Annélides marins de Guadeloupe
117 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) | 84 | 17,07% | 71 | 58,2% | 71 | 58,68% | 71 | 58,68% |
Tricart & Foubert (2000) | 49 | 9,96% | 34 | 27,87% | 34 | 28,1% | 34 | 28,1% |
Dauvin et al. (2003) | 24 | 4,88% | 20 | 16,39% | 20 | 16,53% | 19 | 15,7% |
Pleijel (2007) | 24 | 4,88% | 16 | 13,11% | 16 | 13,22% | 16 | 13,22% |
Nelson-Smith et al. (2014) | 16 | 3,25% | 10 | 8,2% | 10 | 8,26% | 10 | 8,26% |
Bourcier (1988) | 14 | 2,85% | 11 | 9,02% | 11 | 9,09% | 10 | 8,26% |
Godet et al. (2010) | 12 | 2,44% | 9 | 7,38% | 9 | 7,44% | 8 | 6,61% |
Ifremer (2009) | 11 | 2,24% | 9 | 7,38% | 9 | 7,44% | 9 | 7,44% |
Amoureux (1985) | 9 | 1,83% | 3 | 2,46% | 3 | 2,48% | 3 | 2,48% |
Erséus (1990) | 7 | 1,42% | 6 | 4,92% | 6 | 4,96% | 6 | 4,96% |
Questel & Le Quellec (2012) | 7 | 1,42% | 6 | 4,92% | 6 | 4,96% | 6 | 4,96% |
Questel (2020) | 7 | 1,42% | 6 | 4,92% | 6 | 4,96% | 6 | 4,96% |
Erséus & Strehlow (1986) | 6 | 1,22% | 6 | 4,92% | 6 | 4,96% | 6 | 4,96% |
Gout (1991) | 6 | 1,22% | 5 | 4,1% | 5 | 4,13% | 5 | 4,13% |
Claparède (1864) | 5 | 1,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Salazar-Vallejo (2018) | 5 | 1,02% | 3 | 2,46% | 3 | 2,48% | 3 | 2,48% |
Bourmaud (2003) | 4 | 0,81% | 4 | 3,28% | 4 | 3,31% | 4 | 3,31% |
Claparède (1863) | 4 | 0,81% | 0 | 0% | 0 | 0% | 0 | 0% |
Diaz & Cuzange (2009) | 4 | 0,81% | 3 | 2,46% | 3 | 2,48% | 3 | 2,48% |
Erséus (1984) | 4 | 0,81% | 4 | 3,28% | 4 | 3,31% | 4 | 3,31% |
Guille & Laubier (1966) | 4 | 0,81% | 3 | 2,46% | 3 | 2,48% | 2 | 1,65% |
Hove (1975) | 4 | 0,81% | 4 | 3,28% | 4 | 3,31% | 4 | 3,31% |
Martin (2011) | 4 | 0,81% | 4 | 3,28% | 4 | 3,31% | 4 | 3,31% |
Naim (1985) | 4 | 0,81% | 2 | 1,64% | 2 | 1,65% | 2 | 1,65% |
Solís-Weiss & Alcántara (2009) | 4 | 0,81% | 3 | 2,46% | 3 | 2,48% | 3 | 2,48% |
Vonboletzky & Dohle (1967) | 4 | 0,81% | 2 | 1,64% | 2 | 1,65% | 2 | 1,65% |
Arnaud (1974) | 3 | 0,61% | 2 | 1,64% | 2 | 1,65% | 2 | 1,65% |
Cambert et al. (2011) | 3 | 0,61% | 3 | 2,46% | 3 | 2,48% | 3 | 2,48% |
Conde-Vela (2021) | 3 | 0,61% | 3 | 2,46% | 3 | 2,48% | 3 | 2,48% |
Dupont et al. (2023) | 3 | 0,61% | 3 | 2,46% | 3 | 2,48% | 3 | 2,48% |
Gillet (1986) | 3 | 0,61% | 3 | 2,46% | 3 | 2,48% | 3 | 2,48% |
Peyrot-Clausade (1976) | 3 | 0,61% | 3 | 2,46% | 3 | 2,48% | 3 | 2,48% |
Saint-Joseph (1888) | 3 | 0,61% | 0 | 0% | 0 | 0% | 0 | 0% |
Wesenberg-Lund (1958) | 3 | 0,61% | 3 | 2,46% | 3 | 2,48% | 3 | 2,48% |
Augener (1922) | 2 | 0,41% | 0 | 0% | 0 | 0% | 0 | 0% |
Bellan (1972) | 2 | 0,41% | 1 | 0,82% | 1 | 0,83% | 1 | 0,83% |
Ben-Eliahu (1976) | 2 | 0,41% | 2 | 1,64% | 2 | 1,65% | 2 | 1,65% |
Boisseau & Lubet (1955) | 2 | 0,41% | 1 | 0,82% | 1 | 0,83% | 1 | 0,83% |
Bush (1907) | 2 | 0,41% | 0 | 0% | 0 | 0% | 0 | 0% |
Dupont et al. (2023) | 2 | 0,41% | 2 | 1,64% | 2 | 1,65% | 2 | 1,65% |
Erseus (1984) | 2 | 0,41% | 2 | 1,64% | 2 | 1,65% | 2 | 1,65% |
Fauvel (1926) | 2 | 0,41% | 2 | 1,64% | 2 | 1,65% | 2 | 1,65% |
Gravina et al. (2015) | 2 | 0,41% | 0 | 0% | 0 | 0% | 0 | 0% |
Grube (1846) | 2 | 0,41% | 0 | 0% | 0 | 0% | 0 | 0% |
Grube (1863) | 2 | 0,41% | 1 | 0,82% | 1 | 0,83% | 1 | 0,83% |
Harvard University Museum & Morris P.J. (2020) | 2 | 0,41% | 1 | 0,82% | 1 | 0,83% | 1 | 0,83% |
Jones (1962) | 2 | 0,41% | 0 | 0% | 0 | 0% | 0 | 0% |
Kinberg ([1867]) | 2 | 0,41% | 0 | 0% | 0 | 0% | 0 | 0% |
Kritzler (1971) | 2 | 0,41% | 2 | 1,64% | 2 | 1,65% | 2 | 1,65% |
Mackie (1984) | 2 | 0,41% | 2 | 1,64% | 2 | 1,65% | 2 | 1,65% |
Maréchal & Trégarot (2012) | 2 | 0,41% | 2 | 1,64% | 2 | 1,65% | 2 | 1,65% |
Potts (1910) | 2 | 0,41% | 2 | 1,64% | 2 | 1,65% | 2 | 1,65% |
Renaud-Mornant & Gourbault (1984) | 2 | 0,41% | 2 | 1,64% | 2 | 1,65% | 2 | 1,65% |
Rioja (1947) | 2 | 0,41% | 0 | 0% | 0 | 0% | 0 | 0% |
Salazar-Vallejo (2011) | 2 | 0,41% | 2 | 1,64% | 2 | 1,65% | 2 | 1,65% |
Sarda et al. (2009) | 2 | 0,41% | 2 | 1,64% | 2 | 1,65% | 2 | 1,65% |
Thomassin (1970) | 2 | 0,41% | 2 | 1,64% | 2 | 1,65% | 2 | 1,65% |
Treadwell (1943) | 2 | 0,41% | 0 | 0% | 0 | 0% | 0 | 0% |
Treadwell (1943) | 2 | 0,41% | 0 | 0% | 0 | 0% | 0 | 0% |
Aguirrezabalaga & Ceberio (2005) | 1 | 0,2% | 1 | 0,82% | 1 | 0,83% | 1 | 0,83% |
Cahiers de Biologie Marine, 18: 391-411.">Amoureux (1977) | 1 | 0,2% | 1 | 0,82% | 1 | 0,83% | 1 | 0,83% |
Augener (1914) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Augener (1931) | 1 | 0,2% | 1 | 0,82% | 1 | 0,83% | 1 | 0,83% |
Beddard (1905) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Bellan (1960) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Bigot (2006) | 1 | 0,2% | 1 | 0,82% | 1 | 0,83% | 1 | 0,83% |
Bonnet & Jullien (1936) | 1 | 0,2% | 1 | 0,82% | 1 | 0,83% | 1 | 0,83% |
Breton (2014) | 1 | 0,2% | 1 | 0,82% | 1 | 0,83% | 1 | 0,83% |
Cabioch et al. (1968) | 1 | 0,2% | 1 | 0,82% | 1 | 0,83% | 1 | 0,83% |
Caullery (1944) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Chávez-López (2021) | 1 | 0,2% | 1 | 0,82% | 1 | 0,83% | 1 | 0,83% |
Csuzdi & Pavlíček (2009) | 1 | 0,2% | 1 | 0,82% | 1 | 0,83% | 1 | 0,83% |
Csuzdi et al. (2017) | 1 | 0,2% | 1 | 0,82% | 1 | 0,83% | 1 | 0,83% |
Duchêne (1984) | 1 | 0,2% | 1 | 0,82% | 1 | 0,83% | 1 | 0,83% |
Eisen (1895) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Erséus (1997) | 1 | 0,2% | 1 | 0,82% | 1 | 0,83% | 1 | 0,83% |
Fabricius (1780) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Fauvel (1909) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Fauvel (1914) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Fauvel (1952) | 1 | 0,2% | 1 | 0,82% | 1 | 0,83% | 1 | 0,83% |
Gates (1943) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Hartman (1951) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Hartman (1952) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Hartmann-Schroder & Zibrowius (1998) | 1 | 0,2% | 1 | 0,82% | 1 | 0,83% | 1 | 0,83% |
Hartmann-Schroder (1960) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Hébrard et al. (2022) | 1 | 0,2% | 1 | 0,82% | 1 | 0,83% | 1 | 0,83% |
Hoagland (1919) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Iroso (1921) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Izuka (1912) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Jourdan (2020) | 1 | 0,2% | 1 | 0,82% | 1 | 0,83% | 1 | 0,83% |
Lavesque et al. (2017) | 1 | 0,2% | 1 | 0,82% | 1 | 0,83% | 1 | 0,83% |
Linnaeus (1767) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Mesnil (1896) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Michaelsen (1913) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Moore (1907) | 1 | 0,2% | 1 | 0,82% | 1 | 0,83% | 1 | 0,83% |
Müller (2004) | 1 | 0,2% | 1 | 0,82% | 1 | 0,83% | 1 | 0,83% |
Narayaninsamy (2020) | 1 | 0,2% | 1 | 0,82% | 1 | 0,83% | 1 | 0,83% |
Orrell (2019) | 1 | 0,2% | 1 | 0,82% | 1 | 0,83% | 1 | 0,83% |
Pallas (1788) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Pawlik (1988) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Pixell (1913) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Quatrefages (1866) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Ramage et al. (2023) | 1 | 0,2% | 1 | 0,82% | 1 | 0,83% | 1 | 0,83% |
Remane (1925) | 1 | 0,2% | 1 | 0,82% | 1 | 0,83% | 1 | 0,83% |
Renaud-Mornant et al. (1971) | 1 | 0,2% | 1 | 0,82% | 1 | 0,83% | 0 | 0% |
Rioja (1958) | 1 | 0,2% | 1 | 0,82% | 1 | 0,83% | 1 | 0,83% |
Saint-Joseph (1896) | 1 | 0,2% | 1 | 0,82% | 1 | 0,83% | 1 | 0,83% |
Salazar-vallejo et al. (2017) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Shen et al. (1993) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Stephenson (1915) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Theodorides & Desportes (1978) | 1 | 0,2% | 1 | 0,82% | 1 | 0,83% | 1 | 0,83% |
Treadwell (1926) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Uicn et al. (2019) | 1 | 0,2% | 1 | 0,82% | 1 | 0,83% | 1 | 0,83% |
Warren et al. (1994) | 1 | 0,2% | 1 | 0,82% | 1 | 0,83% | 1 | 0,83% |
Wirén (1883) | 1 | 0,2% | 1 | 0,82% | 1 | 0,83% | 1 | 0,83% |
Zibrowius (1968) | 1 | 0,2% | 1 | 0,82% | 1 | 0,83% | 1 | 0,83% |
Zibrowius (1971) | 1 | 0,2% | 1 | 0,82% | 1 | 0,83% | 1 | 0,83% |