Annélides polychètes de métropole
621 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
Référence | Total | Valides | Espèces | Taxons terminaux | ||||
---|---|---|---|---|---|---|---|---|
nb | % | nb | % | nb | % | nb | % | |
Dauvin et al. (2003) | 567 | 15.24% | 423 | 33.84% | 419 | 33.84% | 419 | 33.82% |
Ifremer (2009) | 221 | 5.94% | 168 | 13.44% | 168 | 13.57% | 167 | 13.48% |
Nelson-Smith et al. (2014) | 179 | 4.81% | 105 | 8.4% | 105 | 8.48% | 101 | 8.15% |
Bourcier (1988) | 139 | 3.74% | 90 | 7.2% | 90 | 7.27% | 90 | 7.26% |
Godet et al. (2010) | 139 | 3.74% | 109 | 8.72% | 109 | 8.8% | 108 | 8.72% |
Pleijel (2007) | 82 | 2.2% | 52 | 4.16% | 52 | 4.2% | 51 | 4.12% |
Guille & Laubier (1966) | 73 | 1.96% | 44 | 3.52% | 44 | 3.55% | 44 | 3.55% |
Claparède (1864) | 63 | 1.69% | 10 | 0.8% | 10 | 0.81% | 10 | 0.81% |
Saint-Joseph (1888) | 50 | 1.34% | 17 | 1.36% | 17 | 1.37% | 17 | 1.37% |
Quatrefages (1866) | 48 | 1.29% | 24 | 1.92% | 24 | 1.94% | 24 | 1.94% |
Aguirrezabalaga & Gil (2009) | 43 | 1.16% | 22 | 1.76% | 20 | 1.62% | 22 | 1.78% |
Claparède (1863) | 42 | 1.13% | 14 | 1.12% | 14 | 1.13% | 14 | 1.13% |
Rignault & Chevallier (2017) | 41 | 1.1% | 35 | 2.8% | 35 | 2.83% | 35 | 2.82% |
Dean (2012) | 37 | 0.99% | 30 | 2.4% | 30 | 2.42% | 30 | 2.42% |
Breton (2014) | 34 | 0.91% | 32 | 2.56% | 32 | 2.58% | 32 | 2.58% |
Zibrowius (1968) | 31 | 0.83% | 9 | 0.72% | 9 | 0.73% | 8 | 0.65% |
Cabioch et al. (1968) | 28 | 0.75% | 22 | 1.76% | 22 | 1.78% | 22 | 1.78% |
Gout (1991) | 28 | 0.75% | 24 | 1.92% | 24 | 1.94% | 24 | 1.94% |
Nygren (2004) | 23 | 0.62% | 19 | 1.52% | 19 | 1.53% | 19 | 1.53% |
Martin (2011) | 22 | 0.59% | 18 | 1.44% | 18 | 1.45% | 18 | 1.45% |
Mesnil (1896) | 21 | 0.56% | 9 | 0.72% | 9 | 0.73% | 9 | 0.73% |
Bourmaud (2003) | 20 | 0.54% | 11 | 0.88% | 11 | 0.89% | 11 | 0.89% |
Cambert et al. (2011) | 20 | 0.54% | 17 | 1.36% | 17 | 1.37% | 17 | 1.37% |
Lavesque et al. (2019) | 20 | 0.54% | 20 | 1.6% | 20 | 1.62% | 20 | 1.61% |
Marion & Bobretzky (1875) | 20 | 0.54% | 10 | 0.8% | 10 | 0.81% | 10 | 0.81% |
Pearman et al. (2020) | 20 | 0.54% | 16 | 1.28% | 16 | 1.29% | 15 | 1.21% |
Sarda et al. (2009) | 19 | 0.51% | 9 | 0.72% | 9 | 0.73% | 8 | 0.65% |
Lavesque et al. (2021) | 18 | 0.48% | 18 | 1.44% | 18 | 1.45% | 18 | 1.45% |
Naim (1985) | 18 | 0.48% | 10 | 0.8% | 10 | 0.81% | 10 | 0.81% |
Arnaud (1974) | 17 | 0.46% | 11 | 0.88% | 11 | 0.89% | 11 | 0.89% |
Grube (1863) | 17 | 0.46% | 5 | 0.4% | 5 | 0.4% | 5 | 0.4% |
Tricart & Foubert (2000) | 17 | 0.46% | 11 | 0.88% | 11 | 0.89% | 10 | 0.81% |
Cazaux (1972) | 16 | 0.43% | 8 | 0.64% | 6 | 0.48% | 8 | 0.65% |
DCE-Benthos Network, French Mediterranen Lagoon Monitoring Network (2022) | 16 | 0.43% | 16 | 1.28% | 16 | 1.29% | 16 | 1.29% |
Lavesque et al. (2020) | 16 | 0.43% | 16 | 1.28% | 16 | 1.29% | 16 | 1.29% |
Barnich & Fiege (2001) | 15 | 0.4% | 0 | 0% | 0 | 0% | 0 | 0% |
Duchêne (1984) | 15 | 0.4% | 12 | 0.96% | 12 | 0.97% | 10 | 0.81% |
Fauvel (1950) | 15 | 0.4% | 10 | 0.8% | 10 | 0.81% | 10 | 0.81% |
Goulletquer (2016) | 15 | 0.4% | 14 | 1.12% | 14 | 1.13% | 14 | 1.13% |
Ifremer (2019) | 15 | 0.4% | 14 | 1.12% | 14 | 1.13% | 14 | 1.13% |
Saint-joseph (1898) | 14 | 0.38% | 4 | 0.32% | 4 | 0.32% | 4 | 0.32% |
Aguirrezabalaga & Ceberio (2005) | 13 | 0.35% | 10 | 0.8% | 10 | 0.81% | 10 | 0.81% |
Posidonia oceanica Delile. Recueil des Travaux de la Station Marine d'Endoume, 35(51): 43-105.">Harmelin (1964) | 13 | 0.35% | 12 | 0.96% | 12 | 0.97% | 12 | 0.97% |
Mao et al. (2020) | 13 | 0.35% | 12 | 0.96% | 12 | 0.97% | 12 | 0.97% |
Marion (1876) | 13 | 0.35% | 0 | 0% | 0 | 0% | 0 | 0% |
Poupin et al. (1999) | 13 | 0.35% | 10 | 0.8% | 10 | 0.81% | 10 | 0.81% |
Bellan (1972) | 12 | 0.32% | 5 | 0.4% | 5 | 0.4% | 5 | 0.4% |
Davoult et al. (1999) | 12 | 0.32% | 9 | 0.72% | 9 | 0.73% | 9 | 0.73% |
Aguirrezabalaga & Carrera-Parra (2006) | 11 | 0.3% | 11 | 0.88% | 11 | 0.89% | 11 | 0.89% |
Bigot (2006) | 11 | 0.3% | 10 | 0.8% | 10 | 0.81% | 10 | 0.81% |
Fauvel (1925) | 11 | 0.3% | 9 | 0.72% | 9 | 0.73% | 9 | 0.73% |
Gil (2011) | 11 | 0.3% | 10 | 0.8% | 10 | 0.81% | 10 | 0.81% |
Ifremer (2021) | 11 | 0.3% | 11 | 0.88% | 11 | 0.89% | 11 | 0.89% |
Olivier et al. (2011) | 11 | 0.3% | 11 | 0.88% | 11 | 0.89% | 11 | 0.89% |
Solís-Weiss & Alcántara (2009) | 11 | 0.3% | 10 | 0.8% | 10 | 0.81% | 10 | 0.81% |
Vonboletzky & Dohle (1967) | 11 | 0.3% | 7 | 0.56% | 7 | 0.57% | 5 | 0.4% |
Aguado et al. (2019) | 10 | 0.27% | 10 | 0.8% | 10 | 0.81% | 10 | 0.81% |
Bellan (1975) | 10 | 0.27% | 8 | 0.64% | 8 | 0.65% | 7 | 0.56% |
Boisseau & Lubet (1955) | 10 | 0.27% | 7 | 0.56% | 7 | 0.57% | 7 | 0.56% |
Gil (2011) | 10 | 0.27% | 9 | 0.72% | 9 | 0.73% | 9 | 0.73% |
Swedmark (1959) | 10 | 0.27% | 9 | 0.72% | 9 | 0.73% | 9 | 0.73% |
Barnich & Fiege (2000) | 9 | 0.24% | 8 | 0.64% | 8 | 0.65% | 8 | 0.65% |
Beauchamp (1914) | 9 | 0.24% | 2 | 0.16% | 2 | 0.16% | 2 | 0.16% |
Fauvel (1926) | 9 | 0.24% | 8 | 0.64% | 8 | 0.65% | 7 | 0.56% |
Hartman (1965) | 9 | 0.24% | 6 | 0.48% | 6 | 0.48% | 6 | 0.48% |
Hartmann-Schroder (1960) | 9 | 0.24% | 2 | 0.16% | 2 | 0.16% | 2 | 0.16% |
Mesnil & Caullery (1918) | 9 | 0.24% | 2 | 0.16% | 2 | 0.16% | 2 | 0.16% |
Caullery & Mesnil (1897) | 8 | 0.21% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Day (1961) | 8 | 0.21% | 8 | 0.64% | 8 | 0.65% | 7 | 0.56% |
Dewarumez et al. (2011) | 8 | 0.21% | 8 | 0.64% | 8 | 0.65% | 8 | 0.65% |
Ifremer (2020) | 8 | 0.21% | 8 | 0.64% | 8 | 0.65% | 8 | 0.65% |
Jouin (1966) | 8 | 0.21% | 2 | 0.16% | 2 | 0.16% | 2 | 0.16% |
Saint-Joseph (1894) | 8 | 0.21% | 2 | 0.16% | 2 | 0.16% | 2 | 0.16% |
Solís-Weiss et al. (2004) | 8 | 0.21% | 4 | 0.32% | 4 | 0.32% | 4 | 0.32% |
Zibrowius (1971) | 8 | 0.21% | 8 | 0.64% | 8 | 0.65% | 8 | 0.65% |
Chamberlin (1919) | 7 | 0.19% | 6 | 0.48% | 6 | 0.48% | 6 | 0.48% |
Fauvel (1952) | 7 | 0.19% | 4 | 0.32% | 4 | 0.32% | 4 | 0.32% |
Lavesque et al. (2020) | 7 | 0.19% | 7 | 0.56% | 7 | 0.57% | 7 | 0.56% |
Perkins (1981) | 7 | 0.19% | 4 | 0.32% | 4 | 0.32% | 4 | 0.32% |
Peyrot-Clausade (1976) | 7 | 0.19% | 6 | 0.48% | 6 | 0.48% | 6 | 0.48% |
Saint-joseph (1906) | 7 | 0.19% | 4 | 0.32% | 4 | 0.32% | 4 | 0.32% |
Sato (2013) | 7 | 0.19% | 0 | 0% | 0 | 0% | 0 | 0% |
Sato-Okoshi et al. (2022) | 7 | 0.19% | 7 | 0.56% | 7 | 0.57% | 7 | 0.56% |
Southern (1914) | 7 | 0.19% | 3 | 0.24% | 3 | 0.24% | 3 | 0.24% |
Treadwell (1943) | 7 | 0.19% | 0 | 0% | 0 | 0% | 0 | 0% |
Amoureux (1982) | 6 | 0.16% | 3 | 0.24% | 3 | 0.24% | 3 | 0.24% |
Audouin et al. (1833) | 6 | 0.16% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Bigot et al. (2006) | 6 | 0.16% | 5 | 0.4% | 5 | 0.4% | 5 | 0.4% |
Bush (1905) | 6 | 0.16% | 0 | 0% | 0 | 0% | 0 | 0% |
Conte (2023) | 6 | 0.16% | 6 | 0.48% | 6 | 0.48% | 6 | 0.48% |
Dattagupta (1981) | 6 | 0.16% | 6 | 0.48% | 6 | 0.48% | 6 | 0.48% |
Fourt et al. (2017) | 6 | 0.16% | 6 | 0.48% | 6 | 0.48% | 6 | 0.48% |
Lavesque et al. (2017) | 6 | 0.16% | 4 | 0.32% | 4 | 0.32% | 4 | 0.32% |
Magalhães et al. (2024) | 6 | 0.16% | 6 | 0.48% | 6 | 0.48% | 6 | 0.48% |
McIntosh (1885) | 6 | 0.16% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Meißner (2005) | 6 | 0.16% | 6 | 0.48% | 6 | 0.48% | 6 | 0.48% |
Miura (1980) | 6 | 0.16% | 6 | 0.48% | 6 | 0.48% | 6 | 0.48% |
Salazar-Vallejo (2014) | 6 | 0.16% | 6 | 0.48% | 6 | 0.48% | 6 | 0.48% |
Sikorski et al. (2021) | 6 | 0.16% | 6 | 0.48% | 6 | 0.48% | 6 | 0.48% |
Blake & Maciolek (1987) | 5 | 0.13% | 2 | 0.16% | 2 | 0.16% | 2 | 0.16% |
Boisseau (1952) | 5 | 0.13% | 4 | 0.32% | 4 | 0.32% | 4 | 0.32% |
Cerca et al. (2020) | 5 | 0.13% | 5 | 0.4% | 5 | 0.4% | 5 | 0.4% |
Davoult (1990) | 5 | 0.13% | 5 | 0.4% | 5 | 0.4% | 5 | 0.4% |
Etcheberry & Abraham (2009) | 5 | 0.13% | 2 | 0.16% | 2 | 0.16% | 2 | 0.16% |
Heinen (1911) | 5 | 0.13% | 0 | 0% | 0 | 0% | 0 | 0% |
Keferstein (1862) | 5 | 0.13% | 0 | 0% | 0 | 0% | 0 | 0% |
Linnaeus (1758) | 5 | 0.13% | 2 | 0.16% | 2 | 0.16% | 2 | 0.16% |
Westheide (1973) | 5 | 0.13% | 4 | 0.32% | 4 | 0.32% | 4 | 0.32% |
Barnich & Fiege (2009) | 4 | 0.11% | 4 | 0.32% | 4 | 0.32% | 4 | 0.32% |
Breton et al. (2003) | 4 | 0.11% | 2 | 0.16% | 2 | 0.16% | 2 | 0.16% |
Carrera-Parra (2006) | 4 | 0.11% | 4 | 0.32% | 4 | 0.32% | 4 | 0.32% |
Carrera-Parra (2006) | 4 | 0.11% | 3 | 0.24% | 3 | 0.24% | 3 | 0.24% |
Caullery & Mesnil (1896) | 4 | 0.11% | 2 | 0.16% | 2 | 0.16% | 2 | 0.16% |
Caullery & Mesnil (1916) | 4 | 0.11% | 0 | 0% | 0 | 0% | 0 | 0% |
Caziot (1921) | 4 | 0.11% | 2 | 0.16% | 2 | 0.16% | 2 | 0.16% |
Claparède (1868) | 4 | 0.11% | 2 | 0.16% | 2 | 0.16% | 2 | 0.16% |
Claparède (1870) | 4 | 0.11% | 0 | 0% | 0 | 0% | 0 | 0% |
Collectif & Bebest (2019) | 4 | 0.11% | 4 | 0.32% | 4 | 0.32% | 4 | 0.32% |
Costa (1861) | 4 | 0.11% | 0 | 0% | 0 | 0% | 0 | 0% |
Day (1960) | 4 | 0.11% | 3 | 0.24% | 3 | 0.24% | 3 | 0.24% |
Fabricius (1780) | 4 | 0.11% | 0 | 0% | 0 | 0% | 0 | 0% |
Fauvel (1923) | 4 | 0.11% | 0 | 0% | 0 | 0% | 0 | 0% |
Fauvel (1926) | 4 | 0.11% | 2 | 0.16% | 2 | 0.16% | 2 | 0.16% |
Gidholm (1962) | 4 | 0.11% | 2 | 0.16% | 2 | 0.16% | 2 | 0.16% |
Glémarec (1966) | 4 | 0.11% | 4 | 0.32% | 4 | 0.32% | 4 | 0.32% |
Herpin (1925) | 4 | 0.11% | 4 | 0.32% | 4 | 0.32% | 4 | 0.32% |
Horst (1908) | 4 | 0.11% | 0 | 0% | 0 | 0% | 0 | 0% |
Ifremer (2024) | 4 | 0.11% | 4 | 0.32% | 4 | 0.32% | 4 | 0.32% |
Iroso (1921) | 4 | 0.11% | 0 | 0% | 0 | 0% | 0 | 0% |
Izuka (1912) | 4 | 0.11% | 0 | 0% | 0 | 0% | 0 | 0% |
Latry et al. (2024) | 4 | 0.11% | 4 | 0.32% | 1 | 0.08% | 4 | 0.32% |
Levi (1953) | 4 | 0.11% | 2 | 0.16% | 2 | 0.16% | 2 | 0.16% |
Linnaeus (1767) | 4 | 0.11% | 2 | 0.16% | 2 | 0.16% | 2 | 0.16% |
Mackie (1984) | 4 | 0.11% | 4 | 0.32% | 4 | 0.32% | 4 | 0.32% |
Meyer et al. (2007) | 4 | 0.11% | 2 | 0.16% | 2 | 0.16% | 2 | 0.16% |
Müller (1776) | 4 | 0.11% | 0 | 0% | 0 | 0% | 0 | 0% |
Naville (1933) | 4 | 0.11% | 4 | 0.32% | 4 | 0.32% | 4 | 0.32% |
Quatrefages (1843) | 4 | 0.11% | 4 | 0.32% | 4 | 0.32% | 4 | 0.32% |
Ruta & Pleijel (2006) | 4 | 0.11% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Saint-Joseph (1887) | 4 | 0.11% | 2 | 0.16% | 2 | 0.16% | 2 | 0.16% |
Salazar-Vallejo (2018) | 4 | 0.11% | 2 | 0.16% | 2 | 0.16% | 2 | 0.16% |
Wesenberg-Lund (1949) | 4 | 0.11% | 0 | 0% | 0 | 0% | 0 | 0% |
Arias & Paxton (2015) | 3 | 0.08% | 3 | 0.24% | 3 | 0.24% | 3 | 0.24% |
Augener (1918) | 3 | 0.08% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Bellan & Reys (1967) | 3 | 0.08% | 3 | 0.24% | 3 | 0.24% | 3 | 0.24% |
Bhaud & Gremare (1991) | 3 | 0.08% | 3 | 0.24% | 3 | 0.24% | 3 | 0.24% |
Blake & Kudenov (1978) | 3 | 0.08% | 3 | 0.24% | 3 | 0.24% | 3 | 0.24% |
Blake (2016) | 3 | 0.08% | 3 | 0.24% | 3 | 0.24% | 3 | 0.24% |
Bonifacio et al. (2015) | 3 | 0.08% | 3 | 0.24% | 3 | 0.24% | 3 | 0.24% |
Callier et al. (2009) | 3 | 0.08% | 2 | 0.16% | 2 | 0.16% | 2 | 0.16% |
Caullery & Mesnil (1915) | 3 | 0.08% | 3 | 0.24% | 3 | 0.24% | 3 | 0.24% |
Caullery (1915) | 3 | 0.08% | 3 | 0.24% | 3 | 0.24% | 3 | 0.24% |
Cazaux (1985) | 3 | 0.08% | 3 | 0.24% | 3 | 0.24% | 3 | 0.24% |
Cha et al. (1997) | 3 | 0.08% | 3 | 0.24% | 3 | 0.24% | 3 | 0.24% |
Charles et al. (2003) | 3 | 0.08% | 3 | 0.24% | 3 | 0.24% | 3 | 0.24% |
Chasse & Picard (1968) | 3 | 0.08% | 3 | 0.24% | 3 | 0.24% | 3 | 0.24% |
Cognetti (1957) | 3 | 0.08% | 0 | 0% | 0 | 0% | 0 | 0% |
Cognetti (1961) | 3 | 0.08% | 0 | 0% | 0 | 0% | 0 | 0% |
Dauvin (1978) | 3 | 0.08% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Day (1963) | 3 | 0.08% | 2 | 0.16% | 2 | 0.16% | 2 | 0.16% |
delle Chiaje (1828) | 3 | 0.08% | 0 | 0% | 0 | 0% | 0 | 0% |
Dujardin (1851) | 3 | 0.08% | 0 | 0% | 0 | 0% | 0 | 0% |
Ehlers (1864) | 3 | 0.08% | 2 | 0.16% | 2 | 0.16% | 2 | 0.16% |
Fage & Legendre (1933) | 3 | 0.08% | 3 | 0.24% | 3 | 0.24% | 3 | 0.24% |
Fauvel (1913) | 3 | 0.08% | 3 | 0.24% | 3 | 0.24% | 3 | 0.24% |
Fauvel (1914) | 3 | 0.08% | 3 | 0.24% | 3 | 0.24% | 3 | 0.24% |
Fauvel (1923) | 3 | 0.08% | 0 | 0% | 0 | 0% | 0 | 0% |
Fonseca-Genevois & Cazaux (1987) | 3 | 0.08% | 3 | 0.24% | 3 | 0.24% | 3 | 0.24% |
Fransen (1983) | 3 | 0.08% | 3 | 0.24% | 3 | 0.24% | 3 | 0.24% |
Giard (1904) | 3 | 0.08% | 0 | 0% | 0 | 0% | 0 | 0% |
Gillandt (1979) | 3 | 0.08% | 0 | 0% | 0 | 0% | 0 | 0% |
Gillet (1991) | 3 | 0.08% | 3 | 0.24% | 3 | 0.24% | 3 | 0.24% |
Glémarec & Monniot (1966) | 3 | 0.08% | 2 | 0.16% | 2 | 0.16% | 2 | 0.16% |
Gravier (1896) | 3 | 0.08% | 2 | 0.16% | 2 | 0.16% | 2 | 0.16% |
Grube (1860) | 3 | 0.08% | 0 | 0% | 0 | 0% | 0 | 0% |
Guérin & Kerambrun (1985) | 3 | 0.08% | 3 | 0.24% | 3 | 0.24% | 3 | 0.24% |
Guerin (1990) | 3 | 0.08% | 3 | 0.24% | 3 | 0.24% | 3 | 0.24% |
Harris (1969) | 3 | 0.08% | 3 | 0.24% | 3 | 0.24% | 3 | 0.24% |
Haswell (1920) | 3 | 0.08% | 2 | 0.16% | 2 | 0.16% | 2 | 0.16% |
Ifremer (2022) | 3 | 0.08% | 3 | 0.24% | 3 | 0.24% | 3 | 0.24% |
Jirkov et al. (2018) | 3 | 0.08% | 3 | 0.24% | 3 | 0.24% | 3 | 0.24% |
Johnson (1901) | 3 | 0.08% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Jolly et al. (2013) | 3 | 0.08% | 0 | 0% | 0 | 0% | 0 | 0% |
Kuznetsov et al. (2021) | 3 | 0.08% | 3 | 0.24% | 3 | 0.24% | 3 | 0.24% |
Labrune et al. (2019) | 3 | 0.08% | 3 | 0.24% | 3 | 0.24% | 3 | 0.24% |
Langerhans (1884) | 3 | 0.08% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Laubier (1974) | 3 | 0.08% | 3 | 0.24% | 3 | 0.24% | 3 | 0.24% |
Levi (1954) | 3 | 0.08% | 0 | 0% | 0 | 0% | 0 | 0% |
Maciolek (1985) | 3 | 0.08% | 3 | 0.24% | 3 | 0.24% | 3 | 0.24% |
Maciolek (2000) | 3 | 0.08% | 3 | 0.24% | 3 | 0.24% | 3 | 0.24% |
Mackie (1994) | 3 | 0.08% | 3 | 0.24% | 3 | 0.24% | 3 | 0.24% |
Martin & Romano (2021) | 3 | 0.08% | 3 | 0.24% | 3 | 0.24% | 3 | 0.24% |
Martin et al. (2022) | 3 | 0.08% | 2 | 0.16% | 2 | 0.16% | 2 | 0.16% |
Massé et al. (2023) | 3 | 0.08% | 3 | 0.24% | 2 | 0.16% | 3 | 0.24% |
Michaelsen (1897) | 3 | 0.08% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Montagu (1819) | 3 | 0.08% | 0 | 0% | 0 | 0% | 0 | 0% |
Olivier et al. (2015) | 3 | 0.08% | 3 | 0.24% | 3 | 0.24% | 3 | 0.24% |
Pleijel (1987) | 3 | 0.08% | 3 | 0.24% | 3 | 0.24% | 3 | 0.24% |
Pleijel (1993) | 3 | 0.08% | 0 | 0% | 0 | 0% | 0 | 0% |
Prenant (1924) | 3 | 0.08% | 0 | 0% | 0 | 0% | 0 | 0% |
Quievreux (1963) | 3 | 0.08% | 0 | 0% | 0 | 0% | 0 | 0% |
Remane (1925) | 3 | 0.08% | 3 | 0.24% | 3 | 0.24% | 3 | 0.24% |
Risso (1826) | 3 | 0.08% | 3 | 0.24% | 3 | 0.24% | 3 | 0.24% |
Rullier (1972) | 3 | 0.08% | 0 | 0% | 0 | 0% | 0 | 0% |
Salazar-Vallejo et al. (2007) | 3 | 0.08% | 3 | 0.24% | 3 | 0.24% | 3 | 0.24% |
Salazar-Vallejo (2017) | 3 | 0.08% | 3 | 0.24% | 3 | 0.24% | 3 | 0.24% |
Salazar-Vallejo (2020) | 3 | 0.08% | 2 | 0.16% | 2 | 0.16% | 2 | 0.16% |
San et al. (1996) | 3 | 0.08% | 3 | 0.24% | 3 | 0.24% | 3 | 0.24% |
San et al. (2000) | 3 | 0.08% | 3 | 0.24% | 3 | 0.24% | 3 | 0.24% |
Savigny (1822) | 3 | 0.08% | 2 | 0.16% | 2 | 0.16% | 2 | 0.16% |
Siewing (1955) | 3 | 0.08% | 0 | 0% | 0 | 0% | 0 | 0% |
Söderström (1920) | 3 | 0.08% | 3 | 0.24% | 3 | 0.24% | 3 | 0.24% |
Sun & Yang (1981) | 3 | 0.08% | 0 | 0% | 0 | 0% | 0 | 0% |
Teixeira et al. (2022) | 3 | 0.08% | 3 | 0.24% | 3 | 0.24% | 3 | 0.24% |
Teixeira et al. (2023) | 3 | 0.08% | 3 | 0.24% | 3 | 0.24% | 3 | 0.24% |
Villalobos-Guerrero & Carrera-Parra (2015) | 3 | 0.08% | 3 | 0.24% | 3 | 0.24% | 3 | 0.24% |
Von & Nordheim (1992) | 3 | 0.08% | 0 | 0% | 0 | 0% | 0 | 0% |
Zhadan et al. (2023) | 3 | 0.08% | 3 | 0.24% | 3 | 0.24% | 3 | 0.24% |
Aguirrezabalaga & Ceberio (2003) | 2 | 0.05% | 2 | 0.16% | 2 | 0.16% | 2 | 0.16% |
Aguirrezabalaga et al. (2001) | 2 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
Apstein (19OO) | 2 | 0.05% | 2 | 0.16% | 2 | 0.16% | 2 | 0.16% |
Ayata et al. (2009) | 2 | 0.05% | 2 | 0.16% | 2 | 0.16% | 2 | 0.16% |
Bachelet & Laubier (1994) | 2 | 0.05% | 2 | 0.16% | 2 | 0.16% | 2 | 0.16% |
Banse (1956) | 2 | 0.05% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Banse (1957) | 2 | 0.05% | 2 | 0.16% | 2 | 0.16% | 2 | 0.16% |
Barnich et al. (2000) | 2 | 0.05% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Bellan & Costa (1988) | 2 | 0.05% | 2 | 0.16% | 2 | 0.16% | 2 | 0.16% |
Bellan (1960) | 2 | 0.05% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Ben-eliahu (1972) | 2 | 0.05% | 2 | 0.16% | 2 | 0.16% | 2 | 0.16% |
Bhaud et al. (1994) | 2 | 0.05% | 2 | 0.16% | 2 | 0.16% | 2 | 0.16% |
Bhaud et al. (2002) | 2 | 0.05% | 2 | 0.16% | 2 | 0.16% | 2 | 0.16% |
Blake & Lavesque (2017) | 2 | 0.05% | 2 | 0.16% | 2 | 0.16% | 2 | 0.16% |
Blanchet et al. (2004) | 2 | 0.05% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Brito et al. (2000) | 2 | 0.05% | 2 | 0.16% | 2 | 0.16% | 2 | 0.16% |
Cantone & Bellan (1996) | 2 | 0.05% | 2 | 0.16% | 2 | 0.16% | 2 | 0.16% |
Carazzi (1893) | 2 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
Castelli et al. (1987) | 2 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
Caullery (1944) | 2 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
Cépède (1814) | 2 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
Cépède (1914) | 2 | 0.05% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Chamberlin (1919) | 2 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
Charrier (1924) | 2 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
Claparède (1868) | 2 | 0.05% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Clavier (1983) | 2 | 0.05% | 2 | 0.16% | 2 | 0.16% | 2 | 0.16% |
Clavier (1984) | 2 | 0.05% | 2 | 0.16% | 2 | 0.16% | 2 | 0.16% |
Dahlgren & Pleijel (1995) | 2 | 0.05% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Dauvin & Lee (1983) | 2 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
Day (1954) | 2 | 0.05% | 2 | 0.16% | 2 | 0.16% | 2 | 0.16% |
Delle Chiaje (1841-1844) | 2 | 0.05% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Desbruyeres & Laubier (1977) | 2 | 0.05% | 2 | 0.16% | 2 | 0.16% | 2 | 0.16% |
Dewarumez et al. (1992) | 2 | 0.05% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Droual et al. (2024) | 2 | 0.05% | 2 | 0.16% | 2 | 0.16% | 2 | 0.16% |
Dubois et al. (2007) | 2 | 0.05% | 2 | 0.16% | 2 | 0.16% | 2 | 0.16% |
Ehlers (1908) | 2 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
Ehrhold et al. (2010) | 2 | 0.05% | 2 | 0.16% | 2 | 0.16% | 2 | 0.16% |
Eibye-Jacobsen (1987) | 2 | 0.05% | 2 | 0.16% | 2 | 0.16% | 2 | 0.16% |
Faasse & Giangrande (2012) | 2 | 0.05% | 2 | 0.16% | 2 | 0.16% | 2 | 0.16% |
Fauchald et al. (2012) | 2 | 0.05% | 2 | 0.16% | 2 | 0.16% | 2 | 0.16% |
Fauchald (1975) | 2 | 0.05% | 2 | 0.16% | 2 | 0.16% | 2 | 0.16% |
Fauvel (1909) | 2 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
Fauvel (1916) | 2 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
Fauvel (1924) | 2 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
Fauvel (1927) | 2 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
Fauvel (1953) | 2 | 0.05% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Fitzhugh (1990) | 2 | 0.05% | 2 | 0.16% | 2 | 0.16% | 2 | 0.16% |
Foster (1971) | 2 | 0.05% | 2 | 0.16% | 2 | 0.16% | 2 | 0.16% |
Gaillande (1970) | 2 | 0.05% | 2 | 0.16% | 2 | 0.16% | 2 | 0.16% |
Gallien (1936) | 2 | 0.05% | 2 | 0.16% | 2 | 0.16% | 2 | 0.16% |
George & Petersen (1991) | 2 | 0.05% | 2 | 0.16% | 2 | 0.16% | 2 | 0.16% |
Gravier & Dantan (1934) | 2 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
Gravier (1900) | 2 | 0.05% | 2 | 0.16% | 2 | 0.16% | 2 | 0.16% |
Gravier (1900) | 2 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
Grube (1846) | 2 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
Gruet (1985) | 2 | 0.05% | 2 | 0.16% | 2 | 0.16% | 2 | 0.16% |
Guerin (1970) | 2 | 0.05% | 2 | 0.16% | 2 | 0.16% | 2 | 0.16% |
Guizien et al. (2006) | 2 | 0.05% | 2 | 0.16% | 2 | 0.16% | 2 | 0.16% |
Hall-spencer et al. (2018) | 2 | 0.05% | 2 | 0.16% | 2 | 0.16% | 2 | 0.16% |
Harmelin (1968) | 2 | 0.05% | 2 | 0.16% | 2 | 0.16% | 2 | 0.16% |
Hartman (1951) | 2 | 0.05% | 2 | 0.16% | 2 | 0.16% | 2 | 0.16% |
Hartmann-Schroder (1977) | 2 | 0.05% | 2 | 0.16% | 2 | 0.16% | 2 | 0.16% |
Haswell (1885) | 2 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
Hay-Schmidt (1995) | 2 | 0.05% | 2 | 0.16% | 2 | 0.16% | 2 | 0.16% |
He (1987) | 2 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
Ifremer (2023) | 2 | 0.05% | 2 | 0.16% | 1 | 0.08% | 2 | 0.16% |
Imajima (1990) | 2 | 0.05% | 2 | 0.16% | 2 | 0.16% | 2 | 0.16% |
Izuka (1914) | 2 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
Jones (1956) | 2 | 0.05% | 2 | 0.16% | 2 | 0.16% | 2 | 0.16% |
Jouin (1963) | 2 | 0.05% | 2 | 0.16% | 2 | 0.16% | 2 | 0.16% |
Jouin (1966) | 2 | 0.05% | 2 | 0.16% | 2 | 0.16% | 2 | 0.16% |
Jourde et al. (2020) | 2 | 0.05% | 2 | 0.16% | 2 | 0.16% | 2 | 0.16% |
Katzmann et al. (1974) | 2 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
Kinberg (1856) | 2 | 0.05% | 2 | 0.16% | 2 | 0.16% | 2 | 0.16% |
Kinberg ([1867]) | 2 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
Knight-jones & Knight-jones (1977) | 2 | 0.05% | 1 | 0.08% | 0 | 0% | 1 | 0.08% |
Koechlin (1977) | 2 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
Laborda & Vieitez (1984) | 2 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
Lagadeuc et al. (1990) | 2 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
Langerhans (1879) | 2 | 0.05% | 2 | 0.16% | 2 | 0.16% | 2 | 0.16% |
Laubier & Ramos (1973) | 2 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
Laubier (1961) | 2 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
Laubier (1961) | 2 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
Laubier (1963) | 2 | 0.05% | 2 | 0.16% | 2 | 0.16% | 2 | 0.16% |
Lavesque et al. (2015) | 2 | 0.05% | 2 | 0.16% | 2 | 0.16% | 2 | 0.16% |
Lavesque et al. (2017) | 2 | 0.05% | 2 | 0.16% | 2 | 0.16% | 2 | 0.16% |
Lavesque et al. (2020) | 2 | 0.05% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Licher (1994) | 2 | 0.05% | 2 | 0.16% | 2 | 0.16% | 2 | 0.16% |
Mackie et al. (2005) | 2 | 0.05% | 2 | 0.16% | 2 | 0.16% | 2 | 0.16% |
Magagnini (1966) | 2 | 0.05% | 2 | 0.16% | 2 | 0.16% | 2 | 0.16% |
Malaquin (1893) | 2 | 0.05% | 2 | 0.16% | 2 | 0.16% | 2 | 0.16% |
Malmgren (1867) | 2 | 0.05% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Marenzeller (1879) | 2 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
Marenzeller (1884) | 2 | 0.05% | 2 | 0.16% | 2 | 0.16% | 2 | 0.16% |
Marinescu (1964) | 2 | 0.05% | 2 | 0.16% | 2 | 0.16% | 2 | 0.16% |
Marion (1875) | 2 | 0.05% | 2 | 0.16% | 2 | 0.16% | 2 | 0.16% |
Marion (1883) | 2 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
Martin et al. (2020) | 2 | 0.05% | 2 | 0.16% | 2 | 0.16% | 2 | 0.16% |
Mazieres et al. (2017) | 2 | 0.05% | 2 | 0.16% | 2 | 0.16% | 2 | 0.16% |
McIntosh (1876) | 2 | 0.05% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Mcintosh (1908) | 2 | 0.05% | 2 | 0.16% | 2 | 0.16% | 2 | 0.16% |
Medernach et al. (2000) | 2 | 0.05% | 2 | 0.16% | 2 | 0.16% | 2 | 0.16% |
Mesnil & Caullery (1917) | 2 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
Mesnil (1893) | 2 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
Mesnil (1897) | 2 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
M'intosh (1876) | 2 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
Müller (2004) | 2 | 0.05% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Olivier et al. (2012) | 2 | 0.05% | 2 | 0.16% | 2 | 0.16% | 2 | 0.16% |
Paik (1973) | 2 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
Pearson (1970) | 2 | 0.05% | 2 | 0.16% | 2 | 0.16% | 2 | 0.16% |
Peres & Rancurel (1948) | 2 | 0.05% | 2 | 0.16% | 2 | 0.16% | 2 | 0.16% |
Pflugfelder (1933) | 2 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
Pierantoni (1908) | 2 | 0.05% | 2 | 0.16% | 2 | 0.16% | 2 | 0.16% |
Potts (1910) | 2 | 0.05% | 2 | 0.16% | 2 | 0.16% | 2 | 0.16% |
Potts (1914) | 2 | 0.05% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Prenant (1925) | 2 | 0.05% | 2 | 0.16% | 2 | 0.16% | 2 | 0.16% |
Prenant (1926) | 2 | 0.05% | 2 | 0.16% | 2 | 0.16% | 2 | 0.16% |
Purschke & Joerdens (2007) | 2 | 0.05% | 2 | 0.16% | 2 | 0.16% | 2 | 0.16% |
Purschke (2002) | 2 | 0.05% | 2 | 0.16% | 2 | 0.16% | 2 | 0.16% |
Questel (2020) | 2 | 0.05% | 2 | 0.16% | 2 | 0.16% | 2 | 0.16% |
Radashevsky et al. (2022) | 2 | 0.05% | 2 | 0.16% | 2 | 0.16% | 2 | 0.16% |
Rathke (1843) | 2 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
Reish (1959) | 2 | 0.05% | 2 | 0.16% | 2 | 0.16% | 2 | 0.16% |
Renier (1804) | 2 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
Revel et al. (2024) | 2 | 0.05% | 2 | 0.16% | 2 | 0.16% | 2 | 0.16% |
Rice et al. (2008) | 2 | 0.05% | 2 | 0.16% | 2 | 0.16% | 2 | 0.16% |
Riisgård et al. (2002) | 2 | 0.05% | 2 | 0.16% | 2 | 0.16% | 2 | 0.16% |
Rioja (1918) | 2 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
Rota (1998) | 2 | 0.05% | 2 | 0.16% | 2 | 0.16% | 2 | 0.16% |
Ruta et al. (2007) | 2 | 0.05% | 2 | 0.16% | 2 | 0.16% | 2 | 0.16% |
Saint-joseph (1895) | 2 | 0.05% | 2 | 0.16% | 2 | 0.16% | 2 | 0.16% |
Saint-joseph (1899) | 2 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
Salazar-vallejo (2008) | 2 | 0.05% | 2 | 0.16% | 2 | 0.16% | 2 | 0.16% |
San et al. (1990) | 2 | 0.05% | 2 | 0.16% | 2 | 0.16% | 2 | 0.16% |
Sarto et al. (2000) | 2 | 0.05% | 2 | 0.16% | 2 | 0.16% | 2 | 0.16% |
Schneider (1887) | 2 | 0.05% | 2 | 0.16% | 2 | 0.16% | 2 | 0.16% |
Southern (1909) | 2 | 0.05% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Southward (1977) | 2 | 0.05% | 2 | 0.16% | 2 | 0.16% | 2 | 0.16% |
Swedmark (1952) | 2 | 0.05% | 2 | 0.16% | 2 | 0.16% | 2 | 0.16% |
Teramoto et al. (2013) | 2 | 0.05% | 2 | 0.16% | 2 | 0.16% | 2 | 0.16% |
Treadwell (1943) | 2 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
Verrill (1876) | 2 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
Von Nordheim (1989) | 2 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
Webster (1879) | 2 | 0.05% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Wesenberg-lund (1936) | 2 | 0.05% | 2 | 0.16% | 2 | 0.16% | 2 | 0.16% |
Westheide & Nordheim von (1985) | 2 | 0.05% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Westheide (1967) | 2 | 0.05% | 2 | 0.16% | 2 | 0.16% | 2 | 0.16% |
Wilson (1958) | 2 | 0.05% | 2 | 0.16% | 2 | 0.16% | 2 | 0.16% |
Zhadan et al. (2012) | 2 | 0.05% | 2 | 0.16% | 2 | 0.16% | 2 | 0.16% |
Zibrowius (1968) | 2 | 0.05% | 2 | 0.16% | 2 | 0.16% | 1 | 0.08% |
Allspach & Neuhaus (2021) | 1 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Cahiers de Biologie Marine, 18: 391-411.">Amoureux (1977) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Amouroux (1974) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Annenkova (1928) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Arias & Paxton (2013) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Armenante (1903) | 1 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Augener (1913) | 1 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Augener (1914) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Bachelet (1990) | 1 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Banse & Hobson (1968) | 1 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Banse (1959) | 1 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Bartoli (1974) | 1 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Bastida-zavala et al. (2003) | 1 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Bellan (1971) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Bergstrom (1916) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Berkeley & Berkeley (1950) | 1 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Berkeley (1927) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Bhaud & Duchene (1976) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Bhaud (1969) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Blake & Maciolek (1984) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Blake & Woodwick (1971) | 1 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Bobin & Prenant (1953) | 1 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Bocquet & Stock (1958) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Bonnet & Jullien (1936) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Bonse et al. (1996) | 1 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Bosc (1802) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Boyle & Seaver (2010) | 1 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Breton & Vincent (1999) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Buchanan (1890) | 1 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Cantone (1981) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Carrington (1865) | 1 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Castelli (1985) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Caullery & Mesnil (1918) | 1 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Chamberlin (1920) | 1 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Charles et al. (2014) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Cinar & Giangrande (2018) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Cognetti (1953) | 1 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Conté (2022) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Daguzan (1969) | 1 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Dauvin et al. (2007) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Dehorne (1933) | 1 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Delachaux (1921) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Delle & Chiaje (1828) | 1 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Despartes & Theodorides (1986) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Devin et al. (2006) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Diaz & Cuzange (2009) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Dole-Olivier et al. (2015) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Duchêne (1984) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Dujardin (1839) | 1 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Ehlers (1868) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
. Memoirs of the Museum of Comparative Zoology at Harvard College. 15: 335 pp.">Ehlers (1887) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Ehlers (1901) | 1 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Eisig (1887) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Eliason (1920) | 1 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Eliason (1955) | 1 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Eliason (1962) | 1 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Elosegui et al. (1998) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
European Nucleotide Archive (2019) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Fage & Legendre (1925) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Faucheux (2023) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Fauvel (1895) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Fauvel (1910) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Fauvel (1920) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Fauvel (1923) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Fauvel (1928) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Filippi (1861) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Fischer (1925) | 1 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Fitzhugh et al. (1994) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Foettinger (1884) | 1 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Fraipont (1887) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Friedrich (1937) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Friedrich (1939) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Friedrich (1950) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Fruget & Beisel (2016) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Gadeau de Kerville (1900) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Garrec et al. (2016) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Gaudy & Thomassin (2006) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Gee & Knight-Jones (1962) | 1 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Gee (1964) | 1 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Giangrande et al. (2017) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Giard (1878) | 1 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Gillet (2001) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Glémarec (1969) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Gouillieux et al. (2022) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Gravina et al. (1998) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Greca (1946) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Greeff (1879) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Grémare et al. (1998) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Grémare et al. (1998) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Grube (1840) | 1 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Grube (1855) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Grube (1862) | 1 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Grube (1870) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Gruet et al. (1976) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Guyonnet & Borg (2015) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Hannerz (1956) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Hansen (1879) | 1 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Harlock & Laubier (1966) | 1 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Hartman (1936) | 1 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Hartman (1955) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Hartman (1961) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Hartman (1969) | 1 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Hartmann (1940) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Hartmann-schroder (1962) | 1 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Hartmann-schroder (1963) | 1 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Heath (1930) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Hempelmann (1906) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Hérubel (1903) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Hessle (1925) | 1 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Hoagland (1920) | 1 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Horst (1917) | 1 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Horst (1919) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Horst (1920) | 1 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Hugo et al. (2016) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Huxley (1855) | 1 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Ikeda (1924) | 1 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Imajima & Hartman (1964) | 1 | 0.03% | 1 | 0.08% | 0 | 0% | 1 | 0.08% |
Izuka (1911) | 1 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Jagersten (1940) | 1 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Jägersten 1952) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Johnston (1838) | 1 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Johnston (1839) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Johnston (1840) | 1 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Johnston (1840) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Jouin (1973) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Jourde et al. (2012) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Julien (1928) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Keferstein (1861) | 1 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Kelaher & Rouse (2003) | 1 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Knöllner (1934) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Kükenthal (1887) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Labbé & Racovitza (1897) | 1 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Labrune et al. (2007) | 1 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Lamarck (1818) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Langerhans (1880) | 1 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Lankester (1866) | 1 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Laubier (1962) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Lavesque et al. (2025) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Levinsen (1893) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Linnaeus (1767) | 1 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Lizé (2021) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Loc'h et al. (2008) | 1 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
López et al. (1997) | 1 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Mackay & Gibson (1999) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Mackie (1991) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Malmgren (1865) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Malmgren (1866) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Marcano & Bhaud (1995) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Marenzeller (1874) | 1 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Marenzeller (1875) | 1 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Marenzeller (1895) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Marion & Robretzky (1875) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Martin et al. (1996) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Martin (1996) | 1 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Martins et al. (2012) | 1 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
McIntosh (1897) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Mcintosh (1923) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Mcintosh (1924) | 1 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Meissner et al. (2020) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Meyer (1929) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
MGnify (2017) | 1 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Miura & Shirayama (1992) | 1 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
, 12: 59-198.">Monro (1936) | 1 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Monro (1938) | 1 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Montagu (1813) | 1 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Moore (1907) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Proceedings of the Academy of Natural Sciences of Philadelphia. 62: 328-402.">Moore (1910) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Mortimer et al. (2021) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Müller (1858) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Nebout et al. (2011) | 1 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Nolte (1938) | 1 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Nygren et al. (2010) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
O'Connor (1987) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Okuda (1934) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Orrell (2019) | 1 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Orrhage & Sundberg (1990) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Oug (2011) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Pallas (1766) | 1 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Pallas (1774) | 1 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Pallas (1788) | 1 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Pezy & Dauvin (2018) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Philippi (1844) | 1 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Pires et al. (2010) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Pixell (1913) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Pleijel (2001) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Puytorac (1955) | 1 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Puytorac (1955) | 1 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Quatrefages (1850) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Quatrefages (1866) | 1 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Quatrefages (1866) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Questel & Le Quellec (2012) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Radashevsky (2005) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Ramos (1976) | 1 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Rasmussen (1973) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Ravara et al. (2004) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Reisinger (1925) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Remane (1928) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Renaud-Mornant & Gourbault (1984) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Renaud-Mornant et al. (1971) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Rioja (1917) | 1 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Rioja (1917) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Rioja (1918) | 1 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Rosa (1908) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Rosa (1908) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Rouse (1993) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Saint-Joseph (1896) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Saint-Joseph (1899) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Saiz-Salinas & Amouroux (2010) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Salensky (1907) | 1 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
San et al. (1988) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Sars (1872) | 1 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Schmidt (1848) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Schneider (1868) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Serrano & al. (2003) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Sikorskii (1999) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Sikorskii (2002) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Simboura et al. (2010) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Southern (1921) | 1 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Southward (1956) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Spilmont et al. (2018) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Straughan (1967) | 1 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Tamai (1986) | 1 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Tchang (1931) | 1 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Teixeira et al. (2022) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Théel (1879) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Theodorides & Desportes (1978) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Thomassin (1970) | 1 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Thompson (1844) | 1 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Tiralongo et al. (2022) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Treadwell (1921) | 1 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Treadwell (1926) | 1 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Treadwell (1931) | 1 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Treadwell (1931) | 1 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Treandwell (1932) | 1 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Uchida (1978) | 1 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Van Beneden P. J. & Hesse C. E. (1863) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Vejdovsky (1878) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Verril (1881) | 1 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Warren & Parker (1994) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Warren et al. (1994) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Warren (1976) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Wesenberg-Lund (1939) | 1 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Westheide (1965) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Westheide (1967) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Wilke (1953) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Wilson (1959) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Wilson (1988) | 1 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Wirén (1883) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Wolff (1973) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Worsaae et al. (2009) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Worsaae et al. (2019) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Zenetos et al. (2012) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |
Zibrowius (1978) | 1 | 0.03% | 1 | 0.08% | 1 | 0.08% | 1 | 0.08% |