Crustacés des îles subantarctiques
237 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
Référence | Total | Valides | Espèces | Taxons terminaux | ||||
---|---|---|---|---|---|---|---|---|
nb | % | nb | % | nb | % | nb | % | |
Bellan-Santini & Ledoyer (1974) | 66 | 8,04% | 53 | 12,02% | 53 | 12,13% | 52 | 11,9% |
Ifremer (2009) | 43 | 5,24% | 28 | 6,35% | 28 | 6,41% | 27 | 6,18% |
Arnaud (1974) | 39 | 4,75% | 27 | 6,12% | 26 | 5,95% | 26 | 5,95% |
Stebbing (1888) | 38 | 4,63% | 23 | 5,22% | 23 | 5,26% | 23 | 5,26% |
Vanhöffen (1914) | 37 | 4,51% | 9 | 2,04% | 9 | 2,06% | 9 | 2,06% |
Choudhury & Brandt (2009) | 34 | 4,14% | 34 | 7,71% | 34 | 7,78% | 34 | 7,78% |
Kussakin & Vasina (1980) | 32 | 3,9% | 20 | 4,54% | 19 | 4,35% | 19 | 4,35% |
Kensley (1980) | 29 | 3,53% | 15 | 3,4% | 14 | 3,2% | 14 | 3,2% |
Stebbing (1888) | 29 | 3,53% | 12 | 2,72% | 12 | 2,75% | 12 | 2,75% |
Kussakin & Vasina (1982) | 28 | 3,41% | 11 | 2,49% | 11 | 2,52% | 11 | 2,52% |
Amar & Roman (1974) | 22 | 2,68% | 13 | 2,95% | 12 | 2,75% | 12 | 2,75% |
Pugh et al. (2002) | 20 | 2,44% | 17 | 3,85% | 17 | 3,89% | 17 | 3,89% |
Choudhury & Brandt (2009) | 18 | 2,19% | 16 | 3,63% | 16 | 3,66% | 15 | 3,43% |
Laubitz (1995) | 17 | 2,07% | 17 | 3,85% | 17 | 3,89% | 17 | 3,89% |
Kensley (1989) | 16 | 1,95% | 14 | 3,17% | 14 | 3,2% | 14 | 3,2% |
Beddard (1886) | 15 | 1,83% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Studer (1878) | 14 | 1,71% | 8 | 1,81% | 8 | 1,83% | 8 | 1,83% |
Monod & Dollfus (1932) | 13 | 1,58% | 8 | 1,81% | 8 | 1,83% | 8 | 1,83% |
Ledoyer (1995) | 12 | 1,46% | 10 | 2,27% | 10 | 2,29% | 10 | 2,29% |
D'acoz & Degrave (2018) | 10 | 1,22% | 10 | 2,27% | 10 | 2,29% | 10 | 2,29% |
Kim & Boxshall (2021) | 10 | 1,22% | 10 | 2,27% | 10 | 2,29% | 10 | 2,29% |
Brandt (1990) | 9 | 1,1% | 8 | 1,81% | 7 | 1,6% | 8 | 1,83% |
Broyer et al. (2007) | 9 | 1,1% | 9 | 2,04% | 9 | 2,06% | 9 | 2,06% |
Kensley (1976) | 9 | 1,1% | 5 | 1,13% | 5 | 1,14% | 5 | 1,14% |
Miers (1875) | 9 | 1,1% | 4 | 0,91% | 4 | 0,92% | 4 | 0,92% |
Bellan-Santini (1972) | 8 | 0,97% | 7 | 1,59% | 7 | 1,6% | 6 | 1,37% |
Bellan-Santini (1972) | 8 | 0,97% | 7 | 1,59% | 7 | 1,6% | 7 | 1,6% |
Macpherson (2004) | 8 | 0,97% | 8 | 1,81% | 8 | 1,83% | 8 | 1,83% |
Petryashev (2007) | 8 | 0,97% | 8 | 1,81% | 8 | 1,83% | 8 | 1,83% |
Cousins et al. (2013) | 7 | 0,85% | 6 | 1,36% | 6 | 1,37% | 6 | 1,37% |
Martens & Savatenalinton (2011) | 7 | 0,85% | 0 | 0% | 0 | 0% | 0 | 0% |
Sars (1883) | 7 | 0,85% | 4 | 0,91% | 4 | 0,92% | 4 | 0,92% |
Corbari et al. (2020) | 6 | 0,73% | 5 | 1,13% | 5 | 1,14% | 5 | 1,14% |
Hodgson (1910) | 6 | 0,73% | 3 | 0,68% | 3 | 0,69% | 3 | 0,69% |
Chappuis (1959) | 5 | 0,61% | 2 | 0,45% | 2 | 0,46% | 2 | 0,46% |
D'udekem & D'acoz (2008) | 5 | 0,61% | 5 | 1,13% | 5 | 1,14% | 5 | 1,14% |
British Museum (Natural History), London. 228-261.">Hodgson (1902) | 5 | 0,61% | 0 | 0% | 0 | 0% | 0 | 0% |
Just & Wilson (2004) | 5 | 0,61% | 5 | 1,13% | 5 | 1,14% | 5 | 1,14% |
Kussakin (1967) | 5 | 0,61% | 2 | 0,45% | 2 | 0,46% | 2 | 0,46% |
Macpherson et al. (2002) | 5 | 0,61% | 0 | 0% | 0 | 0% | 0 | 0% |
Merrin (2004) | 5 | 0,61% | 5 | 1,13% | 5 | 1,14% | 5 | 1,14% |
Monod (1925) | 5 | 0,61% | 5 | 1,13% | 5 | 1,14% | 5 | 1,14% |
Schellenberg (1926) | 5 | 0,61% | 4 | 0,91% | 4 | 0,92% | 4 | 0,92% |
Science Report of Shima Marineland, 5: 1-122.">Shiino (1978) | 5 | 0,61% | 4 | 0,91% | 4 | 0,92% | 4 | 0,92% |
Soyer et al. (1987) | 5 | 0,61% | 5 | 1,13% | 5 | 1,14% | 5 | 1,14% |
Ahyong (2014) | 4 | 0,49% | 4 | 0,91% | 4 | 0,92% | 4 | 0,92% |
Alekseev et al. (2021) | 4 | 0,49% | 2 | 0,45% | 2 | 0,46% | 2 | 0,46% |
Barnard (1932) | 4 | 0,49% | 4 | 0,91% | 4 | 0,92% | 4 | 0,92% |
Brady (1910) | 4 | 0,49% | 3 | 0,68% | 3 | 0,69% | 3 | 0,69% |
Keable (2006) | 4 | 0,49% | 4 | 0,91% | 4 | 0,92% | 4 | 0,92% |
Kotov (2007) | 4 | 0,49% | 4 | 0,91% | 4 | 0,92% | 4 | 0,92% |
Miers (1875) | 4 | 0,49% | 2 | 0,45% | 2 | 0,46% | 2 | 0,46% |
Nelson-Smith et al. (2014) | 4 | 0,49% | 3 | 0,68% | 3 | 0,69% | 3 | 0,69% |
Pfeffer (1887) | 4 | 0,49% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Schellenberg (1926) | 4 | 0,49% | 2 | 0,45% | 2 | 0,46% | 2 | 0,46% |
Schotte et al. (1995 onwards) | 4 | 0,49% | 4 | 0,91% | 4 | 0,92% | 4 | 0,92% |
Smet (2015) | 4 | 0,49% | 4 | 0,91% | 4 | 0,92% | 4 | 0,92% |
Stock (1986) | 4 | 0,49% | 4 | 0,91% | 4 | 0,92% | 4 | 0,92% |
Truchot (1974) | 4 | 0,49% | 4 | 0,91% | 4 | 0,92% | 4 | 0,92% |
Arnaud et al. (1972) | 3 | 0,37% | 2 | 0,45% | 2 | 0,46% | 2 | 0,46% |
Balvay (2009) | 3 | 0,37% | 3 | 0,68% | 3 | 0,69% | 3 | 0,69% |
Barnard (1914) | 3 | 0,37% | 3 | 0,68% | 3 | 0,69% | 3 | 0,69% |
Bovée et al. (1973) | 3 | 0,37% | 3 | 0,68% | 3 | 0,69% | 3 | 0,69% |
Brady (1875) | 3 | 0,37% | 0 | 0% | 0 | 0% | 0 | 0% |
Brandt (1998) | 3 | 0,37% | 3 | 0,68% | 3 | 0,69% | 3 | 0,69% |
Champeau & Thiéry (1990) | 3 | 0,37% | 3 | 0,68% | 3 | 0,69% | 3 | 0,69% |
Chappuis (1940) | 3 | 0,37% | 3 | 0,68% | 3 | 0,69% | 3 | 0,69% |
Chevreux (1887) | 3 | 0,37% | 2 | 0,45% | 2 | 0,46% | 2 | 0,46% |
Gomez Simes (1981) | 3 | 0,37% | 0 | 0% | 0 | 0% | 0 | 0% |
Gutt et al. (2007) | 3 | 0,37% | 3 | 0,68% | 3 | 0,69% | 2 | 0,46% |
Kiefer (1944) | 3 | 0,37% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Larsen (2000) | 3 | 0,37% | 3 | 0,68% | 3 | 0,69% | 3 | 0,69% |
Lemaitre (2014) | 3 | 0,37% | 3 | 0,68% | 3 | 0,69% | 3 | 0,69% |
Mackay (2014) | 3 | 0,37% | 2 | 0,45% | 2 | 0,46% | 2 | 0,46% |
Pélosse (1930) | 3 | 0,37% | 0 | 0% | 0 | 0% | 0 | 0% |
Questel (2020) | 3 | 0,37% | 2 | 0,45% | 2 | 0,46% | 2 | 0,46% |
Shulenberger & Barnard (1976) | 3 | 0,37% | 2 | 0,45% | 2 | 0,46% | 2 | 0,46% |
The Annals & Magazine of Natural History, Serie 5 ; volume 11: 203-207.">Stebbing (1883) | 3 | 0,37% | 2 | 0,45% | 2 | 0,46% | 2 | 0,46% |
Tattersall (1955) | 3 | 0,37% | 3 | 0,68% | 3 | 0,69% | 3 | 0,69% |
Annals & Magazine of Natural History Series 7, 17: 452-458.">Walker (1906) | 3 | 0,37% | 2 | 0,45% | 2 | 0,46% | 2 | 0,46% |
Bodiou & Colomines (1986) | 2 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
Bodiou & Colomines (1988) | 2 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
Bourcier (1988) | 2 | 0,24% | 2 | 0,45% | 2 | 0,46% | 2 | 0,46% |
Brehm (1955) | 2 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
Broyer (1985) | 2 | 0,24% | 2 | 0,45% | 2 | 0,46% | 2 | 0,46% |
Champeau (1967) | 2 | 0,24% | 2 | 0,45% | 2 | 0,46% | 2 | 0,46% |
Chevreux (1905) | 2 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
Chevreux (1906) | 2 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
Coineau (1977) | 2 | 0,24% | 2 | 0,45% | 2 | 0,46% | 2 | 0,46% |
Conlan (1990) | 2 | 0,24% | 2 | 0,45% | 2 | 0,46% | 2 | 0,46% |
Dana (1852) | 2 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
Doflein (1904) | 2 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
Fourt et al. (2017) | 2 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
Godet et al. (2010) | 2 | 0,24% | 2 | 0,45% | 2 | 0,46% | 2 | 0,46% |
Gouillieux (2018) | 2 | 0,24% | 2 | 0,45% | 2 | 0,46% | 2 | 0,46% |
Grindley (1971) | 2 | 0,24% | 2 | 0,45% | 2 | 0,46% | 2 | 0,46% |
Grygier (1990) | 2 | 0,24% | 2 | 0,45% | 2 | 0,46% | 2 | 0,46% |
Hansen (1905) | 2 | 0,24% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Hayashi (2006) | 2 | 0,24% | 2 | 0,45% | 2 | 0,46% | 2 | 0,46% |
Kensley (1975) | 2 | 0,24% | 2 | 0,45% | 2 | 0,46% | 2 | 0,46% |
Kim & Boxshall (2020) | 2 | 0,24% | 2 | 0,45% | 2 | 0,46% | 2 | 0,46% |
Kottmann et al. (2013) | 2 | 0,24% | 2 | 0,45% | 2 | 0,46% | 2 | 0,46% |
Krapp-Schickel & Ruffo (2006) | 2 | 0,24% | 2 | 0,45% | 2 | 0,46% | 2 | 0,46% |
Kusakin & Vasina (1980) | 2 | 0,24% | 2 | 0,45% | 2 | 0,46% | 2 | 0,46% |
Kussakin & Vasina (1982) | 2 | 0,24% | 2 | 0,45% | 2 | 0,46% | 2 | 0,46% |
Ledoyer (1977) | 2 | 0,24% | 2 | 0,45% | 2 | 0,46% | 2 | 0,46% |
Ledoyer (1993) | 2 | 0,24% | 2 | 0,45% | 2 | 0,46% | 2 | 0,46% |
Linnaeus (1758) | 2 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
Lowry (2007) | 2 | 0,24% | 2 | 0,45% | 2 | 0,46% | 2 | 0,46% |
Machordom et al. (2022) | 2 | 0,24% | 2 | 0,45% | 2 | 0,46% | 2 | 0,46% |
Macpherson & Segonzac (2005) | 2 | 0,24% | 2 | 0,45% | 2 | 0,46% | 2 | 0,46% |
Martin (2011) | 2 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
Monard (1925) | 2 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
Monod (1930) | 2 | 0,24% | 2 | 0,45% | 2 | 0,46% | 2 | 0,46% |
Monod (1931) | 2 | 0,24% | 2 | 0,45% | 2 | 0,46% | 2 | 0,46% |
Montagu (1808) | 2 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
Pelosse (1925) | 2 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
Pelosse (1927) | 2 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
Poupin et al. (1999) | 2 | 0,24% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Risso (1816) | 2 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
Schellenberg (1931) | 2 | 0,24% | 2 | 0,45% | 2 | 0,46% | 2 | 0,46% |
Schultz (1981) | 2 | 0,24% | 2 | 0,45% | 2 | 0,46% | 2 | 0,46% |
Sheppard (1957) | 2 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
Studer (1879) | 2 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
Studer (1884) | 2 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
Wagele (1987) | 2 | 0,24% | 2 | 0,45% | 2 | 0,46% | 2 | 0,46% |
Wilson & Wagele (1994) | 2 | 0,24% | 2 | 0,45% | 2 | 0,46% | 2 | 0,46% |
Annals of Natural History, (6)(xiii): pp. 225-245, 321-331, & 400-411.">Alcock (1894) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Arnaud (1972) | 1 | 0,12% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Arnaud (2015) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Arnaud (2015) | 1 | 0,12% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Australian Museum (2020) | 1 | 0,12% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Bachelet et al. (2003) | 1 | 0,12% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Barnard (1914) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Annals & Magazine of Natural History Series 10, 7: 426-430.">Barnard (1931) | 1 | 0,12% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Barrois (1889) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Batisse & Dragesco (1967) | 1 | 0,12% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Bayly (1992) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Beddard (1884) | 1 | 0,12% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Beurois (1971) | 1 | 0,12% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Bocher (2002) | 1 | 0,12% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Boeck (1865) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Bosc (1801-1802) | 1 | 0,12% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Brandt & Bruce (2006) | 1 | 0,12% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Brandt (1991) | 1 | 0,12% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Brandt (2007) | 1 | 0,12% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Brocchi (1877) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Broyer (1983) | 1 | 0,12% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Bruce & Brandt (2006) | 1 | 0,12% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Burukovsky & Pakhomov (2009) | 1 | 0,12% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Caziot (1921) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Chevreux (1888) | 1 | 0,12% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Chevreux (1912) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Chilton (1912) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Chun (1902-1903) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Clemente (2014) | 1 | 0,12% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Coudray & Noël (2014) | 1 | 0,12% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Dana (1852) | 1 | 0,12% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Davoult et al. (1999) | 1 | 0,12% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Defaye & Deharveng (2024) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Defaye & Dussart (2011) | 1 | 0,12% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Dussart (1963) | 1 | 0,12% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Evenhuis (2003) | 1 | 0,12% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Fischer (1884) | 1 | 0,12% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Gerken & Mccarthy (2008) | 1 | 0,12% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Giesbrecht (1902) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Gourret (1891) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Guinot & Macpherson (1988) | 1 | 0,12% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Guinot (2011) | 1 | 0,12% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Haswell (1879) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Hayashi & Yaldwyn (1998) | 1 | 0,12% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Holt & Tattersall (1906) | 1 | 0,12% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Holthuis (1991) | 1 | 0,12% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Hullé et al. (2018) | 1 | 0,12% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Huys (2009) | 1 | 0,12% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Jones (2007) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Jurine (1820) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Just & Wilson (2021) | 1 | 0,12% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Kerhervé (1914) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Labbé (1926) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Lair & Gay (1990) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Lang (1933) | 1 | 0,12% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Latreille (1825-[1828]) | 1 | 0,12% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Laubitz (1991) | 1 | 0,12% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Ledoyer (1969) | 1 | 0,12% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Lemaitre (1989) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Lenz & Strunck (1914) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Macpherson (1988) | 1 | 0,12% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Marazanoff (1965) | 1 | 0,12% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Marchini et al. (2015) | 1 | 0,12% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
McCain (1972) | 1 | 0,12% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Medina et al. (2008) | 1 | 0,12% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Monard (1928) | 1 | 0,12% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Myers & Moore (1983) | 1 | 0,12% | 1 | 0,23% | 0 | 0% | 1 | 0,23% |
