Paguroidea
Pagures ou bernard l'hermite, cénobites et crabe des cocotiers (Paguroidea).
163 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 | 44,73% | 334 | 88,13% | 334 | 88,13% | 334 | 88,13% |
| Poupin (2024) | 31 | 4,14% | 31 | 8,18% | 31 | 8,18% | 31 | 8,18% |
| Poupin & Corbari (2016) | 30 | 4,01% | 30 | 7,92% | 30 | 7,92% | 30 | 7,92% |
| Lemaitre (2014) | 28 | 3,74% | 28 | 7,39% | 28 | 7,39% | 28 | 7,39% |
| Poupin et al. (2013) | 25 | 3,34% | 25 | 6,6% | 25 | 6,6% | 25 | 6,6% |
| Poupin (2015) | 22 | 2,94% | 22 | 5,8% | 22 | 5,8% | 22 | 5,8% |
| Komai (2010) | 20 | 2,67% | 20 | 5,28% | 20 | 5,28% | 20 | 5,28% |
| Lemaitre (1994) | 19 | 2,54% | 9 | 2,37% | 9 | 2,37% | 9 | 2,37% |
| Forest (1987) | 16 | 2,14% | 14 | 3,69% | 14 | 3,69% | 14 | 3,69% |
| Lemaitre (2013) | 16 | 2,14% | 16 | 4,22% | 16 | 4,22% | 16 | 4,22% |
| Questel (2020) | 16 | 2,14% | 16 | 4,22% | 16 | 4,22% | 16 | 4,22% |
| Lemaitre (1996) | 13 | 1,74% | 11 | 2,9% | 11 | 2,9% | 11 | 2,9% |
| Mclaughlin (1997) | 13 | 1,74% | 10 | 2,64% | 10 | 2,64% | 10 | 2,64% |
| Poupin (1997) | 13 | 1,74% | 13 | 3,43% | 13 | 3,43% | 13 | 3,43% |
| Bourcier (1988) | 12 | 1,6% | 9 | 2,37% | 9 | 2,37% | 9 | 2,37% |
| Nelson-Smith et al. (2014) | 12 | 1,6% | 9 | 2,37% | 9 | 2,37% | 9 | 2,37% |
| Saint & Laurent (1972) | 12 | 1,6% | 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 | 1,47% | 0 | 0% | 0 | 0% | 0 | 0% |
| Poupin et al. (2013) | 11 | 1,47% | 11 | 2,9% | 11 | 2,9% | 11 | 2,9% |
| Carré (2006) | 10 | 1,34% | 9 | 2,37% | 9 | 2,37% | 9 | 2,37% |
| 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 | 1,34% | 10 | 2,64% | 10 | 2,64% | 10 | 2,64% |
| Lemaitre (1989) | 10 | 1,34% | 8 | 2,11% | 8 | 2,11% | 8 | 2,11% |
| Poupin & Mclaughlin (1998) | 10 | 1,34% | 10 | 2,64% | 10 | 2,64% | 10 | 2,64% |
| Lemaitre et al. (2017) | 8 | 1,07% | 8 | 2,11% | 8 | 2,11% | 8 | 2,11% |
| Mclaughlin (2000) | 8 | 1,07% | 8 | 2,11% | 8 | 2,11% | 8 | 2,11% |
| Poupin (1994) | 8 | 1,07% | 7 | 1,85% | 7 | 1,85% | 7 | 1,85% |
| Ramage (2017) | 8 | 1,07% | 8 | 2,11% | 8 | 2,11% | 8 | 2,11% |
| Risso (1827) | 8 | 1,07% | 2 | 0,53% | 2 | 0,53% | 2 | 0,53% |
| Mclaughlin & Haig (1989) | 7 | 0,93% | 7 | 1,85% | 7 | 1,85% | 7 | 1,85% |
| Mclaughlin (2004) | 7 | 0,93% | 7 | 1,85% | 7 | 1,85% | 7 | 1,85% |
| Corbari et al. (2020) | 6 | 0,8% | 6 | 1,58% | 6 | 1,58% | 6 | 1,58% |
| Forest (1951) | 6 | 0,8% | 6 | 1,58% | 6 | 1,58% | 6 | 1,58% |
| Forest (1954) | 6 | 0,8% | 3 | 0,79% | 3 | 0,79% | 3 | 0,79% |
| Haig & Mclaughlin (1991) | 6 | 0,8% | 5 | 1,32% | 5 | 1,32% | 5 | 1,32% |
| Lemaitre (1999) | 6 | 0,8% | 6 | 1,58% | 6 | 1,58% | 6 | 1,58% |
| Mclaughlin (1981) | 6 | 0,8% | 6 | 1,58% | 6 | 1,58% | 6 | 1,58% |
| Mclaughlin (2007) | 6 | 0,8% | 5 | 1,32% | 5 | 1,32% | 5 | 1,32% |
| Risso (1816) | 6 | 0,8% | 0 | 0% | 0 | 0% | 0 | 0% |
| Forest et al. (2000) | 5 | 0,67% | 5 | 1,32% | 5 | 1,32% | 5 | 1,32% |
| Godet et al. (2010) | 5 | 0,67% | 5 | 1,32% | 5 | 1,32% | 5 | 1,32% |
| Komai & Poupin (2013) | 5 | 0,67% | 5 | 1,32% | 5 | 1,32% | 5 | 1,32% |
| Komai (1999) | 5 | 0,67% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lemaitre (2004) | 5 | 0,67% | 4 | 1,06% | 4 | 1,06% | 4 | 1,06% |
| Orrell (2019) | 5 | 0,67% | 5 | 1,32% | 5 | 1,32% | 5 | 1,32% |
| Alcock (1905) | 4 | 0,53% | 1 | 0,26% | 1 | 0,26% | 1 | 0,26% |
| Almon et al. (2022) | 4 | 0,53% | 4 | 1,06% | 4 | 1,06% | 4 | 1,06% |
| Balss (1911) | 4 | 0,53% | 0 | 0% | 0 | 0% | 0 | 0% |
| Corbari et al. (2015) | 4 | 0,53% | 4 | 1,06% | 4 | 1,06% | 4 | 1,06% |
| Fourt et al. (2017) | 4 | 0,53% | 4 | 1,06% | 4 | 1,06% | 4 | 1,06% |
| Komai & Osawa (2006) | 4 | 0,53% | 4 | 1,06% | 4 | 1,06% | 4 | 1,06% |
| Komai & Poupin (2012) | 4 | 0,53% | 4 | 1,06% | 4 | 1,06% | 4 | 1,06% |
| Leach (1815-1875) | 4 | 0,53% | 2 | 0,53% | 2 | 0,53% | 2 | 0,53% |
| Lemaitre (1997) | 4 | 0,53% | 4 | 1,06% | 4 | 1,06% | 4 | 1,06% |
| Lemaitre (2006) | 4 | 0,53% | 4 | 1,06% | 4 | 1,06% | 4 | 1,06% |
| Lemaitre (2020) | 4 | 0,53% | 4 | 1,06% | 4 | 1,06% | 4 | 1,06% |
| Mclaughlin (1986) | 4 | 0,53% | 2 | 0,53% | 2 | 0,53% | 2 | 0,53% |
| Mclaughlin (2006) | 4 | 0,53% | 4 | 1,06% | 4 | 1,06% | 4 | 1,06% |
| Nobili (1906) | 4 | 0,53% | 0 | 0% | 0 | 0% | 0 | 0% |
| Questel & Le Quellec (2012) | 4 | 0,53% | 4 | 1,06% | 4 | 1,06% | 4 | 1,06% |
| Tricart & Foubert (2000) | 4 | 0,53% | 4 | 1,06% | 4 | 1,06% | 4 | 1,06% |
| Wass (1963) | 4 | 0,53% | 0 | 0% | 0 | 0% | 0 | 0% |
| Wooster (1982) | 4 | 0,53% | 4 | 1,06% | 4 | 1,06% | 4 | 1,06% |
| Asakura & Paulay (2003) | 3 | 0,4% | 3 | 0,79% | 3 | 0,79% | 3 | 0,79% |
| Bourjon et al. (2018) | 3 | 0,4% | 3 | 0,79% | 3 | 0,79% | 3 | 0,79% |
| Breton (2014) | 3 | 0,4% | 3 | 0,79% | 3 | 0,79% | 3 | 0,79% |
| Buitendijk (1937) | 3 | 0,4% | 3 | 0,79% | 3 | 0,79% | 3 | 0,79% |
| Chace (1962) | 3 | 0,4% | 3 | 0,79% | 3 | 0,79% | 3 | 0,79% |
| Forest (1997) | 3 | 0,4% | 0 | 0% | 0 | 0% | 0 | 0% |
| Holthuis (1977) | 3 | 0,4% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ifremer (2009) | 3 | 0,4% | 3 | 0,79% | 3 | 0,79% | 3 | 0,79% |
| Lemaitre & Poupin (2003) | 3 | 0,4% | 3 | 0,79% | 3 | 0,79% | 3 | 0,79% |
| Lemaitre (1998) | 3 | 0,4% | 3 | 0,79% | 3 | 0,79% | 3 | 0,79% |
| Lemaitre (2004) | 3 | 0,4% | 2 | 0,53% | 2 | 0,53% | 2 | 0,53% |
| Miers (1878) | 3 | 0,4% | 0 | 0% | 0 | 0% | 0 | 0% |
| Milne-edwards (1891) | 3 | 0,4% | 0 | 0% | 0 | 0% | 0 | 0% |
| Poupin & Bouchard (2006) | 3 | 0,4% | 3 | 0,79% | 3 | 0,79% | 3 | 0,79% |
| Poupin & Lemaitre (2022) | 3 | 0,4% | 3 | 0,79% | 3 | 0,79% | 3 | 0,79% |
| Poupin & Mclaughlin (1996) | 3 | 0,4% | 3 | 0,79% | 3 | 0,79% | 3 | 0,79% |
| Poupin et al. (2013) | 3 | 0,4% | 3 | 0,79% | 3 | 0,79% | 3 | 0,79% |
| Poupin et al. (2022) | 3 | 0,4% | 3 | 0,79% | 3 | 0,79% | 3 | 0,79% |
| Poupin (2018) | 3 | 0,4% | 3 | 0,79% | 3 | 0,79% | 3 | 0,79% |
| Asakura (2005) | 2 | 0,27% | 2 | 0,53% | 2 | 0,53% | 2 | 0,53% |
| Bouvier (1899) | 2 | 0,27% | 1 | 0,26% | 1 | 0,26% | 1 | 0,26% |
| Clark & Harrison (2021) | 2 | 0,27% | 1 | 0,26% | 1 | 0,26% | 1 | 0,26% |
| Craig & Felder (2022) | 2 | 0,27% | 2 | 0,53% | 2 | 0,53% | 2 | 0,53% |
| Forest & Saint Laurent | 2 | 0,27% | 2 | 0,53% | 2 | 0,53% | 2 | 0,53% |
| Forest (1992) | 2 | 0,27% | 2 | 0,53% | 2 | 0,53% | 2 | 0,53% |
| Kensley (1973) | 2 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
| Komai & Rahayu (2013) | 2 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lemaitre & Campos (1993) | 2 | 0,27% | 2 | 0,53% | 2 | 0,53% | 2 | 0,53% |
| Lemaitre & Mclaughlin (1996) | 2 | 0,27% | 2 | 0,53% | 2 | 0,53% | 2 | 0,53% |
| Lemaitre (1986) | 2 | 0,27% | 2 | 0,53% | 2 | 0,53% | 2 | 0,53% |
| Lemaitre (2010) | 2 | 0,27% | 2 | 0,53% | 2 | 0,53% | 2 | 0,53% |
| Lemaitre (2011) | 2 | 0,27% | 2 | 0,53% | 2 | 0,53% | 2 | 0,53% |
| Lemaitre (2015) | 2 | 0,27% | 2 | 0,53% | 2 | 0,53% | 2 | 0,53% |
| Linnaeus (1758) | 2 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
| Maillaud et al. (2015) | 2 | 0,27% | 2 | 0,53% | 2 | 0,53% | 2 | 0,53% |
| Malay et al. (2012) | 2 | 0,27% | 2 | 0,53% | 2 | 0,53% | 2 | 0,53% |
| Mclaughlin & Haig (1996) | 2 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mclaughlin & Hoover (1996) | 2 | 0,27% | 2 | 0,53% | 2 | 0,53% | 2 | 0,53% |
| Mclaughlin & Lemaitre (2008) | 2 | 0,27% | 2 | 0,53% | 2 | 0,53% | 2 | 0,53% |
| Mclaughlin & Provenzano (1974) | 2 | 0,27% | 2 | 0,53% | 2 | 0,53% | 2 | 0,53% |
| Mclaughlin et al. (1998) | 2 | 0,27% | 1 | 0,26% | 1 | 0,26% | 1 | 0,26% |
| Mclaughlin (2004) | 2 | 0,27% | 1 | 0,26% | 1 | 0,26% | 1 | 0,26% |
| Paulmier (1996) | 2 | 0,27% | 1 | 0,26% | 1 | 0,26% | 1 | 0,26% |
| Pérez (1931) | 2 | 0,27% | 1 | 0,26% | 1 | 0,26% | 1 | 0,26% |
| Poupin & Lemaitre (2003) | 2 | 0,27% | 2 | 0,53% | 2 | 0,53% | 2 | 0,53% |
| Poupin (2001) | 2 | 0,27% | 2 | 0,53% | 2 | 0,53% | 2 | 0,53% |
| Rahayu (2011) | 2 | 0,27% | 2 | 0,53% | 2 | 0,53% | 2 | 0,53% |
| Richer et al. (2013) | 2 | 0,27% | 2 | 0,53% | 2 | 0,53% | 2 | 0,53% |
| Roux (1828) | 2 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
| Saussure (1857) | 2 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
| Terao (1913) | 2 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
| Zarenkov (1989) | 2 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
| Annals of Natural History, (6)(xiii): pp. 225-245, 321-331, & 400-411.">Alcock (1894) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Altès (1962) | 1 | 0,13% | 1 | 0,26% | 1 | 0,26% | 1 | 0,26% |
| Asakura (2001) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Asakura (2006) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Balss (1912) | 1 | 0,13% | 1 | 0,26% | 1 | 0,26% | 1 | 0,26% |
| Bulletin of the Vanderbilt Marine Museum, 3: 1-221.">Boone (1930) | 1 | 0,13% | 1 | 0,26% | 1 | 0,26% | 1 | 0,26% |
| Changeux & Deboutteville (1955) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Clément (1874) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Coudray & Noël (2014) | 1 | 0,13% | 1 | 0,26% | 1 | 0,26% | 1 | 0,26% |
| Coudray & Noël (2014) | 1 | 0,13% | 1 | 0,26% | 1 | 0,26% | 1 | 0,26% |
| Coudray & Noël (2014) | 1 | 0,13% | 1 | 0,26% | 1 | 0,26% | 1 | 0,26% |
| Coudray & Noël (2014) | 1 | 0,13% | 1 | 0,26% | 1 | 0,26% | 1 | 0,26% |
| Coudray & Noël (2014) | 1 | 0,13% | 1 | 0,26% | 1 | 0,26% | 1 | 0,26% |
| Coudray & Noël (2014) | 1 | 0,13% | 1 | 0,26% | 1 | 0,26% | 1 | 0,26% |
| Coudray & Noël (2014) | 1 | 0,13% | 1 | 0,26% | 1 | 0,26% | 1 | 0,26% |
| Coudray & Noël (2014) | 1 | 0,13% | 1 | 0,26% | 1 | 0,26% | 1 | 0,26% |
| Coudray & Noël (2014) | 1 | 0,13% | 1 | 0,26% | 1 | 0,26% | 1 | 0,26% |
| Crisp & Fischer-piette (1959) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Crosnier (1976) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Davoult (1990) | 1 | 0,13% | 1 | 0,26% | 1 | 0,26% | 1 | 0,26% |
| DCE-Benthos Network, French Mediterranen Lagoon Monitoring Network (2022) | 1 | 0,13% | 1 | 0,26% | 1 | 0,26% | 1 | 0,26% |
| Edmondson (1952) | 1 | 0,13% | 1 | 0,26% | 1 | 0,26% | 1 | 0,26% |
| Fabricius (1787) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Forest (1958) | 1 | 0,13% | 1 | 0,26% | 1 | 0,26% | 1 | 0,26% |
| Forest (1984) | 1 | 0,13% | 1 | 0,26% | 1 | 0,26% | 1 | 0,26% |
| Forest (2015) | 1 | 0,13% | 1 | 0,26% | 1 | 0,26% | 1 | 0,26% |
| Gong & Paulay (2018) | 1 | 0,13% | 1 | 0,26% | 1 | 0,26% | 1 | 0,26% |
| Journal of the Asiatic Society of Bengal, lxv: 516-536.">Henderson (1896) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ifremer (2022) | 1 | 0,13% | 1 | 0,26% | 1 | 0,26% | 1 | 0,26% |
| Latreille (1812) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Marchal (1891) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Martin (2003) | 1 | 0,13% | 1 | 0,26% | 1 | 0,26% | 1 | 0,26% |
| Miers (1879) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Miers (1881) | 1 | 0,13% | 1 | 0,26% | 1 | 0,26% | 1 | 0,26% |
| Milne-edwards & Bouvier (1897) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Noël (2015) | 1 | 0,13% | 1 | 0,26% | 1 | 0,26% | 1 | 0,26% |
| Noël (2015) | 1 | 0,13% | 1 | 0,26% | 1 | 0,26% | 1 | 0,26% |
| Noël (2016) | 1 | 0,13% | 1 | 0,26% | 1 | 0,26% | 1 | 0,26% |
| Noël (2016) | 1 | 0,13% | 1 | 0,26% | 1 | 0,26% | 1 | 0,26% |
| Eupagurus bernhardus" et sur quelques-uns de ses parasites. Bulletin de la Société zoologique de France, 52: 99-104.">Pérez (1927) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pérez (1929) | 1 | 0,13% | 1 | 0,26% | 1 | 0,26% | 1 | 0,26% |
| Ross & Zamponi (1983) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sanchez (1977) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Schmitt (1933) | 1 | 0,13% | 1 | 0,26% | 1 | 0,26% | 1 | 0,26% |
| Terao (1914) | 1 | 0,13% | 1 | 0,26% | 1 | 0,26% | 1 | 0,26% |
| Thompson (1943) | 1 | 0,13% | 1 | 0,26% | 1 | 0,26% | 1 | 0,26% |
| Memoirs of the Australian Museum, 4 (3): 203-225.">Whitelegge (1901) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Australian Museum Memoir. 4(2): 135-199">Whitelegge (1901) | 1 | 0,13% | 1 | 0,26% | 1 | 0,26% | 1 | 0,26% |
| Yokoyama (2013) | 1 | 0,13% | 1 | 0,26% | 1 | 0,26% | 1 | 0,26% |
