Décapodes de France métropolitaine
Decapoda de France métropolitaine
418 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) | 108 | 5,79% | 90 | 18,26% | 90 | 18,56% | 90 | 18,44% |
Nelson-Smith et al. (2014) | 104 | 5,58% | 90 | 18,26% | 90 | 18,56% | 88 | 18,03% |
Risso (1816) | 96 | 5,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Godet et al. (2010) | 66 | 3,54% | 61 | 12,37% | 61 | 12,58% | 60 | 12,3% |
Poupin et al. (1999) | 61 | 3,27% | 41 | 8,32% | 41 | 8,45% | 40 | 8,2% |
Fourt et al. (2017) | 46 | 2,47% | 42 | 8,52% | 42 | 8,66% | 42 | 8,61% |
Ifremer (2009) | 37 | 1,98% | 26 | 5,27% | 26 | 5,36% | 25 | 5,12% |
Leach (1815-1875) | 36 | 1,93% | 14 | 2,84% | 14 | 2,89% | 14 | 2,87% |
Risso (1827) | 35 | 1,88% | 7 | 1,42% | 7 | 1,44% | 7 | 1,43% |
Bourcier (1988) | 33 | 1,77% | 29 | 5,88% | 29 | 5,98% | 28 | 5,74% |
Breton (2014) | 30 | 1,61% | 29 | 5,88% | 29 | 5,98% | 29 | 5,94% |
Poupin & Corbari (2016) | 30 | 1,61% | 23 | 4,67% | 23 | 4,74% | 23 | 4,71% |
Holthuis (1977) | 28 | 1,5% | 0 | 0% | 0 | 0% | 0 | 0% |
Linnaeus (1758) | 22 | 1,18% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Clark & Harrison (2021) | 17 | 0,91% | 7 | 1,42% | 7 | 1,44% | 7 | 1,43% |
Goulletquer (2016) | 17 | 0,91% | 17 | 3,45% | 17 | 3,51% | 17 | 3,48% |
Macpherson & Segonzac (2005) | 17 | 0,91% | 13 | 2,64% | 13 | 2,68% | 13 | 2,66% |
Rignault & Chevallier (2017) | 17 | 0,91% | 14 | 2,84% | 14 | 2,89% | 14 | 2,87% |
Bulletin of the Museum of Comparative Zoology at Harvard College. 8(2): 1-68, Pl. 1-2.">Milne-Edwards (1880) | 10 | 0,54% | 3 | 0,61% | 3 | 0,62% | 3 | 0,61% |
Poupin (1994) | 10 | 0,54% | 9 | 1,83% | 9 | 1,86% | 9 | 1,84% |
Guéguen (2000) | 9 | 0,48% | 7 | 1,42% | 7 | 1,44% | 7 | 1,43% |
Paulmier (1996) | 9 | 0,48% | 5 | 1,01% | 5 | 1,03% | 5 | 1,02% |
Poupin et al. (2018) | 9 | 0,48% | 8 | 1,62% | 8 | 1,65% | 8 | 1,64% |
Crosnier (1976) | 8 | 0,43% | 7 | 1,42% | 7 | 1,44% | 7 | 1,43% |
Meynard (2011) | 8 | 0,43% | 4 | 0,81% | 4 | 0,82% | 4 | 0,82% |
Corbari et al. (2015) | 6 | 0,32% | 5 | 1,01% | 5 | 1,03% | 5 | 1,02% |
Dewarumez et al. (2011) | 6 | 0,32% | 5 | 1,01% | 5 | 1,03% | 5 | 1,02% |
Low & Tan (2011) | 6 | 0,32% | 0 | 0% | 0 | 0% | 0 | 0% |
Manning & Holthuis (1989) | 6 | 0,32% | 6 | 1,22% | 6 | 1,24% | 6 | 1,23% |
Bate (1888) | 5 | 0,27% | 4 | 0,81% | 4 | 0,82% | 4 | 0,82% |
Crosnier & Forest (1973) | 5 | 0,27% | 2 | 0,41% | 2 | 0,41% | 1 | 0,2% |
Risso (1822) | 5 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Almon et al. (2022) | 4 | 0,21% | 4 | 0,81% | 4 | 0,82% | 4 | 0,82% |
Boisseau & Lubet (1955) | 4 | 0,21% | 4 | 0,81% | 4 | 0,82% | 4 | 0,82% |
Carré (2006) | 4 | 0,21% | 4 | 0,81% | 4 | 0,82% | 4 | 0,82% |
Corbari et al. (2020) | 4 | 0,21% | 4 | 0,81% | 4 | 0,82% | 4 | 0,82% |
Bulletin of the Museum at Harvard College, 24 : 149-220.">Faxon (1893) | 4 | 0,21% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Machordom et al. (2022) | 4 | 0,21% | 4 | 0,81% | 4 | 0,82% | 4 | 0,82% |
Macpherson (2007) | 4 | 0,21% | 4 | 0,81% | 4 | 0,82% | 4 | 0,82% |
Man (1914) | 4 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Parpet & Gelder (2020) | 4 | 0,21% | 4 | 0,81% | 4 | 0,82% | 4 | 0,82% |
Poupin et al. (2013) | 4 | 0,21% | 3 | 0,61% | 3 | 0,62% | 3 | 0,61% |
Poupin et al. (2013) | 4 | 0,21% | 3 | 0,61% | 3 | 0,62% | 3 | 0,61% |
Questel (2020) | 4 | 0,21% | 4 | 0,81% | 4 | 0,82% | 4 | 0,82% |
Rice & De Saint Laurent (1986) | 4 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Stephensen (1923) | 4 | 0,21% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Aguesse (1960) | 3 | 0,16% | 3 | 0,61% | 3 | 0,62% | 3 | 0,61% |
Annals of Natural History, (6)(xiii): pp. 225-245, 321-331, & 400-411.">Alcock (1894) | 3 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Azevedo Ferreira de & Tavares (2019) | 3 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Crisp & Fischer-piette (1959) | 3 | 0,16% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Fabricius (1775) | 3 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1787) | 3 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Forest (1978) | 3 | 0,16% | 3 | 0,61% | 3 | 0,62% | 3 | 0,61% |
Guinot et al. (2018) | 3 | 0,16% | 3 | 0,61% | 3 | 0,62% | 3 | 0,61% |
Holthuis (2001) | 3 | 0,16% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Jaume & Brehier (2005) | 3 | 0,16% | 3 | 0,61% | 3 | 0,62% | 3 | 0,61% |
Linnaeus (1761) | 3 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Pérez (1931) | 3 | 0,16% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Risso (1827) | 3 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Roux (1828) | 3 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Tan & Low (2014) | 3 | 0,16% | 2 | 0,41% | 2 | 0,41% | 2 | 0,41% |
Vereshchaka et al. (2020) | 3 | 0,16% | 2 | 0,41% | 2 | 0,41% | 2 | 0,41% |
Wirtz & Diesel (1983) | 3 | 0,16% | 3 | 0,61% | 3 | 0,62% | 3 | 0,61% |
Zilli (2021) | 3 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Allain & Morice (1971) | 2 | 0,11% | 2 | 0,41% | 2 | 0,41% | 2 | 0,41% |
Alvarez (1968) | 2 | 0,11% | 2 | 0,41% | 2 | 0,41% | 2 | 0,41% |
Baba & Macpherson (2017) | 2 | 0,11% | 2 | 0,41% | 2 | 0,41% | 2 | 0,41% |
Baba et al. (2008) | 2 | 0,11% | 2 | 0,41% | 2 | 0,41% | 2 | 0,41% |
Barnard (1950) | 2 | 0,11% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Borradaile (1915) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Botello et al. (2013) | 2 | 0,11% | 2 | 0,41% | 2 | 0,41% | 2 | 0,41% |
Comptes rendus hebdomadaires des séances de l'Académie des sciences, 141: 746-749.">Bouvier (1905) | 2 | 0,11% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Bruce (1998) | 2 | 0,11% | 2 | 0,41% | 2 | 0,41% | 2 | 0,41% |
Burukovskii (1977) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Chan & Crosnier (1991) | 2 | 0,11% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Chassard-Bouchaud et al. (1985) | 2 | 0,11% | 2 | 0,41% | 2 | 0,41% | 2 | 0,41% |
Chevaldonné et al. (2008) | 2 | 0,11% | 2 | 0,41% | 2 | 0,41% | 2 | 0,41% |
Churchill (1942) | 2 | 0,11% | 2 | 0,41% | 2 | 0,41% | 2 | 0,41% |
Crosnier (1962) | 2 | 0,11% | 2 | 0,41% | 2 | 0,41% | 2 | 0,41% |
Dauvin et al. (2009) | 2 | 0,11% | 2 | 0,41% | 2 | 0,41% | 2 | 0,41% |
Davoult (1990) | 2 | 0,11% | 2 | 0,41% | 2 | 0,41% | 2 | 0,41% |
Fage (1937) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Forest et al. (1955) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Gaillande & Lagardère (1966) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Grandjean et al. (2021) | 2 | 0,11% | 2 | 0,41% | 2 | 0,41% | 2 | 0,41% |
Guérin-Méneville (1855) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Proceedings of the Zoological Society of London, 1903 1) : 52-79.">Hansen (1903) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Heller (1863) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Hines et al. (1995) | 2 | 0,11% | 2 | 0,41% | 2 | 0,41% | 2 | 0,41% |
Holthuis (1952) | 2 | 0,11% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Koukouras et al. (2002) | 2 | 0,11% | 2 | 0,41% | 2 | 0,41% | 2 | 0,41% |
Krøyer (1855) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Linnaeus (1767) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Lowe et al. (2007) | 2 | 0,11% | 2 | 0,41% | 2 | 0,41% | 2 | 0,41% |
Lucas (1846) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Martin (2011) | 2 | 0,11% | 2 | 0,41% | 2 | 0,41% | 2 | 0,41% |
Miers (1881) | 2 | 0,11% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Milne-Edwards (1853) | 2 | 0,11% | 2 | 0,41% | 2 | 0,41% | 2 | 0,41% |
Milne-Edwards (1881) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Monod (1933) | 2 | 0,11% | 2 | 0,41% | 2 | 0,41% | 2 | 0,41% |
Mouchet (1931) | 2 | 0,11% | 2 | 0,41% | 2 | 0,41% | 2 | 0,41% |
Muñoz et al. (2009) | 2 | 0,11% | 2 | 0,41% | 2 | 0,41% | 2 | 0,41% |
Neveu (2009) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Ng & Richers de Forges (2015) | 2 | 0,11% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Ng et al. (2008) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Ngoc-Ho (2011) | 2 | 0,11% | 2 | 0,41% | 2 | 0,41% | 2 | 0,41% |
Noel (1978) | 2 | 0,11% | 2 | 0,41% | 2 | 0,41% | 2 | 0,41% |
Noël & Guinot (2007) | 2 | 0,11% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Olivi (1792) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Olivier (1791-[1792]) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Pennant (1777) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Pezy et al. (2017) | 2 | 0,11% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Pretus (1990) | 2 | 0,11% | 2 | 0,41% | 2 | 0,41% | 2 | 0,41% |
Questel & Le Quellec (2012) | 2 | 0,11% | 2 | 0,41% | 2 | 0,41% | 2 | 0,41% |
Robles et al. (2007) | 2 | 0,11% | 2 | 0,41% | 2 | 0,41% | 2 | 0,41% |
Rosecchi et al. (1998) | 2 | 0,11% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Roupsard & Caillot (2018) | 2 | 0,11% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Sanz-Brau & Mesquita-Oanes (2019) | 2 | 0,11% | 2 | 0,41% | 2 | 0,41% | 2 | 0,41% |
Shirley & Wolcott (1991) | 2 | 0,11% | 2 | 0,41% | 2 | 0,41% | 2 | 0,41% |
Sollaud (1959) | 2 | 0,11% | 2 | 0,41% | 2 | 0,41% | 2 | 0,41% |
Stebbing (1917) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Annals & Magazine of Natural History Series 9, 6: 220-226.">Sund (1920) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Turkay (1976) | 2 | 0,11% | 2 | 0,41% | 2 | 0,41% | 2 | 0,41% |
Van Guelpen (2016) | 2 | 0,11% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Van et al. (1985) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Vivares & Sprague (1979) | 2 | 0,11% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Abbe (1974) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Altès (1962) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Amanieu & Dantec (1961) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Anastasiadou et al. (2006) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Andrieux (1968) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Anker & Noël (1999) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Anonyme. (2004) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Ary et al. (1985) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Asakura & Watanabe (2005) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Aubert & Sauriau (2015) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Azevedo de & Tavares (2020) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Baba et al. (2018) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Bate (1888) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Béguer et al. (2007) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Béguer et al. (2011) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Béguer, (2010) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Beltran (1982) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Boone (1927) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Bouchard (2021) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Bouvier (1901) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Bouvier (1905) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Bouvier (1906) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Bouvier (1913) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Breton et al. (2002) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Brumbaugh & Mcconaugha (1995) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Burukovsky (1987) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Canu (1891) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Chace (1939) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Chace (1940) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Chan et al. (2016) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Chan (1991) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Chatton & Lwoff (1930) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Chen et al. (2016) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Chevaldonné & Pretus (2021) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Chevaldonne et al. (2023) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Chucholl & Daudey (2008) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Clément (1874) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Cocco (1832) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Colas (2019) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Collas et al. (2011) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Collas et al. (2012) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Costes (1890) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Costlow et al. (1958) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Costlow (1967) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Coudray & Noël (2014) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Coudray & Noël (2014) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Coudray & Noël (2014) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Coudray & Noël (2014) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Coudray & Noël (2014) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Coudray & Noël (2014) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Coudray & Noël (2014) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Coudray & Noël (2014) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Coudray & Noël (2014) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Coudray & Noël (2014) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Coudray & Noël (2014) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Coudray & Noël (2014) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Coudray & Noël (2014) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Coudray & Noël (2014) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Coudray & Noël (2014) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Coudray & Noël (2014) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Coudray & Noël (2014) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Coudray & Noël (2014) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Coudray & Noël (2014) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Coudray & Noël (2014) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Coudray & Noël (2014) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Coudray & Noël (2014) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Coudray & Noël (2014) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Coudray & Noël (2014) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Coudray & Noël (2014) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Coudray & Noël (2014) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Coudray & Noël (2014) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Coudray & Noël (2014) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Coudray & Noël (2014) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Coudray & Noël (2014) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Coudray & Noël (2014) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Coudray & Noël (2014) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Coudray & Noël (2014) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
"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) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Cronin (1949) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Crosnier (2002) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Curd et al. (2015) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
D’Acoz et al. (2022) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Dall (2001) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Daugherty (1952) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Dauvin & Delhay (2010) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Dauvin et al. (1991) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Dauvin (2012) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Davis et al. (2004) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
DCE-Benthos Network, French Mediterranen Lagoon Monitoring Network (2022) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Deblock & Prevot (1968) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Deblock et al. (1960) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
D'incao (1998) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Dittel et al. (2006) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Drach & Forest (1954) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
d'Udekem d'Acoz & Sorbe (2004) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
d'Udekem d'Acoz (1999) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Dworschak et al. (2000) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
D'acoz & Degrave (2018) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Esmark (1866) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Fabricius (1781) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1798) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Fage & Legendre (1933) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Filipová et al. (2013) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Fingerman (1955) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Fischer (1925) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Forest & Zariquiey (1964) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Forest (1957) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Forest (1963) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Forward et al. (2003) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Foxton (1971) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Freeman et al. (1987) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Gadeau de Kerville (1890) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Galil et al. (2016) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Galil (2000) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Gallien (1936) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Garcia Raso et al. (2011) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Gelder et al. (2012) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Gonzalez-ortegon et al. (2020) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Gothland et al. (2013) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Gothland et al. (2014) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Gould (1841) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Gray & Newcombe (1938) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Gruvel (1911) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Gueguen (2001) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Guinot (1969) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Gunter (1938) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Gurney (1939) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Hansen (1922) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Havens et al. (2009) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Herbst (1782-1790) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Hesse & Mangot (2015) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Holthuis (1955) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Huguet (1973) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Ives (1891) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Johnson (1867) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Jourde et al. (2012) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Judkins & Kensley (2008) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Kouba et al. (2014) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Krøyer (1855) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Kruger et al. (2019) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Labrune et al. (2019) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Laffitte et al. (2023) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Lankester (1903) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Latreille ([1802]) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Latreille (1812) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Leach (1814) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Lebeau (1976) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Legall & Poupin (2014) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Lenz & Strunck (1914) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Li (2008) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Lindner & Anderson (1941) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Lochhead & Newcombe (1942) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Lyko (2017) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Machino (1996) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Man (1902) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Man (1931) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Mancinelli et al. (2017) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Mancinelli et al. (2017) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Marchal (1891) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Martin (2003) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Matsuzaki et al. (2009) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Maury (1973) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Milne-edwards & Bouvier (1897) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Milne-Edwards (1890) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Milne-edwards (1891) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Montagu (1808) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Newcombe et al. (1949) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Nobili (1905) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Noel & Amoureux (1977) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Noël & Anker (2016) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Noël & Boulad (2018) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Noël, Anker (2016) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Noël, Breton (2016) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Noël (2013) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Noël (2014) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Noël (2014) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Noël (2015) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Noël (2015) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Noël (2015) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Noël (2015) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Noël (2015) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Noël (2015) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Noël (2015) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Noël (2015) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Noël (2015) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Noël (2015) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Noël (2015) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Noël (2015) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Noël (2015) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Noël (2015) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Noël (2015) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Noël (2015) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Noël (2015) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Noël (2015) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Noël (2015) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Noël (2015) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Noël (2015) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Noël (2015) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Noël (2015) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Noël (2015) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Noël (2015) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Noël (2015) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Noël (2015) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Noël (2015) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Noël (2015) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Noël (2015) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Noël (2015) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Noël (2015) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Noël (2015) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Noël (2015) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Noël (2015) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Noël (2015) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Noël (2015) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Noël (2015) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Noël (2015) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Noël (2015) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Noël (2015) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Noël (2015) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Noël (2015) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Noël (2015) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Noël (2016) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Noël (2016) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Noël (2016) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Noël (2016) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Noël (2016) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Noël (2016) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Noël (2016) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Noël (2016) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Noël (2016) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Noël (2016) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Noël (2017) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Noël (2017) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Noël (2017) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Noël (2017) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Noël (2017) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Noël (2017) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Ortmann (1893) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Paris (1918) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Parisi (1915) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Parpet & Gelder (2018) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Pastore (1996) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Père, & Noël (2017) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Pérez (1921) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Pérez (1922) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Pérez (1924) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Eupagurus bernhardus" et sur quelques-uns de ses parasites. Bulletin de la Société zoologique de France, 52: 99-104.">Pérez (1927) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Pérez (1929) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Pérez (1943) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Pezy & Dauvin (2015) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Pezy & Dauvin (2018) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Pezy et al. (2015) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Pezy et al. (2017) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Pezy et al. (2019) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Pfaller et al. (2019) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Pigeot et al. (2019) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Poisson (1924) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Poupin et al. (2013) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Poupin et al. (2022) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Poupin et al. (2022) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Poupin (2015) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Poupin (2018) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Puissauve, Collas, & Grandjean (2015) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Puissauve, Legros, Noël & Collas (2015) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
PUISSAUVE Renaud, COLLAS Marc & GRANDJEAN Frédéric (2013) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Rathbun et al. (1921) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Rathbun (1896) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Rathbun (1906) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Rathbun (1907) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Règlement d'exécution (UE) 2016/1141 | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Rodrigues da Costa (1968) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Roger (1938) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Ross & Zamponi (1983) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Roudez et al. (2008) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Ryer et al. (1997) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Sadek et al. (2018) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Sandoz & Rogers (1944) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Schmitt (1939) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Schrank et al. (1803) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Scopoli (1763) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Sellier et al. (2016) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Sket & Zakšek (2009) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Smith (1885) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Thongda et al. (2015) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Tricart & Foubert (2000) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Tursi et al. (2004) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Uicn et al. (2019) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Vincent (1986) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Vincent (2002) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Weissburg & Zimmer-faust (1994) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Wolcott et al. (2005) | 1 | 0,05% | 1 | 0,2% | 1 | 0,21% | 1 | 0,2% |
Wood-mason & Alcock (1891) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Yokoya (1933) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |