Bernards l’Hermite, galathées et porcellanes
276 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) | 693 | 40,01% | 552 | 58,47% | 552 | 58,47% | 552 | 58,47% |
Machordom et al. (2022) | 150 | 8,66% | 150 | 15,89% | 150 | 15,89% | 150 | 15,89% |
Macpherson & Robainas-Barcia (2015) | 126 | 7,27% | 126 | 13,35% | 126 | 13,35% | 126 | 13,35% |
Macpherson (1994) | 107 | 6,18% | 0 | 0% | 0 | 0% | 0 | 0% |
Poupin & Corbari (2016) | 72 | 4,16% | 60 | 6,36% | 60 | 6,36% | 60 | 6,36% |
Rodríguez-Flores et al. (2021) | 62 | 3,58% | 62 | 6,57% | 62 | 6,57% | 62 | 6,57% |
Bulletin of the Museum of Comparative Zoology at Harvard College. 8(2): 1-68, Pl. 1-2.">Milne-Edwards (1880) | 53 | 3,06% | 2 | 0,21% | 2 | 0,21% | 2 | 0,21% |
Macpherson (2007) | 49 | 2,83% | 49 | 5,19% | 49 | 5,19% | 49 | 5,19% |
Corbari et al. (2020) | 43 | 2,48% | 28 | 2,97% | 28 | 2,97% | 28 | 2,97% |
Macpherson & de Saint Laurent (1991) | 42 | 2,42% | 0 | 0% | 0 | 0% | 0 | 0% |
Rodríguez-flores et al. (2019) | 37 | 2,14% | 37 | 3,92% | 37 | 3,92% | 37 | 3,92% |
Poupin et al. (2013) | 36 | 2,08% | 36 | 3,81% | 36 | 3,81% | 36 | 3,81% |
Poupin & Lemaitre (2014) | 34 | 1,96% | 34 | 3,6% | 34 | 3,6% | 34 | 3,6% |
Lemaitre (2014) | 28 | 1,62% | 28 | 2,97% | 28 | 2,97% | 28 | 2,97% |
Poupin (2015) | 27 | 1,56% | 27 | 2,86% | 27 | 2,86% | 27 | 2,86% |
Questel (2020) | 26 | 1,5% | 26 | 2,75% | 26 | 2,75% | 26 | 2,75% |
Poupin (1994) | 22 | 1,27% | 15 | 1,59% | 15 | 1,59% | 15 | 1,59% |
Komai (2010) | 20 | 1,15% | 20 | 2,12% | 20 | 2,12% | 20 | 2,12% |
Nelson-Smith et al. (2014) | 20 | 1,15% | 17 | 1,8% | 17 | 1,8% | 17 | 1,8% |
Lemaitre (1994) | 19 | 1,1% | 9 | 0,95% | 9 | 0,95% | 9 | 0,95% |
Macpherson & Segonzac (2005) | 19 | 1,1% | 15 | 1,59% | 15 | 1,59% | 15 | 1,59% |
Poupin (2018) | 17 | 0,98% | 11 | 1,17% | 11 | 1,17% | 11 | 1,17% |
Corbari et al. (2015) | 16 | 0,92% | 8 | 0,85% | 8 | 0,85% | 8 | 0,85% |
Forest (1987) | 16 | 0,92% | 14 | 1,48% | 14 | 1,48% | 14 | 1,48% |
Lemaitre (2013) | 16 | 0,92% | 16 | 1,69% | 16 | 1,69% | 16 | 1,69% |
Ifremer (2009) | 15 | 0,87% | 12 | 1,27% | 12 | 1,27% | 12 | 1,27% |
Poupin et al. (2013) | 15 | 0,87% | 15 | 1,59% | 15 | 1,59% | 15 | 1,59% |
Macpherson et al. (2002) | 14 | 0,81% | 0 | 0% | 0 | 0% | 0 | 0% |
Macpherson et al. (2024) | 14 | 0,81% | 14 | 1,48% | 14 | 1,48% | 14 | 1,48% |
Bourcier (1988) | 13 | 0,75% | 10 | 1,06% | 10 | 1,06% | 10 | 1,06% |
Carré (2006) | 13 | 0,75% | 12 | 1,27% | 12 | 1,27% | 12 | 1,27% |
Lemaitre (1996) | 13 | 0,75% | 11 | 1,17% | 11 | 1,17% | 11 | 1,17% |
Macpherson (2004) | 13 | 0,75% | 2 | 0,21% | 2 | 0,21% | 2 | 0,21% |
Mclaughlin (1997) | 13 | 0,75% | 10 | 1,06% | 10 | 1,06% | 10 | 1,06% |
Poupin (1997) | 13 | 0,75% | 13 | 1,38% | 13 | 1,38% | 13 | 1,38% |
Ahyong (2014) | 12 | 0,69% | 12 | 1,27% | 12 | 1,27% | 12 | 1,27% |
Cabezas et al. (2010) | 12 | 0,69% | 12 | 1,27% | 12 | 1,27% | 12 | 1,27% |
Rodríguez-Flores et al. (2018) | 12 | 0,69% | 9 | 0,95% | 9 | 0,95% | 9 | 0,95% |
Saint & Laurent (1972) | 12 | 0,69% | 0 | 0% | 0 | 0% | 0 | 0% |
Godet et al. (2010) | 11 | 0,64% | 11 | 1,17% | 11 | 1,17% | 11 | 1,17% |
Haig (1989) | 11 | 0,64% | 9 | 0,95% | 9 | 0,95% | 9 | 0,95% |
Paguropsis Henderson, 1888, with the description of a new genus and five new species (Crustacea, Anomura, Diogenidae). ZooKeys, (752): 17-97.">Lemaitre et al. (2018) | 10 | 0,58% | 10 | 1,06% | 10 | 1,06% | 10 | 1,06% |
Lemaitre (1989) | 10 | 0,58% | 8 | 0,85% | 8 | 0,85% | 8 | 0,85% |
Macpherson & Baba (2010) | 10 | 0,58% | 10 | 1,06% | 10 | 1,06% | 10 | 1,06% |
Macpherson & Baba (2012) | 10 | 0,58% | 10 | 1,06% | 10 | 1,06% | 10 | 1,06% |
Macpherson (2012) | 10 | 0,58% | 10 | 1,06% | 10 | 1,06% | 10 | 1,06% |
Poupin & Mclaughlin (1998) | 10 | 0,58% | 10 | 1,06% | 10 | 1,06% | 10 | 1,06% |
Chace (1962) | 9 | 0,52% | 8 | 0,85% | 8 | 0,85% | 8 | 0,85% |
Macpherson & Robainas-barcia (2013) | 9 | 0,52% | 9 | 0,95% | 9 | 0,95% | 9 | 0,95% |
Mccallum et al. (2021) | 9 | 0,52% | 0 | 0% | 0 | 0% | 0 | 0% |
Risso (1816) | 9 | 0,52% | 0 | 0% | 0 | 0% | 0 | 0% |
Rodríguez-Flores et al. (2022) | 9 | 0,52% | 6 | 0,64% | 6 | 0,64% | 6 | 0,64% |
Breton (2014) | 8 | 0,46% | 8 | 0,85% | 8 | 0,85% | 8 | 0,85% |
Lemaitre et al. (2017) | 8 | 0,46% | 8 | 0,85% | 8 | 0,85% | 8 | 0,85% |
Mclaughlin (2000) | 8 | 0,46% | 8 | 0,85% | 8 | 0,85% | 8 | 0,85% |
Ramage (2017) | 8 | 0,46% | 8 | 0,85% | 8 | 0,85% | 8 | 0,85% |
Risso (1827) | 8 | 0,46% | 2 | 0,21% | 2 | 0,21% | 2 | 0,21% |
Macpherson et al. (2017) | 7 | 0,4% | 0 | 0% | 0 | 0% | 0 | 0% |
Macpherson et al. (2023) | 7 | 0,4% | 7 | 0,74% | 7 | 0,74% | 7 | 0,74% |
Macpherson (2000) | 7 | 0,4% | 2 | 0,21% | 2 | 0,21% | 2 | 0,21% |
Mclaughlin & Haig (1989) | 7 | 0,4% | 7 | 0,74% | 7 | 0,74% | 7 | 0,74% |
Mclaughlin (2004) | 7 | 0,4% | 7 | 0,74% | 7 | 0,74% | 7 | 0,74% |
Forest (1951) | 6 | 0,35% | 6 | 0,64% | 6 | 0,64% | 6 | 0,64% |
Forest (1954) | 6 | 0,35% | 3 | 0,32% | 3 | 0,32% | 3 | 0,32% |
Fourt et al. (2017) | 6 | 0,35% | 6 | 0,64% | 6 | 0,64% | 6 | 0,64% |
Haig & Mclaughlin (1991) | 6 | 0,35% | 5 | 0,53% | 5 | 0,53% | 5 | 0,53% |
Leach (1815-1875) | 6 | 0,35% | 2 | 0,21% | 2 | 0,21% | 2 | 0,21% |
Lemaitre (1999) | 6 | 0,35% | 6 | 0,64% | 6 | 0,64% | 6 | 0,64% |
Macpherson & Machordom (2005) | 6 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
Macpherson (1996) | 6 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
Macpherson (2006) | 6 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
Macpherson (2013) | 6 | 0,35% | 2 | 0,21% | 2 | 0,21% | 2 | 0,21% |
Mclaughlin (1981) | 6 | 0,35% | 6 | 0,64% | 6 | 0,64% | 6 | 0,64% |
Mclaughlin (2007) | 6 | 0,35% | 5 | 0,53% | 5 | 0,53% | 5 | 0,53% |
Nobili (1906) | 6 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
Orrell (2019) | 6 | 0,35% | 6 | 0,64% | 6 | 0,64% | 6 | 0,64% |
Poupin et al. (2022) | 6 | 0,35% | 5 | 0,53% | 5 | 0,53% | 5 | 0,53% |
Forest et al. (2000) | 5 | 0,29% | 5 | 0,53% | 5 | 0,53% | 5 | 0,53% |
Komai & Poupin (2013) | 5 | 0,29% | 5 | 0,53% | 5 | 0,53% | 5 | 0,53% |
Komai (1999) | 5 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
Lemaitre (2004) | 5 | 0,29% | 4 | 0,42% | 4 | 0,42% | 4 | 0,42% |
Macpherson & Baba (2006) | 5 | 0,29% | 5 | 0,53% | 5 | 0,53% | 5 | 0,53% |
Macpherson (2009) | 5 | 0,29% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Tricart & Foubert (2000) | 5 | 0,29% | 5 | 0,53% | 5 | 0,53% | 5 | 0,53% |
Alcock (1905) | 4 | 0,23% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Almon et al. (2022) | 4 | 0,23% | 4 | 0,42% | 4 | 0,42% | 4 | 0,42% |
Balss (1911) | 4 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Cabezas et al. (2011) | 4 | 0,23% | 4 | 0,42% | 4 | 0,42% | 4 | 0,42% |
Haig & Kropp (1987) | 4 | 0,23% | 4 | 0,42% | 4 | 0,42% | 4 | 0,42% |
Hiller & Werding (2016) | 4 | 0,23% | 4 | 0,42% | 4 | 0,42% | 4 | 0,42% |
Holthuis (1977) | 4 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Komai & Osawa (2006) | 4 | 0,23% | 4 | 0,42% | 4 | 0,42% | 4 | 0,42% |
Komai & Poupin (2012) | 4 | 0,23% | 4 | 0,42% | 4 | 0,42% | 4 | 0,42% |
Lemaitre (1997) | 4 | 0,23% | 4 | 0,42% | 4 | 0,42% | 4 | 0,42% |
Lemaitre (2006) | 4 | 0,23% | 4 | 0,42% | 4 | 0,42% | 4 | 0,42% |
Lemaitre (2020) | 4 | 0,23% | 4 | 0,42% | 4 | 0,42% | 4 | 0,42% |
Macpherson & Cleva (2010) | 4 | 0,23% | 4 | 0,42% | 4 | 0,42% | 4 | 0,42% |
Mclaughlin (1986) | 4 | 0,23% | 2 | 0,21% | 2 | 0,21% | 2 | 0,21% |
Mclaughlin (2006) | 4 | 0,23% | 4 | 0,42% | 4 | 0,42% | 4 | 0,42% |
Poupin et al. (2013) | 4 | 0,23% | 4 | 0,42% | 4 | 0,42% | 4 | 0,42% |
Questel & Le Quellec (2012) | 4 | 0,23% | 4 | 0,42% | 4 | 0,42% | 4 | 0,42% |
Rice & De Saint Laurent (1986) | 4 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Rodriguez-flores et al. (2019) | 4 | 0,23% | 3 | 0,32% | 3 | 0,32% | 3 | 0,32% |
Wass (1963) | 4 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Wooster (1982) | 4 | 0,23% | 4 | 0,42% | 4 | 0,42% | 4 | 0,42% |
Annals of Natural History, (6)(xiii): pp. 225-245, 321-331, & 400-411.">Alcock (1894) | 3 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Asakura & Paulay (2003) | 3 | 0,17% | 3 | 0,32% | 3 | 0,32% | 3 | 0,32% |
Azevedo Ferreira de & Tavares (2019) | 3 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Baba (1979) | 3 | 0,17% | 3 | 0,32% | 3 | 0,32% | 3 | 0,32% |
Baba (2005) | 3 | 0,17% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Bourjon et al. (2018) | 3 | 0,17% | 3 | 0,32% | 3 | 0,32% | 3 | 0,32% |
Buitendijk (1937) | 3 | 0,17% | 3 | 0,32% | 3 | 0,32% | 3 | 0,32% |
Forest (1997) | 3 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Lemaitre & Poupin (2003) | 3 | 0,17% | 3 | 0,32% | 3 | 0,32% | 3 | 0,32% |
Lemaitre (1998) | 3 | 0,17% | 3 | 0,32% | 3 | 0,32% | 3 | 0,32% |
Lemaitre (2004) | 3 | 0,17% | 2 | 0,21% | 2 | 0,21% | 2 | 0,21% |
Macpherson (1993) | 3 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Milne-edwards (1891) | 3 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Paulmier (1996) | 3 | 0,17% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Poore & Andreakis (2012) | 3 | 0,17% | 3 | 0,32% | 3 | 0,32% | 3 | 0,32% |
Poore & Andreakis (2014) | 3 | 0,17% | 3 | 0,32% | 3 | 0,32% | 3 | 0,32% |
Poupin & Bouchard (2006) | 3 | 0,17% | 3 | 0,32% | 3 | 0,32% | 3 | 0,32% |
Poupin & Lemaitre (2022) | 3 | 0,17% | 3 | 0,32% | 3 | 0,32% | 3 | 0,32% |
Poupin & Mclaughlin (1996) | 3 | 0,17% | 3 | 0,32% | 3 | 0,32% | 3 | 0,32% |
Rodriguez-Flores et al. (2017) | 3 | 0,17% | 3 | 0,32% | 3 | 0,32% | 3 | 0,32% |
Asakura (2005) | 2 | 0,12% | 2 | 0,21% | 2 | 0,21% | 2 | 0,21% |
Baba et al. (2008) | 2 | 0,12% | 2 | 0,21% | 2 | 0,21% | 2 | 0,21% |
Baker (1905) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Benedict (1902) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Boone (1927) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Borradaile (1898) | 2 | 0,12% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Bouvier (1899) | 2 | 0,12% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Clark & Harrison (2021) | 2 | 0,12% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Craig & Felder (2022) | 2 | 0,12% | 2 | 0,21% | 2 | 0,21% | 2 | 0,21% |
Davoult (1990) | 2 | 0,12% | 2 | 0,21% | 2 | 0,21% | 2 | 0,21% |
Forest & Saint Laurent | 2 | 0,12% | 2 | 0,21% | 2 | 0,21% | 2 | 0,21% |
Forest (1992) | 2 | 0,12% | 2 | 0,21% | 2 | 0,21% | 2 | 0,21% |
Haig (1957) | 2 | 0,12% | 2 | 0,21% | 2 | 0,21% | 2 | 0,21% |
Kensley (1973) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Koukouras et al. (2002) | 2 | 0,12% | 2 | 0,21% | 2 | 0,21% | 2 | 0,21% |
Kropp (1983) | 2 | 0,12% | 2 | 0,21% | 2 | 0,21% | 2 | 0,21% |
Lemaitre & Campos (1993) | 2 | 0,12% | 2 | 0,21% | 2 | 0,21% | 2 | 0,21% |
Lemaitre & Mclaughlin (1996) | 2 | 0,12% | 2 | 0,21% | 2 | 0,21% | 2 | 0,21% |
Lemaitre (1986) | 2 | 0,12% | 2 | 0,21% | 2 | 0,21% | 2 | 0,21% |
Lemaitre (2010) | 2 | 0,12% | 2 | 0,21% | 2 | 0,21% | 2 | 0,21% |
Lemaitre (2011) | 2 | 0,12% | 2 | 0,21% | 2 | 0,21% | 2 | 0,21% |
Lemaitre (2015) | 2 | 0,12% | 2 | 0,21% | 2 | 0,21% | 2 | 0,21% |
Linnaeus (1758) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Macpherson et al. (2016) | 2 | 0,12% | 2 | 0,21% | 2 | 0,21% | 2 | 0,21% |
Maillaud et al. (2015) | 2 | 0,12% | 2 | 0,21% | 2 | 0,21% | 2 | 0,21% |
Malay et al. (2012) | 2 | 0,12% | 2 | 0,21% | 2 | 0,21% | 2 | 0,21% |
Mclaughlin & Haig (1996) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Mclaughlin & Hoover (1996) | 2 | 0,12% | 2 | 0,21% | 2 | 0,21% | 2 | 0,21% |
Mclaughlin & Lemaitre (2008) | 2 | 0,12% | 2 | 0,21% | 2 | 0,21% | 2 | 0,21% |
Mclaughlin et al. (1998) | 2 | 0,12% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Mclaughlin (2004) | 2 | 0,12% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Miyake & Baba (1967) | 2 | 0,12% | 2 | 0,21% | 2 | 0,21% | 2 | 0,21% |
Osawa (1996) | 2 | 0,12% | 2 | 0,21% | 2 | 0,21% | 2 | 0,21% |
Osawa (2016) | 2 | 0,12% | 2 | 0,21% | 2 | 0,21% | 2 | 0,21% |
Pérez (1931) | 2 | 0,12% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Poupin & Lemaitre (2003) | 2 | 0,12% | 2 | 0,21% | 2 | 0,21% | 2 | 0,21% |
Poupin (2001) | 2 | 0,12% | 2 | 0,21% | 2 | 0,21% | 2 | 0,21% |
Rahayu (2011) | 2 | 0,12% | 2 | 0,21% | 2 | 0,21% | 2 | 0,21% |
Richer et al. (2013) | 2 | 0,12% | 2 | 0,21% | 2 | 0,21% | 2 | 0,21% |
Rodríguez-flores et al. (2018) | 2 | 0,12% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Roux (1828) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Sankarankutty (1963) | 2 | 0,12% | 2 | 0,21% | 2 | 0,21% | 2 | 0,21% |
Saussure (1857) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Stimpson (1858) | 2 | 0,12% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Terao (1913) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Werding & Hiller (2004) | 2 | 0,12% | 2 | 0,21% | 2 | 0,21% | 2 | 0,21% |
Werding (1996) | 2 | 0,12% | 2 | 0,21% | 2 | 0,21% | 2 | 0,21% |
Zarenkov (1989) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Ahyong & Poore (2004) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Altès (1962) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Asakura (2001) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Asakura (2006) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Azevedo de & Tavares (2020) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Baba (1982) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Baba (1990) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Balss (1912) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Barnard (1950) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Boisseau & Lubet (1955) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Bulletin of the Vanderbilt Marine Museum, 3: 1-221.">Boone (1930) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Boone (1932) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Bourdillon-Casanova (1956) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Bouvier (1914) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Clément (1874) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Coudray & Noël (2014) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Coudray & Noël (2014) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Coudray & Noël (2014) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Coudray & Noël (2014) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Coudray & Noël (2014) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Coudray & Noël (2014) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Coudray & Noël (2014) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Coudray & Noël (2014) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Coudray & Noël (2014) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Coudray & Noël (2014) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Coudray & Noël (2014) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Coudray & Noël (2014) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Coudray & Noël (2014) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Coudray & Noël (2014) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Coudray & Noël (2014) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Coudray & Noël (2014) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Coudray & Noël (2014) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Coudray & Noël (2014) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Crisp & Fischer-piette (1959) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Crosnier (1976) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Dana (1852) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
DCE-Benthos Network, French Mediterranen Lagoon Monitoring Network (2022) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
de Man (1902) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Edmondson (1952) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Fabricius (1787) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Forest (1958) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Forest (1984) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Forest (2015) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Gong & Paulay (2018) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Guéguen (2000) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Haig (1981) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Heller (1862) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Journal of the Asiatic Society of Bengal, lxv: 516-536.">Henderson (1896) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Hernandez et al. (2007) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Ifremer (2022) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Johnson (1970) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Kropp (1986) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Latreille (1812) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Leach (1820) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Linnaeus (1761) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Annals of Natural History, (7)(xv): 233-268.">MacGilchrist (1905) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Macpherson (1999) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Man (1902) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Marchal (1891) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Martin (2003) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Miers (1878) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Miers (1879) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Miers (1881) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Milne-edwards & Bouvier (1897) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Miyake (1961) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Mouchet (1931) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Nobili (1905) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Noël (2015) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Noël (2015) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Noël (2015) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Noël (2015) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Noël (2015) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Noël (2015) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Noël (2015) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Noël (2015) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Noël (2015) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Noël (2015) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Noël (2015) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Noël (2015) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Noël (2015) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Noël (2016) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Noël (2016) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Paulay & Brown (2019) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Pérez (1921) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Pérez (1922) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Eupagurus bernhardus" et sur quelques-uns de ses parasites. Bulletin de la Société zoologique de France, 52: 99-104.">Pérez (1927) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Pérez (1929) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Poore (2014) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Poupin et al. (2022) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Rodrigues da Costa (1968) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Ross & Zamponi (1983) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Sanchez (1977) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Schmitt (1933) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Schnabel & Ahyong (2019) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Terao (1914) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Thompson (1943) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Werding & Hiller (2007) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Werding (1982) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
White (1851) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Australian Museum Memoir. 4(2): 135-199">Whitelegge (1901) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Memoirs of the Australian Museum, 4 (3): 203-225.">Whitelegge (1901) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Yokoyama (2013) | 1 | 0,06% | 1 | 0,11% | 1 | 0,11% | 1 | 0,11% |
Zilli (2021) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |