Annélides marins de Polynésie française
112 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
Référence | Total | Valides | Espèces | Taxons terminaux | ||||
---|---|---|---|---|---|---|---|---|
nb | % | nb | % | nb | % | nb | % | |
Pleijel (2007) | 48 | 9,18% | 31 | 18,34% | 31 | 18,56% | 31 | 18,56% |
Naim (1985) | 36 | 6,88% | 22 | 13,02% | 22 | 13,17% | 22 | 13,17% |
Chamberlin (1919) | 31 | 5,93% | 23 | 13,61% | 23 | 13,77% | 23 | 13,77% |
Dauvin et al. (2003) | 26 | 4,97% | 19 | 11,24% | 19 | 11,38% | 18 | 10,78% |
Bourmaud (2003) | 23 | 4,4% | 13 | 7,69% | 13 | 7,78% | 13 | 7,78% |
Salazar-Vallejo (2020) | 18 | 3,44% | 18 | 10,65% | 18 | 10,78% | 18 | 10,78% |
Dean (2012) | 17 | 3,25% | 17 | 10,06% | 17 | 10,18% | 17 | 10,18% |
Claparède (1864) | 16 | 3,06% | 2 | 1,18% | 2 | 1,2% | 2 | 1,2% |
Bourcier (1988) | 14 | 2,68% | 10 | 5,92% | 10 | 5,99% | 10 | 5,99% |
Peyrot-Clausade (1976) | 14 | 2,68% | 12 | 7,1% | 12 | 7,19% | 12 | 7,19% |
Paulay & Brown (2019) | 13 | 2,49% | 12 | 7,1% | 12 | 7,19% | 12 | 7,19% |
Chamberlin (1919) | 12 | 2,29% | 1 | 0,59% | 1 | 0,6% | 1 | 0,6% |
Salazar-Vallejo (2018) | 12 | 2,29% | 10 | 5,92% | 10 | 5,99% | 10 | 5,99% |
Pearman et al. (2020) | 11 | 2,1% | 10 | 5,92% | 9 | 5,39% | 10 | 5,99% |
Ifremer (2009) | 9 | 1,72% | 7 | 4,14% | 7 | 4,19% | 7 | 4,19% |
Solís-Weiss & Alcántara (2009) | 9 | 1,72% | 8 | 4,73% | 8 | 4,79% | 8 | 4,79% |
Gout (1991) | 8 | 1,53% | 5 | 2,96% | 5 | 2,99% | 5 | 2,99% |
Rullier (1972) | 8 | 1,53% | 3 | 1,78% | 3 | 1,8% | 3 | 1,8% |
Godet et al. (2010) | 7 | 1,34% | 5 | 2,96% | 5 | 2,99% | 5 | 2,99% |
Salazar-Vallejo (2023) | 7 | 1,34% | 7 | 4,14% | 7 | 4,19% | 7 | 4,19% |
Orrell (2019) | 6 | 1,15% | 4 | 2,37% | 4 | 2,4% | 4 | 2,4% |
Fauvel (1919) | 5 | 0,96% | 0 | 0% | 0 | 0% | 0 | 0% |
Glasby et al. (2011) | 5 | 0,96% | 3 | 1,78% | 3 | 1,8% | 3 | 1,8% |
Guille & Laubier (1966) | 5 | 0,96% | 3 | 1,78% | 3 | 1,8% | 3 | 1,8% |
Nelson-Smith et al. (2014) | 5 | 0,96% | 3 | 1,78% | 3 | 1,8% | 3 | 1,8% |
Rignault & Chevallier (2017) | 5 | 0,96% | 4 | 2,37% | 4 | 2,4% | 4 | 2,4% |
Tricart & Foubert (2000) | 5 | 0,96% | 2 | 1,18% | 2 | 1,2% | 2 | 1,2% |
Hartmann-Schroder (1960) | 4 | 0,76% | 0 | 0% | 0 | 0% | 0 | 0% |
Hutchings et al. (1998) | 4 | 0,76% | 4 | 2,37% | 4 | 2,4% | 4 | 2,4% |
Kinberg (1865) | 4 | 0,76% | 4 | 2,37% | 4 | 2,4% | 4 | 2,4% |
Kinberg ([1867]) | 4 | 0,76% | 2 | 1,18% | 2 | 1,2% | 2 | 1,2% |
Treadwell (1943) | 4 | 0,76% | 0 | 0% | 0 | 0% | 0 | 0% |
Arnaud (1974) | 3 | 0,57% | 1 | 0,59% | 1 | 0,6% | 1 | 0,6% |
Cambert et al. (2011) | 3 | 0,57% | 2 | 1,18% | 2 | 1,2% | 2 | 1,2% |
Grube (1863) | 3 | 0,57% | 2 | 1,18% | 2 | 1,2% | 2 | 1,2% |
Harvard University Museum & Morris P.J. (2020) | 3 | 0,57% | 2 | 1,18% | 2 | 1,2% | 2 | 1,2% |
Jouin (1979) | 3 | 0,57% | 3 | 1,78% | 3 | 1,8% | 3 | 1,8% |
Monro (1939) | 3 | 0,57% | 3 | 1,78% | 3 | 1,8% | 3 | 1,8% |
Watson & Russell (1989) | 3 | 0,57% | 3 | 1,78% | 3 | 1,8% | 3 | 1,8% |
Augener (1918) | 2 | 0,38% | 1 | 0,59% | 1 | 0,6% | 1 | 0,6% |
Barnich & Fiege (2001) | 2 | 0,38% | 0 | 0% | 0 | 0% | 0 | 0% |
Beauchamp (1914) | 2 | 0,38% | 0 | 0% | 0 | 0% | 0 | 0% |
Bellan (1972) | 2 | 0,38% | 0 | 0% | 0 | 0% | 0 | 0% |
Bigot (2006) | 2 | 0,38% | 1 | 0,59% | 1 | 0,6% | 0 | 0% |
Claparède (1863) | 2 | 0,38% | 0 | 0% | 0 | 0% | 0 | 0% |
Conde-Vela (2021) | 2 | 0,38% | 2 | 1,18% | 2 | 1,2% | 2 | 1,2% |
Day (1957) | 2 | 0,38% | 2 | 1,18% | 2 | 1,2% | 2 | 1,2% |
Fauchald (1992) | 2 | 0,38% | 2 | 1,18% | 2 | 1,2% | 2 | 1,2% |
Gravier (1905) | 2 | 0,38% | 2 | 1,18% | 2 | 1,2% | 2 | 1,2% |
Jouin (1992) | 2 | 0,38% | 0 | 0% | 0 | 0% | 0 | 0% |
Kinberg (1856) | 2 | 0,38% | 0 | 0% | 0 | 0% | 0 | 0% |
Kinberg (1866) | 2 | 0,38% | 0 | 0% | 0 | 0% | 0 | 0% |
Marion (1876) | 2 | 0,38% | 0 | 0% | 0 | 0% | 0 | 0% |
Monro (1928) | 2 | 0,38% | 0 | 0% | 0 | 0% | 0 | 0% |
Natural History Museum of London (2020) | 2 | 0,38% | 2 | 1,18% | 2 | 1,2% | 2 | 1,2% |
Pettibone (1986) | 2 | 0,38% | 2 | 1,18% | 2 | 1,2% | 2 | 1,2% |
Pettibone (1993) | 2 | 0,38% | 2 | 1,18% | 2 | 1,2% | 2 | 1,2% |
Renaud-Mornant et al. (1971) | 2 | 0,38% | 2 | 1,18% | 2 | 1,2% | 2 | 1,2% |
Rosa (1891) | 2 | 0,38% | 0 | 0% | 0 | 0% | 0 | 0% |
Sarda et al. (2009) | 2 | 0,38% | 2 | 1,18% | 2 | 1,2% | 2 | 1,2% |
Treadwell (1943) | 2 | 0,38% | 0 | 0% | 0 | 0% | 0 | 0% |
Tustison et al. (2020) | 2 | 0,38% | 2 | 1,18% | 2 | 1,2% | 2 | 1,2% |
Watson et al. (2019) | 2 | 0,38% | 2 | 1,18% | 2 | 1,2% | 2 | 1,2% |
Allspach & Neuhaus (2021) | 1 | 0,19% | 1 | 0,59% | 1 | 0,6% | 1 | 0,6% |
Cahiers de Biologie Marine, 18: 391-411.">Amoureux (1977) | 1 | 0,19% | 1 | 0,59% | 1 | 0,6% | 1 | 0,6% |
Augener (1913) | 1 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Australian Museum (2020) | 1 | 0,19% | 1 | 0,59% | 1 | 0,6% | 1 | 0,6% |
Bailey-Brock et al. (2010) | 1 | 0,19% | 1 | 0,59% | 1 | 0,6% | 1 | 0,6% |
Bellan (1975) | 1 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Bergstrom (1916) | 1 | 0,19% | 1 | 0,59% | 1 | 0,6% | 1 | 0,6% |
Blake & Kudenov (1978) | 1 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Boisseau & Lubet (1955) | 1 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Breton (2014) | 1 | 0,19% | 1 | 0,59% | 1 | 0,6% | 1 | 0,6% |
Caullery & Mesnil (1918) | 1 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Caziot (1921) | 1 | 0,19% | 1 | 0,59% | 1 | 0,6% | 1 | 0,6% |
Davoult et al. (1999) | 1 | 0,19% | 1 | 0,59% | 1 | 0,6% | 1 | 0,6% |
Duchêne (1984) | 1 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Dujardin (1839) | 1 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Fauvel (1920) | 1 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Fauvel (1925) | 1 | 0,19% | 1 | 0,59% | 1 | 0,6% | 1 | 0,6% |
Friedrich (1937) | 1 | 0,19% | 1 | 0,59% | 1 | 0,6% | 1 | 0,6% |
Greeff (1879) | 1 | 0,19% | 1 | 0,59% | 1 | 0,6% | 1 | 0,6% |
Grube (1878) | 1 | 0,19% | 1 | 0,59% | 1 | 0,6% | 1 | 0,6% |
Harlock & Laubier (1966) | 1 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Hartman (1949) | 1 | 0,19% | 1 | 0,59% | 1 | 0,6% | 1 | 0,6% |
Hartman (1951) | 1 | 0,19% | 1 | 0,59% | 0 | 0% | 1 | 0,6% |
Hessle (1925) | 1 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Hoagland (1920) | 1 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Izuka (1912) | 1 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Johnson (1897) | 1 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Jouin (1970) | 1 | 0,19% | 1 | 0,59% | 1 | 0,6% | 1 | 0,6% |
Lamarck (1818) | 1 | 0,19% | 1 | 0,59% | 1 | 0,6% | 1 | 0,6% |
Müller (2004) | 1 | 0,19% | 1 | 0,59% | 1 | 0,6% | 1 | 0,6% |
Nolte (1938) | 1 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
O'Connor (1987) | 1 | 0,19% | 1 | 0,59% | 1 | 0,6% | 1 | 0,6% |
Olivier et al. (2015) | 1 | 0,19% | 1 | 0,59% | 1 | 0,6% | 1 | 0,6% |
Paxton & Bailey-Brock (1986) | 1 | 0,19% | 1 | 0,59% | 1 | 0,6% | 1 | 0,6% |
Perkins (1980) | 1 | 0,19% | 1 | 0,59% | 1 | 0,6% | 1 | 0,6% |
Piotrowski et al. (2024) | 1 | 0,19% | 1 | 0,59% | 1 | 0,6% | 1 | 0,6% |
Plate (1916) | 1 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Poupin et al. (1999) | 1 | 0,19% | 1 | 0,59% | 1 | 0,6% | 1 | 0,6% |
Questel (2020) | 1 | 0,19% | 1 | 0,59% | 1 | 0,6% | 1 | 0,6% |
Renon & Lefèvre (1985) | 1 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Rosa (1908) | 1 | 0,19% | 1 | 0,59% | 1 | 0,6% | 1 | 0,6% |
Saint-Joseph (1888) | 1 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Sato-Okoshi et al. (2022) | 1 | 0,19% | 1 | 0,59% | 1 | 0,6% | 1 | 0,6% |
Schmarda (1861) | 1 | 0,19% | 1 | 0,59% | 1 | 0,6% | 1 | 0,6% |
Seidler (1923) | 1 | 0,19% | 1 | 0,59% | 1 | 0,6% | 1 | 0,6% |
Solís-Weiss et al. (2004) | 1 | 0,19% | 1 | 0,59% | 1 | 0,6% | 1 | 0,6% |
Southern (1921) | 1 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Treadwell (1943) | 1 | 0,19% | 1 | 0,59% | 1 | 0,6% | 1 | 0,6% |
Watson & Russell (1998) | 1 | 0,19% | 1 | 0,59% | 1 | 0,6% | 1 | 0,6% |