Scléractiniaires de métropole
43 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
Référence | Total | Valides | Espèces | Taxons terminaux | ||||
---|---|---|---|---|---|---|---|---|
nb | % | nb | % | nb | % | nb | % | |
Reveillaud et al. (2008) | 34 | 17,44% | 32 | 58,18% | 32 | 59,26% | 32 | 59,26% |
Fourt et al. (2017) | 18 | 9,23% | 16 | 29,09% | 16 | 29,63% | 16 | 29,63% |
Ifremer (2009) | 13 | 6,67% | 10 | 18,18% | 10 | 18,52% | 10 | 18,52% |
Zibrowius (1968) | 11 | 5,64% | 7 | 12,73% | 7 | 12,96% | 7 | 12,96% |
Milne-Edwards (1848) | 8 | 4,1% | 1 | 1,82% | 1 | 1,85% | 1 | 1,85% |
Martin (2011) | 7 | 3,59% | 5 | 9,09% | 5 | 9,26% | 5 | 9,26% |
Cairns (1999) | 6 | 3,08% | 5 | 9,09% | 5 | 9,26% | 5 | 9,26% |
Kitahara (2011) | 6 | 3,08% | 6 | 10,91% | 6 | 11,11% | 6 | 11,11% |
Zibrowius (1974) | 5 | 2,56% | 3 | 5,45% | 3 | 5,56% | 3 | 5,56% |
Godet et al. (2010) | 4 | 2,05% | 4 | 7,27% | 4 | 7,41% | 4 | 7,41% |
AAMP (2010) | 3 | 1,54% | 3 | 5,45% | 3 | 5,56% | 3 | 5,56% |
Bourcier (1988) | 3 | 1,54% | 3 | 5,45% | 3 | 5,56% | 3 | 5,56% |
Nelson-Smith et al. (2014) | 3 | 1,54% | 3 | 5,45% | 3 | 5,56% | 3 | 5,56% |
Pourtales (1868) | 3 | 1,54% | 0 | 0% | 0 | 0% | 0 | 0% |
Pourtalès (1880) | 3 | 1,54% | 3 | 5,45% | 3 | 5,56% | 3 | 5,56% |
Fautin (2013) | 2 | 1,03% | 2 | 3,64% | 2 | 3,7% | 2 | 3,7% |
Low & Evenhuis (2013) | 2 | 1,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Moseley ([1880]) | 2 | 1,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Peralta & Fautin (2013) | 2 | 1,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Questel (2020) | 2 | 1,03% | 2 | 3,64% | 2 | 3,7% | 1 | 1,85% |
Tricart & Foubert (2000) | 2 | 1,03% | 2 | 3,64% | 2 | 3,7% | 0 | 0% |
Zibrowius (1980) | 2 | 1,03% | 2 | 3,64% | 2 | 3,7% | 2 | 3,7% |
Andouche et al. (2020) | 1 | 0,51% | 1 | 1,82% | 1 | 1,85% | 1 | 1,85% |
Cairns (1979) | 1 | 0,51% | 1 | 1,82% | 1 | 1,85% | 1 | 1,85% |
Cairns (2000) | 1 | 0,51% | 1 | 1,82% | 1 | 1,85% | 1 | 1,85% |
Cecchini (1914) | 1 | 0,51% | 1 | 1,82% | 1 | 1,85% | 1 | 1,85% |
Chevaldonné et al. (2015) | 1 | 0,51% | 1 | 1,82% | 1 | 1,85% | 1 | 1,85% |
DORIS (2012) | 1 | 0,51% | 1 | 1,82% | 1 | 1,85% | 1 | 1,85% |
Duchassaing et al. (1860) | 1 | 0,51% | 1 | 1,82% | 1 | 1,85% | 0 | 0% |
Ellis & Solander (1786) | 1 | 0,51% | 0 | 0% | 0 | 0% | 0 | 0% |
Fortic et al. (2023) | 1 | 0,51% | 1 | 1,82% | 1 | 1,85% | 1 | 1,85% |
Goulletquer (2016) | 1 | 0,51% | 1 | 1,82% | 1 | 1,85% | 1 | 1,85% |
Hoeksema & Vicente (2014) | 1 | 0,51% | 1 | 1,82% | 1 | 1,85% | 1 | 1,85% |
IUCN (2014) | 1 | 0,51% | 1 | 1,82% | 1 | 1,85% | 1 | 1,85% |
Lacaze-Duthiers (1897) | 1 | 0,51% | 1 | 1,82% | 1 | 1,85% | 1 | 1,85% |
Linnaeus (1758) | 1 | 0,51% | 1 | 1,82% | 1 | 1,85% | 1 | 1,85% |
Linnaeus (1767) | 1 | 0,51% | 0 | 0% | 0 | 0% | 0 | 0% |
Proceedings of the Royal Society of London, 24: 543-569.">Moseley (1876) | 1 | 0,51% | 1 | 1,82% | 1 | 1,85% | 1 | 1,85% |
Nolf & Cahuzac (2009) | 1 | 0,51% | 1 | 1,82% | 1 | 1,85% | 1 | 1,85% |
Questel & Le Quellec (2012) | 1 | 0,51% | 1 | 1,82% | 1 | 1,85% | 0 | 0% |
Risso (1826) | 1 | 0,51% | 1 | 1,82% | 1 | 1,85% | 1 | 1,85% |
Roule (1900) | 1 | 0,51% | 1 | 1,82% | 1 | 1,85% | 1 | 1,85% |
Zibrowius (1982) | 1 | 0,51% | 0 | 0% | 0 | 0% | 0 | 0% |