Poissons de Guadeloupe
231 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) | 270 | 10,39% | 268 | 57,63% | 268 | 58,39% | 265 | 57,61% |
Smith (1997) | 251 | 9,66% | 231 | 49,68% | 225 | 49,02% | 231 | 50,22% |
Questel & Le Quellec (2012) | 247 | 9,5% | 236 | 50,75% | 236 | 51,42% | 234 | 50,87% |
Bouchon-Navaro et al. (2005) | 224 | 8,62% | 184 | 39,57% | 184 | 40,09% | 183 | 39,78% |
Bouchon-Navaro & Louis (1986) | 115 | 4,42% | 98 | 21,08% | 98 | 21,35% | 98 | 21,3% |
Diaz & Cuzange (2009) | 102 | 3,92% | 94 | 20,22% | 94 | 20,48% | 94 | 20,43% |
Brugneaux & Pérès (2006) | 83 | 3,19% | 75 | 16,13% | 75 | 16,34% | 75 | 16,3% |
Fricke et al. (2011) | 49 | 1,89% | 47 | 10,11% | 47 | 10,24% | 45 | 9,78% |
Rousseau (2010) | 47 | 1,81% | 45 | 9,68% | 45 | 9,8% | 45 | 9,78% |
Fricke et al. (2009) | 46 | 1,77% | 42 | 9,03% | 42 | 9,15% | 39 | 8,48% |
Siu et al. (2017) | 41 | 1,58% | 37 | 7,96% | 37 | 8,06% | 36 | 7,83% |
Béarez et al. (2017) | 35 | 1,35% | 35 | 7,53% | 35 | 7,63% | 33 | 7,17% |
Louis et al. (1992) | 33 | 1,27% | 25 | 5,38% | 25 | 5,45% | 24 | 5,22% |
Wickel & Jamon (2010) | 32 | 1,23% | 30 | 6,45% | 30 | 6,54% | 29 | 6,3% |
Poey (1858-61) | 31 | 1,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Collette & Nauen (1983) | 27 | 1,04% | 27 | 5,81% | 23 | 5,01% | 27 | 5,87% |
Compagno (1984) | 21 | 0,81% | 21 | 4,52% | 21 | 4,58% | 21 | 4,57% |
Fourriére et al. (2014) | 21 | 0,81% | 21 | 4,52% | 21 | 4,58% | 21 | 4,57% |
Questel (2017) | 21 | 0,81% | 21 | 4,52% | 21 | 4,58% | 21 | 4,57% |
Bouchon-Navaro et al. (1992) | 20 | 0,77% | 17 | 3,66% | 17 | 3,7% | 16 | 3,48% |
Delrieu-Trottin et al. (2015) | 19 | 0,73% | 19 | 4,09% | 18 | 3,92% | 19 | 4,13% |
Bacchet et al. (2007) | 17 | 0,65% | 16 | 3,44% | 16 | 3,49% | 16 | 3,48% |
Le Bail et al. (2012) | 17 | 0,65% | 17 | 3,66% | 17 | 3,7% | 17 | 3,7% |
Monti et al. (2010) | 17 | 0,65% | 15 | 3,23% | 15 | 3,27% | 15 | 3,26% |
Rafinesque Schmaltz (1810) | 17 | 0,65% | 2 | 0,43% | 2 | 0,44% | 2 | 0,43% |
Cuvier & Valenciennes (1833) | 16 | 0,62% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Linnaeus (1758) | 16 | 0,62% | 2 | 0,43% | 2 | 0,44% | 2 | 0,43% |
Whitehead et al. (1988) | 16 | 0,62% | 16 | 3,44% | 16 | 3,49% | 16 | 3,48% |
Heemstra & Randall (1993) | 15 | 0,58% | 15 | 3,23% | 15 | 3,27% | 15 | 3,26% |
Lim et al. (2002) | 15 | 0,58% | 13 | 2,8% | 13 | 2,83% | 13 | 2,83% |
Allen (1985) | 13 | 0,5% | 13 | 2,8% | 13 | 2,83% | 13 | 2,83% |
UICN Comité français, OFB & MNHN (2021) | 13 | 0,5% | 13 | 2,8% | 13 | 2,83% | 13 | 2,83% |
Berry & Smith-Vaniz (1978) | 12 | 0,46% | 12 | 2,58% | 12 | 2,61% | 12 | 2,61% |
Compagno (1984) | 12 | 0,46% | 12 | 2,58% | 12 | 2,61% | 12 | 2,61% |
Kulbicki et al. (2000) | 11 | 0,42% | 9 | 1,94% | 9 | 1,96% | 8 | 1,74% |
Cohen et al. (1990) | 10 | 0,38% | 10 | 2,15% | 10 | 2,18% | 10 | 2,17% |
Cuvier & Valenciennes ([1832]) | 10 | 0,38% | 0 | 0% | 0 | 0% | 0 | 0% |
Fricke et al. (2013) | 10 | 0,38% | 10 | 2,15% | 10 | 2,18% | 9 | 1,96% |
Kulbicki (comm. pers., 2011) | 10 | 0,38% | 8 | 1,72% | 8 | 1,74% | 8 | 1,74% |
Nakamura (1985) | 10 | 0,38% | 10 | 2,15% | 10 | 2,18% | 10 | 2,17% |
Soubeyran (2008) | 10 | 0,38% | 10 | 2,15% | 10 | 2,18% | 10 | 2,17% |
Béarez & Séret (2009) | 9 | 0,35% | 8 | 1,72% | 8 | 1,74% | 8 | 1,74% |
Richard et al. (1982) | 9 | 0,35% | 4 | 0,86% | 4 | 0,87% | 4 | 0,87% |
Béarez & Bouffandeau (2019) | 8 | 0,31% | 8 | 1,72% | 8 | 1,74% | 7 | 1,52% |
Charbonnel (1990) | 8 | 0,31% | 6 | 1,29% | 6 | 1,31% | 4 | 0,87% |
Whitehead (1985) | 8 | 0,31% | 8 | 1,72% | 8 | 1,74% | 8 | 1,74% |
Pezold et al. (2015) | 7 | 0,27% | 7 | 1,51% | 7 | 1,53% | 7 | 1,52% |
Randall & Vergara (1978) | 7 | 0,27% | 7 | 1,51% | 5 | 1,09% | 7 | 1,52% |
Vaslet & Agrnsm (2018) | 7 | 0,27% | 7 | 1,51% | 7 | 1,53% | 7 | 1,52% |
Williams et al. (2006) | 7 | 0,27% | 6 | 1,29% | 6 | 1,31% | 5 | 1,09% |
Chabanet & Durville (2005) | 6 | 0,23% | 5 | 1,08% | 5 | 1,09% | 5 | 1,09% |
Cuvier & Valenciennes (1830-1832) | 6 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Gronow (1854) | 6 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Müller & Henle (1841) | 6 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Risso (1810) | 6 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Simian et al. (2022) | 6 | 0,23% | 6 | 1,29% | 6 | 1,31% | 6 | 1,3% |
Bloch & Schneider (1801) | 5 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Keith et al. (2006) | 5 | 0,19% | 5 | 1,08% | 5 | 1,09% | 5 | 1,09% |
Keith et al. (2013) | 5 | 0,19% | 5 | 1,08% | 5 | 1,09% | 5 | 1,09% |
Transactions of the Zoological Society of London, 1839: 1-20.">Lowe (1839) | 5 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Polanco & Acero (2016) | 5 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Questel (2023) | 5 | 0,19% | 5 | 1,08% | 5 | 1,09% | 5 | 1,09% |
Risso (1827) | 5 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Séret (1997) | 5 | 0,19% | 5 | 1,08% | 5 | 1,09% | 5 | 1,09% |
Snodgrass & Heller (1905) | 5 | 0,19% | 2 | 0,43% | 2 | 0,44% | 2 | 0,43% |
Swainson (1839) | 5 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Allen (comm. pers., 2009) | 4 | 0,15% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Cuvier & Valenciennes (1847) | 4 | 0,15% | 2 | 0,43% | 2 | 0,44% | 2 | 0,43% |
Fourt et al. (2017) | 4 | 0,15% | 4 | 0,86% | 4 | 0,87% | 4 | 0,87% |
Keith et al. (2002) | 4 | 0,15% | 2 | 0,43% | 2 | 0,44% | 2 | 0,43% |
Klunzinger (1871) | 4 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Lacepède (1800) | 4 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Lacepède (1801) | 4 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Morris (2012) | 4 | 0,15% | 4 | 0,86% | 4 | 0,87% | 4 | 0,87% |
Randall & Earle (2000) | 4 | 0,15% | 4 | 0,86% | 3 | 0,65% | 4 | 0,87% |
Uicn et al. (2019) | 4 | 0,15% | 4 | 0,86% | 4 | 0,87% | 4 | 0,87% |
Chabanaud (1927) | 3 | 0,12% | 3 | 0,65% | 3 | 0,65% | 3 | 0,65% |
Cuvier & Valenciennes (1839) | 3 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Cuvier & Valenciennes (1846) | 3 | 0,12% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Firmat et al. (2012) | 3 | 0,12% | 3 | 0,65% | 3 | 0,65% | 3 | 0,65% |
Gargominy et al. (1996) | 3 | 0,12% | 3 | 0,65% | 3 | 0,65% | 3 | 0,65% |
Hutchinson et al. (2019) | 3 | 0,12% | 3 | 0,65% | 3 | 0,65% | 3 | 0,65% |
Kottelat ( 2013) | 3 | 0,12% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Legand (1950) | 3 | 0,12% | 2 | 0,43% | 2 | 0,44% | 2 | 0,43% |
Maréchal & Trégarot (2012) | 3 | 0,12% | 2 | 0,43% | 2 | 0,44% | 2 | 0,43% |
Maréchal et al. (2006) | 3 | 0,12% | 3 | 0,65% | 3 | 0,65% | 3 | 0,65% |
Møller et al. (2005) | 3 | 0,12% | 3 | 0,65% | 3 | 0,65% | 3 | 0,65% |
Questel (2022) | 3 | 0,12% | 3 | 0,65% | 3 | 0,65% | 3 | 0,65% |
Rignault & Chevallier (2017) | 3 | 0,12% | 2 | 0,43% | 2 | 0,44% | 2 | 0,43% |
Swainson (1838) | 3 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Valenciennes (1836-1844) | 3 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Alley et al. (2023) | 2 | 0,08% | 2 | 0,43% | 2 | 0,44% | 2 | 0,43% |
Anonyme (2016) | 2 | 0,08% | 2 | 0,43% | 2 | 0,44% | 2 | 0,43% |
Bleeker (1852) | 2 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Bowdich (1825) | 2 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Brosse et al. (2021) | 2 | 0,08% | 2 | 0,43% | 2 | 0,44% | 2 | 0,43% |
Brugneaux & Pérès (2005) | 2 | 0,08% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Durand (2016) | 2 | 0,08% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Evermann & Clark (1928) | 2 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Fontan (2019) | 2 | 0,08% | 2 | 0,43% | 2 | 0,44% | 2 | 0,43% |
Fowler (1919) | 2 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Geoffroy Saint-Hilaire ([1817]) | 2 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Goode & Bean (1896) | 2 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Harrison et al. (2007) | 2 | 0,08% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Hildebrand (1948) | 2 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Keith et al. (1999) | 2 | 0,08% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Keith (2002) | 2 | 0,08% | 2 | 0,43% | 2 | 0,44% | 2 | 0,43% |
Lacepède (1802) | 2 | 0,08% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Lowe (1838) | 2 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Macdonald & Barron (1868) | 2 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Maréchal & Pérès (2007) | 2 | 0,08% | 2 | 0,43% | 2 | 0,44% | 2 | 0,43% |
Marquet et al. (2003) | 2 | 0,08% | 2 | 0,43% | 2 | 0,44% | 2 | 0,43% |
Marshall et al. (2009) | 2 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Mitchill (1815) | 2 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Monti et al. (2018) | 2 | 0,08% | 2 | 0,43% | 2 | 0,44% | 2 | 0,43% |
Nardo (1827) | 2 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Palko et al. (1982) | 2 | 0,08% | 2 | 0,43% | 2 | 0,44% | 2 | 0,43% |
Pallas (1770) | 2 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Parenti (2021) | 2 | 0,08% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Poey (1851-1854) | 2 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Rafinesque (1810) | 2 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Reis et al. (2003) | 2 | 0,08% | 2 | 0,43% | 2 | 0,44% | 2 | 0,43% |
Spix & Agassiz (1829-31) | 2 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Tavera et al. (2018) | 2 | 0,08% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Weber (1913) | 2 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Yokoyama (2013) | 2 | 0,08% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Agassiz (1833-1843) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Atwood (1869) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Bancroft (1832) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Bean (1912) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Bennett (1831) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Bernal & Rocha (2011) | 1 | 0,04% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Bertin (1928) | 1 | 0,04% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Bleeker (1865) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Bloch & Schneider (1801) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Bloch (1785-1795) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Bloch (1793) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Bonnaterre (1788) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Bouchon & Lemoine (2003) | 1 | 0,04% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Brito Capello (1867) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Brugneaux & Pérès (2005) | 1 | 0,04% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Capape et al. (2002) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Causse & Hautecoeur (2006) | 1 | 0,04% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Cuvier (1829) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Denys et al. (2022) | 1 | 0,04% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Etcheberry & Abraham (2009) | 1 | 0,04% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Faber (1829) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Forest (1946) | 1 | 0,04% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Forskål (1775) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Fowler (1900) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Francour & Mouine (2008) | 1 | 0,04% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Garman (1899) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Gill (1862) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Girard (1859) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Girondot et al. (2015) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Gmelin (1789) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Goode & Bean (1882) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Goulletquer (2016) | 1 | 0,04% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Günther (1860) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Ifremer (2009) | 1 | 0,04% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Iglésias et al. (2021) | 1 | 0,04% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
IUCN (2014) | 1 | 0,04% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Jamonneau et al. (2025) | 1 | 0,04% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Jordan & Evermann (1903) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Jordan & Gilbert (1882) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Jordan & Gilbert (1884) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Jordan & Jordan (1922) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Jordan et al. (1927) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Jordan (1888) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Kaup (1856) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Keith & Marquet (2011) | 1 | 0,04% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Keith et al. (2014) | 1 | 0,04% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Kiszka et al. (2009) | 1 | 0,04% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Legendre (1937) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Lesson (1830-1831) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Lesueur (1822) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Letourneur et al. (2004) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Linnaeus (1766) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Lizé (2018) | 1 | 0,04% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Lorvelec & Pascal (2009) | 1 | 0,04% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Lowe et al. (2007) | 1 | 0,04% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Lowe (1834) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Proceedings of the general meetings for scientific business of the Zoological Society of London, 1839: 76-92.">Lowe (1839) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Lowe (1841) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Lowe (1843) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Mahé et al. (2013) | 1 | 0,04% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Malm (1877) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Mckenzie (2016) | 1 | 0,04% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Meek & Hildebrand (1923) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Mourier (2012) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Murray (1884) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Nelson-Smith et al. (2014) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Owen (1853) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Pearman et al. (2020) | 1 | 0,04% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Philippi (1887) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Poey (1863) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Preynat (2013) | 1 | 0,04% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
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 | 0,04% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Annales de la Société de Sciences naturelles de la Charente-Maritime, 10(2): 225-236.">Quéro et al. (2011) | 1 | 0,04% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Quéro & Delmas (1982) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Quero & Laborde (1996) | 1 | 0,04% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Quero et al. (1998) | 1 | 0,04% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Quero et al. (2013) | 1 | 0,04% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Quero (1998) | 1 | 0,04% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Questel (2014) | 1 | 0,04% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Questel (2017) | 1 | 0,04% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Ranzani (1839) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Richardson (1846) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Robins & Sylva (1963) | 1 | 0,04% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Rosen (1911) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Runde (2016) | 1 | 0,04% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Rüppell (1835) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Sawai et al. (2018) | 1 | 0,04% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Schinz (1822) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Sellier et al. (2016) | 1 | 0,04% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Séret (1993) | 1 | 0,04% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Séret (2014) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Smith-Vaniz & Carpenter (2007) | 1 | 0,04% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Smith-vaniz & Jelks (2014) | 1 | 0,04% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Steindachner (1861) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Steindachner (1867) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Tregarot et al. (2015) | 1 | 0,04% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Van & Kampen (1907) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Vaslet et al. (2010) | 1 | 0,04% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Vernoux (1988) | 1 | 0,04% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |
Walbaum (1792) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Whitley (1929) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Whitley (1933) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Whitley (1937) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Whitley (1948) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Wickel et al. (2014) | 1 | 0,04% | 1 | 0,22% | 1 | 0,22% | 1 | 0,22% |