Poissons marins de Clipperton
202 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
| Référence | Total | Valides | Espèces | Taxons terminaux | ||||
|---|---|---|---|---|---|---|---|---|
| nb | % | nb | % | nb | % | nb | % | |
| Fourriére et al. (2014) | 132 | 8,47% | 128 | 59,53% | 127 | 59,62% | 128 | 60,09% |
| Fricke et al. (2011) | 111 | 7,12% | 107 | 49,77% | 107 | 50,23% | 107 | 50,23% |
| Siu et al. (2017) | 106 | 6,8% | 103 | 47,91% | 103 | 48,36% | 103 | 48,36% |
| Fricke et al. (2009) | 94 | 6,03% | 90 | 41,86% | 90 | 42,25% | 90 | 42,25% |
| Wickel & Jamon (2010) | 76 | 4,88% | 71 | 33,02% | 71 | 33,33% | 71 | 33,33% |
| Delrieu-Trottin et al. (2015) | 67 | 4,3% | 63 | 29,3% | 63 | 29,58% | 63 | 29,58% |
| Béarez & Séret (2009) | 63 | 4,04% | 60 | 27,91% | 60 | 28,17% | 60 | 28,17% |
| Williams et al. (2006) | 47 | 3,02% | 46 | 21,4% | 46 | 21,6% | 46 | 21,6% |
| Bacchet et al. (2007) | 46 | 2,95% | 40 | 18,6% | 40 | 18,78% | 40 | 18,78% |
| Fricke et al. (2013) | 38 | 2,44% | 38 | 17,67% | 38 | 17,84% | 38 | 17,84% |
| Kulbicki et al. (2000) | 38 | 2,44% | 33 | 15,35% | 33 | 15,49% | 32 | 15,02% |
| Béarez et al. (2017) | 34 | 2,18% | 34 | 15,81% | 34 | 15,96% | 34 | 15,96% |
| Chabanet & Durville (2005) | 30 | 1,93% | 25 | 11,63% | 25 | 11,74% | 25 | 11,74% |
| Questel (2020) | 28 | 1,8% | 27 | 12,56% | 27 | 12,68% | 26 | 12,21% |
| Cuvier & Valenciennes (1833) | 26 | 1,67% | 1 | 0,47% | 1 | 0,47% | 1 | 0,47% |
| Kulbicki (comm. pers., 2011) | 26 | 1,67% | 20 | 9,3% | 20 | 9,39% | 20 | 9,39% |
| Questel & Le Quellec (2012) | 25 | 1,6% | 23 | 10,7% | 23 | 10,8% | 22 | 10,33% |
| Poey (1858-61) | 21 | 1,35% | 0 | 0% | 0 | 0% | 0 | 0% |
| Collette & Nauen (1983) | 19 | 1,22% | 19 | 8,84% | 19 | 8,92% | 19 | 8,92% |
| Richard et al. (1982) | 19 | 1,22% | 7 | 3,26% | 7 | 3,29% | 6 | 2,82% |
| Béarez & Bouffandeau (2019) | 16 | 1,03% | 16 | 7,44% | 16 | 7,51% | 16 | 7,51% |
| Rafinesque Schmaltz (1810) | 14 | 0,9% | 3 | 1,4% | 3 | 1,41% | 3 | 1,41% |
| Bouchon-Navaro et al. (2005) | 13 | 0,83% | 10 | 4,65% | 10 | 4,69% | 10 | 4,69% |
| Linnaeus (1758) | 12 | 0,77% | 4 | 1,86% | 4 | 1,88% | 4 | 1,88% |
| Smith (1997) | 12 | 0,77% | 10 | 4,65% | 10 | 4,69% | 10 | 4,69% |
| Snodgrass & Heller (1905) | 12 | 0,77% | 5 | 2,33% | 5 | 2,35% | 5 | 2,35% |
| Allen (comm. pers., 2009) | 11 | 0,71% | 8 | 3,72% | 8 | 3,76% | 7 | 3,29% |
| Müller & Henle (1841) | 9 | 0,58% | 0 | 0% | 0 | 0% | 0 | 0% |
| Compagno (1984) | 8 | 0,51% | 8 | 3,72% | 8 | 3,76% | 8 | 3,76% |
| Compagno (1984) | 8 | 0,51% | 8 | 3,72% | 8 | 3,76% | 8 | 3,76% |
| Gronow (1854) | 7 | 0,45% | 0 | 0% | 0 | 0% | 0 | 0% |
| Legand (1950) | 7 | 0,45% | 3 | 1,4% | 3 | 1,41% | 3 | 1,41% |
| Transactions of the Zoological Society of London, 1839: 1-20.">Lowe (1839) | 7 | 0,45% | 0 | 0% | 0 | 0% | 0 | 0% |
| Risso (1827) | 7 | 0,45% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bloch & Schneider (1801) | 6 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cuvier & Valenciennes ([1832]) | 6 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
| Nardo (1827) | 6 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
| Randall & Earle (2000) | 6 | 0,39% | 5 | 2,33% | 5 | 2,35% | 5 | 2,35% |
| Cuvier & Valenciennes (1846) | 5 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
| Klunzinger (1871) | 5 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rousseau (2010) | 5 | 0,32% | 5 | 2,33% | 5 | 2,35% | 5 | 2,35% |
| Bonaparte (1837) | 4 | 0,26% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bouchon-Navaro & Louis (1986) | 4 | 0,26% | 3 | 1,4% | 3 | 1,41% | 3 | 1,41% |
| Charbonnel (1990) | 4 | 0,26% | 4 | 1,86% | 4 | 1,88% | 4 | 1,88% |
| Rafinesque (1810) | 4 | 0,26% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rüppell (1835) | 4 | 0,26% | 1 | 0,47% | 1 | 0,47% | 1 | 0,47% |
| Swainson (1839) | 4 | 0,26% | 0 | 0% | 0 | 0% | 0 | 0% |
| Vaslet & Agrnsm (2018) | 4 | 0,26% | 4 | 1,86% | 4 | 1,88% | 4 | 1,88% |
| Allen & Robertson (1995) | 3 | 0,19% | 3 | 1,4% | 3 | 1,41% | 3 | 1,41% |
| Allen & Robertson (1995) | 3 | 0,19% | 3 | 1,4% | 3 | 1,41% | 3 | 1,41% |
| Allen & Robertson (1999) | 3 | 0,19% | 3 | 1,4% | 3 | 1,41% | 3 | 1,41% |
| Allen (1995) | 3 | 0,19% | 3 | 1,4% | 3 | 1,41% | 3 | 1,41% |
| Bonnaterre (1788) | 3 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
| Brugneaux & Pérès (2006) | 3 | 0,19% | 3 | 1,4% | 3 | 1,41% | 3 | 1,41% |
| Cuvier & Valenciennes (1830-1832) | 3 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fowler (1919) | 3 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hemida et al. (2003) | 3 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hutchinson et al. (2019) | 3 | 0,19% | 3 | 1,4% | 3 | 1,41% | 3 | 1,41% |
| Kiszka et al. (2009) | 3 | 0,19% | 2 | 0,93% | 2 | 0,94% | 2 | 0,94% |
| Lacepède (1801) | 3 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lacepède (1803) | 3 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lorvelec & Pascal (2009) | 3 | 0,19% | 3 | 1,4% | 3 | 1,41% | 3 | 1,41% |
| Philippi (1887) | 3 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
| Philippi (1902) | 3 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
| protection du biotope des eaux territoriales de l'île de Clipperton dénommée « aire marine protégée dans les eaux territoriales de l'île de Clipperton » | 3 | 0,19% | 3 | 1,4% | 3 | 1,41% | 3 | 1,41% |
| Schaefer (1987) | 3 | 0,19% | 3 | 1,4% | 3 | 1,41% | 3 | 1,41% |
| Springer (1962) | 3 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
| Berry & Smith-Vaniz (1978) | 2 | 0,13% | 2 | 0,93% | 2 | 0,94% | 2 | 0,94% |
| Bleeker (1852) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bloch & Schneider (1801) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Clua & Planes (2019) | 2 | 0,13% | 2 | 0,93% | 2 | 0,94% | 2 | 0,94% |
| Clua et al. (2019) | 2 | 0,13% | 2 | 0,93% | 2 | 0,94% | 2 | 0,94% |
| Collette (2003) | 2 | 0,13% | 2 | 0,93% | 2 | 0,94% | 2 | 0,94% |
| Craig et al. (2006) | 2 | 0,13% | 2 | 0,93% | 2 | 0,94% | 2 | 0,94% |
| Diaz & Cuzange (2009) | 2 | 0,13% | 2 | 0,93% | 2 | 0,94% | 2 | 0,94% |
| Evermann & Clark (1928) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fourt et al. (2017) | 2 | 0,13% | 2 | 0,93% | 2 | 0,94% | 2 | 0,94% |
| Fricke et al. (2024) | 2 | 0,13% | 2 | 0,93% | 2 | 0,94% | 2 | 0,94% |
| Garman (1913) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gmelin (1789) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Greenfield (1965) | 2 | 0,13% | 2 | 0,93% | 2 | 0,94% | 2 | 0,94% |
| Griffith & Smith (1834) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Günther (1880) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Keith et al. (2013) | 2 | 0,13% | 2 | 0,93% | 2 | 0,94% | 2 | 0,94% |
| Kner & Steindachner (1867) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Letourneur et al. (2004) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Macdonald & Barron (1868) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Marshall et al. (2009) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Menzies (1791) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Millot et al. (2023) | 2 | 0,13% | 2 | 0,93% | 2 | 0,94% | 2 | 0,94% |
| Muss et al. (2001) | 2 | 0,13% | 2 | 0,93% | 2 | 0,94% | 2 | 0,94% |
| Nakamura (1985) | 2 | 0,13% | 2 | 0,93% | 2 | 0,94% | 2 | 0,94% |
| Palko et al. (1982) | 2 | 0,13% | 2 | 0,93% | 2 | 0,94% | 2 | 0,94% |
| Pallas (1770) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pearman et al. (2020) | 2 | 0,13% | 2 | 0,93% | 2 | 0,94% | 2 | 0,94% |
| Pennant (1776) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Perez Canto (1886) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Poey (1851-1854) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Quero et al. (2013) | 2 | 0,13% | 2 | 0,93% | 2 | 0,94% | 2 | 0,94% |
| Rignault & Chevallier (2017) | 2 | 0,13% | 2 | 0,93% | 2 | 0,94% | 2 | 0,94% |
| Risso (1810) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Schultz (1943) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Simian et al. (2022) | 2 | 0,13% | 2 | 0,93% | 2 | 0,94% | 2 | 0,94% |
| Smith (1849) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Annali del Museo Civico di Storia Naturale di Genova 18: 465-590, tavv. I-III.">Vinciguerra (1883) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Walbaum (1792) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Weber (1913) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Whitley (1937) | 2 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Wickel et al. (2014) | 2 | 0,13% | 2 | 0,93% | 2 | 0,94% | 2 | 0,94% |
| Agassiz (1833-1843) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Allen (1997) | 1 | 0,06% | 1 | 0,47% | 1 | 0,47% | 1 | 0,47% |
| Atwood (1869) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Baldwin (1963) | 1 | 0,06% | 1 | 0,47% | 1 | 0,47% | 1 | 0,47% |
| Beebe & Tee-van (1932) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bennett (1831) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bertin (1928) | 1 | 0,06% | 1 | 0,47% | 1 | 0,47% | 1 | 0,47% |
| Blainville (1816) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bleeker (1865) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bloch (1785-1795) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bloch (1793) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bodilis et al. (2011) | 1 | 0,06% | 1 | 0,47% | 1 | 0,47% | 1 | 0,47% |
| Bouchon-Navaro et al. (1992) | 1 | 0,06% | 1 | 0,47% | 1 | 0,47% | 1 | 0,47% |
| Brünnich (1768) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Clua et al. (2016) | 1 | 0,06% | 1 | 0,47% | 1 | 0,47% | 1 | 0,47% |
| Collet et al. (2017) | 1 | 0,06% | 1 | 0,47% | 1 | 0,47% | 1 | 0,47% |
| Cooper (1863) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Curd et al. (2015) | 1 | 0,06% | 1 | 0,47% | 1 | 0,47% | 1 | 0,47% |
| Cuvier (1829) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Day (1865) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Desbrosses (1935) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Eudeline (2022) | 1 | 0,06% | 1 | 0,47% | 1 | 0,47% | 1 | 0,47% |
| Euphrasen (1791) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Faber (1829) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Forest (1946) | 1 | 0,06% | 1 | 0,47% | 1 | 0,47% | 1 | 0,47% |
| Fraser-brunner (1950) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fritzsche (1980) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Garman (1913) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gilbert (1891) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gill (1862) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gill (1863) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gill (1863) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ginsburg (1947) | 1 | 0,06% | 1 | 0,47% | 1 | 0,47% | 1 | 0,47% |
| Girondot et al. (2015) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Goulletquer (2016) | 1 | 0,06% | 1 | 0,47% | 1 | 0,47% | 1 | 0,47% |
| Günther (1866) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Proceedings of the Zoological Society of London, 1907: 1035-1037.">Hopkinson (1907) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jordan & Evermann (1903) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jordan & Gilbert (1882) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jordan & Jordan (1922) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jordan & Meek (1885) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jordan (1884) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Keith et al. (2002) | 1 | 0,06% | 1 | 0,47% | 1 | 0,47% | 1 | 0,47% |
| Keith et al. (2006) | 1 | 0,06% | 1 | 0,47% | 1 | 0,47% | 1 | 0,47% |
| Kishinouye (1920) | 1 | 0,06% | 1 | 0,47% | 1 | 0,47% | 1 | 0,47% |
| Lacepède (1798) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lacepède (1800) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Last et al. (2016) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Legendre (1937) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lesson (1830-1831) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lesueur (1822) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Liénard (1840) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Linnaeus (1766) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Louis et al. (1992) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lowe (1834) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Proceedings of the general meetings for scientific business of the Zoological Society of London, 1839: 76-92.">Lowe (1839) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lowe (1841) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lowe (1843) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Malm (1877) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Meek & Hildebrand (1923) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Moreau (1881) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mourier (2012) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Murray (1884) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Murray (1887) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Nelson-Smith et al. (2014) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Noël, Meunier (2010) | 1 | 0,06% | 1 | 0,47% | 1 | 0,47% | 1 | 0,47% |
| Noronha (1926) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Notarbartolo et al. (2020) | 1 | 0,06% | 1 | 0,47% | 1 | 0,47% | 1 | 0,47% |
| Ogilby (1908) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Osbeck (1765) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Osburn & Nichols (1816) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Owen (1853) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pellegrin (1912) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Annales de la Société de Sciences naturelles de la Charente-Maritime, 10(2): 225-236.">Quéro et al. (2011) | 1 | 0,06% | 1 | 0,47% | 1 | 0,47% | 1 | 0,47% |
| Questel (2023) | 1 | 0,06% | 1 | 0,47% | 1 | 0,47% | 1 | 0,47% |
| Ranzani (1839) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Richardson (1846) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Richer de Forges et al. (2005) | 1 | 0,06% | 1 | 0,47% | 1 | 0,47% | 1 | 0,47% |
| Sawai et al. (2018) | 1 | 0,06% | 1 | 0,47% | 1 | 0,47% | 1 | 0,47% |
| Séret (1997) | 1 | 0,06% | 1 | 0,47% | 1 | 0,47% | 1 | 0,47% |
| Séret (2014) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Snyder (1904) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Springer (1941) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Steindachner (1867) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Storer (1839) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Uyeno et al. (1983) | 1 | 0,06% | 1 | 0,47% | 1 | 0,47% | 1 | 0,47% |
| Van & Kampen (1907) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Victor et al. (2001) | 1 | 0,06% | 1 | 0,47% | 1 | 0,47% | 1 | 0,47% |
| Waite (1904) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Whitley (1929) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Whitley (1931) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Whitley (1933) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Whitley (1937) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
