Annélides polychètes de Polynésie française
111 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 | 9,21% | 31 | 18,45% | 31 | 18,67% | 31 | 18,67% |
| Naim (1985) | 36 | 6,91% | 22 | 13,1% | 22 | 13,25% | 22 | 13,25% |
| Chamberlin (1919) | 31 | 5,95% | 23 | 13,69% | 23 | 13,86% | 23 | 13,86% |
| Dauvin et al. (2003) | 26 | 4,99% | 19 | 11,31% | 19 | 11,45% | 18 | 10,84% |
| Bourmaud (2003) | 23 | 4,41% | 13 | 7,74% | 13 | 7,83% | 13 | 7,83% |
| Salazar-Vallejo (2020) | 18 | 3,45% | 18 | 10,71% | 18 | 10,84% | 18 | 10,84% |
| Dean (2012) | 17 | 3,26% | 17 | 10,12% | 17 | 10,24% | 17 | 10,24% |
| Claparède (1864) | 16 | 3,07% | 2 | 1,19% | 2 | 1,2% | 2 | 1,2% |
| Bourcier (1988) | 14 | 2,69% | 10 | 5,95% | 10 | 6,02% | 10 | 6,02% |
| Peyrot-Clausade (1976) | 14 | 2,69% | 12 | 7,14% | 12 | 7,23% | 12 | 7,23% |
| Paulay & Brown (2019) | 13 | 2,5% | 12 | 7,14% | 12 | 7,23% | 12 | 7,23% |
| Chamberlin (1919) | 12 | 2,3% | 1 | 0,6% | 1 | 0,6% | 1 | 0,6% |
| Salazar-Vallejo (2018) | 12 | 2,3% | 10 | 5,95% | 10 | 6,02% | 10 | 6,02% |
| Pearman et al. (2020) | 11 | 2,11% | 10 | 5,95% | 9 | 5,42% | 10 | 6,02% |
| Ifremer (2009) | 9 | 1,73% | 7 | 4,17% | 7 | 4,22% | 7 | 4,22% |
| Solís-Weiss & Alcántara (2009) | 9 | 1,73% | 8 | 4,76% | 8 | 4,82% | 8 | 4,82% |
| Gout (1991) | 8 | 1,54% | 5 | 2,98% | 5 | 3,01% | 5 | 3,01% |
| Rullier (1972) | 8 | 1,54% | 3 | 1,79% | 3 | 1,81% | 3 | 1,81% |
| Godet et al. (2010) | 7 | 1,34% | 5 | 2,98% | 5 | 3,01% | 5 | 3,01% |
| Salazar-Vallejo (2023) | 7 | 1,34% | 7 | 4,17% | 7 | 4,22% | 7 | 4,22% |
| Orrell (2019) | 6 | 1,15% | 4 | 2,38% | 4 | 2,41% | 4 | 2,41% |
| Fauvel (1919) | 5 | 0,96% | 0 | 0% | 0 | 0% | 0 | 0% |
| Glasby et al. (2011) | 5 | 0,96% | 3 | 1,79% | 3 | 1,81% | 3 | 1,81% |
| Guille & Laubier (1966) | 5 | 0,96% | 3 | 1,79% | 3 | 1,81% | 3 | 1,81% |
| Nelson-Smith et al. (2014) | 5 | 0,96% | 3 | 1,79% | 3 | 1,81% | 3 | 1,81% |
| Rignault & Chevallier (2017) | 5 | 0,96% | 4 | 2,38% | 4 | 2,41% | 4 | 2,41% |
| Tricart & Foubert (2000) | 5 | 0,96% | 2 | 1,19% | 2 | 1,2% | 2 | 1,2% |
| Hartmann-Schroder (1960) | 4 | 0,77% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hutchings et al. (1998) | 4 | 0,77% | 4 | 2,38% | 4 | 2,41% | 4 | 2,41% |
| Kinberg (1865) | 4 | 0,77% | 4 | 2,38% | 4 | 2,41% | 4 | 2,41% |
| Kinberg ([1867]) | 4 | 0,77% | 2 | 1,19% | 2 | 1,2% | 2 | 1,2% |
| Treadwell (1943) | 4 | 0,77% | 0 | 0% | 0 | 0% | 0 | 0% |
| Arnaud (1974) | 3 | 0,58% | 1 | 0,6% | 1 | 0,6% | 1 | 0,6% |
| Cambert et al. (2011) | 3 | 0,58% | 2 | 1,19% | 2 | 1,2% | 2 | 1,2% |
| Grube (1863) | 3 | 0,58% | 2 | 1,19% | 2 | 1,2% | 2 | 1,2% |
| Harvard University Museum & Morris P.J. (2020) | 3 | 0,58% | 2 | 1,19% | 2 | 1,2% | 2 | 1,2% |
| Jouin (1979) | 3 | 0,58% | 3 | 1,79% | 3 | 1,81% | 3 | 1,81% |
| Monro (1939) | 3 | 0,58% | 3 | 1,79% | 3 | 1,81% | 3 | 1,81% |
| Watson & Russell (1989) | 3 | 0,58% | 3 | 1,79% | 3 | 1,81% | 3 | 1,81% |
| Augener (1918) | 2 | 0,38% | 1 | 0,6% | 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 | 0,6% | 1 | 0,6% | 0 | 0% |
| Claparède (1863) | 2 | 0,38% | 0 | 0% | 0 | 0% | 0 | 0% |
| Conde-Vela (2021) | 2 | 0,38% | 2 | 1,19% | 2 | 1,2% | 2 | 1,2% |
| Day (1957) | 2 | 0,38% | 2 | 1,19% | 2 | 1,2% | 2 | 1,2% |
| Fauchald (1992) | 2 | 0,38% | 2 | 1,19% | 2 | 1,2% | 2 | 1,2% |
| Gravier (1905) | 2 | 0,38% | 2 | 1,19% | 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 | 1,19% | 2 | 1,2% | 2 | 1,2% |
| Pettibone (1986) | 2 | 0,38% | 2 | 1,19% | 2 | 1,2% | 2 | 1,2% |
| Pettibone (1993) | 2 | 0,38% | 2 | 1,19% | 2 | 1,2% | 2 | 1,2% |
| Renaud-Mornant et al. (1971) | 2 | 0,38% | 2 | 1,19% | 2 | 1,2% | 2 | 1,2% |
| Sarda et al. (2009) | 2 | 0,38% | 2 | 1,19% | 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 | 1,19% | 2 | 1,2% | 2 | 1,2% |
| Watson et al. (2019) | 2 | 0,38% | 2 | 1,19% | 2 | 1,2% | 2 | 1,2% |
| Allspach & Neuhaus (2021) | 1 | 0,19% | 1 | 0,6% | 1 | 0,6% | 1 | 0,6% |
| Cahiers de Biologie Marine, 18: 391-411.">Amoureux (1977) | 1 | 0,19% | 1 | 0,6% | 1 | 0,6% | 1 | 0,6% |
| Augener (1913) | 1 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
| Australian Museum (2020) | 1 | 0,19% | 1 | 0,6% | 1 | 0,6% | 1 | 0,6% |
| Bailey-Brock et al. (2010) | 1 | 0,19% | 1 | 0,6% | 1 | 0,6% | 1 | 0,6% |
| Bellan (1975) | 1 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bergstrom (1916) | 1 | 0,19% | 1 | 0,6% | 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 | 0,6% | 1 | 0,6% | 1 | 0,6% |
| Caullery & Mesnil (1918) | 1 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
| Caziot (1921) | 1 | 0,19% | 1 | 0,6% | 1 | 0,6% | 1 | 0,6% |
| Davoult et al. (1999) | 1 | 0,19% | 1 | 0,6% | 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 | 0,6% | 1 | 0,6% | 1 | 0,6% |
| Friedrich (1937) | 1 | 0,19% | 1 | 0,6% | 1 | 0,6% | 1 | 0,6% |
| Greeff (1879) | 1 | 0,19% | 1 | 0,6% | 1 | 0,6% | 1 | 0,6% |
| Grube (1878) | 1 | 0,19% | 1 | 0,6% | 1 | 0,6% | 1 | 0,6% |
| Harlock & Laubier (1966) | 1 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hartman (1949) | 1 | 0,19% | 1 | 0,6% | 1 | 0,6% | 1 | 0,6% |
| Hartman (1951) | 1 | 0,19% | 1 | 0,6% | 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 | 0,6% | 1 | 0,6% | 1 | 0,6% |
| Lamarck (1818) | 1 | 0,19% | 1 | 0,6% | 1 | 0,6% | 1 | 0,6% |
| Müller (2004) | 1 | 0,19% | 1 | 0,6% | 1 | 0,6% | 1 | 0,6% |
| Nolte (1938) | 1 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
| O'Connor (1987) | 1 | 0,19% | 1 | 0,6% | 1 | 0,6% | 1 | 0,6% |
| Olivier et al. (2015) | 1 | 0,19% | 1 | 0,6% | 1 | 0,6% | 1 | 0,6% |
| Paxton & Bailey-Brock (1986) | 1 | 0,19% | 1 | 0,6% | 1 | 0,6% | 1 | 0,6% |
| Perkins (1980) | 1 | 0,19% | 1 | 0,6% | 1 | 0,6% | 1 | 0,6% |
| Piotrowski et al. (2024) | 1 | 0,19% | 1 | 0,6% | 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 | 0,6% | 1 | 0,6% | 1 | 0,6% |
| Questel (2020) | 1 | 0,19% | 1 | 0,6% | 1 | 0,6% | 1 | 0,6% |
| Renon & Lefèvre (1985) | 1 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rosa (1908) | 1 | 0,19% | 1 | 0,6% | 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 | 0,6% | 1 | 0,6% | 1 | 0,6% |
| Schmarda (1861) | 1 | 0,19% | 1 | 0,6% | 1 | 0,6% | 1 | 0,6% |
| Seidler (1923) | 1 | 0,19% | 1 | 0,6% | 1 | 0,6% | 1 | 0,6% |
| Solís-Weiss et al. (2004) | 1 | 0,19% | 1 | 0,6% | 1 | 0,6% | 1 | 0,6% |
| Southern (1921) | 1 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
| Treadwell (1943) | 1 | 0,19% | 1 | 0,6% | 1 | 0,6% | 1 | 0,6% |
| Watson & Russell (1998) | 1 | 0,19% | 1 | 0,6% | 1 | 0,6% | 1 | 0,6% |
