Crustacés des îles subantarctiques
231 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 | 8,09% | 53 | 12,07% | 53 | 12,18% | 52 | 11,95% |
| Ifremer (2009) | 43 | 5,27% | 28 | 6,38% | 28 | 6,44% | 27 | 6,21% |
| Arnaud (1974) | 39 | 4,78% | 27 | 6,15% | 26 | 5,98% | 26 | 5,98% |
| Stebbing (1888) | 38 | 4,66% | 23 | 5,24% | 23 | 5,29% | 23 | 5,29% |
| Vanhöffen (1914) | 37 | 4,53% | 9 | 2,05% | 9 | 2,07% | 9 | 2,07% |
| Choudhury & Brandt (2009) | 34 | 4,17% | 34 | 7,74% | 34 | 7,82% | 34 | 7,82% |
| Kussakin & Vasina (1980) | 32 | 3,92% | 20 | 4,56% | 19 | 4,37% | 19 | 4,37% |
| Kensley (1980) | 29 | 3,55% | 15 | 3,42% | 14 | 3,22% | 14 | 3,22% |
| Stebbing (1888) | 29 | 3,55% | 12 | 2,73% | 12 | 2,76% | 12 | 2,76% |
| Kussakin & Vasina (1982) | 28 | 3,43% | 11 | 2,51% | 11 | 2,53% | 11 | 2,53% |
| Amar & Roman (1974) | 22 | 2,7% | 13 | 2,96% | 12 | 2,76% | 12 | 2,76% |
| Pugh et al. (2002) | 20 | 2,45% | 17 | 3,87% | 17 | 3,91% | 17 | 3,91% |
| Choudhury & Brandt (2009) | 18 | 2,21% | 16 | 3,64% | 16 | 3,68% | 15 | 3,45% |
| Laubitz (1995) | 17 | 2,08% | 17 | 3,87% | 17 | 3,91% | 17 | 3,91% |
| Kensley (1989) | 16 | 1,96% | 14 | 3,19% | 14 | 3,22% | 14 | 3,22% |
| Beddard (1886) | 15 | 1,84% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
| Studer (1878) | 14 | 1,72% | 8 | 1,82% | 8 | 1,84% | 8 | 1,84% |
| Monod & Dollfus (1932) | 13 | 1,59% | 8 | 1,82% | 8 | 1,84% | 8 | 1,84% |
| Ledoyer (1995) | 12 | 1,47% | 10 | 2,28% | 10 | 2,3% | 10 | 2,3% |
| D'acoz & Degrave (2018) | 10 | 1,23% | 10 | 2,28% | 10 | 2,3% | 10 | 2,3% |
| Kim & Boxshall (2021) | 10 | 1,23% | 10 | 2,28% | 10 | 2,3% | 10 | 2,3% |
| Brandt (1990) | 9 | 1,1% | 8 | 1,82% | 7 | 1,61% | 8 | 1,84% |
| Miers (1875) | 9 | 1,1% | 4 | 0,91% | 4 | 0,92% | 4 | 0,92% |
| Bellan-Santini (1972) | 8 | 0,98% | 7 | 1,59% | 7 | 1,61% | 6 | 1,38% |
| Bellan-Santini (1972) | 8 | 0,98% | 7 | 1,59% | 7 | 1,61% | 7 | 1,61% |
| Broyer et al. (2007) | 8 | 0,98% | 8 | 1,82% | 8 | 1,84% | 8 | 1,84% |
| Macpherson (2004) | 8 | 0,98% | 8 | 1,82% | 8 | 1,84% | 8 | 1,84% |
| Petryashev (2007) | 8 | 0,98% | 8 | 1,82% | 8 | 1,84% | 8 | 1,84% |
| Cousins et al. (2013) | 7 | 0,86% | 6 | 1,37% | 6 | 1,38% | 6 | 1,38% |
| Martens & Savatenalinton (2011) | 7 | 0,86% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sars (1883) | 7 | 0,86% | 4 | 0,91% | 4 | 0,92% | 4 | 0,92% |
| Corbari et al. (2020) | 6 | 0,74% | 5 | 1,14% | 5 | 1,15% | 5 | 1,15% |
| Hodgson (1910) | 6 | 0,74% | 3 | 0,68% | 3 | 0,69% | 3 | 0,69% |
| Kensley (1976) | 6 | 0,74% | 2 | 0,46% | 2 | 0,46% | 2 | 0,46% |
| Chappuis (1959) | 5 | 0,61% | 2 | 0,46% | 2 | 0,46% | 2 | 0,46% |
| D'udekem & D'acoz (2008) | 5 | 0,61% | 5 | 1,14% | 5 | 1,15% | 5 | 1,15% |
| 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 | 1,14% | 5 | 1,15% | 5 | 1,15% |
| Kussakin (1967) | 5 | 0,61% | 2 | 0,46% | 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 | 1,14% | 5 | 1,15% | 5 | 1,15% |
| Monod (1925) | 5 | 0,61% | 5 | 1,14% | 5 | 1,15% | 5 | 1,15% |
| 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 | 1,14% | 5 | 1,15% | 5 | 1,15% |
| Ahyong (2014) | 4 | 0,49% | 4 | 0,91% | 4 | 0,92% | 4 | 0,92% |
| Alekseev et al. (2021) | 4 | 0,49% | 2 | 0,46% | 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 | 0,46% | 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 | 0,46% | 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 | 0,46% | 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% |
| Chappuis (1940) | 3 | 0,37% | 3 | 0,68% | 3 | 0,69% | 3 | 0,69% |
| Chevreux (1887) | 3 | 0,37% | 2 | 0,46% | 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 | 0,46% | 2 | 0,46% | 2 | 0,46% |
| Pélosse (1930) | 3 | 0,37% | 0 | 0% | 0 | 0% | 0 | 0% |
| Questel (2020) | 3 | 0,37% | 2 | 0,46% | 2 | 0,46% | 2 | 0,46% |
| Shulenberger & Barnard (1976) | 3 | 0,37% | 2 | 0,46% | 2 | 0,46% | 2 | 0,46% |
| The Annals & Magazine of Natural History, Serie 5 ; volume 11: 203-207.">Stebbing (1883) | 3 | 0,37% | 2 | 0,46% | 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 | 0,46% | 2 | 0,46% | 2 | 0,46% |
| Bodiou & Colomines (1986) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bodiou & Colomines (1988) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bourcier (1988) | 2 | 0,25% | 2 | 0,46% | 2 | 0,46% | 2 | 0,46% |
| Brehm (1955) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
| Broyer (1985) | 2 | 0,25% | 2 | 0,46% | 2 | 0,46% | 2 | 0,46% |
| Champeau (1967) | 2 | 0,25% | 2 | 0,46% | 2 | 0,46% | 2 | 0,46% |
| Chevreux (1905) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
| Chevreux (1906) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
| Coineau (1977) | 2 | 0,25% | 2 | 0,46% | 2 | 0,46% | 2 | 0,46% |
| Conlan (1990) | 2 | 0,25% | 2 | 0,46% | 2 | 0,46% | 2 | 0,46% |
| Dana (1852) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
| Doflein (1904) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fourt et al. (2017) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
| Godet et al. (2010) | 2 | 0,25% | 2 | 0,46% | 2 | 0,46% | 2 | 0,46% |
| Grindley (1971) | 2 | 0,25% | 2 | 0,46% | 2 | 0,46% | 2 | 0,46% |
| Grygier (1990) | 2 | 0,25% | 2 | 0,46% | 2 | 0,46% | 2 | 0,46% |
| Hansen (1905) | 2 | 0,25% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
| Hayashi (2006) | 2 | 0,25% | 2 | 0,46% | 2 | 0,46% | 2 | 0,46% |
| Kensley (1975) | 2 | 0,25% | 2 | 0,46% | 2 | 0,46% | 2 | 0,46% |
| Kim & Boxshall (2020) | 2 | 0,25% | 2 | 0,46% | 2 | 0,46% | 2 | 0,46% |
| Kottmann et al. (2013) | 2 | 0,25% | 2 | 0,46% | 2 | 0,46% | 2 | 0,46% |
| Krapp-Schickel & Ruffo (2006) | 2 | 0,25% | 2 | 0,46% | 2 | 0,46% | 2 | 0,46% |
| Kusakin & Vasina (1980) | 2 | 0,25% | 2 | 0,46% | 2 | 0,46% | 2 | 0,46% |
| Kussakin & Vasina (1982) | 2 | 0,25% | 2 | 0,46% | 2 | 0,46% | 2 | 0,46% |
| Ledoyer (1977) | 2 | 0,25% | 2 | 0,46% | 2 | 0,46% | 2 | 0,46% |
| Ledoyer (1993) | 2 | 0,25% | 2 | 0,46% | 2 | 0,46% | 2 | 0,46% |
| Linnaeus (1758) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lowry (2007) | 2 | 0,25% | 2 | 0,46% | 2 | 0,46% | 2 | 0,46% |
| Machordom et al. (2022) | 2 | 0,25% | 2 | 0,46% | 2 | 0,46% | 2 | 0,46% |
| Macpherson & Segonzac (2005) | 2 | 0,25% | 2 | 0,46% | 2 | 0,46% | 2 | 0,46% |
| Martin (2011) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
| Monard (1925) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
| Monod (1930) | 2 | 0,25% | 2 | 0,46% | 2 | 0,46% | 2 | 0,46% |
| Monod (1931) | 2 | 0,25% | 2 | 0,46% | 2 | 0,46% | 2 | 0,46% |
| Montagu (1808) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pelosse (1925) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pelosse (1927) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
| Poupin et al. (1999) | 2 | 0,25% | 1 | 0,23% | 1 | 0,23% | 1 | 0,23% |
| Risso (1816) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
| Schellenberg (1931) | 2 | 0,25% | 2 | 0,46% | 2 | 0,46% | 2 | 0,46% |
| Schultz (1981) | 2 | 0,25% | 2 | 0,46% | 2 | 0,46% | 2 | 0,46% |
| Sheppard (1957) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
| Studer (1879) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
| Studer (1884) | 2 | 0,25% | 0 | 0% | 0 | 0% | 0 | 0% |
| Wagele (1987) | 2 | 0,25% | 2 | 0,46% | 2 | 0,46% | 2 | 0,46% |
| Wilson & Wagele (1994) | 2 | 0,25% | 2 | 0,46% | 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 & 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% |
| 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% |
| 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% |
| 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% |