Natural History Museum of London (2020) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Newman (1979) | 1 | 0,12% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Ng & Castro (2016) | 1 | 0,12% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Noël (2017) | 1 | 0,12% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Bulletin of the Museum of Comparative Zoology at Harvard College, 25: 99-111.">Ortmann (1894) | 1 | 0,12% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Pagano (2009) | 1 | 0,12% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Paris (1916) | 1 | 0,12% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Paulmier (2019) | 1 | 0,12% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Pelosse (1927) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Poisson & Legueux (1926) | 1 | 0,12% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Poupin (1994) | 1 | 0,12% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Poupin (2010) | 1 | 0,12% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Questel & Le Quellec (2012) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Questel (2014) | 1 | 0,12% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Raoux et al. (2020) | 1 | 0,12% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Richardson (1906) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Richardson (1908) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Richer de Forges (1983) | 1 | 0,12% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Rignault & Chevallier (2017) | 1 | 0,12% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Rose (1925) | 1 | 0,12% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Roy (1922) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Roy (1927) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Roy (1931) | 1 | 0,12% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Rühe (1914) | 1 | 0,12% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
San Vicente & Monniot (2014) | 1 | 0,12% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Schmeil (1893) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Schnabel et al. (2017) | 1 | 0,12% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Schultz (1978) | 1 | 0,12% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Séchet & Noël (2015) | 1 | 0,12% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Shornikov (1982) | 1 | 0,12% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Smet (2003) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Stebbing (1902) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Stephensen (1947) | 1 | 0,12% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Stimpson (1858) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Studer (1884) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Natural History Report (Zoology), 3(8): 191-258.">Tattersall (1921) | 1 | 0,12% | 1 | 0,23% | 1 | 0,23% | 0 | 0% |
Teodorczyk & Wägele (1994) | 1 | 0,12% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Thiébaud (1927) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Thomson (1900) | 1 | 0,12% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Van Damme & Dumont (2008) | 1 | 0,12% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Wagele (2015) | 1 | 0,12% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
Journal of the Linnean Society of London, Zoology. 29: 38-64.">Walker (1903) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Walker-Smith & Poore (2001) | 1 | 0,12% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |