Décapodes de Mayotte
234 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
| Référence | Total | Valides | Espèces | Taxons terminaux | ||||
|---|---|---|---|---|---|---|---|---|
| nb | % | nb | % | nb | % | nb | % | |
| Poupin (2010) | 1383 | 81,93% | 1265 | 214,04% | 1265 | 215,5% | 1258 | 214,31% |
| Poupin et al. (2018) | 365 | 21,62% | 347 | 58,71% | 346 | 58,94% | 347 | 59,11% |
| Poupin et al. (2013) | 143 | 8,47% | 130 | 22% | 130 | 22,15% | 128 | 21,81% |
| Poupin (2015) | 83 | 4,92% | 80 | 13,54% | 80 | 13,63% | 80 | 13,63% |
| Poupin et al. (2013) | 57 | 3,38% | 55 | 9,31% | 55 | 9,37% | 54 | 9,2% |
| Corbari et al. (2020) | 18 | 1,07% | 13 | 2,2% | 13 | 2,21% | 13 | 2,21% |
| Keith et al. (2006) | 18 | 1,07% | 18 | 3,05% | 18 | 3,07% | 18 | 3,07% |
| Li (2008) | 16 | 0,95% | 13 | 2,2% | 13 | 2,21% | 13 | 2,21% |
| Keith et al. (2013) | 15 | 0,89% | 15 | 2,54% | 15 | 2,56% | 15 | 2,56% |
| Rathbun (1907) | 14 | 0,83% | 6 | 1,02% | 6 | 1,02% | 6 | 1,02% |
| Poupin et al. (2022) | 13 | 0,77% | 12 | 2,03% | 12 | 2,04% | 12 | 2,04% |
| Ramage (2017) | 13 | 0,77% | 13 | 2,2% | 13 | 2,21% | 13 | 2,21% |
| "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) | 11 | 0,65% | 6 | 1,02% | 6 | 1,02% | 6 | 1,02% |
| Nobili (1906) | 10 | 0,59% | 2 | 0,34% | 2 | 0,34% | 2 | 0,34% |
| Rathbun (1906) | 10 | 0,59% | 3 | 0,51% | 3 | 0,51% | 3 | 0,51% |
| Poupin et al. (2013) | 9 | 0,53% | 8 | 1,35% | 8 | 1,36% | 8 | 1,36% |
| Bourjon et al. (2018) | 8 | 0,47% | 8 | 1,35% | 8 | 1,36% | 8 | 1,36% |
| Paris. pp. [i]-xii, 9-320 ; [Atlas] Crustacés, 5 planches ; Insectes, 21 planches.">Guérin-Méneville ([1829-1838]) | 8 | 0,47% | 2 | 0,34% | 2 | 0,34% | 2 | 0,34% |
| Guinot et al. (2018) | 8 | 0,47% | 8 | 1,35% | 8 | 1,36% | 8 | 1,36% |
| Lagarde (2008) | 8 | 0,47% | 8 | 1,35% | 8 | 1,36% | 8 | 1,36% |
| Chace (1962) | 7 | 0,41% | 6 | 1,02% | 6 | 1,02% | 6 | 1,02% |
| Crosnier (1976) | 7 | 0,41% | 5 | 0,85% | 5 | 0,85% | 5 | 0,85% |
| Poupin et al. (1999) | 7 | 0,41% | 4 | 0,68% | 4 | 0,68% | 4 | 0,68% |
| Poupin (2024) | 7 | 0,41% | 7 | 1,18% | 7 | 1,19% | 7 | 1,19% |
| Roux (1926) | 7 | 0,41% | 6 | 1,02% | 6 | 1,02% | 6 | 1,02% |
| Cleva & Poupin (2012) | 6 | 0,36% | 6 | 1,02% | 6 | 1,02% | 6 | 1,02% |
| Crosnier (1965) | 6 | 0,36% | 5 | 0,85% | 5 | 0,85% | 5 | 0,85% |
| Linnaeus (1758) | 6 | 0,36% | 0 | 0% | 0 | 0% | 0 | 0% |
| Macpherson & Robainas-Barcia (2015) | 6 | 0,36% | 6 | 1,02% | 6 | 1,02% | 6 | 1,02% |
| Man (1902) | 6 | 0,36% | 3 | 0,51% | 3 | 0,51% | 3 | 0,51% |
| Questel (2020) | 6 | 0,36% | 6 | 1,02% | 6 | 1,02% | 6 | 1,02% |
| Ahyong (2014) | 5 | 0,3% | 5 | 0,85% | 5 | 0,85% | 5 | 0,85% |
| Borradaile (1915) | 5 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bruce (1967) | 5 | 0,3% | 3 | 0,51% | 3 | 0,51% | 3 | 0,51% |
| Forest (1987) | 5 | 0,3% | 5 | 0,85% | 5 | 0,85% | 5 | 0,85% |
| Keith & Vigneux (2002) | 5 | 0,3% | 5 | 0,85% | 5 | 0,85% | 5 | 0,85% |
| Keith et al. (1999) | 5 | 0,3% | 5 | 0,85% | 5 | 0,85% | 5 | 0,85% |
| Marquet (2002) | 5 | 0,3% | 5 | 0,85% | 5 | 0,85% | 5 | 0,85% |
| Poupin et al. (2022) | 5 | 0,3% | 5 | 0,85% | 5 | 0,85% | 5 | 0,85% |
| Rignault & Chevallier (2017) | 5 | 0,3% | 4 | 0,68% | 4 | 0,68% | 4 | 0,68% |
| Stimpson (1860) | 5 | 0,3% | 5 | 0,85% | 5 | 0,85% | 5 | 0,85% |
| Tricart & Foubert (2000) | 5 | 0,3% | 5 | 0,85% | 5 | 0,85% | 5 | 0,85% |
| Uicn et al. (2019) | 5 | 0,3% | 5 | 0,85% | 5 | 0,85% | 5 | 0,85% |
| Ward (1939) | 5 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ward (1942) | 5 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anker & Baeza (2021) | 4 | 0,24% | 4 | 0,68% | 4 | 0,68% | 4 | 0,68% |
| Bruce (1990) | 4 | 0,24% | 4 | 0,68% | 4 | 0,68% | 4 | 0,68% |
| Chan et al. (2021) | 4 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
| Crosnier (2002) | 4 | 0,24% | 4 | 0,68% | 4 | 0,68% | 3 | 0,51% |
| Dana (1852) | 4 | 0,24% | 3 | 0,51% | 3 | 0,51% | 3 | 0,51% |
| Fabricius (1798) | 4 | 0,24% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Forest (1954) | 4 | 0,24% | 3 | 0,51% | 3 | 0,51% | 3 | 0,51% |
| Galil et al. (2018) | 4 | 0,24% | 4 | 0,68% | 4 | 0,68% | 4 | 0,68% |
| Galil (2005) | 4 | 0,24% | 4 | 0,68% | 4 | 0,68% | 4 | 0,68% |
| Ifremer (2009) | 4 | 0,24% | 3 | 0,51% | 3 | 0,51% | 3 | 0,51% |
| Komai & Poupin (2012) | 4 | 0,24% | 4 | 0,68% | 4 | 0,68% | 4 | 0,68% |
| Komai (2010) | 4 | 0,24% | 4 | 0,68% | 4 | 0,68% | 4 | 0,68% |
| Lemaitre (2014) | 4 | 0,24% | 4 | 0,68% | 4 | 0,68% | 4 | 0,68% |
| Macpherson & Cleva (2010) | 4 | 0,24% | 4 | 0,68% | 4 | 0,68% | 4 | 0,68% |
| Macpherson et al. (2017) | 4 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mulochau et al. (2019) | 4 | 0,24% | 4 | 0,68% | 4 | 0,68% | 4 | 0,68% |
| Nobili (1905) | 4 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
| Odhner (1925) | 4 | 0,24% | 2 | 0,34% | 2 | 0,34% | 2 | 0,34% |
| Questel (2017) | 4 | 0,24% | 4 | 0,68% | 4 | 0,68% | 4 | 0,68% |
| Rodríguez-flores et al. (2019) | 4 | 0,24% | 4 | 0,68% | 4 | 0,68% | 4 | 0,68% |
| Serene (1984) | 4 | 0,24% | 4 | 0,68% | 4 | 0,68% | 4 | 0,68% |
| Vereshchaka et al. (2020) | 4 | 0,24% | 3 | 0,51% | 3 | 0,51% | 3 | 0,51% |
| Ward (1941) | 4 | 0,24% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Bordaille (1902) | 3 | 0,18% | 2 | 0,34% | 2 | 0,34% | 2 | 0,34% |
| Clark (2002) | 3 | 0,18% | 3 | 0,51% | 3 | 0,51% | 3 | 0,51% |
| Edmondson (1925) | 3 | 0,18% | 0 | 0% | 0 | 0% | 0 | 0% |
| Edmondson (1951) | 3 | 0,18% | 3 | 0,51% | 3 | 0,51% | 3 | 0,51% |
| Fabricius (1787) | 3 | 0,18% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Griffin & Tranter (1986) | 3 | 0,18% | 2 | 0,34% | 2 | 0,34% | 2 | 0,34% |
| Guinot (1957) | 3 | 0,18% | 0 | 0% | 0 | 0% | 0 | 0% |
| Guinot (1964) | 3 | 0,18% | 2 | 0,34% | 2 | 0,34% | 2 | 0,34% |
| Haig (1989) | 3 | 0,18% | 2 | 0,34% | 2 | 0,34% | 2 | 0,34% |
| Hayashi (1995) | 3 | 0,18% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ifremer (2022) | 3 | 0,18% | 3 | 0,51% | 3 | 0,51% | 3 | 0,51% |
| Komai & Osawa (2006) | 3 | 0,18% | 3 | 0,51% | 3 | 0,51% | 3 | 0,51% |
| Machordom et al. (2022) | 3 | 0,18% | 3 | 0,51% | 3 | 0,51% | 3 | 0,51% |
| Mclaughlin & Haig (1989) | 3 | 0,18% | 3 | 0,51% | 3 | 0,51% | 3 | 0,51% |
| Mclay (2001) | 3 | 0,18% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Milne-Edwards (1865) | 3 | 0,18% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Olivier (1791-[1792]) | 3 | 0,18% | 0 | 0% | 0 | 0% | 0 | 0% |
| Poore & Dworschak (2018) | 3 | 0,18% | 3 | 0,51% | 3 | 0,51% | 3 | 0,51% |
| Poupin & Bouchard (2010) | 3 | 0,18% | 0 | 0% | 0 | 0% | 0 | 0% |
| Questel & Le Quellec (2012) | 3 | 0,18% | 3 | 0,51% | 3 | 0,51% | 3 | 0,51% |
| Rathbun (1914) | 3 | 0,18% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rodríguez-Flores et al. (2021) | 3 | 0,18% | 3 | 0,51% | 3 | 0,51% | 3 | 0,51% |
| Sakai (1961) | 3 | 0,18% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Spiridonov et al. (2021) | 3 | 0,18% | 3 | 0,51% | 3 | 0,51% | 3 | 0,51% |
| Aguilera (2002) | 2 | 0,12% | 2 | 0,34% | 2 | 0,34% | 2 | 0,34% |
| Alcock (1905) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anker (2019) | 2 | 0,12% | 2 | 0,34% | 2 | 0,34% | 2 | 0,34% |
| Balss (1938) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Barnard (1950) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Barnard (1962) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bordaille (1903) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bruce (1978) | 2 | 0,12% | 2 | 0,34% | 2 | 0,34% | 2 | 0,34% |
| Buitendijk (1937) | 2 | 0,12% | 2 | 0,34% | 2 | 0,34% | 2 | 0,34% |
| Cabezas et al. (2011) | 2 | 0,12% | 2 | 0,34% | 2 | 0,34% | 2 | 0,34% |
| Calman (1909) | 2 | 0,12% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Cambert et al. (2011) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Chan & Crosnier (1991) | 2 | 0,12% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Chan et al. (2013) | 2 | 0,12% | 2 | 0,34% | 2 | 0,34% | 2 | 0,34% |
| Choy & Marquet (2002) | 2 | 0,12% | 2 | 0,34% | 2 | 0,34% | 2 | 0,34% |
| Crosnier (1962) | 2 | 0,12% | 2 | 0,34% | 2 | 0,34% | 2 | 0,34% |
| Crosnier (1991) | 2 | 0,12% | 2 | 0,34% | 2 | 0,34% | 2 | 0,34% |
| Duris & Bruce (1995) | 2 | 0,12% | 2 | 0,34% | 2 | 0,34% | 2 | 0,34% |
| Edmondson (1954) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bulletin of the Museum at Harvard College, 24 : 149-220.">Faxon (1893) | 2 | 0,12% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Forcellini et al. (2012) | 2 | 0,12% | 2 | 0,34% | 2 | 0,34% | 2 | 0,34% |
| Fourt et al. (2017) | 2 | 0,12% | 2 | 0,34% | 2 | 0,34% | 2 | 0,34% |
| Gordon (1968) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Goulletquer (2016) | 2 | 0,12% | 2 | 0,34% | 2 | 0,34% | 2 | 0,34% |
| Goy & Randall (1986) | 2 | 0,12% | 2 | 0,34% | 2 | 0,34% | 2 | 0,34% |
| Goy (2015) | 2 | 0,12% | 2 | 0,34% | 2 | 0,34% | 2 | 0,34% |
| Hayashi (2009) | 2 | 0,12% | 2 | 0,34% | 2 | 0,34% | 2 | 0,34% |
| Heller (1861) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Klunzinger (1913) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Komai & Anker (2010) | 2 | 0,12% | 2 | 0,34% | 2 | 0,34% | 2 | 0,34% |
| Komai & Ng (2012) | 2 | 0,12% | 2 | 0,34% | 2 | 0,34% | 2 | 0,34% |
| Komai (2008) | 2 | 0,12% | 2 | 0,34% | 2 | 0,34% | 2 | 0,34% |
| Kubo (1949) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lemaitre (1989) | 2 | 0,12% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Lemaitre (1994) | 2 | 0,12% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Maillaud et al. (2015) | 2 | 0,12% | 2 | 0,34% | 2 | 0,34% | 2 | 0,34% |
| Malay et al. (2012) | 2 | 0,12% | 2 | 0,34% | 2 | 0,34% | 2 | 0,34% |
| Man (1914) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mazancourt et al. (2019) | 2 | 0,12% | 2 | 0,34% | 2 | 0,34% | 2 | 0,34% |
| Mclaughlin (1986) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Milne-Edwards (1878) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Naderloo & Türkay (2010) | 2 | 0,12% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Naderloo (2013) | 2 | 0,12% | 2 | 0,34% | 2 | 0,34% | 2 | 0,34% |
| Ng & Richers de Forges (2015) | 2 | 0,12% | 2 | 0,34% | 2 | 0,34% | 2 | 0,34% |
| Nobili (1904) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Paulson (1875) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Poore & Andreakis (2012) | 2 | 0,12% | 2 | 0,34% | 2 | 0,34% | 2 | 0,34% |
| Poupin & Corbari (2016) | 2 | 0,12% | 2 | 0,34% | 2 | 0,34% | 2 | 0,34% |
| Poupin (1994) | 2 | 0,12% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Risso (1816) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rodriguez et al. (2019) | 2 | 0,12% | 2 | 0,34% | 2 | 0,34% | 2 | 0,34% |
| Sakai (1983) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Schmitt (1939) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Shih et al. (2016) | 2 | 0,12% | 2 | 0,34% | 2 | 0,34% | 2 | 0,34% |
| Stebbing (1917) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Takeda (1971) | 2 | 0,12% | 2 | 0,34% | 2 | 0,34% | 2 | 0,34% |
| Ward (1934) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Wood-Mason & Alcock(1891) | 2 | 0,12% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Yokoya (1936) | 2 | 0,12% | 2 | 0,34% | 2 | 0,34% | 2 | 0,34% |
| Zarenkov (1989) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Alcock (1896) | 1 | 0,06% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Baba (1990) | 1 | 0,06% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Baba (2005) | 1 | 0,06% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Balss (1933) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Barathieu et al. (2019) | 1 | 0,06% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Barathieu et al. (2023) | 1 | 0,06% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Boone (1927) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Boone (1927) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bouvier (1914) | 1 | 0,06% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Boyko (2000) | 1 | 0,06% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Bruce (1966) | 1 | 0,06% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Bruce (1974) | 1 | 0,06% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Burkenroad (1936) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cabezas et al. (2010) | 1 | 0,06% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Carré (2006) | 1 | 0,06% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Chace (1976) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Chen et al. (2016) | 1 | 0,06% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Chia (1997) | 1 | 0,06% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Corbari et al. (2015) | 1 | 0,06% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| de Man (1902) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Edmondson (1931) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Edmondson (1952) | 1 | 0,06% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Ferry et al. (2017) | 1 | 0,06% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Forest (1958) | 1 | 0,06% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Froglia (1978) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Galil (2003) | 1 | 0,06% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Gout (1991) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Goy & Devaney (1980) | 1 | 0,06% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Gravier (1920) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Guinot et al. (1982) | 1 | 0,06% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Guinot et al. (1985) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Guinot (1958) | 1 | 0,06% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Harada (1961) | 1 | 0,06% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Holthuis (1952) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Holthuis (1960) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Holthuis (1969) | 1 | 0,06% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Holthuis (1977) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jayachandran & Raji (2004) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kamita (1967) | 1 | 0,06% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Keith & Marquet (2011) | 1 | 0,06% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Komai (1999) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Komai (2004) | 1 | 0,06% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Kossmann (1877) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Leach (1820) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lebeau (1976) | 1 | 0,06% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Lee et al. (2019) | 1 | 0,06% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Lemaitre (1996) | 1 | 0,06% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Lemaitre (2013) | 1 | 0,06% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Maccagno (1936) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Macpherson et al. (2002) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Macpherson (2009) | 1 | 0,06% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Marin (2007) | 1 | 0,06% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Marin (2012) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mary (2017) | 1 | 0,06% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Miers (1881) | 1 | 0,06% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Naderloo et al. (2011) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Nobili (1901) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Noël (2015) | 1 | 0,06% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Noël (2016) | 1 | 0,06% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Noël (2017) | 1 | 0,06% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Noël (2017) | 1 | 0,06% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Olivier (1811) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ortmann (1890) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ortmann (1897) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Osawa & Poupin (2013) | 1 | 0,06% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Paulmier (1996) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pearman et al. (2020) | 1 | 0,06% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Peters (1852) | 1 | 0,06% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Poupin (1997) | 1 | 0,06% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Poupin (2008) | 1 | 0,06% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Rahayu (2016) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rüppell (1830) | 1 | 0,06% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Sakai (1969) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Short & Marquet (1998) | 1 | 0,06% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Stebbing (1923) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Stimpson (1860) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Takeda (2003) | 1 | 0,06% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Tavares & Amouroux (2003) | 1 | 0,06% | 1 | 0,17% | 1 | 0,17% | 1 | 0,17% |
| Terao (1913) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Tirmizi (1960) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Zarenkov (1994) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Zehnter (1895) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
