Crustacés marins de Mayotte
Branchiopoda, Oligostraca et Multicrustacea marins (sens large) de Mayotte
287 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) | 1406 | 74,47% | 1287 | 185,71% | 1287 | 186,79% | 1280 | 185,78% |
| Poupin et al. (2018) | 360 | 19,07% | 342 | 49,35% | 341 | 49,49% | 342 | 49,64% |
| Poupin et al. (2013) | 145 | 7,68% | 131 | 18,9% | 131 | 19,01% | 129 | 18,72% |
| Poupin (2015) | 81 | 4,29% | 78 | 11,26% | 78 | 11,32% | 78 | 11,32% |
| Poupin et al. (2013) | 56 | 2,97% | 54 | 7,79% | 54 | 7,84% | 53 | 7,69% |
| Kornicker (1992) | 54 | 2,86% | 54 | 7,79% | 54 | 7,84% | 54 | 7,84% |
| Gaudy & Thomassin (2006) | 41 | 2,17% | 33 | 4,76% | 33 | 4,79% | 33 | 4,79% |
| Babinot & Kouyoumontzakis (1995) | 23 | 1,22% | 17 | 2,45% | 17 | 2,47% | 17 | 2,47% |
| Colin (2000) | 23 | 1,22% | 22 | 3,17% | 22 | 3,19% | 22 | 3,19% |
| Pagano (2009) | 22 | 1,17% | 21 | 3,03% | 21 | 3,05% | 21 | 3,05% |
| Corbari et al. (2020) | 18 | 0,95% | 13 | 1,88% | 13 | 1,89% | 13 | 1,89% |
| Poupin et al. (1999) | 17 | 0,9% | 13 | 1,88% | 13 | 1,89% | 13 | 1,89% |
| Keith et al. (2006) | 16 | 0,85% | 16 | 2,31% | 16 | 2,32% | 16 | 2,32% |
| Li (2008) | 16 | 0,85% | 13 | 1,88% | 13 | 1,89% | 13 | 1,89% |
| Renon & Lefèvre (1985) | 16 | 0,85% | 15 | 2,16% | 15 | 2,18% | 15 | 2,18% |
| Poupin et al. (2022) | 14 | 0,74% | 13 | 1,88% | 13 | 1,89% | 13 | 1,89% |
| Rathbun (1907) | 14 | 0,74% | 6 | 0,87% | 6 | 0,87% | 6 | 0,87% |
| Keith et al. (2013) | 13 | 0,69% | 13 | 1,88% | 13 | 1,89% | 13 | 1,89% |
| "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 | 0,58% | 6 | 0,87% | 6 | 0,87% | 6 | 0,87% |
| Nobili (1906) | 10 | 0,53% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
| Rathbun (1906) | 10 | 0,53% | 3 | 0,43% | 3 | 0,44% | 3 | 0,44% |
| Poupin et al. (2013) | 9 | 0,48% | 8 | 1,15% | 8 | 1,16% | 8 | 1,16% |
| Ramage (2017) | 9 | 0,48% | 9 | 1,3% | 9 | 1,31% | 9 | 1,31% |
| Bourjon et al. (2018) | 8 | 0,42% | 8 | 1,15% | 8 | 1,16% | 8 | 1,16% |
| Paris. pp. [i]-xii, 9-320 ; [Atlas] Crustacés, 5 planches ; Insectes, 21 planches.">Guérin-Méneville ([1829-1838]) | 8 | 0,42% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
| Guinot et al. (2018) | 8 | 0,42% | 8 | 1,15% | 8 | 1,16% | 8 | 1,16% |
| Lagarde (2008) | 8 | 0,42% | 8 | 1,15% | 8 | 1,16% | 8 | 1,16% |
| Man (1902) | 8 | 0,42% | 3 | 0,43% | 3 | 0,44% | 3 | 0,44% |
| Chace (1962) | 7 | 0,37% | 6 | 0,87% | 6 | 0,87% | 6 | 0,87% |
| Crosnier (1976) | 7 | 0,37% | 5 | 0,72% | 5 | 0,73% | 5 | 0,73% |
| Linnaeus (1758) | 7 | 0,37% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rignault & Chevallier (2017) | 7 | 0,37% | 6 | 0,87% | 6 | 0,87% | 6 | 0,87% |
| Cleva & Poupin (2012) | 6 | 0,32% | 6 | 0,87% | 6 | 0,87% | 6 | 0,87% |
| Crosnier (1965) | 6 | 0,32% | 5 | 0,72% | 5 | 0,73% | 5 | 0,73% |
| Laubitz (1995) | 6 | 0,32% | 6 | 0,87% | 6 | 0,87% | 6 | 0,87% |
| Macpherson & Robainas-Barcia (2015) | 6 | 0,32% | 6 | 0,87% | 6 | 0,87% | 6 | 0,87% |
| Maddocks (2007) | 6 | 0,32% | 4 | 0,58% | 4 | 0,58% | 4 | 0,58% |
| Questel (2020) | 6 | 0,32% | 6 | 0,87% | 6 | 0,87% | 6 | 0,87% |
| Roux (1926) | 6 | 0,32% | 5 | 0,72% | 5 | 0,73% | 5 | 0,73% |
| Ahyong (2014) | 5 | 0,26% | 5 | 0,72% | 5 | 0,73% | 5 | 0,73% |
| Borradaile (1915) | 5 | 0,26% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bruce (1967) | 5 | 0,26% | 3 | 0,43% | 3 | 0,44% | 3 | 0,44% |
| Collin (2000) | 5 | 0,26% | 5 | 0,72% | 5 | 0,73% | 5 | 0,73% |
| Forest (1987) | 5 | 0,26% | 5 | 0,72% | 5 | 0,73% | 5 | 0,73% |
| Ifremer (2009) | 5 | 0,26% | 3 | 0,43% | 3 | 0,44% | 3 | 0,44% |
| Keith & Vigneux (2002) | 5 | 0,26% | 5 | 0,72% | 5 | 0,73% | 5 | 0,73% |
| Keith et al. (1999) | 5 | 0,26% | 5 | 0,72% | 5 | 0,73% | 5 | 0,73% |
| Poupin et al. (2022) | 5 | 0,26% | 5 | 0,72% | 5 | 0,73% | 5 | 0,73% |
| Rosé (1924) | 5 | 0,26% | 3 | 0,43% | 3 | 0,44% | 3 | 0,44% |
| Stimpson (1860) | 5 | 0,26% | 5 | 0,72% | 5 | 0,73% | 5 | 0,73% |
| Tricart & Foubert (2000) | 5 | 0,26% | 5 | 0,72% | 5 | 0,73% | 5 | 0,73% |
| Uicn et al. (2019) | 5 | 0,26% | 5 | 0,72% | 5 | 0,73% | 5 | 0,73% |
| Ward (1939) | 5 | 0,26% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ward (1942) | 5 | 0,26% | 0 | 0% | 0 | 0% | 0 | 0% |
| Whatley & Keeler (1989) | 5 | 0,26% | 4 | 0,58% | 4 | 0,58% | 4 | 0,58% |
| Anker & Baeza (2021) | 4 | 0,21% | 4 | 0,58% | 4 | 0,58% | 4 | 0,58% |
| Binet (1984) | 4 | 0,21% | 4 | 0,58% | 4 | 0,58% | 4 | 0,58% |
| Bruce (1990) | 4 | 0,21% | 4 | 0,58% | 4 | 0,58% | 4 | 0,58% |
| Chan et al. (2021) | 4 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
| Crosnier (2002) | 4 | 0,21% | 4 | 0,58% | 4 | 0,58% | 3 | 0,44% |
| Dana (1852) | 4 | 0,21% | 3 | 0,43% | 3 | 0,44% | 3 | 0,44% |
| Fabricius (1798) | 4 | 0,21% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
| Galil et al. (2018) | 4 | 0,21% | 4 | 0,58% | 4 | 0,58% | 4 | 0,58% |
| Galil (2005) | 4 | 0,21% | 4 | 0,58% | 4 | 0,58% | 4 | 0,58% |
| Komai & Poupin (2012) | 4 | 0,21% | 4 | 0,58% | 4 | 0,58% | 4 | 0,58% |
| Komai (2010) | 4 | 0,21% | 4 | 0,58% | 4 | 0,58% | 4 | 0,58% |
| Lemaitre (2014) | 4 | 0,21% | 4 | 0,58% | 4 | 0,58% | 4 | 0,58% |
| Macpherson & Cleva (2010) | 4 | 0,21% | 4 | 0,58% | 4 | 0,58% | 4 | 0,58% |
| Macpherson et al. (2017) | 4 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
| Manning (1978) | 4 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
| Marquet (2002) | 4 | 0,21% | 4 | 0,58% | 4 | 0,58% | 4 | 0,58% |
| Mulochau et al. (2019) | 4 | 0,21% | 4 | 0,58% | 4 | 0,58% | 4 | 0,58% |
| Nobili (1905) | 4 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
| Odhner (1925) | 4 | 0,21% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
| Poupin et al. (2019) | 4 | 0,21% | 4 | 0,58% | 4 | 0,58% | 4 | 0,58% |
| Questel (2017) | 4 | 0,21% | 4 | 0,58% | 4 | 0,58% | 4 | 0,58% |
| Rodríguez-flores et al. (2019) | 4 | 0,21% | 4 | 0,58% | 4 | 0,58% | 4 | 0,58% |
| Rose (1925) | 4 | 0,21% | 3 | 0,43% | 3 | 0,44% | 3 | 0,44% |
| Serene (1984) | 4 | 0,21% | 4 | 0,58% | 4 | 0,58% | 4 | 0,58% |
| Vereshchaka et al. (2020) | 4 | 0,21% | 3 | 0,43% | 3 | 0,44% | 3 | 0,44% |
| Ward (1941) | 4 | 0,21% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
| Bordaille (1902) | 3 | 0,16% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
| Chatton (1912) | 3 | 0,16% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
| Clark (2002) | 3 | 0,16% | 3 | 0,43% | 3 | 0,44% | 3 | 0,44% |
| Collin (2002) | 3 | 0,16% | 3 | 0,43% | 3 | 0,44% | 3 | 0,44% |
| Edmondson (1925) | 3 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Edmondson (1951) | 3 | 0,16% | 3 | 0,43% | 3 | 0,44% | 3 | 0,44% |
| Fabricius (1787) | 3 | 0,16% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
| Gerken (2018) | 3 | 0,16% | 3 | 0,43% | 3 | 0,44% | 3 | 0,44% |
| Gout (1991) | 3 | 0,16% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
| Griffin & Tranter (1986) | 3 | 0,16% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
| Grygier (1985) | 3 | 0,16% | 3 | 0,43% | 3 | 0,44% | 3 | 0,44% |
| Guinot (1957) | 3 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Guinot (1964) | 3 | 0,16% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
| Haig (1989) | 3 | 0,16% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
| Hayashi (1995) | 3 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ifremer (2022) | 3 | 0,16% | 3 | 0,43% | 3 | 0,44% | 3 | 0,44% |
| Jellinek (1993) | 3 | 0,16% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
| Kilgallen & Lowry (2014) | 3 | 0,16% | 3 | 0,43% | 3 | 0,44% | 3 | 0,44% |
| Komai & Osawa (2006) | 3 | 0,16% | 3 | 0,43% | 3 | 0,44% | 3 | 0,44% |
| Kornicker (1983) | 3 | 0,16% | 3 | 0,43% | 3 | 0,44% | 3 | 0,44% |
| Lucatelli et al. (2012) | 3 | 0,16% | 3 | 0,43% | 3 | 0,44% | 3 | 0,44% |
| Machordom et al. (2022) | 3 | 0,16% | 3 | 0,43% | 3 | 0,44% | 3 | 0,44% |
| Maddocks (1969) | 3 | 0,16% | 3 | 0,43% | 3 | 0,44% | 3 | 0,44% |
| Manning (1968) | 3 | 0,16% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
| Manning (1978) | 3 | 0,16% | 3 | 0,43% | 3 | 0,44% | 3 | 0,44% |
| Mclaughlin & Haig (1989) | 3 | 0,16% | 3 | 0,43% | 3 | 0,44% | 3 | 0,44% |
| Mclay (2001) | 3 | 0,16% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
| Milne-Edwards (1865) | 3 | 0,16% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
| Moosa (1991) | 3 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Olivier (1791-[1792]) | 3 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Poore & Dworschak (2018) | 3 | 0,16% | 3 | 0,43% | 3 | 0,44% | 3 | 0,44% |
| Poupin & Bouchard (2010) | 3 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Questel & Le Quellec (2012) | 3 | 0,16% | 3 | 0,43% | 3 | 0,44% | 3 | 0,44% |
| Rathbun (1914) | 3 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rodríguez-Flores et al. (2021) | 3 | 0,16% | 3 | 0,43% | 3 | 0,44% | 3 | 0,44% |
| Rose (1933) | 3 | 0,16% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
| Sakai (1961) | 3 | 0,16% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
| Spiridonov et al. (2021) | 3 | 0,16% | 3 | 0,43% | 3 | 0,44% | 3 | 0,44% |
| Aguilera (2002) | 2 | 0,11% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
| Ahyong (2017) | 2 | 0,11% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
| Alcock (1905) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anker (2019) | 2 | 0,11% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
| Baird (1843) | 2 | 0,11% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
| Balss (1938) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Barnard (1950) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Barnard (1962) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bordaille (1903) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Brady (1868) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bruce (1978) | 2 | 0,11% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
| Buitendijk (1937) | 2 | 0,11% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
| Cabezas et al. (2011) | 2 | 0,11% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
| Calman (1909) | 2 | 0,11% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
| Carl (1907) | 2 | 0,11% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
| Chan & Crosnier (1991) | 2 | 0,11% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
| Chan et al. (2013) | 2 | 0,11% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
| Choy & Marquet (2002) | 2 | 0,11% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
| Claus (1866) | 2 | 0,11% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
| Crosnier (1962) | 2 | 0,11% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
| Crosnier (1991) | 2 | 0,11% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
| Duris & Bruce (1995) | 2 | 0,11% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
| Edmondson (1954) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bulletin of the Museum at Harvard College, 24 : 149-220.">Faxon (1893) | 2 | 0,11% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
| Forcellini et al. (2012) | 2 | 0,11% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
| Forest (1954) | 2 | 0,11% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
| Fourt et al. (2017) | 2 | 0,11% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
| Fyan (1916) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gordon (1968) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Goulletquer (2016) | 2 | 0,11% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
| Goy & Randall (1986) | 2 | 0,11% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
| Goy (2015) | 2 | 0,11% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
| Hartmann (1964) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hayashi (2009) | 2 | 0,11% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
| Heller (1861) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Klunzinger (1913) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Komai & Anker (2010) | 2 | 0,11% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
| Komai & Ng (2012) | 2 | 0,11% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
| Komai (2008) | 2 | 0,11% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
| Kubo (1949) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ledoyer (1982) | 2 | 0,11% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
| Lemaitre (1989) | 2 | 0,11% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
| Lemaitre (1994) | 2 | 0,11% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
| Maillaud et al. (2015) | 2 | 0,11% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
| Malay et al. (2012) | 2 | 0,11% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
| Man (1914) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mayer (1898) | 2 | 0,11% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
| Mazancourt et al. (2019) | 2 | 0,11% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
| Mclaughlin (1986) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Michel et al. (1971) | 2 | 0,11% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
| Milne-Edwards (1878) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Naderloo & Türkay (2010) | 2 | 0,11% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
| Ng & Richers de Forges (2015) | 2 | 0,11% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
| Nobili (1904) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Oliveira (1945) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Paulson (1875) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Poore & Andreakis (2012) | 2 | 0,11% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
| Poupin & Corbari (2016) | 2 | 0,11% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
| Poupin (1994) | 2 | 0,11% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
| Renon (1989) | 2 | 0,11% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
| Risso (1816) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rodriguez et al. (2019) | 2 | 0,11% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
| Rose (1926) | 2 | 0,11% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
| Sakai (1983) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Schmitt (1939) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Shih et al. (2016) | 2 | 0,11% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
| Stebbing (1917) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Takeda (1971) | 2 | 0,11% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
| Ward (1934) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Wood-Mason & Alcock(1891) | 2 | 0,11% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
| Yokoya (1936) | 2 | 0,11% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
| Zarenkov (1989) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Zhao et al. (1985) | 2 | 0,11% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
| Ahyong (2001) | 1 | 0,05% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
| Alcock (1896) | 1 | 0,05% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
| Baba (1990) | 1 | 0,05% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
| Baba (2005) | 1 | 0,05% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
| Balss (1933) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Barathieu et al. (2019) | 1 | 0,05% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
| Barathieu et al. (2023) | 1 | 0,05% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
| Bernasconi (2000) | 1 | 0,05% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
| Boone (1927) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Boone (1927) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bouvier (1914) | 1 | 0,05% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
| Boxshall & Huys (2007) | 1 | 0,05% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
| Boyko (2000) | 1 | 0,05% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
| Bruce (1966) | 1 | 0,05% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
| Bruce (1974) | 1 | 0,05% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
| Burkenroad (1936) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cabezas et al. (2010) | 1 | 0,05% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
| Cambert et al. (2011) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Carré (2006) | 1 | 0,05% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
| Chace (1976) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Chen et al. (2016) | 1 | 0,05% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
| Chia (1997) | 1 | 0,05% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
| Claus (1863) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Claus (1863) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Corbari et al. (2015) | 1 | 0,05% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
| Day (1978) | 1 | 0,05% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
| de Man (1902) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Edmondson (1931) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Edmondson (1952) | 1 | 0,05% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
| Ferry et al. (2017) | 1 | 0,05% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
| Forest (1958) | 1 | 0,05% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
| Froglia (1978) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Galil (2003) | 1 | 0,05% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
| Goy & Devaney (1980) | 1 | 0,05% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
| Gravier (1920) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Guinot et al. (1982) | 1 | 0,05% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
| Guinot et al. (1985) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Guinot (1958) | 1 | 0,05% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
| Hansen (1926) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Harada (1961) | 1 | 0,05% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
| Holthuis (1941) | 1 | 0,05% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
| Holthuis (1952) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Holthuis (1960) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Holthuis (1977) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jayachandran & Raji (2004) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kamita (1967) | 1 | 0,05% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
| Komai (1999) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Komai (2004) | 1 | 0,05% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
| Kornicker (2015) | 1 | 0,05% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
| Kossmann (1877) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Leach (1820) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lebeau (1976) | 1 | 0,05% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
| Lee et al. (2019) | 1 | 0,05% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
| Lemaitre (1996) | 1 | 0,05% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
| Lemaitre (2013) | 1 | 0,05% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
| Lowry (2007) | 1 | 0,05% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
| Maccagno (1936) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Macpherson et al. (2002) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Macpherson (2009) | 1 | 0,05% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
| Marin (2007) | 1 | 0,05% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
| Marin (2012) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Markham (2015) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Marukawa (1908) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mary (2017) | 1 | 0,05% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
| Miers (1881) | 1 | 0,05% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
| Müller (1990) | 1 | 0,05% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
| Naderloo et al. (2011) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Nobili (1901) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Noël (2015) | 1 | 0,05% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
| Noël (2016) | 1 | 0,05% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
| Noël (2017) | 1 | 0,05% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
| Noël (2017) | 1 | 0,05% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
| Olivier (1811) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ortmann (1890) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ortmann (1897) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pagano et al. (2012) | 1 | 0,05% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
| Paulmier (1996) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Paulmier (2009) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Peters (1852) | 1 | 0,05% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
| Philippi (1843) | 1 | 0,05% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
| Poupin (1997) | 1 | 0,05% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
| Poupin (2008) | 1 | 0,05% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
| Rahayu (2016) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Renon (1977) | 1 | 0,05% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
| Rüppell (1830) | 1 | 0,05% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
| Sakai (1969) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Short & Marquet (1998) | 1 | 0,05% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
| Stebbing (1923) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Stimpson (1860) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Takeda (2003) | 1 | 0,05% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
| Tavares & Amouroux (2003) | 1 | 0,05% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
| Terao (1913) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Tirmizi (1960) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Zarenkov (1994) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Zehnter (1895) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
