Oursins
Echinoidea
106 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
Référence | Total | Valides | Espèces | Taxons terminaux | ||||
---|---|---|---|---|---|---|---|---|
nb | % | nb | % | nb | % | nb | % | |
Ducarme (2023) | 66 | 5,57% | 64 | 22,54% | 64 | 22,94% | 62 | 22,22% |
Améziane (2007) | 45 | 3,8% | 38 | 13,38% | 38 | 13,62% | 38 | 13,62% |
Clark & Rowe (1971) | 34 | 2,87% | 27 | 9,51% | 27 | 9,68% | 27 | 9,68% |
Ameziane et al. (2020) | 31 | 2,62% | 31 | 10,92% | 31 | 11,11% | 31 | 11,11% |
Guille et al. (1986) | 26 | 2,19% | 21 | 7,39% | 21 | 7,53% | 21 | 7,53% |
Martin (2011) | 26 | 2,19% | 26 | 9,15% | 26 | 9,32% | 26 | 9,32% |
Koehler (1921) | 23 | 1,94% | 18 | 6,34% | 18 | 6,45% | 18 | 6,45% |
Conand et al. (2018) | 20 | 1,69% | 20 | 7,04% | 20 | 7,17% | 19 | 6,81% |
Nelson-Smith et al. (2014) | 20 | 1,69% | 14 | 4,93% | 14 | 5,02% | 14 | 5,02% |
Bourmaud (2003) | 19 | 1,6% | 17 | 5,99% | 17 | 6,09% | 17 | 6,09% |
Linnaeus (1758) | 16 | 1,35% | 1 | 0,35% | 1 | 0,36% | 1 | 0,36% |
Brugneaux & Pérès (2006) | 14 | 1,18% | 14 | 4,93% | 14 | 5,02% | 14 | 5,02% |
Conand & ARVAM (2005) | 14 | 1,18% | 13 | 4,58% | 13 | 4,66% | 13 | 4,66% |
Questel (2020) | 14 | 1,18% | 14 | 4,93% | 14 | 5,02% | 14 | 5,02% |
Mironov (2014) | 13 | 1,1% | 13 | 4,58% | 11 | 3,94% | 12 | 4,3% |
Questel & Le Quellec (2012) | 13 | 1,1% | 13 | 4,58% | 13 | 4,66% | 13 | 4,66% |
Ifremer (2009) | 12 | 1,01% | 10 | 3,52% | 10 | 3,58% | 9 | 3,23% |
Solís-Marín & Laguarda Figueras (2009) | 11 | 0,93% | 11 | 3,87% | 11 | 3,94% | 11 | 3,94% |
Orrell (2019) | 10 | 0,84% | 10 | 3,52% | 9 | 3,23% | 10 | 3,58% |
Arnaud (1974) | 9 | 0,76% | 7 | 2,46% | 7 | 2,51% | 6 | 2,15% |
Conand et al. (2016) | 9 | 0,76% | 8 | 2,82% | 8 | 2,87% | 8 | 2,87% |
Bocquet (1953) | 8 | 0,68% | 5 | 1,76% | 5 | 1,79% | 5 | 1,79% |
Proceedings of the American Academy of Arts and Sciences. new series, 6: 190-212.">Agassiz (1879) | 7 | 0,59% | 4 | 1,41% | 4 | 1,43% | 4 | 1,43% |
Pierrat et al. (2012) | 7 | 0,59% | 7 | 2,46% | 7 | 2,51% | 7 | 2,51% |
Bourcier (1988) | 6 | 0,51% | 5 | 1,76% | 5 | 1,79% | 5 | 1,79% |
Diaz & Cuzange (2009) | 6 | 0,51% | 5 | 1,76% | 5 | 1,79% | 5 | 1,79% |
Fourt et al. (2017) | 6 | 0,51% | 6 | 2,11% | 6 | 2,15% | 6 | 2,15% |
Paulay & Brown (2019) | 6 | 0,51% | 5 | 1,76% | 5 | 1,79% | 5 | 1,79% |
Arnaud (1964) | 5 | 0,42% | 2 | 0,7% | 2 | 0,72% | 2 | 0,72% |
Australian Museum (2020) | 5 | 0,42% | 5 | 1,76% | 5 | 1,79% | 5 | 1,79% |
Harvard University Museum & Morris P.J. (2020) | 5 | 0,42% | 3 | 1,06% | 3 | 1,08% | 3 | 1,08% |
Kronen et al. (2008) | 5 | 0,42% | 5 | 1,76% | 5 | 1,79% | 5 | 1,79% |
Anthony (1925) | 4 | 0,34% | 4 | 1,41% | 4 | 1,43% | 4 | 1,43% |
Brugneaux & Pibot (2012) | 4 | 0,34% | 3 | 1,06% | 3 | 1,08% | 3 | 1,08% |
Chabanet et al. (2007) | 4 | 0,34% | 3 | 1,06% | 3 | 1,08% | 3 | 1,08% |
Chagnoux (2022) | 4 | 0,34% | 4 | 1,41% | 4 | 1,43% | 4 | 1,43% |
Conand et al. (2013) | 4 | 0,34% | 4 | 1,41% | 4 | 1,43% | 4 | 1,43% |
Grolière et al. (1980) | 4 | 0,34% | 3 | 1,06% | 3 | 1,08% | 3 | 1,08% |
Kroh et al. (2012) | 4 | 0,34% | 4 | 1,41% | 4 | 1,43% | 4 | 1,43% |
Studer (1876) | 4 | 0,34% | 0 | 0% | 0 | 0% | 0 | 0% |
Conand & Ducarme (2018) | 3 | 0,25% | 2 | 0,7% | 2 | 0,72% | 2 | 0,72% |
Gutt et al. (2007) | 3 | 0,25% | 2 | 0,7% | 2 | 0,72% | 1 | 0,36% |
Lamarck (1816) | 3 | 0,25% | 1 | 0,35% | 1 | 0,36% | 1 | 0,36% |
Müller (1776) | 3 | 0,25% | 1 | 0,35% | 1 | 0,36% | 1 | 0,36% |
Mulochau & Conand (2008) | 3 | 0,25% | 3 | 1,06% | 3 | 1,08% | 3 | 1,08% |
Serafy (1979) | 3 | 0,25% | 3 | 1,06% | 3 | 1,08% | 3 | 1,08% |
Bulletin of the Museum of Comparative Zoölogy at Harvard College. 5: 181-195.">Agassiz (1878) | 2 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Bulletin of the Museum of Comparative Zoology at Harvard College. 8(2): 69-84.">Agassiz (1880) | 2 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Anker & Corbari (2020) | 2 | 0,17% | 2 | 0,7% | 2 | 0,72% | 2 | 0,72% |
Bigot et al. (2006) | 2 | 0,17% | 2 | 0,7% | 2 | 0,72% | 2 | 0,72% |
Bigot et al. (2006) | 2 | 0,17% | 2 | 0,7% | 2 | 0,72% | 2 | 0,72% |
Breton (2014) | 2 | 0,17% | 2 | 0,7% | 2 | 0,72% | 2 | 0,72% |
Byrne & O'Hara (2017) | 2 | 0,17% | 2 | 0,7% | 2 | 0,72% | 2 | 0,72% |
Cherbonnier & Guille (1975) | 2 | 0,17% | 2 | 0,7% | 2 | 0,72% | 2 | 0,72% |
Cherbonnier (1959) | 2 | 0,17% | 1 | 0,35% | 1 | 0,36% | 1 | 0,36% |
Coppard & Schultz (2006) | 2 | 0,17% | 2 | 0,7% | 2 | 0,72% | 2 | 0,72% |
David & Mooi (2000) | 2 | 0,17% | 2 | 0,7% | 2 | 0,72% | 2 | 0,72% |
Fenaux (1965) | 2 | 0,17% | 2 | 0,7% | 2 | 0,72% | 2 | 0,72% |
Gasco (1876) | 2 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Godet et al. (2010) | 2 | 0,17% | 2 | 0,7% | 2 | 0,72% | 2 | 0,72% |
Mah (2020) | 2 | 0,17% | 2 | 0,7% | 2 | 0,72% | 2 | 0,72% |
Mills et al. (2018) | 2 | 0,17% | 2 | 0,7% | 2 | 0,72% | 2 | 0,72% |
Mironov (2006) | 2 | 0,17% | 1 | 0,35% | 1 | 0,36% | 1 | 0,36% |
Régis (1979) | 2 | 0,17% | 2 | 0,7% | 2 | 0,72% | 2 | 0,72% |
Verrill (1876) | 2 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Agassiz (1872-1874) | 1 | 0,08% | 1 | 0,35% | 1 | 0,36% | 1 | 0,36% |
Agassiz (1881) | 1 | 0,08% | 1 | 0,35% | 1 | 0,36% | 1 | 0,36% |
Anonyme (2015) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Bollard et al. (2013) | 1 | 0,08% | 1 | 0,35% | 1 | 0,36% | 1 | 0,36% |
Bronstein (2017) | 1 | 0,08% | 1 | 0,35% | 1 | 0,36% | 1 | 0,36% |
Canu (1891) | 1 | 0,08% | 1 | 0,35% | 1 | 0,36% | 1 | 0,36% |
Cépède (1914) | 1 | 0,08% | 1 | 0,35% | 1 | 0,36% | 1 | 0,36% |
Clark & Courtman-stock (1976) | 1 | 0,08% | 1 | 0,35% | 1 | 0,36% | 1 | 0,36% |
Clark (1907) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
David et al. (2015) | 1 | 0,08% | 1 | 0,35% | 1 | 0,36% | 0 | 0% |
Düben & Koren (1846) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabri-ruiz et al. (2019) | 1 | 0,08% | 1 | 0,35% | 1 | 0,36% | 1 | 0,36% |
Gadeau de Kerville (1900) | 1 | 0,08% | 1 | 0,35% | 1 | 0,36% | 1 | 0,36% |
Hardouin Michelin (1844) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Jose et al. (2015) | 1 | 0,08% | 1 | 0,35% | 1 | 0,36% | 1 | 0,36% |
Knorr & Müller (1766) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Koehler (1883) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Koehler (1926) | 1 | 0,08% | 1 | 0,35% | 1 | 0,36% | 1 | 0,36% |
Kroh (2017) | 1 | 0,08% | 1 | 0,35% | 1 | 0,36% | 1 | 0,36% |
Kroh (2017) | 1 | 0,08% | 1 | 0,35% | 1 | 0,36% | 1 | 0,36% |
Kroh (2017) | 1 | 0,08% | 1 | 0,35% | 1 | 0,36% | 1 | 0,36% |
Kroh (2017) | 1 | 0,08% | 1 | 0,35% | 1 | 0,36% | 1 | 0,36% |
Lessios et al. (1996) | 1 | 0,08% | 1 | 0,35% | 1 | 0,36% | 1 | 0,36% |
Michelin (1862) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Minin (2012) | 1 | 0,08% | 1 | 0,35% | 1 | 0,36% | 1 | 0,36% |
Monod & Dollfus (1932) | 1 | 0,08% | 1 | 0,35% | 1 | 0,36% | 1 | 0,36% |
Mortensen (1907) | 1 | 0,08% | 1 | 0,35% | 1 | 0,36% | 1 | 0,36% |
Mortensen (1921) | 1 | 0,08% | 1 | 0,35% | 1 | 0,36% | 1 | 0,36% |
Mortensen (1936) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Natural History Museum of London (2020) | 1 | 0,08% | 1 | 0,35% | 1 | 0,36% | 1 | 0,36% |
Pennant (1777) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Philippi (1845) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Pierrat (2019) | 1 | 0,08% | 1 | 0,35% | 1 | 0,36% | 1 | 0,36% |
Bulletin du Museum national d'Histoire naturelle, 14A, 2 : 405-441.">Ridder et al. (1992) | 1 | 0,08% | 1 | 0,35% | 1 | 0,36% | 1 | 0,36% |
Saucède (2017) | 1 | 0,08% | 1 | 0,35% | 1 | 0,36% | 1 | 0,36% |
Saucède (2017) | 1 | 0,08% | 1 | 0,35% | 1 | 0,36% | 1 | 0,36% |
Saucède (2017) | 1 | 0,08% | 1 | 0,35% | 1 | 0,36% | 1 | 0,36% |
Saucède (2017) | 1 | 0,08% | 1 | 0,35% | 1 | 0,36% | 1 | 0,36% |
Saucède (2017) | 1 | 0,08% | 1 | 0,35% | 1 | 0,36% | 1 | 0,36% |
Saucède (2017) | 1 | 0,08% | 1 | 0,35% | 1 | 0,36% | 1 | 0,36% |
Weinberg & Ridder (1998) | 1 | 0,08% | 1 | 0,35% | 1 | 0,36% | 1 | 0,36% |