Bryozoaires et brachiopodes
294 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
| Référence | Total | Valides | Espèces | Taxons terminaux | ||||
|---|---|---|---|---|---|---|---|---|
| nb | % | nb | % | nb | % | nb | % | |
| Gordon (2007) | 341 | 18,35% | 317 | 32,41% | 313 | 32,3% | 316 | 32,58% |
| Gordon & D'hondt (1997) | 149 | 8,02% | 140 | 14,31% | 137 | 14,14% | 140 | 14,43% |
| Julien (1881) | 84 | 4,52% | 31 | 3,17% | 31 | 3,2% | 31 | 3,2% |
| Emig (2016) | 80 | 4,31% | 26 | 2,66% | 26 | 2,68% | 26 | 2,68% |
| Ifremer (2009) | 79 | 4,25% | 71 | 7,26% | 71 | 7,33% | 71 | 7,32% |
| D'Hondt (1986) | 68 | 3,66% | 42 | 4,29% | 36 | 3,72% | 42 | 4,33% |
| Gordon (1993) | 63 | 3,39% | 63 | 6,44% | 63 | 6,5% | 63 | 6,49% |
| D'hondt & Gordon (1996) | 54 | 2,91% | 39 | 3,99% | 33 | 3,41% | 36 | 3,71% |
| Nelson-Smith et al. (2014) | 54 | 2,91% | 44 | 4,5% | 44 | 4,54% | 43 | 4,43% |
| D'Hondt & Gordon (1999) | 51 | 2,74% | 51 | 5,21% | 51 | 5,26% | 51 | 5,26% |
| d'Hondt (1984) | 35 | 1,88% | 33 | 3,37% | 33 | 3,41% | 33 | 3,4% |
| d'Hondt (1995) | 35 | 1,88% | 29 | 2,97% | 29 | 2,99% | 29 | 2,99% |
| Zoology, x: 216 pp..">Busk (1884) | 34 | 1,83% | 7 | 0,72% | 7 | 0,72% | 7 | 0,72% |
| Richer de Forges et al. (2005) | 34 | 1,83% | 28 | 2,86% | 28 | 2,89% | 28 | 2,89% |
| Mao et al. (2020) | 33 | 1,78% | 27 | 2,76% | 27 | 2,79% | 27 | 2,78% |
| Bourcier (1988) | 29 | 1,56% | 22 | 2,25% | 22 | 2,27% | 21 | 2,16% |
| Arnaud (1974) | 28 | 1,51% | 15 | 1,53% | 15 | 1,55% | 15 | 1,55% |
| Godet et al. (2010) | 22 | 1,18% | 19 | 1,94% | 19 | 1,96% | 18 | 1,86% |
| Androsova (1972) | 21 | 1,13% | 10 | 1,02% | 10 | 1,03% | 10 | 1,03% |
| Breton (2014) | 21 | 1,13% | 17 | 1,74% | 17 | 1,75% | 17 | 1,75% |
| D'hondt (1976) | 21 | 1,13% | 14 | 1,43% | 14 | 1,44% | 14 | 1,44% |
| Linnaeus (1758) | 20 | 1,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Zezina (1987) | 19 | 1,02% | 17 | 1,74% | 17 | 1,75% | 17 | 1,75% |
| Philipps (1900) | 18 | 0,97% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bitner (2015) | 17 | 0,91% | 17 | 1,74% | 17 | 1,75% | 17 | 1,75% |
| d'Hondt & Mascarell (2010) | 16 | 0,86% | 14 | 1,43% | 14 | 1,44% | 14 | 1,44% |
| Harmelin et al. (2019) | 15 | 0,81% | 12 | 1,23% | 12 | 1,24% | 12 | 1,24% |
| Harmer (1957) | 15 | 0,81% | 9 | 0,92% | 9 | 0,93% | 9 | 0,93% |
| d'Hondt & Mascarell (2004) | 14 | 0,75% | 11 | 1,12% | 11 | 1,14% | 11 | 1,13% |
| d'Hondt & Mascarell (2010) | 14 | 0,75% | 13 | 1,33% | 12 | 1,24% | 13 | 1,34% |
| Fehlauer-ale et al. (2015) | 14 | 0,75% | 14 | 1,43% | 14 | 1,44% | 14 | 1,44% |
| Fourt et al. (2017) | 14 | 0,75% | 14 | 1,43% | 14 | 1,44% | 14 | 1,44% |
| Busk (1876) | 13 | 0,7% | 6 | 0,61% | 6 | 0,62% | 6 | 0,62% |
| Canu & Bassler (1929) | 13 | 0,7% | 8 | 0,82% | 8 | 0,83% | 8 | 0,82% |
| Gordon (1984) | 13 | 0,7% | 11 | 1,12% | 11 | 1,14% | 10 | 1,03% |
| Harmelin & Rosso (2023) | 13 | 0,7% | 13 | 1,33% | 13 | 1,34% | 13 | 1,34% |
| d'Hondt (2009) | 12 | 0,65% | 10 | 1,02% | 10 | 1,03% | 10 | 1,03% |
| Harmer (1926) | 12 | 0,65% | 9 | 0,92% | 9 | 0,93% | 9 | 0,93% |
| Cooper (1981) | 11 | 0,59% | 7 | 0,72% | 7 | 0,72% | 7 | 0,72% |
| Goulletquer (2016) | 11 | 0,59% | 11 | 1,12% | 11 | 1,14% | 11 | 1,13% |
| Redier (1971) | 11 | 0,59% | 7 | 0,72% | 7 | 0,72% | 7 | 0,72% |
| d'Hondt (1979) | 10 | 0,54% | 10 | 1,02% | 10 | 1,03% | 10 | 1,03% |
| Julien (1882) | 10 | 0,54% | 4 | 0,41% | 4 | 0,41% | 4 | 0,41% |
| Lepoint et al. (2019) | 10 | 0,54% | 9 | 0,92% | 9 | 0,93% | 9 | 0,93% |
| Bitner (2008) | 9 | 0,48% | 9 | 0,92% | 9 | 0,93% | 9 | 0,93% |
| Bock (2020) | 9 | 0,48% | 9 | 0,92% | 9 | 0,93% | 9 | 0,93% |
| d'Hondt & Goyffon (1993) | 9 | 0,48% | 8 | 0,82% | 8 | 0,83% | 8 | 0,82% |
| Gautier (1953) | 9 | 0,48% | 5 | 0,51% | 5 | 0,52% | 5 | 0,52% |
| Álvarez (1992) | 8 | 0,43% | 8 | 0,82% | 8 | 0,83% | 8 | 0,82% |
| Bishop & Househam (1987) | 8 | 0,43% | 3 | 0,31% | 3 | 0,31% | 3 | 0,31% |
| Bitner (2014) | 8 | 0,43% | 8 | 0,82% | 8 | 0,83% | 8 | 0,82% |
| Dewarumez et al. (2011) | 8 | 0,43% | 6 | 0,61% | 6 | 0,62% | 6 | 0,62% |
| Harmelin (1984) | 7 | 0,38% | 7 | 0,72% | 7 | 0,72% | 7 | 0,72% |
| Bitner (2010) | 6 | 0,32% | 5 | 0,51% | 5 | 0,52% | 5 | 0,52% |
| Blauwe (2010) | 6 | 0,32% | 5 | 0,51% | 5 | 0,52% | 5 | 0,52% |
| Emig (2018) | 6 | 0,32% | 6 | 0,61% | 6 | 0,62% | 6 | 0,62% |
| Harmelin & Aristegui (1988) | 6 | 0,32% | 2 | 0,2% | 2 | 0,21% | 0 | 0% |
| Hastings (1943) | 6 | 0,32% | 4 | 0,41% | 4 | 0,41% | 4 | 0,41% |
| Julien (1885) | 6 | 0,32% | 2 | 0,2% | 2 | 0,21% | 2 | 0,21% |
| Lamouroux (1816) | 6 | 0,32% | 3 | 0,31% | 3 | 0,31% | 3 | 0,31% |
| Pearman et al. (2020) | 6 | 0,32% | 4 | 0,41% | 4 | 0,41% | 4 | 0,41% |
| Schwaha & Gordon (2024) | 6 | 0,32% | 6 | 0,61% | 6 | 0,62% | 6 | 0,62% |
| Busk (1852) | 5 | 0,27% | 3 | 0,31% | 3 | 0,31% | 3 | 0,31% |
| Davoult et al. (1999) | 5 | 0,27% | 3 | 0,31% | 3 | 0,31% | 3 | 0,31% |
| d'Hondt & Redier (1977) | 5 | 0,27% | 3 | 0,31% | 3 | 0,31% | 3 | 0,31% |
| Echalier & Prenant (1951) | 5 | 0,27% | 5 | 0,51% | 5 | 0,52% | 5 | 0,52% |
| Harmelin et al. (2003) | 5 | 0,27% | 3 | 0,31% | 3 | 0,31% | 3 | 0,31% |
| Harmelin (2020) | 5 | 0,27% | 5 | 0,51% | 5 | 0,52% | 5 | 0,52% |
| Linnaeus (1767) | 5 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rosso et al. (2020) | 5 | 0,27% | 5 | 0,51% | 5 | 0,52% | 5 | 0,52% |
| Waters (1909) | 5 | 0,27% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
| Androsova (1972) | 4 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
| Balavoine (1958) | 4 | 0,22% | 4 | 0,41% | 4 | 0,41% | 4 | 0,41% |
| Bishop (1988) | 4 | 0,22% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
| Bitner (2007) | 4 | 0,22% | 4 | 0,41% | 4 | 0,41% | 4 | 0,41% |
| D'hondt & Hayward (1981) | 4 | 0,22% | 3 | 0,31% | 3 | 0,31% | 3 | 0,31% |
| Ellis & Solander (1786) | 4 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
| Laurin (1997) | 4 | 0,22% | 4 | 0,41% | 4 | 0,41% | 4 | 0,41% |
| Reverter-gil et al. (2016) | 4 | 0,22% | 4 | 0,41% | 4 | 0,41% | 4 | 0,41% |
| Rignault & Chevallier (2017) | 4 | 0,22% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
| Risso (1826) | 4 | 0,22% | 3 | 0,31% | 3 | 0,31% | 3 | 0,31% |
| Simon et al. (2019) | 4 | 0,22% | 4 | 0,41% | 4 | 0,41% | 4 | 0,41% |
| Soule et al. (1995) | 4 | 0,22% | 2 | 0,2% | 2 | 0,21% | 2 | 0,21% |
| Vieira et al. (2013) | 4 | 0,22% | 4 | 0,41% | 4 | 0,41% | 4 | 0,41% |
| Bobin & Prenant (1965) | 3 | 0,16% | 3 | 0,31% | 3 | 0,31% | 3 | 0,31% |
| Canu & Bassler (1930) | 3 | 0,16% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
| D'Hondt (1983) | 3 | 0,16% | 3 | 0,31% | 3 | 0,31% | 3 | 0,31% |
| D'Hondt (1987) | 3 | 0,16% | 3 | 0,31% | 3 | 0,31% | 3 | 0,31% |
| D'Hondt (2010) | 3 | 0,16% | 3 | 0,31% | 3 | 0,31% | 3 | 0,31% |
| Dyrynda et al. (2000) | 3 | 0,16% | 3 | 0,31% | 3 | 0,31% | 3 | 0,31% |
| Fernandez et al. (1993) | 3 | 0,16% | 3 | 0,31% | 3 | 0,31% | 3 | 0,31% |
| Gordon (1986) | 3 | 0,16% | 3 | 0,31% | 3 | 0,31% | 3 | 0,31% |
| Harmelin (1976) | 3 | 0,16% | 3 | 0,31% | 3 | 0,31% | 3 | 0,31% |
| Harmelin (1990) | 3 | 0,16% | 3 | 0,31% | 3 | 0,31% | 3 | 0,31% |
| Joliet (1877) | 3 | 0,16% | 2 | 0,2% | 2 | 0,21% | 2 | 0,21% |
| . (i-vii 1-431).">Levinsen (1909) | 3 | 0,16% | 2 | 0,2% | 2 | 0,21% | 2 | 0,21% |
| Martino & Rosso (2021) | 3 | 0,16% | 3 | 0,31% | 3 | 0,31% | 3 | 0,31% |
| Ryland et al. (2009) | 3 | 0,16% | 3 | 0,31% | 3 | 0,31% | 3 | 0,31% |
| Tricart & Foubert (2000) | 3 | 0,16% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
| Alvarez (1991) | 2 | 0,11% | 2 | 0,2% | 2 | 0,21% | 2 | 0,21% |
| Álvarez (1994) | 2 | 0,11% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
| Alvarez (1995) | 2 | 0,11% | 2 | 0,2% | 2 | 0,21% | 2 | 0,21% |
| Audouin (1826) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Berning et al. (2021) | 2 | 0,11% | 2 | 0,2% | 2 | 0,21% | 2 | 0,21% |
| Bitner & Cohen (2015) | 2 | 0,11% | 2 | 0,2% | 2 | 0,21% | 2 | 0,21% |
| Bitner et al. (2007) | 2 | 0,11% | 2 | 0,2% | 2 | 0,21% | 2 | 0,21% |
| Bitner (2011) | 2 | 0,11% | 2 | 0,2% | 2 | 0,21% | 2 | 0,21% |
| Bitner (2019) | 2 | 0,11% | 2 | 0,2% | 2 | 0,21% | 2 | 0,21% |
| Bock (2021) | 2 | 0,11% | 2 | 0,2% | 2 | 0,21% | 2 | 0,21% |
| Boissel & Urtizberea (2024) | 2 | 0,11% | 2 | 0,2% | 2 | 0,21% | 2 | 0,21% |
| Borg (1944) | 2 | 0,11% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
| Buski (1881) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Canu & Bassler (1927) | 2 | 0,11% | 2 | 0,2% | 2 | 0,21% | 2 | 0,21% |
| Castric-fey (1971) | 2 | 0,11% | 2 | 0,2% | 2 | 0,21% | 2 | 0,21% |
| Cook & Chimonides (1994) | 2 | 0,11% | 2 | 0,2% | 2 | 0,21% | 2 | 0,21% |
| De Blauwe (2005) | 2 | 0,11% | 2 | 0,2% | 2 | 0,21% | 2 | 0,21% |
| Decker et al. (2021) | 2 | 0,11% | 2 | 0,2% | 2 | 0,21% | 2 | 0,21% |
| Deshayes (1863) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| D'Hondt & Occhipinti Ambrogi (1985) | 2 | 0,11% | 2 | 0,2% | 2 | 0,21% | 2 | 0,21% |
| D'hondt (2006) | 2 | 0,11% | 2 | 0,2% | 2 | 0,21% | 2 | 0,21% |
| d'Hondt (2012) | 2 | 0,11% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
| D'hondt (2017) | 2 | 0,11% | 2 | 0,2% | 2 | 0,21% | 2 | 0,21% |
| Di Martino et al. (2020) | 2 | 0,11% | 2 | 0,2% | 2 | 0,21% | 2 | 0,21% |
| Fleming (1828) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Florence et al. (2007) | 2 | 0,11% | 2 | 0,2% | 2 | 0,21% | 2 | 0,21% |
| Galil & Gevili (2014) | 2 | 0,11% | 2 | 0,2% | 2 | 0,21% | 2 | 0,21% |
| Gmelin (1791) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gordon (1982) | 2 | 0,11% | 2 | 0,2% | 2 | 0,21% | 2 | 0,21% |
| Gordon (1988) | 2 | 0,11% | 2 | 0,2% | 2 | 0,21% | 2 | 0,21% |
| Gordon (1993) | 2 | 0,11% | 2 | 0,2% | 2 | 0,21% | 2 | 0,21% |
| Harmelin (1977) | 2 | 0,11% | 2 | 0,2% | 2 | 0,21% | 2 | 0,21% |
| Harmelin (1977) | 2 | 0,11% | 2 | 0,2% | 2 | 0,21% | 2 | 0,21% |
| Harmelin (2006) | 2 | 0,11% | 2 | 0,2% | 2 | 0,21% | 2 | 0,21% |
| Harmer (1934) | 2 | 0,11% | 2 | 0,2% | 2 | 0,21% | 2 | 0,21% |
| Hastings (1929) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hastings (1944) | 2 | 0,11% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
| Hayward (2004) | 2 | 0,11% | 2 | 0,2% | 2 | 0,21% | 2 | 0,21% |
| Hirose (2011) | 2 | 0,11% | 2 | 0,2% | 2 | 0,21% | 2 | 0,21% |
| Proceedings of the Zoological Society of London, 1907: 1035-1037.">Hopkinson (1907) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Impact-Mer et al. (2011) | 2 | 0,11% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
| Johnston (1847) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jullien (1888) | 2 | 0,11% | 2 | 0,2% | 2 | 0,21% | 2 | 0,21% |
| Lamouroux (1821) | 2 | 0,11% | 2 | 0,2% | 2 | 0,21% | 2 | 0,21% |
| Leca & D’hondt (1993) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Logan et al. (2015) | 2 | 0,11% | 2 | 0,2% | 2 | 0,21% | 2 | 0,21% |
| Lopez-Fe (2006) | 2 | 0,11% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
| Loxton (2017) | 2 | 0,11% | 2 | 0,2% | 2 | 0,21% | 2 | 0,21% |
| Martin (2011) | 2 | 0,11% | 2 | 0,2% | 2 | 0,21% | 2 | 0,21% |
| MGnify (2017) | 2 | 0,11% | 2 | 0,2% | 2 | 0,21% | 2 | 0,21% |
| Moyano (1991) | 2 | 0,11% | 2 | 0,2% | 2 | 0,21% | 2 | 0,21% |
| Norman (1868) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Notteghem (1999) | 2 | 0,11% | 2 | 0,2% | 2 | 0,21% | 2 | 0,21% |
| Osburn (1952) | 2 | 0,11% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
| Philippi (1844) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Powell (1967) | 2 | 0,11% | 2 | 0,2% | 2 | 0,21% | 2 | 0,21% |
| Ristedt (1985) | 2 | 0,11% | 2 | 0,2% | 2 | 0,21% | 2 | 0,21% |
| Ryland (1960) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Schwaha et al. (2024) | 2 | 0,11% | 2 | 0,2% | 2 | 0,21% | 2 | 0,21% |
| Sellier et al. (2016) | 2 | 0,11% | 2 | 0,2% | 2 | 0,21% | 2 | 0,21% |
| Souto et al. (2019) | 2 | 0,11% | 2 | 0,2% | 2 | 0,21% | 2 | 0,21% |
| Taylor et al. (2021) | 2 | 0,11% | 2 | 0,2% | 2 | 0,21% | 2 | 0,21% |
| Thornely (1907) | 2 | 0,11% | 2 | 0,2% | 2 | 0,21% | 2 | 0,21% |
| Ulman et al. (2017) | 2 | 0,11% | 2 | 0,2% | 2 | 0,21% | 2 | 0,21% |
| Vaucher (1803) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Vieira et al. (2014) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Waters (1879) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Waters (1903) | 2 | 0,11% | 2 | 0,2% | 2 | 0,21% | 2 | 0,21% |
| Winston & Woollacott (2008) | 2 | 0,11% | 2 | 0,2% | 2 | 0,21% | 2 | 0,21% |
| Alder (1857) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| André et al. (2014) | 1 | 0,05% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
| Ballesteros et al. (2009) | 1 | 0,05% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
| Bassler (1936) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Beauchamp (1918) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Berning & Kuklinski (2008) | 1 | 0,05% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
| Bitner (2006) | 1 | 0,05% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
| Blauwe & Faasse (2001) | 1 | 0,05% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
| Blauwe (2002) | 1 | 0,05% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
| Blauwe (2006) | 1 | 0,05% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
| Breton & D'hondt (2004) | 1 | 0,05% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
| Busk (151) | 1 | 0,05% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
| Busk (1852) | 1 | 0,05% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
| Busk (1854) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Busk (1859) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Busk (1861) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Calvet (1906) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Calvet (1906) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Canu & Bassler (1925) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cépède (1914) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Chevaldonné et al. (2015) | 1 | 0,05% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
| Clausade (1969) | 1 | 0,05% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
| Cook (2001) | 1 | 0,05% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
| Curd et al. (2015) | 1 | 0,05% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
| David & Pouyet (1974) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Delle & Chiaje (1828) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Denisenko (2019) | 1 | 0,05% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
| d'Hondt & Clauss (1999) | 1 | 0,05% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
| D'hondt & Goyffon (1991) | 1 | 0,05% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
| D'hondt & Goyffon (2005) | 1 | 0,05% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
| D'hondt et al. (2004) | 1 | 0,05% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
| Bulletin du Muséum national d'histoire naturelle. 42: 232-256.">D'hondt (1970) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| D'hondt (1974) | 1 | 0,05% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
| d'Hondt (1985) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| D'hondt (2000) | 1 | 0,05% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
| Dolan (2014) | 1 | 0,05% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
| Bulletin de la Société zoologique de France, 48: 161-163.">Dollfus (1923) | 1 | 0,05% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
| D'hondt & Harmelin (1993) | 1 | 0,05% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
| Emig (2014) | 1 | 0,05% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
| Fabricius (1780) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fiala-medioni (1973) | 1 | 0,05% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
| Foster (1972) | 1 | 0,05% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
| Galil & Occhipinti-ambrogi (2009) | 1 | 0,05% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
| Gautier (1952) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gautier (1954) | 1 | 0,05% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
| Gordon & Braga (1994) | 1 | 0,05% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
| Gordon & D'hondt (1997) | 1 | 0,05% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
| Harmelin & D'Hondt (1982) | 1 | 0,05% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
| Harmelin (1973) | 1 | 0,05% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
| Harmelin (1973) | 1 | 0,05% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
| Harmer (1933) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hass (1948) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hassall (1841) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hayward & McKinney (2002) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hayward & Ryland (1995) | 1 | 0,05% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
| Hayward & Thorpe (1989) | 1 | 0,05% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
| Hayward (1979) | 1 | 0,05% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
| Hincks (1860) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hincks (1862) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hincks (1862) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hincks (1879) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hincks (1880 | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hondt & Condé (1996) | 1 | 0,05% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
| Ices (2022) | 1 | 0,05% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
| Ifremer (2020) | 1 | 0,05% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
| Ifremer (2021) | 1 | 0,05% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
| Johnston (1838) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Johnston (1840) | 1 | 0,05% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
| Joliet (1888) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jullien (1886) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kirkpatrick (1890) | 1 | 0,05% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
| Kluge (1962) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Labat (2023) | 1 | 0,05% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
| Lamarck (1816) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Landsborough (1852) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lepoint et al. (2014) | 1 | 0,05% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
| Linnaeus (1761) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Linnaeus (1767) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lizé (2018) | 1 | 0,05% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
| Lizé (2018) | 1 | 0,05% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
| Lizé (2018) | 1 | 0,05% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
| Lizé (2018) | 1 | 0,05% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
| Lodola et al. (2012) | 1 | 0,05% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
| Lodola et al. (2015) | 1 | 0,05% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
| López et al. (1993) | 1 | 0,05% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
| Lovèn (1846) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| MacGillivray (1869) | 1 | 0,05% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
| MacGillivray (1886) | 1 | 0,05% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
| Manzoni (1870) | 1 | 0,05% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
| Marchini et al. (2015) | 1 | 0,05% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
| Massard & Geimer (2005) | 1 | 0,05% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
| Matricardi et al. (1991) | 1 | 0,05% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
| Moll (1803) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Monod & Dollfus (1932) | 1 | 0,05% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
| Moyano (1983) | 1 | 0,05% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
| Müller (2004) | 1 | 0,05% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
| Norman (1864) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Norman (1867) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Norman (1869) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Økland & Økland (2000) | 1 | 0,05% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
| Ortmann (1890) | 1 | 0,05% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
| Osburn (1950) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Packard (1863) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pallas (1766) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pesson (1938) | 1 | 0,05% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
| Prouho (1889) | 1 | 0,05% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
| Ramalho et al. (2018) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Reuss (1848) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Reverter-gil & Fernández-pulpeiro (1995) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Reverter-gil & Souto (2019) | 1 | 0,05% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
| Rogick (1955) | 1 | 0,05% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
| Rosso (2002) | 1 | 0,05% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
| Ryland & Gordon (1977) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ryland (1964) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sartoretto (2012) | 1 | 0,05% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
| Silén (1946) | 1 | 0,05% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
| Soule & Soule (1968) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Souto et al. (2007) | 1 | 0,05% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
| Souto et al. (2010) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Tenison Woods (1880) | 1 | 0,05% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
| Uicn et al. (2019) | 1 | 0,05% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
| Waters (1913) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Winston et al. (2000) | 1 | 0,05% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
| Zabala et al. (1993) | 1 | 0,05% | 1 | 0,1% | 1 | 0,1% | 1 | 0,1% |
| Zibrowius (1968) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Zilli (2021) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
