Annélides marins de la Réunion
96 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 | 11,68% | 26 | 30,95% | 26 | 31,33% | 26 | 31,33% |
Pleijel (2007) | 30 | 8,98% | 16 | 19,05% | 16 | 19,28% | 16 | 19,28% |
Dauvin et al. (2003) | 22 | 6,59% | 19 | 22,62% | 19 | 22,89% | 19 | 22,89% |
Bigot (2006) | 20 | 5,99% | 14 | 16,67% | 13 | 15,66% | 14 | 16,87% |
Naim (1985) | 18 | 5,39% | 9 | 10,71% | 9 | 10,84% | 9 | 10,84% |
Cambert et al. (2011) | 17 | 5,09% | 15 | 17,86% | 15 | 18,07% | 14 | 16,87% |
Claparède (1864) | 16 | 4,79% | 1 | 1,19% | 1 | 1,2% | 1 | 1,2% |
Bourcier (1988) | 15 | 4,49% | 11 | 13,1% | 11 | 13,25% | 11 | 13,25% |
Ifremer (2009) | 15 | 4,49% | 14 | 16,67% | 14 | 16,87% | 14 | 16,87% |
Bigot et al. (2006) | 11 | 3,29% | 8 | 9,52% | 8 | 9,64% | 7 | 8,43% |
Godet et al. (2010) | 10 | 2,99% | 9 | 10,71% | 9 | 10,84% | 9 | 10,84% |
Nelson-Smith et al. (2014) | 9 | 2,69% | 6 | 7,14% | 6 | 7,23% | 6 | 7,23% |
Solís-Weiss & Alcántara (2009) | 8 | 2,4% | 7 | 8,33% | 7 | 8,43% | 7 | 8,43% |
Dean (2012) | 7 | 2,1% | 7 | 8,33% | 7 | 8,43% | 7 | 8,43% |
Carrera-Parra (2006) | 6 | 1,8% | 4 | 4,76% | 4 | 4,82% | 4 | 4,82% |
Gout (1991) | 6 | 1,8% | 2 | 2,38% | 2 | 2,41% | 2 | 2,41% |
Guille & Laubier (1966) | 6 | 1,8% | 4 | 4,76% | 4 | 4,82% | 4 | 4,82% |
Arnaud (1974) | 5 | 1,5% | 4 | 4,76% | 4 | 4,82% | 4 | 4,82% |
Glasby et al. (2011) | 5 | 1,5% | 3 | 3,57% | 3 | 3,61% | 3 | 3,61% |
Peyrot-Clausade (1976) | 5 | 1,5% | 3 | 3,57% | 3 | 3,61% | 3 | 3,61% |
Claparède (1863) | 4 | 1,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Fauvel (1950) | 4 | 1,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Rignault & Chevallier (2017) | 4 | 1,2% | 3 | 3,57% | 3 | 3,61% | 3 | 3,61% |
Tricart & Foubert (2000) | 4 | 1,2% | 2 | 2,38% | 2 | 2,41% | 2 | 2,41% |
Blake & Kudenov (1978) | 3 | 0,9% | 0 | 0% | 0 | 0% | 0 | 0% |
Fauvel (1952) | 3 | 0,9% | 1 | 1,19% | 1 | 1,2% | 1 | 1,2% |
Hartmann-Schroder & Zibrowius (1998) | 3 | 0,9% | 3 | 3,57% | 3 | 3,61% | 3 | 3,61% |
Hoagland (1920) | 3 | 0,9% | 0 | 0% | 0 | 0% | 0 | 0% |
Salazar-Vallejo (2018) | 3 | 0,9% | 3 | 3,57% | 3 | 3,61% | 3 | 3,61% |
Ten Hove & Smith (1990) | 3 | 0,9% | 3 | 3,57% | 3 | 3,61% | 3 | 3,61% |
Watson & Russell (1989) | 3 | 0,9% | 3 | 3,57% | 3 | 3,61% | 3 | 3,61% |
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 | 2,38% | 2 | 2,41% | 2 | 2,41% |
Cazaux (1972) | 2 | 0,6% | 2 | 2,38% | 2 | 2,41% | 2 | 2,41% |
Clavier (1984) | 2 | 0,6% | 2 | 2,38% | 2 | 2,41% | 2 | 2,41% |
Conde-Vela (2021) | 2 | 0,6% | 2 | 2,38% | 2 | 2,41% | 2 | 2,41% |
Davoult (1990) | 2 | 0,6% | 2 | 2,38% | 2 | 2,41% | 2 | 2,41% |
Day (1957) | 2 | 0,6% | 2 | 2,38% | 2 | 2,41% | 2 | 2,41% |
Day (1961) | 2 | 0,6% | 1 | 1,19% | 1 | 1,2% | 1 | 1,2% |
Fourt et al. (2017) | 2 | 0,6% | 2 | 2,38% | 2 | 2,41% | 2 | 2,41% |
Grube (1846) | 2 | 0,6% | 0 | 0% | 0 | 0% | 0 | 0% |
Grube (1863) | 2 | 0,6% | 2 | 2,38% | 2 | 2,41% | 2 | 2,41% |
Ifremer (2023) | 2 | 0,6% | 2 | 2,38% | 2 | 2,41% | 2 | 2,41% |
Izuka (1912) | 2 | 0,6% | 0 | 0% | 0 | 0% | 0 | 0% |
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 | 2,38% | 2 | 2,41% | 2 | 2,41% |
Saint-Joseph (1888) | 2 | 0,6% | 0 | 0% | 0 | 0% | 0 | 0% |
Salazar-Vallejo (2020) | 2 | 0,6% | 2 | 2,38% | 2 | 2,41% | 2 | 2,41% |
Sarda et al. (2009) | 2 | 0,6% | 2 | 2,38% | 2 | 2,41% | 2 | 2,41% |
Southern (1921) | 2 | 0,6% | 2 | 2,38% | 2 | 2,41% | 2 | 2,41% |
Stock (1986) | 2 | 0,6% | 0 | 0% | 0 | 0% | 0 | 0% |
Aguirrezabalaga & Ceberio (2005) | 1 | 0,3% | 1 | 1,19% | 1 | 1,2% | 1 | 1,2% |
Cahiers de Biologie Marine, 18: 391-411.">Amoureux (1977) | 1 | 0,3% | 1 | 1,19% | 1 | 1,2% | 1 | 1,2% |
Audouin et al. (1833) | 1 | 0,3% | 1 | 1,19% | 1 | 1,2% | 1 | 1,2% |
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 | 1,19% | 1 | 1,2% | 1 | 1,2% |
Bhaud & Duchene (1976) | 1 | 0,3% | 1 | 1,19% | 1 | 1,2% | 1 | 1,2% |
Bhaud (1969) | 1 | 0,3% | 1 | 1,19% | 1 | 1,2% | 1 | 1,2% |
Boisseau & Lubet (1955) | 1 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
Carrera-Parra (2006) | 1 | 0,3% | 1 | 1,19% | 1 | 1,2% | 1 | 1,2% |
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 | 1,19% | 1 | 1,2% | 1 | 1,2% |
Day (1960) | 1 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
Day (1963) | 1 | 0,3% | 1 | 1,19% | 1 | 1,2% | 1 | 1,2% |
Fauvel (1910) | 1 | 0,3% | 1 | 1,19% | 1 | 1,2% | 1 | 1,2% |
Fauvel (1926) | 1 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
Fauvel (1926) | 1 | 0,3% | 1 | 1,19% | 1 | 1,2% | 1 | 1,2% |
Fauvel (1928) | 1 | 0,3% | 1 | 1,19% | 1 | 1,2% | 1 | 1,2% |
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 | 1,19% | 1 | 1,2% | 1 | 1,2% |
GT DCE Réunion | 1 | 0,3% | 1 | 1,19% | 1 | 1,2% | 1 | 1,2% |
Hartman (1949) | 1 | 0,3% | 1 | 1,19% | 1 | 1,2% | 1 | 1,2% |
Hartman (1965) | 1 | 0,3% | 1 | 1,19% | 1 | 1,2% | 1 | 1,2% |
Hartmann-Schroder (1960) | 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 | 1,19% | 1 | 1,2% | 1 | 1,2% |
Lamarck (1818) | 1 | 0,3% | 1 | 1,19% | 1 | 1,2% | 1 | 1,2% |
Linnaeus (1758) | 1 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
Linnaeus (1767) | 1 | 0,3% | 1 | 1,19% | 1 | 1,2% | 1 | 1,2% |
Mesnil (1896) | 1 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
Müller (2004) | 1 | 0,3% | 1 | 1,19% | 1 | 1,2% | 1 | 1,2% |
Perkins (1980) | 1 | 0,3% | 1 | 1,19% | 1 | 1,2% | 1 | 1,2% |
Piotrowski et al. (2024) | 1 | 0,3% | 1 | 1,19% | 1 | 1,2% | 1 | 1,2% |
Potts (1914) | 1 | 0,3% | 1 | 1,19% | 1 | 1,2% | 1 | 1,2% |
Quatrefages (1866) | 1 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
Richer de Forges et al. (2005) | 1 | 0,3% | 1 | 1,19% | 1 | 1,2% | 1 | 1,2% |
Solís-Weiss et al. (2004) | 1 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
Szederjesi et al. (2019) | 1 | 0,3% | 1 | 1,19% | 1 | 1,2% | 1 | 1,2% |