Paguroidea
Pagures ou bernard l'hermite, cénobites et crabe des cocotiers (Paguroidea).
159 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) | 335 | 46,4% | 334 | 92,01% | 334 | 92,01% | 334 | 92,01% |
Poupin & Corbari (2016) | 30 | 4,16% | 30 | 8,26% | 30 | 8,26% | 30 | 8,26% |
Lemaitre (2014) | 28 | 3,88% | 28 | 7,71% | 28 | 7,71% | 28 | 7,71% |
Poupin et al. (2013) | 25 | 3,46% | 25 | 6,89% | 25 | 6,89% | 25 | 6,89% |
Poupin (2015) | 22 | 3,05% | 22 | 6,06% | 22 | 6,06% | 22 | 6,06% |
Komai (2010) | 20 | 2,77% | 20 | 5,51% | 20 | 5,51% | 20 | 5,51% |
Lemaitre (1994) | 19 | 2,63% | 9 | 2,48% | 9 | 2,48% | 9 | 2,48% |
Forest (1987) | 16 | 2,22% | 14 | 3,86% | 14 | 3,86% | 14 | 3,86% |
Lemaitre (2013) | 16 | 2,22% | 16 | 4,41% | 16 | 4,41% | 16 | 4,41% |
Questel (2020) | 16 | 2,22% | 16 | 4,41% | 16 | 4,41% | 16 | 4,41% |
Lemaitre (1996) | 13 | 1,8% | 11 | 3,03% | 11 | 3,03% | 11 | 3,03% |
Mclaughlin (1997) | 13 | 1,8% | 10 | 2,75% | 10 | 2,75% | 10 | 2,75% |
Poupin (1997) | 13 | 1,8% | 13 | 3,58% | 13 | 3,58% | 13 | 3,58% |
Bourcier (1988) | 12 | 1,66% | 9 | 2,48% | 9 | 2,48% | 9 | 2,48% |
Nelson-Smith et al. (2014) | 12 | 1,66% | 9 | 2,48% | 9 | 2,48% | 9 | 2,48% |
Saint & Laurent (1972) | 12 | 1,66% | 0 | 0% | 0 | 0% | 0 | 0% |
Bulletin of the Museum of Comparative Zoology at Harvard College. 8(2): 1-68, Pl. 1-2.">Milne-Edwards (1880) | 11 | 1,52% | 0 | 0% | 0 | 0% | 0 | 0% |
Poupin et al. (2013) | 11 | 1,52% | 11 | 3,03% | 11 | 3,03% | 11 | 3,03% |
Carré (2006) | 10 | 1,39% | 9 | 2,48% | 9 | 2,48% | 9 | 2,48% |
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 | 1,39% | 10 | 2,75% | 10 | 2,75% | 10 | 2,75% |
Lemaitre (1989) | 10 | 1,39% | 8 | 2,2% | 8 | 2,2% | 8 | 2,2% |
Poupin & Mclaughlin (1998) | 10 | 1,39% | 10 | 2,75% | 10 | 2,75% | 10 | 2,75% |
Lemaitre et al. (2017) | 8 | 1,11% | 8 | 2,2% | 8 | 2,2% | 8 | 2,2% |
Mclaughlin (2000) | 8 | 1,11% | 8 | 2,2% | 8 | 2,2% | 8 | 2,2% |
Poupin (1994) | 8 | 1,11% | 7 | 1,93% | 7 | 1,93% | 7 | 1,93% |
Ramage (2017) | 8 | 1,11% | 8 | 2,2% | 8 | 2,2% | 8 | 2,2% |
Risso (1827) | 8 | 1,11% | 2 | 0,55% | 2 | 0,55% | 2 | 0,55% |
Mclaughlin & Haig (1989) | 7 | 0,97% | 7 | 1,93% | 7 | 1,93% | 7 | 1,93% |
Mclaughlin (2004) | 7 | 0,97% | 7 | 1,93% | 7 | 1,93% | 7 | 1,93% |
Corbari et al. (2020) | 6 | 0,83% | 6 | 1,65% | 6 | 1,65% | 6 | 1,65% |
Forest (1951) | 6 | 0,83% | 6 | 1,65% | 6 | 1,65% | 6 | 1,65% |
Forest (1954) | 6 | 0,83% | 3 | 0,83% | 3 | 0,83% | 3 | 0,83% |
Haig & Mclaughlin (1991) | 6 | 0,83% | 5 | 1,38% | 5 | 1,38% | 5 | 1,38% |
Lemaitre (1999) | 6 | 0,83% | 6 | 1,65% | 6 | 1,65% | 6 | 1,65% |
Mclaughlin (1981) | 6 | 0,83% | 6 | 1,65% | 6 | 1,65% | 6 | 1,65% |
Mclaughlin (2007) | 6 | 0,83% | 5 | 1,38% | 5 | 1,38% | 5 | 1,38% |
Risso (1816) | 6 | 0,83% | 0 | 0% | 0 | 0% | 0 | 0% |
Forest et al. (2000) | 5 | 0,69% | 5 | 1,38% | 5 | 1,38% | 5 | 1,38% |
Godet et al. (2010) | 5 | 0,69% | 5 | 1,38% | 5 | 1,38% | 5 | 1,38% |
Komai & Poupin (2013) | 5 | 0,69% | 5 | 1,38% | 5 | 1,38% | 5 | 1,38% |
Komai (1999) | 5 | 0,69% | 0 | 0% | 0 | 0% | 0 | 0% |
Lemaitre (2004) | 5 | 0,69% | 4 | 1,1% | 4 | 1,1% | 4 | 1,1% |
Orrell (2019) | 5 | 0,69% | 5 | 1,38% | 5 | 1,38% | 5 | 1,38% |
Alcock (1905) | 4 | 0,55% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
Almon et al. (2022) | 4 | 0,55% | 4 | 1,1% | 4 | 1,1% | 4 | 1,1% |
Balss (1911) | 4 | 0,55% | 0 | 0% | 0 | 0% | 0 | 0% |
Corbari et al. (2015) | 4 | 0,55% | 4 | 1,1% | 4 | 1,1% | 4 | 1,1% |
Fourt et al. (2017) | 4 | 0,55% | 4 | 1,1% | 4 | 1,1% | 4 | 1,1% |
Komai & Osawa (2006) | 4 | 0,55% | 4 | 1,1% | 4 | 1,1% | 4 | 1,1% |
Komai & Poupin (2012) | 4 | 0,55% | 4 | 1,1% | 4 | 1,1% | 4 | 1,1% |
Leach (1815-1875) | 4 | 0,55% | 2 | 0,55% | 2 | 0,55% | 2 | 0,55% |
Lemaitre (1997) | 4 | 0,55% | 4 | 1,1% | 4 | 1,1% | 4 | 1,1% |
Lemaitre (2006) | 4 | 0,55% | 4 | 1,1% | 4 | 1,1% | 4 | 1,1% |
Lemaitre (2020) | 4 | 0,55% | 4 | 1,1% | 4 | 1,1% | 4 | 1,1% |
Mclaughlin (1986) | 4 | 0,55% | 2 | 0,55% | 2 | 0,55% | 2 | 0,55% |
Mclaughlin (2006) | 4 | 0,55% | 4 | 1,1% | 4 | 1,1% | 4 | 1,1% |
Nobili (1906) | 4 | 0,55% | 0 | 0% | 0 | 0% | 0 | 0% |
Questel & Le Quellec (2012) | 4 | 0,55% | 4 | 1,1% | 4 | 1,1% | 4 | 1,1% |
Tricart & Foubert (2000) | 4 | 0,55% | 4 | 1,1% | 4 | 1,1% | 4 | 1,1% |
Wass (1963) | 4 | 0,55% | 0 | 0% | 0 | 0% | 0 | 0% |
Wooster (1982) | 4 | 0,55% | 4 | 1,1% | 4 | 1,1% | 4 | 1,1% |
Asakura & Paulay (2003) | 3 | 0,42% | 3 | 0,83% | 3 | 0,83% | 3 | 0,83% |
Bourjon et al. (2018) | 3 | 0,42% | 3 | 0,83% | 3 | 0,83% | 3 | 0,83% |
Breton (2014) | 3 | 0,42% | 3 | 0,83% | 3 | 0,83% | 3 | 0,83% |
Buitendijk (1937) | 3 | 0,42% | 3 | 0,83% | 3 | 0,83% | 3 | 0,83% |
Chace (1962) | 3 | 0,42% | 3 | 0,83% | 3 | 0,83% | 3 | 0,83% |
Forest (1997) | 3 | 0,42% | 0 | 0% | 0 | 0% | 0 | 0% |
Holthuis (1977) | 3 | 0,42% | 0 | 0% | 0 | 0% | 0 | 0% |
Ifremer (2009) | 3 | 0,42% | 3 | 0,83% | 3 | 0,83% | 3 | 0,83% |
Lemaitre & Poupin (2003) | 3 | 0,42% | 3 | 0,83% | 3 | 0,83% | 3 | 0,83% |
Lemaitre (1998) | 3 | 0,42% | 3 | 0,83% | 3 | 0,83% | 3 | 0,83% |
Lemaitre (2004) | 3 | 0,42% | 2 | 0,55% | 2 | 0,55% | 2 | 0,55% |
Milne-edwards (1891) | 3 | 0,42% | 0 | 0% | 0 | 0% | 0 | 0% |
Poupin & Bouchard (2006) | 3 | 0,42% | 3 | 0,83% | 3 | 0,83% | 3 | 0,83% |
Poupin & Lemaitre (2022) | 3 | 0,42% | 3 | 0,83% | 3 | 0,83% | 3 | 0,83% |
Poupin & Mclaughlin (1996) | 3 | 0,42% | 3 | 0,83% | 3 | 0,83% | 3 | 0,83% |
Poupin et al. (2013) | 3 | 0,42% | 3 | 0,83% | 3 | 0,83% | 3 | 0,83% |
Poupin et al. (2022) | 3 | 0,42% | 3 | 0,83% | 3 | 0,83% | 3 | 0,83% |
Poupin (2018) | 3 | 0,42% | 3 | 0,83% | 3 | 0,83% | 3 | 0,83% |
Asakura (2005) | 2 | 0,28% | 2 | 0,55% | 2 | 0,55% | 2 | 0,55% |
Bouvier (1899) | 2 | 0,28% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
Clark & Harrison (2021) | 2 | 0,28% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
Craig & Felder (2022) | 2 | 0,28% | 2 | 0,55% | 2 | 0,55% | 2 | 0,55% |
Forest & Saint Laurent | 2 | 0,28% | 2 | 0,55% | 2 | 0,55% | 2 | 0,55% |
Forest (1992) | 2 | 0,28% | 2 | 0,55% | 2 | 0,55% | 2 | 0,55% |
Kensley (1973) | 2 | 0,28% | 0 | 0% | 0 | 0% | 0 | 0% |
Lemaitre & Campos (1993) | 2 | 0,28% | 2 | 0,55% | 2 | 0,55% | 2 | 0,55% |
Lemaitre & Mclaughlin (1996) | 2 | 0,28% | 2 | 0,55% | 2 | 0,55% | 2 | 0,55% |
Lemaitre (1986) | 2 | 0,28% | 2 | 0,55% | 2 | 0,55% | 2 | 0,55% |
Lemaitre (2010) | 2 | 0,28% | 2 | 0,55% | 2 | 0,55% | 2 | 0,55% |
Lemaitre (2011) | 2 | 0,28% | 2 | 0,55% | 2 | 0,55% | 2 | 0,55% |
Lemaitre (2015) | 2 | 0,28% | 2 | 0,55% | 2 | 0,55% | 2 | 0,55% |
Linnaeus (1758) | 2 | 0,28% | 0 | 0% | 0 | 0% | 0 | 0% |
Maillaud et al. (2015) | 2 | 0,28% | 2 | 0,55% | 2 | 0,55% | 2 | 0,55% |
Malay et al. (2012) | 2 | 0,28% | 2 | 0,55% | 2 | 0,55% | 2 | 0,55% |
Mclaughlin & Haig (1996) | 2 | 0,28% | 0 | 0% | 0 | 0% | 0 | 0% |
Mclaughlin & Hoover (1996) | 2 | 0,28% | 2 | 0,55% | 2 | 0,55% | 2 | 0,55% |
Mclaughlin & Lemaitre (2008) | 2 | 0,28% | 2 | 0,55% | 2 | 0,55% | 2 | 0,55% |
Mclaughlin et al. (1998) | 2 | 0,28% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
Mclaughlin (2004) | 2 | 0,28% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
Paulmier (1996) | 2 | 0,28% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
Pérez (1931) | 2 | 0,28% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
Poupin & Lemaitre (2003) | 2 | 0,28% | 2 | 0,55% | 2 | 0,55% | 2 | 0,55% |
Poupin (2001) | 2 | 0,28% | 2 | 0,55% | 2 | 0,55% | 2 | 0,55% |
Rahayu (2011) | 2 | 0,28% | 2 | 0,55% | 2 | 0,55% | 2 | 0,55% |
Richer et al. (2013) | 2 | 0,28% | 2 | 0,55% | 2 | 0,55% | 2 | 0,55% |
Roux (1828) | 2 | 0,28% | 0 | 0% | 0 | 0% | 0 | 0% |
Saussure (1857) | 2 | 0,28% | 0 | 0% | 0 | 0% | 0 | 0% |
Terao (1913) | 2 | 0,28% | 0 | 0% | 0 | 0% | 0 | 0% |
Zarenkov (1989) | 2 | 0,28% | 0 | 0% | 0 | 0% | 0 | 0% |
Annals of Natural History, (6)(xiii): pp. 225-245, 321-331, & 400-411.">Alcock (1894) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Altès (1962) | 1 | 0,14% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
Asakura (2001) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Asakura (2006) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Balss (1912) | 1 | 0,14% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
Bulletin of the Vanderbilt Marine Museum, 3: 1-221.">Boone (1930) | 1 | 0,14% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
Clément (1874) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Coudray & Noël (2014) | 1 | 0,14% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
Coudray & Noël (2014) | 1 | 0,14% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
Coudray & Noël (2014) | 1 | 0,14% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
Coudray & Noël (2014) | 1 | 0,14% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
Coudray & Noël (2014) | 1 | 0,14% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
Coudray & Noël (2014) | 1 | 0,14% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
Coudray & Noël (2014) | 1 | 0,14% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
Coudray & Noël (2014) | 1 | 0,14% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
Coudray & Noël (2014) | 1 | 0,14% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
Crisp & Fischer-piette (1959) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Crosnier (1976) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Davoult (1990) | 1 | 0,14% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
DCE-Benthos Network, French Mediterranen Lagoon Monitoring Network (2022) | 1 | 0,14% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
Edmondson (1952) | 1 | 0,14% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
Fabricius (1787) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Forest (1958) | 1 | 0,14% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
Forest (1984) | 1 | 0,14% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
Forest (2015) | 1 | 0,14% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
Gong & Paulay (2018) | 1 | 0,14% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
Journal of the Asiatic Society of Bengal, lxv: 516-536.">Henderson (1896) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Ifremer (2022) | 1 | 0,14% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
Latreille (1812) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Marchal (1891) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Martin (2003) | 1 | 0,14% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
Miers (1878) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Miers (1879) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Miers (1881) | 1 | 0,14% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
Milne-edwards & Bouvier (1897) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Noël (2015) | 1 | 0,14% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
Noël (2015) | 1 | 0,14% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
Noël (2016) | 1 | 0,14% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
Noël (2016) | 1 | 0,14% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
Eupagurus bernhardus" et sur quelques-uns de ses parasites. Bulletin de la Société zoologique de France, 52: 99-104.">Pérez (1927) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Pérez (1929) | 1 | 0,14% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
Ross & Zamponi (1983) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Sanchez (1977) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Schmitt (1933) | 1 | 0,14% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
Terao (1914) | 1 | 0,14% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
Thompson (1943) | 1 | 0,14% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
Australian Museum Memoir. 4(2): 135-199">Whitelegge (1901) | 1 | 0,14% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
Memoirs of the Australian Museum, 4 (3): 203-225.">Whitelegge (1901) | 1 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Yokoyama (2013) | 1 | 0,14% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |