Echinodermes de Martinique
52 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
Référence | Total | Valides | Espèces | Taxons terminaux | ||||
---|---|---|---|---|---|---|---|---|
nb | % | nb | % | nb | % | nb | % | |
Lyman (1883) | 27 | 7,3% | 12 | 11,76% | 12 | 11,88% | 12 | 11,88% |
Brugneaux & Pérès (2006) | 26 | 7,03% | 22 | 21,57% | 22 | 21,78% | 22 | 21,78% |
Harvard University Museum & Morris P.J. (2020) | 21 | 5,68% | 19 | 18,63% | 19 | 18,81% | 19 | 18,81% |
Questel (2020) | 20 | 5,41% | 19 | 18,63% | 19 | 18,81% | 19 | 18,81% |
Questel & Le Quellec (2012) | 19 | 5,14% | 18 | 17,65% | 18 | 17,82% | 18 | 17,82% |
Orrell (2019) | 14 | 3,78% | 14 | 13,73% | 14 | 13,86% | 14 | 13,86% |
Brugneaux & Pibot (2012) | 12 | 3,24% | 10 | 9,8% | 9 | 8,91% | 10 | 9,9% |
Ducarme (2023) | 10 | 2,7% | 10 | 9,8% | 10 | 9,9% | 10 | 9,9% |
Paulay & Brown (2019) | 10 | 2,7% | 9 | 8,82% | 9 | 8,91% | 9 | 8,91% |
Ameziane et al. (2020) | 9 | 2,43% | 9 | 8,82% | 9 | 8,91% | 9 | 8,91% |
Clark (1915) | 9 | 2,43% | 7 | 6,86% | 7 | 6,93% | 7 | 6,93% |
IUCN (2013) | 9 | 2,43% | 9 | 8,82% | 9 | 8,91% | 9 | 8,91% |
Diaz & Cuzange (2009) | 8 | 2,16% | 7 | 6,86% | 7 | 6,93% | 7 | 6,93% |
Walenkamp (1979) | 5 | 1,35% | 5 | 4,9% | 5 | 4,95% | 5 | 4,95% |
Grolière et al. (1980) | 4 | 1,08% | 3 | 2,94% | 3 | 2,97% | 3 | 2,97% |
Miloslavich, P., Díaz, J. M., Klein, E., Alvarado, J. J., Díaz, C., Gobin, J., ... & Ortiz, M. (2010). Marine biodiversity in the Caribbean: regional estimates and distribution patterns. PloS one, 5(8), e11916">Miloslavich et al. (2010) | 4 | 1,08% | 4 | 3,92% | 4 | 3,96% | 4 | 3,96% |
Hernández-herrejón et al. (2008) | 3 | 0,81% | 3 | 2,94% | 3 | 2,97% | 3 | 2,97% |
Linnaeus (1758) | 3 | 0,81% | 0 | 0% | 0 | 0% | 0 | 0% |
Pawson et al. (2009) | 3 | 0,81% | 1 | 0,98% | 1 | 0,99% | 1 | 0,99% |
Améziane (2007) | 2 | 0,54% | 1 | 0,98% | 1 | 0,99% | 1 | 0,99% |
Carpenter (1884) | 2 | 0,54% | 0 | 0% | 0 | 0% | 0 | 0% |
Clark & Rowe (1971) | 2 | 0,54% | 2 | 1,96% | 2 | 1,98% | 2 | 1,98% |
Conand et al. (2013) | 2 | 0,54% | 1 | 0,98% | 1 | 0,99% | 1 | 0,99% |
Conand et al. (2018) | 2 | 0,54% | 2 | 1,96% | 2 | 1,98% | 2 | 1,98% |
Guille et al. (1986) | 2 | 0,54% | 1 | 0,98% | 1 | 0,99% | 1 | 0,99% |
Mironov et al. (2014) | 2 | 0,54% | 2 | 1,96% | 2 | 1,98% | 2 | 1,98% |
Natural History Museum of London (2020) | 2 | 0,54% | 2 | 1,96% | 2 | 1,98% | 2 | 1,98% |
Verrill (1867) | 2 | 0,54% | 0 | 0% | 0 | 0% | 0 | 0% |
Bollard et al. (2013) | 1 | 0,27% | 1 | 0,98% | 1 | 0,99% | 1 | 0,99% |
Borrero-Pérez et al. (2008) | 1 | 0,27% | 1 | 0,98% | 1 | 0,99% | 1 | 0,99% |
Clark et al. (493-507) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Conand & ARVAM (2005) | 1 | 0,27% | 1 | 0,98% | 1 | 0,99% | 1 | 0,99% |
Conand et al. (2010) | 1 | 0,27% | 1 | 0,98% | 1 | 0,99% | 1 | 0,99% |
Conand et al. (2014) | 1 | 0,27% | 1 | 0,98% | 1 | 0,99% | 1 | 0,99% |
Downey (1973) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Ferry et al. (2020) | 1 | 0,27% | 1 | 0,98% | 1 | 0,99% | 1 | 0,99% |
Géry Parent | 1 | 0,27% | 1 | 0,98% | 1 | 0,99% | 1 | 0,99% |
Guille & Vadon (1985) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Hendler & Brugneaux (2013) | 1 | 0,27% | 1 | 0,98% | 1 | 0,99% | 1 | 0,99% |
Ifremer (2022) | 1 | 0,27% | 1 | 0,98% | 1 | 0,99% | 1 | 0,99% |
Impact-Mer et al. (2011) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Koehler (1921) | 1 | 0,27% | 1 | 0,98% | 1 | 0,99% | 1 | 0,99% |
Laguarda-Figueras et al. (2013) | 1 | 0,27% | 1 | 0,98% | 1 | 0,99% | 1 | 0,99% |
Lyman (1869) | 1 | 0,27% | 1 | 0,98% | 1 | 0,99% | 1 | 0,99% |
Lyman (1875) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Maréchal & Trégarot (2012) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Marenzeller & Von (1892) | 1 | 0,27% | 1 | 0,98% | 1 | 0,99% | 1 | 0,99% |
Marsh (1974) | 1 | 0,27% | 1 | 0,98% | 1 | 0,99% | 1 | 0,99% |
Nelson-Smith et al. (2014) | 1 | 0,27% | 1 | 0,98% | 1 | 0,99% | 1 | 0,99% |
Uicn et al. (2019) | 1 | 0,27% | 1 | 0,98% | 1 | 0,99% | 1 | 0,99% |
Vergonzanne (1977) | 1 | 0,27% | 1 | 0,98% | 1 | 0,99% | 1 | 0,99% |
Verrill (1915) | 1 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |