Vertébrés de Saint-Martin
835 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) | 287 | 15,51% | 280 | 66,67% | 257 | 66,75% | 274 | 70,8% |
Questel & Le Quellec (2012) | 257 | 13,88% | 246 | 58,57% | 234 | 60,78% | 233 | 60,21% |
Bouchon-Navaro et al. (2005) | 176 | 9,51% | 148 | 35,24% | 148 | 38,44% | 148 | 38,24% |
Yokoyama (2013) | 167 | 9,02% | 144 | 34,29% | 132 | 34,29% | 133 | 34,37% |
UICN Comité français, OFB & MNHN (2021) | 120 | 6,48% | 120 | 28,57% | 120 | 31,17% | 102 | 26,36% |
Levesque & Delcroix (2018) | 119 | 6,43% | 114 | 27,14% | 100 | 25,97% | 111 | 28,68% |
Uicn et al. (2017) | 118 | 6,37% | 113 | 26,9% | 109 | 28,31% | 94 | 24,29% |
Diaz & Cuzange (2009) | 106 | 5,73% | 98 | 23,33% | 98 | 25,45% | 96 | 24,81% |
Bouchon-Navaro & Louis (1986) | 96 | 5,19% | 81 | 19,29% | 81 | 21,04% | 81 | 20,93% |
Linnaeus (1758) | 72 | 3,89% | 22 | 5,24% | 22 | 5,71% | 16 | 4,13% |
Remsen et al. (2013) | 69 | 3,73% | 67 | 15,95% | 67 | 17,4% | 57 | 14,73% |
Brugneaux & Pérès (2006) | 67 | 3,62% | 61 | 14,52% | 61 | 15,84% | 61 | 15,76% |
Uicn et al. (2015) | 56 | 3,03% | 56 | 13,33% | 56 | 14,55% | 46 | 11,89% |
Henderson & Breuil (2012) | 55 | 2,97% | 40 | 9,52% | 36 | 9,35% | 40 | 10,34% |
Belfan & Conde (2016) | 46 | 2,49% | 44 | 10,48% | 30 | 7,79% | 43 | 11,11% |
Rinaldi (2016) | 40 | 2,16% | 40 | 9,52% | 40 | 10,39% | 24 | 6,2% |
Etcheberry & Abraham (2009) | 37 | 2% | 32 | 7,62% | 32 | 8,31% | 30 | 7,75% |
Dewynter et al. (2022) | 34 | 1,84% | 33 | 7,86% | 31 | 8,05% | 31 | 8,01% |
Carzon et al. (2016) | 30 | 1,62% | 30 | 7,14% | 30 | 7,79% | 18 | 4,65% |
Estrade et al. (2016) | 30 | 1,62% | 30 | 7,14% | 30 | 7,79% | 18 | 4,65% |
Rousseau (2010) | 30 | 1,62% | 28 | 6,67% | 28 | 7,27% | 28 | 7,24% |
Dewynter et al. (2023) | 28 | 1,51% | 28 | 6,67% | 27 | 7,01% | 26 | 6,72% |
Questel et al. (2023) | 27 | 1,46% | 27 | 6,43% | 26 | 6,75% | 25 | 6,46% |
Massary et al. (2017) | 26 | 1,4% | 22 | 5,24% | 21 | 5,45% | 20 | 5,17% |
Questel et al. (2023) | 26 | 1,4% | 26 | 6,19% | 26 | 6,75% | 24 | 6,2% |
Breuil (2002) | 25 | 1,35% | 12 | 2,86% | 12 | 3,12% | 12 | 3,1% |
Lorvelec et al. (2007) | 25 | 1,35% | 20 | 4,76% | 20 | 5,19% | 18 | 4,65% |
Dewynter (2021) | 23 | 1,24% | 23 | 5,48% | 23 | 5,97% | 23 | 5,94% |
Massary et al. (2018) | 23 | 1,24% | 21 | 5% | 20 | 5,19% | 19 | 4,91% |
Weimerskirch et al. (2009) | 23 | 1,24% | 19 | 4,52% | 19 | 4,94% | 17 | 4,39% |
Uicn et al. (2020) | 22 | 1,19% | 22 | 5,24% | 22 | 5,71% | 18 | 4,65% |
Mertens & Wermuth (1960) | 21 | 1,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Clements (2012) | 18 | 0,97% | 18 | 4,29% | 17 | 4,42% | 18 | 4,65% |
Gmelin (1789) | 18 | 0,97% | 4 | 0,95% | 4 | 1,04% | 4 | 1,03% |
Louis et al. (1992) | 18 | 0,97% | 11 | 2,62% | 11 | 2,86% | 11 | 2,84% |
Fricke et al. (2009) | 17 | 0,92% | 16 | 3,81% | 16 | 4,16% | 16 | 4,13% |
Van Dijk et al. (2012) | 17 | 0,92% | 12 | 2,86% | 12 | 3,12% | 12 | 3,1% |
Fricke et al. (2011) | 16 | 0,86% | 16 | 3,81% | 16 | 4,16% | 16 | 4,13% |
Girard (2007) | 16 | 0,86% | 9 | 2,14% | 8 | 2,08% | 9 | 2,33% |
Hoff & Daszkiewicz (2001) | 16 | 0,86% | 13 | 3,1% | 13 | 3,38% | 8 | 2,07% |
Dewynter et al. (2023) | 15 | 0,81% | 15 | 3,57% | 15 | 3,9% | 14 | 3,62% |
Massary et al. (2021) | 15 | 0,81% | 14 | 3,33% | 14 | 3,64% | 13 | 3,36% |
Siu et al. (2017) | 15 | 0,81% | 14 | 3,33% | 14 | 3,64% | 14 | 3,62% |
Tostain et al. (2013) | 15 | 0,81% | 11 | 2,62% | 10 | 2,6% | 11 | 2,84% |
Dewynter et al. (2019) | 14 | 0,76% | 14 | 3,33% | 14 | 3,64% | 13 | 3,36% |
Genoways et al. (2007) | 14 | 0,76% | 14 | 3,33% | 6 | 1,56% | 8 | 2,07% |
Wickel & Jamon (2010) | 14 | 0,76% | 13 | 3,1% | 13 | 3,38% | 13 | 3,36% |
Clements et al. (2015) | 13 | 0,7% | 12 | 2,86% | 2 | 0,52% | 11 | 2,84% |
Proceedings of the Zoological Society of London, 1907: 1035-1037.">Hopkinson (1907) | 13 | 0,7% | 2 | 0,48% | 2 | 0,52% | 2 | 0,52% |
Linnaeus (1766) | 13 | 0,7% | 2 | 0,48% | 1 | 0,26% | 1 | 0,26% |
Smith (1997) | 13 | 0,7% | 13 | 3,1% | 13 | 3,38% | 13 | 3,36% |
Aulagnier (2009) | 12 | 0,65% | 12 | 2,86% | 12 | 3,12% | 10 | 2,58% |
Barré (2021) | 12 | 0,65% | 12 | 2,86% | 12 | 3,12% | 12 | 3,1% |
Catzeflis (2012) | 12 | 0,65% | 12 | 2,86% | 12 | 3,12% | 5 | 1,29% |
Compagno (1984) | 12 | 0,65% | 12 | 2,86% | 12 | 3,12% | 12 | 3,1% |
Barau et al. (2005) | 11 | 0,59% | 9 | 2,14% | 9 | 2,34% | 7 | 1,81% |
Bouchon-Navaro et al. (1992) | 11 | 0,59% | 9 | 2,14% | 9 | 2,34% | 9 | 2,33% |
Dewynter et al. (2021) | 11 | 0,59% | 11 | 2,62% | 11 | 2,86% | 7 | 1,81% |
Dickinson & Remsen (2013) | 11 | 0,59% | 10 | 2,38% | 7 | 1,82% | 10 | 2,58% |
Soubeyran et al. (2011) | 11 | 0,59% | 11 | 2,62% | 11 | 2,86% | 11 | 2,84% |
Charrassin (2016) | 10 | 0,54% | 10 | 2,38% | 10 | 2,6% | 6 | 1,55% |
Charrassin (2016) | 10 | 0,54% | 10 | 2,38% | 10 | 2,6% | 6 | 1,55% |
Jarrett & Shirihai (2014) | 10 | 0,54% | 10 | 2,38% | 10 | 2,6% | 6 | 1,55% |
Moutou (2016) | 10 | 0,54% | 10 | 2,38% | 10 | 2,6% | 6 | 1,55% |
Spitz et al. (2016) | 10 | 0,54% | 10 | 2,38% | 10 | 2,6% | 6 | 1,55% |
Thoisy & Bordin (2016) | 10 | 0,54% | 10 | 2,38% | 10 | 2,6% | 6 | 1,55% |
Uicn et al. (2015) | 10 | 0,54% | 9 | 2,14% | 9 | 2,34% | 8 | 2,07% |
Urtizberea (2016) | 10 | 0,54% | 10 | 2,38% | 10 | 2,6% | 6 | 1,55% |
Béarez et al. (2017) | 9 | 0,49% | 9 | 2,14% | 9 | 2,34% | 9 | 2,33% |
Bochaton et al. (2021) | 9 | 0,49% | 8 | 1,9% | 8 | 2,08% | 8 | 2,07% |
Bordin et al. (2021) | 9 | 0,49% | 9 | 2,14% | 9 | 2,34% | 5 | 1,29% |
Hedges & Conn (2012) | 9 | 0,49% | 8 | 1,9% | 8 | 2,08% | 8 | 2,07% |
Theuerkauf et al. (2010) | 9 | 0,49% | 9 | 2,14% | 9 | 2,34% | 9 | 2,33% |
Aulagnier et al. (2017) | 8 | 0,43% | 8 | 1,9% | 8 | 2,08% | 8 | 2,07% |
Breuil et al. (2010) | 8 | 0,43% | 6 | 1,43% | 5 | 1,3% | 6 | 1,55% |
Collette & Nauen (1983) | 8 | 0,43% | 8 | 1,9% | 8 | 2,08% | 8 | 2,07% |
Gargominy et al. (1996) | 8 | 0,43% | 8 | 1,9% | 8 | 2,08% | 8 | 2,07% |
Garrigue (2007) | 8 | 0,43% | 8 | 1,9% | 8 | 2,08% | 5 | 1,29% |
Poey (1858-61) | 8 | 0,43% | 0 | 0% | 0 | 0% | 0 | 0% |
Rocamora (2004) | 8 | 0,43% | 8 | 1,9% | 7 | 1,82% | 7 | 1,81% |
Yokoyama (2012) | 8 | 0,43% | 6 | 1,43% | 6 | 1,56% | 6 | 1,55% |
Breuil (2009) | 7 | 0,38% | 6 | 1,43% | 6 | 1,56% | 6 | 1,55% |
Deblock et al. (1960) | 7 | 0,38% | 3 | 0,71% | 3 | 0,78% | 3 | 0,78% |
Delrieu-Trottin et al. (2015) | 7 | 0,38% | 7 | 1,67% | 7 | 1,82% | 7 | 1,81% |
Dewynter et al. (2019) | 7 | 0,38% | 7 | 1,67% | 7 | 1,82% | 6 | 1,55% |
Fourriére et al. (2014) | 7 | 0,38% | 7 | 1,67% | 7 | 1,82% | 7 | 1,81% |
Gannier (2001) | 7 | 0,38% | 7 | 1,67% | 7 | 1,82% | 4 | 1,03% |
Gannier (2002) | 7 | 0,38% | 7 | 1,67% | 7 | 1,82% | 4 | 1,03% |
Gannier (2009) | 7 | 0,38% | 7 | 1,67% | 7 | 1,82% | 4 | 1,03% |
G.E.M.M. (2012) | 7 | 0,38% | 7 | 1,67% | 7 | 1,82% | 4 | 1,03% |
Gill (1995) | 7 | 0,38% | 7 | 1,67% | 7 | 1,82% | 6 | 1,55% |
González-sánchez et al. (2021) | 7 | 0,38% | 6 | 1,43% | 6 | 1,56% | 5 | 1,29% |
Guth (1971) | 7 | 0,38% | 6 | 1,43% | 6 | 1,56% | 4 | 1,03% |
Pedersen et al. (2013) | 7 | 0,38% | 7 | 1,67% | 7 | 1,82% | 0 | 0% |
Pezold et al. (2015) | 7 | 0,38% | 7 | 1,67% | 7 | 1,82% | 7 | 1,81% |
Probst et al. (2022) | 7 | 0,38% | 7 | 1,67% | 7 | 1,82% | 7 | 1,81% |
Thibault et al. (2014) | 7 | 0,38% | 7 | 1,67% | 7 | 1,82% | 6 | 1,55% |
Vaslet & Agrnsm (2018) | 7 | 0,38% | 7 | 1,67% | 7 | 1,82% | 7 | 1,81% |
Bacchet et al. (2007) | 6 | 0,32% | 5 | 1,19% | 5 | 1,3% | 5 | 1,29% |
Camiñas et al. (2021) | 6 | 0,32% | 6 | 1,43% | 6 | 1,56% | 6 | 1,55% |
Commission de l’Avifaune Française (2016) | 6 | 0,32% | 6 | 1,43% | 6 | 1,56% | 5 | 1,29% |
Del Hoyo & Collar (2014) | 6 | 0,32% | 4 | 0,95% | 4 | 1,04% | 4 | 1,03% |
Dulau-Drouot et al. (2008) | 6 | 0,32% | 6 | 1,43% | 6 | 1,56% | 3 | 0,78% |
Gannier (2000) | 6 | 0,32% | 6 | 1,43% | 6 | 1,56% | 3 | 0,78% |
Gmelin (1788) | 6 | 0,32% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Heemstra & Randall (1993) | 6 | 0,32% | 6 | 1,43% | 6 | 1,56% | 6 | 1,55% |
Jourdan (2020) | 6 | 0,32% | 6 | 1,43% | 5 | 1,3% | 5 | 1,29% |
Kiszka et al.(2007) | 6 | 0,32% | 6 | 1,43% | 6 | 1,56% | 3 | 0,78% |
Kulbicki et al. (2000) | 6 | 0,32% | 5 | 1,19% | 5 | 1,3% | 5 | 1,29% |
Laran et al. (2011) | 6 | 0,32% | 6 | 1,43% | 6 | 1,56% | 4 | 1,03% |
Lescure et al. (2012) | 6 | 0,32% | 6 | 1,43% | 5 | 1,3% | 5 | 1,29% |
Lowe et al. (2007) | 6 | 0,32% | 6 | 1,43% | 5 | 1,3% | 6 | 1,55% |
Massary et al. (2019) | 6 | 0,32% | 6 | 1,43% | 6 | 1,56% | 5 | 1,29% |
Massary et al. (2020) | 6 | 0,32% | 6 | 1,43% | 6 | 1,56% | 6 | 1,55% |
Muratet (2015) | 6 | 0,32% | 6 | 1,43% | 5 | 1,3% | 5 | 1,29% |
Prévost & Mougin (1970) | 6 | 0,32% | 6 | 1,43% | 6 | 1,56% | 5 | 1,29% |
Probst (2001) | 6 | 0,32% | 5 | 1,19% | 5 | 1,3% | 4 | 1,03% |
Rhodin et al. (2017) | 6 | 0,32% | 4 | 0,95% | 4 | 1,04% | 4 | 1,03% |
Richard et al. (1982) | 6 | 0,32% | 3 | 0,71% | 3 | 0,78% | 3 | 0,78% |
Béarez & Bouffandeau (2019) | 5 | 0,27% | 5 | 1,19% | 5 | 1,3% | 5 | 1,29% |
Bioinsight/diren & Guyane (2006) | 5 | 0,27% | 5 | 1,19% | 5 | 1,3% | 5 | 1,29% |
Bour et al. (2008) | 5 | 0,27% | 5 | 1,19% | 5 | 1,3% | 4 | 1,03% |
Busala et al. (2024) | 5 | 0,27% | 2 | 0,48% | 2 | 0,52% | 1 | 0,26% |
Casale et al. (2021) | 5 | 0,27% | 5 | 1,19% | 5 | 1,3% | 5 | 1,29% |
Chabanet & Durville (2005) | 5 | 0,27% | 4 | 0,95% | 4 | 1,04% | 4 | 1,03% |
Chevalier (2006) | 5 | 0,27% | 5 | 1,19% | 5 | 1,3% | 5 | 1,29% |
Ciccione et al. (2011) | 5 | 0,27% | 5 | 1,19% | 5 | 1,3% | 5 | 1,29% |
Crillon & Cuzange (2020) | 5 | 0,27% | 5 | 1,19% | 5 | 1,3% | 5 | 1,29% |
Dewynter & Claessens (2020) | 5 | 0,27% | 5 | 1,19% | 5 | 1,3% | 3 | 0,78% |
Duffaut et al. (2011) | 5 | 0,27% | 5 | 1,19% | 5 | 1,3% | 5 | 1,29% |
Entraygues (2014) | 5 | 0,27% | 5 | 1,19% | 5 | 1,3% | 5 | 1,29% |
Étaix-bonnin et al. (2011) | 5 | 0,27% | 5 | 1,19% | 5 | 1,3% | 5 | 1,29% |
Fraga & Carvalho (2021) | 5 | 0,27% | 4 | 0,95% | 4 | 1,04% | 4 | 1,03% |
Fretey & Triplet (2022) | 5 | 0,27% | 5 | 1,19% | 5 | 1,3% | 5 | 1,29% |
Fricke et al. (2013) | 5 | 0,27% | 5 | 1,19% | 5 | 1,3% | 5 | 1,29% |
Kiszka et al. (2010) | 5 | 0,27% | 5 | 1,19% | 5 | 1,3% | 3 | 0,78% |
Larsen et al. (2006) | 5 | 0,27% | 5 | 1,19% | 0 | 0% | 5 | 1,29% |
Le Bail et al. (2012) | 5 | 0,27% | 5 | 1,19% | 5 | 1,3% | 5 | 1,29% |
Le Scao et al. (2011) | 5 | 0,27% | 5 | 1,19% | 5 | 1,3% | 5 | 1,29% |
Lee & Walsh-McGehee (2000) | 5 | 0,27% | 5 | 1,19% | 0 | 0% | 5 | 1,29% |
Levesque & Delcroix (2016) | 5 | 0,27% | 4 | 0,95% | 2 | 0,52% | 4 | 1,03% |
Nakamura (1985) | 5 | 0,27% | 5 | 1,19% | 5 | 1,3% | 5 | 1,29% |
Questel (2017) | 5 | 0,27% | 5 | 1,19% | 5 | 1,3% | 5 | 1,29% |
Read & Farman (2018) | 5 | 0,27% | 5 | 1,19% | 5 | 1,3% | 5 | 1,29% |
Read et al. (2023) | 5 | 0,27% | 5 | 1,19% | 5 | 1,3% | 5 | 1,29% |
Ronot (2007) | 5 | 0,27% | 4 | 0,95% | 3 | 0,78% | 4 | 1,03% |
Routtier et al. (2023) | 5 | 0,27% | 3 | 0,71% | 3 | 0,78% | 3 | 0,78% |
Samaran & Guinet (2009) | 5 | 0,27% | 5 | 1,19% | 5 | 1,3% | 4 | 1,03% |
Sauvignet et al. (2000) | 5 | 0,27% | 5 | 1,19% | 5 | 1,3% | 5 | 1,29% |
Swainson (1839) | 5 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Uicn et al. (2019) | 5 | 0,27% | 5 | 1,19% | 5 | 1,3% | 5 | 1,29% |
Allen (1985) | 4 | 0,22% | 4 | 0,95% | 4 | 1,04% | 4 | 1,03% |
Arnold & Ovenden (2014) | 4 | 0,22% | 4 | 0,95% | 4 | 1,04% | 3 | 0,78% |
Barrioz & Morinière (2007) | 4 | 0,22% | 4 | 0,95% | 4 | 1,04% | 4 | 1,03% |
Bauer & Sadlier (2000) | 4 | 0,22% | 3 | 0,71% | 3 | 0,78% | 3 | 0,78% |
Béarez & Séret (2009) | 4 | 0,22% | 3 | 0,71% | 3 | 0,78% | 3 | 0,78% |
Berry & Smith-Vaniz (1978) | 4 | 0,22% | 4 | 0,95% | 4 | 1,04% | 4 | 1,03% |
Birdlife International (2016) | 4 | 0,22% | 4 | 0,95% | 4 | 1,04% | 4 | 1,03% |
Bloch & Schneider (1801) | 4 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Breuil (2013) | 4 | 0,22% | 2 | 0,48% | 2 | 0,52% | 2 | 0,52% |
Butaud (2021) | 4 | 0,22% | 4 | 0,95% | 4 | 1,04% | 4 | 1,03% |
Charbonnel (1990) | 4 | 0,22% | 2 | 0,48% | 2 | 0,52% | 2 | 0,52% |
Collier et al. (2002) | 4 | 0,22% | 4 | 0,95% | 3 | 0,78% | 2 | 0,52% |
Desbrosses & Etcheberry (1987) | 4 | 0,22% | 3 | 0,71% | 3 | 0,78% | 2 | 0,52% |
Ehrhardt (1971) | 4 | 0,22% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Fort & Barrière (2021) | 4 | 0,22% | 4 | 0,95% | 4 | 1,04% | 4 | 1,03% |
Fourt et al. (2017) | 4 | 0,22% | 4 | 0,95% | 4 | 1,04% | 4 | 1,03% |
Frenot et al. (2005) | 4 | 0,22% | 4 | 0,95% | 4 | 1,04% | 4 | 1,03% |
Fretey & Lescure (1999) | 4 | 0,22% | 4 | 0,95% | 4 | 1,04% | 4 | 1,03% |
Gentry et al. (2004) | 4 | 0,22% | 3 | 0,71% | 3 | 0,78% | 3 | 0,78% |
Köhler & Vesely (2011) | 4 | 0,22% | 4 | 0,95% | 4 | 1,04% | 4 | 1,03% |
Lambert (1988) | 4 | 0,22% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Lim et al. (2002) | 4 | 0,22% | 2 | 0,48% | 2 | 0,52% | 2 | 0,52% |
Monti et al. (2010) | 4 | 0,22% | 2 | 0,48% | 2 | 0,52% | 2 | 0,52% |
Morris (2012) | 4 | 0,22% | 4 | 0,95% | 4 | 1,04% | 4 | 1,03% |
Müller & Henle (1841) | 4 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Perrin et al. (2002) | 4 | 0,22% | 4 | 0,95% | 4 | 1,04% | 3 | 0,78% |
Powell & Henderson (2023) | 4 | 0,22% | 3 | 0,71% | 3 | 0,78% | 3 | 0,78% |
Probst (1997) | 4 | 0,22% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Probst (1998) | 4 | 0,22% | 3 | 0,71% | 3 | 0,78% | 3 | 0,78% |
Rafinesque Schmaltz (1810) | 4 | 0,22% | 2 | 0,48% | 2 | 0,52% | 2 | 0,52% |
Swanepoel & Genoways (1983) | 4 | 0,22% | 4 | 0,95% | 4 | 1,04% | 0 | 0% |
Vieillot (1819) | 4 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Williams et al. (2006) | 4 | 0,22% | 3 | 0,71% | 3 | 0,78% | 3 | 0,78% |
Angin et al. (2024) | 3 | 0,16% | 3 | 0,71% | 0 | 0% | 3 | 0,78% |
Aubouin et al. (2016) | 3 | 0,16% | 3 | 0,71% | 3 | 0,78% | 3 | 0,78% |
Baker et al. (1978) | 3 | 0,16% | 3 | 0,71% | 0 | 0% | 3 | 0,78% |
Blanc (1909) | 3 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Burneleau (1983) | 3 | 0,16% | 3 | 0,71% | 3 | 0,78% | 3 | 0,78% |
Carstens et al. (2004) | 3 | 0,16% | 3 | 0,71% | 3 | 0,78% | 0 | 0% |
Catzeflis (2018) | 3 | 0,16% | 3 | 0,71% | 3 | 0,78% | 3 | 0,78% |
Champagne et al. (1997) | 3 | 0,16% | 3 | 0,71% | 2 | 0,52% | 3 | 0,78% |
Delcroix et al. (2011) | 3 | 0,16% | 3 | 0,71% | 3 | 0,78% | 3 | 0,78% |
Dubief & Gallais (2011) | 3 | 0,16% | 3 | 0,71% | 3 | 0,78% | 3 | 0,78% |
Duguy et al. (1998) | 3 | 0,16% | 3 | 0,71% | 3 | 0,78% | 3 | 0,78% |
Duguy et al. (2007) | 3 | 0,16% | 3 | 0,71% | 3 | 0,78% | 3 | 0,78% |
Duguy (1988) | 3 | 0,16% | 3 | 0,71% | 3 | 0,78% | 3 | 0,78% |
Duguy (1994) | 3 | 0,16% | 3 | 0,71% | 3 | 0,78% | 3 | 0,78% |
Duguy (1997) | 3 | 0,16% | 3 | 0,71% | 3 | 0,78% | 3 | 0,78% |
Girondot (2011) | 3 | 0,16% | 3 | 0,71% | 3 | 0,78% | 3 | 0,78% |
Goicoechea et al. (2016) | 3 | 0,16% | 2 | 0,48% | 2 | 0,52% | 0 | 0% |
Hedges (2022) | 3 | 0,16% | 3 | 0,71% | 3 | 0,78% | 3 | 0,78% |
Humphries et al. (2019) | 3 | 0,16% | 3 | 0,71% | 3 | 0,78% | 0 | 0% |
IUCN (2012) | 3 | 0,16% | 3 | 0,71% | 3 | 0,78% | 2 | 0,52% |
Karadjian et al. (2022) | 3 | 0,16% | 3 | 0,71% | 3 | 0,78% | 3 | 0,78% |
Maréchal et al. (2006) | 3 | 0,16% | 3 | 0,71% | 3 | 0,78% | 3 | 0,78% |
Méheust et al. (2018) | 3 | 0,16% | 3 | 0,71% | 3 | 0,78% | 3 | 0,78% |
Morinière & Dell'amico (2011) | 3 | 0,16% | 3 | 0,71% | 3 | 0,78% | 3 | 0,78% |
Nicholson et al. (2012) | 3 | 0,16% | 3 | 0,71% | 3 | 0,78% | 3 | 0,78% |
Oustalet (1895) | 3 | 0,16% | 2 | 0,48% | 2 | 0,52% | 0 | 0% |
Pascal et al. 2006 | 3 | 0,16% | 3 | 0,71% | 2 | 0,52% | 3 | 0,78% |
Poisson (1999) | 3 | 0,16% | 3 | 0,71% | 3 | 0,78% | 3 | 0,78% |
Probst et al. (2000) | 3 | 0,16% | 3 | 0,71% | 3 | 0,78% | 3 | 0,78% |
Questel (2017) | 3 | 0,16% | 3 | 0,71% | 3 | 0,78% | 3 | 0,78% |
Questel (2023) | 3 | 0,16% | 3 | 0,71% | 3 | 0,78% | 3 | 0,78% |
Randall & Vergara (1978) | 3 | 0,16% | 3 | 0,71% | 3 | 0,78% | 3 | 0,78% |
Read & Jean (2021) | 3 | 0,16% | 3 | 0,71% | 3 | 0,78% | 3 | 0,78% |
Robineau & Duhamel (2006) | 3 | 0,16% | 3 | 0,71% | 3 | 0,78% | 2 | 0,52% |
Safford & Hawkins (2013) | 3 | 0,16% | 3 | 0,71% | 3 | 0,78% | 2 | 0,52% |
Sanchez (2020) | 3 | 0,16% | 3 | 0,71% | 3 | 0,78% | 2 | 0,52% |
Shirihai (2003) | 3 | 0,16% | 3 | 0,71% | 3 | 0,78% | 2 | 0,52% |
Simian et al. (2022) | 3 | 0,16% | 3 | 0,71% | 3 | 0,78% | 3 | 0,78% |
Tirvengadum & Bour (1985) | 3 | 0,16% | 2 | 0,48% | 2 | 0,52% | 2 | 0,52% |
Tostain (1980) | 3 | 0,16% | 2 | 0,48% | 2 | 0,52% | 2 | 0,52% |
UICN Comité français, OFB, MNHN & GEPOMAY (2025) | 3 | 0,16% | 3 | 0,71% | 3 | 0,78% | 2 | 0,52% |
van den Burg et al. (2021) | 3 | 0,16% | 2 | 0,48% | 2 | 0,52% | 2 | 0,52% |
Wallach (2020) | 3 | 0,16% | 2 | 0,48% | 2 | 0,52% | 2 | 0,52% |
AAMP (2012) | 2 | 0,11% | 2 | 0,48% | 2 | 0,52% | 0 | 0% |
Aulagnier (2021) | 2 | 0,11% | 2 | 0,48% | 2 | 0,52% | 2 | 0,52% |
Ausilio & Zotier (1989) | 2 | 0,11% | 2 | 0,48% | 2 | 0,52% | 2 | 0,52% |
Baldi et al. (2022) | 2 | 0,11% | 2 | 0,48% | 2 | 0,52% | 2 | 0,52% |
Bartoli (1972) | 2 | 0,11% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Bauer (1987) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Bénito-espinal (1990) | 2 | 0,11% | 2 | 0,48% | 2 | 0,52% | 2 | 0,52% |
Bochaton et al. (2016) | 2 | 0,11% | 2 | 0,48% | 2 | 0,52% | 2 | 0,52% |
Bochaton et al. (2018) | 2 | 0,11% | 2 | 0,48% | 2 | 0,52% | 2 | 0,52% |
Boddaert & Daubenton (1783) | 2 | 0,11% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Boer et al. (1999) | 2 | 0,11% | 2 | 0,48% | 2 | 0,52% | 2 | 0,52% |
Breuil & Ibéné (2008) | 2 | 0,11% | 2 | 0,48% | 2 | 0,52% | 2 | 0,52% |
Breuil (2021) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Brugneaux & Pérès (2005) | 2 | 0,11% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Caceres & Salamolard (2021) | 2 | 0,11% | 2 | 0,48% | 2 | 0,52% | 2 | 0,52% |
Censky & Paulson (1992) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Chapuis et al. (2004) | 2 | 0,11% | 2 | 0,48% | 2 | 0,52% | 2 | 0,52% |
Chartier et al. (2007) | 2 | 0,11% | 2 | 0,48% | 2 | 0,52% | 0 | 0% |
Cheke (1987) | 2 | 0,11% | 2 | 0,48% | 2 | 0,52% | 2 | 0,52% |
Cheon et al. (2023) | 2 | 0,11% | 2 | 0,48% | 0 | 0% | 2 | 0,52% |
Chevallier et al. (2023) | 2 | 0,11% | 2 | 0,48% | 2 | 0,52% | 2 | 0,52% |
Compagno (1984) | 2 | 0,11% | 2 | 0,48% | 2 | 0,52% | 2 | 0,52% |
Cope (1869) | 2 | 0,11% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Cuvier (1829) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
dal Molin (2009) | 2 | 0,11% | 2 | 0,48% | 2 | 0,52% | 2 | 0,52% |
Daniel et al. (2020) | 2 | 0,11% | 2 | 0,48% | 2 | 0,52% | 0 | 0% |
Davant (1967) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Dewynter et al. (2020) | 2 | 0,11% | 2 | 0,48% | 2 | 0,52% | 2 | 0,52% |
Donovan (1816) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Duguy et al. (1997) | 2 | 0,11% | 2 | 0,48% | 2 | 0,52% | 2 | 0,52% |
Duguy et al. (1999) | 2 | 0,11% | 2 | 0,48% | 2 | 0,52% | 2 | 0,52% |
Duguy et al. (2000) | 2 | 0,11% | 2 | 0,48% | 2 | 0,52% | 2 | 0,52% |
Duguy et al. (2002) | 2 | 0,11% | 2 | 0,48% | 2 | 0,52% | 2 | 0,52% |
Duguy et al. (2003) | 2 | 0,11% | 2 | 0,48% | 2 | 0,52% | 2 | 0,52% |
Duguy et al. (2004) | 2 | 0,11% | 2 | 0,48% | 2 | 0,52% | 2 | 0,52% |
Duguy et al. (2006) | 2 | 0,11% | 2 | 0,48% | 2 | 0,52% | 2 | 0,52% |
Duguy (1987) | 2 | 0,11% | 2 | 0,48% | 2 | 0,52% | 2 | 0,52% |
Duguy (1990) | 2 | 0,11% | 2 | 0,48% | 2 | 0,52% | 2 | 0,52% |
Duguy (1992) | 2 | 0,11% | 2 | 0,48% | 2 | 0,52% | 2 | 0,52% |
Duguy (1993) | 2 | 0,11% | 2 | 0,48% | 2 | 0,52% | 2 | 0,52% |
Duguy (1995) | 2 | 0,11% | 2 | 0,48% | 2 | 0,52% | 2 | 0,52% |
Duguy (1996) | 2 | 0,11% | 2 | 0,48% | 2 | 0,52% | 2 | 0,52% |
Durand (2016) | 2 | 0,11% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Fontan (2019) | 2 | 0,11% | 2 | 0,48% | 2 | 0,52% | 2 | 0,52% |
Furminieux (2019) | 2 | 0,11% | 2 | 0,48% | 2 | 0,52% | 2 | 0,52% |
Gibson & Baker (2012) | 2 | 0,11% | 2 | 0,48% | 2 | 0,52% | 2 | 0,52% |
Gilot et al. (1992) | 2 | 0,11% | 2 | 0,48% | 2 | 0,52% | 2 | 0,52% |
Giovannotti et al. (2017) | 2 | 0,11% | 2 | 0,48% | 2 | 0,52% | 2 | 0,52% |
Girondo (2023) | 2 | 0,11% | 2 | 0,48% | 2 | 0,52% | 2 | 0,52% |
Gonzalez et al. (2009) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Gourreau et al. (1998) | 2 | 0,11% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Gronow (1854) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Hamdan et al. (2023) | 2 | 0,11% | 2 | 0,48% | 2 | 0,52% | 2 | 0,52% |
Hass (1991) | 2 | 0,11% | 2 | 0,48% | 2 | 0,52% | 2 | 0,52% |
Holbrook (1855) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Humeau et al. (2020) | 2 | 0,11% | 2 | 0,48% | 2 | 0,52% | 0 | 0% |
Impact-mer (2011) | 2 | 0,11% | 2 | 0,48% | 2 | 0,52% | 2 | 0,52% |
Ingels et al. (2003) | 2 | 0,11% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Jouan (1863) | 2 | 0,11% | 2 | 0,48% | 2 | 0,52% | 2 | 0,52% |
Kasamatsu & Joyce (1995) | 2 | 0,11% | 2 | 0,48% | 2 | 0,52% | 2 | 0,52% |
Keith et al. (2006) | 2 | 0,11% | 2 | 0,48% | 2 | 0,52% | 2 | 0,52% |
Keith et al. (2013) | 2 | 0,11% | 2 | 0,48% | 2 | 0,52% | 2 | 0,52% |
Kemp (2023) | 2 | 0,11% | 2 | 0,48% | 2 | 0,52% | 2 | 0,52% |
Kock et al. (2006) | 2 | 0,11% | 2 | 0,48% | 2 | 0,52% | 2 | 0,52% |
Kojadinovic et al. (2007) | 2 | 0,11% | 2 | 0,48% | 2 | 0,52% | 0 | 0% |
Kulbicki (comm. pers., 2011) | 2 | 0,11% | 2 | 0,48% | 2 | 0,52% | 2 | 0,52% |
Lacepède (1800) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Lacepède (1802) | 2 | 0,11% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Lacoste (de) (2020) | 2 | 0,11% | 2 | 0,48% | 2 | 0,52% | 2 | 0,52% |
Laurenti (1768) | 2 | 0,11% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Leaper et al. (2008) | 2 | 0,11% | 2 | 0,48% | 2 | 0,52% | 2 | 0,52% |
Levesque & Clergeau (2002) | 2 | 0,11% | 2 | 0,48% | 2 | 0,52% | 2 | 0,52% |
Levesque & Delcroix (2013) | 2 | 0,11% | 2 | 0,48% | 0 | 0% | 2 | 0,52% |
Linné (1766) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Lorvelec & Pascal (2009) | 2 | 0,11% | 2 | 0,48% | 2 | 0,52% | 2 | 0,52% |
Lorvelec et al. (2004) | 2 | 0,11% | 2 | 0,48% | 2 | 0,52% | 2 | 0,52% |
Maréchal & Trégarot (2012) | 2 | 0,11% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Marquet et al. (2003) | 2 | 0,11% | 2 | 0,48% | 2 | 0,52% | 2 | 0,52% |
Marshall et al. (2009) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Mas-Coma et al. (1989) | 2 | 0,11% | 2 | 0,48% | 2 | 0,52% | 2 | 0,52% |
Mathews (1914) | 2 | 0,11% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
McNair & Cramer-Burke (2006) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Merrem (1820) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Mothes et al. (2019) | 2 | 0,11% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Nardo (1827) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Olson & Normand (2014) | 2 | 0,11% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Patou et al. (2009) | 2 | 0,11% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Peron (2014) | 2 | 0,11% | 2 | 0,48% | 2 | 0,52% | 2 | 0,52% |
Pezy et al. (2022) | 2 | 0,11% | 2 | 0,48% | 2 | 0,52% | 2 | 0,52% |
Pinto-coelho et al. (2021) | 2 | 0,11% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Pons et al. (2005) | 2 | 0,11% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Powell et al. (2008) | 2 | 0,11% | 2 | 0,48% | 2 | 0,52% | 0 | 0% |
Probst et al. (2001) | 2 | 0,11% | 2 | 0,48% | 2 | 0,52% | 2 | 0,52% |
Rafinesque (1810) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Revilliod (1914) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Reynolds & Henderson (2018) | 2 | 0,11% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Rinaldi et al. (2011) | 2 | 0,11% | 2 | 0,48% | 2 | 0,52% | 2 | 0,52% |
Risso (1827) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Robineau (2005) | 2 | 0,11% | 2 | 0,48% | 2 | 0,52% | 1 | 0,26% |
Rossi-santos et al. (2007) | 2 | 0,11% | 2 | 0,48% | 2 | 0,52% | 1 | 0,26% |
Roux (1913) | 2 | 0,11% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Saint et al. (1978) | 2 | 0,11% | 2 | 0,48% | 2 | 0,52% | 2 | 0,52% |
Simmons (2005) | 2 | 0,11% | 2 | 0,48% | 0 | 0% | 2 | 0,52% |
Snodgrass & Heller (1905) | 2 | 0,11% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Thévenot (2014) | 2 | 0,11% | 2 | 0,48% | 2 | 0,52% | 2 | 0,52% |
Thiele et al. (1999) | 2 | 0,11% | 2 | 0,48% | 2 | 0,52% | 2 | 0,52% |
Thiele et al. (2004) | 2 | 0,11% | 2 | 0,48% | 2 | 0,52% | 1 | 0,26% |
Thunberg (1787) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Timm & Genoways (2003) | 2 | 0,11% | 2 | 0,48% | 1 | 0,26% | 1 | 0,26% |
Tunstall (1880) | 2 | 0,11% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Van Canneytet al. (2008) | 2 | 0,11% | 2 | 0,48% | 2 | 0,52% | 2 | 0,52% |
van den Burg et al. (2021) | 2 | 0,11% | 2 | 0,48% | 2 | 0,52% | 2 | 0,52% |
Vanderwerf et al. (2006) | 2 | 0,11% | 2 | 0,48% | 2 | 0,52% | 2 | 0,52% |
Vieira (2022) | 2 | 0,11% | 2 | 0,48% | 2 | 0,52% | 2 | 0,52% |
Viel (2021) | 2 | 0,11% | 2 | 0,48% | 2 | 0,52% | 2 | 0,52% |
Villanueva et al. (2021) | 2 | 0,11% | 2 | 0,48% | 2 | 0,52% | 2 | 0,52% |
Weimerskirch et al. (2009) | 2 | 0,11% | 2 | 0,48% | 2 | 0,52% | 2 | 0,52% |
Wilson (1813) | 2 | 0,11% | 2 | 0,48% | 2 | 0,52% | 2 | 0,52% |
Abhaya & Probst (2009) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Abhaya et al. (1998) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 0 | 0% |
Agarwal et al. (2021) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Agassiz (1833-1843) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Agassiz (1857) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Ainley et al. (2007) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Al-hasson & Ali (2020) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Allen (comm. pers., 2009) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Alley et al. (2023) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Almeida & Vasconcelos (2023) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Almeida et al. (2019) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Andrew et al. (2008) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Angin (2017) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Angin (2017) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Anonyme. (2004) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Anonyme. (2004) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 0 | 0% |
Anonyme (2008) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Anonyme. (2012) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Anonyme. (2012) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2012) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Anonyme. (2012) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Anonyme. (2012) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Anonyme. (2012) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Anonyme. (2012) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Anonyme. (2012) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Anonyme. (2012) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2012) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Anonyme. (2012) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Anonyme. (2012) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Anonyme. (2012) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 0 | 0% |
Anonyme. (2012) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Anonyme. (2012) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Anonyme. (2012) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2012) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Anonyme. (2012) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Anonyme. (2012) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Anonyme. (2012) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 0 | 0% |
Anonyme. (2012) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Anonyme. (2012) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Anonyme. (2012) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Anonyme. (2012) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2012) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Aquarium de La Rochelle (2017) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Astudillo et al. (2021) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Atkinson (2023) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Atwood (1869) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Bailenger et al. (1965) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Bailon et al. (2015) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Baldi et al. (2023) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Balle et al. (2021) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Bance (2022) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Bancroft (1832) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Barbancey & Probst (1998) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Barbancey (2001) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Barbancey (2001) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Barbour (1912) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Barre et al. (1991) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 0 | 0% |
Bassett (2022) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Bauer et al. (2010) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Bavay (1873) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Bavay (1899) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Beaucournu (1968) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Beauvieux et al. (2024) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Becerra et al. (2024) | 1 | 0,05% | 1 | 0,24% | 0 | 0% | 1 | 0,26% |
Behm et al. (2022) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Bernal & Rocha (2011) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Bertault (1988) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Bertrand & Drogou (2000) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Bertrand et al. (2001) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Bertrand (1982) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Best et al. (1995) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 0 | 0% |
Birdlife International (2012) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Birdlife International (2016) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Birdlife International (2017) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Bloch & Schneider (1801) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Bochaton et al. (2016) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Bochaton et al. (2020) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Boer (2000) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Bonnaterre (1788) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Bonnaterre (1789) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Borcyk et al. (2023) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Borsa (1997) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Boschert & Dronneau (1998) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Bourgade (2020) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Bourgade (2021) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Branch (2010) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 0 | 0% |
Brandt (1838) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Breuil & Serre-collet (2012) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Breuil et al. (2022) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Brito Capello (1867) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Brosse et al. (2021) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Brown (2008) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Brun (1958) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Brunes et al. (2021) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Bucol & Bucol (2019) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Bush et al. (2021) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Caceres (2002) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Calenge et al. (2010) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 0 | 0% |
Callou (2003) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Capalleras & Carretero (2000) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 0 | 0% |
Capape et al. (2002) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Caut et al. (2008) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
CEN Nouvelle-Calédonie (2021) | 1 | 0,05% | 1 | 0,24% | 0 | 0% | 1 | 0,26% |
Censky (1988) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Cerchio et al. (2009) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 0 | 0% |
Chabanaud (1927) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Chambault et al. (2020) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Chastel et al. (1981) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Chastel et al. (2003) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Cheke & Hume (2008) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Cheke (2010) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Chesser et al. (2016) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Chevreux & de Guerne (1893) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Cheylan et al. (2022) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Chibon (1961) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Chibon (1962) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
CHN (2017) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Chocobar et al. (2023) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Ciccione (2001) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Ciccione (2001) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Clements (1992) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Clergeau & Pascal (2003) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Coatmeur (1999) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Colin (1992) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Collectif (2009) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 0 | 0% |
Collet & Duguy (1981) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Collette (2003) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Cope (1862) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Cope (1864) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Cope (1869) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Coues (1862) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Counihan et al. (2012) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 0 | 0% |
Crochet et al. (2022) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Crouzier (2009) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Csabaï (2020) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Cubillos-abrahams et al. (2021) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Cuvier & Valenciennes (1830-1832) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Cuvier & Valenciennes ([1832]) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Cuvier & Valenciennes (1846) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Dalleau et al. (2014) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Danforth (1935) | 1 | 0,05% | 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 | 0,05% | 1 | 0,24% | 1 | 0,26% | 0 | 0% |
Daudin (1802) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 0 | 0% |
Daudin (1803) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Dauvin (1990) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Davis (1973) | 1 | 0,05% | 1 | 0,24% | 0 | 0% | 1 | 0,26% |
de Massary et al. (2015) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 0 | 0% |
Deblock (1966) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Debout (2001) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Deflandre (2007) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Deflorenne et al. (2012) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Delacour (1963) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Delaney & Warner (2017) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Delcroix et al. (2008) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Deliveyne et al. (2023) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Deniau & Provost (2020) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Denys et al. (2022) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Des et al. (2021) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Dewynter (2020) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Dieme et al. (2015) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Dollfus (1966) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Dore (2017) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Dreff & Delliere (1994) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Dubois & Cugnasse (2015) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Dubois & Frétey (2024) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Dubois & Louvet (2014) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Dubois et al. (2008) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Ducatez & Devore (2023) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Duguy & Duron (1981) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Duguy & Duron (1982) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Duguy & Duron (1983) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Duguy & Duron (1984) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Duguy & Duron (1985) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Duguy et al. (1980) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Duguy et al. (2000) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Duguy (1983) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Duguy (1986) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Duguy (1988) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Duguy (1989) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Duméril & Bibron (1839) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Duméril & Bibron (1837) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Duméril & Bribron (1841) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Duméril et al. (1854) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Efe et al. (2009) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 0 | 0% |
Ersts & Rosenbaum (2003) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 0 | 0% |
Eschscholtz (1829) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Eyton (1838) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabre & Orsini (2016) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Ficetola & Scali (2010) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 0 | 0% |
Fleming & Jackson (2011) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 0 | 0% |
Flitti & Rocha (2014) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Francour & Mouine (2008) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Franzini et al. (2018) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Fremont (2002) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Fretey & Bour (1980) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Fretey et al. (2023) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Fretey (1980) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Fretey (2003) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Frétey (2022) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Frétey (2023) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Fritz & Havaš (2007) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Gallien (2011) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
García-padrón & Quevedo (2022) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Gérigny et al. (2020) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Gernigon (2008) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Gill & Thiele (1997) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Gill (1862) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Gillespie (1997) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Girard (1859) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Girondot et al. (2015) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Godet et al. (2021) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Golvan (1956) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
González et al. (2018) | 1 | 0,05% | 1 | 0,24% | 0 | 0% | 1 | 0,26% |
Goulletquer (2016) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Grant (1958) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Gray (1846) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Gray (1850) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Guinet (1991) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Guinet (2004) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Gunderson et al. (2020) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Hedges et al. (2014) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Heimlich-boran (1993) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Hein et al. (2010) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Hellebuyck et al. (2017) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Henao-osorio et al. (2021) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Herzberg (2018) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Hong et al. (2022) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Houttuyn (1782) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Howard et al. (2001) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Howell & Clements (2019) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Hudson et al. (2021) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Ibéné et al. (2007) | 1 | 0,05% | 1 | 0,24% | 0 | 0% | 1 | 0,26% |
Iglésias et al. (2021) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Iković et al. (2023) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 0 | 0% |
Ineich & Bauer (1992) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Ineich et al. (2017) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Ineich (2016) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Isbell & Enstam Jaffe (2013) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
IUCN (2014) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Jairam et al. (2016) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Jamonneau et al. (2025) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Janse et al. (2020) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Jehl et al. (1980) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Jim et al. (2022) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Johnson & Wolman (1984) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 0 | 0% |
Johnson (1973) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Judson et al. (2018) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Karaa et al. (2016) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Kasamatsu et al. (2000) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 0 | 0% |
Keith & Marquet (2011) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Keith et al. (2002) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Keith et al. (1999) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Keith (2002) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
King (1962) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Kiszka et al. (2009) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 0 | 0% |
Heron, 36(1): 31-34.">Kiszka (2003) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 0 | 0% |
Kock & Stephan (1986) | 1 | 0,05% | 1 | 0,24% | 0 | 0% | 1 | 0,26% |
Koleska & Jablonski (2018) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Kornilev et al. (2020) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 0 | 0% |
Labach et al. (2021) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 0 | 0% |
Lacoste (2021) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Lacoste (2021) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Lancastre et al. (1976) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Laran et al. (2012) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Lataste (1877) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Latham (1787) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Lazell (1972) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Le Corre & Jouventin (1999) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 0 | 0% |
Leaper et al. (2008) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 0 | 0% |
Legendre (1937) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Léger & Mouzels (1917) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Léger (2003) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Léger (2008) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Legouez (2010) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Leimroth et al. (2022) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Lescure et al. (2016) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Lescure et al. (2020) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Lescure (2018) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Lesson (1830-1831) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Lesson (1831) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Lesson (1839) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Letacq (1924) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Levesque & Mathurin (2008) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Levesque (2013) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Liardet & d'Auzon (2004) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Liardet (2004) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Liebart et al. (2021) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Lim (1997) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 0 | 0% |
Lizé (2018) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Loisier et al. (2021) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Loison (1989) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Lorvelec & Vigne (2003) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Lorvelec & Vigne (2003) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Lorvelec et al. (2003) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Lorvelec et al. (2009) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Lorvelec et al. (2013) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Lorvelec et al. (2016) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Lorvelec et al. (2017) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Lorvelec et al. (2021) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Louette & Cousin (1999) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Louisin & Probst (1996) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Transactions of the Zoological Society of London, 1839: 1-20.">Lowe (1839) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Maciel et al. (2021) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Mageski et al. (2017) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Mahé et al. (2013) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Maillard & David (2014) | 1 | 0,05% | 1 | 0,24% | 0 | 0% | 1 | 0,26% |
Malm (1877) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Mancino et al. (2022) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Marchandeau & Letty (2021) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Marchandeau et al. (2003) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Marinho (2022) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Marion & Clergeau (2003) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 0 | 0% |
Marion & Marion (1982) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 0 | 0% |
Marion (2003) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 0 | 0% |
Martin et al. (2021) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Martinet et al. (1765) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Massary (2012) | 1 | 0,05% | 1 | 0,24% | 0 | 0% | 1 | 0,26% |
Matsuoka et al. (2005) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 0 | 0% |
Mctavish (2002) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Medetian & Miaud (2024) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Ménard et al. (2000) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Meneses et al. (2019) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Momont (1998) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Montagu (1813) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Moon & Kamath (2019) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Moreau de Jonnès (1818) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Mourier (2012) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Murase et al. (2002) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 0 | 0% |
Murphy et al. (1978) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Murray (1884) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Nadal & Tariel (2008) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Nassi et al. (1975) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Nelson-Smith et al. (2014) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Nicol et al. (2000) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 0 | 0% |
Noël (2024) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 0 | 0% |
Noël (2017) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Nuttall (1834) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Oliveira et al. (2018) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Oliver (2011) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Oremus (2009) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Owen (1853) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
pallas (1764) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Pallas (1770) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Paperna & Landsberg (1989) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Parker & Fitzgerald (2024) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Pascal & Vigne (2003) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Pascal & Vigne (2003) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Pascal & Vigne (2003) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Pascal et al. (2003) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Pascal et al. (2003) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Pearman et al. (2016) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 0 | 0% |
Pearman et al. (2020) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Pearson & Prévot (1971) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Peck & Wilcoxen (2018) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Pérez-delgadillo & Lara-reséndiz (2024) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Perkins (1928) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Perrin et al. (1994) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Peters (1930) | 1 | 0,05% | 1 | 0,24% | 0 | 0% | 1 | 0,26% |
Philippi (1887) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Philippot et al. (2019) | 1 | 0,05% | 1 | 0,24% | 0 | 0% | 1 | 0,26% |
Pitman & Ensor (2003) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Pons et al. (1999) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Pontoppidan (1763) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Pool (2013) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 0 | 0% |
Potin (2013) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Praderi et al. (1992) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Prato et al. (2022) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Prevot (1971) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Preynat (2013) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Probst (1997) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Probst (1999) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Probst (2001) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Probst (2007) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
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 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Puissauve, Comolet-tirman & Whal (2015) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Quéro & Delmas (1982) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Questel & Boggio (2012) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Questel & Boggio (2012) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Questel & Vitry (2012) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Questel et al. (2012) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Questel (2011) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Questel (2012) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Questel (2012) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Questel (2013) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Questel (2018) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 0 | 0% |
Questel (2022) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Randi et al. (2001) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Read et al. (2015) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Recoder et al. (2018) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Reeber (2015) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Reinert et al. (2021) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Reis et al. (2003) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Renaud et al. (2013) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Revuelta et al. (2015) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Rhodin & Carr (2009) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Rignault & Chevallier (2017) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Rimblot et al. (1985) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Ringler et al. (2021) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Robert et al. (2002) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Robineau (1989) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Roche & Guinet (2007) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Rodrigues et al. (2021) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Romero et al. (2010) | 1 | 0,05% | 1 | 0,24% | 0 | 0% | 1 | 0,26% |
Roos (2000) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Roques (1991) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Rosenbaum & Collins (2006) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 0 | 0% |
Roughgarden (1974) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Roux & Coll. (2017) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Roznik et al. (2021) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Cormoran, 15(4): 218.">Rundle & Rundle (2007) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Rüppell (1835) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Russell & Bauer (2002) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Ruys & Coord (2012) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Sanchez & Probst (2016) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Sanchez et al. (2004) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Sanchez et al. (2019) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Savouré-Soubelet et al. (in prep.) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Sawai et al. (2018) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Sayah et al. (2023) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Schneider (1783) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Schoepff (1792) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Schuchmann (1981) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Schweigger (1812) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Scopoli (1786) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Sellier et al. (2016) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Séret (1997) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Séret (2014) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Servan & Arvy (1997) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 0 | 0% |
Servan (1976) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Shaver et al. (2019) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Shaw (1802) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Shukla et al. (2024) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Slater et al. (2014) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Smith et al. (2005) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Smith-vaniz & Jelks (2014) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Snyder et al. (2019) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Socolovschi et al. (2012) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Sonsino (1893) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Soubeyran (2008) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Sparrman (1784) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Spix (1824) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Steadman & Bollt (2010) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 0 | 0% |
Stelfox et al. (2020) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Stoleson & Beissinger (2001) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Swainson (1838) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 0 | 0% |
Sy & Ibañes (2020) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Széles et al. (2018) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Tejedor (2006) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 0 | 0% |
Terrasse & Terrasse (1969) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Thawley & Kolbe (2020) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Thawley et al. (2019) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Thibault et al. (2023) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Thoisy et al. (2003) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 0 | 0% |
Thorpe & Malhotra (2023) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Toohey et al. (2022) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Townsend et al. (2000) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Tregarot et al. (2015) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Tschudi (1838) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Turpin & Probst (1998) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 0 | 0% |
Turpin et al. (2001) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Uicn et al. (2016) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Van Den Burg et al. (2018) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Van den burg et al. (2022) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Vandellius (1761) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Vanderwerf et al. (2004) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Verreaux & Des Murs (1860) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Veysset (2003) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 0 | 0% |
Vieillot (1816) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Vieillot (1817) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Vieillot (1819) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Von May et al. (2021) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Waayers et al. (2011) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Wahl & Barbraud (2005) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Walbaum (1792) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Wallach (2009) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Wang & Liu (2016) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 0 | 0% |
Wasilewski et al. (2022) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Weerdt (2023) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 0 | 0% |
Weterings & Vetter (2017) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Whitley (1929) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Wied (1839) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Wiegmann (1834) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Williams et al. (2009) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 0 | 0% |
Williams et al. (2019) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Works & Olson (2018) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 0 | 0% |
Yengle (2021) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Yésou (2003) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Yésou (2003) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
Yésou (2003) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |
(2022) | 1 | 0,05% | 1 | 0,24% | 1 | 0,26% | 1 | 0,26% |