Poissons osseux d’eau douce
507 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
Référence | Total | Valides | Espèces | Taxons terminaux | ||||
---|---|---|---|---|---|---|---|---|
nb | % | nb | % | nb | % | nb | % | |
Le Bail et al. (2012) | 372 | 8,21% | 350 | 40,94% | 350 | 41,32% | 348 | 41,04% |
Fricke et al. (2011) | 107 | 2,36% | 93 | 10,88% | 93 | 10,98% | 93 | 10,97% |
Keith et al. (2006) | 66 | 1,46% | 51 | 5,96% | 49 | 5,79% | 50 | 5,9% |
Keith et al. (2013) | 52 | 1,15% | 46 | 5,38% | 46 | 5,43% | 46 | 5,42% |
Séret (1997) | 51 | 1,13% | 43 | 5,03% | 43 | 5,08% | 43 | 5,07% |
Fricke et al. (2009) | 45 | 0,99% | 36 | 4,21% | 35 | 4,13% | 34 | 4,01% |
Keith et al. (2011) | 43 | 0,95% | 38 | 4,44% | 38 | 4,49% | 38 | 4,48% |
Siu et al. (2017) | 43 | 0,95% | 37 | 4,33% | 37 | 4,37% | 37 | 4,36% |
Wickel & Jamon (2010) | 30 | 0,66% | 24 | 2,81% | 23 | 2,72% | 24 | 2,83% |
Soubeyran (2008) | 26 | 0,57% | 22 | 2,57% | 22 | 2,6% | 22 | 2,59% |
Sidlauskas & Vari (2012) | 24 | 0,53% | 24 | 2,81% | 24 | 2,83% | 24 | 2,83% |
Uicn et al. (2017) | 23 | 0,51% | 22 | 2,57% | 22 | 2,6% | 22 | 2,59% |
Keith et al. (2002) | 22 | 0,49% | 17 | 1,99% | 17 | 2,01% | 17 | 2% |
Keith et al. (2009) | 21 | 0,46% | 16 | 1,87% | 16 | 1,89% | 16 | 1,89% |
Questel (2020) | 21 | 0,46% | 21 | 2,46% | 21 | 2,48% | 21 | 2,48% |
Lim et al. (2002) | 20 | 0,44% | 16 | 1,87% | 16 | 1,89% | 16 | 1,89% |
Pascal et al. (2006) | 20 | 0,44% | 19 | 2,22% | 19 | 2,24% | 19 | 2,24% |
Béarez et al. (2017) | 19 | 0,42% | 17 | 1,99% | 17 | 2,01% | 17 | 2% |
Eigenmann (1912) | 19 | 0,42% | 11 | 1,29% | 11 | 1,3% | 11 | 1,3% |
Kaup (1856) | 19 | 0,42% | 0 | 0% | 0 | 0% | 0 | 0% |
Linnaeus (1758) | 19 | 0,42% | 6 | 0,7% | 6 | 0,71% | 6 | 0,71% |
Kulbicki (comm. pers., 2011) | 17 | 0,38% | 15 | 1,75% | 15 | 1,77% | 15 | 1,77% |
Monti et al. (2010) | 17 | 0,38% | 15 | 1,75% | 15 | 1,77% | 15 | 1,77% |
Pallas [1814] | 17 | 0,38% | 0 | 0% | 0 | 0% | 0 | 0% |
Duméril (1870) | 16 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
Questel & Le Quellec (2012) | 15 | 0,33% | 15 | 1,75% | 15 | 1,77% | 15 | 1,77% |
Reis et al. (2003) | 13 | 0,29% | 12 | 1,4% | 12 | 1,42% | 12 | 1,42% |
UICN Comité français, OFB & MNHN (2021) | 13 | 0,29% | 13 | 1,52% | 13 | 1,53% | 13 | 1,53% |
Covain et al. (2012) | 12 | 0,26% | 12 | 1,4% | 12 | 1,42% | 12 | 1,42% |
Louis et al. (1992) | 12 | 0,26% | 9 | 1,05% | 9 | 1,06% | 8 | 0,94% |
Marceniuk & Menezes (2007) | 12 | 0,26% | 11 | 1,29% | 11 | 1,3% | 11 | 1,3% |
Brosse et al. (2021) | 11 | 0,24% | 11 | 1,29% | 11 | 1,3% | 11 | 1,3% |
Cuvier & Valenciennes (1848) | 11 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
Keith & Marquet (2011) | 11 | 0,24% | 11 | 1,29% | 11 | 1,3% | 11 | 1,3% |
Walbaum (1792) | 11 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
Costa (2011) | 10 | 0,22% | 9 | 1,05% | 9 | 1,06% | 9 | 1,06% |
Cuvier & Valenciennes (1829) | 10 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Denys et al. (2022) | 10 | 0,22% | 7 | 0,82% | 7 | 0,83% | 7 | 0,83% |
Géry et al. (1991) | 10 | 0,22% | 8 | 0,94% | 8 | 0,94% | 8 | 0,94% |
Nelson-Smith et al. (2014) | 10 | 0,22% | 7 | 0,82% | 7 | 0,83% | 7 | 0,83% |
Smith (1997) | 10 | 0,22% | 6 | 0,7% | 4 | 0,47% | 6 | 0,71% |
Cuvier (1829) | 9 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Freyhof et al. (2005) | 9 | 0,2% | 8 | 0,94% | 8 | 0,94% | 8 | 0,94% |
Keith et al. (2014) | 9 | 0,2% | 8 | 0,94% | 8 | 0,94% | 8 | 0,94% |
Lacepède (1803) | 9 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Bouchon-Navaro et al. (2005) | 8 | 0,18% | 8 | 0,94% | 8 | 0,94% | 8 | 0,94% |
Causse et al. (2023) | 8 | 0,18% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Fisch-Muller et al. (2012) | 8 | 0,18% | 6 | 0,7% | 6 | 0,71% | 6 | 0,71% |
Gery et al. (1996) | 8 | 0,18% | 0 | 0% | 0 | 0% | 0 | 0% |
Legand (1950) | 8 | 0,18% | 4 | 0,47% | 4 | 0,47% | 4 | 0,47% |
Persat & Keith (1997) | 8 | 0,18% | 8 | 0,94% | 8 | 0,94% | 8 | 0,94% |
Bacchet et al. (2007) | 7 | 0,15% | 7 | 0,82% | 7 | 0,83% | 7 | 0,83% |
Duhamel et al. (2005) | 7 | 0,15% | 7 | 0,82% | 7 | 0,83% | 7 | 0,83% |
Gargominy et al. (1996) | 7 | 0,15% | 7 | 0,82% | 7 | 0,83% | 7 | 0,83% |
Günther (1866) | 7 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Huber (1991) | 7 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Keith (2002) | 7 | 0,15% | 7 | 0,82% | 7 | 0,83% | 7 | 0,83% |
Kottelat & Freyhof (2007) | 7 | 0,15% | 6 | 0,7% | 6 | 0,71% | 6 | 0,71% |
Kottelat & Persat (2005) | 7 | 0,15% | 7 | 0,82% | 7 | 0,83% | 7 | 0,83% |
Preynat (2013) | 7 | 0,15% | 7 | 0,82% | 7 | 0,83% | 7 | 0,83% |
Breton (2014) | 6 | 0,13% | 6 | 0,7% | 6 | 0,71% | 6 | 0,71% |
Charbonnel (1990) | 6 | 0,13% | 4 | 0,47% | 4 | 0,47% | 4 | 0,47% |
Cuvier & Valenciennes (1836) | 6 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Delrieu-Trottin et al. (2015) | 6 | 0,13% | 3 | 0,35% | 3 | 0,35% | 3 | 0,35% |
Šimková et al. (2013) | 6 | 0,13% | 6 | 0,7% | 6 | 0,71% | 6 | 0,71% |
Lowe et al. (2007) | 6 | 0,13% | 6 | 0,7% | 6 | 0,71% | 6 | 0,71% |
Pellegrin (1903) | 6 | 0,13% | 6 | 0,7% | 6 | 0,71% | 6 | 0,71% |
Boeseman (1971) | 5 | 0,11% | 4 | 0,47% | 4 | 0,47% | 4 | 0,47% |
Bouchon-Navaro & Louis (1986) | 5 | 0,11% | 5 | 0,58% | 5 | 0,59% | 5 | 0,59% |
Bouchon-Navaro et al. (1992) | 5 | 0,11% | 4 | 0,47% | 4 | 0,47% | 4 | 0,47% |
Cuvier & Valenciennes (1846) | 5 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Denys et al. (2014) | 5 | 0,11% | 5 | 0,58% | 5 | 0,59% | 5 | 0,59% |
Frenot et al. (2005) | 5 | 0,11% | 4 | 0,47% | 4 | 0,47% | 4 | 0,47% |
Jourdan (2020) | 5 | 0,11% | 4 | 0,47% | 4 | 0,47% | 4 | 0,47% |
Keith & Mennesson (2020) | 5 | 0,11% | 4 | 0,47% | 4 | 0,47% | 4 | 0,47% |
Keith et al. (1999) | 5 | 0,11% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Antonelli, Venezia. 128 pp.">Nardo (1847) | 5 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Rafinesque (1810) | 5 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Risso (1827) | 5 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Williams et al. (2006) | 5 | 0,11% | 4 | 0,47% | 4 | 0,47% | 4 | 0,47% |
Bartoli & Prévot (1986) | 4 | 0,09% | 3 | 0,35% | 3 | 0,35% | 3 | 0,35% |
Bonaparte (1837) | 4 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Chevallier et al. (2023) | 4 | 0,09% | 4 | 0,47% | 4 | 0,47% | 4 | 0,47% |
Couch (1877) | 4 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Covain & Fisch-Muller (2012) | 4 | 0,09% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Denys et al. (2020) | 4 | 0,09% | 4 | 0,47% | 4 | 0,47% | 4 | 0,47% |
Eigenmann (1908) | 4 | 0,09% | 3 | 0,35% | 3 | 0,35% | 3 | 0,35% |
Etcheberry & Abraham (2009) | 4 | 0,09% | 4 | 0,47% | 4 | 0,47% | 4 | 0,47% |
Fricke et al. (2013) | 4 | 0,09% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Gmelin (1789) | 4 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Günther (1861) | 4 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Heckel & Kner (1858) | 4 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Heitmans et al. (1983) | 4 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Jordan (1894) | 4 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Keith & Mennesson (2023) | 4 | 0,09% | 4 | 0,47% | 4 | 0,47% | 4 | 0,47% |
Keith et al. (2011) | 4 | 0,09% | 4 | 0,47% | 4 | 0,47% | 4 | 0,47% |
Kottelat ( 2013) | 4 | 0,09% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Kulbicki et al. (2000) | 4 | 0,09% | 3 | 0,35% | 3 | 0,35% | 3 | 0,35% |
Lucena & Malabarba (2010) | 4 | 0,09% | 4 | 0,47% | 4 | 0,47% | 4 | 0,47% |
Mattox et al. (2006) | 4 | 0,09% | 4 | 0,47% | 4 | 0,47% | 4 | 0,47% |
Nardo (1827) | 4 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Oliver & Reichenbach-Klinke (1973) | 4 | 0,09% | 3 | 0,35% | 3 | 0,35% | 3 | 0,35% |
Pascal et al. (2003) | 4 | 0,09% | 4 | 0,47% | 4 | 0,47% | 4 | 0,47% |
Pinna & Keith (2019) | 4 | 0,09% | 4 | 0,47% | 4 | 0,47% | 4 | 0,47% |
Ponton & Merigoux (2000) | 4 | 0,09% | 4 | 0,47% | 4 | 0,47% | 4 | 0,47% |
Puyo (1948) | 4 | 0,09% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Raibaut et al. (1979) | 4 | 0,09% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Reinhardt (1837) | 4 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Vaillant (1899) | 4 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Wagner (1828) | 4 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Băcescu & Băcescu-Meşter (1964) | 3 | 0,07% | 3 | 0,35% | 3 | 0,35% | 3 | 0,35% |
Betancur-r et al. (2008) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Boeseman (1982) | 3 | 0,07% | 3 | 0,35% | 3 | 0,35% | 3 | 0,35% |
Brugneaux & Pérès (2006) | 3 | 0,07% | 3 | 0,35% | 3 | 0,35% | 3 | 0,35% |
Diaz & Cuzange (2009) | 3 | 0,07% | 3 | 0,35% | 3 | 0,35% | 3 | 0,35% |
Firmat et al. (2012) | 3 | 0,07% | 3 | 0,35% | 3 | 0,35% | 3 | 0,35% |
Géry et al. (1988) | 3 | 0,07% | 3 | 0,35% | 3 | 0,35% | 3 | 0,35% |
Géry et al. (1995) | 3 | 0,07% | 3 | 0,35% | 3 | 0,35% | 3 | 0,35% |
Géry (1959) | 3 | 0,07% | 3 | 0,35% | 3 | 0,35% | 3 | 0,35% |
Keith et al. (2006) | 3 | 0,07% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Keith et al. (2020) | 3 | 0,07% | 3 | 0,35% | 3 | 0,35% | 3 | 0,35% |
Keith et al. (2020) | 3 | 0,07% | 3 | 0,35% | 3 | 0,35% | 3 | 0,35% |
Kottelat (2007) | 3 | 0,07% | 3 | 0,35% | 3 | 0,35% | 3 | 0,35% |
Lacepède (1802) | 3 | 0,07% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Lopez-fernandez & Winemiller (2003) | 3 | 0,07% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Marquet et al. (2003) | 3 | 0,07% | 3 | 0,35% | 3 | 0,35% | 3 | 0,35% |
Mennesson & Keith (2017) | 3 | 0,07% | 3 | 0,35% | 3 | 0,35% | 3 | 0,35% |
Mennesson & Keith (2020) | 3 | 0,07% | 3 | 0,35% | 3 | 0,35% | 3 | 0,35% |
Mitchill (1815) | 3 | 0,07% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Nijssen & Isbrucker (1983) | 3 | 0,07% | 3 | 0,35% | 3 | 0,35% | 3 | 0,35% |
Nilsson (1832) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Nordmann (1840-1842) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Pampoulie et al. (2001) | 3 | 0,07% | 3 | 0,35% | 3 | 0,35% | 3 | 0,35% |
Pelosse (1927) | 3 | 0,07% | 3 | 0,35% | 3 | 0,35% | 3 | 0,35% |
Persat et al. (2019) | 3 | 0,07% | 3 | 0,35% | 3 | 0,35% | 3 | 0,35% |
Planquette et al. (1996) | 3 | 0,07% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Rapp et al. (2001) | 3 | 0,07% | 3 | 0,35% | 3 | 0,35% | 3 | 0,35% |
Regan (1916) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Smales et al. (2007) | 3 | 0,07% | 3 | 0,35% | 3 | 0,35% | 2 | 0,24% |
Toledo-piza & Menezes (1996) | 3 | 0,07% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Westby (1988) | 3 | 0,07% | 3 | 0,35% | 3 | 0,35% | 3 | 0,35% |
Yokoyama (2013) | 3 | 0,07% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Zarske et al. (2004) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Zarske et al. (2006) | 3 | 0,07% | 3 | 0,35% | 3 | 0,35% | 3 | 0,35% |
Alley et al. (2023) | 2 | 0,04% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Andrade et al. (2018) | 2 | 0,04% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Anonyme (2016) | 2 | 0,04% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Baird & Girard (1853) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Barthélémy (1926) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Benejam et al. (2008) | 2 | 0,04% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Berrebi et al. (2018) | 2 | 0,04% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Berry & Smith-Vaniz (1978) | 2 | 0,04% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Beslagic et al. (2013) | 2 | 0,04% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Bianco (2014) | 2 | 0,04% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Bloch (1782-1784) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Bonaparte (1846) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Caillot et al. (1999) | 2 | 0,04% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Chen et al. (2001) | 2 | 0,04% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Costa (1829-1853) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Cuvier & Valenciennes (1835) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Cuvier & Valenciennes (1846) | 2 | 0,04% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Dawson & Fourmanoir (1981) | 2 | 0,04% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
de Morais et al. (2024) | 2 | 0,04% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
de Santana & Vari (2010) | 2 | 0,04% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Denys et al. (2013) | 2 | 0,04% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Denys et al. (2021) | 2 | 0,04% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Dingerkus & Seret (1992) | 2 | 0,04% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Dingerkus & Séret (1992) | 2 | 0,04% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Doadrio & Madeira (2004) | 2 | 0,04% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Durand (2016) | 2 | 0,04% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Euzet & Lambert (1974) | 2 | 0,04% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Feutry et al. (2012) | 2 | 0,04% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Fowler (1903) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Garcia-ayala et al. (2024) | 2 | 0,04% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Gauliard et al. (2019) | 2 | 0,04% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Gentry et al. (2004) | 2 | 0,04% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Geoffroy Saint-Hilaire ([1817]) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Gery & Planquette (1983) | 2 | 0,04% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Gery et al. (1998) | 2 | 0,04% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Gery (1992) | 2 | 0,04% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Girard (1859) | 2 | 0,04% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Girard (1859) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Guichenot (1850) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Guichenot (1859) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Günther (1861) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Harrison et al. (2007) | 2 | 0,04% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Heckel (1836) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Hopkins (1991) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Isbrucker & Nijssen (1984) | 2 | 0,04% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Jégu et al. (2003) | 2 | 0,04% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Jordan (1896) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Karaman (1971) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Keith & Marquet (2005) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Keith & Marquet (2006) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Keith & Marquet (2007) | 2 | 0,04% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Keith & Mennesson (2021) | 2 | 0,04% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Keith & Meunier (2000) | 2 | 0,04% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Keith et al. (2000) | 2 | 0,04% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Keith et al. (2007) | 2 | 0,04% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Keith et al. (2009) | 2 | 0,04% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Keith et al. (2010) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Kullander (1982) | 2 | 0,04% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Kullander (2012) | 2 | 0,04% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Laffaille et al. (1999) | 2 | 0,04% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Lavier (1936) | 2 | 0,04% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Linnaeus (1766) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Loot et al. (2001) | 2 | 0,04% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Lujan et al. (2017) | 2 | 0,04% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Malm (1877) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
McClelland (1844) | 2 | 0,04% | 2 | 0,23% | 2 | 0,24% | 0 | 0% |
Mennesson et al. (2019) | 2 | 0,04% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Meunier et al. (2011) | 2 | 0,04% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Meunier et al. (2014) | 2 | 0,04% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Monti et al. (2018) | 2 | 0,04% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Moreau (1881) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Muller & Isbrucker (1993) | 2 | 0,04% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Myers (1960) | 2 | 0,04% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Nijssen & Isbrucker (1980) | 2 | 0,04% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Nijssen & Isbrucker (1990) | 2 | 0,04% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Pallas (1770) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Pampoulie et al. (1999) | 2 | 0,04% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Pampoulie et al. (1999) | 2 | 0,04% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Parenti & Maciolek (1996) | 2 | 0,04% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Parenti (2021) | 2 | 0,04% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Parisi & Lundberg (2009) | 2 | 0,04% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Pascal et al. (1994) | 2 | 0,04% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Pellegrin (1902) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Pellegrin (1908) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Pinna & Keith (2003) | 2 | 0,04% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Risso (1810) | 2 | 0,04% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Rousseau (2010) | 2 | 0,04% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Schomburgk (1841) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Seegers & Huber (1981) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Sellier et al. (2016) | 2 | 0,04% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Shaw & Nodder (1795-1796) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Sideleva (2009) | 2 | 0,04% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Staentzel et al. (2023) | 2 | 0,04% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Tavera et al. (2018) | 2 | 0,04% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Teichert et al. (2013) | 2 | 0,04% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Uicn et al. (2020) | 2 | 0,04% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Valenciennes (1836-1844) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Vallot (1836) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Vari et al. (2003) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Vari et al. (2012) | 2 | 0,04% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Vari (1991) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Watson et al. (2005) | 2 | 0,04% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Whitehead et al. (1988) | 2 | 0,04% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Xia & Durand (2016) | 2 | 0,04% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Zarske et al. (2010) | 2 | 0,04% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Zarske (2012) | 2 | 0,04% | 2 | 0,23% | 2 | 0,24% | 2 | 0,24% |
Acolas et al. (2018) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Adam (2020) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Alexander & Seehausen (2021) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Allardi & Chancerel (1988) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Allardi (1980) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Andrade et al. (2016) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2004) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Anonyme. (2004) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Anonyme. (2004) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Anonyme. (2004) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2004) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Anonyme. (2004) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2004) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Anonyme. (2004) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2004) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Anonyme. (2004) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2004) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Anonyme. (2004) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Anonyme. (2004) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Anonyme. (2004) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Anonyme. (2004) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Anonyme (2011) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Audige (1927) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Bail (2009) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Bartáková et al. (2019) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Béarez & Séret (2009) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Beaulaton et al. (2017) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Bianco & Delmastro (2011) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Bianco (2002) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Bleeker (1854) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Bleeker (1854) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Bleeker (1854) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Bleeker (1856) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Bleeker (1865) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Bloch & Schneider (1801) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Bloch & Schneider (1801) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Bloch (1782) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Bloch (1784) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Bloch (1785-1795) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Bloch (1785-1795) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Bloch (1792) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Bloch (1794) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Bonnaterre (1788) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Bouchon & Lemoine (2003) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Boujard et al. (1988) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Boujard (1992) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Boulenger (1912) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Bragoni et al. (1983) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Bravničar et al. (2020) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Cesco et al. (2001) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Chabanaud (1927) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Chabanet & Durville (2005) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Charbonnier (2011) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Chassaing et al. (2018) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Cocco (1885) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Conway et al. (2017) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Cope (1870) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Cormier (1984) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Coulon & Sautet (1931) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Couteyen (2006) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Craig et al. (2017) | 1 | 0,02% | 1 | 0,12% | 0 | 0% | 1 | 0,12% |
Crampton & Albert (2003) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Cuinet et al. (2024) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Cuvier & Valenciennes (1847) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Dawson (1978) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Dekay (1842) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Dekay (1842) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Denys & Manné (2019) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Denys & Manné (2024) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Denys et al. (2018) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Denys (2017) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Desse-berset & Williot (2011) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Desse-Berset & Williot (2012) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Desse-Berset & Williot (2012) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Desse-Berset (2012) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Desse-Berset (2012) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Dingerkus et al. (1991) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Doadrio et al. (2007) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Dubut et al. (2012) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Duquenne-delobel et al. (2022) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Ebner et al. (2016) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Eichwald (1831) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Esposito et al. (2023) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
European Nucleotide Archive (2019) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Fabricius (1780) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Fernandes et al. (2005) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Firmat & Alibert (2011) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Forskål (1775) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Fourriére et al. (2014) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Fraser-brunner (1947) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Froese & Pauly (2020) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Fuento & Deso (2023) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Georget (2011) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Georget (2013) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Gergaud et al. (2015) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Gery (1961) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Gill (1858) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Gill (1862) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Gory (1972) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Goulletquer (2016) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Gozlan et al. (2010) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Gozlan (2015) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Gray (1851) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Grenand et al. (2015) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Günther (1862) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Günther (1864) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Günther (1876) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Hanzelovà & Gerdeaux (2003) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Haÿ et al. (2022) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Haÿ et al. (2023) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Heckel (1847) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Hein et al. (2010) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Hoedeman (1961) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Proceedings of the Zoological Society of London, 1907: 1035-1037.">Hopkinson (1907) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Jamonneau et al. (2025) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Jégu (2004) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Jeanroy & Denys (2019) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Jegu et al. (2004) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Jégu (1998) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Jégu (2000) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Jordan (1892) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Jordan (1894) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Jourde et al. (2017) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Jufaili et al. (2022) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Kaup (1856) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Keith & Dorson (2003) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Keith & Dorson (2003) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Keith & Dorson (2003) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Keith & Dorson (2003) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Keith & Dorson (2003) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Keith & Dorson (2003) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Keith & Dorson (2003) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Keith & Dorson (2003) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Keith & Machino (2003) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Keith & Mennesson (2023) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Keith et al. (2002) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Keith et al. (2020) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Keith (2000) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Keith (2003) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Keith (2003) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Keith (2003) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Keith (2003) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Keith (2003) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Keith (2003) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Keith (2003) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Keith (2003) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Keith (2003) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Keith (2003) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Keith (2003) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Keith (2003) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Keith (2003) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Keith (2003) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Keith (2003) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Keith (2003) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Keith (2003) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Keith (2003) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Keith (2003) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Keith (2003) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Keith (2003) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Keith (2003) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Kronen et al. (2009) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Krøyer (1838-40) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Krøyer (1846-53) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Krøyer (1852-53) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Lacepède (1801) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Laffaille et al. (2000) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Lefèbvre et al. (2019) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Lehmann et al. (2014) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Lesueur (1818) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Letourneur et al. (2004) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Loiselle & Stiassny (2007) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Lorvelec & Pascal (2009) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Lowe (1838) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Transactions of the Zoological Society of London, 1839: 1-20.">Lowe (1839) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Lowe (1874) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Lundberg et al. (2012) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Lütken (1875) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Machino (2003) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Maeda et al. (2011) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Maillard (1973) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Malm (1861) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
. Onema, Délégation Interrégionale du Nord-Est. 37 pp. + annexes.">Manné (2014) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Marceniuk et al. (2012) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Maréchal & Pérès (2007) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Maréchal & Trégarot (2012) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Masseboeuf & Denys (2023) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Masseboeuf et al. (2020) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Matsuzaki et al. (2009) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Meeus et al. (1993) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Mennesson & Keith (2020) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Merckx et al. (2000) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Mol et al. (2012) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Moreau (1881) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Moreira & Lima (2011) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Müller & Troschel (1844) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Neilson & Stepien (2009) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Norman (1926) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Norman (1929) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Ocea & Consult' (2015) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Pampoulie et al. (2000) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Pellegrin (1900) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Pellegrin (1907) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Pellegrin (1923) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Pellegrin (1932) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Peters (1852) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Petit (1954) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Pieters & Dickinson (2005) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Poey (1858-61) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Préau et al. (2017) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Puissauve & Poulet (2015) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Puissauve, Legros & Costedoat (2015) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Puissauve, Legros & Poulet (2015) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
PUISSAUVE Renaud & BAGLINIERE Jean-Luc (2013) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
PUISSAUVE Renaud & BAGLINIERE Jean-Luc (2013) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Putelat et al. (2021) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Pylaie (1835) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Quéro & Delmas (1982) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Questel (2014) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Questel (2017) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Randall & Earle (2000) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Randall & Kulbicki (2006) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Regan (1905) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Règlement d'exécution (UE) 2016/1141 | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Reis et al. (2005) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Richard et al. (1982) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Roule (1902) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Runde (2016) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Rutkayová et al. (2013) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Santana et al. (2019) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Schindler (1998) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Schinz (1840) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Seret & Dingerkus (1992) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Sherborn (1895) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Silva et al. (2016) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Silva-Oliveira et al. (2020) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Silva-oliveira et al. (2021) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Simian et al. (2022) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Smith-vaniz & Jelks (2014) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Snodgrass & Heller (1905) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Spitz et al. (2015) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Steindachner (1865) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Steindachner (1876) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Steindachner (1894) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Steindachner (1900) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Tales et al. (1997) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Vallot (1837) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Van der Stigchel (1947) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Vecchioni et al. (2022) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Vecchioni et al. (2022) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Watson et al. (2001) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Watson (1999) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Weber & Beaufort (1916) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Yan (2020) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
Yarrell (1836) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Yarrell (1836) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Yarrell (1839) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Zarske et al. (2006) | 1 | 0,02% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |