Echinodermes de Mayotte
105 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) | 275 | 29,96% | 273 | 142,19% | 271 | 144,15% | 266 | 141,49% |
| Améziane (2007) | 96 | 10,46% | 81 | 42,19% | 81 | 43,09% | 78 | 41,49% |
| Guille et al. (1986) | 74 | 8,06% | 63 | 32,81% | 63 | 33,51% | 61 | 32,45% |
| Conand & ARVAM (2005) | 43 | 4,68% | 35 | 18,23% | 35 | 18,62% | 34 | 18,09% |
| Clark & Rowe (1971) | 32 | 3,49% | 24 | 12,5% | 24 | 12,77% | 24 | 12,77% |
| Conand et al. (2016) | 31 | 3,38% | 25 | 13,02% | 25 | 13,3% | 22 | 11,7% |
| Bourmaud (2003) | 30 | 3,27% | 23 | 11,98% | 23 | 12,23% | 21 | 11,17% |
| Conand et al. (2010) | 27 | 2,94% | 27 | 14,06% | 27 | 14,36% | 27 | 14,36% |
| Conand et al. (2018) | 21 | 2,29% | 20 | 10,42% | 20 | 10,64% | 20 | 10,64% |
| Eriksson et al. (2010) | 21 | 2,29% | 21 | 10,94% | 21 | 11,17% | 20 | 10,64% |
| Conand et al. (2013) | 19 | 2,07% | 15 | 7,81% | 15 | 7,98% | 15 | 7,98% |
| Guille & Vadon (1985) | 19 | 2,07% | 14 | 7,29% | 14 | 7,45% | 12 | 6,38% |
| Kronen et al. (2008) | 16 | 1,74% | 15 | 7,81% | 15 | 7,98% | 15 | 7,98% |
| Mulochau & Conand (2008) | 15 | 1,63% | 14 | 7,29% | 14 | 7,45% | 14 | 7,45% |
| Mah (2018) | 12 | 1,31% | 12 | 6,25% | 12 | 6,38% | 12 | 6,38% |
| Devaney (1974) | 11 | 1,2% | 6 | 3,12% | 6 | 3,19% | 6 | 3,19% |
| Linnaeus (1758) | 11 | 1,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Solís-Marín & Laguarda Figueras (2009) | 10 | 1,09% | 10 | 5,21% | 10 | 5,32% | 10 | 5,32% |
| Boissin et al. (2016) | 8 | 0,87% | 5 | 2,6% | 5 | 2,66% | 5 | 2,66% |
| Bollard et al. (2013) | 8 | 0,87% | 6 | 3,12% | 5 | 2,66% | 6 | 3,19% |
| Conand et al. (2014) | 8 | 0,87% | 8 | 4,17% | 8 | 4,26% | 8 | 4,26% |
| Marsh (1974) | 8 | 0,87% | 8 | 4,17% | 8 | 4,26% | 8 | 4,26% |
| Stöhr et al. (2008) | 8 | 0,87% | 7 | 3,65% | 7 | 3,72% | 7 | 3,72% |
| Uthicke et al. (2004) | 8 | 0,87% | 8 | 4,17% | 8 | 4,26% | 8 | 4,26% |
| Ameziane et al. (2020) | 7 | 0,76% | 7 | 3,65% | 7 | 3,72% | 7 | 3,72% |
| Chabanet et al. (2007) | 7 | 0,76% | 6 | 3,12% | 6 | 3,19% | 6 | 3,19% |
| Conand et al. (2005) | 6 | 0,65% | 5 | 2,6% | 4 | 2,13% | 5 | 2,66% |
| Ifremer (2009) | 6 | 0,65% | 5 | 2,6% | 5 | 2,66% | 5 | 2,66% |
| Korzhavina & Ivanenko (2019) | 5 | 0,54% | 5 | 2,6% | 5 | 2,66% | 5 | 2,66% |
| Wantiez (2001) | 5 | 0,54% | 5 | 2,6% | 5 | 2,66% | 4 | 2,13% |
| Baker et al. (2018) | 4 | 0,44% | 4 | 2,08% | 4 | 2,13% | 4 | 2,13% |
| Cherbonnier (1980) | 3 | 0,33% | 1 | 0,52% | 1 | 0,53% | 1 | 0,53% |
| Hardouin Michelin (1844) | 3 | 0,33% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mah (2017) | 3 | 0,33% | 3 | 1,56% | 3 | 1,6% | 3 | 1,6% |
| O'hara et al. (2019) | 3 | 0,33% | 3 | 1,56% | 3 | 1,6% | 3 | 1,6% |
| Stöhr (2011) | 3 | 0,33% | 1 | 0,52% | 1 | 0,53% | 1 | 0,53% |
| Bigot et al. (2006) | 2 | 0,22% | 2 | 1,04% | 2 | 1,06% | 2 | 1,06% |
| Bigot et al. (2006) | 2 | 0,22% | 2 | 1,04% | 2 | 1,06% | 2 | 1,06% |
| Brugneaux & Pérès (2006) | 2 | 0,22% | 2 | 1,04% | 2 | 1,06% | 2 | 1,06% |
| Brugneaux & Pibot (2012) | 2 | 0,22% | 2 | 1,04% | 2 | 1,06% | 2 | 1,06% |
| Calabuig (2016) | 2 | 0,22% | 2 | 1,04% | 2 | 1,06% | 2 | 1,06% |
| Clark (1967) | 2 | 0,22% | 2 | 1,04% | 2 | 1,06% | 2 | 1,06% |
| Deichmann (1963) | 2 | 0,22% | 2 | 1,04% | 2 | 1,06% | 2 | 1,06% |
| Hendler & Brugneaux (2013) | 2 | 0,22% | 2 | 1,04% | 2 | 1,06% | 2 | 1,06% |
| Koehler (1921) | 2 | 0,22% | 2 | 1,04% | 2 | 1,06% | 2 | 1,06% |
| Mah (2003) | 2 | 0,22% | 2 | 1,04% | 2 | 1,06% | 2 | 1,06% |
| Martin (2011) | 2 | 0,22% | 2 | 1,04% | 2 | 1,06% | 2 | 1,06% |
| Nelson-Smith et al. (2014) | 2 | 0,22% | 1 | 0,52% | 1 | 0,53% | 1 | 0,53% |
| Rowe & Massin (2006) | 2 | 0,22% | 2 | 1,04% | 2 | 1,06% | 2 | 1,06% |
| Samyn (2013) | 2 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
| Stohr et al. (2013) | 2 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
| Vergonzanne (1977) | 2 | 0,22% | 1 | 0,52% | 1 | 0,53% | 1 | 0,53% |
| Verrill (1867) | 2 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bartsch (2008) | 1 | 0,11% | 1 | 0,52% | 1 | 0,53% | 1 | 0,53% |
| Bocquet (1953) | 1 | 0,11% | 1 | 0,52% | 1 | 0,53% | 1 | 0,53% |
| Bourcier (1988) | 1 | 0,11% | 1 | 0,52% | 1 | 0,53% | 1 | 0,53% |
| Breton (2014) | 1 | 0,11% | 1 | 0,52% | 1 | 0,53% | 1 | 0,53% |
| Bronstein (2017) | 1 | 0,11% | 1 | 0,52% | 1 | 0,53% | 1 | 0,53% |
| Canu (1891) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Chauvet & Lemouellic (2005) | 1 | 0,11% | 1 | 0,52% | 0 | 0% | 1 | 0,53% |
| Clark (1915) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Conand & Mangion (2002) | 1 | 0,11% | 1 | 0,52% | 1 | 0,53% | 1 | 0,53% |
| Crosnier (1959) | 1 | 0,11% | 1 | 0,52% | 1 | 0,53% | 1 | 0,53% |
| Delle & Chiaje (1823-1831) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ducarme (2017) | 1 | 0,11% | 1 | 0,52% | 1 | 0,53% | 1 | 0,53% |
| Ferry et al. (2020) | 1 | 0,11% | 1 | 0,52% | 1 | 0,53% | 1 | 0,53% |
| Godet et al. (2010) | 1 | 0,11% | 1 | 0,52% | 1 | 0,53% | 1 | 0,53% |
| Haszprunar et al. (2017) | 1 | 0,11% | 1 | 0,52% | 1 | 0,53% | 1 | 0,53% |
| Hertlein & Emerson (1957) | 1 | 0,11% | 1 | 0,52% | 1 | 0,53% | 1 | 0,53% |
| Ifremer (2022) | 1 | 0,11% | 1 | 0,52% | 1 | 0,53% | 1 | 0,53% |
| Kroh (2017) | 1 | 0,11% | 1 | 0,52% | 1 | 0,53% | 1 | 0,53% |
| Kroh (2017) | 1 | 0,11% | 1 | 0,52% | 1 | 0,53% | 1 | 0,53% |
| Kroh (2017) | 1 | 0,11% | 1 | 0,52% | 1 | 0,53% | 1 | 0,53% |
| Kronen et al. (2009) | 1 | 0,11% | 1 | 0,52% | 0 | 0% | 1 | 0,53% |
| Lessios et al. (1996) | 1 | 0,11% | 1 | 0,52% | 1 | 0,53% | 1 | 0,53% |
| Lyman (1861) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mah (2015) | 1 | 0,11% | 1 | 0,52% | 1 | 0,53% | 1 | 0,53% |
| Mah (2018) | 1 | 0,11% | 1 | 0,52% | 1 | 0,53% | 1 | 0,53% |
| Mah (2023) | 1 | 0,11% | 1 | 0,52% | 1 | 0,53% | 1 | 0,53% |
| Mulochau et al. (2019) | 1 | 0,11% | 1 | 0,52% | 1 | 0,53% | 1 | 0,53% |
| O’Hara & Thuy (2022) | 1 | 0,11% | 1 | 0,52% | 1 | 0,53% | 1 | 0,53% |
| O'Hara (2015) | 1 | 0,11% | 1 | 0,52% | 1 | 0,53% | 1 | 0,53% |
| O'hara (2015) | 1 | 0,11% | 1 | 0,52% | 1 | 0,53% | 1 | 0,53% |
| O'hara (2015) | 1 | 0,11% | 1 | 0,52% | 1 | 0,53% | 1 | 0,53% |
| O'hara (2015) | 1 | 0,11% | 1 | 0,52% | 1 | 0,53% | 1 | 0,53% |
| O'hara (2015) | 1 | 0,11% | 1 | 0,52% | 1 | 0,53% | 1 | 0,53% |
| O'hara (2015) | 1 | 0,11% | 1 | 0,52% | 1 | 0,53% | 1 | 0,53% |
| O'hara (2015) | 1 | 0,11% | 1 | 0,52% | 1 | 0,53% | 1 | 0,53% |
| O'hara (2015) | 1 | 0,11% | 1 | 0,52% | 1 | 0,53% | 1 | 0,53% |
| O'hara (2015) | 1 | 0,11% | 1 | 0,52% | 1 | 0,53% | 1 | 0,53% |
| O'hara (2015) | 1 | 0,11% | 1 | 0,52% | 1 | 0,53% | 1 | 0,53% |
| O'hara (2015) | 1 | 0,11% | 1 | 0,52% | 1 | 0,53% | 1 | 0,53% |
| O'Loughlin & MacKenzie (2013) | 1 | 0,11% | 1 | 0,52% | 1 | 0,53% | 1 | 0,53% |
| O'loughlin & Rowe (2006) | 1 | 0,11% | 1 | 0,52% | 1 | 0,53% | 1 | 0,53% |
| Questel & Le Quellec (2012) | 1 | 0,11% | 1 | 0,52% | 1 | 0,53% | 1 | 0,53% |
| Questel (2020) | 1 | 0,11% | 1 | 0,52% | 1 | 0,53% | 1 | 0,53% |
| Rignault & Chevallier (2017) | 1 | 0,11% | 1 | 0,52% | 1 | 0,53% | 1 | 0,53% |
| Saucède (2017) | 1 | 0,11% | 1 | 0,52% | 1 | 0,53% | 1 | 0,53% |
| Saucède (2017) | 1 | 0,11% | 1 | 0,52% | 1 | 0,53% | 1 | 0,53% |
| Saucède (2017) | 1 | 0,11% | 1 | 0,52% | 1 | 0,53% | 1 | 0,53% |
| Saucède (2017) | 1 | 0,11% | 1 | 0,52% | 1 | 0,53% | 1 | 0,53% |
| Saucède (2017) | 1 | 0,11% | 1 | 0,52% | 1 | 0,53% | 1 | 0,53% |
| Uicn et al. (2019) | 1 | 0,11% | 1 | 0,52% | 1 | 0,53% | 1 | 0,53% |
| Walenkamp (1979) | 1 | 0,11% | 1 | 0,52% | 1 | 0,53% | 1 | 0,53% |
| Wickel et al. (2016) | 1 | 0,11% | 1 | 0,52% | 1 | 0,53% | 1 | 0,53% |
