Hydrozoaires de métropole
171 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
Référence | Total | Valides | Espèces | Taxons terminaux | ||||
---|---|---|---|---|---|---|---|---|
nb | % | nb | % | nb | % | nb | % | |
Poupin et al. (1999) | 60 | 4,68% | 52 | 15,25% | 52 | 15,25% | 52 | 15,25% |
Nelson-Smith et al. (2014) | 42 | 3,27% | 34 | 9,97% | 34 | 9,97% | 34 | 9,97% |
Bedot (1910) | 38 | 2,96% | 20 | 5,87% | 20 | 5,87% | 20 | 5,87% |
Ifremer (2009) | 29 | 2,26% | 26 | 7,62% | 26 | 7,62% | 26 | 7,62% |
Motz-Kossowska (1910) | 27 | 2,1% | 6 | 1,76% | 6 | 1,76% | 6 | 1,76% |
Galea (2013) | 23 | 1,79% | 19 | 5,57% | 19 | 5,57% | 19 | 5,57% |
Galea (2008) | 16 | 1,25% | 14 | 4,11% | 14 | 4,11% | 14 | 4,11% |
Gravier-Bonnet et al. (2007) | 16 | 1,25% | 12 | 3,52% | 12 | 3,52% | 12 | 3,52% |
Gravier-Bonnet (2007) | 15 | 1,17% | 12 | 3,52% | 12 | 3,52% | 12 | 3,52% |
Linnaeus (1758) | 15 | 1,17% | 3 | 0,88% | 3 | 0,88% | 3 | 0,88% |
Rignault & Chevallier (2017) | 15 | 1,17% | 12 | 3,52% | 12 | 3,52% | 12 | 3,52% |
Godet et al. (2010) | 14 | 1,09% | 12 | 3,52% | 12 | 3,52% | 12 | 3,52% |
Bedot (1914) | 13 | 1,01% | 8 | 2,35% | 8 | 2,35% | 8 | 2,35% |
Breton (2014) | 13 | 1,01% | 12 | 3,52% | 12 | 3,52% | 12 | 3,52% |
Bourmaud (2003) | 12 | 0,94% | 9 | 2,64% | 9 | 2,64% | 9 | 2,64% |
Goulletquer (2016) | 9 | 0,7% | 8 | 2,35% | 8 | 2,35% | 8 | 2,35% |
European Nucleotide Archive (2019) | 8 | 0,62% | 8 | 2,35% | 8 | 2,35% | 8 | 2,35% |
Svoboda & Cornelius (1991) | 8 | 0,62% | 8 | 2,35% | 8 | 2,35% | 8 | 2,35% |
Billard (1923) | 7 | 0,55% | 5 | 1,47% | 5 | 1,47% | 5 | 1,47% |
Caziot (1921) | 7 | 0,55% | 4 | 1,17% | 4 | 1,17% | 4 | 1,17% |
Galea et al. (2021) | 7 | 0,55% | 7 | 2,05% | 7 | 2,05% | 7 | 2,05% |
Galea (2010) | 7 | 0,55% | 5 | 1,47% | 5 | 1,47% | 5 | 1,47% |
Bulletin de la Société Zoologique de France, 38: 282-288, 304-315.">Le Danois (1913) | 7 | 0,55% | 2 | 0,59% | 2 | 0,59% | 2 | 0,59% |
Mccrady (1859) | 7 | 0,55% | 2 | 0,59% | 2 | 0,59% | 2 | 0,59% |
Millard (1977) | 7 | 0,55% | 6 | 1,76% | 6 | 1,76% | 6 | 1,76% |
Pearman et al. (2020) | 7 | 0,55% | 6 | 1,76% | 6 | 1,76% | 6 | 1,76% |
Alder (1859) | 6 | 0,47% | 4 | 1,17% | 4 | 1,17% | 4 | 1,17% |
Memoirs of the Museum of Comparative Zoology at Harvard College Cambridge, 37: 1-243.">Bigelow (1909) | 6 | 0,47% | 3 | 0,88% | 3 | 0,88% | 3 | 0,88% |
Dolan (2014) | 6 | 0,47% | 6 | 1,76% | 6 | 1,76% | 6 | 1,76% |
Gravier-Bonnet & Bourmaud (2005) | 6 | 0,47% | 4 | 1,17% | 4 | 1,17% | 4 | 1,17% |
Nowaczyk et al. (2016) | 6 | 0,47% | 6 | 1,76% | 6 | 1,76% | 6 | 1,76% |
Bouillon & Deroux (1967) | 5 | 0,39% | 5 | 1,47% | 5 | 1,47% | 5 | 1,47% |
Redier (1971) | 5 | 0,39% | 4 | 1,17% | 4 | 1,17% | 4 | 1,17% |
Sauvage (1886) | 5 | 0,39% | 4 | 1,17% | 4 | 1,17% | 4 | 1,17% |
Schuchert (2008) | 5 | 0,39% | 2 | 0,59% | 2 | 0,59% | 2 | 0,59% |
Arnaud (1974) | 4 | 0,31% | 2 | 0,59% | 2 | 0,59% | 2 | 0,59% |
Bouillon (1965) | 4 | 0,31% | 2 | 0,59% | 2 | 0,59% | 2 | 0,59% |
Dewarumez et al. (2011) | 4 | 0,31% | 3 | 0,88% | 3 | 0,88% | 3 | 0,88% |
Lacassagne (1968) | 4 | 0,31% | 4 | 1,17% | 4 | 1,17% | 4 | 1,17% |
Olivier et al. (2015) | 4 | 0,31% | 4 | 1,17% | 4 | 1,17% | 4 | 1,17% |
Schuchert (2017) | 4 | 0,31% | 4 | 1,17% | 4 | 1,17% | 4 | 1,17% |
Swedmark & Teissier (1957) | 4 | 0,31% | 4 | 1,17% | 4 | 1,17% | 4 | 1,17% |
Bedot (1888) | 3 | 0,23% | 3 | 0,88% | 3 | 0,88% | 3 | 0,88% |
Billard (1922) | 3 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Carré (1968) | 3 | 0,23% | 3 | 0,88% | 3 | 0,88% | 3 | 0,88% |
Carré (1968) | 3 | 0,23% | 3 | 0,88% | 3 | 0,88% | 3 | 0,88% |
Carré (1969) | 3 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Carré (1969) | 3 | 0,23% | 3 | 0,88% | 3 | 0,88% | 3 | 0,88% |
Gadeau de Kerville (1900) | 3 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
MGnify (2017) | 3 | 0,23% | 3 | 0,88% | 3 | 0,88% | 3 | 0,88% |
Naumov & Stepanjants (1972) | 3 | 0,23% | 2 | 0,59% | 2 | 0,59% | 2 | 0,59% |
Pallas (1766) | 3 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Péres (1925) | 3 | 0,23% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
Pérez (1920) | 3 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Picard (1958) | 3 | 0,23% | 3 | 0,88% | 3 | 0,88% | 3 | 0,88% |
Picard (1960) | 3 | 0,23% | 3 | 0,88% | 3 | 0,88% | 3 | 0,88% |
Questel & Le Quellec (2012) | 3 | 0,23% | 3 | 0,88% | 3 | 0,88% | 3 | 0,88% |
Questel (2020) | 3 | 0,23% | 3 | 0,88% | 3 | 0,88% | 3 | 0,88% |
Swedmark & Teissier (1958) | 3 | 0,23% | 3 | 0,88% | 3 | 0,88% | 3 | 0,88% |
Teissier (1922) | 3 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Vervoort (1993) | 3 | 0,23% | 3 | 0,88% | 3 | 0,88% | 3 | 0,88% |
Weill & Weill (1935) | 3 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Agassiz & Mayer (1902) | 2 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Agassiz (1849) | 2 | 0,16% | 2 | 0,59% | 2 | 0,59% | 2 | 0,59% |
Albertini-Berhaut (1970) | 2 | 0,16% | 2 | 0,59% | 2 | 0,59% | 2 | 0,59% |
Albertini-berhaut (1970) | 2 | 0,16% | 2 | 0,59% | 2 | 0,59% | 2 | 0,59% |
Alder (1856) | 2 | 0,16% | 2 | 0,59% | 2 | 0,59% | 2 | 0,59% |
Allman (1888) | 2 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Ansín Agís et al. (2014) | 2 | 0,16% | 2 | 0,59% | 2 | 0,59% | 2 | 0,59% |
Proceedings of the United States National Museum, 44: 1-119.">Bigelow (1913) | 2 | 0,16% | 2 | 0,59% | 2 | 0,59% | 2 | 0,59% |
Bourne (1890) | 2 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Buecher (1999) | 2 | 0,16% | 2 | 0,59% | 2 | 0,59% | 2 | 0,59% |
Clarke (1879) | 2 | 0,16% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
Curd et al. (2015) | 2 | 0,16% | 2 | 0,59% | 2 | 0,59% | 2 | 0,59% |
Damas (1934) | 2 | 0,16% | 2 | 0,59% | 2 | 0,59% | 2 | 0,59% |
Ellis & Solander (1786) | 2 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Forbes (1848) | 2 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Fourt et al. (2017) | 2 | 0,16% | 2 | 0,59% | 2 | 0,59% | 2 | 0,59% |
Galea & Ferry (2015) | 2 | 0,16% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
Galea & Schories (2012) | 2 | 0,16% | 2 | 0,59% | 2 | 0,59% | 2 | 0,59% |
Goy (1965) | 2 | 0,16% | 2 | 0,59% | 2 | 0,59% | 2 | 0,59% |
Gravier-Bonnet et al. (2022) | 2 | 0,16% | 2 | 0,59% | 2 | 0,59% | 2 | 0,59% |
Haeckel (1864) | 2 | 0,16% | 2 | 0,59% | 2 | 0,59% | 2 | 0,59% |
Haeckel (1879) | 2 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Hassall (1848) | 2 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Heller (1868) | 2 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Hincks (1855) | 2 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Hincks (1861) | 2 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Hincks (1862) | 2 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Lamarck (1816) | 2 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Lamouroux (1816) | 2 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Licandro et al. (2004) | 2 | 0,16% | 2 | 0,59% | 2 | 0,59% | 2 | 0,59% |
Mao et al. (2020) | 2 | 0,16% | 2 | 0,59% | 2 | 0,59% | 2 | 0,59% |
Modeer (1791) | 2 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Remane (1927) | 2 | 0,16% | 2 | 0,59% | 2 | 0,59% | 2 | 0,59% |
Totton (1930) | 2 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Valkanov (1965) | 2 | 0,16% | 2 | 0,59% | 2 | 0,59% | 2 | 0,59% |
Vanhöffen (1903) | 2 | 0,16% | 2 | 0,59% | 2 | 0,59% | 2 | 0,59% |
Vervoort & Vasseur (1977) | 2 | 0,16% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
Alder (1857) | 1 | 0,08% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
Allman (1859) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Altuna Prados & Álvarez Claudio (1994) | 1 | 0,08% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
Ansin Agis et al. (2001) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Ansín Agís et al. (2009) | 1 | 0,08% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
Arvy (1972) | 1 | 0,08% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
Bale (1888) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Bale (1924) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Balvay (2009) | 1 | 0,08% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
Bigelow (1909) | 1 | 0,08% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
Brugneaux & Pérès (2005) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Cauvin (2010) | 1 | 0,08% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
Cocks (1854) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Collectif & Bebest (2019) | 1 | 0,08% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
Cunningham (1892) | 1 | 0,08% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
Deuss et al. (2013) | 1 | 0,08% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
Eschscholtz (1829) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Forsskål & Niebuhr (1775) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Forsskål (1775) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Fraser (1948) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Galea (2007) | 1 | 0,08% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
Gegenbaur (1857) | 1 | 0,08% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
Gmelin (1791) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Gravier-Bonnet & Bourmaud (2006) | 1 | 0,08% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
Hartlaub (1901) | 1 | 0,08% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
Hincks (1861) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Hincks (1866) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Hincks (1866) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Proceedings of the Zoological Society of London, 1907: 1035-1037.">Hopkinson (1907) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Hughes (1983) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Ifremer (2020) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Ifremer (2022) | 1 | 0,08% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
Kölliker (1853) | 1 | 0,08% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
Kousteni et al. (2019) | 1 | 0,08% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
Krohn (1853) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Lamouroux (1821) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Lankester (1880) | 1 | 0,08% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
Laval (1968) | 1 | 0,08% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
Leloup (1935) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Linnaeus (1761) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Linnaeus (1767) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Linné (1767) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Loeuillet et al. (2017) | 1 | 0,08% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
MacGillivray (1842) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Marchessaux et al. (2017) | 1 | 0,08% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
Mayer (1910) | 1 | 0,08% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
Millard (1957) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Molnar et al. (2008) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Moura et al. (2012) | 1 | 0,08% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
Müller (1776) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Noël, Chevallier (2016) | 1 | 0,08% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
Norman (1867) | 1 | 0,08% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
Orrell (2019) | 1 | 0,08% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
Otto (1823) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Pena et al. (2010) | 1 | 0,08% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
Picard (1951) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Zoologischer Anzeiger, 7: 148-152, 164-169, 185-188, 216-221.">Pieper (1884) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Questel (2022) | 1 | 0,08% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
Rees & White (1957) | 1 | 0,08% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
Renaud-Mornant & Jouin (1965) | 1 | 0,08% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
Roth (1871) | 1 | 0,08% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
Saemundsson (1911) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Sars (1835) | 1 | 0,08% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
Sars (1857) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Sars (1874) | 1 | 0,08% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
Schuchert & Collins (2021) | 1 | 0,08% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
Schuchert (2000) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Schuchert (2008) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Sentz-Braconnot & Carré (1966) | 1 | 0,08% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
Sowerby (1941) | 1 | 0,08% | 1 | 0,29% | 1 | 0,29% | 1 | 0,29% |
Uicn et al. (2019) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Zilli (2021) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |