Annélides marins de Nouvelle-Calédonie
226 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) | 268 | 21,97% | 177 | 49,44% | 175 | 49,44% | 176 | 49,72% |
| Dauvin et al. (2003) | 57 | 4,67% | 42 | 11,73% | 42 | 11,86% | 40 | 11,3% |
| Dean (2012) | 36 | 2,95% | 33 | 9,22% | 33 | 9,32% | 30 | 8,47% |
| Bourcier (1988) | 30 | 2,46% | 21 | 5,87% | 21 | 5,93% | 20 | 5,65% |
| Nelson-Smith et al. (2014) | 29 | 2,38% | 18 | 5,03% | 18 | 5,08% | 17 | 4,8% |
| Naim (1985) | 28 | 2,3% | 17 | 4,75% | 17 | 4,8% | 17 | 4,8% |
| Rullier (1972) | 27 | 2,21% | 18 | 5,03% | 18 | 5,08% | 18 | 5,08% |
| Bourmaud (2003) | 24 | 1,97% | 13 | 3,63% | 13 | 3,67% | 13 | 3,67% |
| Claparède (1864) | 23 | 1,89% | 3 | 0,84% | 3 | 0,85% | 3 | 0,85% |
| Godet et al. (2010) | 19 | 1,56% | 15 | 4,19% | 15 | 4,24% | 14 | 3,95% |
| Salazar-Vallejo (2018) | 18 | 1,48% | 16 | 4,47% | 16 | 4,52% | 16 | 4,52% |
| Ifremer (2009) | 17 | 1,39% | 13 | 3,63% | 13 | 3,67% | 13 | 3,67% |
| Gout (1991) | 16 | 1,31% | 11 | 3,07% | 11 | 3,11% | 10 | 2,82% |
| Rullier & François (1972) | 15 | 1,23% | 15 | 4,19% | 15 | 4,24% | 15 | 4,24% |
| Salazar-Vallejo (2020) | 14 | 1,15% | 10 | 2,79% | 10 | 2,82% | 10 | 2,82% |
| Wit & Erseus (2007) | 14 | 1,15% | 14 | 3,91% | 14 | 3,95% | 14 | 3,95% |
| Cambert et al. (2011) | 13 | 1,07% | 9 | 2,51% | 9 | 2,54% | 9 | 2,54% |
| Erseus & Bergfeldt (2007) | 12 | 0,98% | 12 | 3,35% | 12 | 3,39% | 12 | 3,39% |
| Hanley & Burke (1991) | 12 | 0,98% | 10 | 2,79% | 10 | 2,82% | 10 | 2,82% |
| Richer de Forges et al. (2005) | 12 | 0,98% | 11 | 3,07% | 11 | 3,11% | 11 | 3,11% |
| Tricart & Foubert (2000) | 11 | 0,9% | 6 | 1,68% | 6 | 1,69% | 6 | 1,69% |
| Peyrot-Clausade (1976) | 10 | 0,82% | 9 | 2,51% | 9 | 2,54% | 9 | 2,54% |
| Hartmann-Schroder & Zibrowius (1998) | 9 | 0,74% | 9 | 2,51% | 9 | 2,54% | 9 | 2,54% |
| Hartmann-Schroder (1992) | 9 | 0,74% | 6 | 1,68% | 6 | 1,69% | 6 | 1,69% |
| Leon-Gonzalez & Salazar-Vallejo (2003) | 9 | 0,74% | 9 | 2,51% | 9 | 2,54% | 9 | 2,54% |
| Quatrefages (1866) | 9 | 0,74% | 4 | 1,12% | 4 | 1,13% | 4 | 1,13% |
| Solís-Weiss & Alcántara (2009) | 9 | 0,74% | 8 | 2,23% | 8 | 2,26% | 8 | 2,26% |
| Australian Museum (2020) | 8 | 0,66% | 8 | 2,23% | 8 | 2,26% | 8 | 2,26% |
| Fauvel (1930) | 8 | 0,66% | 2 | 0,56% | 2 | 0,56% | 2 | 0,56% |
| Lechapt & Kirtley (1998) | 8 | 0,66% | 8 | 2,23% | 8 | 2,26% | 8 | 2,26% |
| Rignault & Chevallier (2017) | 8 | 0,66% | 6 | 1,68% | 6 | 1,69% | 6 | 1,69% |
| Arnaud (1974) | 7 | 0,57% | 3 | 0,84% | 3 | 0,85% | 3 | 0,85% |
| Prantoni et al. (2017) | 7 | 0,57% | 7 | 1,96% | 7 | 1,98% | 7 | 1,98% |
| Salazar-Vallejo (2023) | 7 | 0,57% | 7 | 1,96% | 7 | 1,98% | 7 | 1,98% |
| Bellan (1972) | 6 | 0,49% | 2 | 0,56% | 2 | 0,56% | 2 | 0,56% |
| Bellan (1975) | 6 | 0,49% | 4 | 1,12% | 4 | 1,13% | 4 | 1,13% |
| Cazaux (1972) | 6 | 0,49% | 4 | 1,12% | 4 | 1,13% | 4 | 1,13% |
| Claparède (1863) | 6 | 0,49% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
| Guille & Laubier (1966) | 6 | 0,49% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
| Leon-gonzalez & Salazar-vallejo (2003) | 6 | 0,49% | 6 | 1,68% | 6 | 1,69% | 6 | 1,69% |
| Marion (1876) | 6 | 0,49% | 0 | 0% | 0 | 0% | 0 | 0% |
| Willey (1905) | 6 | 0,49% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
| Breton (2014) | 5 | 0,41% | 4 | 1,12% | 4 | 1,13% | 4 | 1,13% |
| Glasby et al. (2011) | 5 | 0,41% | 3 | 0,84% | 3 | 0,85% | 3 | 0,85% |
| Marenzeller (1879) | 5 | 0,41% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
| Treadwell (1926) | 5 | 0,41% | 2 | 0,56% | 2 | 0,56% | 2 | 0,56% |
| Augener (1918) | 4 | 0,33% | 3 | 0,84% | 3 | 0,85% | 3 | 0,85% |
| Bigot (2006) | 4 | 0,33% | 3 | 0,84% | 3 | 0,85% | 3 | 0,85% |
| Boisseau & Lubet (1955) | 4 | 0,33% | 2 | 0,56% | 2 | 0,56% | 2 | 0,56% |
| Carrera-Parra (2006) | 4 | 0,33% | 4 | 1,12% | 4 | 1,13% | 4 | 1,13% |
| Caullery & Mesnil (1916) | 4 | 0,33% | 0 | 0% | 0 | 0% | 0 | 0% |
| Duchêne (1984) | 4 | 0,33% | 2 | 0,56% | 2 | 0,56% | 2 | 0,56% |
| Grube (1863) | 4 | 0,33% | 2 | 0,56% | 2 | 0,56% | 2 | 0,56% |
| Jouin (1970) | 4 | 0,33% | 4 | 1,12% | 4 | 1,13% | 4 | 1,13% |
| Kupriyanova & Ippolitov (2015) | 4 | 0,33% | 4 | 1,12% | 4 | 1,13% | 4 | 1,13% |
| Lechapt (1997) | 4 | 0,33% | 4 | 1,12% | 4 | 1,13% | 4 | 1,13% |
| Martin (2011) | 4 | 0,33% | 4 | 1,12% | 4 | 1,13% | 4 | 1,13% |
| Pruvot (1930) | 4 | 0,33% | 4 | 1,12% | 4 | 1,13% | 4 | 1,13% |
| Questel (2020) | 4 | 0,33% | 4 | 1,12% | 4 | 1,13% | 4 | 1,13% |
| Zibrowius (1968) | 4 | 0,33% | 4 | 1,12% | 4 | 1,13% | 4 | 1,13% |
| Augener (1913) | 3 | 0,25% | 2 | 0,56% | 2 | 0,56% | 2 | 0,56% |
| Dupont et al. (2023) | 3 | 0,25% | 3 | 0,84% | 3 | 0,85% | 3 | 0,85% |
| Erséus & Strehlow (1986) | 3 | 0,25% | 3 | 0,84% | 3 | 0,85% | 3 | 0,85% |
| Fauchald (1992) | 3 | 0,25% | 3 | 0,84% | 3 | 0,85% | 3 | 0,85% |
| Fauvel (1911) | 3 | 0,25% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
| Fauvel (1919) | 3 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fauvel (1926) | 3 | 0,25% | 3 | 0,84% | 3 | 0,85% | 3 | 0,85% |
| Fauvel (1950) | 3 | 0,25% | 3 | 0,84% | 3 | 0,85% | 3 | 0,85% |
| Fauvel (1952) | 3 | 0,25% | 3 | 0,84% | 3 | 0,85% | 3 | 0,85% |
| Giere et al. (2008) | 3 | 0,25% | 3 | 0,84% | 3 | 0,85% | 3 | 0,85% |
| Hartmann-Schroder (1960) | 3 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hartmann-Schroder (1998) | 3 | 0,25% | 3 | 0,84% | 3 | 0,85% | 3 | 0,85% |
| Izuka (1912) | 3 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lechapt (1992) | 3 | 0,25% | 3 | 0,84% | 3 | 0,85% | 3 | 0,85% |
| Lechapt (1992) | 3 | 0,25% | 3 | 0,84% | 3 | 0,85% | 3 | 0,85% |
| Paulay & Brown (2019) | 3 | 0,25% | 3 | 0,84% | 3 | 0,85% | 3 | 0,85% |
| Pixell (1913) | 3 | 0,25% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
| Potts (1910) | 3 | 0,25% | 2 | 0,56% | 2 | 0,56% | 2 | 0,56% |
| Saint-Joseph (1888) | 3 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ten Hove & Smith (1990) | 3 | 0,25% | 3 | 0,84% | 3 | 0,85% | 3 | 0,85% |
| Watson & Russell (1989) | 3 | 0,25% | 3 | 0,84% | 3 | 0,85% | 3 | 0,85% |
| Watson (2015) | 3 | 0,25% | 3 | 0,84% | 3 | 0,85% | 3 | 0,85% |
| Aiyar & Alikunhi (1944) | 2 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Augener (1914) | 2 | 0,16% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
| Barnich & Fiege (2001) | 2 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Beauchamp (1914) | 2 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bush (1905) | 2 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Caullery & Mesnil (1897) | 2 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Caullery (1944) | 2 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Chamberlin (1919) | 2 | 0,16% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
| Conde-Vela (2021) | 2 | 0,16% | 2 | 0,56% | 2 | 0,56% | 2 | 0,56% |
| Day (1951) | 2 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dupont et al. (2023) | 2 | 0,16% | 2 | 0,56% | 2 | 0,56% | 2 | 0,56% |
| Erseus (1989) | 2 | 0,16% | 2 | 0,56% | 2 | 0,56% | 2 | 0,56% |
| Fauvel (1921) | 2 | 0,16% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
| Fauvel (1925) | 2 | 0,16% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
| Glasby et al. (2013) | 2 | 0,16% | 2 | 0,56% | 2 | 0,56% | 2 | 0,56% |
| Gravina et al. (2015) | 2 | 0,16% | 2 | 0,56% | 2 | 0,56% | 2 | 0,56% |
| Grube (1846) | 2 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Guerin (1970) | 2 | 0,16% | 2 | 0,56% | 2 | 0,56% | 2 | 0,56% |
| Hempelmann (1906) | 2 | 0,16% | 2 | 0,56% | 2 | 0,56% | 2 | 0,56% |
| Holthe (1986) | 2 | 0,16% | 2 | 0,56% | 2 | 0,56% | 2 | 0,56% |
| Imagima et al. (1984) | 2 | 0,16% | 2 | 0,56% | 2 | 0,56% | 2 | 0,56% |
| Imajima (1976) | 2 | 0,16% | 2 | 0,56% | 2 | 0,56% | 2 | 0,56% |
| Imajima (1976) | 2 | 0,16% | 2 | 0,56% | 2 | 0,56% | 2 | 0,56% |
| Jouin (1963) | 2 | 0,16% | 2 | 0,56% | 2 | 0,56% | 0 | 0% |
| Kinberg (1856) | 2 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Koechlin (1977) | 2 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lechapt & Gruet (1993) | 2 | 0,16% | 2 | 0,56% | 2 | 0,56% | 2 | 0,56% |
| Lechapt & Kirtley (1996) | 2 | 0,16% | 2 | 0,56% | 2 | 0,56% | 2 | 0,56% |
| M'intosh (1876) | 2 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Monro (1928) | 2 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pettibone (1986) | 2 | 0,16% | 2 | 0,56% | 2 | 0,56% | 2 | 0,56% |
| Pettibone (1989) | 2 | 0,16% | 2 | 0,56% | 2 | 0,56% | 2 | 0,56% |
| Pillai (1960) | 2 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pillai (1965) | 2 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ruta & Pleijel (2006) | 2 | 0,16% | 2 | 0,56% | 2 | 0,56% | 2 | 0,56% |
| Southern (1921) | 2 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Stock (1986) | 2 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Telenius & Shah (2019) | 2 | 0,16% | 2 | 0,56% | 2 | 0,56% | 2 | 0,56% |
| Thiriot-quiévreux (1965) | 2 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Treadwell (1943) | 2 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Verrill (1876) | 2 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Vonboletzky & Dohle (1967) | 2 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Watson & Russell (1991) | 2 | 0,16% | 2 | 0,56% | 2 | 0,56% | 2 | 0,56% |
| Westheide (1974) | 2 | 0,16% | 2 | 0,56% | 2 | 0,56% | 2 | 0,56% |
| Cahiers de Biologie Marine, 18: 391-411.">Amoureux (1977) | 1 | 0,08% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
| Audouin et al. (1833) | 1 | 0,08% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
| Augener (1925) | 1 | 0,08% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
| Augener (1926) | 1 | 0,08% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
| Augener (1927) | 1 | 0,08% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
| Bastida-zavala et al. (2003) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bastida-zavala et al. (2016) | 1 | 0,08% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
| Beddard (1905) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bellan (1960) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bellan (1971) | 1 | 0,08% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
| Fisheries Commonwealth of Australia, 4(2 & 3): 127-162.">Benham (1916) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bergstrom (1916) | 1 | 0,08% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
| Bigot et al. (2006) | 1 | 0,08% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
| Blake (2016) | 1 | 0,08% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
| Bonnet & Jullien (1936) | 1 | 0,08% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
| Bonse et al. (1996) | 1 | 0,08% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
| Boyle & Seaver (2010) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cabioch et al. (1968) | 1 | 0,08% | 1 | 0,28% | 1 | 0,28% | 0 | 0% |
| Caullery & Mesnil (1918) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Claparède (1868) | 1 | 0,08% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
| Csuzdi & Pavlíček (2009) | 1 | 0,08% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
| Csuzdi et al. (2017) | 1 | 0,08% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
| Davoult (1990) | 1 | 0,08% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
| Day (1960) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Day (1963) | 1 | 0,08% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
| DCE-Benthos Network, French Mediterranen Lagoon Monitoring Network (2022) | 1 | 0,08% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
| Diaz & Cuzange (2009) | 1 | 0,08% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
| Dujardin (1839) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Eisen (1895) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Erséus (1981) | 1 | 0,08% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
| Erséus (1997) | 1 | 0,08% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
| European Nucleotide Archive (2019) | 1 | 0,08% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
| Fauvel (1920) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fauvel (1926) | 1 | 0,08% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
| Gates (1943) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gee (1964) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gibson (2009) | 1 | 0,08% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
| Gidholm (1962) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gillet (1991) | 1 | 0,08% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
| Goulletquer (2016) | 1 | 0,08% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
| Gravina et al. (1998) | 1 | 0,08% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
| Grube (1878) | 1 | 0,08% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
| Harlock & Laubier (1966) | 1 | 0,08% | 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 | 0,08% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
| Hartman (1949) | 1 | 0,08% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
| Hartman (1954) | 1 | 0,08% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
| Hartman (1969) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Harvard University Museum & Morris P.J. (2020) | 1 | 0,08% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
| Hoagland (1920) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hoeksema et al. (2014) | 1 | 0,08% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
| Horst (1917) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Horst (1921) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Iroso (1921) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Izuka (1911) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jones (1962) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jourdan (2020) | 1 | 0,08% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
| Keferstein (1862) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kinberg (1865) | 1 | 0,08% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
| Lamarck (1818) | 1 | 0,08% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
| Laubier (1962) | 1 | 0,08% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
| Lavesque et al. (2017) | 1 | 0,08% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
| Linnaeus (1767) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Liu & Erséus (2017) | 1 | 0,08% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
| Maciolek (1985) | 1 | 0,08% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
| Maréchal & Trégarot (2012) | 1 | 0,08% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
| Marion & Robretzky (1875) | 1 | 0,08% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
| Martin et al. (1996) | 1 | 0,08% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
| Mesnil (1896) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Michaelsen (1913) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Monro (1938) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Müller (2004) | 1 | 0,08% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
| Nygren (2004) | 1 | 0,08% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
| Orrell (2019) | 1 | 0,08% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
| Pallas (1788) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Perkins (1980) | 1 | 0,08% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
| Perkins (1981) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pezy & Dauvin (2018) | 1 | 0,08% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
| Philippi (1844) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Piotrowski et al. (2024) | 1 | 0,08% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
| Plate (1916) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Prouzet (2015) | 1 | 0,08% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
| Questel & Le Quellec (2012) | 1 | 0,08% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
| Ramage et al. (2023) | 1 | 0,08% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
| Rathke (1843) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Reish (1968) | 1 | 0,08% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
| Rioja (1918) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Saint-joseph (1906) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Salazar-Vallejo (2022) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Schmarda (1861) | 1 | 0,08% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
| Solís-Weiss et al. (2004) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Southern (1914) | 1 | 0,08% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
| Stephenson (1915) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Straughan (1967) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Tchang (1931) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Treadwell (1931) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Uchida (1978) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Uicn et al. (2019) | 1 | 0,08% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
| Wang & Erseus (2004) | 1 | 0,08% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
| Wesenberg-Lund (1949) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Zibrowius (1971) | 1 | 0,08% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
