Nudibranches
149 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
Référence | Total | Valides | Espèces | Taxons terminaux | ||||
---|---|---|---|---|---|---|---|---|
nb | % | nb | % | nb | % | nb | % | |
Bidgrain (2015) | 268 | 14,23% | 180 | 23,78% | 180 | 23,81% | 180 | 23,81% |
Héros et al. (2007) | 180 | 9,56% | 127 | 16,78% | 127 | 16,8% | 127 | 16,8% |
Lamy & Pointier (2018) | 118 | 6,27% | 100 | 13,21% | 100 | 13,23% | 100 | 13,23% |
Hervé (2010) | 85 | 4,51% | 57 | 7,53% | 57 | 7,54% | 57 | 7,54% |
Michenet & Bosserelle (2013) | 65 | 3,45% | 50 | 6,61% | 50 | 6,61% | 50 | 6,61% |
Nelson-Smith et al. (2014) | 62 | 3,29% | 42 | 5,55% | 42 | 5,56% | 41 | 5,42% |
Tröndlé & Boutet (2009) | 59 | 3,13% | 33 | 4,36% | 33 | 4,37% | 33 | 4,37% |
Risbec (1928) | 57 | 3,03% | 21 | 2,77% | 21 | 2,78% | 21 | 2,78% |
Ortea et al. (2012) | 52 | 2,76% | 36 | 4,76% | 36 | 4,76% | 36 | 4,76% |
Bouchet et al. (2008) | 33 | 1,75% | 30 | 3,96% | 30 | 3,97% | 30 | 3,97% |
Ortea et al. (2018) | 32 | 1,7% | 24 | 3,17% | 24 | 3,17% | 24 | 3,17% |
Rudman (1995) | 22 | 1,17% | 12 | 1,59% | 12 | 1,59% | 12 | 1,59% |
Ortea et al. (2013) | 20 | 1,06% | 8 | 1,06% | 8 | 1,06% | 8 | 1,06% |
Martin (2011) | 18 | 0,96% | 18 | 2,38% | 18 | 2,38% | 18 | 2,38% |
Innabi et al. (2023) | 16 | 0,85% | 16 | 2,11% | 16 | 2,12% | 16 | 2,12% |
Risso (1818) | 16 | 0,85% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Godet et al. (2010) | 13 | 0,69% | 9 | 1,19% | 9 | 1,19% | 9 | 1,19% |
Bourjon et al. (2018) | 12 | 0,64% | 11 | 1,45% | 11 | 1,46% | 11 | 1,46% |
Donohoo et al. (2023) | 10 | 0,53% | 10 | 1,32% | 10 | 1,32% | 10 | 1,32% |
Labbé (1923) | 10 | 0,53% | 0 | 0% | 0 | 0% | 0 | 0% |
Labbé (1931) | 10 | 0,53% | 6 | 0,79% | 3 | 0,4% | 6 | 0,79% |
Deuss et al. (2013) | 9 | 0,48% | 8 | 1,06% | 8 | 1,06% | 8 | 1,06% |
Rudman (1990) | 9 | 0,48% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Arnaud (1974) | 8 | 0,42% | 5 | 0,66% | 5 | 0,66% | 5 | 0,66% |
Valdes & Gosliner (2001) | 8 | 0,42% | 8 | 1,06% | 8 | 1,06% | 8 | 1,06% |
Breton (2014) | 7 | 0,37% | 5 | 0,66% | 5 | 0,66% | 5 | 0,66% |
Fahey & Gosliner (2000) | 7 | 0,37% | 7 | 0,92% | 7 | 0,93% | 7 | 0,93% |
Questel (2020) | 7 | 0,37% | 7 | 0,92% | 7 | 0,93% | 7 | 0,93% |
Rignault & Chevallier (2017) | 7 | 0,37% | 3 | 0,4% | 3 | 0,4% | 3 | 0,4% |
Salvador et al. (2022) | 7 | 0,37% | 7 | 0,92% | 7 | 0,93% | 7 | 0,93% |
Valdés (2001) | 7 | 0,37% | 5 | 0,66% | 5 | 0,66% | 5 | 0,66% |
Vicente & Arnaud (1974) | 7 | 0,37% | 4 | 0,53% | 4 | 0,53% | 4 | 0,53% |
Pruvot-Fol (1930) | 6 | 0,32% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Rudman (1982) | 6 | 0,32% | 5 | 0,66% | 5 | 0,66% | 5 | 0,66% |
Kaiser (2009) | 5 | 0,27% | 4 | 0,53% | 4 | 0,53% | 4 | 0,53% |
Kienberger et al. (2016) | 5 | 0,27% | 3 | 0,4% | 3 | 0,4% | 3 | 0,4% |
Salvat & Bacchet (2011) | 5 | 0,27% | 5 | 0,66% | 5 | 0,66% | 5 | 0,66% |
Valdes & Ortea (1995) | 5 | 0,27% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Brunckhorst & Willan (1989) | 4 | 0,21% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Canu (1891) | 4 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
Fourt et al. (2017) | 4 | 0,21% | 4 | 0,53% | 4 | 0,53% | 4 | 0,53% |
Furfaro et al. (2018) | 4 | 0,21% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Héros (comm. pers., 2011) | 4 | 0,21% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Ortea & Bouchet (1989) | 4 | 0,21% | 4 | 0,53% | 4 | 0,53% | 4 | 0,53% |
Paz-Sedano et al. (2022) | 4 | 0,21% | 4 | 0,53% | 4 | 0,53% | 4 | 0,53% |
Pola et al. (2019) | 4 | 0,21% | 4 | 0,53% | 4 | 0,53% | 4 | 0,53% |
Valdés et al. (2022) | 4 | 0,21% | 4 | 0,53% | 4 | 0,53% | 4 | 0,53% |
Vicente (1974) | 4 | 0,21% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Carmona et al. (2014) | 3 | 0,16% | 3 | 0,4% | 3 | 0,4% | 3 | 0,4% |
Chabanet et al. (2007) | 3 | 0,16% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Epstein et al. (2018) | 3 | 0,16% | 3 | 0,4% | 3 | 0,4% | 3 | 0,4% |
Fize (1961) | 3 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
García-Méndez et al. (2022) | 3 | 0,16% | 3 | 0,4% | 3 | 0,4% | 3 | 0,4% |
Gmelin (1791) | 3 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Proceedings of the Zoological Society of London, 1907: 1035-1037.">Hopkinson (1907) | 3 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Korshunova et al. (2019) | 3 | 0,16% | 3 | 0,4% | 3 | 0,4% | 3 | 0,4% |
Linnaeus (1758) | 3 | 0,16% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Müller (1776) | 3 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Orbigny (1837) | 3 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Avicennia, 20: 21-22.">Ortea & Espinosa (2017) | 3 | 0,16% | 3 | 0,4% | 3 | 0,4% | 3 | 0,4% |
Ortea & Espinosa (2017) | 3 | 0,16% | 3 | 0,4% | 3 | 0,4% | 3 | 0,4% |
Ortea & Moro (2016) | 3 | 0,16% | 3 | 0,4% | 3 | 0,4% | 3 | 0,4% |
Ortea et al. (2015) | 3 | 0,16% | 3 | 0,4% | 3 | 0,4% | 3 | 0,4% |
Ortea (2022) | 3 | 0,16% | 3 | 0,4% | 3 | 0,4% | 3 | 0,4% |
Pola et al. (2008) | 3 | 0,16% | 3 | 0,4% | 3 | 0,4% | 3 | 0,4% |
Pruvot-Fol (1952) | 3 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Richard (1985) | 3 | 0,16% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Rudman (1986) | 3 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Rufray et al. (2021) | 3 | 0,16% | 3 | 0,4% | 3 | 0,4% | 3 | 0,4% |
Sentz-Braconnot & Carré (1966) | 3 | 0,16% | 3 | 0,4% | 3 | 0,4% | 3 | 0,4% |
Soong et al. (2022) | 3 | 0,16% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Tibiriçá et al. (2023) | 3 | 0,16% | 3 | 0,4% | 3 | 0,4% | 3 | 0,4% |
Vicente (1975) | 3 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Wilson & Burghardt (2015) | 3 | 0,16% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Yonow (2012) | 3 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Bouchet & Ortea (1983) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Bryce (2000) | 2 | 0,11% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Caballer & Ortea (2014) | 2 | 0,11% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Caballer & Ortea (2015) | 2 | 0,11% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Caballer & Ortea (2019) | 2 | 0,11% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Caballer Gutiérrez et al. (2016) | 2 | 0,11% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Carmona et al. (2014) | 2 | 0,11% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Carmona (2020) | 2 | 0,11% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Cauvin (2005) | 2 | 0,11% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Cauvin (2007) | 2 | 0,11% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Cauvin (2010) | 2 | 0,11% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Cauvin (2015) | 2 | 0,11% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Caziot (1921) | 2 | 0,11% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Cervera et al. (2010) | 2 | 0,11% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Cunha et al. (2023) | 2 | 0,11% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Gosliner & Fahey (2011) | 2 | 0,11% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Goulletquer (2016) | 2 | 0,11% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Lima et al. (2016) | 2 | 0,11% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Martynov (2006) | 2 | 0,11% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Millen & Hermosillo (2012) | 2 | 0,11% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Ortea et al. (1990) | 2 | 0,11% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Ortea (1982) | 2 | 0,11% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Ortea (2016) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Powell (1960) | 2 | 0,11% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Tardy (1963) | 2 | 0,11% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Chromodoris quadricolor group" of East Africa, with descriptions of two new species of the genus Chromodoris Alder & Hancock, 1855 (Heterobranchia, Nudibranchia). Journal of Zoological Systematics and Evolutionary Research, 58(1): 230-261.">Tibiriçá et al. (2019) | 2 | 0,11% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Toms et al. (2021) | 2 | 0,11% | 2 | 0,26% | 2 | 0,26% | 2 | 0,26% |
Alder & Hancock (1854) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Arvy (1953) | 1 | 0,05% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Boisseau & Lubet (1955) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Carmona et al. (2014) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Cauvin (2009) | 1 | 0,05% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Cauvin (2010) | 1 | 0,05% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Cauvin (2010) | 1 | 0,05% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Cauvin (2012) | 1 | 0,05% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Cauvin (2015) | 1 | 0,05% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Chevaldonné et al. (2015) | 1 | 0,05% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Chun (1889) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Claverie & Kamenos (2008) | 1 | 0,05% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Coves et al. (2024) | 1 | 0,05% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Cuvier (1804) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Delemarre et al. (2016) | 1 | 0,05% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Droual (2018) | 1 | 0,05% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Forum DORIS (2016) | 1 | 0,05% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Furfaro & Mariottini (2019) | 1 | 0,05% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Gadeau de Kerville (1900) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
González-Duarte et al. (2008) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Goud et al. (2020) | 1 | 0,05% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Grall et al. (2015) | 1 | 0,05% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Ifremer (2009) | 1 | 0,05% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Johnston (1838) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Korshunova et al. (2020) | 1 | 0,05% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Kress (1970) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Linnaeus (1761) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Massemin et al. (2009) | 1 | 0,05% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
MGnify (2017) | 1 | 0,05% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Müller (2004) | 1 | 0,05% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Ortea & Caballer (2014) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Ortea et al. (2014) | 1 | 0,05% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Ortea (1979) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Pearman et al. (2020) | 1 | 0,05% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Pola et al. (2006) | 1 | 0,05% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Poupin et al. (1999) | 1 | 0,05% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Renau et al. (2024) | 1 | 0,05% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Salvini-Plawen & Sterrer (1968) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Schmekel (1965) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Schroedl (2000) | 1 | 0,05% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Tardy (1969) | 1 | 0,05% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Trainito et al. (2022) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Uicn et al. (2019) | 1 | 0,05% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Valdes & Hamann (2008) | 1 | 0,05% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Vanhaelen et al. (2014) | 1 | 0,05% | 1 | 0,13% | 1 | 0,13% | 1 | 0,13% |
Vayssière (1919) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Zilli (2021) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |