Reptiles de l'océan Pacifique
482 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
Référence | Total | Valides | Espèces | Taxons terminaux | ||||
---|---|---|---|---|---|---|---|---|
nb | % | nb | % | nb | % | nb | % | |
Bauer & Sadlier (2000) | 85 | 22,73% | 70 | 37,84% | 70 | 38,67% | 68 | 37,36% |
Bauer et al. (2022) | 69 | 18,45% | 69 | 37,3% | 69 | 38,12% | 69 | 37,91% |
Roux (1913) | 52 | 13,9% | 11 | 5,95% | 11 | 6,08% | 11 | 6,04% |
Bernstein et al. (2021) | 33 | 8,82% | 33 | 17,84% | 33 | 18,23% | 33 | 18,13% |
Geneva et al. (2013) | 24 | 6,42% | 22 | 11,89% | 22 | 12,15% | 22 | 12,09% |
Mertens & Wermuth (1960) | 21 | 5,61% | 0 | 0% | 0 | 0% | 0 | 0% |
Uicn et al. (2015) | 19 | 5,08% | 16 | 8,65% | 16 | 8,84% | 16 | 8,79% |
Sadlier et al. (2012) | 18 | 4,81% | 14 | 7,57% | 14 | 7,73% | 14 | 7,69% |
Bauer et al. (2006) | 16 | 4,28% | 16 | 8,65% | 16 | 8,84% | 16 | 8,79% |
Duval et al. (2019) | 16 | 4,28% | 16 | 8,65% | 16 | 8,84% | 16 | 8,79% |
Bauer & Sadlier (1994) | 15 | 4,01% | 11 | 5,95% | 11 | 6,08% | 11 | 6,04% |
Ineich (2007) | 15 | 4,01% | 11 | 5,95% | 10 | 5,52% | 11 | 6,04% |
Van Dijk et al. (2012) | 15 | 4,01% | 12 | 6,49% | 12 | 6,63% | 12 | 6,59% |
Boulenger (1883) | 14 | 3,74% | 6 | 3,24% | 6 | 3,31% | 6 | 3,3% |
Bauer et al. (2012) | 13 | 3,48% | 11 | 5,95% | 11 | 6,08% | 11 | 6,04% |
Bavay (1869) | 13 | 3,48% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Brischoux et al. (2018) | 13 | 3,48% | 11 | 5,95% | 11 | 6,08% | 10 | 5,49% |
Sadlier et al. (2014) | 13 | 3,48% | 13 | 7,03% | 13 | 7,18% | 13 | 7,14% |
Bauer & DeVaney (1987) | 12 | 3,21% | 4 | 2,16% | 4 | 2,21% | 4 | 2,2% |
Gill (1995) | 12 | 3,21% | 11 | 5,95% | 11 | 6,08% | 10 | 5,49% |
Morelon (2015) | 12 | 3,21% | 9 | 4,86% | 9 | 4,97% | 9 | 4,95% |
Deuss & Jourdan (2022) | 11 | 2,94% | 11 | 5,95% | 11 | 6,08% | 11 | 6,04% |
Probst et al. (2022) | 11 | 2,94% | 11 | 5,95% | 11 | 6,08% | 11 | 6,04% |
Sadlier et al. (2009) | 11 | 2,94% | 11 | 5,95% | 11 | 6,08% | 11 | 6,04% |
Dewynter et al. (2023) | 10 | 2,67% | 10 | 5,41% | 10 | 5,52% | 9 | 4,95% |
Goiran et al. (2022) | 10 | 2,67% | 7 | 3,78% | 7 | 3,87% | 6 | 3,3% |
Ineich (2016) | 10 | 2,67% | 8 | 4,32% | 8 | 4,42% | 8 | 4,4% |
Probst (2001) | 10 | 2,67% | 8 | 4,32% | 8 | 4,42% | 7 | 3,85% |
Sadlier et al. (2002) | 10 | 2,67% | 10 | 5,41% | 10 | 5,52% | 10 | 5,49% |
Astrongatt (2017) | 9 | 2,41% | 9 | 4,86% | 9 | 4,97% | 9 | 4,95% |
Dewynter et al. (2022) | 9 | 2,41% | 9 | 4,86% | 9 | 4,97% | 8 | 4,4% |
Henderson & Breuil (2012) | 9 | 2,41% | 6 | 3,24% | 2 | 1,1% | 6 | 3,3% |
Massary et al. (2020) | 9 | 2,41% | 9 | 4,86% | 9 | 4,97% | 9 | 4,95% |
Sadlier et al. (2004) | 9 | 2,41% | 9 | 4,86% | 9 | 4,97% | 9 | 4,95% |
Astrongatt (2019) | 8 | 2,14% | 8 | 4,32% | 8 | 4,42% | 8 | 4,4% |
Blanc et al. (1993) | 8 | 2,14% | 6 | 3,24% | 6 | 3,31% | 5 | 2,75% |
Bocage (1881) | 8 | 2,14% | 3 | 1,62% | 3 | 1,66% | 3 | 1,65% |
Caut et al. (2013) | 8 | 2,14% | 7 | 3,78% | 7 | 3,87% | 7 | 3,85% |
Dewynter et al. (2023) | 8 | 2,14% | 8 | 4,32% | 8 | 4,42% | 7 | 3,85% |
Greer (1974) | 8 | 2,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Massary et al. (2021) | 8 | 2,14% | 8 | 4,32% | 8 | 4,42% | 7 | 3,85% |
Questel et al. (2023) | 8 | 2,14% | 8 | 4,32% | 8 | 4,42% | 7 | 3,85% |
Questel et al. (2023) | 8 | 2,14% | 8 | 4,32% | 8 | 4,42% | 7 | 3,85% |
Sadlier et al. (2014) | 8 | 2,14% | 8 | 4,32% | 8 | 4,42% | 8 | 4,4% |
Zug (1985) | 8 | 2,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme (2015) | 7 | 1,87% | 6 | 3,24% | 6 | 3,31% | 6 | 3,3% |
Dewynter et al. (2019) | 7 | 1,87% | 7 | 3,78% | 7 | 3,87% | 6 | 3,3% |
Gherghel et al. (2016) | 7 | 1,87% | 7 | 3,78% | 7 | 3,87% | 7 | 3,85% |
Massary et al. (2018) | 7 | 1,87% | 7 | 3,78% | 7 | 3,87% | 6 | 3,3% |
Ronot (2007) | 7 | 1,87% | 6 | 3,24% | 5 | 2,76% | 6 | 3,3% |
Sanchez (2020) | 7 | 1,87% | 7 | 3,78% | 7 | 3,87% | 6 | 3,3% |
Uicn et al. (2017) | 7 | 1,87% | 7 | 3,78% | 7 | 3,87% | 6 | 3,3% |
Vences et al. (2001) | 7 | 1,87% | 4 | 2,16% | 4 | 2,21% | 4 | 2,2% |
Zdunek (2022) | 7 | 1,87% | 6 | 3,24% | 6 | 3,31% | 5 | 2,75% |
Camiñas et al. (2021) | 6 | 1,6% | 6 | 3,24% | 6 | 3,31% | 6 | 3,3% |
Cogger & Heatwole (2006) | 6 | 1,6% | 6 | 3,24% | 6 | 3,31% | 6 | 3,3% |
Dewynter et al. (2019) | 6 | 1,6% | 6 | 3,24% | 6 | 3,31% | 5 | 2,75% |
Good et al. (1997) | 6 | 1,6% | 2 | 1,08% | 2 | 1,1% | 2 | 1,1% |
Lescure et al. (2012) | 6 | 1,6% | 6 | 3,24% | 5 | 2,76% | 5 | 2,75% |
Massary et al. (2017) | 6 | 1,6% | 6 | 3,24% | 6 | 3,31% | 5 | 2,75% |
Massary et al. (2019) | 6 | 1,6% | 6 | 3,24% | 6 | 3,31% | 5 | 2,75% |
Muratet (2015) | 6 | 1,6% | 6 | 3,24% | 5 | 2,76% | 5 | 2,75% |
Probst (1997) | 6 | 1,6% | 3 | 1,62% | 3 | 1,66% | 3 | 1,65% |
Questel (2020) | 6 | 1,6% | 6 | 3,24% | 5 | 2,76% | 6 | 3,3% |
Sadlier et al. (1999) | 6 | 1,6% | 6 | 3,24% | 6 | 3,31% | 6 | 3,3% |
Sadlier (1988) | 6 | 1,6% | 3 | 1,62% | 3 | 1,66% | 3 | 1,65% |
Sauvage (1878) | 6 | 1,6% | 0 | 0% | 0 | 0% | 0 | 0% |
Angel (1935) | 5 | 1,34% | 2 | 1,08% | 2 | 1,1% | 2 | 1,1% |
Bauer & Sadlier (2000) | 5 | 1,34% | 2 | 1,08% | 2 | 1,1% | 2 | 1,1% |
Bioinsight/diren & Guyane (2006) | 5 | 1,34% | 5 | 2,7% | 5 | 2,76% | 5 | 2,75% |
Bour et al. (2008) | 5 | 1,34% | 5 | 2,7% | 5 | 2,76% | 4 | 2,2% |
Casale et al. (2021) | 5 | 1,34% | 5 | 2,7% | 5 | 2,76% | 5 | 2,75% |
Chevalier (2006) | 5 | 1,34% | 5 | 2,7% | 5 | 2,76% | 5 | 2,75% |
Ciccione et al. (2011) | 5 | 1,34% | 5 | 2,7% | 5 | 2,76% | 5 | 2,75% |
Crillon & Cuzange (2020) | 5 | 1,34% | 5 | 2,7% | 5 | 2,76% | 5 | 2,75% |
Duffaut et al. (2011) | 5 | 1,34% | 5 | 2,7% | 5 | 2,76% | 5 | 2,75% |
Entraygues (2014) | 5 | 1,34% | 5 | 2,7% | 5 | 2,76% | 5 | 2,75% |
Étaix-bonnin et al. (2011) | 5 | 1,34% | 5 | 2,7% | 5 | 2,76% | 5 | 2,75% |
Fretey & Triplet (2022) | 5 | 1,34% | 5 | 2,7% | 5 | 2,76% | 5 | 2,75% |
Goiran & Shine (2020) | 5 | 1,34% | 4 | 2,16% | 4 | 2,21% | 4 | 2,2% |
González-sánchez et al. (2021) | 5 | 1,34% | 5 | 2,7% | 5 | 2,76% | 4 | 2,2% |
Havery et al. (2018) | 5 | 1,34% | 4 | 2,16% | 4 | 2,21% | 3 | 1,65% |
Lambert (1988) | 5 | 1,34% | 2 | 1,08% | 2 | 1,1% | 2 | 1,1% |
Le Scao et al. (2011) | 5 | 1,34% | 5 | 2,7% | 5 | 2,76% | 5 | 2,75% |
Questel & Le Quellec (2012) | 5 | 1,34% | 4 | 2,16% | 4 | 2,21% | 4 | 2,2% |
Read & Farman (2018) | 5 | 1,34% | 5 | 2,7% | 5 | 2,76% | 5 | 2,75% |
Read et al. (2023) | 5 | 1,34% | 5 | 2,7% | 5 | 2,76% | 5 | 2,75% |
Rhodin et al. (2017) | 5 | 1,34% | 3 | 1,62% | 3 | 1,66% | 3 | 1,65% |
Sadlier et al. (2006) | 5 | 1,34% | 5 | 2,7% | 5 | 2,76% | 5 | 2,75% |
Sadlier et al. (2014) | 5 | 1,34% | 5 | 2,7% | 5 | 2,76% | 5 | 2,75% |
Sadlier et al. (2015) | 5 | 1,34% | 0 | 0% | 0 | 0% | 0 | 0% |
Sauvignet et al. (2000) | 5 | 1,34% | 5 | 2,7% | 5 | 2,76% | 5 | 2,75% |
Tirvengadum & Bour (1985) | 5 | 1,34% | 4 | 2,16% | 4 | 2,21% | 4 | 2,2% |
Arnold & Ovenden (2014) | 4 | 1,07% | 4 | 2,16% | 4 | 2,21% | 3 | 1,65% |
Barrioz & Morinière (2007) | 4 | 1,07% | 4 | 2,16% | 4 | 2,21% | 4 | 2,2% |
Bauer et al. (1998) | 4 | 1,07% | 4 | 2,16% | 4 | 2,21% | 4 | 2,2% |
Bauer et al. (2009) | 4 | 1,07% | 4 | 2,16% | 4 | 2,21% | 4 | 2,2% |
Bauer et al. (2012) | 4 | 1,07% | 3 | 1,62% | 3 | 1,66% | 3 | 1,65% |
Fretey & Lescure (1999) | 4 | 1,07% | 4 | 2,16% | 4 | 2,21% | 4 | 2,2% |
Hoser (2016) | 4 | 1,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Hudel et al. (2020) | 4 | 1,07% | 4 | 2,16% | 4 | 2,21% | 4 | 2,2% |
Ineich et al. (2007) | 4 | 1,07% | 4 | 2,16% | 4 | 2,21% | 3 | 1,65% |
Jourdan (2020) | 4 | 1,07% | 4 | 2,16% | 3 | 1,66% | 3 | 1,65% |
Linnaeus (1758) | 4 | 1,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Probst (1998) | 4 | 1,07% | 3 | 1,62% | 3 | 1,66% | 3 | 1,65% |
Rasmussen & Ineich (2000) | 4 | 1,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Sadlier et al. (2004) | 4 | 1,07% | 4 | 2,16% | 4 | 2,21% | 4 | 2,2% |
Sadlier et al. (2012) | 4 | 1,07% | 4 | 2,16% | 4 | 2,21% | 4 | 2,2% |
Sadlier (1987) | 4 | 1,07% | 4 | 2,16% | 4 | 2,21% | 4 | 2,2% |
Shaw (1802) | 4 | 1,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Udyawer et al. (2023) | 4 | 1,07% | 3 | 1,62% | 3 | 1,66% | 3 | 1,65% |
Wright et al. (2000) | 4 | 1,07% | 4 | 2,16% | 4 | 2,21% | 4 | 2,2% |
Blanc (1909) | 3 | 0,8% | 0 | 0% | 0 | 0% | 0 | 0% |
Breuil et al. (2010) | 3 | 0,8% | 2 | 1,08% | 1 | 0,55% | 2 | 1,1% |
Busala et al. (2024) | 3 | 0,8% | 2 | 1,08% | 2 | 1,1% | 1 | 0,55% |
CEN Nouvelle-Calédonie (2021) | 3 | 0,8% | 3 | 1,62% | 2 | 1,1% | 3 | 1,65% |
Champagne et al. (1997) | 3 | 0,8% | 3 | 1,62% | 2 | 1,1% | 3 | 1,65% |
Cheke (1987) | 3 | 0,8% | 3 | 1,62% | 3 | 1,66% | 3 | 1,65% |
Cuvier (1829) | 3 | 0,8% | 0 | 0% | 0 | 0% | 0 | 0% |
Delcroix et al. (2011) | 3 | 0,8% | 3 | 1,62% | 3 | 1,66% | 3 | 1,65% |
Dubief & Gallais (2011) | 3 | 0,8% | 3 | 1,62% | 3 | 1,66% | 3 | 1,65% |
Duguy et al. (1998) | 3 | 0,8% | 3 | 1,62% | 3 | 1,66% | 3 | 1,65% |
Duguy et al. (2007) | 3 | 0,8% | 3 | 1,62% | 3 | 1,66% | 3 | 1,65% |
Duguy (1988) | 3 | 0,8% | 3 | 1,62% | 3 | 1,66% | 3 | 1,65% |
Duguy (1994) | 3 | 0,8% | 3 | 1,62% | 3 | 1,66% | 3 | 1,65% |
Duguy (1997) | 3 | 0,8% | 3 | 1,62% | 3 | 1,66% | 3 | 1,65% |
Duméril & Bibron (1836) | 3 | 0,8% | 2 | 1,08% | 2 | 1,1% | 2 | 1,1% |
Girard (1858) | 3 | 0,8% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Girondot (2011) | 3 | 0,8% | 3 | 1,62% | 3 | 1,66% | 3 | 1,65% |
Glaw & Rösler (2015) | 3 | 0,8% | 3 | 1,62% | 3 | 1,66% | 3 | 1,65% |
Goiran & Shine (2013) | 3 | 0,8% | 3 | 1,62% | 3 | 1,66% | 3 | 1,65% |
Günther (1872) | 3 | 0,8% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Günther (1873) | 3 | 0,8% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Heatwole & Cogger (2013) | 3 | 0,8% | 2 | 1,08% | 2 | 1,1% | 2 | 1,1% |
Hoff & Daszkiewicz (2001) | 3 | 0,8% | 3 | 1,62% | 3 | 1,66% | 3 | 1,65% |
In: Charpy, L. (coord.) 2009. Clipperton, environnement et biodiversité d'un microcosme océanique. Muséum national d'Histoire naturelle, Paris; IRD, Marseille: 347-380. (Patrimoines naturels; 68).">Ineich et al. (2009) | 3 | 0,8% | 3 | 1,62% | 0 | 0% | 3 | 1,65% |
Jourdan et al. (2014) | 3 | 0,8% | 3 | 1,62% | 3 | 1,66% | 3 | 1,65% |
Maldonado (2017) | 3 | 0,8% | 2 | 1,08% | 2 | 1,1% | 2 | 1,1% |
Méheust et al. (2018) | 3 | 0,8% | 3 | 1,62% | 3 | 1,66% | 3 | 1,65% |
Morinière & Dell'amico (2011) | 3 | 0,8% | 3 | 1,62% | 3 | 1,66% | 3 | 1,65% |
Ohler et al. (2021) | 3 | 0,8% | 1 | 0,54% | 1 | 0,55% | 0 | 0% |
Poisson (1999) | 3 | 0,8% | 3 | 1,62% | 3 | 1,66% | 3 | 1,65% |
Read & Jean (2021) | 3 | 0,8% | 3 | 1,62% | 3 | 1,66% | 3 | 1,65% |
Sadlier et al. (1997) | 3 | 0,8% | 3 | 1,62% | 3 | 1,66% | 3 | 1,65% |
Sadlier et al. (2009) | 3 | 0,8% | 3 | 1,62% | 3 | 1,66% | 3 | 1,65% |
Sanchez & Probst (2016) | 3 | 0,8% | 3 | 1,62% | 3 | 1,66% | 3 | 1,65% |
Seipp & Obst (1994) | 3 | 0,8% | 0 | 0% | 0 | 0% | 0 | 0% |
Shine et al. (2019) | 3 | 0,8% | 3 | 1,62% | 3 | 1,66% | 3 | 1,65% |
Turpin & Probst (1998) | 3 | 0,8% | 3 | 1,62% | 3 | 1,66% | 2 | 1,1% |
Wallach (2020) | 3 | 0,8% | 2 | 1,08% | 2 | 1,1% | 2 | 1,1% |
Alvarez et al. (2023) | 2 | 0,53% | 2 | 1,08% | 2 | 1,1% | 2 | 1,1% |
Baldi et al. (2022) | 2 | 0,53% | 2 | 1,08% | 2 | 1,1% | 2 | 1,1% |
Bauer et al. (2000) | 2 | 0,53% | 0 | 0% | 0 | 0% | 0 | 0% |
Bauer et al. (2006) | 2 | 0,53% | 2 | 1,08% | 2 | 1,1% | 2 | 1,1% |
Bauer et al. (2010) | 2 | 0,53% | 2 | 1,08% | 2 | 1,1% | 2 | 1,1% |
Bauer (1987) | 2 | 0,53% | 0 | 0% | 0 | 0% | 0 | 0% |
Behm et al. (2019) | 2 | 0,53% | 2 | 1,08% | 2 | 1,1% | 2 | 1,1% |
Blom et al. (2019) | 2 | 0,53% | 2 | 1,08% | 2 | 1,1% | 2 | 1,1% |
Bocage (1873) | 2 | 0,53% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Bocage (1873) | 2 | 0,53% | 2 | 1,08% | 2 | 1,1% | 2 | 1,1% |
Böhme (1976) | 2 | 0,53% | 0 | 0% | 0 | 0% | 0 | 0% |
Böhme (1979) | 2 | 0,53% | 0 | 0% | 0 | 0% | 0 | 0% |
Börner (1980) | 2 | 0,53% | 0 | 0% | 0 | 0% | 0 | 0% |
Boulenger (1880) | 2 | 0,53% | 0 | 0% | 0 | 0% | 0 | 0% |
Breuil (2002) | 2 | 0,53% | 0 | 0% | 0 | 0% | 0 | 0% |
Brischoux & Bonnet (2009) | 2 | 0,53% | 2 | 1,08% | 2 | 1,1% | 2 | 1,1% |
Carille (2012) | 2 | 0,53% | 2 | 1,08% | 2 | 1,1% | 2 | 1,1% |
Cheon et al. (2023) | 2 | 0,53% | 2 | 1,08% | 0 | 0% | 2 | 1,1% |
Chevallier et al. (2023) | 2 | 0,53% | 2 | 1,08% | 2 | 1,1% | 2 | 1,1% |
Cole et al. (2005) | 2 | 0,53% | 2 | 1,08% | 2 | 1,1% | 2 | 1,1% |
Dubos et al. (2023) | 2 | 0,53% | 2 | 1,08% | 2 | 1,1% | 2 | 1,1% |
Duguy et al. (1997) | 2 | 0,53% | 2 | 1,08% | 2 | 1,1% | 2 | 1,1% |
Duguy et al. (1999) | 2 | 0,53% | 2 | 1,08% | 2 | 1,1% | 2 | 1,1% |
Duguy et al. (2000) | 2 | 0,53% | 2 | 1,08% | 2 | 1,1% | 2 | 1,1% |
Duguy et al. (2002) | 2 | 0,53% | 2 | 1,08% | 2 | 1,1% | 2 | 1,1% |
Duguy et al. (2003) | 2 | 0,53% | 2 | 1,08% | 2 | 1,1% | 2 | 1,1% |
Duguy et al. (2004) | 2 | 0,53% | 2 | 1,08% | 2 | 1,1% | 2 | 1,1% |
Duguy et al. (2006) | 2 | 0,53% | 2 | 1,08% | 2 | 1,1% | 2 | 1,1% |
Duguy (1987) | 2 | 0,53% | 2 | 1,08% | 2 | 1,1% | 2 | 1,1% |
Duguy (1990) | 2 | 0,53% | 2 | 1,08% | 2 | 1,1% | 2 | 1,1% |
Duguy (1992) | 2 | 0,53% | 2 | 1,08% | 2 | 1,1% | 2 | 1,1% |
Duguy (1993) | 2 | 0,53% | 2 | 1,08% | 2 | 1,1% | 2 | 1,1% |
Duguy (1995) | 2 | 0,53% | 2 | 1,08% | 2 | 1,1% | 2 | 1,1% |
Duguy (1996) | 2 | 0,53% | 2 | 1,08% | 2 | 1,1% | 2 | 1,1% |
Flecks et al. (2012) | 2 | 0,53% | 2 | 1,08% | 2 | 1,1% | 2 | 1,1% |
Gargominy et al. (1996) | 2 | 0,53% | 2 | 1,08% | 2 | 1,1% | 2 | 1,1% |
Girard (2007) | 2 | 0,53% | 1 | 0,54% | 0 | 0% | 1 | 0,55% |
Girondo (2023) | 2 | 0,53% | 2 | 1,08% | 2 | 1,1% | 2 | 1,1% |
Guichenot (1866) | 2 | 0,53% | 2 | 1,08% | 2 | 1,1% | 2 | 1,1% |
Heinicke et al. (2023) | 2 | 0,53% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Henao-osorio et al. (2021) | 2 | 0,53% | 2 | 1,08% | 2 | 1,1% | 2 | 1,1% |
Henkel & Böhme (2001) | 2 | 0,53% | 2 | 1,08% | 2 | 1,1% | 2 | 1,1% |
Ineich & Sadlier (1991) | 2 | 0,53% | 0 | 0% | 0 | 0% | 0 | 0% |
Ineich et al. (2007) | 2 | 0,53% | 2 | 1,08% | 2 | 1,1% | 2 | 1,1% |
Jouan (1863) | 2 | 0,53% | 2 | 1,08% | 2 | 1,1% | 2 | 1,1% |
Klein et al. (2016) | 2 | 0,53% | 2 | 1,08% | 2 | 1,1% | 1 | 0,55% |
Köhler et al. (2024) | 2 | 0,53% | 2 | 1,08% | 2 | 1,1% | 2 | 1,1% |
Lescure (2015) | 2 | 0,53% | 0 | 0% | 0 | 0% | 0 | 0% |
Lesson (1830) | 2 | 0,53% | 0 | 0% | 0 | 0% | 0 | 0% |
Linné (1766) | 2 | 0,53% | 0 | 0% | 0 | 0% | 0 | 0% |
Merrem (1820) | 2 | 0,53% | 0 | 0% | 0 | 0% | 0 | 0% |
Peron (2014) | 2 | 0,53% | 2 | 1,08% | 2 | 1,1% | 2 | 1,1% |
Probst et al. (2000) | 2 | 0,53% | 2 | 1,08% | 2 | 1,1% | 2 | 1,1% |
Probst et al. (2001) | 2 | 0,53% | 2 | 1,08% | 2 | 1,1% | 2 | 1,1% |
Rinaldi et al. (2011) | 2 | 0,53% | 2 | 1,08% | 2 | 1,1% | 2 | 1,1% |
Sadlier & Bauer (2000) | 2 | 0,53% | 2 | 1,08% | 2 | 1,1% | 2 | 1,1% |
Sadlier et al. (1998) | 2 | 0,53% | 0 | 0% | 0 | 0% | 0 | 0% |
Sadlier et al. (2006) | 2 | 0,53% | 2 | 1,08% | 2 | 1,1% | 2 | 1,1% |
Sadlier et al. (2013) | 2 | 0,53% | 2 | 1,08% | 2 | 1,1% | 2 | 1,1% |
Sadlier et al. (2014) | 2 | 0,53% | 2 | 1,08% | 2 | 1,1% | 2 | 1,1% |
Sadlier et al. (2019) | 2 | 0,53% | 2 | 1,08% | 2 | 1,1% | 2 | 1,1% |
Sadlier et al. (2019) | 2 | 0,53% | 2 | 1,08% | 2 | 1,1% | 2 | 1,1% |
Sanchez et al. (2019) | 2 | 0,53% | 2 | 1,08% | 2 | 1,1% | 2 | 1,1% |
Sanders et al. (2013) | 2 | 0,53% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Schneider (1801) | 2 | 0,53% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Sebat et al. (2005) | 2 | 0,53% | 2 | 1,08% | 2 | 1,1% | 2 | 1,1% |
Shine et al. (2002) | 2 | 0,53% | 2 | 1,08% | 2 | 1,1% | 2 | 1,1% |
Skipwith et al. (2014) | 2 | 0,53% | 2 | 1,08% | 2 | 1,1% | 2 | 1,1% |
Solórzano & Sasa (2024) | 2 | 0,53% | 2 | 1,08% | 2 | 1,1% | 2 | 1,1% |
Thunberg (1787) | 2 | 0,53% | 0 | 0% | 0 | 0% | 0 | 0% |
Weterings & Vetter (2017) | 2 | 0,53% | 2 | 1,08% | 2 | 1,1% | 2 | 1,1% |
Zug et al. (2007) | 2 | 0,53% | 2 | 1,08% | 2 | 1,1% | 2 | 1,1% |
Abhaya & Probst (2009) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Abhaya et al. (1998) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 0 | 0% |
Abhaya et al. (2000) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Agassiz (1857) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Al-hasson & Ali (2020) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Anderson (1925) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Andersson (1908) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2004) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Aquarium de La Rochelle (2017) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Armand & Ferlay (2023) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Augros et al. (2017) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Augros et al. (2018) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Austin & Zug (1999) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Baldi et al. (2023) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Balouet & Buffetaut 1987 | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Bance (2022) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Barbancey (2001) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Barbancey (2001) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Barbour (1912) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Bassett et al. (2021) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Bauer & Jackman (2006) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Bauer & Russell (1986) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Bauer & Russell (1987) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Bauer & Russell (1991) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Bauer et al. (1992) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Bauer et al. (2008) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Bauer et al. (2022) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Bauer (1985) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Baxter-gilbert et al. (2021) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Beauvieux et al. (2024) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Becerra et al. (2024) | 1 | 0,27% | 1 | 0,54% | 0 | 0% | 1 | 0,55% |
Behm et al. (2022) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Bertrand & Drogou (2000) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Bertrand et al. (2001) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Bleeker (1860) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Blom (2015) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Boettger (1880) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Bonnaterre (1789) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Borroto-páez (2018) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Boulenger (1878) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Boulenger (1900) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Bourgade (2021) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Brisbane et al. (2021) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Brocchi (1876) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Brongniart (1800) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Brown & Gibbons (1986) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Capalleras & Carretero (2000) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 0 | 0% |
Catala (1950) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Caut et al. (2008) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Cazanove et al. (2023) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Chambault et al. (2020) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Cheke (2010) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Chevreux & de Guerne (1893) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Ciccione (2000) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Ciccione (2001) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Ciccione (2001) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Claudin et al. (2022) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Clause et al. (2017) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Colin (1992) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Collazos-astudillo et al. (2022) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Crowe-riddell et al. (2021) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Cummings et al. (2021) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Dal Zotto et al. (2024) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Dalleau et al. (2014) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
D´angiolella et al. (2021) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Daudin (1803) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Dauvin (1990) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
de Massary et al. (2015) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 0 | 0% |
de Vis (1905) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Delcroix et al. (2008) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Deso et al. (2020) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Deso (2001) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Deuss et al. (2024) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Dewynter et al. (2020) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Dotsenko (2011) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Dubos et al. (2020) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Duguy & Duron (1981) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Duguy & Duron (1982) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Duguy & Duron (1983) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Duguy & Duron (1984) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Duguy & Duron (1985) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Duguy et al. (1980) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Duguy et al. (2000) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Duguy (1983) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Duguy (1986) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Duguy (1988) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Duguy (1989) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Duméril & Bibron (1844) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Duméril & Duméril (1851) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Duméril (1853) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Eschscholtz (1829) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Ficetola & Scali (2010) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 0 | 0% |
Finnerty et al. (2021) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Fretey & Bour (1980) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Fretey et al. (2023) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Fretey (1980) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Fretey (2003) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Frétey (2022) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Fritz & Havaš (2007) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Gallien-lamarche (2018) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Garman (1899) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Gérigny et al. (2020) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Girard (1997) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Goiran & Shine (2014) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Goiran et al. (2013) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Goiran et al. (2018) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Goiran et al. (2020) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Goiran et al. (2020) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Goiran et al. (2022) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Goldberg et al. (2011) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
González et al. (2018) | 1 | 0,27% | 1 | 0,54% | 0 | 0% | 1 | 0,55% |
Grant-mackie et al. (2003) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Gray (1842) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Griffing et al. (2022) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Heatwole et al. (2005) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Hedges et al. (2014) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Heinicke et al. (2010) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Herzberg (2018) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Holden & Ineich (2018) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Holden et al. (2014) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Holt et al. (2007) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Iković et al. (2023) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 0 | 0% |
Ineich & Bauer (1992) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Ineich & Blanc (1988) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Ineich & Fischer (2016) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Ineich & Giraud (2019) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Ineich & Laboute (2002) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Ineich et al. (2014) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Ineich et al. (2017) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Ineich et al. (2017) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Ineich et al. (2018) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Ineich et al. (2019) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Ineich (1987) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Ineich (1999) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Ineich (2009) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Ineich (2015) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Ineich (2018) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Jacquinot & Guichenot (1853) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Jim et al. (2022) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Jouan (1864) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Jowers et al. (2022) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Karaa et al. (2016) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Karin et al. (2021) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Kharin & Dotsenko (2012) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Kharin (1983) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Kharin (1984) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Kordi & Shabanipour (2012) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Kornilev et al. (2020) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 0 | 0% |
Krefft (1869) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Lacépède (1804) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Lanza & Boscherini (2000) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Lapwong et al. (2021) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Lescure et al. (2016) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Lescure et al. (2020) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Lesson (1826-1830) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Liardet & d'Auzon (2004) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Liardet (2004) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Liebart et al. (2021) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Liebgold et al. (2019) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Lillywhite & Menon (2019) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Loisier et al. (2021) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Lorvelec & Pascal (2009) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 0 | 0% |
Lorvelec & Pascal (2009) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Lorvelec et al. (2009) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Lorvelec et al. (2011) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Lorvelec et al. (2016) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Lorvelec et al. (2017) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Louisin & Probst (1996) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Loveridge (1941) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Lowe et al. (2007) | 1 | 0,27% | 1 | 0,54% | 0 | 0% | 1 | 0,55% |
Lynch et al. (2021) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Lynch et al. (2023) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Maillard & David (2014) | 1 | 0,27% | 1 | 0,54% | 0 | 0% | 1 | 0,55% |
Mancino et al. (2022) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Martin et al. (2021) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Massary (2012) | 1 | 0,27% | 1 | 0,54% | 0 | 0% | 1 | 0,55% |
Mckay & Milenkaya (2020) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Medetian & Miaud (2024) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Mertens (1928) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Meyen (1834) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Montrousier (1860) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Moutou (1995) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Murphy et al. (1978) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Oliver (2011) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Ota & Ineich (2006) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Parker (1926) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Parmentier et al. (2017) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Pascal et al. 2006 | 1 | 0,27% | 1 | 0,54% | 0 | 0% | 1 | 0,55% |
Perkins (1928) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Peters (1869) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Philippot et al. (2019) | 1 | 0,27% | 1 | 0,54% | 0 | 0% | 1 | 0,55% |
Porcel et al. (2021) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Prato et al. (2022) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Probst (1995) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Probst (1997) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Probst (1997) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Probst (2007) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Read et al. (2015) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Revuelta et al. (2015) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Reynolds & Henderson (2018) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Reynolds et al. (2014) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Rhodin & Carr (2009) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Rimblot et al. (1985) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Rocha et al. (2022) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Romero et al. (2010) | 1 | 0,27% | 1 | 0,54% | 0 | 0% | 1 | 0,55% |
Roos (2000) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Rüppell (1835) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Russel & Bauer (1986) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Russell & Bauer (1991) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Sadlier & Bauer (1997) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Sadlier & Bauer (1999) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Sadlier & Bauer (2002) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Sadlier et al. (2002) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Sadlier et al. (2014) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Schneider (1783) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Schneider (1799) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Schoepff (1792) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Schwaner & Brown (1984) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Schweigger (1812) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Seipp & Klemmer (1994) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Servan & Arvy (1997) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 0 | 0% |
Servan (1976) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Shaver et al. (2019) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Shea et al. (2021) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Shine & Gorian (2021) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Shine et al. (2012) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Shine et al. (2019) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Shine et al. (2019) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Shine et al. (2020) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Shine et al. (2021) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Shine et al. (2022) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Shine et al. (2022) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Shine et al. (2023) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Slavenko et al. (2021) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Snyder et al. (2019) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Sonsino (1893) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Steindachner (1870) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Stelfox et al. (2020) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Tan et al. (2019) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Tchékémian & Leleu (2024) | 1 | 0,27% | 1 | 0,54% | 0 | 0% | 1 | 0,55% |
Thibault et al. (2017) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Thibault et al. (2023) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Turpin & Probst (1997) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Udyawer et al. (2020) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Uicn et al. (2020) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
van den Burg et al. (2021) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Vandelli (1761) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Veysset (2003) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 0 | 0% |
Waayers et al. (2011) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Wallach (2009) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Wang & Qiu (2022) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Weerdt et al. (2021) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Wehsener & Noss (2022) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Werner (1898) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Werner (1899) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Werner (1910) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Werner (1980) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 1 | 0,55% |
Wied (1839) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Works & Olson (2018) | 1 | 0,27% | 1 | 0,54% | 1 | 0,55% | 0 | 0% |
Yokoyama (2012) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |