Bryozoaires de métropole
197 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
Référence | Total | Valides | Espèces | Taxons terminaux | ||||
---|---|---|---|---|---|---|---|---|
nb | % | nb | % | nb | % | nb | % | |
Julien (1881) | 83 | 9,83% | 31 | 7,81% | 31 | 7,87% | 31 | 7,87% |
Ifremer (2009) | 59 | 6,99% | 53 | 13,35% | 53 | 13,45% | 53 | 13,45% |
Nelson-Smith et al. (2014) | 51 | 6,04% | 42 | 10,58% | 42 | 10,66% | 41 | 10,41% |
Mao et al. (2020) | 33 | 3,91% | 27 | 6,8% | 27 | 6,85% | 27 | 6,85% |
Godet et al. (2010) | 22 | 2,61% | 19 | 4,79% | 19 | 4,82% | 18 | 4,57% |
Bourcier (1988) | 21 | 2,49% | 15 | 3,78% | 15 | 3,81% | 14 | 3,55% |
Breton (2014) | 21 | 2,49% | 17 | 4,28% | 17 | 4,31% | 17 | 4,31% |
Linnaeus (1758) | 19 | 2,25% | 0 | 0% | 0 | 0% | 0 | 0% |
Harmelin et al. (2019) | 15 | 1,78% | 12 | 3,02% | 12 | 3,05% | 12 | 3,05% |
Gordon (2007) | 13 | 1,54% | 12 | 3,02% | 12 | 3,05% | 12 | 3,05% |
Harmelin & Rosso (2023) | 13 | 1,54% | 13 | 3,27% | 13 | 3,3% | 13 | 3,3% |
Fehlauer-ale et al. (2015) | 11 | 1,3% | 11 | 2,77% | 11 | 2,79% | 11 | 2,79% |
Goulletquer (2016) | 11 | 1,3% | 11 | 2,77% | 11 | 2,79% | 11 | 2,79% |
d'Hondt (1979) | 10 | 1,18% | 10 | 2,52% | 10 | 2,54% | 10 | 2,54% |
Julien (1882) | 10 | 1,18% | 4 | 1,01% | 4 | 1,02% | 4 | 1,02% |
Lepoint et al. (2019) | 10 | 1,18% | 9 | 2,27% | 9 | 2,28% | 9 | 2,28% |
d'Hondt & Goyffon (1993) | 9 | 1,07% | 8 | 2,02% | 8 | 2,03% | 8 | 2,03% |
Gautier (1953) | 9 | 1,07% | 5 | 1,26% | 5 | 1,27% | 5 | 1,27% |
Álvarez (1992) | 8 | 0,95% | 8 | 2,02% | 8 | 2,03% | 8 | 2,03% |
Bishop & Househam (1987) | 8 | 0,95% | 3 | 0,76% | 3 | 0,76% | 3 | 0,76% |
Dewarumez et al. (2011) | 8 | 0,95% | 6 | 1,51% | 6 | 1,52% | 6 | 1,52% |
Fourt et al. (2017) | 8 | 0,95% | 8 | 2,02% | 8 | 2,03% | 8 | 2,03% |
Harmelin (1984) | 7 | 0,83% | 7 | 1,76% | 7 | 1,78% | 7 | 1,78% |
Blauwe (2010) | 6 | 0,71% | 5 | 1,26% | 5 | 1,27% | 5 | 1,27% |
d'Hondt (1995) | 6 | 0,71% | 5 | 1,26% | 5 | 1,27% | 5 | 1,27% |
Harmelin & Aristegui (1988) | 6 | 0,71% | 2 | 0,5% | 2 | 0,51% | 0 | 0% |
Julien (1885) | 6 | 0,71% | 2 | 0,5% | 2 | 0,51% | 2 | 0,51% |
Pearman et al. (2020) | 6 | 0,71% | 4 | 1,01% | 4 | 1,02% | 4 | 1,02% |
Davoult et al. (1999) | 5 | 0,59% | 3 | 0,76% | 3 | 0,76% | 3 | 0,76% |
Echalier & Prenant (1951) | 5 | 0,59% | 5 | 1,26% | 5 | 1,27% | 5 | 1,27% |
Harmelin (2020) | 5 | 0,59% | 5 | 1,26% | 5 | 1,27% | 5 | 1,27% |
Linnaeus (1767) | 5 | 0,59% | 0 | 0% | 0 | 0% | 0 | 0% |
Rosso et al. (2020) | 5 | 0,59% | 5 | 1,26% | 5 | 1,27% | 5 | 1,27% |
Balavoine (1958) | 4 | 0,47% | 4 | 1,01% | 4 | 1,02% | 4 | 1,02% |
Bishop (1988) | 4 | 0,47% | 1 | 0,25% | 1 | 0,25% | 1 | 0,25% |
D'hondt & Hayward (1981) | 4 | 0,47% | 3 | 0,76% | 3 | 0,76% | 3 | 0,76% |
d'Hondt & Mascarell (2010) | 4 | 0,47% | 3 | 0,76% | 3 | 0,76% | 3 | 0,76% |
Ellis & Solander (1786) | 4 | 0,47% | 0 | 0% | 0 | 0% | 0 | 0% |
Redier (1971) | 4 | 0,47% | 2 | 0,5% | 2 | 0,51% | 2 | 0,51% |
Reverter-gil et al. (2016) | 4 | 0,47% | 4 | 1,01% | 4 | 1,02% | 4 | 1,02% |
Rignault & Chevallier (2017) | 4 | 0,47% | 1 | 0,25% | 1 | 0,25% | 1 | 0,25% |
Vieira et al. (2013) | 4 | 0,47% | 4 | 1,01% | 4 | 1,02% | 4 | 1,02% |
Arnaud (1974) | 3 | 0,36% | 3 | 0,76% | 3 | 0,76% | 3 | 0,76% |
Bobin & Prenant (1965) | 3 | 0,36% | 3 | 0,76% | 3 | 0,76% | 3 | 0,76% |
Bock (2020) | 3 | 0,36% | 3 | 0,76% | 3 | 0,76% | 3 | 0,76% |
Busk (1876) | 3 | 0,36% | 2 | 0,5% | 2 | 0,51% | 2 | 0,51% |
D'Hondt (1987) | 3 | 0,36% | 3 | 0,76% | 3 | 0,76% | 3 | 0,76% |
D'Hondt (2010) | 3 | 0,36% | 3 | 0,76% | 3 | 0,76% | 3 | 0,76% |
Dyrynda et al. (2000) | 3 | 0,36% | 3 | 0,76% | 3 | 0,76% | 3 | 0,76% |
Fernandez et al. (1993) | 3 | 0,36% | 3 | 0,76% | 3 | 0,76% | 3 | 0,76% |
Harmelin (1976) | 3 | 0,36% | 3 | 0,76% | 3 | 0,76% | 3 | 0,76% |
Harmelin (1990) | 3 | 0,36% | 3 | 0,76% | 3 | 0,76% | 3 | 0,76% |
Joliet (1877) | 3 | 0,36% | 2 | 0,5% | 2 | 0,51% | 2 | 0,51% |
Martino & Rosso (2021) | 3 | 0,36% | 3 | 0,76% | 3 | 0,76% | 3 | 0,76% |
Ryland et al. (2009) | 3 | 0,36% | 3 | 0,76% | 3 | 0,76% | 3 | 0,76% |
Alvarez (1991) | 2 | 0,24% | 2 | 0,5% | 2 | 0,51% | 2 | 0,51% |
Álvarez (1994) | 2 | 0,24% | 1 | 0,25% | 1 | 0,25% | 1 | 0,25% |
Alvarez (1995) | 2 | 0,24% | 2 | 0,5% | 2 | 0,51% | 2 | 0,51% |
Audouin (1826) | 2 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
Berning et al. (2021) | 2 | 0,24% | 2 | 0,5% | 2 | 0,51% | 2 | 0,51% |
Busk (1852) | 2 | 0,24% | 1 | 0,25% | 1 | 0,25% | 1 | 0,25% |
Zoology, x: 216 pp..">Busk (1884) | 2 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
Canu & Bassler (1930) | 2 | 0,24% | 1 | 0,25% | 1 | 0,25% | 1 | 0,25% |
Castric-fey (1971) | 2 | 0,24% | 2 | 0,5% | 2 | 0,51% | 2 | 0,51% |
De Blauwe (2005) | 2 | 0,24% | 2 | 0,5% | 2 | 0,51% | 2 | 0,51% |
Decker et al. (2021) | 2 | 0,24% | 2 | 0,5% | 2 | 0,51% | 2 | 0,51% |
D'Hondt & Occhipinti Ambrogi (1985) | 2 | 0,24% | 2 | 0,5% | 2 | 0,51% | 2 | 0,51% |
d'Hondt (1984) | 2 | 0,24% | 2 | 0,5% | 2 | 0,51% | 2 | 0,51% |
Di Martino et al. (2020) | 2 | 0,24% | 2 | 0,5% | 2 | 0,51% | 2 | 0,51% |
Fleming (1828) | 2 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
Galil & Gevili (2014) | 2 | 0,24% | 2 | 0,5% | 2 | 0,51% | 2 | 0,51% |
Harmelin (1977) | 2 | 0,24% | 2 | 0,5% | 2 | 0,51% | 2 | 0,51% |
Harmelin (1977) | 2 | 0,24% | 2 | 0,5% | 2 | 0,51% | 2 | 0,51% |
Hastings (1944) | 2 | 0,24% | 1 | 0,25% | 1 | 0,25% | 1 | 0,25% |
Johnston (1847) | 2 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
Lamouroux (1816) | 2 | 0,24% | 1 | 0,25% | 1 | 0,25% | 1 | 0,25% |
Lamouroux (1821) | 2 | 0,24% | 2 | 0,5% | 2 | 0,51% | 2 | 0,51% |
Lopez-Fe (2006) | 2 | 0,24% | 1 | 0,25% | 1 | 0,25% | 1 | 0,25% |
Loxton (2017) | 2 | 0,24% | 2 | 0,5% | 2 | 0,51% | 2 | 0,51% |
MGnify (2017) | 2 | 0,24% | 2 | 0,5% | 2 | 0,51% | 2 | 0,51% |
Norman (1868) | 2 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
Notteghem (1999) | 2 | 0,24% | 2 | 0,5% | 2 | 0,51% | 2 | 0,51% |
Richer de Forges et al. (2005) | 2 | 0,24% | 1 | 0,25% | 1 | 0,25% | 1 | 0,25% |
Ryland (1960) | 2 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
Sellier et al. (2016) | 2 | 0,24% | 2 | 0,5% | 2 | 0,51% | 2 | 0,51% |
Souto et al. (2019) | 2 | 0,24% | 2 | 0,5% | 2 | 0,51% | 2 | 0,51% |
Ulman et al. (2017) | 2 | 0,24% | 2 | 0,5% | 2 | 0,51% | 2 | 0,51% |
Vaucher (1803) | 2 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
Vieira et al. (2014) | 2 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
Waters (1879) | 2 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
Alder (1857) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
André et al. (2014) | 1 | 0,12% | 1 | 0,25% | 1 | 0,25% | 1 | 0,25% |
Ballesteros et al. (2009) | 1 | 0,12% | 1 | 0,25% | 1 | 0,25% | 1 | 0,25% |
Beauchamp (1918) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Berning & Kuklinski (2008) | 1 | 0,12% | 1 | 0,25% | 1 | 0,25% | 1 | 0,25% |
Blauwe & Faasse (2001) | 1 | 0,12% | 1 | 0,25% | 1 | 0,25% | 1 | 0,25% |
Blauwe (2002) | 1 | 0,12% | 1 | 0,25% | 1 | 0,25% | 1 | 0,25% |
Blauwe (2006) | 1 | 0,12% | 1 | 0,25% | 1 | 0,25% | 1 | 0,25% |
Boissel & Urtizberea (2024) | 1 | 0,12% | 1 | 0,25% | 1 | 0,25% | 1 | 0,25% |
Breton & D'hondt (2004) | 1 | 0,12% | 1 | 0,25% | 1 | 0,25% | 1 | 0,25% |
Busk (151) | 1 | 0,12% | 1 | 0,25% | 1 | 0,25% | 1 | 0,25% |
Busk (1854) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Busk (1859) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Busk (1861) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Calvet (1906) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Calvet (1906) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Canu & Bassler (1925) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Cépède (1914) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Clausade (1969) | 1 | 0,12% | 1 | 0,25% | 1 | 0,25% | 1 | 0,25% |
Curd et al. (2015) | 1 | 0,12% | 1 | 0,25% | 1 | 0,25% | 1 | 0,25% |
David & Pouyet (1974) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Delle & Chiaje (1828) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Denisenko (2019) | 1 | 0,12% | 1 | 0,25% | 1 | 0,25% | 1 | 0,25% |
d'Hondt & Clauss (1999) | 1 | 0,12% | 1 | 0,25% | 1 | 0,25% | 1 | 0,25% |
D'hondt & Goyffon (1991) | 1 | 0,12% | 1 | 0,25% | 1 | 0,25% | 1 | 0,25% |
D'hondt & Goyffon (2005) | 1 | 0,12% | 1 | 0,25% | 1 | 0,25% | 1 | 0,25% |
d'Hondt & Mascarell (2010) | 1 | 0,12% | 1 | 0,25% | 1 | 0,25% | 1 | 0,25% |
D'hondt et al. (2004) | 1 | 0,12% | 1 | 0,25% | 1 | 0,25% | 1 | 0,25% |
Bulletin du Muséum national d'histoire naturelle. 42: 232-256.">D'hondt (1970) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
D'hondt (1974) | 1 | 0,12% | 1 | 0,25% | 1 | 0,25% | 1 | 0,25% |
d'Hondt (1985) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
D'hondt (2000) | 1 | 0,12% | 1 | 0,25% | 1 | 0,25% | 1 | 0,25% |
d'Hondt (2009) | 1 | 0,12% | 1 | 0,25% | 1 | 0,25% | 1 | 0,25% |
Dolan (2014) | 1 | 0,12% | 1 | 0,25% | 1 | 0,25% | 1 | 0,25% |
Bulletin de la Société zoologique de France, 48: 161-163.">Dollfus (1923) | 1 | 0,12% | 1 | 0,25% | 1 | 0,25% | 1 | 0,25% |
D'hondt & Harmelin (1993) | 1 | 0,12% | 1 | 0,25% | 1 | 0,25% | 1 | 0,25% |
Fabricius (1780) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Fiala-medioni (1973) | 1 | 0,12% | 1 | 0,25% | 1 | 0,25% | 1 | 0,25% |
Galil & Occhipinti-ambrogi (2009) | 1 | 0,12% | 1 | 0,25% | 1 | 0,25% | 1 | 0,25% |
Gautier (1952) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Gautier (1954) | 1 | 0,12% | 1 | 0,25% | 1 | 0,25% | 1 | 0,25% |
Harmelin & D'Hondt (1982) | 1 | 0,12% | 1 | 0,25% | 1 | 0,25% | 1 | 0,25% |
Harmelin (1973) | 1 | 0,12% | 1 | 0,25% | 1 | 0,25% | 1 | 0,25% |
Harmelin (1973) | 1 | 0,12% | 1 | 0,25% | 1 | 0,25% | 1 | 0,25% |
Harmer (1933) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Hass (1948) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Hassall (1841) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Hayward & McKinney (2002) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Hayward & Ryland (1995) | 1 | 0,12% | 1 | 0,25% | 1 | 0,25% | 1 | 0,25% |
Hayward (1979) | 1 | 0,12% | 1 | 0,25% | 1 | 0,25% | 1 | 0,25% |
Hincks (1860) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Hincks (1862) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Hincks (1862) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Hincks (1879) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Hincks (1880 | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Hondt & Condé (1996) | 1 | 0,12% | 1 | 0,25% | 1 | 0,25% | 1 | 0,25% |
Ices (2022) | 1 | 0,12% | 1 | 0,25% | 1 | 0,25% | 1 | 0,25% |
Ifremer (2020) | 1 | 0,12% | 1 | 0,25% | 1 | 0,25% | 1 | 0,25% |
Ifremer (2021) | 1 | 0,12% | 1 | 0,25% | 1 | 0,25% | 1 | 0,25% |
Johnston (1838) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Johnston (1840) | 1 | 0,12% | 1 | 0,25% | 1 | 0,25% | 1 | 0,25% |
Joliet (1888) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Jullien (1886) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Labat (2023) | 1 | 0,12% | 1 | 0,25% | 1 | 0,25% | 1 | 0,25% |
Lamarck (1816) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Landsborough (1852) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Lepoint et al. (2014) | 1 | 0,12% | 1 | 0,25% | 1 | 0,25% | 1 | 0,25% |
Linnaeus (1761) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Linnaeus (1767) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Lizé (2018) | 1 | 0,12% | 1 | 0,25% | 1 | 0,25% | 1 | 0,25% |
Lizé (2018) | 1 | 0,12% | 1 | 0,25% | 1 | 0,25% | 1 | 0,25% |
Lizé (2018) | 1 | 0,12% | 1 | 0,25% | 1 | 0,25% | 1 | 0,25% |
Lizé (2018) | 1 | 0,12% | 1 | 0,25% | 1 | 0,25% | 1 | 0,25% |
Lodola et al. (2012) | 1 | 0,12% | 1 | 0,25% | 1 | 0,25% | 1 | 0,25% |
Lodola et al. (2015) | 1 | 0,12% | 1 | 0,25% | 1 | 0,25% | 1 | 0,25% |
López et al. (1993) | 1 | 0,12% | 1 | 0,25% | 1 | 0,25% | 1 | 0,25% |
Manzoni (1870) | 1 | 0,12% | 1 | 0,25% | 1 | 0,25% | 1 | 0,25% |
Marchini et al. (2015) | 1 | 0,12% | 1 | 0,25% | 1 | 0,25% | 1 | 0,25% |
Massard & Geimer (2005) | 1 | 0,12% | 1 | 0,25% | 1 | 0,25% | 1 | 0,25% |
Matricardi et al. (1991) | 1 | 0,12% | 1 | 0,25% | 1 | 0,25% | 1 | 0,25% |
Moll (1803) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Müller (2004) | 1 | 0,12% | 1 | 0,25% | 1 | 0,25% | 1 | 0,25% |
Norman (1864) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Norman (1867) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Norman (1869) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Økland & Økland (2000) | 1 | 0,12% | 1 | 0,25% | 1 | 0,25% | 1 | 0,25% |
Ortmann (1890) | 1 | 0,12% | 1 | 0,25% | 1 | 0,25% | 1 | 0,25% |
Packard (1863) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Pallas (1766) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Pesson (1938) | 1 | 0,12% | 1 | 0,25% | 1 | 0,25% | 1 | 0,25% |
Prouho (1889) | 1 | 0,12% | 1 | 0,25% | 1 | 0,25% | 1 | 0,25% |
Ramalho et al. (2018) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Reuss (1848) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Reverter-gil & Fernández-pulpeiro (1995) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Reverter-gil & Souto (2019) | 1 | 0,12% | 1 | 0,25% | 1 | 0,25% | 1 | 0,25% |
Rosso (2002) | 1 | 0,12% | 1 | 0,25% | 1 | 0,25% | 1 | 0,25% |
Ryland & Gordon (1977) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Ryland (1964) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Silén (1946) | 1 | 0,12% | 1 | 0,25% | 1 | 0,25% | 1 | 0,25% |
Soule & Soule (1968) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Souto et al. (2007) | 1 | 0,12% | 1 | 0,25% | 1 | 0,25% | 1 | 0,25% |
Souto et al. (2010) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Uicn et al. (2019) | 1 | 0,12% | 1 | 0,25% | 1 | 0,25% | 1 | 0,25% |
Winston et al. (2000) | 1 | 0,12% | 1 | 0,25% | 1 | 0,25% | 1 | 0,25% |
Zabala et al. (1993) | 1 | 0,12% | 1 | 0,25% | 1 | 0,25% | 1 | 0,25% |
Zibrowius (1968) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Zilli (2021) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |