Décapodes des îles Eparses
158 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) | 821 | 78,64% | 753 | 235,31% | 753 | 237,54% | 750 | 236,59% |
Poupin et al. (2018) | 236 | 22,61% | 223 | 69,69% | 223 | 70,35% | 223 | 70,35% |
Poupin et al. (2013) | 175 | 16,76% | 159 | 49,69% | 159 | 50,16% | 157 | 49,53% |
Poupin (2015) | 103 | 9,87% | 99 | 30,94% | 99 | 31,23% | 99 | 31,23% |
Poupin et al. (2013) | 76 | 7,28% | 71 | 22,19% | 71 | 22,4% | 70 | 22,08% |
Corbari et al. (2020) | 16 | 1,53% | 14 | 4,38% | 14 | 4,42% | 14 | 4,42% |
Rathbun (1907) | 12 | 1,15% | 6 | 1,88% | 6 | 1,89% | 6 | 1,89% |
Guinot et al. (2018) | 10 | 0,96% | 9 | 2,81% | 9 | 2,84% | 9 | 2,84% |
Li (2008) | 10 | 0,96% | 7 | 2,19% | 7 | 2,21% | 7 | 2,21% |
Bourjon et al. (2018) | 9 | 0,86% | 9 | 2,81% | 9 | 2,84% | 9 | 2,84% |
Ramage (2017) | 9 | 0,86% | 8 | 2,5% | 8 | 2,52% | 8 | 2,52% |
Macpherson & Robainas-Barcia (2015) | 7 | 0,67% | 7 | 2,19% | 7 | 2,21% | 7 | 2,21% |
Nobili (1906) | 7 | 0,67% | 5 | 1,56% | 5 | 1,58% | 5 | 1,58% |
Paris. pp. [i]-xii, 9-320 ; [Atlas] Crustacés, 5 planches ; Insectes, 21 planches.">Guérin-Méneville ([1829-1838]) | 6 | 0,57% | 2 | 0,62% | 2 | 0,63% | 2 | 0,63% |
Poupin et al. (2013) | 6 | 0,57% | 5 | 1,56% | 5 | 1,58% | 5 | 1,58% |
Rathbun (1906) | 6 | 0,57% | 1 | 0,31% | 1 | 0,32% | 1 | 0,32% |
Ahyong (2014) | 5 | 0,48% | 5 | 1,56% | 5 | 1,58% | 5 | 1,58% |
Crosnier (1965) | 5 | 0,48% | 5 | 1,56% | 5 | 1,58% | 5 | 1,58% |
Komai & Poupin (2013) | 5 | 0,48% | 5 | 1,56% | 5 | 1,58% | 5 | 1,58% |
Poupin et al. (2022) | 5 | 0,48% | 5 | 1,56% | 5 | 1,58% | 5 | 1,58% |
Questel (2020) | 5 | 0,48% | 5 | 1,56% | 5 | 1,58% | 5 | 1,58% |
Uicn et al. (2019) | 5 | 0,48% | 5 | 1,56% | 5 | 1,58% | 5 | 1,58% |
Anker & Baeza (2021) | 4 | 0,38% | 4 | 1,25% | 4 | 1,26% | 4 | 1,26% |
Chace (1962) | 4 | 0,38% | 4 | 1,25% | 4 | 1,26% | 4 | 1,26% |
"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) | 4 | 0,38% | 1 | 0,31% | 1 | 0,32% | 1 | 0,32% |
Forest (1954) | 4 | 0,38% | 3 | 0,94% | 3 | 0,95% | 3 | 0,95% |
Linnaeus (1758) | 4 | 0,38% | 0 | 0% | 0 | 0% | 0 | 0% |
Questel (2017) | 4 | 0,38% | 4 | 1,25% | 4 | 1,26% | 4 | 1,26% |
Rodríguez-flores et al. (2019) | 4 | 0,38% | 4 | 1,25% | 4 | 1,26% | 4 | 1,26% |
Tricart & Foubert (2000) | 4 | 0,38% | 4 | 1,25% | 4 | 1,26% | 4 | 1,26% |
Ward (1939) | 4 | 0,38% | 0 | 0% | 0 | 0% | 0 | 0% |
Ward (1942) | 4 | 0,38% | 0 | 0% | 0 | 0% | 0 | 0% |
Bordaille (1903) | 3 | 0,29% | 1 | 0,31% | 1 | 0,32% | 1 | 0,32% |
Cleva & Poupin (2012) | 3 | 0,29% | 3 | 0,94% | 3 | 0,95% | 3 | 0,95% |
Crosnier (2002) | 3 | 0,29% | 3 | 0,94% | 3 | 0,95% | 3 | 0,95% |
Dana (1852) | 3 | 0,29% | 2 | 0,62% | 2 | 0,63% | 2 | 0,63% |
Edmondson (1925) | 3 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
Forest (1951) | 3 | 0,29% | 3 | 0,94% | 3 | 0,95% | 3 | 0,95% |
Haig (1989) | 3 | 0,29% | 2 | 0,62% | 2 | 0,63% | 2 | 0,63% |
Keith et al. (2013) | 3 | 0,29% | 3 | 0,94% | 3 | 0,95% | 3 | 0,95% |
Macpherson (2007) | 3 | 0,29% | 3 | 0,94% | 3 | 0,95% | 3 | 0,95% |
Ng & Shih (2015) | 3 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
Poore & Dworschak (2018) | 3 | 0,29% | 3 | 0,94% | 3 | 0,95% | 3 | 0,95% |
Poupin & Bouchard (2010) | 3 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
Rathbun (1914) | 3 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
Rignault & Chevallier (2017) | 3 | 0,29% | 2 | 0,62% | 2 | 0,63% | 2 | 0,63% |
Roux (1926) | 3 | 0,29% | 3 | 0,94% | 3 | 0,95% | 3 | 0,95% |
Ward (1941) | 3 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
Aguilera (2002) | 2 | 0,19% | 2 | 0,62% | 2 | 0,63% | 2 | 0,63% |
Anker (2019) | 2 | 0,19% | 2 | 0,62% | 2 | 0,63% | 2 | 0,63% |
Anker (2022) | 2 | 0,19% | 2 | 0,62% | 2 | 0,63% | 2 | 0,63% |
Berry (1979) | 2 | 0,19% | 2 | 0,62% | 2 | 0,63% | 2 | 0,63% |
Borradaile (1915) | 2 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Bruce (1978) | 2 | 0,19% | 2 | 0,62% | 2 | 0,63% | 2 | 0,63% |
Cabezas et al. (2010) | 2 | 0,19% | 2 | 0,62% | 2 | 0,63% | 2 | 0,63% |
Clark (2002) | 2 | 0,19% | 2 | 0,62% | 2 | 0,63% | 2 | 0,63% |
Crosnier (1962) | 2 | 0,19% | 2 | 0,62% | 2 | 0,63% | 2 | 0,63% |
Crosnier (1976) | 2 | 0,19% | 1 | 0,31% | 1 | 0,32% | 1 | 0,32% |
Crosnier (1991) | 2 | 0,19% | 2 | 0,62% | 2 | 0,63% | 2 | 0,63% |
Duris & Bruce (1995) | 2 | 0,19% | 2 | 0,62% | 2 | 0,63% | 2 | 0,63% |
Fourt et al. (2017) | 2 | 0,19% | 2 | 0,62% | 2 | 0,63% | 2 | 0,63% |
Griffin & Tranter (1986) | 2 | 0,19% | 1 | 0,31% | 1 | 0,32% | 1 | 0,32% |
Ifremer (2009) | 2 | 0,19% | 2 | 0,62% | 2 | 0,63% | 2 | 0,63% |
Kensley (1973) | 2 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Klunzinger (1913) | 2 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Lemaitre (1999) | 2 | 0,19% | 2 | 0,62% | 2 | 0,63% | 2 | 0,63% |
Maillaud et al. (2015) | 2 | 0,19% | 2 | 0,62% | 2 | 0,63% | 2 | 0,63% |
Milne-Edwards (1878) | 2 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Ng & Richers de Forges (2015) | 2 | 0,19% | 2 | 0,62% | 2 | 0,63% | 2 | 0,63% |
Nobili (1905) | 2 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Odhner (1925) | 2 | 0,19% | 1 | 0,31% | 1 | 0,32% | 1 | 0,32% |
Olivier (1791-[1792]) | 2 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Poupin (1997) | 2 | 0,19% | 2 | 0,62% | 2 | 0,63% | 2 | 0,63% |
Questel & Le Quellec (2012) | 2 | 0,19% | 2 | 0,62% | 2 | 0,63% | 2 | 0,63% |
Rathbun (1911) | 2 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Rodriguez et al. (2019) | 2 | 0,19% | 2 | 0,62% | 2 | 0,63% | 2 | 0,63% |
Saint & Laurent (1972) | 2 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Saito & Anker (2014) | 2 | 0,19% | 2 | 0,62% | 2 | 0,63% | 2 | 0,63% |
Schmitt (1939) | 2 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Shahdadi & Schubart (2020) | 2 | 0,19% | 2 | 0,62% | 2 | 0,63% | 2 | 0,63% |
Terao (1913) | 2 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Ward (1934) | 2 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Wooster (1982) | 2 | 0,19% | 2 | 0,62% | 2 | 0,63% | 2 | 0,63% |
Zarenkov (1989) | 2 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Researches on Crustacea. Special Number, 2, 1-203.">Baba (1988) | 1 | 0,1% | 1 | 0,31% | 1 | 0,32% | 1 | 0,32% |
Baba (1990) | 1 | 0,1% | 1 | 0,31% | 1 | 0,32% | 1 | 0,32% |
Balss (1933) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Barnard (1950) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Boone (1927) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Bordaille (1902) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Bouvier (1914) | 1 | 0,1% | 1 | 0,31% | 1 | 0,32% | 1 | 0,32% |
Boyko (2000) | 1 | 0,1% | 1 | 0,31% | 1 | 0,32% | 1 | 0,32% |
Bruce (1967) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Bruce (1974) | 1 | 0,1% | 1 | 0,31% | 1 | 0,32% | 1 | 0,32% |
Calman (1909) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Cambert et al. (2011) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Carré (2006) | 1 | 0,1% | 1 | 0,31% | 1 | 0,32% | 1 | 0,32% |
Corbari et al. (2015) | 1 | 0,1% | 1 | 0,31% | 1 | 0,32% | 1 | 0,32% |
Davie (1995) | 1 | 0,1% | 1 | 0,31% | 1 | 0,32% | 1 | 0,32% |
Davie (1997) | 1 | 0,1% | 1 | 0,31% | 1 | 0,32% | 1 | 0,32% |
Edmondson (1931) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1787) | 1 | 0,1% | 1 | 0,31% | 1 | 0,32% | 1 | 0,32% |
Fabricius (1798) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Ferry et al. (2017) | 1 | 0,1% | 1 | 0,31% | 1 | 0,32% | 1 | 0,32% |
Forest (1958) | 1 | 0,1% | 1 | 0,31% | 1 | 0,32% | 1 | 0,32% |
Forest (1987) | 1 | 0,1% | 1 | 0,31% | 1 | 0,32% | 1 | 0,32% |
Goulletquer (2016) | 1 | 0,1% | 1 | 0,31% | 1 | 0,32% | 1 | 0,32% |
Goy (2015) | 1 | 0,1% | 1 | 0,31% | 1 | 0,32% | 1 | 0,32% |
Guinot et al. (1985) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Guinot (1958) | 1 | 0,1% | 1 | 0,31% | 1 | 0,32% | 1 | 0,32% |
Haig & Kropp (1987) | 1 | 0,1% | 1 | 0,31% | 1 | 0,32% | 1 | 0,32% |
Heller (1861) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Heller (1862) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Holthuis (1952) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Holthuis (1960) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Keith & Vigneux (2002) | 1 | 0,1% | 1 | 0,31% | 1 | 0,32% | 1 | 0,32% |
Keith et al. (2006) | 1 | 0,1% | 1 | 0,31% | 1 | 0,32% | 1 | 0,32% |
Komai & Osawa (2006) | 1 | 0,1% | 1 | 0,31% | 1 | 0,32% | 1 | 0,32% |
Komai (1999) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Komai (2010) | 1 | 0,1% | 1 | 0,31% | 1 | 0,32% | 1 | 0,32% |
Latreille (1812) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Leach (1820) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Leene (1936) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Lemaitre (1989) | 1 | 0,1% | 1 | 0,31% | 1 | 0,32% | 1 | 0,32% |
Lemaitre (1994) | 1 | 0,1% | 1 | 0,31% | 1 | 0,32% | 1 | 0,32% |
Lemaitre (2004) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Lewinsohn (1979) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Machordom et al. (2022) | 1 | 0,1% | 1 | 0,31% | 1 | 0,32% | 1 | 0,32% |
Macpherson et al. (2017) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Macpherson (2009) | 1 | 0,1% | 1 | 0,31% | 1 | 0,32% | 1 | 0,32% |
Man (1902) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Marchal (1891) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Marin (2012) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Marquet (2002) | 1 | 0,1% | 1 | 0,31% | 1 | 0,32% | 1 | 0,32% |
Mclay (1991) | 1 | 0,1% | 1 | 0,31% | 1 | 0,32% | 1 | 0,32% |
Miers (1881) | 1 | 0,1% | 1 | 0,31% | 1 | 0,32% | 1 | 0,32% |
Milne-Edwards (1865) | 1 | 0,1% | 1 | 0,31% | 1 | 0,32% | 1 | 0,32% |
Naderloo & Türkay (2010) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Naderloo et al. (2011) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Nobili (1904) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Noël (2014) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Noël (2014) | 1 | 0,1% | 1 | 0,31% | 1 | 0,32% | 1 | 0,32% |
Noël (2015) | 1 | 0,1% | 1 | 0,31% | 1 | 0,32% | 1 | 0,32% |
Noël (2017) | 1 | 0,1% | 1 | 0,31% | 1 | 0,32% | 1 | 0,32% |
Ortmann (1897) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Peters (1852) | 1 | 0,1% | 1 | 0,31% | 1 | 0,32% | 1 | 0,32% |
Pezy et al. (2017) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Pfaller et al. (2019) | 1 | 0,1% | 1 | 0,31% | 1 | 0,32% | 1 | 0,32% |
Poupin et al. (2022) | 1 | 0,1% | 1 | 0,31% | 1 | 0,32% | 1 | 0,32% |
Poupin (2008) | 1 | 0,1% | 1 | 0,31% | 1 | 0,32% | 1 | 0,32% |
Richer et al. (1996) | 1 | 0,1% | 1 | 0,31% | 1 | 0,32% | 1 | 0,32% |
Sakai (1969) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Serene (1984) | 1 | 0,1% | 1 | 0,31% | 1 | 0,32% | 1 | 0,32% |
Shih et al. (2016) | 1 | 0,1% | 1 | 0,31% | 1 | 0,32% | 1 | 0,32% |
Stebbing (1923) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Stimpson (1860) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Tavares & Amouroux (2003) | 1 | 0,1% | 1 | 0,31% | 1 | 0,32% | 1 | 0,32% |
Ward (1933) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |