Annélides marins de la Réunion
98 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
| Référence | Total | Valides | Espèces | Taxons terminaux | ||||
|---|---|---|---|---|---|---|---|---|
| nb | % | nb | % | nb | % | nb | % | |
| Bourmaud (2003) | 39 | 11,71% | 26 | 30,59% | 26 | 30,95% | 26 | 30,95% |
| Pleijel (2007) | 30 | 9,01% | 16 | 18,82% | 16 | 19,05% | 16 | 19,05% |
| Dauvin et al. (2003) | 22 | 6,61% | 19 | 22,35% | 19 | 22,62% | 19 | 22,62% |
| Bigot (2006) | 20 | 6,01% | 14 | 16,47% | 13 | 15,48% | 14 | 16,67% |
| Naim (1985) | 18 | 5,41% | 9 | 10,59% | 9 | 10,71% | 9 | 10,71% |
| Cambert et al. (2011) | 17 | 5,11% | 15 | 17,65% | 15 | 17,86% | 14 | 16,67% |
| Claparède (1864) | 16 | 4,8% | 1 | 1,18% | 1 | 1,19% | 1 | 1,19% |
| Bourcier (1988) | 15 | 4,5% | 11 | 12,94% | 11 | 13,1% | 11 | 13,1% |
| Ifremer (2009) | 15 | 4,5% | 14 | 16,47% | 14 | 16,67% | 14 | 16,67% |
| Bigot et al. (2006) | 11 | 3,3% | 8 | 9,41% | 8 | 9,52% | 7 | 8,33% |
| Godet et al. (2010) | 10 | 3% | 9 | 10,59% | 9 | 10,71% | 9 | 10,71% |
| Nelson-Smith et al. (2014) | 9 | 2,7% | 6 | 7,06% | 6 | 7,14% | 6 | 7,14% |
| Solís-Weiss & Alcántara (2009) | 8 | 2,4% | 7 | 8,24% | 7 | 8,33% | 7 | 8,33% |
| Dean (2012) | 7 | 2,1% | 7 | 8,24% | 7 | 8,33% | 7 | 8,33% |
| Carrera-Parra (2006) | 6 | 1,8% | 4 | 4,71% | 4 | 4,76% | 4 | 4,76% |
| Gout (1991) | 6 | 1,8% | 2 | 2,35% | 2 | 2,38% | 2 | 2,38% |
| Guille & Laubier (1966) | 6 | 1,8% | 4 | 4,71% | 4 | 4,76% | 4 | 4,76% |
| Arnaud (1974) | 5 | 1,5% | 4 | 4,71% | 4 | 4,76% | 4 | 4,76% |
| Glasby et al. (2011) | 5 | 1,5% | 3 | 3,53% | 3 | 3,57% | 3 | 3,57% |
| Peyrot-Clausade (1976) | 5 | 1,5% | 3 | 3,53% | 3 | 3,57% | 3 | 3,57% |
| Salazar-Vallejo et al. (2024) | 5 | 1,5% | 5 | 5,88% | 5 | 5,95% | 5 | 5,95% |
| Claparède (1863) | 4 | 1,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fauvel (1950) | 4 | 1,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pearman et al. (2020) | 4 | 1,2% | 4 | 4,71% | 4 | 4,76% | 4 | 4,76% |
| Rignault & Chevallier (2017) | 4 | 1,2% | 3 | 3,53% | 3 | 3,57% | 3 | 3,57% |
| Tricart & Foubert (2000) | 4 | 1,2% | 2 | 2,35% | 2 | 2,38% | 2 | 2,38% |
| Blake & Kudenov (1978) | 3 | 0,9% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fauvel (1952) | 3 | 0,9% | 1 | 1,18% | 1 | 1,19% | 1 | 1,19% |
| Hartmann-Schroder & Zibrowius (1998) | 3 | 0,9% | 3 | 3,53% | 3 | 3,57% | 3 | 3,57% |
| Hoagland (1920) | 3 | 0,9% | 0 | 0% | 0 | 0% | 0 | 0% |
| Salazar-Vallejo (2018) | 3 | 0,9% | 3 | 3,53% | 3 | 3,57% | 3 | 3,57% |
| Ten Hove & Smith (1990) | 3 | 0,9% | 3 | 3,53% | 3 | 3,57% | 3 | 3,57% |
| Watson & Russell (1989) | 3 | 0,9% | 3 | 3,53% | 3 | 3,57% | 3 | 3,57% |
| Augener (1918) | 2 | 0,6% | 0 | 0% | 0 | 0% | 0 | 0% |
| Barnich & Fiege (2001) | 2 | 0,6% | 0 | 0% | 0 | 0% | 0 | 0% |
| Breton (2014) | 2 | 0,6% | 2 | 2,35% | 2 | 2,38% | 2 | 2,38% |
| Cazaux (1972) | 2 | 0,6% | 2 | 2,35% | 2 | 2,38% | 2 | 2,38% |
| Clavier (1984) | 2 | 0,6% | 2 | 2,35% | 2 | 2,38% | 2 | 2,38% |
| Conde-Vela (2021) | 2 | 0,6% | 2 | 2,35% | 2 | 2,38% | 2 | 2,38% |
| Davoult (1990) | 2 | 0,6% | 2 | 2,35% | 2 | 2,38% | 2 | 2,38% |
| Day (1957) | 2 | 0,6% | 2 | 2,35% | 2 | 2,38% | 2 | 2,38% |
| Day (1961) | 2 | 0,6% | 1 | 1,18% | 1 | 1,19% | 1 | 1,19% |
| Fourt et al. (2017) | 2 | 0,6% | 2 | 2,35% | 2 | 2,38% | 2 | 2,38% |
| Grube (1846) | 2 | 0,6% | 0 | 0% | 0 | 0% | 0 | 0% |
| Grube (1863) | 2 | 0,6% | 2 | 2,35% | 2 | 2,38% | 2 | 2,38% |
| Ifremer (2023) | 2 | 0,6% | 2 | 2,35% | 2 | 2,38% | 2 | 2,38% |
| Marion (1876) | 2 | 0,6% | 0 | 0% | 0 | 0% | 0 | 0% |
| Monro (1928) | 2 | 0,6% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pettibone (1986) | 2 | 0,6% | 2 | 2,35% | 2 | 2,38% | 2 | 2,38% |
| Saint-Joseph (1888) | 2 | 0,6% | 0 | 0% | 0 | 0% | 0 | 0% |
| Salazar-Vallejo (2020) | 2 | 0,6% | 2 | 2,35% | 2 | 2,38% | 2 | 2,38% |
| Sarda et al. (2009) | 2 | 0,6% | 2 | 2,35% | 2 | 2,38% | 2 | 2,38% |
| Southern (1921) | 2 | 0,6% | 2 | 2,35% | 2 | 2,38% | 2 | 2,38% |
| Stock (1986) | 2 | 0,6% | 0 | 0% | 0 | 0% | 0 | 0% |
| Aguirrezabalaga & Ceberio (2005) | 1 | 0,3% | 1 | 1,18% | 1 | 1,19% | 1 | 1,19% |
| Cahiers de Biologie Marine, 18: 391-411.">Amoureux (1977) | 1 | 0,3% | 1 | 1,18% | 1 | 1,19% | 1 | 1,19% |
| Audouin et al. (1833) | 1 | 0,3% | 1 | 1,18% | 1 | 1,19% | 1 | 1,19% |
| Augener (1906) | 1 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
| Augener (1913) | 1 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
| Banse & Hobson (1968) | 1 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
| Beauchamp (1914) | 1 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bellan (1972) | 1 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bergstrom (1916) | 1 | 0,3% | 1 | 1,18% | 1 | 1,19% | 1 | 1,19% |
| Bhaud & Duchene (1976) | 1 | 0,3% | 1 | 1,18% | 1 | 1,19% | 1 | 1,19% |
| Bhaud (1969) | 1 | 0,3% | 1 | 1,18% | 1 | 1,19% | 1 | 1,19% |
| Boisseau & Lubet (1955) | 1 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
| Carrera-Parra (2006) | 1 | 0,3% | 1 | 1,18% | 1 | 1,19% | 1 | 1,19% |
| Caullery & Mesnil (1918) | 1 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
| Chamberlin (1919) | 1 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dauvin (1978) | 1 | 0,3% | 1 | 1,18% | 1 | 1,19% | 1 | 1,19% |
| Day (1960) | 1 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
| Day (1963) | 1 | 0,3% | 1 | 1,18% | 1 | 1,19% | 1 | 1,19% |
| Fauvel (1910) | 1 | 0,3% | 1 | 1,18% | 1 | 1,19% | 1 | 1,19% |
| Fauvel (1926) | 1 | 0,3% | 1 | 1,18% | 1 | 1,19% | 1 | 1,19% |
| Fauvel (1926) | 1 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fauvel (1928) | 1 | 0,3% | 1 | 1,18% | 1 | 1,19% | 1 | 1,19% |
| Fauvel (1953) | 1 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
| Foster (1971) | 1 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gaudy & Thomassin (2006) | 1 | 0,3% | 1 | 1,18% | 1 | 1,19% | 1 | 1,19% |
| GT DCE Réunion | 1 | 0,3% | 1 | 1,18% | 1 | 1,19% | 1 | 1,19% |
| Hartman (1949) | 1 | 0,3% | 1 | 1,18% | 1 | 1,19% | 1 | 1,19% |
| Hartman (1965) | 1 | 0,3% | 1 | 1,18% | 1 | 1,19% | 1 | 1,19% |
| Hartmann-Schroder (1960) | 1 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
| Izuka (1912) | 1 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
| Johnson (1901) | 1 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kinberg (1865) | 1 | 0,3% | 1 | 1,18% | 1 | 1,19% | 1 | 1,19% |
| Lamarck (1818) | 1 | 0,3% | 1 | 1,18% | 1 | 1,19% | 1 | 1,19% |
| Linnaeus (1758) | 1 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
| Linnaeus (1767) | 1 | 0,3% | 1 | 1,18% | 1 | 1,19% | 1 | 1,19% |
| Mesnil (1896) | 1 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
| Müller (2004) | 1 | 0,3% | 1 | 1,18% | 1 | 1,19% | 1 | 1,19% |
| Perkins (1980) | 1 | 0,3% | 1 | 1,18% | 1 | 1,19% | 1 | 1,19% |
| Piotrowski et al. (2024) | 1 | 0,3% | 1 | 1,18% | 1 | 1,19% | 1 | 1,19% |
| Potts (1914) | 1 | 0,3% | 1 | 1,18% | 1 | 1,19% | 1 | 1,19% |
| Quatrefages (1866) | 1 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
| Richer de Forges et al. (2005) | 1 | 0,3% | 1 | 1,18% | 1 | 1,19% | 1 | 1,19% |
| Solís-Weiss et al. (2004) | 1 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
| Szederjesi et al. (2019) | 1 | 0,3% | 1 | 1,18% | 1 | 1,19% | 1 | 1,19% |
