Bryozoaires
Bryozoa
263 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 | 20,77% | 317 | 35,86% | 313 | 35,77% | 316 | 36,07% |
Gordon & D'hondt (1997) | 149 | 9,07% | 140 | 15,84% | 137 | 15,66% | 140 | 15,98% |
Julien (1881) | 84 | 5,12% | 31 | 3,51% | 31 | 3,54% | 31 | 3,54% |
D'Hondt (1986) | 68 | 4,14% | 42 | 4,75% | 36 | 4,11% | 42 | 4,79% |
Gordon (1993) | 63 | 3,84% | 63 | 7,13% | 63 | 7,2% | 63 | 7,19% |
Ifremer (2009) | 60 | 3,65% | 54 | 6,11% | 54 | 6,17% | 54 | 6,16% |
D'hondt & Gordon (1996) | 54 | 3,29% | 39 | 4,41% | 33 | 3,77% | 36 | 4,11% |
D'Hondt & Gordon (1999) | 51 | 3,11% | 51 | 5,77% | 51 | 5,83% | 51 | 5,82% |
Nelson-Smith et al. (2014) | 51 | 3,11% | 42 | 4,75% | 42 | 4,8% | 41 | 4,68% |
d'Hondt (1984) | 35 | 2,13% | 33 | 3,73% | 33 | 3,77% | 33 | 3,77% |
d'Hondt (1995) | 35 | 2,13% | 29 | 3,28% | 29 | 3,31% | 29 | 3,31% |
Zoology, x: 216 pp..">Busk (1884) | 34 | 2,07% | 7 | 0,79% | 7 | 0,8% | 7 | 0,8% |
Mao et al. (2020) | 33 | 2,01% | 27 | 3,05% | 27 | 3,09% | 27 | 3,08% |
Arnaud (1974) | 27 | 1,64% | 14 | 1,58% | 14 | 1,6% | 14 | 1,6% |
Godet et al. (2010) | 22 | 1,34% | 19 | 2,15% | 19 | 2,17% | 18 | 2,05% |
Androsova (1972) | 21 | 1,28% | 10 | 1,13% | 10 | 1,14% | 10 | 1,14% |
Bourcier (1988) | 21 | 1,28% | 15 | 1,7% | 15 | 1,71% | 14 | 1,6% |
Breton (2014) | 21 | 1,28% | 17 | 1,92% | 17 | 1,94% | 17 | 1,94% |
Linnaeus (1758) | 19 | 1,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Philipps (1900) | 18 | 1,1% | 0 | 0% | 0 | 0% | 0 | 0% |
d'Hondt & Mascarell (2010) | 16 | 0,97% | 14 | 1,58% | 14 | 1,6% | 14 | 1,6% |
Harmelin et al. (2019) | 15 | 0,91% | 12 | 1,36% | 12 | 1,37% | 12 | 1,37% |
Harmer (1957) | 15 | 0,91% | 9 | 1,02% | 9 | 1,03% | 9 | 1,03% |
d'Hondt & Mascarell (2004) | 14 | 0,85% | 11 | 1,24% | 11 | 1,26% | 11 | 1,26% |
d'Hondt & Mascarell (2010) | 14 | 0,85% | 13 | 1,47% | 12 | 1,37% | 13 | 1,48% |
Fehlauer-ale et al. (2015) | 14 | 0,85% | 14 | 1,58% | 14 | 1,6% | 14 | 1,6% |
Busk (1876) | 13 | 0,79% | 6 | 0,68% | 6 | 0,69% | 6 | 0,68% |
Canu & Bassler (1929) | 13 | 0,79% | 8 | 0,9% | 8 | 0,91% | 8 | 0,91% |
Gordon (1984) | 13 | 0,79% | 11 | 1,24% | 11 | 1,26% | 10 | 1,14% |
Harmelin & Rosso (2023) | 13 | 0,79% | 13 | 1,47% | 13 | 1,49% | 13 | 1,48% |
d'Hondt (2009) | 12 | 0,73% | 10 | 1,13% | 10 | 1,14% | 10 | 1,14% |
Harmer (1926) | 12 | 0,73% | 9 | 1,02% | 9 | 1,03% | 9 | 1,03% |
Goulletquer (2016) | 11 | 0,67% | 11 | 1,24% | 11 | 1,26% | 11 | 1,26% |
Redier (1971) | 11 | 0,67% | 7 | 0,79% | 7 | 0,8% | 7 | 0,8% |
Richer de Forges et al. (2005) | 11 | 0,67% | 7 | 0,79% | 7 | 0,8% | 7 | 0,8% |
d'Hondt (1979) | 10 | 0,61% | 10 | 1,13% | 10 | 1,14% | 10 | 1,14% |
Julien (1882) | 10 | 0,61% | 4 | 0,45% | 4 | 0,46% | 4 | 0,46% |
Lepoint et al. (2019) | 10 | 0,61% | 9 | 1,02% | 9 | 1,03% | 9 | 1,03% |
Bock (2020) | 9 | 0,55% | 9 | 1,02% | 9 | 1,03% | 9 | 1,03% |
d'Hondt & Goyffon (1993) | 9 | 0,55% | 8 | 0,9% | 8 | 0,91% | 8 | 0,91% |
Gautier (1953) | 9 | 0,55% | 5 | 0,57% | 5 | 0,57% | 5 | 0,57% |
Álvarez (1992) | 8 | 0,49% | 8 | 0,9% | 8 | 0,91% | 8 | 0,91% |
Bishop & Househam (1987) | 8 | 0,49% | 3 | 0,34% | 3 | 0,34% | 3 | 0,34% |
Dewarumez et al. (2011) | 8 | 0,49% | 6 | 0,68% | 6 | 0,69% | 6 | 0,68% |
Fourt et al. (2017) | 8 | 0,49% | 8 | 0,9% | 8 | 0,91% | 8 | 0,91% |
Harmelin (1984) | 7 | 0,43% | 7 | 0,79% | 7 | 0,8% | 7 | 0,8% |
Blauwe (2010) | 6 | 0,37% | 5 | 0,57% | 5 | 0,57% | 5 | 0,57% |
Harmelin & Aristegui (1988) | 6 | 0,37% | 2 | 0,23% | 2 | 0,23% | 0 | 0% |
Hastings (1943) | 6 | 0,37% | 4 | 0,45% | 4 | 0,46% | 4 | 0,46% |
Julien (1885) | 6 | 0,37% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
Lamouroux (1816) | 6 | 0,37% | 3 | 0,34% | 3 | 0,34% | 3 | 0,34% |
Pearman et al. (2020) | 6 | 0,37% | 4 | 0,45% | 4 | 0,46% | 4 | 0,46% |
Schwaha & Gordon (2024) | 6 | 0,37% | 6 | 0,68% | 6 | 0,69% | 6 | 0,68% |
Busk (1852) | 5 | 0,3% | 3 | 0,34% | 3 | 0,34% | 3 | 0,34% |
Davoult et al. (1999) | 5 | 0,3% | 3 | 0,34% | 3 | 0,34% | 3 | 0,34% |
d'Hondt & Redier (1977) | 5 | 0,3% | 3 | 0,34% | 3 | 0,34% | 3 | 0,34% |
Echalier & Prenant (1951) | 5 | 0,3% | 5 | 0,57% | 5 | 0,57% | 5 | 0,57% |
Harmelin (2020) | 5 | 0,3% | 5 | 0,57% | 5 | 0,57% | 5 | 0,57% |
Linnaeus (1767) | 5 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
Rosso et al. (2020) | 5 | 0,3% | 5 | 0,57% | 5 | 0,57% | 5 | 0,57% |
Waters (1909) | 5 | 0,3% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Androsova (1972) | 4 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
Balavoine (1958) | 4 | 0,24% | 4 | 0,45% | 4 | 0,46% | 4 | 0,46% |
Bishop (1988) | 4 | 0,24% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
D'hondt & Hayward (1981) | 4 | 0,24% | 3 | 0,34% | 3 | 0,34% | 3 | 0,34% |
Ellis & Solander (1786) | 4 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
Reverter-gil et al. (2016) | 4 | 0,24% | 4 | 0,45% | 4 | 0,46% | 4 | 0,46% |
Rignault & Chevallier (2017) | 4 | 0,24% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Soule et al. (1995) | 4 | 0,24% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
Vieira et al. (2013) | 4 | 0,24% | 4 | 0,45% | 4 | 0,46% | 4 | 0,46% |
Bobin & Prenant (1965) | 3 | 0,18% | 3 | 0,34% | 3 | 0,34% | 3 | 0,34% |
Canu & Bassler (1930) | 3 | 0,18% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
D'Hondt (1983) | 3 | 0,18% | 3 | 0,34% | 3 | 0,34% | 3 | 0,34% |
D'Hondt (1987) | 3 | 0,18% | 3 | 0,34% | 3 | 0,34% | 3 | 0,34% |
D'Hondt (2010) | 3 | 0,18% | 3 | 0,34% | 3 | 0,34% | 3 | 0,34% |
Dyrynda et al. (2000) | 3 | 0,18% | 3 | 0,34% | 3 | 0,34% | 3 | 0,34% |
Fernandez et al. (1993) | 3 | 0,18% | 3 | 0,34% | 3 | 0,34% | 3 | 0,34% |
Gordon (1986) | 3 | 0,18% | 3 | 0,34% | 3 | 0,34% | 3 | 0,34% |
Harmelin (1976) | 3 | 0,18% | 3 | 0,34% | 3 | 0,34% | 3 | 0,34% |
Harmelin (1990) | 3 | 0,18% | 3 | 0,34% | 3 | 0,34% | 3 | 0,34% |
Joliet (1877) | 3 | 0,18% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
. (i-vii 1-431).">Levinsen (1909) | 3 | 0,18% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
Martino & Rosso (2021) | 3 | 0,18% | 3 | 0,34% | 3 | 0,34% | 3 | 0,34% |
Ryland et al. (2009) | 3 | 0,18% | 3 | 0,34% | 3 | 0,34% | 3 | 0,34% |
Alvarez (1991) | 2 | 0,12% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
Álvarez (1994) | 2 | 0,12% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Alvarez (1995) | 2 | 0,12% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
Audouin (1826) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Berning et al. (2021) | 2 | 0,12% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
Bock (2021) | 2 | 0,12% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
Boissel & Urtizberea (2024) | 2 | 0,12% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
Borg (1944) | 2 | 0,12% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Buski (1881) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Canu & Bassler (1927) | 2 | 0,12% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
Castric-fey (1971) | 2 | 0,12% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
Cook & Chimonides (1994) | 2 | 0,12% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
De Blauwe (2005) | 2 | 0,12% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
Decker et al. (2021) | 2 | 0,12% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
D'Hondt & Occhipinti Ambrogi (1985) | 2 | 0,12% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
D'hondt (2006) | 2 | 0,12% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
d'Hondt (2012) | 2 | 0,12% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
D'hondt (2017) | 2 | 0,12% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
Di Martino et al. (2020) | 2 | 0,12% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
Fleming (1828) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Florence et al. (2007) | 2 | 0,12% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
Galil & Gevili (2014) | 2 | 0,12% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
Gordon (1982) | 2 | 0,12% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
Gordon (1988) | 2 | 0,12% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
Gordon (1993) | 2 | 0,12% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
Harmelin (1977) | 2 | 0,12% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
Harmelin (1977) | 2 | 0,12% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
Harmelin (2006) | 2 | 0,12% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
Harmer (1934) | 2 | 0,12% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
Hastings (1929) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Hastings (1944) | 2 | 0,12% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Hayward (2004) | 2 | 0,12% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
Hirose (2011) | 2 | 0,12% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
Impact-Mer et al. (2011) | 2 | 0,12% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Johnston (1847) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Jullien (1888) | 2 | 0,12% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
Lamouroux (1821) | 2 | 0,12% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
Leca & D’hondt (1993) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Lopez-Fe (2006) | 2 | 0,12% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Loxton (2017) | 2 | 0,12% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
MGnify (2017) | 2 | 0,12% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
Moyano (1991) | 2 | 0,12% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
Norman (1868) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Notteghem (1999) | 2 | 0,12% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
Osburn (1952) | 2 | 0,12% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Powell (1967) | 2 | 0,12% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
Ristedt (1985) | 2 | 0,12% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
Ryland (1960) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Schwaha et al. (2024) | 2 | 0,12% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
Sellier et al. (2016) | 2 | 0,12% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
Souto et al. (2019) | 2 | 0,12% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
Taylor et al. (2021) | 2 | 0,12% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
Thornely (1907) | 2 | 0,12% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
Ulman et al. (2017) | 2 | 0,12% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
Vaucher (1803) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Vieira et al. (2014) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Waters (1879) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Waters (1903) | 2 | 0,12% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
Winston & Woollacott (2008) | 2 | 0,12% | 2 | 0,23% | 2 | 0,23% | 2 | 0,23% |
Alder (1857) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
André et al. (2014) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Ballesteros et al. (2009) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Bassler (1936) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Beauchamp (1918) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Berning & Kuklinski (2008) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Blauwe & Faasse (2001) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Blauwe (2002) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Blauwe (2006) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Breton & D'hondt (2004) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Busk (151) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Busk (1852) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Busk (1854) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Busk (1859) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Busk (1861) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Calvet (1906) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Calvet (1906) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Canu & Bassler (1925) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Cépède (1914) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Clausade (1969) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Cook (2001) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Curd et al. (2015) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
David & Pouyet (1974) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Delle & Chiaje (1828) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Denisenko (2019) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
d'Hondt & Clauss (1999) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
D'hondt & Goyffon (1991) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
D'hondt & Goyffon (2005) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
D'hondt et al. (2004) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Bulletin du Muséum national d'histoire naturelle. 42: 232-256.">D'hondt (1970) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
D'hondt (1974) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
d'Hondt (1985) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
D'hondt (2000) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Dolan (2014) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Bulletin de la Société zoologique de France, 48: 161-163.">Dollfus (1923) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
D'hondt & Harmelin (1993) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Fabricius (1780) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Fiala-medioni (1973) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Galil & Occhipinti-ambrogi (2009) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Gautier (1952) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Gautier (1954) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Gordon & Braga (1994) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Gordon & D'hondt (1997) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Harmelin & D'Hondt (1982) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Harmelin (1973) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Harmelin (1973) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Harmer (1933) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Hass (1948) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Hassall (1841) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Hayward & McKinney (2002) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Hayward & Ryland (1995) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Hayward & Thorpe (1989) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Hayward (1979) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Hincks (1860) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Hincks (1862) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Hincks (1862) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Hincks (1879) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Hincks (1880 | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Hondt & Condé (1996) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Ices (2022) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Ifremer (2020) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Ifremer (2021) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Johnston (1838) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Johnston (1840) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Joliet (1888) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Jullien (1886) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Kirkpatrick (1890) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Kluge (1962) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Labat (2023) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Lamarck (1816) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Landsborough (1852) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Lepoint et al. (2014) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Linnaeus (1761) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Linnaeus (1767) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Lizé (2018) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Lizé (2018) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Lizé (2018) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Lizé (2018) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Lodola et al. (2012) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Lodola et al. (2015) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
López et al. (1993) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
MacGillivray (1869) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
MacGillivray (1886) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Manzoni (1870) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Marchini et al. (2015) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Massard & Geimer (2005) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Matricardi et al. (1991) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Moll (1803) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Monod & Dollfus (1932) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Moyano (1983) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Müller (2004) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Norman (1864) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Norman (1867) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Norman (1869) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Økland & Økland (2000) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Ortmann (1890) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Osburn (1950) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Packard (1863) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Pallas (1766) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Pesson (1938) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Prouho (1889) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Ramalho et al. (2018) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Reuss (1848) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Reverter-gil & Fernández-pulpeiro (1995) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Reverter-gil & Souto (2019) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Rogick (1955) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Rosso (2002) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Ryland & Gordon (1977) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Ryland (1964) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Silén (1946) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Soule & Soule (1968) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Souto et al. (2007) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Souto et al. (2010) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Tenison Woods (1880) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Uicn et al. (2019) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Waters (1913) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Winston et al. (2000) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Zabala et al. (1993) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Zibrowius (1968) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Zilli (2021) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |