Annélides polychètes de Guadeloupe
104 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
Référence | Total | Valides | Espèces | Taxons terminaux | ||||
---|---|---|---|---|---|---|---|---|
nb | % | nb | % | nb | % | nb | % | |
Dean (2012) | 82 | 17,9% | 69 | 62,73% | 69 | 63,3% | 69 | 63,3% |
Tricart & Foubert (2000) | 49 | 10,7% | 34 | 30,91% | 34 | 31,19% | 34 | 31,19% |
Pleijel (2007) | 24 | 5,24% | 16 | 14,55% | 16 | 14,68% | 16 | 14,68% |
Dauvin et al. (2003) | 23 | 5,02% | 19 | 17,27% | 19 | 17,43% | 18 | 16,51% |
Nelson-Smith et al. (2014) | 16 | 3,49% | 10 | 9,09% | 10 | 9,17% | 10 | 9,17% |
Bourcier (1988) | 14 | 3,06% | 11 | 10% | 11 | 10,09% | 10 | 9,17% |
Godet et al. (2010) | 12 | 2,62% | 9 | 8,18% | 9 | 8,26% | 8 | 7,34% |
Ifremer (2009) | 11 | 2,4% | 9 | 8,18% | 9 | 8,26% | 9 | 8,26% |
Amoureux (1985) | 9 | 1,97% | 3 | 2,73% | 3 | 2,75% | 3 | 2,75% |
Questel & Le Quellec (2012) | 7 | 1,53% | 6 | 5,45% | 6 | 5,5% | 6 | 5,5% |
Questel (2020) | 7 | 1,53% | 6 | 5,45% | 6 | 5,5% | 6 | 5,5% |
Gout (1991) | 6 | 1,31% | 5 | 4,55% | 5 | 4,59% | 5 | 4,59% |
Claparède (1864) | 5 | 1,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Salazar-Vallejo (2018) | 5 | 1,09% | 3 | 2,73% | 3 | 2,75% | 3 | 2,75% |
Bourmaud (2003) | 4 | 0,87% | 4 | 3,64% | 4 | 3,67% | 4 | 3,67% |
Claparède (1863) | 4 | 0,87% | 0 | 0% | 0 | 0% | 0 | 0% |
Diaz & Cuzange (2009) | 4 | 0,87% | 3 | 2,73% | 3 | 2,75% | 3 | 2,75% |
Guille & Laubier (1966) | 4 | 0,87% | 3 | 2,73% | 3 | 2,75% | 2 | 1,83% |
Hove (1975) | 4 | 0,87% | 4 | 3,64% | 4 | 3,67% | 4 | 3,67% |
Martin (2011) | 4 | 0,87% | 4 | 3,64% | 4 | 3,67% | 4 | 3,67% |
Naim (1985) | 4 | 0,87% | 2 | 1,82% | 2 | 1,83% | 2 | 1,83% |
Pearman et al. (2020) | 4 | 0,87% | 4 | 3,64% | 4 | 3,67% | 4 | 3,67% |
Solís-Weiss & Alcántara (2009) | 4 | 0,87% | 3 | 2,73% | 3 | 2,75% | 3 | 2,75% |
Vonboletzky & Dohle (1967) | 4 | 0,87% | 2 | 1,82% | 2 | 1,83% | 2 | 1,83% |
Arnaud (1974) | 3 | 0,66% | 2 | 1,82% | 2 | 1,83% | 2 | 1,83% |
Bhaud & Gremare (1991) | 3 | 0,66% | 3 | 2,73% | 3 | 2,75% | 3 | 2,75% |
Cambert et al. (2011) | 3 | 0,66% | 3 | 2,73% | 3 | 2,75% | 3 | 2,75% |
Cha et al. (1997) | 3 | 0,66% | 3 | 2,73% | 3 | 2,75% | 3 | 2,75% |
Conde-Vela (2021) | 3 | 0,66% | 3 | 2,73% | 3 | 2,75% | 3 | 2,75% |
Gillet (1986) | 3 | 0,66% | 3 | 2,73% | 3 | 2,75% | 3 | 2,75% |
Peyrot-Clausade (1976) | 3 | 0,66% | 3 | 2,73% | 3 | 2,75% | 3 | 2,75% |
Saint-Joseph (1888) | 3 | 0,66% | 0 | 0% | 0 | 0% | 0 | 0% |
Wesenberg-Lund (1958) | 3 | 0,66% | 3 | 2,73% | 3 | 2,75% | 3 | 2,75% |
Augener (1922) | 2 | 0,44% | 0 | 0% | 0 | 0% | 0 | 0% |
Bellan (1972) | 2 | 0,44% | 1 | 0,91% | 1 | 0,92% | 1 | 0,92% |
Ben-Eliahu (1976) | 2 | 0,44% | 2 | 1,82% | 2 | 1,83% | 2 | 1,83% |
Boisseau & Lubet (1955) | 2 | 0,44% | 1 | 0,91% | 1 | 0,92% | 1 | 0,92% |
Bush (1907) | 2 | 0,44% | 0 | 0% | 0 | 0% | 0 | 0% |
Fauvel (1926) | 2 | 0,44% | 2 | 1,82% | 2 | 1,83% | 2 | 1,83% |
Gravina et al. (2015) | 2 | 0,44% | 0 | 0% | 0 | 0% | 0 | 0% |
Grube (1846) | 2 | 0,44% | 0 | 0% | 0 | 0% | 0 | 0% |
Grube (1863) | 2 | 0,44% | 1 | 0,91% | 1 | 0,92% | 1 | 0,92% |
Harvard University Museum & Morris P.J. (2020) | 2 | 0,44% | 1 | 0,91% | 1 | 0,92% | 1 | 0,92% |
Jones (1962) | 2 | 0,44% | 0 | 0% | 0 | 0% | 0 | 0% |
Kinberg ([1867]) | 2 | 0,44% | 0 | 0% | 0 | 0% | 0 | 0% |
Kritzler (1971) | 2 | 0,44% | 2 | 1,82% | 2 | 1,83% | 2 | 1,83% |
Mackie (1984) | 2 | 0,44% | 2 | 1,82% | 2 | 1,83% | 2 | 1,83% |
Maréchal & Trégarot (2012) | 2 | 0,44% | 2 | 1,82% | 2 | 1,83% | 2 | 1,83% |
Montagu (1819) | 2 | 0,44% | 0 | 0% | 0 | 0% | 0 | 0% |
Potts (1910) | 2 | 0,44% | 2 | 1,82% | 2 | 1,83% | 2 | 1,83% |
Rioja (1947) | 2 | 0,44% | 0 | 0% | 0 | 0% | 0 | 0% |
Salazar-Vallejo (2011) | 2 | 0,44% | 2 | 1,82% | 2 | 1,83% | 2 | 1,83% |
Sarda et al. (2009) | 2 | 0,44% | 2 | 1,82% | 2 | 1,83% | 2 | 1,83% |
Thomassin (1970) | 2 | 0,44% | 2 | 1,82% | 2 | 1,83% | 2 | 1,83% |
Treadwell (1943) | 2 | 0,44% | 0 | 0% | 0 | 0% | 0 | 0% |
Treadwell (1943) | 2 | 0,44% | 0 | 0% | 0 | 0% | 0 | 0% |
Aguirrezabalaga & Ceberio (2005) | 1 | 0,22% | 1 | 0,91% | 1 | 0,92% | 1 | 0,92% |
Cahiers de Biologie Marine, 18: 391-411.">Amoureux (1977) | 1 | 0,22% | 1 | 0,91% | 1 | 0,92% | 1 | 0,92% |
Augener (1914) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Augener (1931) | 1 | 0,22% | 1 | 0,91% | 1 | 0,92% | 1 | 0,92% |
Bellan (1960) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Bigot (2006) | 1 | 0,22% | 1 | 0,91% | 1 | 0,92% | 1 | 0,92% |
Bonnet & Jullien (1936) | 1 | 0,22% | 1 | 0,91% | 1 | 0,92% | 1 | 0,92% |
Breton (2014) | 1 | 0,22% | 1 | 0,91% | 1 | 0,92% | 1 | 0,92% |
Caullery (1944) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Chávez-López (2021) | 1 | 0,22% | 1 | 0,91% | 1 | 0,92% | 1 | 0,92% |
Collectif & Bebest (2019) | 1 | 0,22% | 1 | 0,91% | 1 | 0,92% | 1 | 0,92% |
Duchêne (1984) | 1 | 0,22% | 1 | 0,91% | 1 | 0,92% | 1 | 0,92% |
Fabricius (1780) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Fauvel (1909) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Fauvel (1914) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Fauvel (1952) | 1 | 0,22% | 1 | 0,91% | 1 | 0,92% | 1 | 0,92% |
Hartman (1951) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Hartman (1952) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Hartmann-Schroder & Zibrowius (1998) | 1 | 0,22% | 1 | 0,91% | 1 | 0,92% | 1 | 0,92% |
Hartmann-Schroder (1960) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Hébrard et al. (2022) | 1 | 0,22% | 1 | 0,91% | 1 | 0,92% | 1 | 0,92% |
Hoagland (1919) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Iroso (1921) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Izuka (1912) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Lavesque et al. (2017) | 1 | 0,22% | 1 | 0,91% | 1 | 0,92% | 1 | 0,92% |
Linnaeus (1767) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Mesnil (1896) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Moore (1907) | 1 | 0,22% | 1 | 0,91% | 1 | 0,92% | 1 | 0,92% |
Müller (2004) | 1 | 0,22% | 1 | 0,91% | 1 | 0,92% | 1 | 0,92% |
Narayaninsamy (2020) | 1 | 0,22% | 1 | 0,91% | 1 | 0,92% | 1 | 0,92% |
Orrell (2019) | 1 | 0,22% | 1 | 0,91% | 1 | 0,92% | 1 | 0,92% |
Pallas (1788) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Pawlik (1988) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Pixell (1913) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Quatrefages (1866) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Renaud-Mornant & Gourbault (1984) | 1 | 0,22% | 1 | 0,91% | 1 | 0,92% | 1 | 0,92% |
Renaud-Mornant et al. (1971) | 1 | 0,22% | 1 | 0,91% | 1 | 0,92% | 0 | 0% |
Rioja (1958) | 1 | 0,22% | 1 | 0,91% | 1 | 0,92% | 1 | 0,92% |
Saint-Joseph (1896) | 1 | 0,22% | 1 | 0,91% | 1 | 0,92% | 1 | 0,92% |
Salazar-vallejo et al. (2017) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Shen et al. (1993) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Theodorides & Desportes (1978) | 1 | 0,22% | 1 | 0,91% | 1 | 0,92% | 1 | 0,92% |
Treadwell (1926) | 1 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Uicn et al. (2019) | 1 | 0,22% | 1 | 0,91% | 1 | 0,92% | 1 | 0,92% |
Warren et al. (1994) | 1 | 0,22% | 1 | 0,91% | 1 | 0,92% | 1 | 0,92% |
Wirén (1883) | 1 | 0,22% | 1 | 0,91% | 1 | 0,92% | 1 | 0,92% |
Zibrowius (1968) | 1 | 0,22% | 1 | 0,91% | 1 | 0,92% | 1 | 0,92% |
Zibrowius (1971) | 1 | 0,22% | 1 | 0,91% | 1 | 0,92% | 1 | 0,92% |