Crustacés marins de la Réunion
Branchiopoda, Oligostraca et Multicrustacea marins (sens large) de la Réunion
341 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
Référence | Total | Valides | Espèces | Taxons terminaux | ||||
---|---|---|---|---|---|---|---|---|
nb | % | nb | % | nb | % | nb | % | |
Poupin (2010) | 1453 | 81,04% | 1329 | 193,73% | 1328 | 194,72% | 1321 | 193,7% |
Poupin et al. (2018) | 180 | 10,04% | 169 | 24,64% | 168 | 24,63% | 169 | 24,78% |
Poupin et al. (2013) | 124 | 6,92% | 113 | 16,47% | 113 | 16,57% | 112 | 16,42% |
Poupin (2015) | 74 | 4,13% | 70 | 10,2% | 70 | 10,26% | 70 | 10,26% |
Poupin et al. (2013) | 35 | 1,95% | 32 | 4,66% | 32 | 4,69% | 31 | 4,55% |
Crosnier (1976) | 29 | 1,62% | 23 | 3,35% | 23 | 3,37% | 23 | 3,37% |
Colin (2000) | 24 | 1,34% | 23 | 3,35% | 23 | 3,37% | 23 | 3,37% |
Rathbun (1907) | 21 | 1,17% | 9 | 1,31% | 9 | 1,32% | 9 | 1,32% |
Babinot & Kouyoumontzakis (1995) | 17 | 0,95% | 12 | 1,75% | 12 | 1,76% | 12 | 1,76% |
Keith et al. (2006) | 17 | 0,95% | 16 | 2,33% | 16 | 2,35% | 16 | 2,35% |
Bourjon et al. (2018) | 16 | 0,89% | 16 | 2,33% | 16 | 2,35% | 16 | 2,35% |
Corbari et al. (2020) | 15 | 0,84% | 13 | 1,9% | 13 | 1,91% | 13 | 1,91% |
Li (2008) | 15 | 0,84% | 12 | 1,75% | 12 | 1,76% | 12 | 1,76% |
Poupin et al. (2013) | 15 | 0,84% | 14 | 2,04% | 14 | 2,05% | 14 | 2,05% |
Whatley & Keeler (1989) | 15 | 0,84% | 13 | 1,9% | 13 | 1,91% | 13 | 1,91% |
Poupin et al. (2022) | 14 | 0,78% | 14 | 2,04% | 14 | 2,05% | 14 | 2,05% |
Keith et al. (2013) | 13 | 0,73% | 13 | 1,9% | 13 | 1,91% | 13 | 1,91% |
Müller (1990) | 12 | 0,67% | 12 | 1,75% | 12 | 1,76% | 12 | 1,76% |
"The Fauna and Geography of the Maldive and Laccadive Archipelagoes" edited by J. Stanley Gardiner, Cambridge, 4to, vol. ii, part 4: 852-921, pls. lxx-lxxxvii, text-figg. 127-139.: 852-921.">Coutiere (1905) | 11 | 0,61% | 4 | 0,58% | 4 | 0,59% | 4 | 0,59% |
Macpherson & Robainas-Barcia (2015) | 11 | 0,61% | 11 | 1,6% | 11 | 1,61% | 11 | 1,61% |
Nobili (1906) | 11 | 0,61% | 5 | 0,73% | 5 | 0,73% | 5 | 0,73% |
Foster & Buckeridge (1994) | 10 | 0,56% | 6 | 0,87% | 6 | 0,88% | 6 | 0,88% |
Lagarde (2008) | 10 | 0,56% | 10 | 1,46% | 10 | 1,47% | 10 | 1,47% |
Poupin & Corbari (2016) | 10 | 0,56% | 10 | 1,46% | 10 | 1,47% | 10 | 1,47% |
Poupin et al. (2022) | 10 | 0,56% | 9 | 1,31% | 9 | 1,32% | 9 | 1,32% |
Bozic (1965) | 9 | 0,5% | 6 | 0,87% | 6 | 0,88% | 6 | 0,88% |
Keith et al. (1999) | 9 | 0,5% | 9 | 1,31% | 9 | 1,32% | 9 | 1,32% |
Macpherson et al. (2002) | 9 | 0,5% | 0 | 0% | 0 | 0% | 0 | 0% |
Ramage (2017) | 9 | 0,5% | 9 | 1,31% | 9 | 1,32% | 9 | 1,32% |
Fourt et al. (2017) | 8 | 0,45% | 8 | 1,17% | 8 | 1,17% | 8 | 1,17% |
Paris. pp. [i]-xii, 9-320 ; [Atlas] Crustacés, 5 planches ; Insectes, 21 planches.">Guérin-Méneville ([1829-1838]) | 8 | 0,45% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
Guinot et al. (2018) | 8 | 0,45% | 8 | 1,17% | 8 | 1,17% | 8 | 1,17% |
Linnaeus (1758) | 8 | 0,45% | 0 | 0% | 0 | 0% | 0 | 0% |
Rathbun (1906) | 8 | 0,45% | 4 | 0,58% | 4 | 0,59% | 4 | 0,59% |
Collin (2000) | 7 | 0,39% | 7 | 1,02% | 7 | 1,03% | 7 | 1,03% |
Poupin (1994) | 7 | 0,39% | 6 | 0,87% | 6 | 0,88% | 6 | 0,88% |
Questel (2020) | 7 | 0,39% | 7 | 1,02% | 7 | 1,03% | 7 | 1,03% |
Rodríguez-Flores et al. (2021) | 7 | 0,39% | 7 | 1,02% | 7 | 1,03% | 7 | 1,03% |
Chace (1962) | 6 | 0,33% | 6 | 0,87% | 6 | 0,88% | 6 | 0,88% |
Coutures (2001) | 6 | 0,33% | 6 | 0,87% | 6 | 0,88% | 6 | 0,88% |
Guinot (1985) | 6 | 0,33% | 6 | 0,87% | 6 | 0,88% | 6 | 0,88% |
Machordom et al. (2022) | 6 | 0,33% | 6 | 0,87% | 6 | 0,88% | 6 | 0,88% |
Macpherson (2007) | 6 | 0,33% | 6 | 0,87% | 6 | 0,88% | 6 | 0,88% |
Müller (1991) | 6 | 0,33% | 6 | 0,87% | 6 | 0,88% | 6 | 0,88% |
Müller (1991) | 6 | 0,33% | 0 | 0% | 0 | 0% | 0 | 0% |
Risso (1816) | 6 | 0,33% | 0 | 0% | 0 | 0% | 0 | 0% |
Roux (1926) | 6 | 0,33% | 5 | 0,73% | 5 | 0,73% | 5 | 0,73% |
Tricart & Foubert (2000) | 6 | 0,33% | 6 | 0,87% | 6 | 0,88% | 6 | 0,88% |
Cleva & Poupin (2012) | 5 | 0,28% | 5 | 0,73% | 5 | 0,73% | 5 | 0,73% |
Collin (2002) | 5 | 0,28% | 5 | 0,73% | 5 | 0,73% | 5 | 0,73% |
Crosnier (1965) | 5 | 0,28% | 5 | 0,73% | 5 | 0,73% | 5 | 0,73% |
Fabricius (1798) | 5 | 0,28% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Keith & Vigneux (2002) | 5 | 0,28% | 5 | 0,73% | 5 | 0,73% | 5 | 0,73% |
Komai (2010) | 5 | 0,28% | 5 | 0,73% | 5 | 0,73% | 5 | 0,73% |
Kropp (1988) | 5 | 0,28% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Kubo (1949) | 5 | 0,28% | 0 | 0% | 0 | 0% | 0 | 0% |
Laubitz (1995) | 5 | 0,28% | 5 | 0,73% | 5 | 0,73% | 5 | 0,73% |
Maddocks (2007) | 5 | 0,28% | 3 | 0,44% | 3 | 0,44% | 3 | 0,44% |
Nobili (1905) | 5 | 0,28% | 0 | 0% | 0 | 0% | 0 | 0% |
Ribes (1989) | 5 | 0,28% | 4 | 0,58% | 4 | 0,59% | 4 | 0,59% |
Stimpson (1860) | 5 | 0,28% | 5 | 0,73% | 5 | 0,73% | 5 | 0,73% |
Ahyong (2014) | 4 | 0,22% | 4 | 0,58% | 4 | 0,59% | 4 | 0,59% |
Anker & Baeza (2021) | 4 | 0,22% | 4 | 0,58% | 4 | 0,59% | 4 | 0,59% |
Bouvier (1914) | 4 | 0,22% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
Bruce (1967) | 4 | 0,22% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
Chan et al. (2021) | 4 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Crosnier (2002) | 4 | 0,22% | 3 | 0,44% | 3 | 0,44% | 2 | 0,29% |
Edmondson (1925) | 4 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Galil et al. (2018) | 4 | 0,22% | 4 | 0,58% | 4 | 0,59% | 4 | 0,59% |
Jellinek (1993) | 4 | 0,22% | 4 | 0,58% | 4 | 0,59% | 4 | 0,59% |
Komai (2008) | 4 | 0,22% | 4 | 0,58% | 4 | 0,59% | 4 | 0,59% |
Mclaughlin & Haig (1989) | 4 | 0,22% | 4 | 0,58% | 4 | 0,59% | 4 | 0,59% |
Bulletin of the Museum of Comparative Zoology at Harvard College. 8(2): 1-68, Pl. 1-2.">Milne-Edwards (1880) | 4 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Müller (1991) | 4 | 0,22% | 4 | 0,58% | 4 | 0,59% | 4 | 0,59% |
Paulmier (1996) | 4 | 0,22% | 3 | 0,44% | 3 | 0,44% | 3 | 0,44% |
Poore & Dworschak (2018) | 4 | 0,22% | 4 | 0,58% | 4 | 0,59% | 4 | 0,59% |
Ward (1942) | 4 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Barnard (1950) | 3 | 0,17% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
Bigot (2006) | 3 | 0,17% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
Bourcier (1988) | 3 | 0,17% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
Bozić (1964) | 3 | 0,17% | 3 | 0,44% | 3 | 0,44% | 3 | 0,44% |
Brady (1868) | 3 | 0,17% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Bruce (1979) | 3 | 0,17% | 3 | 0,44% | 3 | 0,44% | 3 | 0,44% |
Chan (1991) | 3 | 0,17% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
Chevreux (1887) | 3 | 0,17% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Edmondson (1954) | 3 | 0,17% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Grygier (1985) | 3 | 0,17% | 3 | 0,44% | 3 | 0,44% | 3 | 0,44% |
Guinot & Richer de Forges (1981) | 3 | 0,17% | 3 | 0,44% | 3 | 0,44% | 3 | 0,44% |
Lemaitre (1989) | 3 | 0,17% | 3 | 0,44% | 3 | 0,44% | 3 | 0,44% |
Lucatelli et al. (2012) | 3 | 0,17% | 3 | 0,44% | 3 | 0,44% | 3 | 0,44% |
Macpherson et al. (2017) | 3 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Macpherson (1988) | 3 | 0,17% | 3 | 0,44% | 3 | 0,44% | 3 | 0,44% |
Man (1902) | 3 | 0,17% | 3 | 0,44% | 3 | 0,44% | 3 | 0,44% |
Manning (1978) | 3 | 0,17% | 3 | 0,44% | 3 | 0,44% | 3 | 0,44% |
Marquet (2002) | 3 | 0,17% | 3 | 0,44% | 3 | 0,44% | 3 | 0,44% |
Milne-Edwards (1865) | 3 | 0,17% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Müller (1990) | 3 | 0,17% | 3 | 0,44% | 3 | 0,44% | 3 | 0,44% |
Mulochau et al. (2019) | 3 | 0,17% | 3 | 0,44% | 3 | 0,44% | 3 | 0,44% |
Ngoc-Ho (1989) | 3 | 0,17% | 3 | 0,44% | 3 | 0,44% | 3 | 0,44% |
Nobili (1904) | 3 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Odhner (1925) | 3 | 0,17% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Olivier (1791-[1792]) | 3 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Poupin et al. (1999) | 3 | 0,17% | 3 | 0,44% | 3 | 0,44% | 3 | 0,44% |
Questel & Le Quellec (2012) | 3 | 0,17% | 3 | 0,44% | 3 | 0,44% | 3 | 0,44% |
Rathbun (1914) | 3 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Rignault & Chevallier (2017) | 3 | 0,17% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
Schmitt (1939) | 3 | 0,17% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Spiridonov et al. (2021) | 3 | 0,17% | 3 | 0,44% | 3 | 0,44% | 3 | 0,44% |
Tavares (1994) | 3 | 0,17% | 3 | 0,44% | 3 | 0,44% | 3 | 0,44% |
Tavares (2006) | 3 | 0,17% | 3 | 0,44% | 3 | 0,44% | 3 | 0,44% |
Vereshchaka et al. (2020) | 3 | 0,17% | 3 | 0,44% | 3 | 0,44% | 3 | 0,44% |
Ward (1939) | 3 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Ward (1941) | 3 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Aguilera (2002) | 2 | 0,11% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
Ahyong (2017) | 2 | 0,11% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
Baez et al. (2022) | 2 | 0,11% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
Barnard (1962) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Baudry et al. (2022) | 2 | 0,11% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
Benson & Maddocks (1964) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Bigot et al. (2006) | 2 | 0,11% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Bordaille (1903) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Borradaile (1915) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Boyko & Harvey (1999) | 2 | 0,11% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
Bruce (2006) | 2 | 0,11% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
Burkenroad (1959) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Calman (1909) | 2 | 0,11% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Report Fisheries and Marine Biological Survey Cape Town, 4(3): 1-26.">Calman (1925) | 2 | 0,11% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
Carré (2006) | 2 | 0,11% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
Champion (1973) | 2 | 0,11% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
Chan & Crosnier (1991) | 2 | 0,11% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Chen et al. (2016) | 2 | 0,11% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
Choy & Marquet (2002) | 2 | 0,11% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
Corbari et al. (2015) | 2 | 0,11% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Dana (1852) | 2 | 0,11% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
Bulletin of the Museum at Harvard College, 24 : 149-220.">Faxon (1893) | 2 | 0,11% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Forcellini et al. (2012) | 2 | 0,11% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
Forest (1954) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Fujino & Miyake (1969) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Gordon (1968) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Griffin & Tranter (1986) | 2 | 0,11% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
Guéguen (2000) | 2 | 0,11% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
Guinot (1964) | 2 | 0,11% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
Guinot (1976) | 2 | 0,11% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
, 50: 47-86.">Gutu (2007) | 2 | 0,11% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
, 52: 101-125.">Gutu (2009) | 2 | 0,11% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
, 55(1): 27-40.">Gutu (2012) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Harada (1961) | 2 | 0,11% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
Hayashi (2009) | 2 | 0,11% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
Hiller & Werding (2016) | 2 | 0,11% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
Huys & Gee (1996) | 2 | 0,11% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
Huys & Lee (1999) | 2 | 0,11% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
Kemp (1922) | 2 | 0,11% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
Kensley (1977) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Kiefer (1960) | 2 | 0,11% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
Komai & Ng (2012) | 2 | 0,11% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
Komai & Osawa (2006) | 2 | 0,11% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
Komai (2004) | 2 | 0,11% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
Kubo (1955) | 2 | 0,11% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
Laurie (1906) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Lemaitre (1994) | 2 | 0,11% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
Lemaitre (1996) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Lucas (1846) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Maddocks (1969) | 2 | 0,11% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
Malay et al. (2012) | 2 | 0,11% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
Manning (1978) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Mazancourt et al. (2019) | 2 | 0,11% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
Mclaughlin (1986) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Mendoza & Devi (2017) | 2 | 0,11% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
Milne-Edwards (1878) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Müller (1992) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Nelson-Smith et al. (2014) | 2 | 0,11% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Nguyen (2010) | 2 | 0,11% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Ortmann (1892) | 2 | 0,11% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
Perez & Farfante (1977) | 2 | 0,11% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
Perez & Farfante (1980) | 2 | 0,11% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
Poupin (1997) | 2 | 0,11% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
Poupin (2008) | 2 | 0,11% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
Rathbun (1911) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Richer et al. (1996) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Risso (1827) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Rodriguez et al. (2019) | 2 | 0,11% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
Saint & Laurent (1972) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Sakai (1983) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Schioedte & Meinert (1884) | 2 | 0,11% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
Schotte et al. (1995 onwards) | 2 | 0,11% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Shahdadi & Schubart (2020) | 2 | 0,11% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
Stebbing (1917) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Stock (1986) | 2 | 0,11% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
Takeda (1977) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Tan & Ng (1996) | 2 | 0,11% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
Thomassin (1973) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Turkay (1978) | 2 | 0,11% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
Van et al. (2011) | 2 | 0,11% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Ward (1934) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Wood-Mason & Alcock(1891) | 2 | 0,11% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Wooster (1982) | 2 | 0,11% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
Yokoya (1936) | 2 | 0,11% | 2 | 0,29% | 2 | 0,29% | 2 | 0,29% |
Zarenkov (1989) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Achituv & Langsam (2009) | 1 | 0,06% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Ahyong & Caldwell (2017) | 1 | 0,06% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Ahyong (2001) | 1 | 0,06% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Aizawa (1974) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Alcock & Anderson (1899) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Annals of Natural History, (6)(xiii): pp. 225-245, 321-331, & 400-411.">Alcock (1894) | 1 | 0,06% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Alcock (1905) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Anker (2010) | 1 | 0,06% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Anker (2017) | 1 | 0,06% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Asakura (2001) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Balss (1911) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Balss (1938) | 1 | 0,06% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Banner & Banner (1966) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Barnard (1914) | 1 | 0,06% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Bernasconi (2000) | 1 | 0,06% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Bulletin of the Vanderbilt Marine Museum, 5: 1-210.">Boone (1934) | 1 | 0,06% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Bordaille (1902) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Bordaille (1916) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Boyko (2000) | 1 | 0,06% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Boyko (2010) | 1 | 0,06% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Breton (2014) | 1 | 0,06% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Bruce & Trautwein (2007) | 1 | 0,06% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Bruce (1966) | 1 | 0,06% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Bruce (1974) | 1 | 0,06% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Bruce (1981) | 1 | 0,06% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Bruce (1988) | 1 | 0,06% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Bruce (2005) | 1 | 0,06% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Burkenroad (1936) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Burukovsky (1993) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Cambert et al. (2011) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Chan et al. (2016) | 1 | 0,06% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Chappuis et al. (1956) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Chia & Ng (2000) | 1 | 0,06% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Costes (1890) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Coutiere (1909) | 1 | 0,06% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Crosnier (1978) | 1 | 0,06% | 1 | 0,15% | 0 | 0% | 1 | 0,15% |
Crosnier (1986) | 1 | 0,06% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Crosnier (2002) | 1 | 0,06% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Dervin et al. (2014) | 1 | 0,06% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Edmondson (1952) | 1 | 0,06% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
European Nucleotide Archive (2019) | 1 | 0,06% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Fabricius ([1777]) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1787) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Fize & Serene (1957) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Forest (1958) | 1 | 0,06% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Galil (2003) | 1 | 0,06% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Gall & Beague (1986) | 1 | 0,06% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Godet et al. (2010) | 1 | 0,06% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Goulletquer (2016) | 1 | 0,06% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Gourret (1891) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Gout (1991) | 1 | 0,06% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Goy & Devaney (1980) | 1 | 0,06% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Goy (2015) | 1 | 0,06% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Gutu (2011) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Haig & Kropp (1987) | 1 | 0,06% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Haller (1880) | 1 | 0,06% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Hayashi (1999) | 1 | 0,06% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Proceedings of the United States National Museum. 35(1654): 489-543; 46 figs.">Holmes (1908) | 1 | 0,06% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Holthuis (1941) | 1 | 0,06% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Holthuis (1952) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Holthuis (1955) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Holthuis (1963) | 1 | 0,06% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Holthuis (1977) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Huang & Shih (2021) | 1 | 0,06% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Ifremer (2009) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Ifremer (2022) | 1 | 0,06% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Jacquemet et al. (2011) | 1 | 0,06% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Javed (1990) | 1 | 0,06% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Jayachandran & Raji (2004) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Jourdan & Mille (2006) | 1 | 0,06% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Jourdan (2020) | 1 | 0,06% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Kamita (1967) | 1 | 0,06% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Keith et al. (2002) | 1 | 0,06% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Klunzinger (1913) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Komai & Poupin (2013) | 1 | 0,06% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Komai & Shimetsugu (2019) | 1 | 0,06% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Komai (1999) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Lalubie et al. (2015) | 1 | 0,06% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Lebeau (1976) | 1 | 0,06% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Ledoyer (1986) | 1 | 0,06% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Lee et al. (2019) | 1 | 0,06% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Leene (1936) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Lemaitre (2004) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Lenz & Strunck (1914) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Lim et al. (2002) | 1 | 0,06% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Annals of Natural History, (7)(xv): 233-268.">MacGilchrist (1905) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Macpherson (2004) | 1 | 0,06% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Malz & Jellinek (1989) | 1 | 0,06% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Tijdschrift der Nederlandsche Dierkundige Vereeniging, 2(3 & 4): 587-614.">Man (1905) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Leiden Notes Mus Jentink, 29: 127-145.">Man (1907) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Man (1911) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Manning & Holthuis (1989) | 1 | 0,06% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Marin (2007) | 1 | 0,06% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Marin (2012) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Mary (2017) | 1 | 0,06% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Mclay (2001) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Melzer (2014) | 1 | 0,06% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Miers (1879) | 1 | 0,06% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Miers (1881) | 1 | 0,06% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Milne-Edwards (1890) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Miquel (1984) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Miyake (1939) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Murienne et al. (2022) | 1 | 0,06% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Nobili (1901) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Nobili (1903) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Noël & Boulad (2018) | 1 | 0,06% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Noël (1986) | 1 | 0,06% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Noël (2013) | 1 | 0,06% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Noël (2014) | 1 | 0,06% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Noël (2014) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Noël (2015) | 1 | 0,06% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Noël (2015) | 1 | 0,06% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Noël (2016) | 1 | 0,06% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Noël (2017) | 1 | 0,06% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Noël (2017) | 1 | 0,06% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Noël et al. (1996) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Šobánová & Duriš (2021) | 1 | 0,06% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Olivier & Latreille (1811) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Olivier (1811) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Ortmann (1890) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Parisi (1916) | 1 | 0,06% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Peters (1852) | 1 | 0,06% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Pezy et al. (2017) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Pfaller et al. (2019) | 1 | 0,06% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Poisson & Legueux (1926) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Ramadan (1938) | 1 | 0,06% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Sakai (1969) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Schnabel & Ahyong (2010) | 1 | 0,06% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Serene (1984) | 1 | 0,06% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Shih et al. (2016) | 1 | 0,06% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Short & Marquet (1998) | 1 | 0,06% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Siebold (1824) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Singh (2021) | 1 | 0,06% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Stebbing (1914) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Stebbing (1915) | 1 | 0,06% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Stebbing (1923) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Stimpson (1860) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Terao (1913) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Thompson (1943) | 1 | 0,06% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Ward (1933) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Werding & Hiller (2007) | 1 | 0,06% | 1 | 0,15% | 1 | 0,15% | 1 | 0,15% |
Yokoya (1933) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Zarenkov (1994) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |