Echinodermes de la Réunion
110 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) | 196 | 20,52% | 194 | 91,51% | 194 | 93,27% | 188 | 90,38% |
Améziane (2007) | 87 | 9,11% | 71 | 33,49% | 71 | 34,13% | 69 | 33,17% |
Guille et al. (1986) | 69 | 7,23% | 58 | 27,36% | 58 | 27,88% | 56 | 26,92% |
Conand et al. (2018) | 51 | 5,34% | 46 | 21,7% | 46 | 22,12% | 45 | 21,63% |
Bourmaud (2003) | 41 | 4,29% | 30 | 14,15% | 30 | 14,42% | 28 | 13,46% |
Conand et al. (2010) | 31 | 3,25% | 31 | 14,62% | 31 | 14,9% | 31 | 14,9% |
Clark & Rowe (1971) | 29 | 3,04% | 22 | 10,38% | 22 | 10,58% | 22 | 10,58% |
Conand et al. (2016) | 26 | 2,72% | 20 | 9,43% | 20 | 9,62% | 18 | 8,65% |
Conand & ARVAM (2005) | 25 | 2,62% | 19 | 8,96% | 19 | 9,13% | 19 | 9,13% |
Jangoux & Aziz (1988) | 23 | 2,41% | 21 | 9,91% | 20 | 9,62% | 21 | 10,1% |
Conand et al. (2013) | 18 | 1,88% | 15 | 7,08% | 15 | 7,21% | 15 | 7,21% |
Eriksson et al. (2010) | 16 | 1,68% | 16 | 7,55% | 16 | 7,69% | 16 | 7,69% |
Bollard et al. (2013) | 15 | 1,57% | 12 | 5,66% | 10 | 4,81% | 12 | 5,77% |
Guille & Vadon (1985) | 15 | 1,57% | 12 | 5,66% | 12 | 5,77% | 11 | 5,29% |
Boissin et al. (2016) | 14 | 1,47% | 10 | 4,72% | 10 | 4,81% | 10 | 4,81% |
Kronen et al. (2008) | 14 | 1,47% | 13 | 6,13% | 13 | 6,25% | 13 | 6,25% |
Solís-Marín & Laguarda Figueras (2009) | 14 | 1,47% | 13 | 6,13% | 13 | 6,25% | 13 | 6,25% |
Mulochau & Conand (2008) | 13 | 1,36% | 12 | 5,66% | 12 | 5,77% | 12 | 5,77% |
Stöhr et al. (2008) | 13 | 1,36% | 12 | 5,66% | 12 | 5,77% | 12 | 5,77% |
Bulletin du Muséum national d'histoire naturelle, 4ème série, section A, 6(3): 583-615. ">Vadon & Guille (1984) |
12 | 1,26% | 9 | 4,25% | 9 | 4,33% | 9 | 4,33% |
Devaney (1974) | 11 | 1,15% | 6 | 2,83% | 6 | 2,88% | 6 | 2,88% |
Conand et al. (2014) | 10 | 1,05% | 10 | 4,72% | 10 | 4,81% | 10 | 4,81% |
Ameziane et al. (2020) | 8 | 0,84% | 7 | 3,3% | 7 | 3,37% | 7 | 3,37% |
Ifremer (2009) | 8 | 0,84% | 4 | 1,89% | 4 | 1,92% | 4 | 1,92% |
Uthicke et al. (2004) | 8 | 0,84% | 8 | 3,77% | 8 | 3,85% | 8 | 3,85% |
Linnaeus (1758) | 7 | 0,73% | 0 | 0% | 0 | 0% | 0 | 0% |
Marsh (1974) | 5 | 0,52% | 5 | 2,36% | 5 | 2,4% | 4 | 1,92% |
O'loughlin & Rowe (2006) | 5 | 0,52% | 5 | 2,36% | 5 | 2,4% | 5 | 2,4% |
Smirnov et al. (2014) | 5 | 0,52% | 2 | 0,94% | 2 | 0,96% | 2 | 0,96% |
Stöhr (2011) | 5 | 0,52% | 2 | 0,94% | 2 | 0,96% | 2 | 0,96% |
Deichmann (1963) | 4 | 0,42% | 3 | 1,42% | 3 | 1,44% | 3 | 1,44% |
O’Hara & Thuy (2022) | 4 | 0,42% | 4 | 1,89% | 4 | 1,92% | 4 | 1,92% |
Chabanet et al. (2007) | 3 | 0,31% | 3 | 1,42% | 3 | 1,44% | 3 | 1,44% |
Conand et al. (2005) | 3 | 0,31% | 2 | 0,94% | 2 | 0,96% | 2 | 0,96% |
Hardouin Michelin (1844) | 3 | 0,31% | 0 | 0% | 0 | 0% | 0 | 0% |
O'hara et al. (2019) | 3 | 0,31% | 3 | 1,42% | 3 | 1,44% | 3 | 1,44% |
Wantiez (2001) | 3 | 0,31% | 3 | 1,42% | 3 | 1,44% | 3 | 1,44% |
Bigot et al. (2006) | 2 | 0,21% | 2 | 0,94% | 2 | 0,96% | 2 | 0,96% |
Bigot et al. (2006) | 2 | 0,21% | 2 | 0,94% | 2 | 0,96% | 2 | 0,96% |
Brugneaux & Pérès (2006) | 2 | 0,21% | 2 | 0,94% | 2 | 0,96% | 2 | 0,96% |
Brugneaux & Pibot (2012) | 2 | 0,21% | 2 | 0,94% | 2 | 0,96% | 2 | 0,96% |
Cherbonnier (1980) | 2 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Clark (1967) | 2 | 0,21% | 2 | 0,94% | 2 | 0,96% | 2 | 0,96% |
Conand & Ducarme (2018) | 2 | 0,21% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Hertlein & Emerson (1957) | 2 | 0,21% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Koehler (1921) | 2 | 0,21% | 2 | 0,94% | 2 | 0,96% | 2 | 0,96% |
Mah (2003) | 2 | 0,21% | 2 | 0,94% | 2 | 0,96% | 2 | 0,96% |
Mah (2018) | 2 | 0,21% | 2 | 0,94% | 2 | 0,96% | 2 | 0,96% |
Martin (2011) | 2 | 0,21% | 2 | 0,94% | 2 | 0,96% | 2 | 0,96% |
Nelson-Smith et al. (2014) | 2 | 0,21% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
O'Hara & Stöhr (2006) | 2 | 0,21% | 2 | 0,94% | 2 | 0,96% | 2 | 0,96% |
Roux (1985) | 2 | 0,21% | 2 | 0,94% | 2 | 0,96% | 2 | 0,96% |
Rowe & Massin (2006) | 2 | 0,21% | 2 | 0,94% | 2 | 0,96% | 2 | 0,96% |
Samyn (2013) | 2 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Sladen (1889) | 2 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Stohr et al. (2013) | 2 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Vergonzanne (1977) | 2 | 0,21% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Bartsch (2008) | 1 | 0,1% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Bigot (2006) | 1 | 0,1% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Bocquet (1953) | 1 | 0,1% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Bourcier (1988) | 1 | 0,1% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Breton (2014) | 1 | 0,1% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Canu (1891) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Clark & Courtman-stock (1976) | 1 | 0,1% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Clark (1915) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Conand & Mangion (2002) | 1 | 0,1% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Conand et al. (2016) | 1 | 0,1% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Crosnier (1959) | 1 | 0,1% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Delle & Chiaje (1823-1831) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Ducarme (2017) | 1 | 0,1% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
European Nucleotide Archive (2019) | 1 | 0,1% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Fasmer (1930) | 1 | 0,1% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Godet et al. (2010) | 1 | 0,1% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Haszprunar et al. (2017) | 1 | 0,1% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Hendler & Brugneaux (2013) | 1 | 0,1% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Ifremer (2023) | 1 | 0,1% | 1 | 0,47% | 0 | 0% | 1 | 0,48% |
Zoologischer Anzeiger, xx: 66-170.">Koehler (1897) | 1 | 0,1% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Koehler (1922) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Lessios et al. (1996) | 1 | 0,1% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Lyman (1878) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Lyman (1883) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Mah (2015) | 1 | 0,1% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Mah (2015) | 1 | 0,1% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Mah (2017) | 1 | 0,1% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Mah (2023) | 1 | 0,1% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Mah (2023) | 1 | 0,1% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Michelin (1862) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Natural History Museum of London (2020) | 1 | 0,1% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
O'Hara (2015) | 1 | 0,1% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
O'hara (2015) | 1 | 0,1% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
O'hara (2015) | 1 | 0,1% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
O'hara (2015) | 1 | 0,1% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
O'hara (2015) | 1 | 0,1% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
O'hara (2015) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
O'hara (2015) | 1 | 0,1% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
O'hara (2015) | 1 | 0,1% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
O'hara (2015) | 1 | 0,1% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Okanishi & Fujita (2013) | 1 | 0,1% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Okanishi & Fujita (2014) | 1 | 0,1% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Okanishi et al. (2013) | 1 | 0,1% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
O'Loughlin & MacKenzie (2013) | 1 | 0,1% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Orrell (2019) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Questel & Le Quellec (2012) | 1 | 0,1% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Questel (2020) | 1 | 0,1% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Rignault & Chevallier (2017) | 1 | 0,1% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
The International Barcode of Life Consortium (2016) | 1 | 0,1% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Thomson (1873) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Vadon & Guille (2015) | 1 | 0,1% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Walenkamp (1979) | 1 | 0,1% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |
Weinberg & Ridder (1998) | 1 | 0,1% | 1 | 0,47% | 1 | 0,48% | 1 | 0,48% |