Crustacés de Clipperton
139 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) | 202 | 41,39% | 184 | 97,87% | 184 | 100% | 184 | 100% |
Pagano (2009) | 53 | 10,86% | 43 | 22,87% | 43 | 23,37% | 43 | 23,37% |
Allison & Holden (1971) | 39 | 7,99% | 30 | 15,96% | 24 | 13,04% | 30 | 16,3% |
Poupin et al. (2018) | 27 | 5,53% | 26 | 13,83% | 26 | 14,13% | 26 | 14,13% |
Chace (1962) | 26 | 5,33% | 22 | 11,7% | 22 | 11,96% | 22 | 11,96% |
Collin (2002) | 26 | 5,33% | 20 | 10,64% | 19 | 10,33% | 20 | 10,87% |
Renon & Lefèvre (1985) | 25 | 5,12% | 25 | 13,3% | 25 | 13,59% | 25 | 13,59% |
Gaudy & Thomassin (2006) | 23 | 4,71% | 20 | 10,64% | 20 | 10,87% | 20 | 10,87% |
Poupin et al. (2013) | 16 | 3,28% | 14 | 7,45% | 14 | 7,61% | 14 | 7,61% |
Poupin et al. (1999) | 13 | 2,66% | 12 | 6,38% | 12 | 6,52% | 12 | 6,52% |
Poupin (2015) | 11 | 2,25% | 11 | 5,85% | 11 | 5,98% | 11 | 5,98% |
Jakiel et al. (2019) | 10 | 2,05% | 10 | 5,32% | 10 | 5,43% | 10 | 5,43% |
Li & Poupin (2009) | 9 | 1,84% | 0 | 0% | 0 | 0% | 0 | 0% |
Haig & Mclaughlin (1991) | 6 | 1,23% | 5 | 2,66% | 5 | 2,72% | 5 | 2,72% |
Perger (2019) | 6 | 1,23% | 4 | 2,13% | 4 | 2,17% | 4 | 2,17% |
Rosé (1924) | 6 | 1,23% | 3 | 1,6% | 3 | 1,63% | 3 | 1,63% |
Schmitt (1939) | 6 | 1,23% | 1 | 0,53% | 1 | 0,54% | 1 | 0,54% |
Coutiere (1909) | 5 | 1,02% | 4 | 2,13% | 4 | 2,17% | 4 | 2,17% |
Paris. pp. [i]-xii, 9-320 ; [Atlas] Crustacés, 5 planches ; Insectes, 21 planches.">Guérin-Méneville ([1829-1838]) | 5 | 1,02% | 2 | 1,06% | 2 | 1,09% | 2 | 1,09% |
Guinot et al. (2018) | 5 | 1,02% | 5 | 2,66% | 5 | 2,72% | 5 | 2,72% |
Questel (2020) | 5 | 1,02% | 5 | 2,66% | 5 | 2,72% | 5 | 2,72% |
Rose (1925) | 5 | 1,02% | 4 | 2,13% | 4 | 2,17% | 4 | 2,17% |
Avila-Garcia et al. (2020) | 4 | 0,82% | 0 | 0% | 0 | 0% | 0 | 0% |
Boone (1927) | 4 | 0,82% | 0 | 0% | 0 | 0% | 0 | 0% |
Carré (2006) | 4 | 0,82% | 4 | 2,13% | 4 | 2,17% | 4 | 2,17% |
Linnaeus (1758) | 4 | 0,82% | 0 | 0% | 0 | 0% | 0 | 0% |
Michel et al. (1971) | 4 | 0,82% | 4 | 2,13% | 4 | 2,17% | 4 | 2,17% |
Poupin et al. (2013) | 4 | 0,82% | 3 | 1,6% | 3 | 1,63% | 3 | 1,63% |
Rathbun (1907) | 4 | 0,82% | 2 | 1,06% | 2 | 1,09% | 2 | 1,09% |
Rose (1926) | 4 | 0,82% | 2 | 1,06% | 2 | 1,09% | 2 | 1,09% |
Chatton (1912) | 3 | 0,61% | 2 | 1,06% | 2 | 1,09% | 2 | 1,09% |
Ehrhardt (1970) | 3 | 0,61% | 0 | 0% | 0 | 0% | 0 | 0% |
Li (2008) | 3 | 0,61% | 3 | 1,6% | 3 | 1,63% | 3 | 1,63% |
Manning (1964) | 3 | 0,61% | 0 | 0% | 0 | 0% | 0 | 0% |
Marin (2010) | 3 | 0,61% | 0 | 0% | 0 | 0% | 0 | 0% |
Poltarukha & Melnik (2012) | 3 | 0,61% | 3 | 1,6% | 3 | 1,63% | 3 | 1,63% |
Poupin & Bouchard (2006) | 3 | 0,61% | 3 | 1,6% | 3 | 1,63% | 3 | 1,63% |
Poupin & Corbari (2016) | 3 | 0,61% | 3 | 1,6% | 3 | 1,63% | 3 | 1,63% |
Rathbun (1902) | 3 | 0,61% | 0 | 0% | 0 | 0% | 0 | 0% |
Renon (1989) | 3 | 0,61% | 3 | 1,6% | 3 | 1,63% | 3 | 1,63% |
Rignault & Chevallier (2017) | 3 | 0,61% | 3 | 1,6% | 3 | 1,63% | 3 | 1,63% |
Rodriguez et al. (2019) | 3 | 0,61% | 1 | 0,53% | 1 | 0,54% | 1 | 0,54% |
Rose (1933) | 3 | 0,61% | 2 | 1,06% | 2 | 1,09% | 2 | 1,09% |
Stephensen (1935) | 3 | 0,61% | 3 | 1,6% | 3 | 1,63% | 3 | 1,63% |
Swain (1967) | 3 | 0,61% | 0 | 0% | 0 | 0% | 0 | 0% |
Tricart & Foubert (2000) | 3 | 0,61% | 3 | 1,6% | 3 | 1,63% | 3 | 1,63% |
Zullo (1969) | 3 | 0,61% | 0 | 0% | 0 | 0% | 0 | 0% |
Aguilera (2002) | 2 | 0,41% | 2 | 1,06% | 2 | 1,09% | 2 | 1,09% |
Alekseev et al. (2021) | 2 | 0,41% | 1 | 0,53% | 1 | 0,54% | 1 | 0,54% |
Baird (1843) | 2 | 0,41% | 2 | 1,06% | 2 | 1,09% | 2 | 1,09% |
Binet (1984) | 2 | 0,41% | 2 | 1,06% | 2 | 1,09% | 2 | 1,09% |
Bold (1963) | 2 | 0,41% | 0 | 0% | 0 | 0% | 0 | 0% |
Bouvier (1899) | 2 | 0,41% | 1 | 0,53% | 1 | 0,54% | 1 | 0,54% |
Bradford (1974) | 2 | 0,41% | 2 | 1,06% | 2 | 1,09% | 2 | 1,09% |
Carbonel et al. (2007) | 2 | 0,41% | 2 | 1,06% | 2 | 1,09% | 2 | 1,09% |
Claus (1866) | 2 | 0,41% | 2 | 1,06% | 2 | 1,09% | 2 | 1,09% |
Cleva & Poupin (2012) | 2 | 0,41% | 2 | 1,06% | 2 | 1,09% | 2 | 1,09% |
Collin (2000) | 2 | 0,41% | 2 | 1,06% | 2 | 1,09% | 2 | 1,09% |
Corbari et al. (2015) | 2 | 0,41% | 2 | 1,06% | 2 | 1,09% | 2 | 1,09% |
Edwards (1944) | 2 | 0,41% | 0 | 0% | 0 | 0% | 0 | 0% |
Finnegan (1931) | 2 | 0,41% | 0 | 0% | 0 | 0% | 0 | 0% |
Haig (1957) | 2 | 0,41% | 2 | 1,06% | 2 | 1,09% | 2 | 1,09% |
Hendrickx (1990) | 2 | 0,41% | 0 | 0% | 0 | 0% | 0 | 0% |
Holthuis (1950) | 2 | 0,41% | 2 | 1,06% | 2 | 1,09% | 2 | 1,09% |
Li (2006) | 2 | 0,41% | 0 | 0% | 0 | 0% | 0 | 0% |
Lucas (1846) | 2 | 0,41% | 0 | 0% | 0 | 0% | 0 | 0% |
Manning (1988) | 2 | 0,41% | 2 | 1,06% | 2 | 1,09% | 2 | 1,09% |
Mclaughlin & Hoover (1996) | 2 | 0,41% | 2 | 1,06% | 2 | 1,09% | 2 | 1,09% |
Omatsola (1972) | 2 | 0,41% | 0 | 0% | 0 | 0% | 0 | 0% |
Pagano et al. (2012) | 2 | 0,41% | 2 | 1,06% | 2 | 1,09% | 2 | 1,09% |
Paulmier (2009) | 2 | 0,41% | 1 | 0,53% | 1 | 0,54% | 1 | 0,54% |
Questel & Le Quellec (2012) | 2 | 0,41% | 2 | 1,06% | 2 | 1,09% | 2 | 1,09% |
Rathbun (1906) | 2 | 0,41% | 0 | 0% | 0 | 0% | 0 | 0% |
Shoemaker (1942) | 2 | 0,41% | 2 | 1,06% | 2 | 1,09% | 2 | 1,09% |
Stimpson (1860) | 2 | 0,41% | 0 | 0% | 0 | 0% | 0 | 0% |
Teeter (1975) | 2 | 0,41% | 0 | 0% | 0 | 0% | 0 | 0% |
Wicksten (1987) | 2 | 0,41% | 2 | 1,06% | 2 | 1,09% | 2 | 1,09% |
Abele (1975) | 1 | 0,2% | 1 | 0,53% | 1 | 0,54% | 1 | 0,54% |
Alvarez et al. (1996) | 1 | 0,2% | 1 | 0,53% | 1 | 0,54% | 1 | 0,54% |
Amon et al. (2017) | 1 | 0,2% | 1 | 0,53% | 1 | 0,54% | 1 | 0,54% |
Balvay (2009) | 1 | 0,2% | 1 | 0,53% | 1 | 0,54% | 1 | 0,54% |
Bate et al. (1981) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Bold (1963) | 1 | 0,2% | 1 | 0,53% | 1 | 0,54% | 1 | 0,54% |
Bulletin of the Vanderbilt Marine Museum, 3: 1-221.">Boone (1930) | 1 | 0,2% | 1 | 0,53% | 1 | 0,54% | 1 | 0,54% |
Boone (1932) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Bouchard & Poupin (2009) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Boxshall & Huys (2007) | 1 | 0,2% | 1 | 0,53% | 1 | 0,54% | 1 | 0,54% |
Brady (1911) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Breton (2014) | 1 | 0,2% | 1 | 0,53% | 1 | 0,54% | 0 | 0% |
Calman (1909) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Caziot (1921) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Champeau (1967) | 1 | 0,2% | 1 | 0,53% | 1 | 0,54% | 1 | 0,54% |
Ciampo (1971) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Claus (1863) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Claus (1863) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Colin (2000) | 1 | 0,2% | 1 | 0,53% | 1 | 0,54% | 1 | 0,54% |
Corbari et al. (2020) | 1 | 0,2% | 1 | 0,53% | 1 | 0,54% | 1 | 0,54% |
"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 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Crosnier (2002) | 1 | 0,2% | 1 | 0,53% | 1 | 0,54% | 1 | 0,54% |
Curd et al. (2015) | 1 | 0,2% | 1 | 0,53% | 1 | 0,54% | 1 | 0,54% |
Dewarumez et al. (2011) | 1 | 0,2% | 1 | 0,53% | 1 | 0,54% | 0 | 0% |
Edmondson (1930) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Bulletin of the Museum at Harvard College, 24 : 149-220.">Faxon (1893) | 1 | 0,2% | 1 | 0,53% | 1 | 0,54% | 1 | 0,54% |
Giesbrecht (1891) | 1 | 0,2% | 1 | 0,53% | 1 | 0,54% | 1 | 0,54% |
Goulletquer (2016) | 1 | 0,2% | 1 | 0,53% | 1 | 0,54% | 1 | 0,54% |
Guinot-dumortier (1960) | 1 | 0,2% | 1 | 0,53% | 1 | 0,54% | 1 | 0,54% |
Harada (1961) | 1 | 0,2% | 1 | 0,53% | 1 | 0,54% | 1 | 0,54% |
Hermoso-salazar & Solis-weiss (2001) | 1 | 0,2% | 1 | 0,53% | 1 | 0,54% | 1 | 0,54% |
Hernandez et al. (2007) | 1 | 0,2% | 1 | 0,53% | 1 | 0,54% | 1 | 0,54% |
Kropp (1989) | 1 | 0,2% | 1 | 0,53% | 1 | 0,54% | 1 | 0,54% |
Legall & Poupin (2014) | 1 | 0,2% | 1 | 0,53% | 1 | 0,54% | 1 | 0,54% |
Maddocks (2007) | 1 | 0,2% | 1 | 0,53% | 1 | 0,54% | 1 | 0,54% |
Man (1902) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Marukawa (1908) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Miers (1881) | 1 | 0,2% | 1 | 0,53% | 1 | 0,54% | 1 | 0,54% |
Milne-Edwards (1878) | 1 | 0,2% | 1 | 0,53% | 1 | 0,54% | 1 | 0,54% |
Nobili (1905) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Noël & Boulad (2018) | 1 | 0,2% | 1 | 0,53% | 1 | 0,54% | 1 | 0,54% |
Noël (2014) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Noël (2014) | 1 | 0,2% | 1 | 0,53% | 1 | 0,54% | 1 | 0,54% |
Noël (2015) | 1 | 0,2% | 1 | 0,53% | 1 | 0,54% | 1 | 0,54% |
Olivier (1791-[1792]) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Olivier (1811) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Ortmann (1890) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Perrier (1929) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Pfaller et al. (2019) | 1 | 0,2% | 1 | 0,53% | 1 | 0,54% | 1 | 0,54% |
Philippi (1843) | 1 | 0,2% | 1 | 0,53% | 1 | 0,54% | 1 | 0,54% |
Poupin et al. (2009) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Pugh et al. (2002) | 1 | 0,2% | 1 | 0,53% | 1 | 0,54% | 1 | 0,54% |
Ramage (2017) | 1 | 0,2% | 1 | 0,53% | 1 | 0,54% | 1 | 0,54% |
Renon (1977) | 1 | 0,2% | 1 | 0,53% | 1 | 0,54% | 1 | 0,54% |
Rose (1925) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Smith (1885) | 1 | 0,2% | 1 | 0,53% | 1 | 0,54% | 1 | 0,54% |
Stimpson (1860) | 1 | 0,2% | 1 | 0,53% | 1 | 0,54% | 1 | 0,54% |
Thompson (1888) | 1 | 0,2% | 1 | 0,53% | 1 | 0,54% | 1 | 0,54% |
Tollu (2009) | 1 | 0,2% | 1 | 0,53% | 1 | 0,54% | 1 | 0,54% |
Van Duzee (1937) | 1 | 0,2% | 1 | 0,53% | 1 | 0,54% | 1 | 0,54% |
Bulletin United States National Museum No 100, 14(4): pp. i-ix 141-441.">Wilson (1950) | 1 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Yokoyama (2013) | 1 | 0,2% | 1 | 0,53% | 1 | 0,54% | 1 | 0,54% |