Reptiles des Antilles-Guyane
816 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 | 25,06% | 137 | 41,14% | 109 | 44,67% | 103 | 36,79% |
Uicn et al. (2017) | 170 | 19,27% | 150 | 45,05% | 150 | 61,48% | 111 | 39,64% |
Henderson & Breuil (2012) | 125 | 14,17% | 76 | 22,82% | 61 | 25% | 67 | 23,93% |
Massary et al. (2021) | 59 | 6,69% | 58 | 17,42% | 32 | 13,11% | 49 | 17,5% |
Linnaeus (1758) | 57 | 6,46% | 6 | 1,8% | 5 | 2,05% | 3 | 1,07% |
Breuil (2002) | 53 | 6,01% | 27 | 8,11% | 17 | 6,97% | 20 | 7,14% |
Fraga & Carvalho (2021) | 47 | 5,33% | 44 | 13,21% | 44 | 18,03% | 31 | 11,07% |
Hedges & Conn (2012) | 47 | 5,33% | 28 | 8,41% | 28 | 11,48% | 24 | 8,57% |
Van Dijk et al. (2012) | 45 | 5,1% | 32 | 9,61% | 28 | 11,48% | 28 | 10% |
Nicholson et al. (2012) | 41 | 4,65% | 28 | 8,41% | 13 | 5,33% | 25 | 8,93% |
Mertens & Wermuth (1960) | 31 | 3,51% | 0 | 0% | 0 | 0% | 0 | 0% |
Dewynter et al. (2022) | 28 | 3,17% | 27 | 8,11% | 25 | 10,25% | 24 | 8,57% |
Dewynter et al. (2019) | 27 | 3,06% | 27 | 8,11% | 23 | 9,43% | 23 | 8,21% |
Dewynter et al. (2023) | 26 | 2,95% | 26 | 7,81% | 25 | 10,25% | 23 | 8,21% |
Questel et al. (2023) | 26 | 2,95% | 26 | 7,81% | 25 | 10,25% | 23 | 8,21% |
Questel et al. (2023) | 25 | 2,83% | 25 | 7,51% | 25 | 10,25% | 22 | 7,86% |
Massary et al. (2017) | 24 | 2,72% | 20 | 6,01% | 19 | 7,79% | 17 | 6,07% |
Dewynter et al. (2023) | 23 | 2,61% | 23 | 6,91% | 23 | 9,43% | 19 | 6,79% |
Massary et al. (2018) | 22 | 2,49% | 20 | 6,01% | 19 | 7,79% | 17 | 6,07% |
Questel (2020) | 22 | 2,49% | 22 | 6,61% | 20 | 8,2% | 21 | 7,5% |
Breuil et al. (2010) | 19 | 2,15% | 15 | 4,5% | 14 | 5,74% | 13 | 4,64% |
Dewynter et al. (2019) | 17 | 1,93% | 16 | 4,8% | 16 | 6,56% | 13 | 4,64% |
Van Dijk et al. (2014) | 17 | 1,93% | 0 | 0% | 0 | 0% | 0 | 0% |
Breuil (2009) | 16 | 1,81% | 11 | 3,3% | 11 | 4,51% | 8 | 2,86% |
Uicn et al. (2015) | 16 | 1,81% | 16 | 4,8% | 16 | 6,56% | 16 | 5,71% |
Szpigel (2024) | 15 | 1,7% | 13 | 3,9% | 13 | 5,33% | 11 | 3,93% |
Questel & Le Quellec (2012) | 14 | 1,59% | 11 | 3,3% | 11 | 4,51% | 10 | 3,57% |
Girard (2007) | 13 | 1,47% | 8 | 2,4% | 7 | 2,87% | 7 | 2,5% |
Grazziotin et al. (2012) | 13 | 1,47% | 11 | 3,3% | 11 | 4,51% | 8 | 2,86% |
Yokoyama (2013) | 11 | 1,25% | 9 | 2,7% | 9 | 3,69% | 8 | 2,86% |
Adalsteinsson et al. (2009) | 10 | 1,13% | 3 | 0,9% | 3 | 1,23% | 3 | 1,07% |
Dewynter et al. (2020) | 10 | 1,13% | 10 | 3% | 10 | 4,1% | 10 | 3,57% |
Goicoechea et al. (2016) | 10 | 1,13% | 6 | 1,8% | 6 | 2,46% | 4 | 1,43% |
Reynolds & Henderson (2018) | 10 | 1,13% | 8 | 2,4% | 7 | 2,87% | 6 | 2,14% |
Bochaton et al. (2021) | 9 | 1,02% | 9 | 2,7% | 9 | 3,69% | 6 | 2,14% |
González-sánchez et al. (2021) | 9 | 1,02% | 9 | 2,7% | 9 | 3,69% | 8 | 2,86% |
Moraes-da-silva et al. (2021) | 9 | 1,02% | 9 | 2,7% | 9 | 3,69% | 5 | 1,79% |
Spix (1825) | 9 | 1,02% | 3 | 0,9% | 3 | 1,23% | 3 | 1,07% |
Laurenti (1768) | 8 | 0,91% | 4 | 1,2% | 3 | 1,23% | 3 | 1,07% |
Lescure et al. (2012) | 8 | 0,91% | 7 | 2,1% | 6 | 2,46% | 6 | 2,14% |
Massary et al. (2019) | 8 | 0,91% | 8 | 2,4% | 8 | 3,28% | 7 | 2,5% |
Muratet (2015) | 8 | 0,91% | 8 | 2,4% | 7 | 2,87% | 7 | 2,5% |
Probst et al. (2022) | 8 | 0,91% | 8 | 2,4% | 8 | 3,28% | 8 | 2,86% |
Bernal & Dubois (2023) | 7 | 0,79% | 6 | 1,8% | 6 | 2,46% | 4 | 1,43% |
Bour et al. (2008) | 7 | 0,79% | 6 | 1,8% | 6 | 2,46% | 5 | 1,79% |
Busala et al. (2024) | 7 | 0,79% | 4 | 1,2% | 3 | 1,23% | 3 | 1,07% |
Camiñas et al. (2021) | 7 | 0,79% | 7 | 2,1% | 7 | 2,87% | 7 | 2,5% |
Golvan (1962) | 7 | 0,79% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Lazell (1964) | 7 | 0,79% | 0 | 0% | 0 | 0% | 0 | 0% |
Muñoz et al. (2013) | 7 | 0,79% | 0 | 0% | 0 | 0% | 0 | 0% |
Pinto-coelho et al. (2021) | 7 | 0,79% | 5 | 1,5% | 5 | 2,05% | 2 | 0,71% |
Probst (2001) | 7 | 0,79% | 6 | 1,8% | 6 | 2,46% | 5 | 1,79% |
Schweigger (1812) | 7 | 0,79% | 0 | 0% | 0 | 0% | 0 | 0% |
Souza-oliveira et al. (2024) | 7 | 0,79% | 6 | 1,8% | 6 | 2,46% | 4 | 1,43% |
Spix (1824) | 7 | 0,79% | 1 | 0,3% | 1 | 0,41% | 0 | 0% |
Casale et al. (2021) | 6 | 0,68% | 6 | 1,8% | 6 | 2,46% | 6 | 2,14% |
Duméril & Bibron (1837) | 6 | 0,68% | 0 | 0% | 0 | 0% | 0 | 0% |
Fretey & Triplet (2022) | 6 | 0,68% | 6 | 1,8% | 6 | 2,46% | 6 | 2,14% |
Hedges et al. (2014) | 6 | 0,68% | 3 | 0,9% | 3 | 1,23% | 3 | 1,07% |
Lazell (1972) | 6 | 0,68% | 0 | 0% | 0 | 0% | 0 | 0% |
Massary et al. (2020) | 6 | 0,68% | 6 | 1,8% | 6 | 2,46% | 6 | 2,14% |
Rhodin et al. (2017) | 6 | 0,68% | 4 | 1,2% | 4 | 1,64% | 4 | 1,43% |
Ronot (2007) | 6 | 0,68% | 5 | 1,5% | 4 | 1,64% | 5 | 1,79% |
Sayah et al. (2023) | 6 | 0,68% | 5 | 1,5% | 5 | 2,05% | 5 | 1,79% |
Schneider (1801) | 6 | 0,68% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Thomas (1964) | 6 | 0,68% | 5 | 1,5% | 0 | 0% | 5 | 1,79% |
Arnold & Ovenden (2014) | 5 | 0,57% | 4 | 1,2% | 4 | 1,64% | 3 | 1,07% |
Barbrour (1915) | 5 | 0,57% | 3 | 0,9% | 2 | 0,82% | 2 | 0,71% |
Barrioz & Morinière (2007) | 5 | 0,57% | 5 | 1,5% | 5 | 2,05% | 5 | 1,79% |
Bioinsight/diren & Guyane (2006) | 5 | 0,57% | 5 | 1,5% | 5 | 2,05% | 5 | 1,79% |
Chevalier (2006) | 5 | 0,57% | 5 | 1,5% | 5 | 2,05% | 5 | 1,79% |
Ciccione et al. (2011) | 5 | 0,57% | 5 | 1,5% | 5 | 2,05% | 5 | 1,79% |
Crillon & Cuzange (2020) | 5 | 0,57% | 5 | 1,5% | 5 | 2,05% | 5 | 1,79% |
Duffaut et al. (2011) | 5 | 0,57% | 5 | 1,5% | 5 | 2,05% | 5 | 1,79% |
Entraygues (2014) | 5 | 0,57% | 5 | 1,5% | 5 | 2,05% | 5 | 1,79% |
Étaix-bonnin et al. (2011) | 5 | 0,57% | 5 | 1,5% | 5 | 2,05% | 5 | 1,79% |
Hamdan et al. (2023) | 5 | 0,57% | 5 | 1,5% | 5 | 2,05% | 3 | 1,07% |
Ineich (2016) | 5 | 0,57% | 5 | 1,5% | 5 | 2,05% | 5 | 1,79% |
Le Scao et al. (2011) | 5 | 0,57% | 5 | 1,5% | 5 | 2,05% | 5 | 1,79% |
Maran & Frétey (2023) | 5 | 0,57% | 5 | 1,5% | 5 | 2,05% | 5 | 1,79% |
Read & Farman (2018) | 5 | 0,57% | 5 | 1,5% | 5 | 2,05% | 5 | 1,79% |
Read et al. (2023) | 5 | 0,57% | 5 | 1,5% | 5 | 2,05% | 5 | 1,79% |
Routtier et al. (2023) | 5 | 0,57% | 5 | 1,5% | 5 | 2,05% | 1 | 0,36% |
Sauvignet et al. (2000) | 5 | 0,57% | 5 | 1,5% | 5 | 2,05% | 5 | 1,79% |
Schlegel (1837) | 5 | 0,57% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Schwartz (1964) | 5 | 0,57% | 3 | 0,9% | 0 | 0% | 3 | 1,07% |
Thorpe & Malhotra (2023) | 5 | 0,57% | 5 | 1,5% | 5 | 2,05% | 4 | 1,43% |
Vieira (2022) | 5 | 0,57% | 5 | 1,5% | 5 | 2,05% | 2 | 0,71% |
Yokoyama (2012) | 5 | 0,57% | 4 | 1,2% | 4 | 1,64% | 3 | 1,07% |
Albuquerque et al. (2022) | 4 | 0,45% | 4 | 1,2% | 2 | 0,82% | 2 | 0,71% |
Arredondo et al. (2020) | 4 | 0,45% | 3 | 0,9% | 3 | 1,23% | 3 | 1,07% |
Bauer & Sadlier (2000) | 4 | 0,45% | 3 | 0,9% | 3 | 1,23% | 3 | 1,07% |
Boie (1827) | 4 | 0,45% | 0 | 0% | 0 | 0% | 0 | 0% |
Breuil (2013) | 4 | 0,45% | 2 | 0,6% | 2 | 0,82% | 1 | 0,36% |
Carrasco et al. (2012) | 4 | 0,45% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Carvalho et al. (2023) | 4 | 0,45% | 4 | 1,2% | 4 | 1,64% | 3 | 1,07% |
Cole & Dessauer (1993) | 4 | 0,45% | 4 | 1,2% | 4 | 1,64% | 4 | 1,43% |
Daudin (1803) | 4 | 0,45% | 0 | 0% | 0 | 0% | 0 | 0% |
Dewynter et al. (2016) | 4 | 0,45% | 4 | 1,2% | 4 | 1,64% | 4 | 1,43% |
Dewynter (2016) | 4 | 0,45% | 4 | 1,2% | 4 | 1,64% | 3 | 1,07% |
Duguy (1988) | 4 | 0,45% | 4 | 1,2% | 4 | 1,64% | 4 | 1,43% |
Duguy (1994) | 4 | 0,45% | 4 | 1,2% | 4 | 1,64% | 4 | 1,43% |
Duguy (1997) | 4 | 0,45% | 4 | 1,2% | 4 | 1,64% | 4 | 1,43% |
Duméril et al. (1854) | 4 | 0,45% | 0 | 0% | 0 | 0% | 0 | 0% |
Fretey & Lescure (1999) | 4 | 0,45% | 4 | 1,2% | 4 | 1,64% | 4 | 1,43% |
Hass (1991) | 4 | 0,45% | 4 | 1,2% | 4 | 1,64% | 3 | 1,07% |
Kallel et al. (2018) | 4 | 0,45% | 3 | 0,9% | 3 | 1,23% | 2 | 0,71% |
Köhler & Vesely (2011) | 4 | 0,45% | 4 | 1,2% | 4 | 1,64% | 4 | 1,43% |
Lambert (1988) | 4 | 0,45% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Lescure et al. (2020) | 4 | 0,45% | 4 | 1,2% | 3 | 1,23% | 4 | 1,43% |
Linné (1766) | 4 | 0,45% | 0 | 0% | 0 | 0% | 0 | 0% |
Massary & Hoogmoed (2001) | 4 | 0,45% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Méheust et al. (2018) | 4 | 0,45% | 4 | 1,2% | 4 | 1,64% | 4 | 1,43% |
Momont (1998) | 4 | 0,45% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Morinière & Dell'amico (2011) | 4 | 0,45% | 4 | 1,2% | 4 | 1,64% | 4 | 1,43% |
Olson & Normand (2014) | 4 | 0,45% | 2 | 0,6% | 2 | 0,82% | 2 | 0,71% |
Pellegrino et al. (2018) | 4 | 0,45% | 4 | 1,2% | 4 | 1,64% | 4 | 1,43% |
Probst (1997) | 4 | 0,45% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Probst (1998) | 4 | 0,45% | 3 | 0,9% | 3 | 1,23% | 3 | 1,07% |
Questel (2017) | 4 | 0,45% | 3 | 0,9% | 3 | 1,23% | 3 | 1,07% |
Rivas et al. (2024) | 4 | 0,45% | 2 | 0,6% | 2 | 0,82% | 1 | 0,36% |
Rojas-runjaic et al. (2021) | 4 | 0,45% | 4 | 1,2% | 4 | 1,64% | 4 | 1,43% |
Sanchez (2020) | 4 | 0,45% | 4 | 1,2% | 4 | 1,64% | 2 | 0,71% |
Souza (2020) | 4 | 0,45% | 4 | 1,2% | 4 | 1,64% | 4 | 1,43% |
Starace (2013) | 4 | 0,45% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Tirvengadum & Bour (1985) | 4 | 0,45% | 3 | 0,9% | 3 | 1,23% | 3 | 1,07% |
Almeida et al. (2022) | 3 | 0,34% | 3 | 0,9% | 3 | 1,23% | 2 | 0,71% |
Angin et al. (2024) | 3 | 0,34% | 3 | 0,9% | 0 | 0% | 3 | 1,07% |
Bailon et al. (2015) | 3 | 0,34% | 2 | 0,6% | 2 | 0,82% | 2 | 0,71% |
Blanc (1909) | 3 | 0,34% | 0 | 0% | 0 | 0% | 0 | 0% |
Bochaton & Hanot (2021) | 3 | 0,34% | 3 | 0,9% | 3 | 1,23% | 2 | 0,71% |
Bochaton et al. (2016) | 3 | 0,34% | 3 | 0,9% | 3 | 1,23% | 2 | 0,71% |
Bochaton et al. (2017) | 3 | 0,34% | 3 | 0,9% | 3 | 1,23% | 3 | 1,07% |
Bonnaterre (1789) | 3 | 0,34% | 0 | 0% | 0 | 0% | 0 | 0% |
Bour (2006) | 3 | 0,34% | 0 | 0% | 0 | 0% | 0 | 0% |
Brunes et al. (2021) | 3 | 0,34% | 2 | 0,6% | 2 | 0,82% | 0 | 0% |
Carvalho et al. (2015) | 3 | 0,34% | 3 | 0,9% | 3 | 1,23% | 3 | 1,07% |
Carvalho et al. (2016) | 3 | 0,34% | 3 | 0,9% | 3 | 1,23% | 3 | 1,07% |
Champagne et al. (1997) | 3 | 0,34% | 3 | 0,9% | 2 | 0,82% | 3 | 1,07% |
Cope (1868) | 3 | 0,34% | 0 | 0% | 0 | 0% | 0 | 0% |
Delcroix et al. (2011) | 3 | 0,34% | 3 | 0,9% | 3 | 1,23% | 3 | 1,07% |
Dubief & Gallais (2011) | 3 | 0,34% | 3 | 0,9% | 3 | 1,23% | 3 | 1,07% |
Duguy et al. (1998) | 3 | 0,34% | 3 | 0,9% | 3 | 1,23% | 3 | 1,07% |
Duguy et al. (1999) | 3 | 0,34% | 3 | 0,9% | 3 | 1,23% | 3 | 1,07% |
Duguy et al. (2000) | 3 | 0,34% | 3 | 0,9% | 3 | 1,23% | 3 | 1,07% |
Duguy et al. (2002) | 3 | 0,34% | 3 | 0,9% | 3 | 1,23% | 3 | 1,07% |
Duguy et al. (2006) | 3 | 0,34% | 3 | 0,9% | 3 | 1,23% | 3 | 1,07% |
Duguy et al. (2007) | 3 | 0,34% | 3 | 0,9% | 3 | 1,23% | 3 | 1,07% |
Duguy (1990) | 3 | 0,34% | 3 | 0,9% | 3 | 1,23% | 3 | 1,07% |
Duguy (1996) | 3 | 0,34% | 3 | 0,9% | 3 | 1,23% | 3 | 1,07% |
Duméril & Bibron (1836) | 3 | 0,34% | 2 | 0,6% | 1 | 0,41% | 1 | 0,36% |
Gamble et al. (2011) | 3 | 0,34% | 2 | 0,6% | 2 | 0,82% | 2 | 0,71% |
Giovannotti et al. (2017) | 3 | 0,34% | 2 | 0,6% | 2 | 0,82% | 2 | 0,71% |
Girondot (2011) | 3 | 0,34% | 3 | 0,9% | 3 | 1,23% | 3 | 1,07% |
Henderson & Powell (2009) | 3 | 0,34% | 1 | 0,3% | 1 | 0,41% | 0 | 0% |
Jadin et al. (2014) | 3 | 0,34% | 2 | 0,6% | 2 | 0,82% | 2 | 0,71% |
Jan (1863) | 3 | 0,34% | 0 | 0% | 0 | 0% | 0 | 0% |
Kemp (2023) | 3 | 0,34% | 3 | 0,9% | 3 | 1,23% | 2 | 0,71% |
La Cepède (1789) | 3 | 0,34% | 0 | 0% | 0 | 0% | 0 | 0% |
Lescure (2018) | 3 | 0,34% | 3 | 0,9% | 3 | 1,23% | 3 | 1,07% |
Macculloch et al. (2009) | 3 | 0,34% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Martins et al. (2019) | 3 | 0,34% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Merrem (1820) | 3 | 0,34% | 0 | 0% | 0 | 0% | 0 | 0% |
Miralles & Carranza (2010) | 3 | 0,34% | 0 | 0% | 0 | 0% | 0 | 0% |
Miralles et al. (2017) | 3 | 0,34% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Mothes et al. (2019) | 3 | 0,34% | 2 | 0,6% | 2 | 0,82% | 2 | 0,71% |
Oliveira et al. (2016) | 3 | 0,34% | 3 | 0,9% | 2 | 0,82% | 2 | 0,71% |
Poisson (1999) | 3 | 0,34% | 3 | 0,9% | 3 | 1,23% | 3 | 1,07% |
Pomar-gómez et al. (2021) | 3 | 0,34% | 3 | 0,9% | 3 | 1,23% | 2 | 0,71% |
Probst et al. (2000) | 3 | 0,34% | 3 | 0,9% | 3 | 1,23% | 3 | 1,07% |
Read & Jean (2021) | 3 | 0,34% | 3 | 0,9% | 3 | 1,23% | 3 | 1,07% |
Rodríguez-rodríguez & Calderón-espinosa (2024) | 3 | 0,34% | 0 | 0% | 0 | 0% | 0 | 0% |
Roughgarden (1995) | 3 | 0,34% | 0 | 0% | 0 | 0% | 0 | 0% |
Roux (1913) | 3 | 0,34% | 2 | 0,6% | 2 | 0,82% | 2 | 0,71% |
Surget-Groba & Thorpe (2013) | 3 | 0,34% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Thorpe et al. (2008) | 3 | 0,34% | 2 | 0,6% | 2 | 0,82% | 1 | 0,36% |
van den Burg et al. (2021) | 3 | 0,34% | 2 | 0,6% | 2 | 0,82% | 1 | 0,36% |
Vidal et al. (1999) | 3 | 0,34% | 3 | 0,9% | 3 | 1,23% | 3 | 1,07% |
Vidal et al. (2010) | 3 | 0,34% | 2 | 0,6% | 2 | 0,82% | 2 | 0,71% |
Wagler (1830) | 3 | 0,34% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Wallach (2020) | 3 | 0,34% | 2 | 0,6% | 2 | 0,82% | 2 | 0,71% |
Araujo & Machado (1980) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Baldi et al. (2022) | 2 | 0,23% | 2 | 0,6% | 2 | 0,82% | 2 | 0,71% |
Balle et al. (2021) | 2 | 0,23% | 2 | 0,6% | 2 | 0,82% | 2 | 0,71% |
Bance (2022) | 2 | 0,23% | 2 | 0,6% | 2 | 0,82% | 2 | 0,71% |
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 & Powell (2024) | 2 | 0,23% | 0 | 0% | 0 | 0% | 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 | 0,71% |
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 | 0,71% |
Bochaton & Bailon (2018) | 2 | 0,23% | 2 | 0,6% | 2 | 0,82% | 2 | 0,71% |
Bochaton et al. (2018) | 2 | 0,23% | 2 | 0,6% | 2 | 0,82% | 2 | 0,71% |
Bochaton et al. (2021) | 2 | 0,23% | 2 | 0,6% | 2 | 0,82% | 2 | 0,71% |
Bourgade (2021) | 2 | 0,23% | 2 | 0,6% | 2 | 0,82% | 2 | 0,71% |
Brasileiro (2021) | 2 | 0,23% | 2 | 0,6% | 2 | 0,82% | 2 | 0,71% |
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 | 0,71% |
Censky & Paulson (1992) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Cheke (1987) | 2 | 0,23% | 2 | 0,6% | 2 | 0,82% | 2 | 0,71% |
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 | 0,71% |
Chevallier et al. (2023) | 2 | 0,23% | 2 | 0,6% | 2 | 0,82% | 2 | 0,71% |
">Claes (2024) | 2 | 0,23% | 2 | 0,6% | 2 | 0,82% | 2 | 0,71% |
Clarac et al. (2024) | 2 | 0,23% | 2 | 0,6% | 2 | 0,82% | 2 | 0,71% |
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 | 0,71% |
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. (1997) | 2 | 0,23% | 2 | 0,6% | 2 | 0,82% | 2 | 0,71% |
Duguy et al. (2003) | 2 | 0,23% | 2 | 0,6% | 2 | 0,82% | 2 | 0,71% |
Duguy et al. (2004) | 2 | 0,23% | 2 | 0,6% | 2 | 0,82% | 2 | 0,71% |
Duguy (1986) | 2 | 0,23% | 2 | 0,6% | 2 | 0,82% | 2 | 0,71% |
Duguy (1987) | 2 | 0,23% | 2 | 0,6% | 2 | 0,82% | 2 | 0,71% |
Duguy (1992) | 2 | 0,23% | 2 | 0,6% | 2 | 0,82% | 2 | 0,71% |
Duguy (1993) | 2 | 0,23% | 2 | 0,6% | 2 | 0,82% | 2 | 0,71% |
Duguy (1995) | 2 | 0,23% | 2 | 0,6% | 2 | 0,82% | 2 | 0,71% |
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% | 0 | 0% | 0 | 0% | 0 | 0% |
Gasc & Rodrigues (1979) | 2 | 0,23% | 2 | 0,6% | 2 | 0,82% | 2 | 0,71% |
Girondo (2023) | 2 | 0,23% | 2 | 0,6% | 2 | 0,82% | 2 | 0,71% |
Gomés et al. (2018) | 2 | 0,23% | 2 | 0,6% | 1 | 0,41% | 2 | 0,71% |
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 | 0,71% |
Havery et al. (2018) | 2 | 0,23% | 2 | 0,6% | 2 | 0,82% | 2 | 0,71% |
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% |
Jouan (1863) | 2 | 0,23% | 2 | 0,6% | 2 | 0,82% | 2 | 0,71% |
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 | 0,71% |
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 | 0,71% |
Martins et al. (2023) | 2 | 0,23% | 2 | 0,6% | 2 | 0,82% | 2 | 0,71% |
Melo-sampaio et al. (2019) | 2 | 0,23% | 2 | 0,6% | 2 | 0,82% | 2 | 0,71% |
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 | 0,71% |
Noël (2024) | 2 | 0,23% | 2 | 0,6% | 2 | 0,82% | 1 | 0,36% |
Oliver (2011) | 2 | 0,23% | 2 | 0,6% | 2 | 0,82% | 2 | 0,71% |
Ortega-de et al. (2023) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Parker & Fitzgerald (2024) | 2 | 0,23% | 2 | 0,6% | 2 | 0,82% | 2 | 0,71% |
Passos et al. (2004) | 2 | 0,23% | 2 | 0,6% | 2 | 0,82% | 2 | 0,71% |
Peron (2014) | 2 | 0,23% | 2 | 0,6% | 2 | 0,82% | 2 | 0,71% |
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 | 0,71% |
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 | 0,71% |
Rinaldi et al. (2011) | 2 | 0,23% | 2 | 0,6% | 2 | 0,82% | 2 | 0,71% |
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 | 0,71% |
Sanchez et al. (2019) | 2 | 0,23% | 2 | 0,6% | 2 | 0,82% | 2 | 0,71% |
Santos (2003) | 2 | 0,23% | 2 | 0,6% | 2 | 0,82% | 2 | 0,71% |
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 | 0,71% |
Silveira & Magnusson (1999) | 2 | 0,23% | 2 | 0,6% | 2 | 0,82% | 2 | 0,71% |
Spix (1824) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Srodawa et al. (2023) | 2 | 0,23% | 2 | 0,6% | 2 | 0,82% | 2 | 0,71% |
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 | 0,71% |
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 | 0,71% |
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% |
Wied-neuwied (1821) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Wüster et al. (2024) | 2 | 0,23% | 2 | 0,6% | 2 | 0,82% | 1 | 0,36% |
Yuki (1993) | 2 | 0,23% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Abhaya & Probst (2003) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Abhaya & Probst (2009) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Abhaya et al. (1998) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 0 | 0% |
Agarwal et al. (2021) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Agassiz (1857) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Agostini et al. (2023) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Albuquerque & Fernandes (2022) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 0 | 0% |
Albuquerque et al. (2018) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Albuquerque et al. (2019) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Aléssio & Herrel (2024) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Al-hasson & Ali (2020) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Almeida & Vasconcelos (2023) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Almeida et al. (2019) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Almeida et al. (2024) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 0 | 0% |
Amaral et al. (2019) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Anaissi & Costa-campos (2021) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Anaissi & Costa-campos (2021) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Andersson (1918) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Angel (1935) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Angin (2017) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Angin (2017) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Anonyme (ICZN) (2019) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2004) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Antonini et al. (2023) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Aquarium de La Rochelle (2017) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Armand & Ferlay (2023) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Astudillo et al. (2021) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 0 | 0% |
Asztalos et al. (2020) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Auguste et al. (2019) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Avila-pires et al. (2013) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Bailey & Carvalho (1946) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Bailey et al. (2023) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Baker & Allain (2020) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Baldi et al. (2023) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Barbancey & Probst (1998) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 0 | 0% |
Barbancey (2001) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Barbancey (2001) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Barbour (1914) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Bassett (2022) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Bauer & Sadlier (1994) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Bauer et al. (2010) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Bauer et al. (2024) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Bauer et al. (2024) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Bavay (1869) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Beauvieux et al. (2024) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Becerra et al. (2024) | 1 | 0,11% | 1 | 0,3% | 0 | 0% | 1 | 0,36% |
Behm et al. (2022) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Bell (1827) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Bell (1827) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Benício (2021) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Bertrand & Drogou (2000) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Bertrand et al. (2001) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Bochaton et al. (2016) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Bochaton et al. (2017) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Bochaton et al. (2020) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Bonnaterre (1790) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Bonnet et al. (1999) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Borcyk et al. (2023) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 0 | 0% |
Borroto-páez (2018) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Boulenger (1883) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Boulenger (1887) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Boulenger (1891) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 0 | 0% |
Boulenger (1896) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Boulenger (1912) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Bour (1973) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Bourgade (2013) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Bourgade (2020) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Bourgade (2020) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Brasileiro et al. (2023) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Breuil & Ibéné (2008) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Breuil & Serre-collet (2012) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Breuil et al. (2022) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 0 | 0% |
Breuil (1999) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Brito-gitirana et al. (2019) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Brongersma (1928) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Burger (1955) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Burneleau (1983) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Busack & Pandya (2001) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Bush et al. (2021) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Caceres (2002) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Cáceres-martínez et al. (2020) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Caldeira Costa et al. (2009) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Camayo & Zúñiga-baos (2023) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 0 | 0% |
Campos et al. (2024) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Capalleras & Carretero (2000) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 0 | 0% |
Carpio et al. (2022) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Carvajal-ocampo et al. (2019) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Caut & Jowers (2015) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Caut et al. (2008) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Caut et al. (2019) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Cavalcante et al. (2022) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 0 | 0% |
CEN Nouvelle-Calédonie (2021) | 1 | 0,11% | 1 | 0,3% | 0 | 0% | 1 | 0,36% |
Censky (1988) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Chambault et al. (2020) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Chance et al. (2024) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Chevallier et al. (2024) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Chevreux & de Guerne (1893) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Chippaux (1986) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Chocobar et al. (2023) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Chua (2018) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Ciccione (2001) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Ciccione (2001) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Cochran (1938) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Coélho et al. (2019) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 0 | 0% |
Colin (1992) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Collazos-astudillo et al. (2022) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Cope (1864) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Cope (1879) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Cope (1894) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Cornuaille et al. (2021) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Costa et al. (2013) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Costal-oliveira et al. (2019) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Cummings et al. (2021) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Cunha et al. (2019) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Cunha et al. (2021) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Cunha (1970) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Curcio et al. (2011) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Cuvier & Voigt (1832) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Cuvier (1807) | 1 | 0,11% | 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 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Da Silva et al. (2018) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Dal Vechio et al. (2015) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Dal Zotto et al. (2024) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Dalleau et al. (2014) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
D´angiolella et al. (2021) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Daudin (1803) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Daudin (1803) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Dauvin (1990) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
David et al. (2002) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
de Andrade (2019) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 0 | 0% |
De Carvalho et al. (2018) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 0 | 0% |
Delafontaine et al. (2018) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Delaney & Warner (2017) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Delcroix et al. (2008) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Deliveyne et al. (2023) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 0 | 0% |
Dewynter & Rufray (2012) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Dewynter & Surugue (2012) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Dewynter et al. (2015) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Dewynter et al. (2019) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Diaz-ricaurte et al. (2018) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 0 | 0% |
Dixon et al. (1993) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Dixon (1983) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Dubois & Frétey (2024) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Dubois et al. (2024) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Dueñas et al. (2021) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 0 | 0% |
Duguy & Duron (1981) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Duguy & Duron (1982) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Duguy & Duron (1983) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Duguy & Duron (1984) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Duguy & Duron (1985) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Duguy et al. (1980) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Duguy et al. (2000) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Duguy (1983) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Duguy (1988) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Duguy (1989) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Duméril & Bibron (1839) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Duméril & Bibron (1839) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Duméril & Bribron (1835) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Duméril et al. (1854) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Dunn & Conant (1936) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Duval et al. (2019) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Eiselt (1963) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Entiauspe-neto & Loebmann (2019) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Entiauspe-neto et al. (2018) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Eschscholtz (1829) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Etheridge (1964) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Fagundes et al. (2021) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Farias et al. (2019) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Fernandes et al. (2023) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Feuillet et al. (2010) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Ficetola & Scali (2010) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 0 | 0% |
Fieldsend et al. (2021) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Figueiredo et al. (2021) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
França & França (2019) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 0 | 0% |
França et al. (2019) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Francisco et al. (2018) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Franco & Ferreira (2003) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Franzen (1996) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Franzini et al. (2019) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Fretey & Bour (1980) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Fretey et al. (2023) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Fretey (1980) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Fretey (1987) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Fretey (2003) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Frétey (2019) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Frétey (2022) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Frétey (2023) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Fritz et al. (2010) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Fritz et al. (2020) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Fujishima (2021) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Gans (1963) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
García-ayachi et al. (2020) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
García-cobos et al. (2021) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Gargominy et al. (1996) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Garman (1880) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Garman (1887) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Garman (1887) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Geneva et al. (2013) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Gérigny et al. (2020) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Gill (1995) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Gomès & Ibéné (2013) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 0 | 0% |
Gomes et al. (2020) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
González et al. (2018) | 1 | 0,11% | 1 | 0,3% | 0 | 0% | 1 | 0,36% |
Gouillard (1973) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Goyannes-araújo et al. (2009) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Graboski et al. (2018) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Graitson et al. (2012) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Grant (1958) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Gray (1831) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Gray (1849) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Gray (1863) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Gray (1873) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Griffin (1917) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Grisales-martínez & Arias-alvarez (2018) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Gros-désormeaux et al. (2017) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Guichenot (1855) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Guilhon et al. (2024) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Guilhon (2023) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Guiller & Vacher (2022) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Gunderson et al. (2020) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Günther (1860) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Günther (1868) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Günther (1872) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Hamdan et al. (2014) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Hedges et al. (2009) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Hedges (2008) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Hedges (2011) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Hellebuyck et al. (2017) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Henao-osorio et al. (2021) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Henderson & Powell (2006) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 0 | 0% |
Henderson et al. (1993) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Hermann (1804) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Herrera-alzate (2023) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Herron et al. (1990) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Herzberg (2018) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Hodges et al. (2024) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Hoge & Romano (1969) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Holbrook (1836) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Hoogmoed & Lescure (1975) | 1 | 0,11% | 1 | 0,3% | 0 | 0% | 1 | 0,36% |
Hoogmoed (1977) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Houttuyn (1782) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Howard et al. (2001) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Howell & Clements (2019) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Hudson et al. (2019) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
ICZN (2010) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Iković et al. (2023) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 0 | 0% |
Ineich & Bauer (1992) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Ineich & Giraud (2019) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Ineich & Massary (1997) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Ineich et al. (2017) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Ineich et al. (2019) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Ineich (1999) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Ineich (2015) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Jadin et al. (2021) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Jairam & Jairam-doerga (2015) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Jairam et al. (2016) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Jan (1858) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Jared et al. (2023) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Jeimi et al. (2008) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Jim et al. (2022) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Johansson et al. (2013) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Jowers et al. (2020) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 0 | 0% |
Judson et al. (2018) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Kadafi et al. (2024) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Karaa et al. (2016) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Karin et al. (2021) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
King (1962) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Klauber (1939) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Koleska & Jablonski (2018) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Kollarits et al. (2013) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Kornilev et al. (2020) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 0 | 0% |
Kuhl (1820) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Kwet (2013) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Lainson et al. (1975) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Lazell (1964) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Lazell (1994) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Lédée & Questel (2013) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Léger & Mouzels (1917) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Legouez (2010) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Leimroth et al. (2022) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Leite et al. (2021) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Lema & Albuquerque (2010) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Lema et al. (2017) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Lescure et al. (2016) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Liardet & d'Auzon (2004) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Liardet (2004) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Lichtenstein & Martens (1856) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Lichtenstein (1823) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Liebart et al. (2021) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Liebgold et al. (2019) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Lima et al. (2019) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 0 | 0% |
Lima et al. (2022) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Lock & Griffiths (2022) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Loisier et al. (2021) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
López (2023) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Lorvelec & Pascal (2009) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Lorvelec & Pascal (2009) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Lorvelec et al. (2009) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Lorvelec et al. (2011) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Lorvelec et al. (2013) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Lorvelec et al. (2016) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Lorvelec et al. (2017) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Lorvelec et al. (2017) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Lorvelec (2011) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Louisin & Probst (1996) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Lowe et al. (2007) | 1 | 0,11% | 1 | 0,3% | 0 | 0% | 1 | 0,36% |
Maciel et al. (2021) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Mageski et al. (2017) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Maillard & David (2014) | 1 | 0,11% | 1 | 0,3% | 0 | 0% | 1 | 0,36% |
Mancino et al. (2022) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Marinho (2022) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Marioni et al. (2019) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Marques-souza et al. (2018) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Marques-souza et al. (2022) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Marquis et al. (2020) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Martin et al. (2021) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Maschio et al. (2021) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 0 | 0% |
Massary & Ineich (1997) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Massary & Ineich (1999) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Massary et al. (2000) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Massary et al. (2001) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Massary (1999) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Massary (2012) | 1 | 0,11% | 1 | 0,3% | 0 | 0% | 1 | 0,36% |
Matz (2005) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Medetian & Miaud (2024) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Mendoça et al. (2016) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Meneses et al. (2019) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 0 | 0% |
Mesquita et al. (2020) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Métrailler (2007) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Meyen (1834) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Miller (1779) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Miralles et al. (2005) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Montingelli et al. (2019) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Moon & Kamath (2019) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Morales et al. (2020) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Moreau de Jonnès (1816) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Moreau de Jonnès (1818) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Müller (1923) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Müller 1924 | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Murphy et al. (2020) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Naveda-rodríguez et al. (2020) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Oliveira et al. (2018) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Oliveira et al. (2021) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Oliveira (2023) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Oliveira-souza et al. (2021) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
O'shaughnessy (1881) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Paperna & Landsberg (1989) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Paré & Lorvelec (2012) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 0 | 0% |
Parker (1935) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Parker (1936) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Parmentier et al. (2017) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Pascal et al. 2006 | 1 | 0,11% | 1 | 0,3% | 0 | 0% | 1 | 0,36% |
Passos & Fernandes (2008) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Passos et al. (2022) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Pérez-delgadillo & Lara-reséndiz (2024) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Perkins (1928) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Monatsberichte der königlich Akademie der Wissenschaften zu Berlin, 1857: 402.">Peters (1858) | 1 | 0,11% | 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 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Peters (1867) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Peters (1869) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Philippot et al. (2019) | 1 | 0,11% | 1 | 0,3% | 0 | 0% | 1 | 0,36% |
Pinto & Fernandes (2012) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Pinto & Fernandes (2017) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Pinto et al. (2019) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Pinto et al. (2023) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Portilla & Lamus (2020) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Powell et al. (2021) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Prato et al. (2022) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Prémel et al. (2022) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 0 | 0% |
Probst & Deso (2001) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Probst et al. (2023) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Probst (1997) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Probst (1999) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 0 | 0% |
Probst (2001) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Probst (2007) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Puissauve, Cohen & De Massary (2015) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Quah & Grismer (2024) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Questel & Boggio (2012) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Questel & Boggio (2012) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Questel & Vitry (2012) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Questel et al. (2012) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Questel (2011) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Questel (2012) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Questel (2012) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Questel (2013) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Questel (2018) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 0 | 0% |
Quiñones-betancourt et al. (2018) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Quintana et al. (2021) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Quintana (2017) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Quinteros-muñoz & Aguayo (2021) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 0 | 0% |
Raddi (1820) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Ramalho et al. (2024) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Read et al. (2015) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Recoder et al. (2018) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Regio & Pontes (2020) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 0 | 0% |
Reinert et al. (2021) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 0 | 0% |
Renner (2002) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Réserve Naturelle de Saint Barthélemy (2014) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Résière et al. (2018) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Reuss (1834) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Revuelta et al. (2015) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Ribeiro-júnior et al. (2019) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Richmond (1966) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Rimblot et al. (1985) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Rivas et al. (2023) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 0 | 0% |
Roberto et al. (2021) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 0 | 0% |
Rocha et al. (2023) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Rocha et al. (2024) | 1 | 0,11% | 1 | 0,3% | 0 | 0% | 1 | 0,36% |
Rodrigues et al. (2021) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Rojas-morales et al. (2021) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Rojas-runjaic et al. (2024) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Romero et al. (2010) | 1 | 0,11% | 1 | 0,3% | 0 | 0% | 1 | 0,36% |
Romero-marcucci et al. (2024) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Roos (2000) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Rösler et al. (2019) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Roux (1929) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Rufray et al. (2015) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Rufz (1859 | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Ruibal (1952) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Rüppell (1835) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Russell & Bauer (2002) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Ruthven (1916) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Sadlier et al. (2012) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Sanches et al. (2019) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Sanches et al. (2020) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Sanchez et al. (2017) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 0 | 0% |
Santana & Teixeira (2020) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Santos et al. (2024) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Savage (2011) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Schargel et al. (2024) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Schlegel (1839) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Schmidt & Walker (1943) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Schmidt (1928) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Schriften der Gesellschaft Naturforschender Freunde zu Berlin, 10(3): 259-283.">Schneider (1792) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Schnell & Swierk (2021) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Schoepff (1792) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Schultze et al. (2020) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Schwartz & Henderson (1991) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Scopoli (1788) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Serrano & Díaz-ricaurte (2018) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 0 | 0% |
Servan & Arvy (1997) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 0 | 0% |
Servan (1976) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Shaver et al. (2019) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Shukla et al. (2024) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Silva & Farias (2019) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Silva et al. (2003) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Silva et al. (2019) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Silva et al. (2021) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Silva et al. (2022) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Snyder et al. (2019) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Sonsino (1893) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Sousa et al. (2021) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Sousa (2019) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Sparrman (1784) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Spix (1824) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Starace & Ineich (2024) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 0 | 0% |
Starace (1997) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Stelfox et al. (2020) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Stephan (2011) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Stoleson & Beissinger (2001) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Suckow (1798) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Sulton (2020) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Tan (2024) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Tavares-pinheiro et al. (2021) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Tavares-pinheiro et al. (2021) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Thawley et al. (2019) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Thibault et al. (2023) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Thomas et al. (2021) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Thorbjarnarson (2010) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Thorpe & Stenson (2003) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Toohey et al. (2022) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Torres Bonilla (2018) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 0 | 0% |
Torres-bonilla et al. (2024) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Torres-carvajal et al. (2020) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 0 | 0% |
Townsend et al. (2000) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Trochet et al. (2024) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Tschudi (1845) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Turpin & Probst (1998) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 0 | 0% |
Uicn et al. (2020) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Valencia & Garzon-tello (2018) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Van Den Burg et al. (2018) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Van den Burg et al. (2020) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Van den burg et al. (2022) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Vandellius (1761) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Vanzolini (1978) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Vargas-ramírez et al. (2020) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Vasconcelos et al. (2006) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Vasconcelos et al. (2024) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Vasconcelos Neto (2020) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Vásquez-cruz & Kelly-hernández (2024) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Venegas-anaya et al. (2008) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Veysset (2003) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 0 | 0% |
Vieira et al. (2023) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Vieira (2015) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Vieira (2023) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Vogt et al. (2013) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Von May et al. (2019) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 0 | 0% |
Von May et al. (2021) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Waayers et al. (2011) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Wallach (2009) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Wang & Qiu (2022) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Wasilewski et al. (2022) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 0 | 0% |
Wells & Herberg (2019) | 1 | 0,11% | 1 | 0,3% | 0 | 0% | 1 | 0,36% |
Werner (1924) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Werner (1980) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Weterings & Vetter (2017) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Wied (1839) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Wied-Neuwied (1824) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Wiegmann (1834) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Wiest (1978) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Williams et al. (2019) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Wilson & Mata-silva (2015) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 0 | 0% |
Works & Olson (2018) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 0 | 0% |
Wucherer (1861) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Wüster et al. (2002) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Yengle (2021) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Zaher & Prudente (1999) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Zambrano et al. (2022) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
Zdunek (2022) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 1 | 0,36% |
(2022) | 1 | 0,11% | 1 | 0,3% | 1 | 0,41% | 0 | 0% |