Reptiles des Antilles-Guyane
743 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
| Référence | Total | Valides | Espèces | Taxons terminaux | ||||
|---|---|---|---|---|---|---|---|---|
| nb | % | nb | % | nb | % | nb | % | |
| Hoff & Daszkiewicz (2001) | 221 | 25,67% | 137 | 41,27% | 109 | 44,86% | 103 | 36,92% |
| Uicn et al. (2017) | 170 | 19,74% | 150 | 45,18% | 150 | 61,73% | 111 | 39,78% |
| Henderson & Breuil (2012) | 125 | 14,52% | 76 | 22,89% | 61 | 25,1% | 67 | 24,01% |
| Massary et al. (2021) | 59 | 6,85% | 58 | 17,47% | 32 | 13,17% | 49 | 17,56% |
| Linnaeus (1758) | 57 | 6,62% | 6 | 1,81% | 5 | 2,06% | 3 | 1,08% |
| Breuil (2002) | 53 | 6,16% | 27 | 8,13% | 17 | 7% | 20 | 7,17% |
| Fraga & Carvalho (2021) | 47 | 5,46% | 44 | 13,25% | 44 | 18,11% | 31 | 11,11% |
| Hedges & Conn (2012) | 47 | 5,46% | 28 | 8,43% | 28 | 11,52% | 24 | 8,6% |
| Van Dijk et al. (2012) | 45 | 5,23% | 32 | 9,64% | 28 | 11,52% | 28 | 10,04% |
| Nicholson et al. (2012) | 41 | 4,76% | 28 | 8,43% | 13 | 5,35% | 25 | 8,96% |
| Mertens & Wermuth (1960) | 31 | 3,6% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dewynter et al. (2019) | 27 | 3,14% | 27 | 8,13% | 23 | 9,47% | 23 | 8,24% |
| Dewynter et al. (2022) | 25 | 2,9% | 25 | 7,53% | 25 | 10,29% | 22 | 7,89% |
| Dewynter et al. (2023) | 25 | 2,9% | 25 | 7,53% | 25 | 10,29% | 22 | 7,89% |
| Questel et al. (2023) | 25 | 2,9% | 25 | 7,53% | 25 | 10,29% | 22 | 7,89% |
| Questel et al. (2023) | 25 | 2,9% | 25 | 7,53% | 25 | 10,29% | 22 | 7,89% |
| Massary et al. (2017) | 24 | 2,79% | 20 | 6,02% | 19 | 7,82% | 17 | 6,09% |
| Dewynter et al. (2023) | 23 | 2,67% | 23 | 6,93% | 23 | 9,47% | 19 | 6,81% |
| Massary et al. (2018) | 22 | 2,56% | 20 | 6,02% | 19 | 7,82% | 17 | 6,09% |
| Questel (2020) | 22 | 2,56% | 22 | 6,63% | 20 | 8,23% | 21 | 7,53% |
| Breuil et al. (2010) | 19 | 2,21% | 15 | 4,52% | 14 | 5,76% | 13 | 4,66% |
| Dewynter et al. (2019) | 17 | 1,97% | 16 | 4,82% | 16 | 6,58% | 13 | 4,66% |
| Van Dijk et al. (2014) | 17 | 1,97% | 0 | 0% | 0 | 0% | 0 | 0% |
| Breuil (2009) | 16 | 1,86% | 11 | 3,31% | 11 | 4,53% | 8 | 2,87% |
| Uicn et al. (2015) | 16 | 1,86% | 16 | 4,82% | 16 | 6,58% | 16 | 5,73% |
| Questel & Le Quellec (2012) | 14 | 1,63% | 11 | 3,31% | 11 | 4,53% | 10 | 3,58% |
| Girard (2007) | 13 | 1,51% | 8 | 2,41% | 7 | 2,88% | 7 | 2,51% |
| Grazziotin et al. (2012) | 13 | 1,51% | 11 | 3,31% | 11 | 4,53% | 8 | 2,87% |
| Yokoyama (2013) | 11 | 1,28% | 9 | 2,71% | 9 | 3,7% | 8 | 2,87% |
| Adalsteinsson et al. (2009) | 10 | 1,16% | 3 | 0,9% | 3 | 1,23% | 3 | 1,08% |
| Dewynter et al. (2020) | 10 | 1,16% | 10 | 3,01% | 10 | 4,12% | 10 | 3,58% |
| Goicoechea et al. (2016) | 10 | 1,16% | 6 | 1,81% | 6 | 2,47% | 4 | 1,43% |
| Reynolds & Henderson (2018) | 10 | 1,16% | 8 | 2,41% | 7 | 2,88% | 6 | 2,15% |
| Bochaton et al. (2021) | 9 | 1,05% | 9 | 2,71% | 9 | 3,7% | 6 | 2,15% |
| González-sánchez et al. (2021) | 9 | 1,05% | 9 | 2,71% | 9 | 3,7% | 8 | 2,87% |
| Moraes-da-silva et al. (2021) | 9 | 1,05% | 9 | 2,71% | 9 | 3,7% | 5 | 1,79% |
| Spix (1825) | 9 | 1,05% | 3 | 0,9% | 3 | 1,23% | 3 | 1,08% |
| Lescure et al. (2012) | 8 | 0,93% | 7 | 2,11% | 6 | 2,47% | 6 | 2,15% |
| Massary et al. (2019) | 8 | 0,93% | 8 | 2,41% | 8 | 3,29% | 7 | 2,51% |
| Muratet (2015) | 8 | 0,93% | 8 | 2,41% | 7 | 2,88% | 7 | 2,51% |
| Probst et al. (2022) | 8 | 0,93% | 8 | 2,41% | 8 | 3,29% | 8 | 2,87% |
| Bernal & Dubois (2023) | 7 | 0,81% | 6 | 1,81% | 6 | 2,47% | 4 | 1,43% |
| Bour et al. (2008) | 7 | 0,81% | 6 | 1,81% | 6 | 2,47% | 5 | 1,79% |
| Camiñas et al. (2021) | 7 | 0,81% | 7 | 2,11% | 7 | 2,88% | 7 | 2,51% |
| Laurenti (1768) | 7 | 0,81% | 4 | 1,2% | 3 | 1,23% | 3 | 1,08% |
| Lazell (1964) | 7 | 0,81% | 0 | 0% | 0 | 0% | 0 | 0% |
| Muñoz et al. (2013) | 7 | 0,81% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pinto-coelho et al. (2021) | 7 | 0,81% | 5 | 1,51% | 5 | 2,06% | 2 | 0,72% |
| Probst (2001) | 7 | 0,81% | 6 | 1,81% | 6 | 2,47% | 5 | 1,79% |
| Schweigger (1812) | 7 | 0,81% | 0 | 0% | 0 | 0% | 0 | 0% |
| Souza-oliveira et al. (2024) | 7 | 0,81% | 6 | 1,81% | 6 | 2,47% | 4 | 1,43% |
| Spix (1824) | 7 | 0,81% | 1 | 0,3% | 1 | 0,41% | 0 | 0% |
| Casale et al. (2021) | 6 | 0,7% | 6 | 1,81% | 6 | 2,47% | 6 | 2,15% |
| Duméril & Bibron (1837) | 6 | 0,7% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fretey & Triplet (2022) | 6 | 0,7% | 6 | 1,81% | 6 | 2,47% | 6 | 2,15% |
| Hedges et al. (2014) | 6 | 0,7% | 3 | 0,9% | 3 | 1,23% | 3 | 1,08% |
| Lazell (1972) | 6 | 0,7% | 0 | 0% | 0 | 0% | 0 | 0% |
| Massary et al. (2020) | 6 | 0,7% | 6 | 1,81% | 6 | 2,47% | 6 | 2,15% |
| Ronot (2007) | 6 | 0,7% | 5 | 1,51% | 4 | 1,65% | 5 | 1,79% |
| Sayah et al. (2023) | 6 | 0,7% | 5 | 1,51% | 5 | 2,06% | 5 | 1,79% |
| Thomas (1964) | 6 | 0,7% | 5 | 1,51% | 0 | 0% | 5 | 1,79% |
| Arnold & Ovenden (2014) | 5 | 0,58% | 4 | 1,2% | 4 | 1,65% | 3 | 1,08% |
| Barbrour (1915) | 5 | 0,58% | 3 | 0,9% | 2 | 0,82% | 2 | 0,72% |
| Barrioz & Morinière (2007) | 5 | 0,58% | 5 | 1,51% | 5 | 2,06% | 5 | 1,79% |
| Bioinsight/diren & Guyane (2006) | 5 | 0,58% | 5 | 1,51% | 5 | 2,06% | 5 | 1,79% |
| Chevalier (2006) | 5 | 0,58% | 5 | 1,51% | 5 | 2,06% | 5 | 1,79% |
| Ciccione et al. (2011) | 5 | 0,58% | 5 | 1,51% | 5 | 2,06% | 5 | 1,79% |
| Crillon & Cuzange (2020) | 5 | 0,58% | 5 | 1,51% | 5 | 2,06% | 5 | 1,79% |
| Duffaut et al. (2011) | 5 | 0,58% | 5 | 1,51% | 5 | 2,06% | 5 | 1,79% |
| Entraygues (2014) | 5 | 0,58% | 5 | 1,51% | 5 | 2,06% | 5 | 1,79% |
| Étaix-bonnin et al. (2011) | 5 | 0,58% | 5 | 1,51% | 5 | 2,06% | 5 | 1,79% |
| Hamdan et al. (2023) | 5 | 0,58% | 5 | 1,51% | 5 | 2,06% | 3 | 1,08% |
| Ineich (2016) | 5 | 0,58% | 5 | 1,51% | 5 | 2,06% | 5 | 1,79% |
| Le Scao et al. (2011) | 5 | 0,58% | 5 | 1,51% | 5 | 2,06% | 5 | 1,79% |
| Maran & Frétey (2023) | 5 | 0,58% | 5 | 1,51% | 5 | 2,06% | 5 | 1,79% |
| Read et al. (2023) | 5 | 0,58% | 5 | 1,51% | 5 | 2,06% | 5 | 1,79% |
| Rhodin et al. (2017) | 5 | 0,58% | 3 | 0,9% | 3 | 1,23% | 3 | 1,08% |
| Routtier et al. (2023) | 5 | 0,58% | 5 | 1,51% | 5 | 2,06% | 1 | 0,36% |
| Sauvignet et al. (2000) | 5 | 0,58% | 5 | 1,51% | 5 | 2,06% | 5 | 1,79% |
| Schlegel (1837) | 5 | 0,58% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Schneider (1801) | 5 | 0,58% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Schwartz (1964) | 5 | 0,58% | 3 | 0,9% | 0 | 0% | 3 | 1,08% |
| Thorpe & Malhotra (2023) | 5 | 0,58% | 5 | 1,51% | 5 | 2,06% | 4 | 1,43% |
| Vieira (2022) | 5 | 0,58% | 5 | 1,51% | 5 | 2,06% | 2 | 0,72% |
| Yokoyama (2012) | 5 | 0,58% | 4 | 1,2% | 4 | 1,65% | 3 | 1,08% |
| Albuquerque et al. (2022) | 4 | 0,46% | 4 | 1,2% | 2 | 0,82% | 2 | 0,72% |
| Arredondo et al. (2020) | 4 | 0,46% | 3 | 0,9% | 3 | 1,23% | 3 | 1,08% |
| Bauer & Sadlier (2000) | 4 | 0,46% | 3 | 0,9% | 3 | 1,23% | 3 | 1,08% |
| Boie (1827) | 4 | 0,46% | 0 | 0% | 0 | 0% | 0 | 0% |
| Breuil (2013) | 4 | 0,46% | 2 | 0,6% | 2 | 0,82% | 1 | 0,36% |
| Carrasco et al. (2012) | 4 | 0,46% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Carvalho et al. (2023) | 4 | 0,46% | 4 | 1,2% | 4 | 1,65% | 3 | 1,08% |
| Cole & Dessauer (1993) | 4 | 0,46% | 4 | 1,2% | 4 | 1,65% | 4 | 1,43% |
| Daudin (1803) | 4 | 0,46% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dewynter et al. (2016) | 4 | 0,46% | 4 | 1,2% | 4 | 1,65% | 4 | 1,43% |
| Dewynter (2016) | 4 | 0,46% | 4 | 1,2% | 4 | 1,65% | 3 | 1,08% |
| Duméril et al. (1854) | 4 | 0,46% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fretey & Lescure (1999) | 4 | 0,46% | 4 | 1,2% | 4 | 1,65% | 4 | 1,43% |
| Hass (1991) | 4 | 0,46% | 4 | 1,2% | 4 | 1,65% | 3 | 1,08% |
| Kallel et al. (2018) | 4 | 0,46% | 3 | 0,9% | 3 | 1,23% | 2 | 0,72% |
| Köhler & Vesely (2011) | 4 | 0,46% | 4 | 1,2% | 4 | 1,65% | 4 | 1,43% |
| Lambert (1988) | 4 | 0,46% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Lescure et al. (2020) | 4 | 0,46% | 4 | 1,2% | 3 | 1,23% | 4 | 1,43% |
| Linné (1766) | 4 | 0,46% | 0 | 0% | 0 | 0% | 0 | 0% |
| Massary & Hoogmoed (2001) | 4 | 0,46% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Méheust et al. (2018) | 4 | 0,46% | 4 | 1,2% | 4 | 1,65% | 4 | 1,43% |
| Momont (1998) | 4 | 0,46% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Morinière & Dell'amico (2011) | 4 | 0,46% | 4 | 1,2% | 4 | 1,65% | 4 | 1,43% |
| Olson & Normand (2014) | 4 | 0,46% | 2 | 0,6% | 2 | 0,82% | 2 | 0,72% |
| Pellegrino et al. (2018) | 4 | 0,46% | 4 | 1,2% | 4 | 1,65% | 4 | 1,43% |
| Probst (1997) | 4 | 0,46% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Probst (1998) | 4 | 0,46% | 3 | 0,9% | 3 | 1,23% | 3 | 1,08% |
| Questel (2017) | 4 | 0,46% | 3 | 0,9% | 3 | 1,23% | 3 | 1,08% |
| Rivas et al. (2024) | 4 | 0,46% | 2 | 0,6% | 2 | 0,82% | 1 | 0,36% |
| Rojas-runjaic et al. (2021) | 4 | 0,46% | 4 | 1,2% | 4 | 1,65% | 4 | 1,43% |
| Sanchez (2020) | 4 | 0,46% | 4 | 1,2% | 4 | 1,65% | 2 | 0,72% |
| Souza (2020) | 4 | 0,46% | 4 | 1,2% | 4 | 1,65% | 4 | 1,43% |
| Starace (2013) | 4 | 0,46% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Tirvengadum & Bour (1985) | 4 | 0,46% | 3 | 0,9% | 3 | 1,23% | 3 | 1,08% |
| Almeida et al. (2022) | 3 | 0,35% | 3 | 0,9% | 3 | 1,23% | 2 | 0,72% |
| Bailon et al. (2015) | 3 | 0,35% | 2 | 0,6% | 2 | 0,82% | 2 | 0,72% |
| Blanc (1909) | 3 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bochaton & Hanot (2021) | 3 | 0,35% | 3 | 0,9% | 3 | 1,23% | 2 | 0,72% |
| Bochaton et al. (2016) | 3 | 0,35% | 3 | 0,9% | 3 | 1,23% | 2 | 0,72% |
| Bochaton et al. (2017) | 3 | 0,35% | 3 | 0,9% | 3 | 1,23% | 3 | 1,08% |
| Bonnaterre (1789) | 3 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bour (2006) | 3 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
| Brunes et al. (2021) | 3 | 0,35% | 2 | 0,6% | 2 | 0,82% | 0 | 0% |
| Carvalho et al. (2015) | 3 | 0,35% | 3 | 0,9% | 3 | 1,23% | 3 | 1,08% |
| Carvalho et al. (2016) | 3 | 0,35% | 3 | 0,9% | 3 | 1,23% | 3 | 1,08% |
| Champagne et al. (1997) | 3 | 0,35% | 3 | 0,9% | 2 | 0,82% | 3 | 1,08% |
| Cope (1868) | 3 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
| Delcroix et al. (2011) | 3 | 0,35% | 3 | 0,9% | 3 | 1,23% | 3 | 1,08% |
| Dubief & Gallais (2011) | 3 | 0,35% | 3 | 0,9% | 3 | 1,23% | 3 | 1,08% |
| Duméril & Bibron (1836) | 3 | 0,35% | 2 | 0,6% | 1 | 0,41% | 1 | 0,36% |
| Gamble et al. (2011) | 3 | 0,35% | 2 | 0,6% | 2 | 0,82% | 2 | 0,72% |
| Giovannotti et al. (2017) | 3 | 0,35% | 2 | 0,6% | 2 | 0,82% | 2 | 0,72% |
| Girondot (2011) | 3 | 0,35% | 3 | 0,9% | 3 | 1,23% | 3 | 1,08% |
| Henderson & Powell (2009) | 3 | 0,35% | 1 | 0,3% | 1 | 0,41% | 0 | 0% |
| Jadin et al. (2014) | 3 | 0,35% | 2 | 0,6% | 2 | 0,82% | 2 | 0,72% |
| Jan (1863) | 3 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kemp (2023) | 3 | 0,35% | 3 | 0,9% | 3 | 1,23% | 2 | 0,72% |
| La Cepède (1789) | 3 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lescure (2018) | 3 | 0,35% | 3 | 0,9% | 3 | 1,23% | 3 | 1,08% |
| Macculloch et al. (2009) | 3 | 0,35% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Martins et al. (2019) | 3 | 0,35% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Merrem (1820) | 3 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
| Miralles & Carranza (2010) | 3 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
| Miralles et al. (2017) | 3 | 0,35% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Mothes et al. (2019) | 3 | 0,35% | 2 | 0,6% | 2 | 0,82% | 2 | 0,72% |
| Oliveira et al. (2016) | 3 | 0,35% | 3 | 0,9% | 2 | 0,82% | 2 | 0,72% |
| Poisson (1999) | 3 | 0,35% | 3 | 0,9% | 3 | 1,23% | 3 | 1,08% |
| Pomar-gómez et al. (2021) | 3 | 0,35% | 3 | 0,9% | 3 | 1,23% | 2 | 0,72% |
| Probst et al. (2000) | 3 | 0,35% | 3 | 0,9% | 3 | 1,23% | 3 | 1,08% |
| Rodríguez-rodríguez & Calderón-espinosa (2024) | 3 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
| Roughgarden (1995) | 3 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
| Roux (1913) | 3 | 0,35% | 2 | 0,6% | 2 | 0,82% | 2 | 0,72% |
| Surget-Groba & Thorpe (2013) | 3 | 0,35% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Thorpe et al. (2008) | 3 | 0,35% | 2 | 0,6% | 2 | 0,82% | 1 | 0,36% |
| van den Burg et al. (2021) | 3 | 0,35% | 2 | 0,6% | 2 | 0,82% | 1 | 0,36% |
| Vidal et al. (1999) | 3 | 0,35% | 3 | 0,9% | 3 | 1,23% | 3 | 1,08% |
| Vidal et al. (2010) | 3 | 0,35% | 2 | 0,6% | 2 | 0,82% | 2 | 0,72% |
| Wagler (1830) | 3 | 0,35% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Wallach (2020) | 3 | 0,35% | 2 | 0,6% | 2 | 0,82% | 2 | 0,72% |
| Baldi et al. (2022) | 2 | 0,23% | 2 | 0,6% | 2 | 0,82% | 2 | 0,72% |
| Balle et al. (2021) | 2 | 0,23% | 2 | 0,6% | 2 | 0,82% | 2 | 0,72% |
| Bance (2022) | 2 | 0,23% | 2 | 0,6% | 2 | 0,82% | 2 | 0,72% |
| Barbour & Noble (1915) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Barré et al. (2016) | 2 | 0,23% | 1 | 0,3% | 1 | 0,41% | 0 | 0% |
| Bauer (1987) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Behm et al. (2019) | 2 | 0,23% | 2 | 0,6% | 2 | 0,82% | 2 | 0,72% |
| Bernarde et al. (2021) | 2 | 0,23% | 2 | 0,6% | 2 | 0,82% | 0 | 0% |
| Blanc et al. (1993) | 2 | 0,23% | 2 | 0,6% | 2 | 0,82% | 2 | 0,72% |
| Bochaton & Bailon (2018) | 2 | 0,23% | 2 | 0,6% | 2 | 0,82% | 2 | 0,72% |
| Bochaton et al. (2018) | 2 | 0,23% | 2 | 0,6% | 2 | 0,82% | 2 | 0,72% |
| Bochaton et al. (2021) | 2 | 0,23% | 2 | 0,6% | 2 | 0,82% | 2 | 0,72% |
| Bourgade (2021) | 2 | 0,23% | 2 | 0,6% | 2 | 0,82% | 2 | 0,72% |
| Brasileiro (2021) | 2 | 0,23% | 2 | 0,6% | 2 | 0,82% | 2 | 0,72% |
| Breuil (2013) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Breuil (2021) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cadle (2009) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Camurugi et al. (2022) | 2 | 0,23% | 2 | 0,6% | 2 | 0,82% | 2 | 0,72% |
| Censky & Paulson (1992) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cheke (1987) | 2 | 0,23% | 2 | 0,6% | 2 | 0,82% | 2 | 0,72% |
| Cheke (2010) | 2 | 0,23% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Cheon et al. (2023) | 2 | 0,23% | 2 | 0,6% | 0 | 0% | 2 | 0,72% |
| Chevallier et al. (2023) | 2 | 0,23% | 2 | 0,6% | 2 | 0,82% | 2 | 0,72% |
| Clarac et al. (2024) | 2 | 0,23% | 2 | 0,6% | 2 | 0,82% | 2 | 0,72% |
| Cope (1860) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cope (1864) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cope (1869) | 2 | 0,23% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Correa & Artigas (1978) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Costa et al. (2022) | 2 | 0,23% | 2 | 0,6% | 1 | 0,41% | 1 | 0,36% |
| Cuvier (1829) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dal Vechioet al. (2021) | 2 | 0,23% | 2 | 0,6% | 2 | 0,82% | 2 | 0,72% |
| D'angiolella et al. (2011) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Daudin (1801) | 2 | 0,23% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Daudin (1802) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Daudin (1802) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| de Massary et al. (2015) | 2 | 0,23% | 1 | 0,3% | 1 | 0,41% | 0 | 0% |
| Duguy et al. (2003) | 2 | 0,23% | 2 | 0,6% | 2 | 0,82% | 2 | 0,72% |
| Duguy et al. (2004) | 2 | 0,23% | 2 | 0,6% | 2 | 0,82% | 2 | 0,72% |
| Duguy (1992) | 2 | 0,23% | 2 | 0,6% | 2 | 0,82% | 2 | 0,72% |
| Duméril et al. (1870-1909) | 2 | 0,23% | 1 | 0,3% | 1 | 0,41% | 0 | 0% |
| Fernandes et al. (2004) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Franzini et al. (2018) | 2 | 0,23% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Freitas (1958) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fritz & Havaš (2007) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gasc & Rodrigues (1979) | 2 | 0,23% | 2 | 0,6% | 2 | 0,82% | 2 | 0,72% |
| Gasc & Rodrigues (1979) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Girondo (2023) | 2 | 0,23% | 2 | 0,6% | 2 | 0,82% | 2 | 0,72% |
| Gomés et al. (2018) | 2 | 0,23% | 2 | 0,6% | 1 | 0,41% | 2 | 0,72% |
| Gray (1851) | 2 | 0,23% | 2 | 0,6% | 1 | 0,41% | 1 | 0,36% |
| Harvey (2008) | 2 | 0,23% | 2 | 0,6% | 2 | 0,82% | 2 | 0,72% |
| Havery et al. (2018) | 2 | 0,23% | 2 | 0,6% | 2 | 0,82% | 2 | 0,72% |
| Hedges et al. (2016) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jadin et al. (2020) | 2 | 0,23% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Jourdan (2020) | 2 | 0,23% | 2 | 0,6% | 1 | 0,41% | 1 | 0,36% |
| Jowers et al. (2013) | 2 | 0,23% | 2 | 0,6% | 2 | 0,82% | 2 | 0,72% |
| Klaczko et al. (2010) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| La Cepède (1788) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lidth de Jeude (1904) | 2 | 0,23% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Lorvelec et al. (2021) | 2 | 0,23% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Maciel et al. (2024) | 2 | 0,23% | 2 | 0,6% | 2 | 0,82% | 2 | 0,72% |
| Martins et al. (2023) | 2 | 0,23% | 2 | 0,6% | 2 | 0,82% | 2 | 0,72% |
| Melo-sampaio et al. (2019) | 2 | 0,23% | 2 | 0,6% | 2 | 0,82% | 2 | 0,72% |
| Moravec et al. (2018) | 2 | 0,23% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Murphy et al. (1978) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Murphy et al. (2019) | 2 | 0,23% | 2 | 0,6% | 2 | 0,82% | 0 | 0% |
| Myers & Cadle (1994) | 2 | 0,23% | 2 | 0,6% | 2 | 0,82% | 2 | 0,72% |
| Oliver (2011) | 2 | 0,23% | 2 | 0,6% | 2 | 0,82% | 2 | 0,72% |
| Passos et al. (2004) | 2 | 0,23% | 2 | 0,6% | 2 | 0,82% | 2 | 0,72% |
| Peron (2014) | 2 | 0,23% | 2 | 0,6% | 2 | 0,82% | 2 | 0,72% |
| Peters (1863) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Probst et al. (2001) | 2 | 0,23% | 2 | 0,6% | 2 | 0,82% | 2 | 0,72% |
| Questel (2011) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rhodin & Carr (2009) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ribeiro-júnior et al. (2020) | 2 | 0,23% | 2 | 0,6% | 2 | 0,82% | 2 | 0,72% |
| Rinaldi et al. (2011) | 2 | 0,23% | 2 | 0,6% | 2 | 0,82% | 2 | 0,72% |
| Rojas-morales et al. (2021) | 2 | 0,23% | 2 | 0,6% | 2 | 0,82% | 0 | 0% |
| Roughgarden (1974) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sanchez & Probst (2016) | 2 | 0,23% | 2 | 0,6% | 2 | 0,82% | 2 | 0,72% |
| Sanchez et al. (2019) | 2 | 0,23% | 2 | 0,6% | 2 | 0,82% | 2 | 0,72% |
| Santos (2003) | 2 | 0,23% | 2 | 0,6% | 2 | 0,82% | 2 | 0,72% |
| Schneider (1783) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Schwartz & Thomas (1975) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sentzen (1796) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Shaw (1802) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Silva (2022) | 2 | 0,23% | 2 | 0,6% | 2 | 0,82% | 2 | 0,72% |
| Silveira & Magnusson (1999) | 2 | 0,23% | 2 | 0,6% | 2 | 0,82% | 2 | 0,72% |
| Spix (1824) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Starace (1995) | 2 | 0,23% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Thawley & Kolbe (2020) | 2 | 0,23% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Thorpe et al. (2010) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Thunberg (1787) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Torres-ramírez et al. (2021) | 2 | 0,23% | 2 | 0,6% | 2 | 0,82% | 1 | 0,36% |
| Troschel (1848) | 2 | 0,23% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Turpin et al. (2001) | 2 | 0,23% | 1 | 0,3% | 0 | 0% | 1 | 0,36% |
| van den Burg et al. (2021) | 2 | 0,23% | 2 | 0,6% | 2 | 0,82% | 2 | 0,72% |
| Villanueva et al. (2021) | 2 | 0,23% | 2 | 0,6% | 2 | 0,82% | 0 | 0% |
| Vuillaume et al. (2015) | 2 | 0,23% | 2 | 0,6% | 2 | 0,82% | 2 | 0,72% |
| Wallach et al. (2014) | 2 | 0,23% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Wied (1825) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Yuki (1993) | 2 | 0,23% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Abhaya & Probst (2003) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Abhaya & Probst (2009) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Abhaya et al. (1998) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 0 | 0% |
| Agarwal et al. (2021) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Agassiz (1857) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Agostini et al. (2023) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Albuquerque & Fernandes (2022) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 0 | 0% |
| Albuquerque et al. (2018) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Albuquerque et al. (2019) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Al-hasson & Ali (2020) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Almeida & Vasconcelos (2023) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Almeida et al. (2019) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Amaral et al. (2019) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Anaissi & Costa-campos (2021) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Anaissi & Costa-campos (2021) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Andersson (1918) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Angin (2017) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Angin (2017) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Anonyme (ICZN) (2019) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anonyme. (2004) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Antonini et al. (2023) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Aquarium de La Rochelle (2017) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Armand & Ferlay (2023) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Astudillo et al. (2021) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 0 | 0% |
| Asztalos et al. (2020) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Auguste et al. (2019) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Avila-pires et al. (2013) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Bailey & Carvalho (1946) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bailey et al. (2023) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Baker & Allain (2020) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Baldi et al. (2023) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Barbancey & Probst (1998) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 0 | 0% |
| Barbancey (2001) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Barbancey (2001) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Barbour (1914) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bassett (2022) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bauer & Sadlier (1994) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Bauer et al. (2010) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Bauer et al. (2024) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Becerra et al. (2024) | 1 | 0,12% | 1 | 0,3% | 0 | 0% | 1 | 0,36% |
| Behm et al. (2022) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bell (1827) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Bell (1827) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Benício (2021) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Bertrand & Drogou (2000) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Bertrand et al. (2001) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Bochaton et al. (2016) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Bochaton et al. (2017) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bochaton et al. (2020) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bonnaterre (1790) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bonnet et al. (1999) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Borcyk et al. (2023) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 0 | 0% |
| Borroto-páez (2018) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Boulenger (1887) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Boulenger (1891) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 0 | 0% |
| Boulenger (1896) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Boulenger (1912) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bour (1973) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bourgade (2013) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Bourgade (2020) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Bourgade (2020) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Brasileiro et al. (2023) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Breuil & Ibéné (2008) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Breuil & Serre-collet (2012) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Breuil et al. (2022) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 0 | 0% |
| Breuil (1999) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Brito-gitirana et al. (2019) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Brongersma (1928) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Burger (1955) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Burneleau (1983) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Busack & Pandya (2001) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Bush et al. (2021) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Caceres (2002) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Cáceres-martínez et al. (2020) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Caldeira Costa et al. (2009) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Camayo & Zúñiga-baos (2023) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 0 | 0% |
| Campos et al. (2024) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Capalleras & Carretero (2000) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 0 | 0% |
| Carpio et al. (2022) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Carvajal-ocampo et al. (2019) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Caut & Jowers (2015) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Caut et al. (2019) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Cavalcante et al. (2022) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 0 | 0% |
| CEN Nouvelle-Calédonie (2021) | 1 | 0,12% | 1 | 0,3% | 0 | 0% | 1 | 0,36% |
| Censky (1988) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Chambault et al. (2020) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Chevallier et al. (2024) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Chevreux & de Guerne (1893) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Chippaux (1986) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Chocobar et al. (2023) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Chua (2018) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Ciccione (2001) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Ciccione (2001) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Cochran (1938) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Coélho et al. (2019) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 0 | 0% |
| Colin (1992) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Collazos-astudillo et al. (2022) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Cope (1864) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cope (1879) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cope (1894) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cornuaille et al. (2021) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Costa et al. (2013) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Costal-oliveira et al. (2019) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Cummings et al. (2021) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Cunha et al. (2019) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Cunha et al. (2021) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Cunha (1970) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Curcio et al. (2011) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cuvier & Voigt (1832) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Cuvier (1807) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Le règne animal distribué d'après son organisation, pour servir de base à l'histoire naturelle des animaux et d'introduction à l'anatomie comparée. Tome 2, contenant les reptiles, les poissons, les mollusques et les annélides. Déterville, Paris. i-xviii+1-532 pp. ">Cuvier (1816) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Da Silva et al. (2018) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Dal Vechio et al. (2015) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Dal Zotto et al. (2024) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Dalleau et al. (2014) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| D´angiolella et al. (2021) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Daudin (1803) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Daudin (1803) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dauvin (1990) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| David et al. (2002) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| de Andrade (2019) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 0 | 0% |
| De Carvalho et al. (2018) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 0 | 0% |
| Delafontaine et al. (2018) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Delaney & Warner (2017) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Delcroix et al. (2008) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Deliveyne et al. (2023) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 0 | 0% |
| Dewynter & Rufray (2012) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Dewynter & Surugue (2012) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Dewynter et al. (2015) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Dewynter et al. (2019) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Diaz-ricaurte et al. (2018) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 0 | 0% |
| Dixon et al. (1993) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dixon (1983) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dubois et al. (2024) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dueñas et al. (2021) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 0 | 0% |
| Duguy (1983) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Duméril & Bibron (1839) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Duméril & Bibron (1839) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Duméril & Bribron (1835) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Duméril et al. (1854) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dunn & Conant (1936) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Duval et al. (2019) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Eiselt (1963) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Entiauspe-neto & Loebmann (2019) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Entiauspe-neto et al. (2018) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Eschscholtz (1829) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Etheridge (1964) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Fagundes et al. (2021) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Farias et al. (2019) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Fernandes et al. (2023) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Feuillet et al. (2010) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Ficetola & Scali (2010) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 0 | 0% |
| Fieldsend et al. (2021) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| França & França (2019) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 0 | 0% |
| França et al. (2019) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Francisco et al. (2018) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Franco & Ferreira (2003) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Franzen (1996) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Franzini et al. (2019) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Fretey & Bour (1980) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Fretey et al. (2023) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Fretey (1980) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Fretey (1987) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Fretey (2003) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Frétey (2019) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Frétey (2022) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Frétey (2023) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Fritz et al. (2010) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Fritz et al. (2020) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fujishima (2021) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Gans (1963) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| García-ayachi et al. (2020) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| García-cobos et al. (2021) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Gargominy et al. (1996) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Garman (1880) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Garman (1887) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Garman (1887) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Geneva et al. (2013) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Gérigny et al. (2020) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Gill (1995) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Gomès & Ibéné (2013) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 0 | 0% |
| Gomes et al. (2020) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| González et al. (2018) | 1 | 0,12% | 1 | 0,3% | 0 | 0% | 1 | 0,36% |
| Gouillard (1973) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Goyannes-araújo et al. (2009) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Graboski et al. (2018) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Graitson et al. (2012) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Grant (1958) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Gray (1831) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gray (1849) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Gray (1863) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gray (1873) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Griffin (1917) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Grisales-martínez & Arias-alvarez (2018) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Gros-désormeaux et al. (2017) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Guichenot (1855) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Guilhon et al. (2024) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Guilhon (2023) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Guiller & Vacher (2022) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Gunderson et al. (2020) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Günther (1860) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Günther (1868) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Günther (1872) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hamdan et al. (2014) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Hedges et al. (2009) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hedges (2008) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hedges (2011) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Hellebuyck et al. (2017) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Henao-osorio et al. (2021) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Henderson & Powell (2006) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 0 | 0% |
