% | 1 | 0,15% | 0 | 0% | 1 | 0,16% |
Behm et al. (2022) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Bernal & Rocha (2011) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Bertault (1988) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Bertrand & Drogou (2000) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Bertrand et al. (2001) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Bertrand (1982) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Best et al. (1995) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 0 | 0% |
Birdlife International (2012) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Birdlife International (2016) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Birdlife International (2016) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Birdlife International (2017) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Blache ([2018]) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Blainville (1816) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Bleeker (1865) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Bloch & Schneider (1801) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Bloch (1785-1795) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Bloch (1785-1795) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Bloch (1790) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Bloch (1793) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Bochaton et al. (2016) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Bochaton et al. (2020) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Bocourt (1868) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Boer (2000) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Boissinot (2009) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Bonnaterre (1788) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Bonnaterre (1789) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Borcyk et al. (2023) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Borsa (1997) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Boschert & Dronneau (1998) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Bouchon & Lemoine (2003) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Bourgade (2020) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Bourgade (2021) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Branch (2010) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 0 | 0% |
Brandt (1838) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Breuil & Serre-collet (2012) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Breuil et al. (2012) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Breuil et al. (2022) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Breuil (1999) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Breuil (2021) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Brito Capello (1867) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Brugneaux & Pérès (2005) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Brun (1958) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Brunes et al. (2021) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Bush et al. (2021) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Caceres (2002) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Calenge et al. (2010) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 0 | 0% |
Callou (2003) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Capalleras & Carretero (2000) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 0 | 0% |
Capape et al. (2002) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Caut et al. (2008) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
CEN Nouvelle-Calédonie (2021) | 1 | 0,03% | 1 | 0,15% | 0 | 0% | 1 | 0,16% |
Censky & Paulson (1992) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Censky (1988) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Cerchio et al. (2009) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 0 | 0% |
Cervigon (1966) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Chambault et al. (2020) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Chastel et al. (1981) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Chastel et al. (2003) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Cheke & Hume (2008) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 0 | 0% |
Cheke (2010) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Chesser et al. (2016) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Chevreux & de Guerne (1893) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Cheylan et al. (2022) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Chibon (1961) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Chibon (1962) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
CHN (2017) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Chocobar et al. (2023) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Ciccione (2001) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Ciccione (2001) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Clements (1992) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Clergeau & Pascal (2003) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Coatmeur (1999) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Colin (1992) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Collectif (2009) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 0 | 0% |
Collet & Duguy (1981) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Collette (2003) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Cope (1864) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Cope (1869) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Coues (1862) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Counihan et al. (2012) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 0 | 0% |
Crochet et al. (2022) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Crouzier (2009) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Csabaï (2020) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 0 | 0% |
Cuevas et al. (2022) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Cuvier & Valenciennes (1828-1830) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Cuvier & Valenciennes (1849) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Cuvier & Voigt (1832) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Dalleau et al. (2014) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Danforth (1935) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
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 | 0,03% | 1 | 0,15% | 1 | 0,16% | 0 | 0% |
Daudin (1800) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Daudin (1802) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 0 | 0% |
Daudin (1803) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Dauvin (1990) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Davis (1973) | 1 | 0,03% | 1 | 0,15% | 0 | 0% | 1 | 0,16% |
Day (1865) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
de Massary et al. (2015) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 0 | 0% |
Deblock (1966) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Debout (2001) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Debout (2009) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Dechelle & Ingels (2007) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Dedukh & Krasikova (2017) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Deflandre (2007) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Deflorenne et al. (2012) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Dekay (1842) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Dekay (1842) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Delacour (1963) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Delaney & Warner (2017) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Delcroix et al. (2008) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Delgado-trejo et al. (2024) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Deniau & Provost (2020) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 0 | 0% |
Denys et al. (2022) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Desbrosses (1934) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Desbrosses (1935) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Dieme et al. (2015) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Dollfus (1966) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Dreff & Delliere (1994) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Drohvalenko et al. (2022) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Dubois & Frétey (2024) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Dubois & Louvet (2014) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Dubois & Ohler (1994) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Ducatez & Devore (2023) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Duguy & Duron (1981) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Duguy & Duron (1982) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Duguy & Duron (1983) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Duguy & Duron (1984) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Duguy & Duron (1985) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Duguy et al. (1980) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Duguy et al. (2000) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Duguy (1983) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Duguy (1986) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Duguy (1988) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Duguy (1989) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Duméril & Bibron (1839) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Duméril & Bibron (1837) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Duméril & Bribron (1841) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Efe et al. (2009) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 0 | 0% |
Ersts & Rosenbaum (2003) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 0 | 0% |
Eschscholtz (1829) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Eyton (1838) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Faber (1829) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabre & Orsini (2016) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Ficetola & Scali (2010) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 0 | 0% |
Fleming & Jackson (2011) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 0 | 0% |
Flitti & Rocha (2014) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 0 | 0% |
Forest (1946) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Fowler (1900) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Francour & Mouine (2008) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Franzini et al. (2018) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Fraser-brunner (1950) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Fremont (2002) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Fretey & Bour (1980) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Fretey et al. (2023) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Fretey (1980) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Fretey (2003) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Frétey (2022) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Frétey (2023) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Fritz & Havaš (2007) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Gallien (2011) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Garman (1913) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Gérigny et al. (2020) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Gernigon (2008) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Gerovasileiou et al. (2020) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Gibson & Baker (2012) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Gill & Thiele (1997) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Gill (1862) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Gillespie (1997) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Girard (1859) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Girondot et al. (2015) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Godet et al. (2021) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
González et al. (2018) | 1 | 0,03% | 1 | 0,15% | 0 | 0% | 1 | 0,16% |
Goode & Bean (1882) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Gouillard (1973) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Goulletquer (2016) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Grant (1958) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Gray (1846) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Gray (1850) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Guermeur (1987) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Guinet (1991) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Guinet (2004) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Gunderson et al. (2020) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Günther (1859) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Guyétant & Moine (1992) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Hamdan et al. (2023) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Heimlich-boran (1993) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Hellebuyck et al. (2017) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Henao-osorio et al. (2021) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Herzberg (2018) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Holsbeek et al. (2008) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Houttuyn (1782) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Howard et al. (2001) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Howell & Clements (2019) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Hudson et al. (2021) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Huey (1927) | 1 | 0,03% | 1 | 0,15% | 0 | 0% | 1 | 0,16% |
Ibéné et al. (2007) | 1 | 0,03% | 1 | 0,15% | 0 | 0% | 1 | 0,16% |
Iglésias et al. (2021) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Iglesias-carrasco et al. (2017) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Iković et al. (2023) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 0 | 0% |
Ineich & Bauer (1992) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Ineich & Giraud (2019) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Ineich et al. (2017) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Ineich (2016) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
IUCN (2014) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Jairam et al. (2016) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Jamonneau et al. (2025) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Jehl et al. (1980) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Jim et al. (2022) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Johnson & Wolman (1984) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 0 | 0% |
Johnson (1973) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Jordan & Evermann (1903) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Jordan & Gilbert (1882) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Jordan & Gilbert (1882) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Jordan & Gilbert (1884) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Jordan (1888) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Judson et al. (2018) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Karaa et al. (2016) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Kasamatsu et al. (2000) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 0 | 0% |
Keith & Marquet (2011) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Keith et al. (1999) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
King (1962) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Kiszka et al. (2009) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 0 | 0% |
Heron, 36(1): 31-34.">Kiszka (2003) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 0 | 0% |
Kock & Stephan (1986) | 1 | 0,03% | 1 | 0,15% | 0 | 0% | 1 | 0,16% |
Kolenda et al. (2024) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Koleska & Jablonski (2018) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Kornilev et al. (2020) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 0 | 0% |
Labach et al. (2021) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 0 | 0% |
Lacepède (1802) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Lacepède (1803) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Lancastre et al. (1976) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Lataste (1877) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Lataste (1877) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Latham (1787) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Lazell (1972) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Le Corre & Jouventin (1999) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 0 | 0% |
Leaper et al. (2008) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 0 | 0% |
Leblond (2003) | 1 | 0,03% | 1 | 0,15% | 0 | 0% | 1 | 0,16% |
Lédée & Questel (2013) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Léger & Mouzels (1917) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Legouez (2010) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Leimroth et al. (2022) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Lescure et al. (2016) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Lescure et al. (2020) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Lescure (2018) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Lesson (1830-1831) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Lesson (1831) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 0 | 0% |
Lesson (1839) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Lesueur (1822) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Letacq (1924) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Letourneur et al. (2004) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Levesque & Mathurin (2008) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Levesque (2001) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Levesque (2013) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Liardet & d'Auzon (2004) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Liardet (2004) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Liebart et al. (2021) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Lim (1997) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 0 | 0% |
Lizé (2018) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Loisier et al. (2021) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Loison (1989) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 0 | 0% |
Lorvelec & Vigne (2003) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Lorvelec et al. (2003) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Lorvelec et al. (2003) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Lorvelec et al. (2009) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Lorvelec et al. (2016) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Lorvelec et al. (2017) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Louisin & Probst (1996) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Lourie et al. (2016) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Lowe (1833) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Lowe (1838) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Lowe (1841) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Lucchini & Pizzigalli (2020) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Maciel et al. (2021) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Mageski et al. (2017) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Mahé et al. (2013) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Maillard & David (2014) | 1 | 0,03% | 1 | 0,15% | 0 | 0% | 1 | 0,16% |
Mancino et al. (2022) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Marchandeau & Letty (2021) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Marchandeau et al. (2003) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Maréchal (2007) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Marinho (2022) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Marion & Clergeau (2003) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 0 | 0% |
Marion & Marion (1982) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 0 | 0% |
Marion (2003) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 0 | 0% |
Marion (2003) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Martin et al. (2021) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Martinet et al. (1765) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Massary (2012) | 1 | 0,03% | 1 | 0,15% | 0 | 0% | 1 | 0,16% |
Matsuoka et al. (2005) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 0 | 0% |
Mcbride et al. (2010) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Medetian & Miaud (2024) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Meek & Hildebrand (1923) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Melin et al. (2003) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Ménard et al. (2000) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Mezhzherin et al. (2023) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Mezhzherin et al. (2024) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Momont (1998) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Montagu (1813) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Moon & Kamath (2019) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Moreau de Jonnès (1818) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Moreau (1881) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Morel (1959) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Morrison (2006) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Mourier (2012) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Muller et al. (2022) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Murase et al. (2002) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 0 | 0% |
Murray (1884) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Murray (1887) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Nadal & Tariel (2008) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 0 | 0% |
Nassi et al. (1975) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Nelson-Smith et al. (2014) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Neveu (1997) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Nicol et al. (2000) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 0 | 0% |
Noël (2024) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 0 | 0% |
Noël (2017) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Oliveira et al. (2018) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Oliver (2011) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
O'reilly (1818) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Oremus (2009) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Osbeck (1765) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Owen (1853) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Pagano & Lorvelec (2003) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
pallas (1764) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Paperna & Landsberg (1989) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Parker & Fitzgerald (2024) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Pascal & Vigne (2003) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Pascal & Vigne (2003) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Pascal & Vigne (2003) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Pascal et al. (2003) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Pearman et al. (2016) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 0 | 0% |
Peck & Wilcoxen (2018) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Perez Canto (1886) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Pérez-delgadillo & Lara-reséndiz (2024) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Perkins (1928) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Perrin et al. (1994) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Peters (1930) | 1 | 0,03% | 1 | 0,15% | 0 | 0% | 1 | 0,16% |
Philippi (1902) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Philippot et al. (2019) | 1 | 0,03% | 1 | 0,15% | 0 | 0% | 1 | 0,16% |
Pitman & Ensor (2003) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Poey (1863) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Pool (2013) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 0 | 0% |
Pop (2024) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Praderi et al. (1992) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Prato et al. (2022) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Preynat (2013) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Probst (1997) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Probst (1997) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Probst (1999) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Probst (2001) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Probst (2007) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Puissauve, Comolet-tirman & Whal (2015) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 0 | 0% |
Purenne (2016) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Quéro & Delmas (1982) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Quero & Laborde (1996) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Quero et al. (1998) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Quero (1998) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Questel & Boggio (2012) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Questel & Boggio (2012) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Questel & Vitry (2012) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Questel et al. (2012) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Questel (2011) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Questel (2012) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Questel (2012) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Questel (2013) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Questel (2014) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Questel (2018) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 0 | 0% |
Questel (2020) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Randi et al. (2001) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Ranzani (1839) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Read et al. (2015) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Recoder et al. (2018) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Reeber (2015) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Reis et al. (2003) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Renaud et al. (2013) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Réserve Naturelle de Saint Barthélemy (2014) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Revuelta et al. (2015) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Rhodin & Carr (2009) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Rimblot et al. (1985) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Ringler et al. (2021) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Robert et al. (2002) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Robineau (1989) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Roche & Guinet (2007) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Rodrigues et al. (2021) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Romero et al. (2010) | 1 | 0,03% | 1 | 0,15% | 0 | 0% | 1 | 0,16% |
Roos (2000) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Roques (1991) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Rosenbaum & Collins (2006) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 0 | 0% |
Roughgarden (1974) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Roux & Coll. (2017) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Roznik et al. (2021) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Rüppell (1835) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Russell & Bauer (2002) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Sanchez & Probst (2016) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Sanchez et al. (2004) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Sanchez et al. (2019) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Sawai et al. (2018) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Sayah et al. (2023) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Schinz (1822) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Schneider (1783) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Schoepff (1792) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Schuchmann (1981) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 0 | 0% |
Schulte et al. (2024) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Schweigger (1812) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Scopoli (1786) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Sellier et al. (2016) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Séret (2014) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Servan & Arvy (1997) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 0 | 0% |
Servan (1976) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Shaver et al. (2019) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Shaw (1802) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Shukla et al. (2024) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Sigalas (1931) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Slater et al. (2014) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Smith et al. (2005) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Smith-Vaniz & Carpenter (2007) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Smith-vaniz & Jelks (2014) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Snyder et al. (2019) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Socha & Ogielska (2010) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Socolovschi et al. (2012) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Sonsino (1893) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Sparrman (1784) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Spiroux (1996) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Spix (1824) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Springer (1941) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Steadman & Bollt (2010) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 0 | 0% |
Steindachner (1861) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Steindachner (1867) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Stelfox et al. (2020) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Swainson (1838) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 0 | 0% |
Széles et al. (2018) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Taton (1877) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Terrasse & Terrasse (1969) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Thawley et al. (2019) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Thévenot (2014) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Thibault et al. (2023) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Thoisy et al. (2003) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 0 | 0% |
Toohey et al. (2022) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Tostain & Dujardin (1988) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Townsend et al. (2000) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Tregarot et al. (2015) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Tschudi (1838) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Turpin & Probst (1998) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 0 | 0% |
Uicn et al. (2016) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
UNEP-WCMC (2005) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Van & Kampen (1907) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Van Den Burg et al. (2018) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Van den burg et al. (2022) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Vandellius (1761) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Vanderwerf et al. (2004) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Vaslet et al. (2010) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Vernoux (1988) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Verreaux & Des Murs (1860) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 0 | 0% |
Veysset (2003) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 0 | 0% |
Vieillot (1816) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Vieillot (1817) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Vieillot (1819) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Vieira (2022) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Viel (2021) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Von May et al. (2021) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Waayers et al. (2011) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Wahl & Barbraud (2005) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 0 | 0% |
Wallach (2009) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Wang & Liu (2016) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 0 | 0% |
Wasilewski et al. (2022) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Weerdt (2023) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 0 | 0% |
Weterings & Vetter (2017) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Whitley (1929) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Whitley (1933) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Whitley (1937) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Wied (1839) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Williams et al. (2009) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 0 | 0% |
Williams et al. (2019) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Works & Olson (2018) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 0 | 0% |
Yengle (2021) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Yésou (2003) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
Yésou (2003) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |
(2022) | 1 | 0,03% | 1 | 0,15% | 1 | 0,16% | 1 | 0,16% |