Nudibranches de métropole
86 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
Référence | Total | Valides | Espèces | Taxons terminaux | ||||
---|---|---|---|---|---|---|---|---|
nb | % | nb | % | nb | % | nb | % | |
Nelson-Smith et al. (2014) | 62 | 8,12% | 42 | 18,1% | 42 | 18,18% | 41 | 17,75% |
Martin (2011) | 18 | 2,36% | 18 | 7,76% | 18 | 7,79% | 18 | 7,79% |
Risso (1818) | 16 | 2,09% | 2 | 0,86% | 2 | 0,87% | 2 | 0,87% |
Godet et al. (2010) | 13 | 1,7% | 9 | 3,88% | 9 | 3,9% | 9 | 3,9% |
Labbé (1923) | 10 | 1,31% | 0 | 0% | 0 | 0% | 0 | 0% |
Labbé (1931) | 10 | 1,31% | 6 | 2,59% | 3 | 1,3% | 6 | 2,6% |
Breton (2014) | 7 | 0,92% | 5 | 2,16% | 5 | 2,16% | 5 | 2,16% |
Rignault & Chevallier (2017) | 7 | 0,92% | 3 | 1,29% | 3 | 1,3% | 3 | 1,3% |
Salvador et al. (2022) | 7 | 0,92% | 7 | 3,02% | 7 | 3,03% | 7 | 3,03% |
Bidgrain (2015) | 6 | 0,79% | 5 | 2,16% | 5 | 2,16% | 5 | 2,16% |
Héros et al. (2007) | 5 | 0,65% | 2 | 0,86% | 2 | 0,87% | 2 | 0,87% |
Kienberger et al. (2016) | 5 | 0,65% | 3 | 1,29% | 3 | 1,3% | 3 | 1,3% |
Michenet & Bosserelle (2013) | 5 | 0,65% | 3 | 1,29% | 3 | 1,3% | 3 | 1,3% |
Valdes & Ortea (1995) | 5 | 0,65% | 1 | 0,43% | 1 | 0,43% | 1 | 0,43% |
Brunckhorst & Willan (1989) | 4 | 0,52% | 1 | 0,43% | 1 | 0,43% | 1 | 0,43% |
Canu (1891) | 4 | 0,52% | 0 | 0% | 0 | 0% | 0 | 0% |
Fourt et al. (2017) | 4 | 0,52% | 4 | 1,72% | 4 | 1,73% | 4 | 1,73% |
Furfaro et al. (2018) | 4 | 0,52% | 1 | 0,43% | 1 | 0,43% | 1 | 0,43% |
Ortea & Bouchet (1989) | 4 | 0,52% | 4 | 1,72% | 4 | 1,73% | 4 | 1,73% |
Pola et al. (2019) | 4 | 0,52% | 4 | 1,72% | 4 | 1,73% | 4 | 1,73% |
Fize (1961) | 3 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
Gmelin (1791) | 3 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
Hervé (2010) | 3 | 0,39% | 2 | 0,86% | 2 | 0,87% | 2 | 0,87% |
Proceedings of the Zoological Society of London, 1907: 1035-1037.">Hopkinson (1907) | 3 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
Korshunova et al. (2019) | 3 | 0,39% | 3 | 1,29% | 3 | 1,3% | 3 | 1,3% |
Lamy & Pointier (2018) | 3 | 0,39% | 1 | 0,43% | 1 | 0,43% | 1 | 0,43% |
Linnaeus (1758) | 3 | 0,39% | 2 | 0,86% | 2 | 0,87% | 2 | 0,87% |
Müller (1776) | 3 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
Orbigny (1837) | 3 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
Ortea et al. (2012) | 3 | 0,39% | 2 | 0,86% | 2 | 0,87% | 2 | 0,87% |
Ortea et al. (2018) | 3 | 0,39% | 1 | 0,43% | 1 | 0,43% | 1 | 0,43% |
Pruvot-Fol (1952) | 3 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
Rufray et al. (2021) | 3 | 0,39% | 3 | 1,29% | 3 | 1,3% | 3 | 1,3% |
Sentz-Braconnot & Carré (1966) | 3 | 0,39% | 3 | 1,29% | 3 | 1,3% | 3 | 1,3% |
Tröndlé & Boutet (2009) | 3 | 0,39% | 2 | 0,86% | 2 | 0,87% | 2 | 0,87% |
Vicente (1975) | 3 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
Caballer Gutiérrez et al. (2016) | 2 | 0,26% | 2 | 0,86% | 2 | 0,87% | 2 | 0,87% |
Carmona (2020) | 2 | 0,26% | 2 | 0,86% | 2 | 0,87% | 2 | 0,87% |
Caziot (1921) | 2 | 0,26% | 1 | 0,43% | 1 | 0,43% | 1 | 0,43% |
Cervera et al. (2010) | 2 | 0,26% | 2 | 0,86% | 2 | 0,87% | 2 | 0,87% |
Goulletquer (2016) | 2 | 0,26% | 2 | 0,86% | 2 | 0,87% | 2 | 0,87% |
Risbec (1928) | 2 | 0,26% | 0 | 0% | 0 | 0% | 0 | 0% |
Tardy (1963) | 2 | 0,26% | 2 | 0,86% | 2 | 0,87% | 2 | 0,87% |
Toms et al. (2021) | 2 | 0,26% | 2 | 0,86% | 2 | 0,87% | 2 | 0,87% |
Alder & Hancock (1854) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Arvy (1953) | 1 | 0,13% | 1 | 0,43% | 1 | 0,43% | 1 | 0,43% |
Boisseau & Lubet (1955) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Carmona et al. (2014) | 1 | 0,13% | 1 | 0,43% | 1 | 0,43% | 1 | 0,43% |
Carmona et al. (2014) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Cauvin (2010) | 1 | 0,13% | 1 | 0,43% | 1 | 0,43% | 1 | 0,43% |
Chevaldonné et al. (2015) | 1 | 0,13% | 1 | 0,43% | 1 | 0,43% | 1 | 0,43% |
Chun (1889) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Claverie & Kamenos (2008) | 1 | 0,13% | 1 | 0,43% | 1 | 0,43% | 1 | 0,43% |
Coves et al. (2024) | 1 | 0,13% | 1 | 0,43% | 1 | 0,43% | 1 | 0,43% |
Cuvier (1804) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Delemarre et al. (2016) | 1 | 0,13% | 1 | 0,43% | 1 | 0,43% | 1 | 0,43% |
Droual (2018) | 1 | 0,13% | 1 | 0,43% | 1 | 0,43% | 1 | 0,43% |
Forum DORIS (2016) | 1 | 0,13% | 1 | 0,43% | 1 | 0,43% | 1 | 0,43% |
Furfaro & Mariottini (2019) | 1 | 0,13% | 1 | 0,43% | 1 | 0,43% | 1 | 0,43% |
Gadeau de Kerville (1900) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
González-Duarte et al. (2008) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Goud et al. (2020) | 1 | 0,13% | 1 | 0,43% | 1 | 0,43% | 1 | 0,43% |
Grall et al. (2015) | 1 | 0,13% | 1 | 0,43% | 1 | 0,43% | 1 | 0,43% |
Ifremer (2009) | 1 | 0,13% | 1 | 0,43% | 1 | 0,43% | 1 | 0,43% |
Johnston (1838) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Kaiser (2009) | 1 | 0,13% | 1 | 0,43% | 1 | 0,43% | 1 | 0,43% |
Korshunova et al. (2020) | 1 | 0,13% | 1 | 0,43% | 1 | 0,43% | 1 | 0,43% |
Kress (1970) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Linnaeus (1761) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
MGnify (2017) | 1 | 0,13% | 1 | 0,43% | 1 | 0,43% | 1 | 0,43% |
Müller (2004) | 1 | 0,13% | 1 | 0,43% | 1 | 0,43% | 1 | 0,43% |
Ortea & Caballer (2014) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Ortea et al. (1990) | 1 | 0,13% | 1 | 0,43% | 1 | 0,43% | 1 | 0,43% |
Ortea et al. (2013) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Ortea (1979) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Poupin et al. (1999) | 1 | 0,13% | 1 | 0,43% | 1 | 0,43% | 1 | 0,43% |
Questel (2020) | 1 | 0,13% | 1 | 0,43% | 1 | 0,43% | 1 | 0,43% |
Renau et al. (2024) | 1 | 0,13% | 1 | 0,43% | 1 | 0,43% | 1 | 0,43% |
Salvini-Plawen & Sterrer (1968) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Schmekel (1965) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Tardy (1969) | 1 | 0,13% | 1 | 0,43% | 1 | 0,43% | 1 | 0,43% |
Trainito et al. (2022) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Uicn et al. (2019) | 1 | 0,13% | 1 | 0,43% | 1 | 0,43% | 1 | 0,43% |
Vanhaelen et al. (2014) | 1 | 0,13% | 1 | 0,43% | 1 | 0,43% | 1 | 0,43% |
Vayssière (1919) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Zilli (2021) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |