Décapodes de Guadeloupe
254 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
| Référence | Total | Valides | Espèces | Taxons terminaux | ||||
|---|---|---|---|---|---|---|---|---|
| nb | % | nb | % | nb | % | nb | % | |
| Poupin & Corbari (2016) | 260 | 18,84% | 234 | 38,36% | 234 | 38,42% | 234 | 38,42% |
| Poupin (2024) | 195 | 14,13% | 194 | 31,8% | 194 | 31,86% | 194 | 31,86% |
| Carmona-Suárez & Poupin (2016) | 119 | 8,62% | 99 | 16,23% | 99 | 16,26% | 99 | 16,26% |
| Questel (2020) | 98 | 7,1% | 97 | 15,9% | 97 | 15,93% | 97 | 15,93% |
| Poupin (2018) | 96 | 6,96% | 84 | 13,77% | 84 | 13,79% | 84 | 13,79% |
| Tricart & Foubert (2000) | 94 | 6,81% | 70 | 11,48% | 70 | 11,49% | 69 | 11,33% |
| Poupin (2010) | 76 | 5,51% | 69 | 11,31% | 69 | 11,33% | 69 | 11,33% |
| Poupin (1994) | 73 | 5,29% | 57 | 9,34% | 57 | 9,36% | 57 | 9,36% |
| Bulletin of the Museum of Comparative Zoology at Harvard College. 8(2): 1-68, Pl. 1-2.">Milne-Edwards (1880) | 69 | 5% | 14 | 2,3% | 14 | 2,3% | 14 | 2,3% |
| Corbari et al. (2015) | 67 | 4,86% | 57 | 9,34% | 57 | 9,36% | 57 | 9,36% |
| Carré (2006) | 52 | 3,77% | 43 | 7,05% | 43 | 7,06% | 43 | 7,06% |
| Paulmier (1996) | 41 | 2,97% | 31 | 5,08% | 31 | 5,09% | 31 | 5,09% |
| Corbari et al. (2020) | 30 | 2,17% | 20 | 3,28% | 20 | 3,28% | 20 | 3,28% |
| Poupin & Lemaitre (2014) | 28 | 2,03% | 28 | 4,59% | 28 | 4,6% | 28 | 4,6% |
| Questel & Le Quellec (2012) | 27 | 1,96% | 22 | 3,61% | 22 | 3,61% | 22 | 3,61% |
| Machordom et al. (2022) | 18 | 1,3% | 18 | 2,95% | 18 | 2,96% | 18 | 2,96% |
| Guéguen (2000) | 14 | 1,01% | 11 | 1,8% | 11 | 1,81% | 11 | 1,81% |
| Monti et al. (2010) | 14 | 1,01% | 13 | 2,13% | 13 | 2,13% | 13 | 2,13% |
| Saussure (1857) | 14 | 1,01% | 4 | 0,66% | 4 | 0,66% | 4 | 0,66% |
| UICN Comité français, OFB & MNHN (2021) | 14 | 1,01% | 14 | 2,3% | 14 | 2,3% | 14 | 2,3% |
| Lim et al. (2002) | 12 | 0,87% | 12 | 1,97% | 12 | 1,97% | 12 | 1,97% |
| Rodríguez-Flores et al. (2018) | 12 | 0,87% | 9 | 1,48% | 9 | 1,48% | 9 | 1,48% |
| Beltran (1982) | 10 | 0,72% | 10 | 1,64% | 10 | 1,64% | 10 | 1,64% |
| Poupin et al. (1999) | 9 | 0,65% | 8 | 1,31% | 8 | 1,31% | 8 | 1,31% |
| Rodríguez-Flores et al. (2022) | 9 | 0,65% | 6 | 0,98% | 6 | 0,99% | 6 | 0,99% |
| Lemaitre et al. (2017) | 8 | 0,58% | 8 | 1,31% | 8 | 1,31% | 8 | 1,31% |
| Anker (2012) | 7 | 0,51% | 7 | 1,15% | 7 | 1,15% | 7 | 1,15% |
| Coutiere (1909) | 7 | 0,51% | 5 | 0,82% | 5 | 0,82% | 4 | 0,66% |
| Crosnier (1976) | 7 | 0,51% | 6 | 0,98% | 6 | 0,99% | 6 | 0,99% |
| Yokoyama (2013) | 7 | 0,51% | 6 | 0,98% | 6 | 0,99% | 6 | 0,99% |
| Baba & Wicksten (2017) | 6 | 0,43% | 6 | 0,98% | 6 | 0,99% | 6 | 0,99% |
| Bracken-Grissom & Felder (2014) | 6 | 0,43% | 6 | 0,98% | 6 | 0,99% | 6 | 0,99% |
| Ifremer (2009) | 6 | 0,43% | 3 | 0,49% | 3 | 0,49% | 3 | 0,49% |
| Mclaughlin (1981) | 6 | 0,43% | 6 | 0,98% | 6 | 0,99% | 6 | 0,99% |
| Pinheiro & Boos (2016) | 6 | 0,43% | 6 | 0,98% | 6 | 0,99% | 6 | 0,99% |
| Poupin et al. (2013) | 6 | 0,43% | 5 | 0,82% | 5 | 0,82% | 5 | 0,82% |
| Questel (2014) | 6 | 0,43% | 6 | 0,98% | 6 | 0,99% | 6 | 0,99% |
| Anker & Baeza (2021) | 5 | 0,36% | 5 | 0,82% | 5 | 0,82% | 5 | 0,82% |
| Linnaeus (1758) | 5 | 0,36% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rodriguez et al. (2019) | 5 | 0,36% | 3 | 0,49% | 3 | 0,49% | 3 | 0,49% |
| Rojas-Beltran (1981) | 5 | 0,36% | 5 | 0,82% | 5 | 0,82% | 5 | 0,82% |
| Uicn et al. (2019) | 5 | 0,36% | 5 | 0,82% | 5 | 0,82% | 5 | 0,82% |
| Ashrafi & Hultgren (2022) | 4 | 0,29% | 4 | 0,66% | 4 | 0,66% | 3 | 0,49% |
| Boone (1927) | 4 | 0,29% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Chen et al. (2016) | 4 | 0,29% | 4 | 0,66% | 4 | 0,66% | 4 | 0,66% |
| Fourt et al. (2017) | 4 | 0,29% | 4 | 0,66% | 4 | 0,66% | 4 | 0,66% |
| Guinot et al. (2018) | 4 | 0,29% | 4 | 0,66% | 4 | 0,66% | 4 | 0,66% |
| Holthuis (1958) | 4 | 0,29% | 4 | 0,66% | 4 | 0,66% | 4 | 0,66% |
| IUCN (2013) | 4 | 0,29% | 4 | 0,66% | 4 | 0,66% | 4 | 0,66% |
| Lemaitre (2020) | 4 | 0,29% | 4 | 0,66% | 4 | 0,66% | 4 | 0,66% |
| Oliviera (1939) | 4 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
| Questel (2017) | 4 | 0,29% | 4 | 0,66% | 4 | 0,66% | 4 | 0,66% |
| Rathbun (1898) | 4 | 0,29% | 4 | 0,66% | 4 | 0,66% | 4 | 0,66% |
| Anker & Corbari (2020) | 3 | 0,22% | 3 | 0,49% | 3 | 0,49% | 3 | 0,49% |
| Anker et al. (2012) | 3 | 0,22% | 3 | 0,49% | 3 | 0,49% | 3 | 0,49% |
| Anker (2017) | 3 | 0,22% | 3 | 0,49% | 3 | 0,49% | 3 | 0,49% |
| Chace (1939) | 3 | 0,22% | 3 | 0,49% | 3 | 0,49% | 3 | 0,49% |
| Diaz & Cuzange (2009) | 3 | 0,22% | 2 | 0,33% | 2 | 0,33% | 2 | 0,33% |
| Goulletquer (2016) | 3 | 0,22% | 3 | 0,49% | 3 | 0,49% | 3 | 0,49% |
| Gueguen (1998) | 3 | 0,22% | 3 | 0,49% | 3 | 0,49% | 3 | 0,49% |
| Rathbun (1924) | 3 | 0,22% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Schmitt (1933) | 3 | 0,22% | 2 | 0,33% | 2 | 0,33% | 2 | 0,33% |
| Stimpson (1871) | 3 | 0,22% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Stimpson (1871) | 3 | 0,22% | 3 | 0,49% | 3 | 0,49% | 3 | 0,49% |
| Tavares (1994) | 3 | 0,22% | 3 | 0,49% | 3 | 0,49% | 3 | 0,49% |
| Anker (2007) | 2 | 0,14% | 2 | 0,33% | 2 | 0,33% | 2 | 0,33% |
| Anker (2014) | 2 | 0,14% | 2 | 0,33% | 2 | 0,33% | 2 | 0,33% |
| Anker (2020) | 2 | 0,14% | 2 | 0,33% | 2 | 0,33% | 2 | 0,33% |
| Benedict (1902) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bray et al. (1990) | 2 | 0,14% | 2 | 0,33% | 2 | 0,33% | 2 | 0,33% |
| Burkenroad (1939) | 2 | 0,14% | 2 | 0,33% | 2 | 0,33% | 2 | 0,33% |
| Chace (1962) | 2 | 0,14% | 2 | 0,33% | 2 | 0,33% | 2 | 0,33% |
| Churchill (1942) | 2 | 0,14% | 2 | 0,33% | 2 | 0,33% | 2 | 0,33% |
| Crane (1943) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Farfante & Bullis (1973) | 2 | 0,14% | 2 | 0,33% | 2 | 0,33% | 2 | 0,33% |
| Farfante (1967) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Farfante (1971) | 2 | 0,14% | 2 | 0,33% | 2 | 0,33% | 2 | 0,33% |
| Forest & Saint Laurent | 2 | 0,14% | 2 | 0,33% | 2 | 0,33% | 2 | 0,33% |
| Garcia (1977) | 2 | 0,14% | 2 | 0,33% | 2 | 0,33% | 2 | 0,33% |
| Goeke (1989) | 2 | 0,14% | 2 | 0,33% | 2 | 0,33% | 2 | 0,33% |
| Gueguen (1995) | 2 | 0,14% | 2 | 0,33% | 2 | 0,33% | 2 | 0,33% |
| Gueguen (1997) | 2 | 0,14% | 2 | 0,33% | 2 | 0,33% | 2 | 0,33% |
| Guinot-dumortier (1960) | 2 | 0,14% | 2 | 0,33% | 2 | 0,33% | 2 | 0,33% |
| Hines et al. (1995) | 2 | 0,14% | 2 | 0,33% | 2 | 0,33% | 2 | 0,33% |
| Holthuis (1974) | 2 | 0,14% | 2 | 0,33% | 2 | 0,33% | 2 | 0,33% |
| Lemaitre & Campos (1993) | 2 | 0,14% | 2 | 0,33% | 2 | 0,33% | 2 | 0,33% |
| Lemaitre & Mclaughlin (1996) | 2 | 0,14% | 2 | 0,33% | 2 | 0,33% | 2 | 0,33% |
| Lemaitre (1986) | 2 | 0,14% | 2 | 0,33% | 2 | 0,33% | 2 | 0,33% |
| Lucas (1846) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Macia & Robinson (2009) | 2 | 0,14% | 2 | 0,33% | 2 | 0,33% | 2 | 0,33% |
| Macpherson et al. (2016) | 2 | 0,14% | 2 | 0,33% | 2 | 0,33% | 2 | 0,33% |
| Macpherson (1988) | 2 | 0,14% | 2 | 0,33% | 2 | 0,33% | 2 | 0,33% |
| Macpherson (2007) | 2 | 0,14% | 2 | 0,33% | 2 | 0,33% | 2 | 0,33% |
| Manning (1969) | 2 | 0,14% | 2 | 0,33% | 2 | 0,33% | 2 | 0,33% |
| Milne-edwards (1837) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Milne-Edwards (1881) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Nobili (1906) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Olivier (1791-[1792]) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Patton et al. (1985) | 2 | 0,14% | 2 | 0,33% | 2 | 0,33% | 2 | 0,33% |
| Poupin et al. (2018) | 2 | 0,14% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Questel (2023) | 2 | 0,14% | 2 | 0,33% | 2 | 0,33% | 2 | 0,33% |
| Rathbun (1901) | 2 | 0,14% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Bulletin de la Société Zoologique de France, xxviii: 63-79.">Richard (1903) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Righi (1965) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Risso (1816) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Robles et al. (2007) | 2 | 0,14% | 2 | 0,33% | 2 | 0,33% | 2 | 0,33% |
| Rodríguez-flores et al. (2018) | 2 | 0,14% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Sarver et al. (1998) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Schmitt (1924) | 2 | 0,14% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Shirley & Wolcott (1991) | 2 | 0,14% | 2 | 0,33% | 2 | 0,33% | 2 | 0,33% |
| Tavares & Melo (2010) | 2 | 0,14% | 2 | 0,33% | 2 | 0,33% | 2 | 0,33% |
| Telford (1980) | 2 | 0,14% | 2 | 0,33% | 2 | 0,33% | 2 | 0,33% |
| Turkay (1975) | 2 | 0,14% | 2 | 0,33% | 2 | 0,33% | 2 | 0,33% |
| Vereshchaka (1994) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| von Hagen (1968) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Wass (1963) | 2 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Werding (1996) | 2 | 0,14% | 2 | 0,33% | 2 | 0,33% | 2 | 0,33% |
| Williams & Child (1989) | 2 | 0,14% | 2 | 0,33% | 2 | 0,33% | 2 | 0,33% |
| Williams (1974) | 2 | 0,14% | 2 | 0,33% | 2 | 0,33% | 2 | 0,33% |
| Williamson et al. (2012) | 2 | 0,14% | 2 | 0,33% | 2 | 0,33% | 2 | 0,33% |
| Abbe (1974) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Bulletin of the Museum of Comparative Zoology at Harvard College. 8(2): 69-84.">Agassiz (1880) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Annals of Natural History, (6)(xiii): pp. 225-245, 321-331, & 400-411.">Alcock (1894) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Amanieu & Dantec (1961) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Anker & Grave (2012) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Anonyme (2008) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Arnaud (2015) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Ary et al. (1985) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Barnard (1950) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bell (1865) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Boone (1930) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bouvier (1901) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Bouvier (1905) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Comptes rendus hebdomadaires des séances de l'Académie des sciences, 141: 746-749.">Bouvier (1905) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bouvier (1905) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Breton (2014) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Bruce (1974) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Brumbaugh & Mcconaugha (1995) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Burkenroad (1936) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Burkenroad (1946) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Carmona-Suarez (2015) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Carmona-Suarez (2015) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Carmona-suarez (2015) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Carvacho (1979) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Chace (1969) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Chan (1991) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Christoffersen (1979) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Coelho (1972) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Costlow et al. (1958) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Costlow (1967) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Coudray & Noël (2014) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Coudray & Noël (2014) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Coudray & Noël (2014) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| "The Fauna and Geography of the Maldive and Laccadive Archipelagoes" edited by J. Stanley Gardiner, Cambridge, 4to, vol. ii, part 4: 852-921, pls. lxx-lxxxvii, text-figg. 127-139.: 852-921.">Coutiere (1905) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cronin (1949) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Crosnier (1986) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Curd et al. (2015) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Daugherty (1952) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Davis et al. (2004) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Dewarumez et al. (2011) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Dittel et al. (2006) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Memoirs of the Museum of Comparative Zoology at Harvard College Cambridge, 27: 177-274.">Edwards & Bouvier (1909) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Fabricius (1793) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fabricius (1793) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fabricius (1798) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ferry et al. (2017) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Fingerman (1955) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Forward et al. (2003) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Fransen (1990) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Freeman et al. (1987) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Galil et al. (2016) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Galil (2000) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Garth (1951) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Gomez (1933) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gonzalez-ortegon et al. (2020) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Goy (2015) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Gray & Newcombe (1938) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Guinot (1969) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Gunter (1938) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Gurney (1943) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Havens et al. (2009) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Holthuis (1950) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Holthuis (1955) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Holthuis (1960) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Holthuis (1962) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Holthuis (1977) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Huff (1979) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Impact-Mer et al. (2011) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Ives (1891) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Johnson (1867) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jones (1969) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kingsley (1878) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Knowlton & Keller (1983) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Labrune et al. (2019) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Lenz & Strunck (1914) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Li (2008) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Lochhead & Newcombe (1942) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Macia & Robinson (2012) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Macpherson & Segonzac (2005) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Mancinelli et al. (2017) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Mancinelli et al. (2017) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Manning & Holthuis (1989) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Miers (1878) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Miers (1879) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Miers (1881) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Milne-edwards & Bouvier (1897) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Milne-edwards (1873-1880) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Milne-Edwards (1878) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Milne-edwards (1883) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Milne-Edwards (1890) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mulochau et al. (2019) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Nelson-Smith et al. (2014) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Newcombe et al. (1949) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Nobili (1905) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Noël & Boulad (2018) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Noël & Prouzet (2017) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Noël (2014) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Noël (2014) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Noël (2015) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Noël (2015) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Noël (2017) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Noël (2017) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Pachelle et al. (2016) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Pêpe et al. (2021) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Pezy et al. (2019) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Pfaller et al. (2019) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Poore (2014) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Poupin & Felder (2015) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Poupin et al. (2013) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rathbun (1892) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rathbun (1896) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Rathbun (1934) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Righi (1967) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rios & Duffy (2007) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Roudez et al. (2008) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Ryer et al. (1997) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Sadek et al. (2018) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Sanchez (1977) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sandoz & Rogers (1944) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Schmitt (1939) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Stimpson (1860) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Tavares & Amouroux (2003) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Tavares & Gouvea (2013) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Thongda et al. (2015) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Tollu (2009) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Torres et al. (2006) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Vereshchaka et al. (2020) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Vincent (1986) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Weckel (2019) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Weissburg & Zimmer-faust (1994) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Werding (1982) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Wolcott et al. (2005) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Yang et al. (2014) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| (1967) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