| Henderson et al. (1993) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Hermann (1804) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Herrera-alzate (2023) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Herron et al. (1990) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Herzberg (2018) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Hoge & Romano (1969) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Holbrook (1836) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hoogmoed & Lescure (1975) | 1 | 0,12% | 1 | 0,3% | 0 | 0% | 1 | 0,36% |
| Hoogmoed (1977) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Houttuyn (1782) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Howard et al. (2001) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Howell & Clements (2019) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hudson et al. (2019) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| ICZN (2010) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Iković et al. (2023) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 0 | 0% |
| Ineich & Bauer (1992) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ineich & Giraud (2019) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Ineich & Massary (1997) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Ineich et al. (2017) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Ineich et al. (2019) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Ineich (1999) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Ineich (2015) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Jadin et al. (2021) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Jairam & Jairam-doerga (2015) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Jairam et al. (2016) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Jan (1858) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jared et al. (2023) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Jeimi et al. (2008) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Jim et al. (2022) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Johansson et al. (2013) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jowers et al. (2020) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 0 | 0% |
| Judson et al. (2018) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Kadafi et al. (2024) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Karaa et al. (2016) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Karin et al. (2021) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| King (1962) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Klauber (1939) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Koleska & Jablonski (2018) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Kollarits et al. (2013) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kornilev et al. (2020) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 0 | 0% |
| Kuhl (1820) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Kwet (2013) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lazell (1964) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lazell (1994) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lédée & Questel (2013) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Legouez (2010) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Leimroth et al. (2022) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Leite et al. (2021) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Lema & Albuquerque (2010) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Lema et al. (2017) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lescure et al. (2016) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Lichtenstein & Martens (1856) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lichtenstein (1823) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Liebart et al. (2021) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Liebgold et al. (2019) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Lima et al. (2019) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 0 | 0% |
| Lima et al. (2022) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Lock & Griffiths (2022) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Loisier et al. (2021) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| López (2023) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Lorvelec & Pascal (2009) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Lorvelec & Pascal (2009) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Lorvelec et al. (2009) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Lorvelec et al. (2011) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Lorvelec et al. (2013) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Lorvelec et al. (2016) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Lorvelec et al. (2017) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Lorvelec et al. (2017) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Lorvelec (2011) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Louisin & Probst (1996) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Lowe et al. (2007) | 1 | 0,12% | 1 | 0,3% | 0 | 0% | 1 | 0,36% |
| Maciel et al. (2021) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Mageski et al. (2017) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Maillard & David (2014) | 1 | 0,12% | 1 | 0,3% | 0 | 0% | 1 | 0,36% |
| Marinho (2022) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Marioni et al. (2019) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Marques-souza et al. (2018) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Marques-souza et al. (2022) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Marquis et al. (2020) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Maschio et al. (2021) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 0 | 0% |
| Massary & Ineich (1997) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Massary & Ineich (1999) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Massary et al. (2000) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Massary et al. (2001) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Massary (1999) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Massary (2012) | 1 | 0,12% | 1 | 0,3% | 0 | 0% | 1 | 0,36% |
| Matz (2005) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mendoça et al. (2016) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Meneses et al. (2019) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 0 | 0% |
| Mesquita et al. (2020) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Métrailler (2007) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Meyen (1834) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Miller (1779) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Miralles et al. (2005) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Montingelli et al. (2019) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Moon & Kamath (2019) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Morales et al. (2020) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Moreau de Jonnès (1816) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Moreau de Jonnès (1818) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Müller (1923) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Müller 1924 | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Murphy et al. (2020) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Naveda-rodríguez et al. (2020) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Oliveira et al. (2018) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Oliveira et al. (2021) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Oliveira (2023) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Oliveira-souza et al. (2021) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| O'shaughnessy (1881) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Paré & Lorvelec (2012) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 0 | 0% |
| Parker (1935) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Parker (1936) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Parmentier et al. (2017) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Pascal et al. 2006 | 1 | 0,12% | 1 | 0,3% | 0 | 0% | 1 | 0,36% |
| Passos & Fernandes (2008) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Passos et al. (2022) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Pérez-delgadillo & Lara-reséndiz (2024) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Monatsberichte der königlich Akademie der Wissenschaften zu Berlin, 1857: 402.">Peters (1858) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cercosaura und die mit dieser Gattung verwandten Eidechsen aus Südamerika. Abhandlungen der Königlichen Akademie der Wissenschaften zu Berlin, 1862: 165-225.">Peters (1863) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Peters (1867) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Peters (1869) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pinto & Fernandes (2012) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pinto & Fernandes (2017) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Pinto et al. (2019) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Pinto et al. (2023) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Portilla & Lamus (2020) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Powell et al. (2021) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Prato et al. (2022) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Prémel et al. (2022) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 0 | 0% |
| Probst & Deso (2001) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Probst et al. (2023) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Probst (1997) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Probst (1999) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 0 | 0% |
| Probst (2001) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Probst (2007) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Puissauve, Cohen & De Massary (2015) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Quah & Grismer (2024) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Questel & Boggio (2012) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Questel & Boggio (2012) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Questel & Vitry (2012) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Questel et al. (2012) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Questel (2011) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Questel (2012) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Questel (2012) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Questel (2013) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Questel (2018) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 0 | 0% |
| Quiñones-betancourt et al. (2018) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Quintana et al. (2021) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Quintana (2017) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Quinteros-muñoz & Aguayo (2021) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 0 | 0% |
| Raddi (1820) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ramalho et al. (2024) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Read et al. (2015) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Recoder et al. (2018) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Regio & Pontes (2020) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 0 | 0% |
| Reinert et al. (2021) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 0 | 0% |
| Renner (2002) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Réserve Naturelle de Saint Barthélemy (2014) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Résière et al. (2018) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Reuss (1834) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Revuelta et al. (2015) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Ribeiro-júnior et al. (2019) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Richmond (1966) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rimblot et al. (1985) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Rivas et al. (2023) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 0 | 0% |
| Roberto et al. (2021) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 0 | 0% |
| Rocha et al. (2023) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Rocha et al. (2024) | 1 | 0,12% | 1 | 0,3% | 0 | 0% | 1 | 0,36% |
| Rodrigues et al. (2021) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Rojas-morales et al. (2021) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Rojas-runjaic et al. (2024) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Romero et al. (2010) | 1 | 0,12% | 1 | 0,3% | 0 | 0% | 1 | 0,36% |
| Romero-marcucci et al. (2024) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Roos (2000) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Rösler et al. (2019) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Roux (1929) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rufray et al. (2015) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Rufz (1859 | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Ruibal (1952) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rüppell (1835) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Russell & Bauer (2002) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Ruthven (1916) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sanches et al. (2019) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Sanches et al. (2020) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Sanchez et al. (2017) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 0 | 0% |
| Santana & Teixeira (2020) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Savage (2011) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Schlegel (1839) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Schmidt & Walker (1943) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Schmidt (1928) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Schriften der Gesellschaft Naturforschender Freunde zu Berlin, 10(3): 259-283.">Schneider (1792) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Schnell & Swierk (2021) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Schoepff (1792) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Schultze et al. (2020) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Schwartz & Henderson (1991) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Scopoli (1788) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Serrano & Díaz-ricaurte (2018) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 0 | 0% |
| Servan & Arvy (1997) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 0 | 0% |
| Servan (1976) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Shaver et al. (2019) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Silva & Farias (2019) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Silva et al. (2003) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Silva et al. (2019) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Silva et al. (2021) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Silva et al. (2022) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Snyder et al. (2019) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Sousa et al. (2021) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Sousa (2019) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Sparrman (1784) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Spix (1824) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Starace (1997) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Stelfox et al. (2020) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Stephan (2011) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Suckow (1798) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sulton (2020) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Tan (2024) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Tavares-pinheiro et al. (2021) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Tavares-pinheiro et al. (2021) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Thawley et al. (2019) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Thibault et al. (2023) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Thomas et al. (2021) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Thorbjarnarson (2010) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Thorpe & Stenson (2003) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Toohey et al. (2022) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Torres Bonilla (2018) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 0 | 0% |
| Torres-carvajal et al. (2020) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 0 | 0% |
| Townsend et al. (2000) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Tschudi (1845) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Turpin & Probst (1998) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 0 | 0% |
| Uicn et al. (2020) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Valencia & Garzon-tello (2018) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Van Den Burg et al. (2018) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Van den Burg et al. (2020) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Van den burg et al. (2022) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Vandelli (1761) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Vanzolini (1978) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Vargas-ramírez et al. (2020) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Vasconcelos et al. (2006) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Vasconcelos Neto (2020) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Vásquez-cruz & Kelly-hernández (2024) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Venegas-anaya et al. (2008) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Veysset (2003) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 0 | 0% |
| Vieira et al. (2023) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Vieira (2023) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Vogt et al. (2013) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Von May et al. (2019) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 0 | 0% |
| Von May et al. (2021) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Waayers et al. (2011) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Wallach (2009) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Wang & Qiu (2022) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Wasilewski et al. (2022) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 0 | 0% |
| Wells & Herberg (2019) | 1 | 0,12% | 1 | 0,3% | 0 | 0% | 1 | 0,36% |
| Werner (1924) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Werner (1980) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Weterings & Vetter (2017) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Wied (1839) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Wied-Neuwied (1824) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Wied-neuwied (1821) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Wiegmann (1834) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Wiest (1978) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Williams et al. (2019) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Wilson & Mata-silva (2015) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 0 | 0% |
| Works & Olson (2018) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 0 | 0% |
| Wucherer (1861) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Wüster et al. (2002) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Yengle (2021) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Zaher & Prudente (1999) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Zambrano et al. (2022) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| Zdunek (2022) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
| (2022) | 1 | 0,12% | 1 | 0,3% | 1 | 0,41% | 0 | 0% |
