Porifères de métropole
Porifera de métropole
278 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
| Référence | Total | Valides | Espèces | Taxons terminaux | ||||
|---|---|---|---|---|---|---|---|---|
| nb | % | nb | % | nb | % | nb | % | |
| Vacelet (1969) | 124 | 4,63% | 75 | 10,82% | 75 | 10,85% | 74 | 10,71% |
| Vacelet (1961) | 105 | 3,92% | 72 | 10,39% | 72 | 10,42% | 72 | 10,42% |
| Haeckel (1872) | 78 | 2,91% | 6 | 0,87% | 6 | 0,87% | 6 | 0,87% |
| Fourt et al. (2017) | 70 | 2,62% | 50 | 7,22% | 50 | 7,24% | 48 | 6,95% |
| Topsent (1892) | 57 | 2,13% | 12 | 1,73% | 12 | 1,74% | 12 | 1,74% |
| Cabioch (1968) | 52 | 1,94% | 24 | 3,46% | 23 | 3,33% | 23 | 3,33% |
| Godet et al. (2010) | 47 | 1,76% | 40 | 5,77% | 40 | 5,79% | 39 | 5,64% |
| Nelson-Smith et al. (2014) | 39 | 1,46% | 29 | 4,18% | 29 | 4,2% | 28 | 4,05% |
| Breton (2014) | 24 | 0,9% | 21 | 3,03% | 21 | 3,04% | 20 | 2,89% |
| Topsent (1890) | 21 | 0,78% | 8 | 1,15% | 8 | 1,16% | 8 | 1,16% |
| Topsent (1896) | 18 | 0,67% | 9 | 1,3% | 9 | 1,3% | 9 | 1,3% |
| Descatoire (1966) | 17 | 0,64% | 8 | 1,15% | 8 | 1,16% | 8 | 1,16% |
| Annu Ist Zool Univ Napoli, 12: 1-93.">Sara & Siribelli (1960) | 17 | 0,64% | 8 | 1,15% | 8 | 1,16% | 8 | 1,16% |
| Schmidt (1862) | 17 | 0,64% | 5 | 0,72% | 5 | 0,72% | 5 | 0,72% |
| Bowerbank (1866) | 16 | 0,6% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
| Sara (1958) | 14 | 0,52% | 6 | 0,87% | 6 | 0,87% | 6 | 0,87% |
| Barucca et al. (2007) | 12 | 0,45% | 10 | 1,44% | 10 | 1,45% | 10 | 1,45% |
| Hansson (1999) | 11 | 0,41% | 8 | 1,15% | 8 | 1,16% | 8 | 1,16% |
| Sara et al. (1992) | 11 | 0,41% | 9 | 1,3% | 9 | 1,3% | 9 | 1,3% |
| Pisera & Vacelet (2011) | 10 | 0,37% | 8 | 1,15% | 8 | 1,16% | 8 | 1,16% |
| Topsent (1890) | 10 | 0,37% | 4 | 0,58% | 4 | 0,58% | 4 | 0,58% |
| Topsent (1928) | 10 | 0,37% | 3 | 0,43% | 3 | 0,43% | 3 | 0,43% |
| Van Soest et al. (2020) | 10 | 0,37% | 5 | 0,72% | 5 | 0,72% | 5 | 0,72% |
| Boury-esnault et al. (1982) | 9 | 0,34% | 7 | 1,01% | 7 | 1,01% | 7 | 1,01% |
| Topsent (1893) | 9 | 0,34% | 5 | 0,72% | 5 | 0,72% | 5 | 0,72% |
| Boisseau & Lubet (1955) | 8 | 0,3% | 4 | 0,58% | 4 | 0,58% | 4 | 0,58% |
| Bourcier (1988) | 8 | 0,3% | 7 | 1,01% | 7 | 1,01% | 7 | 1,01% |
| Annals of Natural History, (4)(xviii): pp. 226-240, 307-324, 388-410, 458-473.">Carter (1876) | 8 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pulitzer-Finali (1977) | 8 | 0,3% | 8 | 1,15% | 8 | 1,16% | 8 | 1,16% |
| Borojevic (1966) | 7 | 0,26% | 5 | 0,72% | 5 | 0,72% | 5 | 0,72% |
| Hancock (1849) | 7 | 0,26% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
| Montagu (1814) | 7 | 0,26% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pearman et al. (2020) | 7 | 0,26% | 4 | 0,58% | 4 | 0,58% | 4 | 0,58% |
| Reveillaud et al. (2012) | 7 | 0,26% | 7 | 1,01% | 7 | 1,01% | 7 | 1,01% |
| Richer de Forges et al. (2005) | 7 | 0,26% | 6 | 0,87% | 6 | 0,87% | 6 | 0,87% |
| Sara (1960) | 7 | 0,26% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
| Topsent (1904) | 7 | 0,26% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
| Boury-Esnault et al. (2017) | 6 | 0,22% | 6 | 0,87% | 6 | 0,87% | 6 | 0,87% |
| Esper ([1791]-1794) | 6 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
| Henkel & Janussen (2011) | 6 | 0,22% | 3 | 0,43% | 3 | 0,43% | 3 | 0,43% |
| Muricy et al. (1996) | 6 | 0,22% | 6 | 0,87% | 6 | 0,87% | 6 | 0,87% |
| , 84: 445-621.">Pulitzer-Finali (1982) | 6 | 0,22% | 3 | 0,43% | 3 | 0,43% | 3 | 0,43% |
| Vacelet & Perez (1998) | 6 | 0,22% | 6 | 0,87% | 6 | 0,87% | 6 | 0,87% |
| Borojevic et al. (1968) | 5 | 0,19% | 4 | 0,58% | 4 | 0,58% | 4 | 0,58% |
| Bowerbank (1874) | 5 | 0,19% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
| Lendenfeld (1891) | 5 | 0,19% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
| Lundbeck (1902) | 5 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
| Schmidt (1868) | 5 | 0,19% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
| Topsent (1927) | 5 | 0,19% | 4 | 0,58% | 4 | 0,58% | 4 | 0,58% |
| Tuzet & Connes (1963) | 5 | 0,19% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
| Vacelet & Perez (2008) | 5 | 0,19% | 4 | 0,58% | 4 | 0,58% | 4 | 0,58% |
| van Soest & Hooper (1993) | 5 | 0,19% | 4 | 0,58% | 4 | 0,58% | 4 | 0,58% |
| Amade et al. (1982) | 4 | 0,15% | 3 | 0,43% | 3 | 0,43% | 3 | 0,43% |
| Borojevic & Boury-Esnault (1987) | 4 | 0,15% | 3 | 0,43% | 3 | 0,43% | 3 | 0,43% |
| Chevaldonné et al. (2015) | 4 | 0,15% | 3 | 0,43% | 3 | 0,43% | 3 | 0,43% |
| Hanitsch (1890) | 4 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hansen (1885) | 4 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
| Johnson (1978) | 4 | 0,15% | 4 | 0,58% | 4 | 0,58% | 4 | 0,58% |
| Johnson (1978) | 4 | 0,15% | 4 | 0,58% | 4 | 0,58% | 4 | 0,58% |
| Johnson (1980) | 4 | 0,15% | 4 | 0,58% | 4 | 0,58% | 4 | 0,58% |
| Johnston (1842) | 4 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mao et al. (2020) | 4 | 0,15% | 4 | 0,58% | 4 | 0,58% | 4 | 0,58% |
| Perrier (1936) | 4 | 0,15% | 4 | 0,58% | 4 | 0,58% | 4 | 0,58% |
| Piscitelli et al. (2011) | 4 | 0,15% | 4 | 0,58% | 4 | 0,58% | 4 | 0,58% |
| Riesgo & Maldonado (2009) | 4 | 0,15% | 4 | 0,58% | 4 | 0,58% | 4 | 0,58% |
| Amu Ist Zool Univ Napoli, 14: 1-62.">Sara & Siribelli (1962) | 4 | 0,15% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
| Schmidt (1864° | 4 | 0,15% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
| Topsent (1891) | 4 | 0,15% | 4 | 0,58% | 4 | 0,58% | 4 | 0,58% |
| Topsent (1893) | 4 | 0,15% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
| Topsent (1898) | 4 | 0,15% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
| Topsent (1925) | 4 | 0,15% | 4 | 0,58% | 4 | 0,58% | 4 | 0,58% |
| Vacelet & Boury-Esnault (1996) | 4 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
| Vacelet et al. (2000) | 4 | 0,15% | 4 | 0,58% | 4 | 0,58% | 4 | 0,58% |
| Aellen & Brandt (1983) | 3 | 0,11% | 3 | 0,43% | 3 | 0,43% | 3 | 0,43% |
| Borojevic & Boury-Esnault (1986) | 3 | 0,11% | 3 | 0,43% | 3 | 0,43% | 3 | 0,43% |
| Bowerbank (1858) | 3 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bowerbank (1864) | 3 | 0,11% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
| Carballo (2000) | 3 | 0,11% | 3 | 0,43% | 3 | 0,43% | 3 | 0,43% |
| Carteron & Pouget (2008) | 3 | 0,11% | 3 | 0,43% | 3 | 0,43% | 3 | 0,43% |
| Chagas & Cavalcanti (2021) | 3 | 0,11% | 3 | 0,43% | 3 | 0,43% | 3 | 0,43% |
| Ciavatta et al. (1994) | 3 | 0,11% | 3 | 0,43% | 3 | 0,43% | 3 | 0,43% |
| Ellis & Solander (1786) | 3 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gadeau de Kerville (1900) | 3 | 0,11% | 3 | 0,43% | 3 | 0,43% | 3 | 0,43% |
| Gallissian (1982) | 3 | 0,11% | 3 | 0,43% | 3 | 0,43% | 3 | 0,43% |
| Gallissian (1983) | 3 | 0,11% | 3 | 0,43% | 3 | 0,43% | 3 | 0,43% |
| Hooper & Van Soest (2002) | 3 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Keller (1889) | 3 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lendenfeld (1897) | 3 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Revues des Travaux de l'Institut des Pêches Maritimes, 22: 225-246.">Levi & Vacelet (1958) | 3 | 0,11% | 3 | 0,43% | 3 | 0,43% | 3 | 0,43% |
| MGnify (2017) | 3 | 0,11% | 3 | 0,43% | 3 | 0,43% | 3 | 0,43% |
| Nardo (1833) | 3 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pérez et al. (2017) | 3 | 0,11% | 3 | 0,43% | 3 | 0,43% | 3 | 0,43% |
| Pouliquen (1972) | 3 | 0,11% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
| Schmidt (1875) | 3 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Stephens (1916) | 3 | 0,11% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
| Topsent (1889) | 3 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Topsent (1891) | 3 | 0,11% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
| Topsent (1892) | 3 | 0,11% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
| Topsent (1900) | 3 | 0,11% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
| Tsurnamal (1969) | 3 | 0,11% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
| Uriz & Maldonado (1993) | 3 | 0,11% | 3 | 0,43% | 3 | 0,43% | 3 | 0,43% |
| Vacelet & Boury-Esnault (1982) | 3 | 0,11% | 3 | 0,43% | 3 | 0,43% | 3 | 0,43% |
| Vacelet & Levi (1958) | 3 | 0,11% | 3 | 0,43% | 3 | 0,43% | 3 | 0,43% |
| Zarrouk et al. (2013) | 3 | 0,11% | 3 | 0,43% | 3 | 0,43% | 3 | 0,43% |
| Alvarado & Bautista (1972) | 2 | 0,07% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
| Arnaud (1974) | 2 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Borojevic & Boury-esnault (1986) | 2 | 0,07% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
| Borojevic (1966) | 2 | 0,07% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
| Bourmaud (2003) | 2 | 0,07% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
| Boury-Esnault & Bézac (2007) | 2 | 0,07% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
| Boury-esnault et al. (2015) | 2 | 0,07% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
| Bowerbank (1862) | 2 | 0,07% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
| Burlando et al. (1992) | 2 | 0,07% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
| Burton (1935) | 2 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Carter (1879) | 2 | 0,07% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
| Duboseq & Tuzet (1944) | 2 | 0,07% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
| Ereskovsky et al. (2011) | 2 | 0,07% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
| INTEGRATIVE AND COMPARATIVE BIOLOGY, 50: 227.">Escobar & Sanchez (2010) | 2 | 0,07% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
| Escobar et al. (2012) | 2 | 0,07% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
| Fabricius (1780) | 2 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ferrario et al. (2010) | 2 | 0,07% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
| Ferrer Hernandez (1916) | 2 | 0,07% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
| Ferretti et al. (2009) | 2 | 0,07% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
| Fristedt (1885) | 2 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fristedt (1887) | 2 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gaino et al. (1987) | 2 | 0,07% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
| Gallissian (1980) | 2 | 0,07% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
| Gautret (1986) | 2 | 0,07% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
| Gentric & Sauleau (2013) | 2 | 0,07% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
| Gilis et al. (2011) | 2 | 0,07% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
| Gilis et al. (2012) | 2 | 0,07% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
| Gray (1867) | 2 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Guzzetti et al. (2019) | 2 | 0,07% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
| Haeckel (1870) | 2 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hermans et al. (2010) | 2 | 0,07% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
| Imesek et al. (2014) | 2 | 0,07% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
| Jones & Pearson (1990) | 2 | 0,07% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
| Koechlin (1977) | 2 | 0,07% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
| Kopp et al. (2011) | 2 | 0,07% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
| Lamarck (1813) | 2 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ledda et al. (2011) | 2 | 0,07% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
| Lehnert (1993) | 2 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lendenfeld (1885) | 2 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lendenfeld (1898) | 2 | 0,07% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
| Levi (1957) | 2 | 0,07% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
| Linnaeus (1759) | 2 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Manconi et al. (2009) | 2 | 0,07% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
| Manuel & Parco (2000) | 2 | 0,07% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
| Mariani et al. (2000) | 2 | 0,07% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
| Mariani et al. (2001) | 2 | 0,07% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
| Mariani et al. (2006) | 2 | 0,07% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
| Meenatchi et al. (2020) | 2 | 0,07% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
| Pallas (1766) | 2 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pansini (1983) | 2 | 0,07% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
| Perez et al. (2006) | 2 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Perez et al. (2011) | 2 | 0,07% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
| Quevrain et al. (2014) | 2 | 0,07% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
| Redmond et al. (2013) | 2 | 0,07% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
| Ridley & Dendy (1886) | 2 | 0,07% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
| Rutzler & Bromley (1981) | 2 | 0,07% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
| Santín et al. (2021) | 2 | 0,07% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
| Sara (1958) | 2 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Schirl (1973) | 2 | 0,07% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
| Schmidt (1866) | 2 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Topsent (1901) | 2 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Topsent (1905) | 2 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Topsent (1924) | 2 | 0,07% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
| Topsent (1932) | 2 | 0,07% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
| Topsent (1937) | 2 | 0,07% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
| Tuzet & Connes (1964) | 2 | 0,07% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
| Tuzet (1964) | 2 | 0,07% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
| Usher et al. (2004) | 2 | 0,07% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
| Vacelet (1964) | 2 | 0,07% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
| Van et al. (2003) | 2 | 0,07% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
| Alcolado & Busutil (2012) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Babic (1921) | 1 | 0,04% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
| Barboza du Bocage (1869) | 1 | 0,04% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
| Berno et al. (2016) | 1 | 0,04% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
| Bidder (1895) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Borley (1931) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Borojevic (1966) | 1 | 0,04% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
| Borojevic (1971) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Borojevic (1971) | 1 | 0,04% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
| Boury-esnault et al. (1994) | 1 | 0,04% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
| Bowerbank & Norman (1882) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bowerbank (1845) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bowerbank (1861) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Breitfuss (1897) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Breitfuss (1912) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Breton (1999) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Breton (2005) | 1 | 0,04% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
| Burton (1930) | 1 | 0,04% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
| Burton (1935) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bulletin of the British Museum (Natural History) Zoology, 2: 215-239.">Burton (1954) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cabioch (1976) | 1 | 0,04% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
| Carter (1871) | 1 | 0,04% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
| Carter (1880) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Carter (1882) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Carter (1882) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Carter (1884) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Carter (1885) | 1 | 0,04% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
| Carteron et al. (2012) | 1 | 0,04% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
| Cebrian & Uriz (2006) | 1 | 0,04% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
| Czerniavsky (1878) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| delle Chiaje (1828) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| DORIS (2012) | 1 | 0,04% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
| Duchassaing & Michelotti (1864) | 1 | 0,04% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
| Ebner (1887) | 1 | 0,04% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
| Forest (1957) | 1 | 0,04% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
| Gazave et al. (2013) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Giard (1890) | 1 | 0,04% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
| Gouillieux et al. (2022) | 1 | 0,04% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
| Goulletquer (2016) | 1 | 0,04% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
| Graeffe (1882) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Grant (1826) | 1 | 0,04% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
| Grant (1826) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hanitsch (1891) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hanitsch (1894) | 1 | 0,04% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
| Hentschel (1914) | 1 | 0,04% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
| Idan et al. (2020) | 1 | 0,04% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
| Ifremer (2009) | 1 | 0,04% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
| Ifremer (2019) | 1 | 0,04% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
| Ifremer (2020) | 1 | 0,04% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
| Ifremer (2021) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kirkpatrick (1900) | 1 | 0,04% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
| Kirkpatrick (1908) | 1 | 0,04% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
| Klautau et al. (2004) | 1 | 0,04% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
| Klautau et al. (2013) | 1 | 0,04% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
| Koehler (1886) | 1 | 0,04% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
| Kölliker (1864) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lackschewitz (1886) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lambe (1896) | 1 | 0,04% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
| Laubenfels (1936) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Levi (1967) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Levinsen (1887) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Linnaeus (1767) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Little (1968) | 1 | 0,04% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
| Marlow et al. (2018) | 1 | 0,04% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
| Martin & Uriz (1993) | 1 | 0,04% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
| Miklucho-Maclay (1868) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Müller (1806) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Norman (1869) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Picton & Goodwin (2007) | 1 | 0,04% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
| Prenant (1926) | 1 | 0,04% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
| Questel (2020) | 1 | 0,04% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
| Ridley & Dendy (1886) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rignault & Chevallier (2017) | 1 | 0,04% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
| Risso ([1827]) | 1 | 0,04% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
| Rosell & Uriz (2002) | 1 | 0,04% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
| Rosique et al. (1996) | 1 | 0,04% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
| Sarà (1953) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sarà (1959) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sarà (1961) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Schleyer et al. (2016) | 1 | 0,04% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
| Schmidt (1869) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Schmidt (1873) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Schmidt (1875) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Schmidt (1880) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Schuffner (1877) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Soubigou et al. (2020) | 1 | 0,04% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
| Stephens (1912) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Templeton (1836) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Thiele (1905) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Topsent (1888) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Topsent (1894) | 1 | 0,04% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
| Topsent (1896) | 1 | 0,04% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
| Topsent (1905) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Topsent (1920) | 1 | 0,04% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
| Topsent (1929) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Tuzet et al. (1952) | 1 | 0,04% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
| Uljanin (1872° | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Vacelet & Arnaud (1972) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Vacelet & Breton (2004) | 1 | 0,04% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
| Vacelet (1958) | 1 | 0,04% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
| Vacelet (1969) | 1 | 0,04% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
| Verrill (1873) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Wiens et al. (1999) | 1 | 0,04% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
| (2005) | 1 | 0,04% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
