Annélides polychètes de Mayotte
95 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
| Référence | Total | Valides | Espèces | Taxons terminaux | ||||
|---|---|---|---|---|---|---|---|---|
| nb | % | nb | % | nb | % | nb | % | |
| Gout (1991) | 48 | 15,53% | 37 | 38,14% | 37 | 38,14% | 37 | 38,14% |
| Cambert et al. (2011) | 40 | 12,94% | 32 | 32,99% | 32 | 32,99% | 32 | 32,99% |
| Dauvin et al. (2003) | 37 | 11,97% | 33 | 34,02% | 33 | 34,02% | 33 | 34,02% |
| Pleijel (2007) | 29 | 9,39% | 16 | 16,49% | 16 | 16,49% | 16 | 16,49% |
| Bourcier (1988) | 20 | 6,47% | 17 | 17,53% | 17 | 17,53% | 17 | 17,53% |
| Ifremer (2009) | 18 | 5,83% | 14 | 14,43% | 14 | 14,43% | 14 | 14,43% |
| Godet et al. (2010) | 17 | 5,5% | 15 | 15,46% | 15 | 15,46% | 15 | 15,46% |
| Dean (2012) | 16 | 5,18% | 16 | 16,49% | 16 | 16,49% | 16 | 16,49% |
| Bigot (2006) | 12 | 3,88% | 10 | 10,31% | 10 | 10,31% | 10 | 10,31% |
| Nelson-Smith et al. (2014) | 12 | 3,88% | 11 | 11,34% | 11 | 11,34% | 11 | 11,34% |
| Guille & Laubier (1966) | 9 | 2,91% | 7 | 7,22% | 7 | 7,22% | 7 | 7,22% |
| Claparède (1864) | 8 | 2,59% | 1 | 1,03% | 1 | 1,03% | 1 | 1,03% |
| Bourmaud (2003) | 7 | 2,27% | 3 | 3,09% | 3 | 3,09% | 3 | 3,09% |
| Naim (1985) | 7 | 2,27% | 4 | 4,12% | 4 | 4,12% | 4 | 4,12% |
| Tricart & Foubert (2000) | 5 | 1,62% | 2 | 2,06% | 2 | 2,06% | 2 | 2,06% |
| Bigot et al. (2006) | 4 | 1,29% | 3 | 3,09% | 3 | 3,09% | 3 | 3,09% |
| Davoult (1990) | 4 | 1,29% | 4 | 4,12% | 4 | 4,12% | 4 | 4,12% |
| Martin (2011) | 4 | 1,29% | 4 | 4,12% | 4 | 4,12% | 4 | 4,12% |
| Solís-Weiss & Alcántara (2009) | 4 | 1,29% | 3 | 3,09% | 3 | 3,09% | 3 | 3,09% |
| Claparède (1863) | 3 | 0,97% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fauvel (1926) | 3 | 0,97% | 3 | 3,09% | 3 | 3,09% | 3 | 3,09% |
| Fauvel (1952) | 3 | 0,97% | 3 | 3,09% | 3 | 3,09% | 3 | 3,09% |
| Rignault & Chevallier (2017) | 3 | 0,97% | 1 | 1,03% | 1 | 1,03% | 1 | 1,03% |
| Rullier (1972) | 3 | 0,97% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sarda et al. (2009) | 3 | 0,97% | 3 | 3,09% | 3 | 3,09% | 3 | 3,09% |
| Ten Hove & Smith (1990) | 3 | 0,97% | 3 | 3,09% | 3 | 3,09% | 3 | 3,09% |
| Aguirrezabalaga & Ceberio (2005) | 2 | 0,65% | 2 | 2,06% | 2 | 2,06% | 2 | 2,06% |
| Augener (1918) | 2 | 0,65% | 2 | 2,06% | 2 | 2,06% | 2 | 2,06% |
| Bellan (1975) | 2 | 0,65% | 2 | 2,06% | 2 | 2,06% | 2 | 2,06% |
| Calabuig (2016) | 2 | 0,65% | 2 | 2,06% | 2 | 2,06% | 2 | 2,06% |
| Carrera-Parra (2006) | 2 | 0,65% | 2 | 2,06% | 2 | 2,06% | 2 | 2,06% |
| Duchêne (1984) | 2 | 0,65% | 2 | 2,06% | 2 | 2,06% | 2 | 2,06% |
| Fauvel (1950) | 2 | 0,65% | 2 | 2,06% | 2 | 2,06% | 2 | 2,06% |
| Grube (1846) | 2 | 0,65% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hartmann-Schroder (1960) | 2 | 0,65% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mackie (1984) | 2 | 0,65% | 2 | 2,06% | 2 | 2,06% | 2 | 2,06% |
| Marion (1876) | 2 | 0,65% | 0 | 0% | 0 | 0% | 0 | 0% |
| McIntosh (1885) | 2 | 0,65% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mesnil (1896) | 2 | 0,65% | 1 | 1,03% | 1 | 1,03% | 1 | 1,03% |
| Pettibone (1986) | 2 | 0,65% | 2 | 2,06% | 2 | 2,06% | 2 | 2,06% |
| Peyrot-Clausade (1976) | 2 | 0,65% | 2 | 2,06% | 2 | 2,06% | 2 | 2,06% |
| Saint-Joseph (1888) | 2 | 0,65% | 0 | 0% | 0 | 0% | 0 | 0% |
| Vonboletzky & Dohle (1967) | 2 | 0,65% | 2 | 2,06% | 2 | 2,06% | 2 | 2,06% |
| Augener (1906) | 1 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
| Beauchamp (1914) | 1 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bhaud & Duchene (1976) | 1 | 0,32% | 1 | 1,03% | 1 | 1,03% | 1 | 1,03% |
| Bhaud (1969) | 1 | 0,32% | 1 | 1,03% | 1 | 1,03% | 1 | 1,03% |
| Boisseau & Lubet (1955) | 1 | 0,32% | 1 | 1,03% | 1 | 1,03% | 1 | 1,03% |
| Breton (2014) | 1 | 0,32% | 1 | 1,03% | 1 | 1,03% | 1 | 1,03% |
| Carrera-Parra (2006) | 1 | 0,32% | 1 | 1,03% | 1 | 1,03% | 1 | 1,03% |
| Caullery & Mesnil (1918) | 1 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
| Claparède (1868) | 1 | 0,32% | 1 | 1,03% | 1 | 1,03% | 1 | 1,03% |
| Dauvin (1978) | 1 | 0,32% | 1 | 1,03% | 1 | 1,03% | 1 | 1,03% |
| Davoult et al. (1999) | 1 | 0,32% | 1 | 1,03% | 1 | 1,03% | 1 | 1,03% |
| Day (1957) | 1 | 0,32% | 1 | 1,03% | 1 | 1,03% | 1 | 1,03% |
| Fabricius (1780) | 1 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fauvel (1895) | 1 | 0,32% | 1 | 1,03% | 1 | 1,03% | 1 | 1,03% |
| Fauvel (1925) | 1 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fauvel (1926) | 1 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fauvel (1928) | 1 | 0,32% | 1 | 1,03% | 1 | 1,03% | 1 | 1,03% |
| Gaudy & Thomassin (2006) | 1 | 0,32% | 1 | 1,03% | 1 | 1,03% | 1 | 1,03% |
| Gillet (1991) | 1 | 0,32% | 1 | 1,03% | 1 | 1,03% | 1 | 1,03% |
| Goulletquer (2016) | 1 | 0,32% | 1 | 1,03% | 1 | 1,03% | 1 | 1,03% |
| Gravier (1904) | 1 | 0,32% | 1 | 1,03% | 1 | 1,03% | 1 | 1,03% |
| Harlock & Laubier (1966) | 1 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
| Posidonia oceanica Delile. Recueil des Travaux de la Station Marine d'Endoume, 35(51): 43-105.">Harmelin (1964) | 1 | 0,32% | 1 | 1,03% | 1 | 1,03% | 1 | 1,03% |
| Hartman (1961) | 1 | 0,32% | 1 | 1,03% | 1 | 1,03% | 1 | 1,03% |
| Hartman (1965) | 1 | 0,32% | 1 | 1,03% | 1 | 1,03% | 1 | 1,03% |
| Hartman (1969) | 1 | 0,32% | 1 | 1,03% | 1 | 1,03% | 1 | 1,03% |
| Hartmann-Schröder (1985) | 1 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hoagland (1920) | 1 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ifremer (2021) | 1 | 0,32% | 1 | 1,03% | 1 | 1,03% | 1 | 1,03% |
| Izuka (1912) | 1 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
| Keferstein (1862) | 1 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kinberg (1856) | 1 | 0,32% | 1 | 1,03% | 1 | 1,03% | 1 | 1,03% |
| Lavesque et al. (2017) | 1 | 0,32% | 1 | 1,03% | 1 | 1,03% | 1 | 1,03% |
| Maciolek (1985) | 1 | 0,32% | 1 | 1,03% | 1 | 1,03% | 1 | 1,03% |
| Marenzeller (1879) | 1 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
| Marion & Robretzky (1875) | 1 | 0,32% | 1 | 1,03% | 1 | 1,03% | 1 | 1,03% |
| Martin et al. (1996) | 1 | 0,32% | 1 | 1,03% | 1 | 1,03% | 1 | 1,03% |
| Miura & Shirayama (1992) | 1 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
| Müller (1858) | 1 | 0,32% | 1 | 1,03% | 1 | 1,03% | 1 | 1,03% |
| Piotrowski et al. (2024) | 1 | 0,32% | 1 | 1,03% | 1 | 1,03% | 1 | 1,03% |
| Potts (1910) | 1 | 0,32% | 1 | 1,03% | 1 | 1,03% | 1 | 1,03% |
| Potts (1914) | 1 | 0,32% | 1 | 1,03% | 1 | 1,03% | 1 | 1,03% |
| Prouzet (2015) | 1 | 0,32% | 1 | 1,03% | 1 | 1,03% | 1 | 1,03% |
| Quatrefages (1866) | 1 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
| Questel (2020) | 1 | 0,32% | 1 | 1,03% | 1 | 1,03% | 1 | 1,03% |
| Rathke (1843) | 1 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
| Savigny (1822) | 1 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
| Söderström (1920) | 1 | 0,32% | 1 | 1,03% | 1 | 1,03% | 1 | 1,03% |
| Solís-Weiss et al. (2004) | 1 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
| Theodorides & Desportes (1978) | 1 | 0,32% | 1 | 1,03% | 1 | 1,03% | 1 | 1,03% |
| Treadwell (1943) | 1 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
| Wirén (1883) | 1 | 0,32% | 1 | 1,03% | 1 | 1,03% | 1 | 1,03% |
