Décapodes de Guyane
139 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
Référence | Total | Valides | Espèces | Taxons terminaux | ||||
---|---|---|---|---|---|---|---|---|
nb | % | nb | % | nb | % | nb | % | |
Corbari et al. (2015) | 97 | 19,92% | 79 | 42,02% | 79 | 42,02% | 79 | 42,02% |
Poupin & Corbari (2016) | 86 | 17,66% | 75 | 39,89% | 75 | 39,89% | 75 | 39,89% |
Tricart & Foubert (2000) | 53 | 10,88% | 38 | 20,21% | 38 | 20,21% | 38 | 20,21% |
Poupin (2010) | 24 | 4,93% | 24 | 12,77% | 24 | 12,77% | 24 | 12,77% |
Questel (2020) | 22 | 4,52% | 21 | 11,17% | 21 | 11,17% | 21 | 11,17% |
Guéguen (2000) | 21 | 4,31% | 17 | 9,04% | 17 | 9,04% | 17 | 9,04% |
Poupin (1994) | 21 | 4,31% | 15 | 7,98% | 15 | 7,98% | 15 | 7,98% |
Paulmier (1996) | 20 | 4,11% | 14 | 7,45% | 14 | 7,45% | 14 | 7,45% |
Bulletin of the Museum of Comparative Zoology at Harvard College. 8(2): 1-68, Pl. 1-2.">Milne-Edwards (1880) | 18 | 3,7% | 5 | 2,66% | 5 | 2,66% | 5 | 2,66% |
Carré (2006) | 14 | 2,87% | 11 | 5,85% | 11 | 5,85% | 11 | 5,85% |
Carmona-Suárez & Poupin (2016) | 13 | 2,67% | 9 | 4,79% | 9 | 4,79% | 9 | 4,79% |
Poupin (2018) | 12 | 2,46% | 11 | 5,85% | 11 | 5,85% | 11 | 5,85% |
Questel & Le Quellec (2012) | 12 | 2,46% | 9 | 4,79% | 9 | 4,79% | 9 | 4,79% |
IUCN (2013) | 11 | 2,26% | 10 | 5,32% | 10 | 5,32% | 10 | 5,32% |
Corbari et al. (2020) | 8 | 1,64% | 5 | 2,66% | 5 | 2,66% | 5 | 2,66% |
Machordom et al. (2022) | 8 | 1,64% | 8 | 4,26% | 8 | 4,26% | 8 | 4,26% |
Anker (2012) | 6 | 1,23% | 6 | 3,19% | 6 | 3,19% | 6 | 3,19% |
Poupin et al. (1999) | 5 | 1,03% | 4 | 2,13% | 4 | 2,13% | 4 | 2,13% |
Uicn et al. (2019) | 5 | 1,03% | 5 | 2,66% | 5 | 2,66% | 5 | 2,66% |
Fourt et al. (2017) | 4 | 0,82% | 4 | 2,13% | 4 | 2,13% | 4 | 2,13% |
Holthuis (1958) | 4 | 0,82% | 4 | 2,13% | 4 | 2,13% | 4 | 2,13% |
Oliviera (1939) | 4 | 0,82% | 0 | 0% | 0 | 0% | 0 | 0% |
Pinheiro & Boos (2016) | 4 | 0,82% | 4 | 2,13% | 4 | 2,13% | 4 | 2,13% |
Questel (2017) | 4 | 0,82% | 4 | 2,13% | 4 | 2,13% | 4 | 2,13% |
Risso (1816) | 4 | 0,82% | 0 | 0% | 0 | 0% | 0 | 0% |
Yokoyama (2013) | 4 | 0,82% | 4 | 2,13% | 4 | 2,13% | 4 | 2,13% |
Almeida et al. (2013) | 3 | 0,62% | 3 | 1,6% | 3 | 1,6% | 3 | 1,6% |
Beltran (1982) | 3 | 0,62% | 3 | 1,6% | 3 | 1,6% | 3 | 1,6% |
Carvalho-batista et al. (2019) | 3 | 0,62% | 3 | 1,6% | 3 | 1,6% | 3 | 1,6% |
Chen et al. (2016) | 3 | 0,62% | 3 | 1,6% | 3 | 1,6% | 3 | 1,6% |
Cronin et al. (2022) | 3 | 0,62% | 3 | 1,6% | 3 | 1,6% | 3 | 1,6% |
Crosnier (1976) | 3 | 0,62% | 2 | 1,06% | 2 | 1,06% | 2 | 1,06% |
Gueguen (1998) | 3 | 0,62% | 3 | 1,6% | 3 | 1,6% | 3 | 1,6% |
Guinot-dumortier (1960) | 3 | 0,62% | 3 | 1,6% | 3 | 1,6% | 3 | 1,6% |
Holthuis (1960) | 3 | 0,62% | 2 | 1,06% | 2 | 1,06% | 2 | 1,06% |
Rhyne & Lin (2006) | 3 | 0,62% | 3 | 1,6% | 3 | 1,6% | 3 | 1,6% |
Rodriguez et al. (2019) | 3 | 0,62% | 2 | 1,06% | 2 | 1,06% | 2 | 1,06% |
Baudry et al. (2022) | 2 | 0,41% | 2 | 1,06% | 2 | 1,06% | 2 | 1,06% |
Boone (1927) | 2 | 0,41% | 0 | 0% | 0 | 0% | 0 | 0% |
Comptes rendus hebdomadaires des séances de l'Académie des sciences, 141: 746-749.">Bouvier (1905) | 2 | 0,41% | 1 | 0,53% | 1 | 0,53% | 1 | 0,53% |
Bray et al. (1990) | 2 | 0,41% | 2 | 1,06% | 2 | 1,06% | 2 | 1,06% |
Carvalho et al. (2010) | 2 | 0,41% | 2 | 1,06% | 2 | 1,06% | 2 | 1,06% |
Crane (1943) | 2 | 0,41% | 0 | 0% | 0 | 0% | 0 | 0% |
Farfante & Bullis (1973) | 2 | 0,41% | 2 | 1,06% | 2 | 1,06% | 2 | 1,06% |
Grave (2007) | 2 | 0,41% | 2 | 1,06% | 2 | 1,06% | 2 | 1,06% |
Gueguen (1995) | 2 | 0,41% | 2 | 1,06% | 2 | 1,06% | 2 | 1,06% |
Gueguen (1997) | 2 | 0,41% | 2 | 1,06% | 2 | 1,06% | 2 | 1,06% |
Guinot et al. (2018) | 2 | 0,41% | 2 | 1,06% | 2 | 1,06% | 2 | 1,06% |
Holthuis (1956) | 2 | 0,41% | 0 | 0% | 0 | 0% | 0 | 0% |
Ifremer (2009) | 2 | 0,41% | 0 | 0% | 0 | 0% | 0 | 0% |
Kensley & Walker (1982) | 2 | 0,41% | 2 | 1,06% | 2 | 1,06% | 2 | 1,06% |
Latreille ([1803]) | 2 | 0,41% | 0 | 0% | 0 | 0% | 0 | 0% |
Lim et al. (2002) | 2 | 0,41% | 2 | 1,06% | 2 | 1,06% | 2 | 1,06% |
Linnaeus (1758) | 2 | 0,41% | 0 | 0% | 0 | 0% | 0 | 0% |
Magalhaes (1988) | 2 | 0,41% | 2 | 1,06% | 2 | 1,06% | 2 | 1,06% |
Manning & Holthuis (1989) | 2 | 0,41% | 2 | 1,06% | 2 | 1,06% | 2 | 1,06% |
Miers (1878) | 2 | 0,41% | 2 | 1,06% | 2 | 1,06% | 2 | 1,06% |
Milne-edwards (1837) | 2 | 0,41% | 0 | 0% | 0 | 0% | 0 | 0% |
Poupin et al. (2013) | 2 | 0,41% | 2 | 1,06% | 2 | 1,06% | 2 | 1,06% |
Rathbun (1898) | 2 | 0,41% | 2 | 1,06% | 2 | 1,06% | 2 | 1,06% |
Bulletin de la Société Zoologique de France, xxviii: 63-79.">Richard (1903) | 2 | 0,41% | 0 | 0% | 0 | 0% | 0 | 0% |
Righi (1965) | 2 | 0,41% | 0 | 0% | 0 | 0% | 0 | 0% |
Risso (1827) | 2 | 0,41% | 0 | 0% | 0 | 0% | 0 | 0% |
Sarver et al. (1998) | 2 | 0,41% | 0 | 0% | 0 | 0% | 0 | 0% |
Saussure (1857) | 2 | 0,41% | 0 | 0% | 0 | 0% | 0 | 0% |
Silva et al. (2020) | 2 | 0,41% | 2 | 1,06% | 2 | 1,06% | 2 | 1,06% |
Stimpson (1871) | 2 | 0,41% | 2 | 1,06% | 2 | 1,06% | 2 | 1,06% |
Tavares & Gusmão (2016) | 2 | 0,41% | 0 | 0% | 0 | 0% | 0 | 0% |
von Hagen (1968) | 2 | 0,41% | 0 | 0% | 0 | 0% | 0 | 0% |
Williams (1974) | 2 | 0,41% | 2 | 1,06% | 2 | 1,06% | 2 | 1,06% |
Annals of Natural History, (6)(xiii): pp. 225-245, 321-331, & 400-411.">Alcock (1894) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Barnard (1950) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Bourcier (1988) | 1 | 0,21% | 1 | 0,53% | 1 | 0,53% | 1 | 0,53% |
Bouvier (1905) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Bouvier (1912) | 1 | 0,21% | 1 | 0,53% | 1 | 0,53% | 1 | 0,53% |
Burkenroad (1936) | 1 | 0,21% | 1 | 0,53% | 1 | 0,53% | 1 | 0,53% |
Chace (1939) | 1 | 0,21% | 1 | 0,53% | 1 | 0,53% | 1 | 0,53% |
Chan (1991) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Coudray & Noël (2014) | 1 | 0,21% | 1 | 0,53% | 1 | 0,53% | 1 | 0,53% |
Crosnier & Forest (1973) | 1 | 0,21% | 1 | 0,53% | 1 | 0,53% | 1 | 0,53% |
Diaz & Cuzange (2009) | 1 | 0,21% | 1 | 0,53% | 1 | 0,53% | 1 | 0,53% |
Annales de la société entomologique de France, 22(2): 205-210.">Dupuis (1986) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Memoirs of the Museum of Comparative Zoology at Harvard College Cambridge, 27: 177-274.">Edwards & Bouvier (1909) | 1 | 0,21% | 1 | 0,53% | 1 | 0,53% | 1 | 0,53% |
Fabricius (1793) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Fabricius (1798) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Ferry et al. (2017) | 1 | 0,21% | 1 | 0,53% | 1 | 0,53% | 1 | 0,53% |
Galil et al. (2016) | 1 | 0,21% | 1 | 0,53% | 1 | 0,53% | 1 | 0,53% |
Galil (2000) | 1 | 0,21% | 1 | 0,53% | 1 | 0,53% | 1 | 0,53% |
Gall & Beague (1986) | 1 | 0,21% | 1 | 0,53% | 1 | 0,53% | 1 | 0,53% |
Gomez (1933) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Goud et al. (2021) | 1 | 0,21% | 1 | 0,53% | 1 | 0,53% | 1 | 0,53% |
Goulletquer (2016) | 1 | 0,21% | 1 | 0,53% | 1 | 0,53% | 1 | 0,53% |
Goy (2015) | 1 | 0,21% | 1 | 0,53% | 1 | 0,53% | 1 | 0,53% |
Gueguen (2001) | 1 | 0,21% | 1 | 0,53% | 1 | 0,53% | 1 | 0,53% |
Guinot (1969) | 1 | 0,21% | 1 | 0,53% | 1 | 0,53% | 1 | 0,53% |
Holthuis (1950) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Holthuis (1952) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Holthuis (1959) | 1 | 0,21% | 1 | 0,53% | 1 | 0,53% | 1 | 0,53% |
Holthuis (1962) | 1 | 0,21% | 1 | 0,53% | 1 | 0,53% | 1 | 0,53% |
Holthuis (1974) | 1 | 0,21% | 1 | 0,53% | 1 | 0,53% | 1 | 0,53% |
Huff (1979) | 1 | 0,21% | 1 | 0,53% | 1 | 0,53% | 1 | 0,53% |
Impact-Mer et al. (2011) | 1 | 0,21% | 1 | 0,53% | 1 | 0,53% | 1 | 0,53% |
Ives (1891) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Johnson (1867) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Jourdan & Mille (2006) | 1 | 0,21% | 1 | 0,53% | 1 | 0,53% | 1 | 0,53% |
Jourdan (2020) | 1 | 0,21% | 1 | 0,53% | 1 | 0,53% | 1 | 0,53% |
Jourde et al. (2017) | 1 | 0,21% | 1 | 0,53% | 1 | 0,53% | 1 | 0,53% |
Keith et al. (2002) | 1 | 0,21% | 1 | 0,53% | 1 | 0,53% | 1 | 0,53% |
Keith et al. (1999) | 1 | 0,21% | 1 | 0,53% | 1 | 0,53% | 1 | 0,53% |
Lagarde (2008) | 1 | 0,21% | 1 | 0,53% | 1 | 0,53% | 1 | 0,53% |
Lalubie et al. (2015) | 1 | 0,21% | 1 | 0,53% | 1 | 0,53% | 1 | 0,53% |
Leach (1817) | 1 | 0,21% | 1 | 0,53% | 1 | 0,53% | 1 | 0,53% |
Lenz & Strunck (1914) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Macpherson (2007) | 1 | 0,21% | 1 | 0,53% | 1 | 0,53% | 1 | 0,53% |
Magalhães & Santos (2021) | 1 | 0,21% | 1 | 0,53% | 1 | 0,53% | 1 | 0,53% |
Milne-edwards (1883) | 1 | 0,21% | 1 | 0,53% | 1 | 0,53% | 1 | 0,53% |
Monti et al. (2010) | 1 | 0,21% | 1 | 0,53% | 1 | 0,53% | 1 | 0,53% |
Murienne et al. (2022) | 1 | 0,21% | 1 | 0,53% | 1 | 0,53% | 1 | 0,53% |
Ng & Castro (2016) | 1 | 0,21% | 1 | 0,53% | 1 | 0,53% | 1 | 0,53% |
Noël (2015) | 1 | 0,21% | 1 | 0,53% | 1 | 0,53% | 1 | 0,53% |
Noël (2015) | 1 | 0,21% | 1 | 0,53% | 1 | 0,53% | 1 | 0,53% |
Noël (2016) | 1 | 0,21% | 1 | 0,53% | 1 | 0,53% | 1 | 0,53% |
Odinetz et al. (1994) | 1 | 0,21% | 1 | 0,53% | 1 | 0,53% | 1 | 0,53% |
Olivier (1791-[1792]) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Pachelle & Tavares (2018) | 1 | 0,21% | 1 | 0,53% | 1 | 0,53% | 1 | 0,53% |
Pereira et al. (2014) | 1 | 0,21% | 1 | 0,53% | 1 | 0,53% | 1 | 0,53% |
Poupin & Lemaitre (2014) | 1 | 0,21% | 1 | 0,53% | 1 | 0,53% | 1 | 0,53% |
Poupin et al. (2018) | 1 | 0,21% | 1 | 0,53% | 1 | 0,53% | 1 | 0,53% |
Questel (2014) | 1 | 0,21% | 1 | 0,53% | 1 | 0,53% | 1 | 0,53% |
Righi (1967) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Rodríguez-Flores et al. (2018) | 1 | 0,21% | 1 | 0,53% | 1 | 0,53% | 1 | 0,53% |
Sadek et al. (2018) | 1 | 0,21% | 1 | 0,53% | 1 | 0,53% | 1 | 0,53% |
Schmitt (1933) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Singh (2021) | 1 | 0,21% | 1 | 0,53% | 1 | 0,53% | 1 | 0,53% |
Tavares & Amouroux (2003) | 1 | 0,21% | 1 | 0,53% | 1 | 0,53% | 1 | 0,53% |
UICN Comité français, OFB & MNHN (2021) | 1 | 0,21% | 1 | 0,53% | 1 | 0,53% | 1 | 0,53% |
Vereshchaka et al. (2020) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Yokoya (1933) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
(1967) | 1 | 0,21% | 1 | 0,53% | 1 | 0,53% | 1 | 0,53% |