Crustacés de la Réunion
373 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) | 1464 | 78,54% | 1340 | 187,94% | 1339 | 188,86% | 1332 | 187,87% |
Poupin et al. (2018) | 182 | 9,76% | 171 | 23,98% | 170 | 23,98% | 171 | 24,12% |
Poupin et al. (2013) | 125 | 6,71% | 114 | 15,99% | 114 | 16,08% | 113 | 15,94% |
Poupin (2015) | 76 | 4,08% | 72 | 10,1% | 72 | 10,16% | 72 | 10,16% |
Poupin et al. (2013) | 36 | 1,93% | 33 | 4,63% | 33 | 4,65% | 32 | 4,51% |
Crosnier (1976) | 29 | 1,56% | 23 | 3,23% | 23 | 3,24% | 23 | 3,24% |
Colin (2000) | 24 | 1,29% | 23 | 3,23% | 23 | 3,24% | 23 | 3,24% |
Rathbun (1907) | 21 | 1,13% | 9 | 1,26% | 9 | 1,27% | 9 | 1,27% |
Babinot & Kouyoumontzakis (1995) | 17 | 0,91% | 12 | 1,68% | 12 | 1,69% | 12 | 1,69% |
Keith et al. (2006) | 17 | 0,91% | 16 | 2,24% | 16 | 2,26% | 16 | 2,26% |
Bourjon et al. (2018) | 16 | 0,86% | 16 | 2,24% | 16 | 2,26% | 16 | 2,26% |
Corbari et al. (2020) | 15 | 0,8% | 13 | 1,82% | 13 | 1,83% | 13 | 1,83% |
Li (2008) | 15 | 0,8% | 12 | 1,68% | 12 | 1,69% | 12 | 1,69% |
Poupin et al. (2013) | 15 | 0,8% | 14 | 1,96% | 14 | 1,97% | 14 | 1,97% |
Whatley & Keeler (1989) | 15 | 0,8% | 13 | 1,82% | 13 | 1,83% | 13 | 1,83% |
Poupin et al. (2022) | 14 | 0,75% | 14 | 1,96% | 14 | 1,97% | 14 | 1,97% |
Ramage (2017) | 14 | 0,75% | 14 | 1,96% | 14 | 1,97% | 14 | 1,97% |
Keith et al. (2013) | 13 | 0,7% | 13 | 1,82% | 13 | 1,83% | 13 | 1,83% |
Poupin (2024) | 13 | 0,7% | 13 | 1,82% | 13 | 1,83% | 13 | 1,83% |
Bozic (1965) | 12 | 0,64% | 6 | 0,84% | 6 | 0,85% | 6 | 0,85% |
Müller (1990) | 12 | 0,64% | 12 | 1,68% | 12 | 1,69% | 12 | 1,69% |
"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 | 0,59% | 4 | 0,56% | 4 | 0,56% | 4 | 0,56% |
Macpherson & Robainas-Barcia (2015) | 11 | 0,59% | 11 | 1,54% | 11 | 1,55% | 11 | 1,55% |
Nobili (1906) | 11 | 0,59% | 5 | 0,7% | 5 | 0,71% | 5 | 0,71% |
Foster & Buckeridge (1994) | 10 | 0,54% | 6 | 0,84% | 6 | 0,85% | 6 | 0,85% |
Lagarde (2008) | 10 | 0,54% | 10 | 1,4% | 10 | 1,41% | 10 | 1,41% |
Poupin & Corbari (2016) | 10 | 0,54% | 10 | 1,4% | 10 | 1,41% | 10 | 1,41% |
Poupin et al. (2022) | 10 | 0,54% | 9 | 1,26% | 9 | 1,27% | 9 | 1,27% |
Keith et al. (1999) | 9 | 0,48% | 9 | 1,26% | 9 | 1,27% | 9 | 1,27% |
Macpherson et al. (2002) | 9 | 0,48% | 0 | 0% | 0 | 0% | 0 | 0% |
Fourt et al. (2017) | 8 | 0,43% | 8 | 1,12% | 8 | 1,13% | 8 | 1,13% |
Paris. pp. [i]-xii, 9-320 ; [Atlas] Crustacés, 5 planches ; Insectes, 21 planches.">Guérin-Méneville ([1829-1838]) | 8 | 0,43% | 2 | 0,28% | 2 | 0,28% | 2 | 0,28% |
Guinot et al. (2018) | 8 | 0,43% | 8 | 1,12% | 8 | 1,13% | 8 | 1,13% |
Linnaeus (1758) | 8 | 0,43% | 0 | 0% | 0 | 0% | 0 | 0% |
Questel (2020) | 8 | 0,43% | 8 | 1,12% | 8 | 1,13% | 8 | 1,13% |
Rathbun (1906) | 8 | 0,43% | 4 | 0,56% | 4 | 0,56% | 4 | 0,56% |
Collin (2000) | 7 | 0,38% | 7 | 0,98% | 7 | 0,99% | 7 | 0,99% |
Poupin (1994) | 7 | 0,38% | 6 | 0,84% | 6 | 0,85% | 6 | 0,85% |
Rodríguez-Flores et al. (2021) | 7 | 0,38% | 7 | 0,98% | 7 | 0,99% | 7 | 0,99% |
Roux (1926) | 7 | 0,38% | 6 | 0,84% | 6 | 0,85% | 6 | 0,85% |
Taiti & Ferrara (1983) | 7 | 0,38% | 6 | 0,84% | 6 | 0,85% | 6 | 0,85% |
Chace (1962) | 6 | 0,32% | 6 | 0,84% | 6 | 0,85% | 6 | 0,85% |
Coutures (2001) | 6 | 0,32% | 6 | 0,84% | 6 | 0,85% | 6 | 0,85% |
Guinot (1985) | 6 | 0,32% | 6 | 0,84% | 6 | 0,85% | 6 | 0,85% |
Machordom et al. (2022) | 6 | 0,32% | 6 | 0,84% | 6 | 0,85% | 6 | 0,85% |
Macpherson (2007) | 6 | 0,32% | 6 | 0,84% | 6 | 0,85% | 6 | 0,85% |
Müller (1991) | 6 | 0,32% | 6 | 0,84% | 6 | 0,85% | 6 | 0,85% |
Müller (1991) | 6 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
Risso (1816) | 6 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
Tricart & Foubert (2000) | 6 | 0,32% | 6 | 0,84% | 6 | 0,85% | 6 | 0,85% |
Chappuis et al. (1956) | 5 | 0,27% | 2 | 0,28% | 2 | 0,28% | 2 | 0,28% |
Cleva & Poupin (2012) | 5 | 0,27% | 5 | 0,7% | 5 | 0,71% | 5 | 0,71% |
Collin (2002) | 5 | 0,27% | 5 | 0,7% | 5 | 0,71% | 5 | 0,71% |
Crosnier (1965) | 5 | 0,27% | 5 | 0,7% | 5 | 0,71% | 5 | 0,71% |
Fabricius (1798) | 5 | 0,27% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
Keith & Vigneux (2002) | 5 | 0,27% | 5 | 0,7% | 5 | 0,71% | 5 | 0,71% |
Komai (2010) | 5 | 0,27% | 5 | 0,7% | 5 | 0,71% | 5 | 0,71% |
Kropp (1988) | 5 | 0,27% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
Kubo (1949) | 5 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Laubitz (1995) | 5 | 0,27% | 5 | 0,7% | 5 | 0,71% | 5 | 0,71% |
Maddocks (2007) | 5 | 0,27% | 3 | 0,42% | 3 | 0,42% | 3 | 0,42% |
Nobili (1905) | 5 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Ribes (1989) | 5 | 0,27% | 4 | 0,56% | 4 | 0,56% | 4 | 0,56% |
Séchet & Noël (2015) | 5 | 0,27% | 2 | 0,28% | 2 | 0,28% | 2 | 0,28% |
Stimpson (1860) | 5 | 0,27% | 5 | 0,7% | 5 | 0,71% | 5 | 0,71% |
Ahyong (2014) | 4 | 0,21% | 4 | 0,56% | 4 | 0,56% | 4 | 0,56% |
Anker & Baeza (2021) | 4 | 0,21% | 4 | 0,56% | 4 | 0,56% | 4 | 0,56% |
Bouvier (1914) | 4 | 0,21% | 2 | 0,28% | 2 | 0,28% | 2 | 0,28% |
Bruce (1967) | 4 | 0,21% | 2 | 0,28% | 2 | 0,28% | 2 | 0,28% |
Chan et al. (2021) | 4 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Crosnier (2002) | 4 | 0,21% | 3 | 0,42% | 3 | 0,42% | 2 | 0,28% |
Dollfus (1895) | 4 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Edmondson (1925) | 4 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Galil et al. (2018) | 4 | 0,21% | 4 | 0,56% | 4 | 0,56% | 4 | 0,56% |
Jellinek (1993) | 4 | 0,21% | 4 | 0,56% | 4 | 0,56% | 4 | 0,56% |
Komai (2008) | 4 | 0,21% | 4 | 0,56% | 4 | 0,56% | 4 | 0,56% |
Mclaughlin & Haig (1989) | 4 | 0,21% | 4 | 0,56% | 4 | 0,56% | 4 | 0,56% |
Bulletin of the Museum of Comparative Zoology at Harvard College. 8(2): 1-68, Pl. 1-2.">Milne-Edwards (1880) | 4 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Müller (1991) | 4 | 0,21% | 4 | 0,56% | 4 | 0,56% | 4 | 0,56% |
Paulmier (1996) | 4 | 0,21% | 3 | 0,42% | 3 | 0,42% | 3 | 0,42% |
Poore & Dworschak (2018) | 4 | 0,21% | 4 | 0,56% | 4 | 0,56% | 4 | 0,56% |
Rigaud et al. (1997) | 4 | 0,21% | 4 | 0,56% | 4 | 0,56% | 4 | 0,56% |
Ward (1942) | 4 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Barnard (1950) | 3 | 0,16% | 2 | 0,28% | 2 | 0,28% | 2 | 0,28% |
Bigot (2006) | 3 | 0,16% | 2 | 0,28% | 2 | 0,28% | 2 | 0,28% |
Bourcier (1988) | 3 | 0,16% | 2 | 0,28% | 2 | 0,28% | 2 | 0,28% |
Bozić (1964) | 3 | 0,16% | 3 | 0,42% | 3 | 0,42% | 3 | 0,42% |
Brady (1868) | 3 | 0,16% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
Bruce (1979) | 3 | 0,16% | 3 | 0,42% | 3 | 0,42% | 3 | 0,42% |
Chan (1991) | 3 | 0,16% | 2 | 0,28% | 2 | 0,28% | 2 | 0,28% |
Chevreux (1887) | 3 | 0,16% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
Edmondson (1954) | 3 | 0,16% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
Forest (1954) | 3 | 0,16% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
Grygier (1985) | 3 | 0,16% | 3 | 0,42% | 3 | 0,42% | 3 | 0,42% |
Guinot & Richer de Forges (1981) | 3 | 0,16% | 3 | 0,42% | 3 | 0,42% | 3 | 0,42% |
Lemaitre (1989) | 3 | 0,16% | 3 | 0,42% | 3 | 0,42% | 3 | 0,42% |
Lucatelli et al. (2012) | 3 | 0,16% | 3 | 0,42% | 3 | 0,42% | 3 | 0,42% |
Macpherson et al. (2017) | 3 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Macpherson (1988) | 3 | 0,16% | 3 | 0,42% | 3 | 0,42% | 3 | 0,42% |
Man (1902) | 3 | 0,16% | 3 | 0,42% | 3 | 0,42% | 3 | 0,42% |
Manning (1978) | 3 | 0,16% | 3 | 0,42% | 3 | 0,42% | 3 | 0,42% |
Marquet (2002) | 3 | 0,16% | 3 | 0,42% | 3 | 0,42% | 3 | 0,42% |
Milne-Edwards (1865) | 3 | 0,16% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
Müller (1990) | 3 | 0,16% | 3 | 0,42% | 3 | 0,42% | 3 | 0,42% |
Mulochau et al. (2019) | 3 | 0,16% | 3 | 0,42% | 3 | 0,42% | 3 | 0,42% |
Ngoc-Ho (1989) | 3 | 0,16% | 3 | 0,42% | 3 | 0,42% | 3 | 0,42% |
Nobili (1904) | 3 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Odhner (1925) | 3 | 0,16% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
Olivier (1791-[1792]) | 3 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Poupin et al. (1999) | 3 | 0,16% | 3 | 0,42% | 3 | 0,42% | 3 | 0,42% |
Poupin (2008) | 3 | 0,16% | 2 | 0,28% | 2 | 0,28% | 2 | 0,28% |
Questel & Le Quellec (2012) | 3 | 0,16% | 3 | 0,42% | 3 | 0,42% | 3 | 0,42% |
Rathbun (1914) | 3 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Rignault & Chevallier (2017) | 3 | 0,16% | 2 | 0,28% | 2 | 0,28% | 2 | 0,28% |
Schmitt (1939) | 3 | 0,16% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
Spiridonov et al. (2021) | 3 | 0,16% | 3 | 0,42% | 3 | 0,42% | 3 | 0,42% |
Tavares (1994) | 3 | 0,16% | 3 | 0,42% | 3 | 0,42% | 3 | 0,42% |
Tavares (2006) | 3 | 0,16% | 3 | 0,42% | 3 | 0,42% | 3 | 0,42% |
Thiéry & Champeau (1994) | 3 | 0,16% | 3 | 0,42% | 3 | 0,42% | 3 | 0,42% |
Vandel (1981) | 3 | 0,16% | 3 | 0,42% | 3 | 0,42% | 3 | 0,42% |
Vereshchaka et al. (2020) | 3 | 0,16% | 3 | 0,42% | 3 | 0,42% | 3 | 0,42% |
Ward (1939) | 3 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Ward (1941) | 3 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Aguilera (2002) | 2 | 0,11% | 2 | 0,28% | 2 | 0,28% | 2 | 0,28% |
Ahyong (2017) | 2 | 0,11% | 2 | 0,28% | 2 | 0,28% | 2 | 0,28% |
Baez et al. (2022) | 2 | 0,11% | 2 | 0,28% | 2 | 0,28% | 2 | 0,28% |
Barnard (1962) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Baudry et al. (2022) | 2 | 0,11% | 2 | 0,28% | 2 | 0,28% | 2 | 0,28% |
Benson & Maddocks (1964) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Bigot et al. (2006) | 2 | 0,11% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
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 | 0,28% | 2 | 0,28% | 2 | 0,28% |
Bruce (2006) | 2 | 0,11% | 2 | 0,28% | 2 | 0,28% | 2 | 0,28% |
Burkenroad (1959) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Calman (1909) | 2 | 0,11% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
Report Fisheries and Marine Biological Survey Cape Town, 4(3): 1-26.">Calman (1925) | 2 | 0,11% | 2 | 0,28% | 2 | 0,28% | 2 | 0,28% |
Carré (2006) | 2 | 0,11% | 2 | 0,28% | 2 | 0,28% | 2 | 0,28% |
Champion (1973) | 2 | 0,11% | 2 | 0,28% | 2 | 0,28% | 2 | 0,28% |
Chan & Crosnier (1991) | 2 | 0,11% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
Chappuis (1956) | 2 | 0,11% | 2 | 0,28% | 2 | 0,28% | 2 | 0,28% |
Chen et al. (2016) | 2 | 0,11% | 2 | 0,28% | 2 | 0,28% | 2 | 0,28% |
Choy & Marquet (2002) | 2 | 0,11% | 2 | 0,28% | 2 | 0,28% | 2 | 0,28% |
Corbari et al. (2015) | 2 | 0,11% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
Dana (1852) | 2 | 0,11% | 2 | 0,28% | 2 | 0,28% | 2 | 0,28% |
Bulletin of the Museum at Harvard College, 24 : 149-220.">Faxon (1893) | 2 | 0,11% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
Forcellini et al. (2012) | 2 | 0,11% | 2 | 0,28% | 2 | 0,28% | 2 | 0,28% |
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 | 0,28% | 2 | 0,28% | 2 | 0,28% |
Guéguen (2000) | 2 | 0,11% | 2 | 0,28% | 2 | 0,28% | 2 | 0,28% |
Guinot (1964) | 2 | 0,11% | 2 | 0,28% | 2 | 0,28% | 2 | 0,28% |
Guinot (1976) | 2 | 0,11% | 2 | 0,28% | 2 | 0,28% | 2 | 0,28% |
, 50: 47-86.">Gutu (2007) | 2 | 0,11% | 2 | 0,28% | 2 | 0,28% | 2 | 0,28% |
, 52: 101-125.">Gutu (2009) | 2 | 0,11% | 2 | 0,28% | 2 | 0,28% | 2 | 0,28% |
, 55(1): 27-40.">Gutu (2012) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Harada (1961) | 2 | 0,11% | 2 | 0,28% | 2 | 0,28% | 2 | 0,28% |
Hayashi (2009) | 2 | 0,11% | 2 | 0,28% | 2 | 0,28% | 2 | 0,28% |
Hiller & Werding (2016) | 2 | 0,11% | 2 | 0,28% | 2 | 0,28% | 2 | 0,28% |
Huys & Gee (1996) | 2 | 0,11% | 2 | 0,28% | 2 | 0,28% | 2 | 0,28% |
Huys & Lee (1999) | 2 | 0,11% | 2 | 0,28% | 2 | 0,28% | 2 | 0,28% |
Jackson (1933) | 2 | 0,11% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
Jourdan (2020) | 2 | 0,11% | 2 | 0,28% | 2 | 0,28% | 2 | 0,28% |
Kemp (1922) | 2 | 0,11% | 2 | 0,28% | 2 | 0,28% | 2 | 0,28% |
Kensley (1977) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Kiefer (1960) | 2 | 0,11% | 2 | 0,28% | 2 | 0,28% | 2 | 0,28% |
Komai & Ng (2012) | 2 | 0,11% | 2 | 0,28% | 2 | 0,28% | 2 | 0,28% |
Komai & Osawa (2006) | 2 | 0,11% | 2 | 0,28% | 2 | 0,28% | 2 | 0,28% |
Komai (2004) | 2 | 0,11% | 2 | 0,28% | 2 | 0,28% | 2 | 0,28% |
Kubo (1955) | 2 | 0,11% | 2 | 0,28% | 2 | 0,28% | 2 | 0,28% |
Laurie (1906) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Lemaitre (1994) | 2 | 0,11% | 2 | 0,28% | 2 | 0,28% | 2 | 0,28% |
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 | 0,28% | 2 | 0,28% | 2 | 0,28% |
Malay et al. (2012) | 2 | 0,11% | 2 | 0,28% | 2 | 0,28% | 2 | 0,28% |
Manning (1978) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Mazancourt et al. (2019) | 2 | 0,11% | 2 | 0,28% | 2 | 0,28% | 2 | 0,28% |
Mclaughlin (1986) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Mendoza & Devi (2017) | 2 | 0,11% | 2 | 0,28% | 2 | 0,28% | 2 | 0,28% |
Meurgey (2011) | 2 | 0,11% | 2 | 0,28% | 2 | 0,28% | 2 | 0,28% |
Miers (1878) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
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 | 0,14% | 1 | 0,14% | 1 | 0,14% |
Nguyen (2010) | 2 | 0,11% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
Ortmann (1892) | 2 | 0,11% | 2 | 0,28% | 2 | 0,28% | 2 | 0,28% |
Perez & Farfante (1977) | 2 | 0,11% | 2 | 0,28% | 2 | 0,28% | 2 | 0,28% |
Perez & Farfante (1980) | 2 | 0,11% | 2 | 0,28% | 2 | 0,28% | 2 | 0,28% |
Poupin et al. (2018) | 2 | 0,11% | 2 | 0,28% | 2 | 0,28% | 2 | 0,28% |
Poupin (1997) | 2 | 0,11% | 2 | 0,28% | 2 | 0,28% | 2 | 0,28% |
Rathbun (1911) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Richardson (1914) | 2 | 0,11% | 2 | 0,28% | 2 | 0,28% | 2 | 0,28% |
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 | 0,28% | 2 | 0,28% | 2 | 0,28% |
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 | 0,28% | 2 | 0,28% | 2 | 0,28% |
Schmalfuss (2003) | 2 | 0,11% | 2 | 0,28% | 2 | 0,28% | 2 | 0,28% |
Schotte et al. (1995 onwards) | 2 | 0,11% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
Shahdadi & Schubart (2020) | 2 | 0,11% | 2 | 0,28% | 2 | 0,28% | 2 | 0,28% |
Stebbing (1917) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Stock (1986) | 2 | 0,11% | 2 | 0,28% | 2 | 0,28% | 2 | 0,28% |
Takeda (1977) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Tan & Ng (1996) | 2 | 0,11% | 2 | 0,28% | 2 | 0,28% | 2 | 0,28% |
Thomassin (1973) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Turkay (1978) | 2 | 0,11% | 2 | 0,28% | 2 | 0,28% | 2 | 0,28% |
Van et al. (2011) | 2 | 0,11% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
Ward (1934) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Wood-Mason & Alcock(1891) | 2 | 0,11% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
Wooster (1982) | 2 | 0,11% | 2 | 0,28% | 2 | 0,28% | 2 | 0,28% |
Yokoya (1936) | 2 | 0,11% | 2 | 0,28% | 2 | 0,28% | 2 | 0,28% |
Zarenkov (1989) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Achituv & Langsam (2009) | 1 | 0,05% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
Ahyong & Caldwell (2017) | 1 | 0,05% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
Ahyong (2001) | 1 | 0,05% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
Aizawa (1974) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Alcock & Anderson (1899) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Annals of Natural History, (6)(xiii): pp. 225-245, 321-331, & 400-411.">Alcock (1894) | 1 | 0,05% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
Alcock (1905) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Anker (2010) | 1 | 0,05% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
Anker (2017) | 1 | 0,05% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
Asakura (2001) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Bagnall (1908) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Balss (1911) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Balss (1938) | 1 | 0,05% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
Banner & Banner (1966) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Barnard (1914) | 1 | 0,05% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
Bernasconi (2000) | 1 | 0,05% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
Bulletin of the Vanderbilt Marine Museum, 5: 1-210.">Boone (1934) | 1 | 0,05% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
Bordaille (1902) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Bordaille (1916) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Boyko (2000) | 1 | 0,05% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
Boyko (2010) | 1 | 0,05% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
Brandt (1833) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Breton (2014) | 1 | 0,05% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
Bruce & Trautwein (2007) | 1 | 0,05% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
Bruce (1966) | 1 | 0,05% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
Bruce (1974) | 1 | 0,05% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
Bruce (1981) | 1 | 0,05% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
Bruce (1988) | 1 | 0,05% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
Bruce (2005) | 1 | 0,05% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
Burkenroad (1936) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Burukovsky (1993) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Cambert et al. (2011) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Chan et al. (2016) | 1 | 0,05% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
Chia & Ng (2000) | 1 | 0,05% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
Cochard et al. (2010) | 1 | 0,05% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
Costes (1890) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Coutiere (1909) | 1 | 0,05% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
Crosnier (1978) | 1 | 0,05% | 1 | 0,14% | 0 | 0% | 1 | 0,14% |
Crosnier (1986) | 1 | 0,05% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
Crosnier (2002) | 1 | 0,05% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
Delsalle & Sechet (2014) | 1 | 0,05% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
Dervin et al. (2014) | 1 | 0,05% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
Edmondson (1952) | 1 | 0,05% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
European Nucleotide Archive (2019) | 1 | 0,05% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
Fabricius ([1777]) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1787) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Fenwick & Webber (2008) | 1 | 0,05% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
Ferrara & Taiti (1979) | 1 | 0,05% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
Fize & Serene (1957) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Forest (1958) | 1 | 0,05% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
Galil (2003) | 1 | 0,05% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
Gall & Beague (1986) | 1 | 0,05% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
Gier (2018) | 1 | 0,05% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
Godet et al. (2010) | 1 | 0,05% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
Goulletquer (2016) | 1 | 0,05% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
Gourret (1891) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Gout (1991) | 1 | 0,05% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
Goy & Devaney (1980) | 1 | 0,05% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
Goy (2015) | 1 | 0,05% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
Gutu (2011) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Haig & Kropp (1987) | 1 | 0,05% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
Haller (1880) | 1 | 0,05% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
Hayashi (1999) | 1 | 0,05% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
Hett (1934) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Proceedings of the United States National Museum. 35(1654): 489-543; 46 figs.">Holmes (1908) | 1 | 0,05% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
Holthuis (1941) | 1 | 0,05% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
Holthuis (1952) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Holthuis (1955) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Holthuis (1963) | 1 | 0,05% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
Holthuis (1977) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Huang & Shih (2021) | 1 | 0,05% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
Huet & Poupin (2020) | 1 | 0,05% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
Ifremer (2009) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Ifremer (2022) | 1 | 0,05% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
Jackson (1941) | 1 | 0,05% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
Jacquemet et al. (2011) | 1 | 0,05% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
Javed (1990) | 1 | 0,05% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
Jayachandran & Raji (2004) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Jourdan & Mille (2006) | 1 | 0,05% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
Kamita (1967) | 1 | 0,05% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
Keith et al. (2002) | 1 | 0,05% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
Klunzinger (1913) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Komai & Poupin (2013) | 1 | 0,05% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
Komai & Shimetsugu (2019) | 1 | 0,05% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
Komai (1999) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Lalubie et al. (2015) | 1 | 0,05% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
Lebeau (1976) | 1 | 0,05% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
Ledoyer (1986) | 1 | 0,05% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
Lee et al. (2019) | 1 | 0,05% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
Leene (1936) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Legrand (1949) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Legrand (1950) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Legrand (1953) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Lemaitre (2004) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Lenz & Strunck (1914) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Lim et al. (2002) | 1 | 0,05% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
Annals of Natural History, (7)(xv): 233-268.">MacGilchrist (1905) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Macpherson (2004) | 1 | 0,05% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
Malz & Jellinek (1989) | 1 | 0,05% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
Tijdschrift der Nederlandsche Dierkundige Vereeniging, 2(3 & 4): 587-614.">Man (1905) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Leiden Notes Mus Jentink, 29: 127-145.">Man (1907) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Man (1911) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Manning & Holthuis (1989) | 1 | 0,05% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
Marin (2007) | 1 | 0,05% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
Marin (2012) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Mary (2017) | 1 | 0,05% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
Mclay (2001) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Melzer (2014) | 1 | 0,05% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
Miers (1879) | 1 | 0,05% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
Miers (1881) | 1 | 0,05% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
Milne-Edwards (1890) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Miquel (1984) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Miyake (1939) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Murienne et al. (2022) | 1 | 0,05% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
Nobili (1901) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Nobili (1903) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Noël & Boulad (2018) | 1 | 0,05% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
Noël (1986) | 1 | 0,05% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
Noël (2013) | 1 | 0,05% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
Noël (2014) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Noël (2014) | 1 | 0,05% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
Noël (2015) | 1 | 0,05% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
Noël (2015) | 1 | 0,05% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
Noël (2016) | 1 | 0,05% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
Noël (2017) | 1 | 0,05% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
Noël (2017) | 1 | 0,05% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
Noël et al. (1996) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Šobánová & Duriš (2021) | 1 | 0,05% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
Olivier & Latreille (1811) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Olivier (1811) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Ortmann (1890) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Parisi (1916) | 1 | 0,05% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
Peters (1852) | 1 | 0,05% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
Pezy et al. (2017) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Pfaller et al. (2019) | 1 | 0,05% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
Poisson & Legueux (1926) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Questel (2014) | 1 | 0,05% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
Ramadan (1938) | 1 | 0,05% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
Ruffo (1956) | 1 | 0,05% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
Sakai (1969) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Schmalfuss (2004) | 1 | 0,05% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
Schnabel & Ahyong (2010) | 1 | 0,05% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
Séchet et al. (2014) | 1 | 0,05% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
Serene (1984) | 1 | 0,05% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
Shih et al. (2016) | 1 | 0,05% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
Short & Marquet (1998) | 1 | 0,05% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
Siebold (1824) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Singh (2021) | 1 | 0,05% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
Stebbing (1914) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Stebbing (1915) | 1 | 0,05% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
Stebbing (1923) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Stimpson (1860) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Terao (1913) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Thompson (1943) | 1 | 0,05% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
Verhoeff (1926) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Ward (1933) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Werding & Hiller (2007) | 1 | 0,05% | 1 | 0,14% | 1 | 0,14% | 1 | 0,14% |
Yokoya (1933) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Zarenkov (1994) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |