Annélides marins de Terre Adélie
Annelida marins (sens large) de Clipperton : inclut les espèces strictement marines (habitat 1) ou pouvant également être retrouvées en eau douce (habitat 4 = eau douce / marin), en eau saumâtre (habitat 6) ou a terre (habitat 5 = marin et terrestre).
69 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
| Référence | Total | Valides | Espèces | Taxons terminaux | ||||
|---|---|---|---|---|---|---|---|---|
| nb | % | nb | % | nb | % | nb | % | |
| Arnaud (1974) | 63 | 20,72% | 37 | 44,58% | 35 | 43,75% | 37 | 46,25% |
| Bellan (1972) | 44 | 14,47% | 22 | 26,51% | 20 | 25% | 22 | 27,5% |
| Fauvel (1950) | 40 | 13,16% | 21 | 25,3% | 21 | 26,25% | 19 | 23,75% |
| Bellan (1975) | 29 | 9,54% | 17 | 20,48% | 16 | 20% | 17 | 21,25% |
| Duchêne (1984) | 23 | 7,57% | 15 | 18,07% | 15 | 18,75% | 14 | 17,5% |
| Dauvin et al. (2003) | 16 | 5,26% | 14 | 16,87% | 14 | 17,5% | 11 | 13,75% |
| McIntosh (1885) | 16 | 5,26% | 4 | 4,82% | 4 | 5% | 4 | 5% |
| Fauvel (1952) | 11 | 3,62% | 5 | 6,02% | 5 | 6,25% | 5 | 6,25% |
| Ifremer (2009) | 11 | 3,62% | 9 | 10,84% | 9 | 11,25% | 8 | 10% |
| Nelson-Smith et al. (2014) | 10 | 3,29% | 6 | 7,23% | 6 | 7,5% | 5 | 6,25% |
| Godet et al. (2010) | 9 | 2,96% | 8 | 9,64% | 8 | 10% | 6 | 7,5% |
| Pleijel (2007) | 9 | 2,96% | 6 | 7,23% | 6 | 7,5% | 6 | 7,5% |
| Bourcier (1988) | 7 | 2,3% | 6 | 7,23% | 6 | 7,5% | 6 | 7,5% |
| Fauvel (1953) | 7 | 2,3% | 3 | 3,61% | 3 | 3,75% | 3 | 3,75% |
| M'intosh (1876) | 7 | 2,3% | 2 | 2,41% | 2 | 2,5% | 2 | 2,5% |
| Tricart & Foubert (2000) | 4 | 1,32% | 3 | 3,61% | 3 | 3,75% | 2 | 2,5% |
| Bhaud & Gremare (1991) | 3 | 0,99% | 3 | 3,61% | 3 | 3,75% | 3 | 3,75% |
| Bourmaud (2003) | 3 | 0,99% | 2 | 2,41% | 2 | 2,5% | 2 | 2,5% |
| Cha et al. (1997) | 3 | 0,99% | 3 | 3,61% | 3 | 3,75% | 3 | 3,75% |
| Kinberg (1856) | 3 | 0,99% | 2 | 2,41% | 2 | 2,5% | 2 | 2,5% |
| Naim (1985) | 3 | 0,99% | 1 | 1,2% | 1 | 1,25% | 1 | 1,25% |
| Pearman et al. (2020) | 3 | 0,99% | 3 | 3,61% | 3 | 3,75% | 1 | 1,25% |
| Averincev (1972) | 2 | 0,66% | 1 | 1,2% | 0 | 0% | 1 | 1,25% |
| Breton (2014) | 2 | 0,66% | 2 | 2,41% | 2 | 2,5% | 2 | 2,5% |
| Caullery & Mesnil (1897) | 2 | 0,66% | 0 | 0% | 0 | 0% | 0 | 0% |
| Claparède (1864) | 2 | 0,66% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dean (2012) | 2 | 0,66% | 2 | 2,41% | 2 | 2,5% | 2 | 2,5% |
| Ehlers (1908) | 2 | 0,66% | 2 | 2,41% | 2 | 2,5% | 2 | 2,5% |
| Gillet (1991) | 2 | 0,66% | 2 | 2,41% | 2 | 2,5% | 2 | 2,5% |
| Grube (1863) | 2 | 0,66% | 2 | 2,41% | 2 | 2,5% | 2 | 2,5% |
| Guille & Laubier (1966) | 2 | 0,66% | 1 | 1,2% | 1 | 1,25% | 1 | 1,25% |
| Koechlin (1977) | 2 | 0,66% | 0 | 0% | 0 | 0% | 0 | 0% |
| Marion (1876) | 2 | 0,66% | 0 | 0% | 0 | 0% | 0 | 0% |
| Meißner (2005) | 2 | 0,66% | 2 | 2,41% | 2 | 2,5% | 2 | 2,5% |
| , 12: 59-198.">Monro (1936) | 2 | 0,66% | 1 | 1,2% | 0 | 0% | 1 | 1,25% |
| Montagu (1819) | 2 | 0,66% | 0 | 0% | 0 | 0% | 0 | 0% |
| Quatrefages (1866) | 2 | 0,66% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rignault & Chevallier (2017) | 2 | 0,66% | 1 | 1,2% | 1 | 1,25% | 1 | 1,25% |
| Rzhavsky (2010) | 2 | 0,66% | 2 | 2,41% | 2 | 2,5% | 2 | 2,5% |
| Saint-Joseph (1888) | 2 | 0,66% | 0 | 0% | 0 | 0% | 0 | 0% |
| Salazar-vallejo (2012) | 2 | 0,66% | 1 | 1,2% | 1 | 1,25% | 1 | 1,25% |
| Solís-Weiss & Alcántara (2009) | 2 | 0,66% | 2 | 2,41% | 2 | 2,5% | 2 | 2,5% |
| Studer (1878) | 2 | 0,66% | 0 | 0% | 0 | 0% | 0 | 0% |
| Verrill (1876) | 2 | 0,66% | 0 | 0% | 0 | 0% | 0 | 0% |
| Vonboletzky & Dohle (1967) | 2 | 0,66% | 2 | 2,41% | 2 | 2,5% | 0 | 0% |
| Cahiers de Biologie Marine, 18: 391-411.">Amoureux (1977) | 1 | 0,33% | 1 | 1,2% | 1 | 1,25% | 1 | 1,25% |
| Banse & Hobson (1968) | 1 | 0,33% | 0 | 0% | 0 | 0% | 0 | 0% |
| Benham (1921) | 1 | 0,33% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bigot et al. (2006) | 1 | 0,33% | 1 | 1,2% | 1 | 1,25% | 1 | 1,25% |
| Claparède (1863) | 1 | 0,33% | 0 | 0% | 0 | 0% | 0 | 0% |
| Davoult (1990) | 1 | 0,33% | 1 | 1,2% | 1 | 1,25% | 1 | 1,25% |
| Ehlers (1897) | 1 | 0,33% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fabricius (1780) | 1 | 0,33% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fauvel (1926) | 1 | 0,33% | 1 | 1,2% | 1 | 1,25% | 0 | 0% |
| Gravier (1906) | 1 | 0,33% | 1 | 1,2% | 1 | 1,25% | 1 | 1,25% |
| Gravier (1906) | 1 | 0,33% | 0 | 0% | 0 | 0% | 0 | 0% |
| GT DCE Réunion | 1 | 0,33% | 1 | 1,2% | 1 | 1,25% | 1 | 1,25% |
| Gutt et al. (2007) | 1 | 0,33% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hartman (1965) | 1 | 0,33% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hartman (1967) | 1 | 0,33% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hessle (1917) | 1 | 0,33% | 1 | 1,2% | 1 | 1,25% | 1 | 1,25% |
| Izuka (1912) | 1 | 0,33% | 0 | 0% | 0 | 0% | 0 | 0% |
| Johnson (1901) | 1 | 0,33% | 0 | 0% | 0 | 0% | 0 | 0% |
| Keferstein (1862) | 1 | 0,33% | 0 | 0% | 0 | 0% | 0 | 0% |
| Monod & Dollfus (1932) | 1 | 0,33% | 1 | 1,2% | 1 | 1,25% | 1 | 1,25% |
| Natural History Museum of London (2020) | 1 | 0,33% | 0 | 0% | 0 | 0% | 0 | 0% |
| Nygren (2004) | 1 | 0,33% | 1 | 1,2% | 1 | 1,25% | 1 | 1,25% |
| Piraino et al. (2003) | 1 | 0,33% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sarda et al. (2009) | 1 | 0,33% | 1 | 1,2% | 1 | 1,25% | 0 | 0% |
