Scléractiniaires
Scleractinia
199 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
| Référence | Total | Valides | Espèces | Taxons terminaux | ||||
|---|---|---|---|---|---|---|---|---|
| nb | % | nb | % | nb | % | nb | % | |
| Pichon (2007) | 313 | 16,68% | 232 | 26,76% | 232 | 26,88% | 232 | 26,88% |
| Pichon & Thomassin (2005) | 202 | 10,76% | 153 | 17,65% | 153 | 17,73% | 153 | 17,73% |
| Pichon et al. (2007) | 171 | 9,11% | 137 | 15,8% | 137 | 15,87% | 137 | 15,87% |
| Faure et al. (2008) | 163 | 8,68% | 134 | 15,46% | 134 | 15,53% | 134 | 15,53% |
| Glynn et al. (2007) | 149 | 7,94% | 117 | 13,49% | 117 | 13,56% | 117 | 13,56% |
| Kitahara (2011) | 119 | 6,34% | 118 | 13,61% | 116 | 13,44% | 118 | 13,67% |
| Tricart & Foubert (2000) | 99 | 5,27% | 82 | 9,46% | 82 | 9,5% | 80 | 9,27% |
| Cairns (1999) | 98 | 5,22% | 91 | 10,5% | 88 | 10,2% | 90 | 10,43% |
| Pichon (comm. pers., 2012) | 82 | 4,37% | 68 | 7,84% | 68 | 7,88% | 68 | 7,88% |
| Uicn et al. (2020) | 66 | 3,52% | 59 | 6,81% | 59 | 6,84% | 59 | 6,84% |
| Questel (2020) | 56 | 2,98% | 53 | 6,11% | 53 | 6,14% | 52 | 6,03% |
| Chevalier & Kuhlmann (1983) | 52 | 2,77% | 31 | 3,58% | 31 | 3,59% | 31 | 3,59% |
| Questel & Le Quellec (2012) | 49 | 2,61% | 41 | 4,73% | 41 | 4,75% | 40 | 4,63% |
| Dana (1846-1849) | 40 | 2,13% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
| Andouche et al. (2020) | 38 | 2,02% | 36 | 4,15% | 36 | 4,17% | 36 | 4,17% |
| Fenner & Muir (2008) | 37 | 1,97% | 31 | 3,58% | 31 | 3,59% | 31 | 3,59% |
| Reveillaud et al. (2008) | 34 | 1,81% | 32 | 3,69% | 32 | 3,71% | 31 | 3,59% |
| Diaz & Cuzange (2009) | 31 | 1,65% | 24 | 2,77% | 24 | 2,78% | 24 | 2,78% |
| Sheppard (1987) | 30 | 1,6% | 8 | 0,92% | 8 | 0,93% | 8 | 0,93% |
| Bigot (comm. pers., 2018) | 26 | 1,39% | 25 | 2,88% | 25 | 2,9% | 25 | 2,9% |
| Fautin (2013) | 22 | 1,17% | 22 | 2,54% | 21 | 2,43% | 21 | 2,43% |
| IUCN (2013) | 21 | 1,12% | 17 | 1,96% | 17 | 1,97% | 17 | 1,97% |
| Quelch (1886) | 20 | 1,07% | 4 | 0,46% | 4 | 0,46% | 4 | 0,46% |
| Gardiner (1899) | 19 | 1,01% | 9 | 1,04% | 9 | 1,04% | 9 | 1,04% |
| Fourt et al. (2017) | 18 | 0,96% | 16 | 1,85% | 16 | 1,85% | 16 | 1,85% |
| Bosserelle et al. (2014) | 17 | 0,91% | 16 | 1,85% | 16 | 1,85% | 16 | 1,85% |
| Flot & Adjeroud (2009) | 17 | 0,91% | 15 | 1,73% | 15 | 1,74% | 15 | 1,74% |
| AAMP (2010) | 15 | 0,8% | 15 | 1,73% | 14 | 1,62% | 15 | 1,74% |
| Kitahara & Cairns (2009) | 15 | 0,8% | 15 | 1,73% | 15 | 1,74% | 15 | 1,74% |
| Kitahara et al. (2010) | 15 | 0,8% | 15 | 1,73% | 15 | 1,74% | 15 | 1,74% |
| Orrell (2019) | 15 | 0,8% | 10 | 1,15% | 10 | 1,16% | 10 | 1,16% |
| Moseley ([1880]) | 14 | 0,75% | 7 | 0,81% | 7 | 0,81% | 7 | 0,81% |
| Ifremer (2009) | 13 | 0,69% | 10 | 1,15% | 10 | 1,16% | 9 | 1,04% |
| Low & Evenhuis (2013) | 13 | 0,69% | 6 | 0,69% | 6 | 0,7% | 6 | 0,7% |
| Zibrowius (1968) | 12 | 0,64% | 8 | 0,92% | 8 | 0,93% | 8 | 0,93% |
| . Rapport GIS "Lag-May" / Conseil Général de Mayotte / Centre d'Océanologie de Marseille. 61 pp.">Thomassin et al. (1998) | 11 | 0,59% | 9 | 1,04% | 9 | 1,04% | 9 | 1,04% |
| National Institute of Water and Atmospheric Research (2016) | 10 | 0,53% | 7 | 0,81% | 7 | 0,81% | 7 | 0,81% |
| Payri et al. (2002) | 10 | 0,53% | 7 | 0,81% | 7 | 0,81% | 7 | 0,81% |
| Milne-Edwards (1848) | 9 | 0,48% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
| Adjeroud et al. (2012) | 8 | 0,43% | 5 | 0,58% | 5 | 0,58% | 5 | 0,58% |
| Arrigoni et al. (2016) | 8 | 0,43% | 8 | 0,92% | 8 | 0,93% | 8 | 0,93% |
| Peralta & Fautin (2013) | 8 | 0,43% | 3 | 0,35% | 3 | 0,35% | 3 | 0,35% |
| Cairns (2000) | 7 | 0,37% | 7 | 0,81% | 7 | 0,81% | 7 | 0,81% |
| Martin (2011) | 7 | 0,37% | 5 | 0,58% | 5 | 0,58% | 5 | 0,58% |
| Cairns (1989) | 6 | 0,32% | 6 | 0,69% | 6 | 0,7% | 6 | 0,7% |
| Cairns (2004) | 6 | 0,32% | 6 | 0,69% | 6 | 0,7% | 6 | 0,7% |
| Duchassaing et al. (1860) | 6 | 0,32% | 2 | 0,23% | 2 | 0,23% | 1 | 0,12% |
| Kitahara & Cairns (2008) | 6 | 0,32% | 6 | 0,69% | 6 | 0,7% | 6 | 0,7% |
| Pourtales (1868) | 6 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pourtalès (1880) | 6 | 0,32% | 4 | 0,46% | 4 | 0,46% | 4 | 0,46% |
| Zibrowius (1974) | 6 | 0,32% | 4 | 0,46% | 4 | 0,46% | 4 | 0,46% |
| Proceedings of the Royal Society of London, 24: 543-569.">Moseley (1876) | 5 | 0,27% | 3 | 0,35% | 3 | 0,35% | 3 | 0,35% |
| Wells (1968) | 5 | 0,27% | 4 | 0,46% | 4 | 0,46% | 4 | 0,46% |
| Arrigoni et al. (2018) | 4 | 0,21% | 4 | 0,46% | 4 | 0,46% | 4 | 0,46% |
| Arrigoni et al. (2020) | 4 | 0,21% | 4 | 0,46% | 4 | 0,46% | 4 | 0,46% |
| Benzoni et al. (2010) | 4 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
| Duchassaing et al. (1864) | 4 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
| Godet et al. (2010) | 4 | 0,21% | 4 | 0,46% | 4 | 0,46% | 4 | 0,46% |
| Goud et al. (2021) | 4 | 0,21% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Quelch (1884) | 4 | 0,21% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
| Uicn et al. (2019) | 4 | 0,21% | 4 | 0,46% | 4 | 0,46% | 4 | 0,46% |
| Vaughan (1906) | 4 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
| Volpi & Benvenuti (2003) | 4 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bourcier (1988) | 3 | 0,16% | 3 | 0,35% | 3 | 0,35% | 3 | 0,35% |
| Carricart-Ganivet & Reyes-Bonilla (1999) | 3 | 0,16% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
| Chevalier (1971) | 3 | 0,16% | 3 | 0,35% | 3 | 0,35% | 3 | 0,35% |
| Devantier et al. (2008) | 3 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Devantier et al. (2014) | 3 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gall (2021) | 3 | 0,16% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Gardiner (1897) | 3 | 0,16% | 3 | 0,35% | 3 | 0,35% | 3 | 0,35% |
| Harvard University Museum & Morris P.J. (2020) | 3 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hoffmeister (1929) | 3 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Impact-Mer et al. (2011) | 3 | 0,16% | 3 | 0,35% | 3 | 0,35% | 3 | 0,35% |
| Johnston & Burgess (2023) | 3 | 0,16% | 3 | 0,35% | 3 | 0,35% | 3 | 0,35% |
| Nelson-Smith et al. (2014) | 3 | 0,16% | 3 | 0,35% | 3 | 0,35% | 3 | 0,35% |
| Vaughan (1907) | 3 | 0,16% | 3 | 0,35% | 3 | 0,35% | 3 | 0,35% |
| Tijdschrift der Nederlandse Dierkundige Vereeniging (Ser. 2), 7: 89-115.">Alcock (1902) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Benzoni & Pichon (2004) | 2 | 0,11% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
| Benzoni et al. (2014) | 2 | 0,11% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
| Benzoni (2013) | 2 | 0,11% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
| Brook (1892) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Brugneaux & Pérès (2006) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cairns & Zibrowius (2016) | 2 | 0,11% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
| Cairns (1977) | 2 | 0,11% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
| Cairns (1979) | 2 | 0,11% | 2 | 0,23% | 1 | 0,12% | 2 | 0,23% |
| Cairns (1995) | 2 | 0,11% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
| Duchassaing & Fonbressin (1870) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ellis & Solander (1786) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gardiner (1900) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hourigan (2020) | 2 | 0,11% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
| Ifremer (2020) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Le Sueur (1817) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lindström (1877) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Linsley et al. (1999) | 2 | 0,11% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
| Mckenna et al. (2009) | 2 | 0,11% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
| Richer de Forges et al. (2005) | 2 | 0,11% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
| Sheppard et al. (2008) | 2 | 0,11% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
| Turak et al. (2008) | 2 | 0,11% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
| Turak et al. (2014) | 2 | 0,11% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
| Umbgrove (1940) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Veron (2000) | 2 | 0,11% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
| Wells (1961) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Wijsman-Best (1970) | 2 | 0,11% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
| Yiu & Qiu (2022) | 2 | 0,11% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
| Zibrowius (1980) | 2 | 0,11% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
| Aronson et al. (2008) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Aronson et al. (2008) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Aronson et al. (2008) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Aronson et al. (2008) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Aronson et al. (2008) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Aronson et al. (2008) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Aronson et al. (2008) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Arrigoni et al. (2016) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Australian Museum (2020) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Bernard (1896) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Bernard (1897) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Bernard (1897) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Brook (1891) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cairns (1979) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Cairns (1998) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cambert et al. (2011) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cecchini (1914) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Chevaldonné et al. (2015) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Cuif et al. (2003) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Dennant (1904) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Devantier et al. (2008) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Devantier et al. (2008) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Devantier et al. (2008) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Devantier et al. (2008) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| deVantier et al. (2008) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| deVantier et al. (2008) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Devantier et al. (2014) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Devantier et al. (2014) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| deVantier et al. (2014) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| deVantier et al. (2014) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| deVantier et al. (2014) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| deVantier et al. (2014) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| DORIS (2012) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Duchassaing & Fontbressin (1850) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Duncan (1865) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Duncan (1876) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Duncan (1889) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| European Nucleotide Archive (2019) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Faure (1982) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Fortic et al. (2023) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Gardiner (1898) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Goulletquer (2016) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Gravier (1910) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Gregory (1895) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Head (1978) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Hoeksema & Vicente (2014) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Hoeksema et al. (2014) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Hoeksema et al. (2014) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Hoeksema et al. (2014) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Hoeksema et al. (2014) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Hoeksema et al. (2014) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hoeksema (2012) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| ICZN (2011) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ifremer (2021) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| IUCN (2014) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Kitahara (2005) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Klunzinger (1879) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lacaze-Duthiers (1897) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Linnaeus (1758) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Linnaeus (1767) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mckenna et al. (2011) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Milne & Edwards (1860) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Milne et al. (1857) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Nemenzo (1976) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Nolf & Cahuzac (2009) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Owens (1994) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Payri et al. (2016) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Pearman et al. (2020) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Pichon et al. (2020) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Pourtalès (1874) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Pyle et al. (2016) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Questel (2022) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Richards et al. (2008) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Richards et al. (2014) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Risso (1826) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Roule (1900) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Sheppard et al. (2008) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sheppard et al. (2014) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Turak et al. (2008) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Vaga et al. (2023) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Van et al. (2008) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Veron & Wallace (1984) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Veron et al. (1977) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Veron (1985) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Veron (1985) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Verrill (1864) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Verrill (1872) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Verrill (1901) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Wallace & Wolstenholme (1998) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Wallace (1994) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Wallace (1999) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Yabe & Sugiyama (1937) | 1 | 0,05% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Zibrowius & Arnaud (1995) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Zibrowius (1982) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
