Espèces de Terre Adélie
Toutes les espèces de Terre Adélie
539 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) | 582 | 19,56% | 360 | 31,17% | 351 | 31,74% | 359 | 32,26% |
Manguin (1960) | 261 | 8,77% | 180 | 15,58% | 129 | 11,66% | 171 | 15,36% |
Bellan-Santini (1972) | 72 | 2,42% | 49 | 4,24% | 49 | 4,43% | 49 | 4,4% |
Uicn et al. (2015) | 71 | 2,39% | 67 | 5,8% | 64 | 5,79% | 55 | 4,94% |
Dettaï et al. (2011) | 64 | 2,15% | 61 | 5,28% | 61 | 5,52% | 61 | 5,48% |
Rinaldi (2016) | 60 | 2,02% | 52 | 4,5% | 52 | 4,7% | 36 | 3,23% |
Arnaud (1972) | 56 | 1,88% | 21 | 1,82% | 21 | 1,9% | 21 | 1,89% |
Blanc-Vernet (1965) | 54 | 1,81% | 34 | 2,94% | 34 | 3,07% | 34 | 3,05% |
Carzon et al. (2016) | 45 | 1,51% | 39 | 3,38% | 39 | 3,53% | 27 | 2,43% |
Estrade et al. (2016) | 45 | 1,51% | 39 | 3,38% | 39 | 3,53% | 27 | 2,43% |
Bellan (1972) | 44 | 1,48% | 22 | 1,9% | 20 | 1,81% | 22 | 1,98% |
d'Udekem d'Acoz & Verheye (2017) | 44 | 1,48% | 43 | 3,72% | 43 | 3,89% | 43 | 3,86% |
Powell (1960) | 42 | 1,41% | 16 | 1,39% | 16 | 1,45% | 16 | 1,44% |
Fauvel (1950) | 40 | 1,34% | 21 | 1,82% | 21 | 1,9% | 19 | 1,71% |
Monniot et al. (2011) | 37 | 1,24% | 37 | 3,2% | 37 | 3,35% | 37 | 3,32% |
Arnaud (1972) | 35 | 1,18% | 33 | 2,86% | 31 | 2,8% | 32 | 2,88% |
Amar & Roman (1974) | 34 | 1,14% | 18 | 1,56% | 16 | 1,45% | 17 | 1,53% |
Monniot & Monniot (1983) | 34 | 1,14% | 31 | 2,68% | 31 | 2,8% | 31 | 2,79% |
Naumov & Stepanjants (1972) | 34 | 1,14% | 12 | 1,04% | 12 | 1,08% | 12 | 1,08% |
Cantera & Arnaud (1985) | 31 | 1,04% | 21 | 1,82% | 21 | 1,9% | 20 | 1,8% |
Gaillard (1954) | 30 | 1,01% | 11 | 0,95% | 11 | 0,99% | 11 | 0,99% |
Bellan (1975) | 29 | 0,97% | 17 | 1,47% | 16 | 1,45% | 17 | 1,53% |
Debenay & Cabioch (2007) | 27 | 0,91% | 21 | 1,82% | 21 | 1,9% | 21 | 1,89% |
Ifremer (2009) | 25 | 0,84% | 18 | 1,56% | 18 | 1,63% | 14 | 1,26% |
Vacelet & Arnaud (1972) | 25 | 0,84% | 14 | 1,21% | 14 | 1,27% | 14 | 1,26% |
Arnaud (1964) | 24 | 0,81% | 17 | 1,47% | 16 | 1,45% | 17 | 1,53% |
Arnaud (1974) | 23 | 0,77% | 16 | 1,39% | 16 | 1,45% | 16 | 1,44% |
Debenay (2013) | 23 | 0,77% | 14 | 1,21% | 14 | 1,27% | 14 | 1,26% |
Duchêne (1984) | 23 | 0,77% | 15 | 1,3% | 15 | 1,36% | 14 | 1,26% |
Androsova (1972) | 21 | 0,71% | 10 | 0,87% | 10 | 0,9% | 10 | 0,9% |
Newell (1984) | 21 | 0,71% | 21 | 1,82% | 21 | 1,9% | 21 | 1,89% |
Ricard (1985) | 21 | 0,71% | 12 | 1,04% | 11 | 0,99% | 8 | 0,72% |
Bellan-Santini (1972) | 20 | 0,67% | 13 | 1,13% | 13 | 1,18% | 13 | 1,17% |
Cherbonnier (1974) | 20 | 0,67% | 9 | 0,78% | 9 | 0,81% | 9 | 0,81% |
Boury-esnault et al. (1982) | 19 | 0,64% | 11 | 0,95% | 11 | 0,99% | 11 | 0,99% |
Gutt et al. (2007) | 19 | 0,64% | 14 | 1,21% | 14 | 1,27% | 12 | 1,08% |
Sara et al. (1992) | 18 | 0,6% | 10 | 0,87% | 10 | 0,9% | 10 | 0,9% |
Dauvin et al. (2003) | 16 | 0,54% | 14 | 1,21% | 14 | 1,27% | 11 | 0,99% |
McIntosh (1885) | 16 | 0,54% | 4 | 0,35% | 4 | 0,36% | 4 | 0,36% |
Charrassin (2016) | 15 | 0,5% | 13 | 1,13% | 13 | 1,18% | 9 | 0,81% |
Charrassin (2016) | 15 | 0,5% | 13 | 1,13% | 13 | 1,18% | 9 | 0,81% |
Corbari et al. (2020) | 15 | 0,5% | 13 | 1,13% | 13 | 1,18% | 13 | 1,17% |
Jarrett & Shirihai (2014) | 15 | 0,5% | 13 | 1,13% | 13 | 1,18% | 9 | 0,81% |
Moutou (2016) | 15 | 0,5% | 13 | 1,13% | 13 | 1,18% | 9 | 0,81% |
Spitz et al. (2016) | 15 | 0,5% | 13 | 1,13% | 13 | 1,18% | 9 | 0,81% |
Thoisy & Bordin (2016) | 15 | 0,5% | 13 | 1,13% | 13 | 1,18% | 9 | 0,81% |
Urtizberea (2016) | 15 | 0,5% | 13 | 1,13% | 13 | 1,18% | 9 | 0,81% |
Zdzitowiecki & Ozouf-Costaz (2013) | 15 | 0,5% | 12 | 1,04% | 12 | 1,08% | 12 | 1,08% |
Zdzitowiecki (2001) | 15 | 0,5% | 13 | 1,13% | 13 | 1,18% | 13 | 1,17% |
Nelson-Smith et al. (2014) | 14 | 0,47% | 9 | 0,78% | 9 | 0,81% | 8 | 0,72% |
Zdzitowiecki et al. (1998) | 14 | 0,47% | 12 | 1,04% | 12 | 1,08% | 12 | 1,08% |
Vénec-Peyré (1985) | 13 | 0,44% | 12 | 1,04% | 12 | 1,08% | 12 | 1,08% |
Bellan-Santini & Ledoyer (1974) | 12 | 0,4% | 12 | 1,04% | 12 | 1,08% | 12 | 1,08% |
Godet et al. (2010) | 12 | 0,4% | 9 | 0,78% | 9 | 0,81% | 7 | 0,63% |
Kussakin & Vasina (1980) | 12 | 0,4% | 7 | 0,61% | 6 | 0,54% | 6 | 0,54% |
Choudhury & Brandt (2009) | 11 | 0,37% | 10 | 0,87% | 10 | 0,9% | 9 | 0,81% |
Duhamel et al. (2005) | 11 | 0,37% | 11 | 0,95% | 11 | 0,99% | 11 | 0,99% |
Fauvel (1952) | 11 | 0,37% | 5 | 0,43% | 5 | 0,45% | 5 | 0,45% |
Linnaeus (1758) | 11 | 0,37% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
Millard (1977) | 11 | 0,37% | 9 | 0,78% | 9 | 0,81% | 9 | 0,81% |
Sladen (1889) | 11 | 0,37% | 7 | 0,61% | 5 | 0,45% | 4 | 0,36% |
Vasselon et al. (2019) | 11 | 0,37% | 7 | 0,61% | 5 | 0,45% | 6 | 0,54% |
Arnaud (1965) | 10 | 0,34% | 5 | 0,43% | 5 | 0,45% | 5 | 0,45% |
Choudhury & Brandt (2009) | 10 | 0,34% | 10 | 0,87% | 10 | 0,9% | 10 | 0,9% |
Hedley (1916) | 10 | 0,34% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Monniot & Dettai (2015) | 10 | 0,34% | 5 | 0,43% | 5 | 0,45% | 5 | 0,45% |
Paulmier (1997) | 10 | 0,34% | 5 | 0,43% | 5 | 0,45% | 4 | 0,36% |
Vicente & Arnaud (1974) | 10 | 0,34% | 6 | 0,52% | 6 | 0,54% | 6 | 0,54% |
Bourcier (1988) | 9 | 0,3% | 7 | 0,61% | 7 | 0,63% | 7 | 0,63% |
Gaillard (1954) | 9 | 0,3% | 4 | 0,35% | 4 | 0,36% | 4 | 0,36% |
Guilcher et al. (1965) | 9 | 0,3% | 5 | 0,43% | 5 | 0,45% | 5 | 0,45% |
M'intosh (1876) | 9 | 0,3% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
Pleijel (2007) | 9 | 0,3% | 6 | 0,52% | 6 | 0,54% | 6 | 0,54% |
Shirihai (2003) | 9 | 0,3% | 8 | 0,69% | 8 | 0,72% | 5 | 0,45% |
Annals & Magazine of Natural History Series 7, 17: 452-458.">Walker (1906) | 9 | 0,3% | 6 | 0,52% | 6 | 0,54% | 6 | 0,54% |
Ausilio & Zotier (1989) | 8 | 0,27% | 7 | 0,61% | 7 | 0,63% | 7 | 0,63% |
Q. J. Micr. Sci. (n.s.), xix: pp. 20 & 261.">Brady (1879) | 8 | 0,27% | 5 | 0,43% | 5 | 0,45% | 5 | 0,45% |
Guilloux et al. (2013) | 8 | 0,27% | 7 | 0,61% | 7 | 0,63% | 6 | 0,54% |
Laskowski et al. (2007) | 8 | 0,27% | 7 | 0,61% | 7 | 0,63% | 7 | 0,63% |
Lohmann (1907) | 8 | 0,27% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
Monniot & Monniot (1974) | 8 | 0,27% | 7 | 0,61% | 7 | 0,63% | 7 | 0,63% |
Monniot (1978) | 8 | 0,27% | 8 | 0,69% | 8 | 0,72% | 8 | 0,72% |
Perrin et al. (2002) | 8 | 0,27% | 7 | 0,61% | 7 | 0,63% | 4 | 0,36% |
Smith (1875) | 8 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Uicn et al. (2017) | 8 | 0,27% | 8 | 0,69% | 8 | 0,72% | 5 | 0,45% |
Fauvel (1953) | 7 | 0,24% | 3 | 0,26% | 3 | 0,27% | 3 | 0,27% |
Kensley (1980) | 7 | 0,24% | 3 | 0,26% | 2 | 0,18% | 2 | 0,18% |
Kim & Boxshall (2021) | 7 | 0,24% | 7 | 0,61% | 7 | 0,63% | 7 | 0,63% |
Ledoyer (1969) | 7 | 0,24% | 7 | 0,61% | 6 | 0,54% | 7 | 0,63% |
Riaux-Gobin (1994) | 7 | 0,24% | 6 | 0,52% | 6 | 0,54% | 6 | 0,54% |
Samaran & Guinet (2009) | 7 | 0,24% | 6 | 0,52% | 5 | 0,45% | 3 | 0,27% |
Stekhoven & Mawson (1955) | 7 | 0,24% | 6 | 0,52% | 6 | 0,54% | 6 | 0,54% |
Aulagnier (2009) | 6 | 0,2% | 6 | 0,52% | 6 | 0,54% | 2 | 0,18% |
Boer et al. (1999) | 6 | 0,2% | 5 | 0,43% | 5 | 0,45% | 4 | 0,36% |
Boer (2000) | 6 | 0,2% | 5 | 0,43% | 4 | 0,36% | 3 | 0,27% |
Bordin et al. (2021) | 6 | 0,2% | 6 | 0,52% | 6 | 0,54% | 2 | 0,18% |
Broyer (1973) | 6 | 0,2% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
Chevreux (1905) | 6 | 0,2% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
Eléaume et al. (2014) | 6 | 0,2% | 5 | 0,43% | 5 | 0,45% | 5 | 0,45% |
Bulletin de la Societe Zoologique de France, 38: 260-271.">Fauré-Fremiet (1913) | 6 | 0,2% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
Gannier (2001) | 6 | 0,2% | 6 | 0,52% | 6 | 0,54% | 3 | 0,27% |
Garrigue (2007) | 6 | 0,2% | 6 | 0,52% | 6 | 0,54% | 3 | 0,27% |
G.E.M.M. (2012) | 6 | 0,2% | 6 | 0,52% | 6 | 0,54% | 3 | 0,27% |
Prévost & Mougin (1970) | 6 | 0,2% | 5 | 0,43% | 5 | 0,45% | 4 | 0,36% |
Ridley & Dendy (1886) | 6 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Robineau & Duhamel (2006) | 6 | 0,2% | 5 | 0,43% | 5 | 0,45% | 2 | 0,18% |
Wittmann & Chevaldonné (2021) | 6 | 0,2% | 6 | 0,52% | 6 | 0,54% | 6 | 0,54% |
Al-Handal et al. (2016) | 5 | 0,17% | 4 | 0,35% | 4 | 0,36% | 3 | 0,27% |
Catzeflis (2012) | 5 | 0,17% | 5 | 0,43% | 5 | 0,45% | 1 | 0,09% |
Cherbonnier & Guille (1975) | 5 | 0,17% | 3 | 0,26% | 3 | 0,27% | 2 | 0,18% |
Desbrosses & Etcheberry (1987) | 5 | 0,17% | 4 | 0,35% | 4 | 0,36% | 1 | 0,09% |
British Museum (Natural History), London. 228-261.">Hodgson (1902) | 5 | 0,17% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Leiper & Atkinson (1914) | 5 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Monod & Dollfus (1932) | 5 | 0,17% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
Pelseneer (1903) | 5 | 0,17% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
Questel (2020) | 5 | 0,17% | 5 | 0,43% | 5 | 0,45% | 4 | 0,36% |
Rossi-santos et al. (2007) | 5 | 0,17% | 4 | 0,35% | 4 | 0,36% | 2 | 0,18% |
Schellenberg (1926) | 5 | 0,17% | 3 | 0,26% | 3 | 0,27% | 3 | 0,27% |
Smith (1876) | 5 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Smith (1885) | 5 | 0,17% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
Uicn et al. (2015) | 5 | 0,17% | 5 | 0,43% | 5 | 0,45% | 5 | 0,45% |
Waren et al. (1986) | 5 | 0,17% | 4 | 0,35% | 4 | 0,36% | 4 | 0,36% |
Androsova (1972) | 4 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Cépède (1914) | 4 | 0,13% | 1 | 0,09% | 1 | 0,09% | 0 | 0% |
Chevreux (1912) | 4 | 0,13% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Cobb (1930) | 4 | 0,13% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
Eleaume et al. (2011) | 4 | 0,13% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
Isenmann et al. (1971) | 4 | 0,13% | 4 | 0,35% | 4 | 0,36% | 4 | 0,36% |
Kasamatsu & Joyce (1995) | 4 | 0,13% | 3 | 0,26% | 3 | 0,27% | 3 | 0,27% |
Kim & Boxshall (2020) | 4 | 0,13% | 4 | 0,35% | 4 | 0,36% | 4 | 0,36% |
Matsuoka et al. (2005) | 4 | 0,13% | 4 | 0,35% | 3 | 0,27% | 2 | 0,18% |
Monniot & Gaill (1978) | 4 | 0,13% | 3 | 0,26% | 3 | 0,27% | 3 | 0,27% |
Munilla et al. (2009) | 4 | 0,13% | 4 | 0,35% | 4 | 0,36% | 3 | 0,27% |
Parr (1950) | 4 | 0,13% | 3 | 0,26% | 3 | 0,27% | 3 | 0,27% |
Pearman et al. (2020) | 4 | 0,13% | 4 | 0,35% | 4 | 0,36% | 2 | 0,18% |
Stebbing (1888) | 4 | 0,13% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
Thiele et al. (1999) | 4 | 0,13% | 3 | 0,26% | 2 | 0,18% | 3 | 0,27% |
Tricart & Foubert (2000) | 4 | 0,13% | 3 | 0,26% | 3 | 0,27% | 2 | 0,18% |
Vanhöffen (1914) | 4 | 0,13% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
Ainley et al. (2007) | 3 | 0,1% | 3 | 0,26% | 3 | 0,27% | 2 | 0,18% |
Banks et al. (2006) | 3 | 0,1% | 3 | 0,26% | 3 | 0,27% | 3 | 0,27% |
Barau et al. (2005) | 3 | 0,1% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
Bhaud & Gremare (1991) | 3 | 0,1% | 3 | 0,26% | 3 | 0,27% | 3 | 0,27% |
Borsa (1997) | 3 | 0,1% | 2 | 0,17% | 2 | 0,18% | 1 | 0,09% |
Bourmaud (2003) | 3 | 0,1% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
Breton (2014) | 3 | 0,1% | 3 | 0,26% | 3 | 0,27% | 3 | 0,27% |
Brunet et al. (2017) | 3 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Carravieri et al. (2016) | 3 | 0,1% | 3 | 0,26% | 3 | 0,27% | 3 | 0,27% |
Carriol & Féral (1985) | 3 | 0,1% | 3 | 0,26% | 3 | 0,27% | 3 | 0,27% |
CEVA (2011) | 3 | 0,1% | 2 | 0,17% | 2 | 0,18% | 1 | 0,09% |
Cha et al. (1997) | 3 | 0,1% | 3 | 0,26% | 3 | 0,27% | 3 | 0,27% |
Chastel & Beaucournu (1992) | 3 | 0,1% | 3 | 0,26% | 3 | 0,27% | 3 | 0,27% |
Clements (2012) | 3 | 0,1% | 3 | 0,26% | 3 | 0,27% | 2 | 0,18% |
Cobb (1914) | 3 | 0,1% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
Coleman (1991) | 3 | 0,1% | 3 | 0,26% | 3 | 0,27% | 3 | 0,27% |
Dewynter et al. (2021) | 3 | 0,1% | 3 | 0,26% | 3 | 0,27% | 2 | 0,18% |
Dulau-Drouot et al. (2008) | 3 | 0,1% | 3 | 0,26% | 3 | 0,27% | 2 | 0,18% |
Faltýnková et al. (2017) | 3 | 0,1% | 3 | 0,26% | 3 | 0,27% | 3 | 0,27% |
Forster (1781) | 3 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Gannier (2002) | 3 | 0,1% | 3 | 0,26% | 3 | 0,27% | 2 | 0,18% |
Gannier (2009) | 3 | 0,1% | 3 | 0,26% | 3 | 0,27% | 2 | 0,18% |
Expedition 1910 Nat History Report Zoology, 6(No. 2): pp. 25-268.">Heron-allen & Earland (1922) | 3 | 0,1% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Iglesias et al. (2012) | 3 | 0,1% | 3 | 0,26% | 3 | 0,27% | 3 | 0,27% |
Just & Wilson (2004) | 3 | 0,1% | 3 | 0,26% | 3 | 0,27% | 3 | 0,27% |
Kinberg (1856) | 3 | 0,1% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
Mawson (1958) | 3 | 0,1% | 3 | 0,26% | 3 | 0,27% | 3 | 0,27% |
Milan (2018) | 3 | 0,1% | 1 | 0,09% | 1 | 0,09% | 0 | 0% |
Monniot (2011) | 3 | 0,1% | 3 | 0,26% | 3 | 0,27% | 3 | 0,27% |
Moore et al. (2016) | 3 | 0,1% | 3 | 0,26% | 3 | 0,27% | 3 | 0,27% |
Naim (1985) | 3 | 0,1% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Pfeffer (1887) | 3 | 0,1% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Questel & Le Quellec (2012) | 3 | 0,1% | 3 | 0,26% | 3 | 0,27% | 2 | 0,18% |
Redier (1971) | 3 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Robineau (2005) | 3 | 0,1% | 3 | 0,26% | 3 | 0,27% | 1 | 0,09% |
Studer (1876) | 3 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Thiele et al. (2004) | 3 | 0,1% | 3 | 0,26% | 2 | 0,18% | 2 | 0,18% |
Thiele (1905) | 3 | 0,1% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Totton (1930) | 3 | 0,1% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
Van de Vijver et al. (1999) | 3 | 0,1% | 2 | 0,17% | 1 | 0,09% | 2 | 0,18% |
Journal of the Linnean Society of London, Zoology. 29: 38-64.">Walker (1903) | 3 | 0,1% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
Wheeler (1940) | 3 | 0,1% | 3 | 0,26% | 3 | 0,27% | 3 | 0,27% |
AAMP (2012) | 2 | 0,07% | 2 | 0,17% | 2 | 0,18% | 0 | 0% |
Améziane et al. (2011) | 2 | 0,07% | 2 | 0,17% | 2 | 0,18% | 1 | 0,09% |
Ameziane et al. (2020) | 2 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
André (1933) | 2 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Averincev (1972) | 2 | 0,07% | 1 | 0,09% | 0 | 0% | 1 | 0,09% |
Baird et al. (2011) | 2 | 0,07% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
Barre et al. (2009) | 2 | 0,07% | 2 | 0,17% | 2 | 0,18% | 1 | 0,09% |
Bay-nouailhat & Bay-nouailhat (2020) | 2 | 0,07% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
Beddard (1886) | 2 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Boer & Simmonds (2000) | 2 | 0,07% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
Bonnet (1977) | 2 | 0,07% | 2 | 0,17% | 2 | 0,18% | 0 | 0% |
Quarterly Journal of Microscopical Science, XXl: 31-71.">Brady (1881) | 2 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Brady (1907) | 2 | 0,07% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
Brandt (1990) | 2 | 0,07% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
Bushueva (1978) | 2 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Caullery & Mesnil (1897) | 2 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Chevreux (1887) | 2 | 0,07% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Claparède (1864) | 2 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Coleman & Andres (1988) | 2 | 0,07% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
Coste et al. (2008) | 2 | 0,07% | 2 | 0,17% | 1 | 0,09% | 2 | 0,18% |
Danis & Jangoux (2008) | 2 | 0,07% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
Dean (2012) | 2 | 0,07% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
Decloitre (1978) | 2 | 0,07% | 2 | 0,17% | 0 | 0% | 2 | 0,18% |
Delord et al. (2008) | 2 | 0,07% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
Diaz & Cuzange (2009) | 2 | 0,07% | 2 | 0,17% | 2 | 0,18% | 0 | 0% |
Earland (1933) | 2 | 0,07% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Edmonds (1972) | 2 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Ehlers (1908) | 2 | 0,07% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
Emison (2000) | 2 | 0,07% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
Fariñas et al. (2015) | 2 | 0,07% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
Frugone et al. (2021) | 2 | 0,07% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
Gannier (2000) | 2 | 0,07% | 2 | 0,17% | 2 | 0,18% | 1 | 0,09% |
Gillet (1991) | 2 | 0,07% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
Gimbel (1919) | 2 | 0,07% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
Goulletquer (2016) | 2 | 0,07% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
Gravier (1913) | 2 | 0,07% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Grube (1863) | 2 | 0,07% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
Guille & Laubier (1966) | 2 | 0,07% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Hastings (1943) | 2 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Heger et al. (2009) | 2 | 0,07% | 2 | 0,17% | 2 | 0,18% | 1 | 0,09% |
Hentschel (1914) | 2 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Herlédan (2023) | 2 | 0,07% | 2 | 0,17% | 2 | 0,18% | 1 | 0,09% |
Herubel (1913) | 2 | 0,07% | 1 | 0,09% | 1 | 0,09% | 0 | 0% |
Hess et al. (2005) | 2 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
IUCN (2012) | 2 | 0,07% | 2 | 0,17% | 2 | 0,18% | 1 | 0,09% |
Johnston & Mawson (1941) | 2 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Johnston & Mawson (1945) | 2 | 0,07% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
Jullien (1888) | 2 | 0,07% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
Kawamura (1994) | 2 | 0,07% | 2 | 0,17% | 2 | 0,18% | 0 | 0% |
Kim & Boxshall (2021) | 2 | 0,07% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
Kiszka et al.(2007) | 2 | 0,07% | 2 | 0,17% | 2 | 0,18% | 1 | 0,09% |
Klages (1993) | 2 | 0,07% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
Kock et al. (2006) | 2 | 0,07% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
Koechlin (1977) | 2 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Kussakin (1967) | 2 | 0,07% | 1 | 0,09% | 0 | 0% | 1 | 0,09% |
Laran et al. (2011) | 2 | 0,07% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
Le Cohu & Maillard (1983) | 2 | 0,07% | 2 | 0,17% | 2 | 0,18% | 1 | 0,09% |
Leaper et al. (2008) | 2 | 0,07% | 2 | 0,17% | 2 | 0,18% | 1 | 0,09% |
Leaper et al. (2008) | 2 | 0,07% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
Levesque & Delcroix (2018) | 2 | 0,07% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
Macleod et al. (2006) | 2 | 0,07% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
Mahé et al. (2016) | 2 | 0,07% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
Maillard (1978) | 2 | 0,07% | 2 | 0,17% | 1 | 0,09% | 1 | 0,09% |
Marion (1876) | 2 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
McCain (1972) | 2 | 0,07% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
Meißner (2005) | 2 | 0,07% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
Merrin (2004) | 2 | 0,07% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
Michel et al. (2020) | 2 | 0,07% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
Miers (1875) | 2 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Rep, 30: 1-160.">Millar (1960) | 2 | 0,07% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
Monnier et al. (2009) | 2 | 0,07% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Monod (1931) | 2 | 0,07% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
, 12: 59-198.">Monro (1936) | 2 | 0,07% | 1 | 0,09% | 0 | 0% | 1 | 0,09% |
Montagu (1808) | 2 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Montagu (1819) | 2 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Moser (1999) | 2 | 0,07% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
O’Loughlin (2009) | 2 | 0,07% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Ono & Moteki (2016) | 2 | 0,07% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
Poupin et al. (1999) | 2 | 0,07% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
Powell (1951) | 2 | 0,07% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
Prudhoe & Bray (1973) | 2 | 0,07% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
Quatrefages (1866) | 2 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Riaux-Gobin & Compère (2008) | 2 | 0,07% | 2 | 0,17% | 2 | 0,18% | 1 | 0,09% |
Ribeiro et al. (2022) | 2 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Richer de Forges et al. (2005) | 2 | 0,07% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Ridley & Dendy (1886) | 2 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Ridoux (1989) | 2 | 0,07% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
Rignault & Chevallier (2017) | 2 | 0,07% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Robineau (1989) | 2 | 0,07% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Rzhavsky (2010) | 2 | 0,07% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
Safford & Hawkins (2013) | 2 | 0,07% | 2 | 0,17% | 1 | 0,09% | 2 | 0,18% |
Saint-Joseph (1888) | 2 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Salazar-vallejo (2012) | 2 | 0,07% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Samaran (2008) | 2 | 0,07% | 2 | 0,17% | 1 | 0,09% | 1 | 0,09% |
Schellenberg (1926) | 2 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Searby & Jouventin (2005) | 2 | 0,07% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
Solís-Weiss & Alcántara (2009) | 2 | 0,07% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
Sollas (1886) | 2 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Stahl et al. (1985) | 2 | 0,07% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
Stebbing (1888) | 2 | 0,07% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
Studer (1878) | 2 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Thurston (1972) | 2 | 0,07% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
Timm (1978) | 2 | 0,07% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Tostain et al. (2013) | 2 | 0,07% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
Tremblay & Cherel (2003) | 2 | 0,07% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
Udekem d’Acoz & Havermans (2012) | 2 | 0,07% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
UICN Comité français, OFB & MNHN (2021) | 2 | 0,07% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
Van Canneytet al. (2008) | 2 | 0,07% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
Verrill (1876) | 2 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Vonboletzky & Dohle (1967) | 2 | 0,07% | 2 | 0,17% | 2 | 0,18% | 0 | 0% |
Waters (1903) | 2 | 0,07% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
Watson (1882) | 2 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Watson (1882) | 2 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Wheeler (1934) | 2 | 0,07% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
Williamson (1868) | 2 | 0,07% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Wright & Studer (1889) | 2 | 0,07% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
Yamaguti (1971) | 2 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Zdzitowiecki (1983) | 2 | 0,07% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
Zdzitowiecki (1984) | 2 | 0,07% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
Zdzitowiecki (1998) | 2 | 0,07% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
Zimmer (1914) | 2 | 0,07% | 2 | 0,17% | 2 | 0,18% | 2 | 0,18% |
Allgen (1929) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Allman (1888) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Cahiers de Biologie Marine, 18: 391-411.">Amoureux (1977) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Andrew et al. (2008) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Anonyme (2015) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Arnaud (1964) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Arnaud (2015) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Bale (1888) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Banse & Hobson (1968) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Barre et al. (1977) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Bastian (1865) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Batisse & Dragesco (1967) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Béarez et al. (2017) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Bedot (1910) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Bedot (1914) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Benham (1921) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Best et al. (1995) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 0 | 0% |
Bester & Roux (1986) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Bey & Ector (2013) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Bigot et al. (2006) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Thécamoebiens du Sol". Hermann, Paris. 103pp.">Bonnet & Thomas (1960) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 0 | 0% |
Bonnet (1965) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 0 | 0% |
Borg (1944) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Brady (1884) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Branch et al. (2007) | 1 | 0,03% | 1 | 0,09% | 0 | 0% | 1 | 0,09% |
Branch (2010) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 0 | 0% |
Brandt (1837) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Brattey et al. (1990) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Brocchi (1877) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Brownell et al. (1999) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Budylenko (1977) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 0 | 0% |
Zoology, x: 216 pp..">Busk (1884) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Annals of Natural History, (4)(xviii): pp. 226-240, 307-324, 388-410, 458-473.">Carter (1876) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Carzon (2012) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Causse et al. (2011) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Cerchio et al. (2009) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 0 | 0% |
Chapman (1916) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Cherel & Boxshall (2004) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Claparède (1863) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Coleman (1996) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Collectif (2009) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 0 | 0% |
Commission de l’Avifaune Française (2016) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Coste & Ricard (1990) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Cottarel et al. (2013) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Cotte et al. (2001) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 0 | 0% |
Counihan et al. (2012) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 0 | 0% |
Courtecuisse (2009) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Cushman (1913) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Cushman (1920) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Cutler & Cutler (1996) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Danel et al. (2023) | 1 | 0,03% | 1 | 0,09% | 0 | 0% | 1 | 0,09% |
Davey (2010) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Davey (2010) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Davey (2010) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Davey (2011) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Davey (2017) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
David et al. (2015) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 0 | 0% |
Davoult (1990) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Decloitre (1960) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Decloitre (1970) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Decloitre (1977) | 1 | 0,03% | 1 | 0,09% | 0 | 0% | 1 | 0,09% |
Deflandre (1927) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Deflandre (1929) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 0 | 0% |
Deflandre (1960) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Dell (1990) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Deméré (2014) | 1 | 0,03% | 1 | 0,09% | 0 | 0% | 1 | 0,09% |
Deuss et al. (2013) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
d'Hondt (1984) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Dubois et al. (2008) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
D'udekem & D'acoz (2008) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
D'udekem et al. (2018) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Duhamel & Welsford (2011) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 0 | 0% |
Dupont et al. (2007) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
D'acoz & Degrave (2018) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Earland (1934) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Ehlers (1897) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Ersts & Rosenbaum (2003) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 0 | 0% |
Fabricius (1780) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Facca & Casabianca (2006) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Fauvel (1926) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 0 | 0% |
Finsch (1876) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Fleming & Jackson (2011) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 0 | 0% |
Flood et al. (2021) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Forster (1844) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Foster (1972) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Friedlaender et al. (2010) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Gaillard (1954) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Gassiole & Monnier (2019) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Geiger (2015) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Gibson (1985) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Gill & Thiele (1997) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Gillespie (1997) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Gmelin (1789) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Golvan (1969) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Goodall et al. (1997) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Gould (1849) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Gout (1991) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Graeve et al. (2001) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Gravier (1906) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Gravier (1906) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Gravier-Bonnet et al. (2022) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Gray (1846) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
GT DCE Réunion | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Guille (2015) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Guille (2015) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Guinet (1991) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Guinet (2004) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Günther (1878) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Hansson (1999) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Hartman (1965) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Hartman (1967) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Hassall (1848) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Hedley et al. (2007) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Heron-allen & Earland (1929) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Heron-allen & Earland (1932) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Héros et al. (2007) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Hessle (1917) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Hodgson (1910) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Hoek (1881) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 0 | 0% |
Hombron & Jacquinot (1841) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Proceedings of the Zoological Society of London, 1907: 1035-1037.">Hopkinson (1907) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Ifremer (2019) | 1 | 0,03% | 1 | 0,09% | 0 | 0% | 1 | 0,09% |
Izuka (1912) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Jacquet et al. (2008) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 0 | 0% |
Jay et al. (2009) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Jehl et al. (1980) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Johnson & Wolman (1984) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 0 | 0% |
Johnson (1901) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Johnston (1938) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Joubin (1905) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Julien (1881) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Justine et al. (2010) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Kasamatsu et al. (2000) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 0 | 0% |
Keferstein (1862) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Kiszka et al. (2009) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 0 | 0% |
Kiszka et al. (2010) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Klages & Gutt (1990) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Koehler (1906) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Koehler (1912) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Kuhl (1820) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Lambert (2004) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Laran et al. (2012) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Larsen (2000) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Leidy (1879) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Lesson (1828) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 0 | 0% |
Levring (1944) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Loerz et al. (2012) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Lorz (2009) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Lowry & Kilgallen (2015) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Ludwig (1898) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Mah (2008) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Mah (2015) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Mah (2015) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Mah (2023) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Mao et al. (2020) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Monniot (1988) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Monniot (2013) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Montagu (1803) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Montfort de Denys (1808) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Motz-Kossowska (1910) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Mougin (1984) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Murase et al. (2002) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 0 | 0% |
Natural History Museum of London (2020) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Nicholls (1939) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Nicol et al. (2000) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 0 | 0% |
Noël (2017) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Nygren (2004) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Okamura & Kitakado (2008) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Packard (1867) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Pancucci-papadopoulou et al. (1999) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Pastor de Ward (1995) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Perry et al. (1999) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 0 | 0% |
Petit (1970) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Piraino et al. (2003) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Pitman & Ensor (2003) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Poisson & Legueux (1926) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Ponder (1983) | 1 | 0,03% | 1 | 0,09% | 0 | 0% | 1 | 0,09% |
Prevost (1970) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Probst (1997) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Raust & Sanford (2007) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Remsen et al. (2013) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Rhumbler (1905) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Riccialdelli et al. (2010) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Richardson (1906) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Richardson (1908) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Ridley & Dendy (1887) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Roche & Guinet (2007) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Rogers & Brown (1999) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Rosenbaum & Collins (2006) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 0 | 0% |
Samaran & Guinet (2010) | 1 | 0,03% | 1 | 0,09% | 0 | 0% | 1 | 0,09% |
Samaran et al. (2010) | 1 | 0,03% | 1 | 0,09% | 0 | 0% | 1 | 0,09% |
Sarda et al. (2009) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 0 | 0% |
Schotte et al. (1995 onwards) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Sekiguchi et al. (1993) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Sellier et al. (2016) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Shukla et al. (2013) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Siciliano & Santos (2003) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Sirovic et al. (2009) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 0 | 0% |
Sladen (1882) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 0 | 0% |
Sluiter (1906) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Smith et al. (2005) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Stampanato (2015) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Stampanato (2015) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Stampanato (2015) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Stampanato (2015) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 0 | 0% |
Stampanato (2015) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Stimpson (1858) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Stranks (1994) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Taki (1961) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Tapolczai et al. (2017) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 0 | 0% |
Taranek (1881) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 0 | 0% |
Taylor et al. (2013) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Thomson (1900) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Tostain & Dujardin (1988) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Tougaard (2010) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Traustedt (1881) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Tröndlé & Boutet (2009) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Trouessart (1894) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Truchot (1974) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
UICN Comité français, OFB, MNHN & GEPOMAY (2025) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Uicn et al. (2019) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Vacelet (1969) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Varela et al. (2007) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Vénec-Peyré & Salvat (1981) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Vollmer et al. (2019) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Waren & Hain (1996) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Warham et al. (1977) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Watson (1881) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Watson (2008) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Weerdt (2023) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 0 | 0% |
Wiencke & Clayton (2002) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Williams et al. (2009) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 0 | 0% |
Zdzitowiecki & Cielecka (1997) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Zdzitowiecki & Cielecka (1997) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Zdzitowiecki et al. (1993) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Zelaya & Geiger (2007) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Zinke et al. (2005) | 1 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |