Crustacés marins de Clipperton
Branchiopoda, Oligostraca et Multicrustacea marins au sens large de Clipperton
135 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) | 201 | 41,79% | 183 | 100,55% | 183 | 102,23% | 183 | 102,23% |
Pagano (2009) | 52 | 10,81% | 42 | 23,08% | 42 | 23,46% | 42 | 23,46% |
Allison & Holden (1971) | 36 | 7,48% | 27 | 14,84% | 21 | 11,73% | 27 | 15,08% |
Poupin et al. (2018) | 27 | 5,61% | 26 | 14,29% | 26 | 14,53% | 26 | 14,53% |
Chace (1962) | 26 | 5,41% | 22 | 12,09% | 22 | 12,29% | 22 | 12,29% |
Collin (2002) | 25 | 5,2% | 18 | 9,89% | 18 | 10,06% | 18 | 10,06% |
Renon & Lefèvre (1985) | 25 | 5,2% | 25 | 13,74% | 25 | 13,97% | 25 | 13,97% |
Gaudy & Thomassin (2006) | 23 | 4,78% | 20 | 10,99% | 20 | 11,17% | 20 | 11,17% |
Poupin et al. (2013) | 16 | 3,33% | 14 | 7,69% | 14 | 7,82% | 14 | 7,82% |
Pearman et al. (2020) | 15 | 3,12% | 14 | 7,69% | 14 | 7,82% | 14 | 7,82% |
Poupin et al. (1999) | 13 | 2,7% | 12 | 6,59% | 12 | 6,7% | 12 | 6,7% |
Poupin (2015) | 11 | 2,29% | 11 | 6,04% | 11 | 6,15% | 11 | 6,15% |
Jakiel et al. (2019) | 10 | 2,08% | 10 | 5,49% | 10 | 5,59% | 10 | 5,59% |
Li & Poupin (2009) | 9 | 1,87% | 0 | 0% | 0 | 0% | 0 | 0% |
Paulmier (2014) | 9 | 1,87% | 9 | 4,95% | 9 | 5,03% | 9 | 5,03% |
Haig & Mclaughlin (1991) | 6 | 1,25% | 5 | 2,75% | 5 | 2,79% | 5 | 2,79% |
Poupin (2024) | 6 | 1,25% | 6 | 3,3% | 6 | 3,35% | 6 | 3,35% |
Rosé (1924) | 6 | 1,25% | 3 | 1,65% | 3 | 1,68% | 3 | 1,68% |
Schmitt (1939) | 6 | 1,25% | 1 | 0,55% | 1 | 0,56% | 1 | 0,56% |
Coutiere (1909) | 5 | 1,04% | 4 | 2,2% | 4 | 2,23% | 4 | 2,23% |
Paris. pp. [i]-xii, 9-320 ; [Atlas] Crustacés, 5 planches ; Insectes, 21 planches.">Guérin-Méneville ([1829-1838]) | 5 | 1,04% | 2 | 1,1% | 2 | 1,12% | 2 | 1,12% |
Questel (2020) | 5 | 1,04% | 5 | 2,75% | 5 | 2,79% | 5 | 2,79% |
Rose (1925) | 5 | 1,04% | 4 | 2,2% | 4 | 2,23% | 4 | 2,23% |
Avila-Garcia et al. (2020) | 4 | 0,83% | 0 | 0% | 0 | 0% | 0 | 0% |
Boone (1927) | 4 | 0,83% | 0 | 0% | 0 | 0% | 0 | 0% |
Carré (2006) | 4 | 0,83% | 4 | 2,2% | 4 | 2,23% | 4 | 2,23% |
Guinot et al. (2018) | 4 | 0,83% | 4 | 2,2% | 4 | 2,23% | 4 | 2,23% |
Linnaeus (1758) | 4 | 0,83% | 0 | 0% | 0 | 0% | 0 | 0% |
Michel et al. (1971) | 4 | 0,83% | 4 | 2,2% | 4 | 2,23% | 4 | 2,23% |
Poupin et al. (2013) | 4 | 0,83% | 3 | 1,65% | 3 | 1,68% | 3 | 1,68% |
Rathbun (1907) | 4 | 0,83% | 2 | 1,1% | 2 | 1,12% | 2 | 1,12% |
Rose (1926) | 4 | 0,83% | 2 | 1,1% | 2 | 1,12% | 2 | 1,12% |
Chatton (1912) | 3 | 0,62% | 2 | 1,1% | 2 | 1,12% | 2 | 1,12% |
Li (2008) | 3 | 0,62% | 3 | 1,65% | 3 | 1,68% | 3 | 1,68% |
Manning (1964) | 3 | 0,62% | 0 | 0% | 0 | 0% | 0 | 0% |
Marin (2010) | 3 | 0,62% | 0 | 0% | 0 | 0% | 0 | 0% |
Poltarukha & Melnik (2012) | 3 | 0,62% | 3 | 1,65% | 3 | 1,68% | 3 | 1,68% |
Poupin & Bouchard (2006) | 3 | 0,62% | 3 | 1,65% | 3 | 1,68% | 3 | 1,68% |
Poupin & Corbari (2016) | 3 | 0,62% | 3 | 1,65% | 3 | 1,68% | 3 | 1,68% |
Rathbun (1902) | 3 | 0,62% | 0 | 0% | 0 | 0% | 0 | 0% |
Renon (1989) | 3 | 0,62% | 3 | 1,65% | 3 | 1,68% | 3 | 1,68% |
Rignault & Chevallier (2017) | 3 | 0,62% | 3 | 1,65% | 3 | 1,68% | 3 | 1,68% |
Rodriguez et al. (2019) | 3 | 0,62% | 1 | 0,55% | 1 | 0,56% | 1 | 0,56% |
Rose (1933) | 3 | 0,62% | 2 | 1,1% | 2 | 1,12% | 2 | 1,12% |
Stephensen (1935) | 3 | 0,62% | 3 | 1,65% | 3 | 1,68% | 3 | 1,68% |
Swain (1967) | 3 | 0,62% | 0 | 0% | 0 | 0% | 0 | 0% |
Tricart & Foubert (2000) | 3 | 0,62% | 3 | 1,65% | 3 | 1,68% | 3 | 1,68% |
Zullo (1969) | 3 | 0,62% | 0 | 0% | 0 | 0% | 0 | 0% |
Aguilera (2002) | 2 | 0,42% | 2 | 1,1% | 2 | 1,12% | 2 | 1,12% |
Baird (1843) | 2 | 0,42% | 2 | 1,1% | 2 | 1,12% | 2 | 1,12% |
Binet (1984) | 2 | 0,42% | 2 | 1,1% | 2 | 1,12% | 2 | 1,12% |
Bold (1963) | 2 | 0,42% | 0 | 0% | 0 | 0% | 0 | 0% |
Bouvier (1899) | 2 | 0,42% | 1 | 0,55% | 1 | 0,56% | 1 | 0,56% |
Bradford (1974) | 2 | 0,42% | 2 | 1,1% | 2 | 1,12% | 2 | 1,12% |
Carbonel et al. (2007) | 2 | 0,42% | 2 | 1,1% | 2 | 1,12% | 2 | 1,12% |
Claus (1866) | 2 | 0,42% | 2 | 1,1% | 2 | 1,12% | 2 | 1,12% |
Cleva & Poupin (2012) | 2 | 0,42% | 2 | 1,1% | 2 | 1,12% | 2 | 1,12% |
Collin (2000) | 2 | 0,42% | 2 | 1,1% | 2 | 1,12% | 2 | 1,12% |
Corbari et al. (2015) | 2 | 0,42% | 2 | 1,1% | 2 | 1,12% | 2 | 1,12% |
Edwards (1944) | 2 | 0,42% | 0 | 0% | 0 | 0% | 0 | 0% |
Finnegan (1931) | 2 | 0,42% | 0 | 0% | 0 | 0% | 0 | 0% |
Haig (1957) | 2 | 0,42% | 2 | 1,1% | 2 | 1,12% | 2 | 1,12% |
Hendrickx (1990) | 2 | 0,42% | 0 | 0% | 0 | 0% | 0 | 0% |
Holthuis (1950) | 2 | 0,42% | 2 | 1,1% | 2 | 1,12% | 2 | 1,12% |
Li (2006) | 2 | 0,42% | 0 | 0% | 0 | 0% | 0 | 0% |
Lucas (1846) | 2 | 0,42% | 0 | 0% | 0 | 0% | 0 | 0% |
Manning (1988) | 2 | 0,42% | 2 | 1,1% | 2 | 1,12% | 2 | 1,12% |
Mclaughlin & Hoover (1996) | 2 | 0,42% | 2 | 1,1% | 2 | 1,12% | 2 | 1,12% |
Omatsola (1972) | 2 | 0,42% | 0 | 0% | 0 | 0% | 0 | 0% |
Pagano et al. (2012) | 2 | 0,42% | 2 | 1,1% | 2 | 1,12% | 2 | 1,12% |
Paulmier (2009) | 2 | 0,42% | 1 | 0,55% | 1 | 0,56% | 1 | 0,56% |
Questel & Le Quellec (2012) | 2 | 0,42% | 2 | 1,1% | 2 | 1,12% | 2 | 1,12% |
Rathbun (1906) | 2 | 0,42% | 0 | 0% | 0 | 0% | 0 | 0% |
Shoemaker (1942) | 2 | 0,42% | 2 | 1,1% | 2 | 1,12% | 2 | 1,12% |
Stimpson (1860) | 2 | 0,42% | 0 | 0% | 0 | 0% | 0 | 0% |
Teeter (1975) | 2 | 0,42% | 0 | 0% | 0 | 0% | 0 | 0% |
Wicksten (1987) | 2 | 0,42% | 2 | 1,1% | 2 | 1,12% | 2 | 1,12% |
Abele (1975) | 1 | 0,21% | 1 | 0,55% | 1 | 0,56% | 1 | 0,56% |
Alvarez et al. (1996) | 1 | 0,21% | 1 | 0,55% | 1 | 0,56% | 1 | 0,56% |
Amon et al. (2017) | 1 | 0,21% | 1 | 0,55% | 1 | 0,56% | 1 | 0,56% |
Bate et al. (1981) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Bold (1963) | 1 | 0,21% | 1 | 0,55% | 1 | 0,56% | 1 | 0,56% |
Bulletin of the Vanderbilt Marine Museum, 3: 1-221.">Boone (1930) | 1 | 0,21% | 1 | 0,55% | 1 | 0,56% | 1 | 0,56% |
Boone (1932) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Boxshall & Huys (2007) | 1 | 0,21% | 1 | 0,55% | 1 | 0,56% | 1 | 0,56% |
Brady (1911) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Breton (2014) | 1 | 0,21% | 1 | 0,55% | 1 | 0,56% | 0 | 0% |
Calman (1909) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Caziot (1921) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Ciampo (1971) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Claus (1863) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Claus (1863) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Colin (2000) | 1 | 0,21% | 1 | 0,55% | 1 | 0,56% | 1 | 0,56% |
Corbari et al. (2020) | 1 | 0,21% | 1 | 0,55% | 1 | 0,56% | 1 | 0,56% |
"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 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Crosnier (2002) | 1 | 0,21% | 1 | 0,55% | 1 | 0,56% | 1 | 0,56% |
Curd et al. (2015) | 1 | 0,21% | 1 | 0,55% | 1 | 0,56% | 1 | 0,56% |
Dewarumez et al. (2011) | 1 | 0,21% | 1 | 0,55% | 1 | 0,56% | 0 | 0% |
Edmondson (1930) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Bulletin of the Museum at Harvard College, 24 : 149-220.">Faxon (1893) | 1 | 0,21% | 1 | 0,55% | 1 | 0,56% | 1 | 0,56% |
Giesbrecht (1891) | 1 | 0,21% | 1 | 0,55% | 1 | 0,56% | 1 | 0,56% |
Goulletquer (2016) | 1 | 0,21% | 1 | 0,55% | 1 | 0,56% | 1 | 0,56% |
Guinot-dumortier (1960) | 1 | 0,21% | 1 | 0,55% | 1 | 0,56% | 1 | 0,56% |
Harada (1961) | 1 | 0,21% | 1 | 0,55% | 1 | 0,56% | 1 | 0,56% |
Hermoso-salazar & Solis-weiss (2001) | 1 | 0,21% | 1 | 0,55% | 1 | 0,56% | 1 | 0,56% |
Hernandez et al. (2007) | 1 | 0,21% | 1 | 0,55% | 1 | 0,56% | 1 | 0,56% |
Kropp (1989) | 1 | 0,21% | 1 | 0,55% | 1 | 0,56% | 1 | 0,56% |
Legall & Poupin (2014) | 1 | 0,21% | 1 | 0,55% | 1 | 0,56% | 1 | 0,56% |
Maddocks (2007) | 1 | 0,21% | 1 | 0,55% | 1 | 0,56% | 1 | 0,56% |
Man (1902) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Marukawa (1908) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Miers (1881) | 1 | 0,21% | 1 | 0,55% | 1 | 0,56% | 1 | 0,56% |
Milne-Edwards (1878) | 1 | 0,21% | 1 | 0,55% | 1 | 0,56% | 1 | 0,56% |
Nobili (1905) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Noël & Boulad (2018) | 1 | 0,21% | 1 | 0,55% | 1 | 0,56% | 1 | 0,56% |
Noël (2014) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Noël (2014) | 1 | 0,21% | 1 | 0,55% | 1 | 0,56% | 1 | 0,56% |
Noël (2015) | 1 | 0,21% | 1 | 0,55% | 1 | 0,56% | 1 | 0,56% |
Olivier (1791-[1792]) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Olivier (1811) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Ortmann (1890) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Perrier (1929) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Pfaller et al. (2019) | 1 | 0,21% | 1 | 0,55% | 1 | 0,56% | 1 | 0,56% |
Philippi (1843) | 1 | 0,21% | 1 | 0,55% | 1 | 0,56% | 1 | 0,56% |
Poupin et al. (2009) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Ramage (2017) | 1 | 0,21% | 1 | 0,55% | 1 | 0,56% | 1 | 0,56% |
Renon (1977) | 1 | 0,21% | 1 | 0,55% | 1 | 0,56% | 1 | 0,56% |
Rose (1925) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Smith (1885) | 1 | 0,21% | 1 | 0,55% | 1 | 0,56% | 1 | 0,56% |
Stimpson (1860) | 1 | 0,21% | 1 | 0,55% | 1 | 0,56% | 1 | 0,56% |
Thompson (1888) | 1 | 0,21% | 1 | 0,55% | 1 | 0,56% | 1 | 0,56% |
Tollu (2009) | 1 | 0,21% | 1 | 0,55% | 1 | 0,56% | 1 | 0,56% |
Van Duzee (1937) | 1 | 0,21% | 1 | 0,55% | 1 | 0,56% | 1 | 0,56% |
Bulletin United States National Museum No 100, 14(4): pp. i-ix 141-441.">Wilson (1950) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Yokoyama (2013) | 1 | 0,21% | 1 | 0,55% | 1 | 0,56% | 1 | 0,56% |