Octocoralliaires
Octocorallia
136 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
Référence | Total | Valides | Espèces | Taxons terminaux | ||||
---|---|---|---|---|---|---|---|---|
nb | % | nb | % | nb | % | nb | % | |
Van Ofwegen (2007) | 172 | 16,6% | 153 | 24,52% | 153 | 24,6% | 153 | 24,6% |
Philippot (1987) | 121 | 11,68% | 106 | 16,99% | 105 | 16,88% | 104 | 16,72% |
Grasshoff (1999) | 109 | 10,52% | 99 | 15,87% | 99 | 15,92% | 99 | 15,92% |
Grasshoff (2007) | 93 | 8,98% | 88 | 14,1% | 88 | 14,15% | 88 | 14,15% |
Schleyer & Benayahu (2016) | 56 | 5,41% | 56 | 8,97% | 56 | 9% | 56 | 9% |
Fourt et al. (2017) | 46 | 4,44% | 46 | 7,37% | 46 | 7,4% | 46 | 7,4% |
Benayahu & van Ofwegen (2012) | 38 | 3,67% | 37 | 5,93% | 37 | 5,95% | 37 | 5,95% |
Bourmaud (2003) | 37 | 3,57% | 29 | 4,65% | 29 | 4,66% | 29 | 4,66% |
Diaz & Cuzange (2009) | 30 | 2,9% | 23 | 3,69% | 23 | 3,7% | 22 | 3,54% |
Andouche et al. (2020) | 26 | 2,51% | 17 | 2,72% | 17 | 2,73% | 17 | 2,73% |
Questel & Le Quellec (2012) | 23 | 2,22% | 18 | 2,88% | 18 | 2,89% | 18 | 2,89% |
Questel (2020) | 23 | 2,22% | 22 | 3,53% | 22 | 3,54% | 22 | 3,54% |
Ifremer (2009) | 20 | 1,93% | 19 | 3,04% | 19 | 3,05% | 19 | 3,05% |
Duchassaing et al. (1860) | 18 | 1,74% | 7 | 1,12% | 7 | 1,13% | 7 | 1,13% |
Schleyer et al. (2016) | 15 | 1,45% | 15 | 2,4% | 15 | 2,41% | 15 | 2,41% |
D'hondt & D'hondt (2020) | 14 | 1,35% | 14 | 2,24% | 13 | 2,09% | 13 | 2,09% |
Hourigan (2020) | 14 | 1,35% | 14 | 2,24% | 14 | 2,25% | 14 | 2,25% |
Martin (2011) | 14 | 1,35% | 14 | 2,24% | 14 | 2,25% | 14 | 2,25% |
Nelson-Smith et al. (2014) | 13 | 1,25% | 11 | 1,76% | 11 | 1,77% | 11 | 1,77% |
Dai & Jeng (2016) | 11 | 1,06% | 10 | 1,6% | 10 | 1,61% | 10 | 1,61% |
Richer de Forges et al. (2005) | 11 | 1,06% | 10 | 1,6% | 10 | 1,61% | 10 | 1,61% |
D'hondt & D'hondt (2018) | 10 | 0,97% | 10 | 1,6% | 8 | 1,29% | 10 | 1,61% |
Verseveldt (1977) | 10 | 0,97% | 10 | 1,6% | 10 | 1,61% | 10 | 1,61% |
Tixier-Durivault & Lafargue (1969) | 9 | 0,87% | 6 | 0,96% | 6 | 0,96% | 6 | 0,96% |
Van Ofwegen (2002) | 9 | 0,87% | 9 | 1,44% | 9 | 1,45% | 9 | 1,45% |
Deichmann (1936) | 8 | 0,77% | 2 | 0,32% | 2 | 0,32% | 2 | 0,32% |
Duchassaing et al. (1864) | 8 | 0,77% | 2 | 0,32% | 2 | 0,32% | 2 | 0,32% |
European Nucleotide Archive (2019) | 8 | 0,77% | 8 | 1,28% | 8 | 1,29% | 8 | 1,29% |
National Institute of Water and Atmospheric Research (2016) | 8 | 0,77% | 6 | 0,96% | 6 | 0,96% | 6 | 0,96% |
Orrell (2019) | 8 | 0,77% | 8 | 1,28% | 8 | 1,29% | 8 | 1,29% |
Goud et al. (2021) | 6 | 0,58% | 5 | 0,8% | 5 | 0,8% | 5 | 0,8% |
Anonyme (2023) | 5 | 0,48% | 5 | 0,8% | 5 | 0,8% | 5 | 0,8% |
Godet et al. (2010) | 5 | 0,48% | 5 | 0,8% | 5 | 0,8% | 5 | 0,8% |
Pallas (1766) | 5 | 0,48% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Taylor & Rogers (2015) | 5 | 0,48% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Ambroso et al. (2013) | 4 | 0,39% | 4 | 0,64% | 4 | 0,64% | 4 | 0,64% |
Bayer & Stefani (1988) | 4 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
Bayer (1996) | 4 | 0,39% | 2 | 0,32% | 2 | 0,32% | 2 | 0,32% |
Carpine & Grasshoff (1975) | 4 | 0,39% | 4 | 0,64% | 4 | 0,64% | 4 | 0,64% |
Duchassaing & Fonbressin (1870) | 4 | 0,39% | 2 | 0,32% | 2 | 0,32% | 2 | 0,32% |
Grasshoff (1996) | 4 | 0,39% | 4 | 0,64% | 4 | 0,64% | 4 | 0,64% |
Ifremer (2022) | 4 | 0,39% | 3 | 0,48% | 3 | 0,48% | 3 | 0,48% |
Linnaeus (1758) | 4 | 0,39% | 3 | 0,48% | 3 | 0,48% | 3 | 0,48% |
Milne et al. (1857) | 4 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
Natural History Museum of London (2020) | 4 | 0,39% | 2 | 0,32% | 2 | 0,32% | 2 | 0,32% |
Quod et al. (1995) | 4 | 0,39% | 4 | 0,64% | 4 | 0,64% | 4 | 0,64% |
Roule (1900) | 4 | 0,39% | 2 | 0,32% | 2 | 0,32% | 2 | 0,32% |
Sartoretto (2012) | 4 | 0,39% | 4 | 0,64% | 4 | 0,64% | 4 | 0,64% |
Stiasny (1951) | 4 | 0,39% | 0 | 0% | 0 | 0% | 0 | 0% |
Bayer (1990) | 3 | 0,29% | 3 | 0,48% | 3 | 0,48% | 3 | 0,48% |
Cairns (2016) | 3 | 0,29% | 3 | 0,48% | 3 | 0,48% | 3 | 0,48% |
Chevaldonné et al. (2015) | 3 | 0,29% | 3 | 0,48% | 3 | 0,48% | 3 | 0,48% |
D'hondt & Tixier-Durivault (1975) | 3 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
Harvard University Museum & Morris P.J. (2020) | 3 | 0,29% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Hiles (1899) | 3 | 0,29% | 3 | 0,48% | 3 | 0,48% | 3 | 0,48% |
Impact-Mer et al. (2011) | 3 | 0,29% | 3 | 0,48% | 3 | 0,48% | 3 | 0,48% |
Moore et al. (2016) | 3 | 0,29% | 3 | 0,48% | 3 | 0,48% | 3 | 0,48% |
Moser (1919) | 3 | 0,29% | 3 | 0,48% | 3 | 0,48% | 3 | 0,48% |
Aurivillius (1931) | 2 | 0,19% | 2 | 0,32% | 2 | 0,32% | 2 | 0,32% |
Bayer et al. (2016) | 2 | 0,19% | 2 | 0,32% | 2 | 0,32% | 2 | 0,32% |
Bayer (1959) | 2 | 0,19% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Cairns (2010) | 2 | 0,19% | 2 | 0,32% | 2 | 0,32% | 2 | 0,32% |
Cordeiro et al. (2018) | 2 | 0,19% | 2 | 0,32% | 2 | 0,32% | 2 | 0,32% |
Dana (1846-1849) | 2 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Devictor & Morton (2010) | 2 | 0,19% | 2 | 0,32% | 2 | 0,32% | 2 | 0,32% |
D'hondt & D'hondt (2019) | 2 | 0,19% | 2 | 0,32% | 2 | 0,32% | 2 | 0,32% |
D'hondt (1986) | 2 | 0,19% | 2 | 0,32% | 2 | 0,32% | 2 | 0,32% |
D'hondt (1992) | 2 | 0,19% | 2 | 0,32% | 2 | 0,32% | 2 | 0,32% |
Duchassaing & Michelin (1846) | 2 | 0,19% | 2 | 0,32% | 2 | 0,32% | 2 | 0,32% |
Grasshoff & Bargibant (2001) | 2 | 0,19% | 2 | 0,32% | 2 | 0,32% | 2 | 0,32% |
Gravier (1913) | 2 | 0,19% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Groot & Weinberg (1982) | 2 | 0,19% | 2 | 0,32% | 2 | 0,32% | 2 | 0,32% |
Linnaeus (1767) | 2 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Macleod et al. (2024) | 2 | 0,19% | 2 | 0,32% | 2 | 0,32% | 2 | 0,32% |
Mao et al. (2020) | 2 | 0,19% | 2 | 0,32% | 2 | 0,32% | 2 | 0,32% |
Mcfadden & Breton Hutchinson (2004) | 2 | 0,19% | 2 | 0,32% | 2 | 0,32% | 2 | 0,32% |
McFadden et al. (2024) | 2 | 0,19% | 2 | 0,32% | 2 | 0,32% | 2 | 0,32% |
Núñez et al. (2000) | 2 | 0,19% | 2 | 0,32% | 2 | 0,32% | 2 | 0,32% |
Pante & France (2010) | 2 | 0,19% | 2 | 0,32% | 2 | 0,32% | 2 | 0,32% |
Pourtales (1868) | 2 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Taylor et al. (2013) | 2 | 0,19% | 2 | 0,32% | 2 | 0,32% | 2 | 0,32% |
Tixier-durivault (1964) | 2 | 0,19% | 2 | 0,32% | 2 | 0,32% | 2 | 0,32% |
Weinberg (2013) | 2 | 0,19% | 2 | 0,32% | 2 | 0,32% | 2 | 0,32% |
Wright & Studer (1889) | 2 | 0,19% | 2 | 0,32% | 2 | 0,32% | 2 | 0,32% |
Zhan (2023) | 2 | 0,19% | 2 | 0,32% | 2 | 0,32% | 2 | 0,32% |
Allspach & Janussen (2020) | 1 | 0,1% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Altuna et al. (2008) | 1 | 0,1% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Arnaud (1974) | 1 | 0,1% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Australian Museum (2020) | 1 | 0,1% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Bayer et al. (2013) | 1 | 0,1% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Bigot (comm. pers., 2018) | 1 | 0,1% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Bigot et al. (2006) | 1 | 0,1% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Bigot (2006) | 1 | 0,1% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Bourdillon (1955) | 1 | 0,1% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Breton (2014) | 1 | 0,1% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Brugneaux & Pérès (2006) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Cairns (2012) | 1 | 0,1% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Casamajor et al. (2021) | 1 | 0,1% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Casamajor et al. (2022) | 1 | 0,1% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Coppari et al. (2020) | 1 | 0,1% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
D'hondt & D'hondt (2017) | 1 | 0,1% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Duchassaing & Fontbressin (1850) | 1 | 0,1% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Ellis & Solander (1786) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Gall (2021) | 1 | 0,1% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Glémarec et al. (1987) | 1 | 0,1% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Gmelin (1791) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Gutt et al. (2007) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Harmelin & Garrabou (2005) | 1 | 0,1% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Hartmann-Schröder (1985) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Proceedings of the Zoological Society of London, 1907: 1035-1037.">Hopkinson (1907) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Ifremer (2020) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Johnson (1861) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Johnston (1847) | 1 | 0,1% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Julien (1881) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Kükenthal (1907) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Lamouroux (1816) | 1 | 0,1% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Lutz & Ginsburg (2007) | 1 | 0,1% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Mackay & Rowden (2016) | 1 | 0,1% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Marion (1878) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Mills et al. (2018) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Noël (2016) | 1 | 0,1% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Obura et al. (2008) | 1 | 0,1% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Peralta & Fautin (2013) | 1 | 0,1% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Pérez (1920) | 1 | 0,1% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Philippi (1835) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Questel (2022) | 1 | 0,1% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Richer de Forges & Pianet (1984) | 1 | 0,1% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Risso ([1827]) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Rudi et al. (1998) | 1 | 0,1% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Stock (1986) | 1 | 0,1% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Rapport GIS "Lag-May" & Centre d'Océanologie de Marseille, pour le compte de DAF Mayotte, SPEM & FFEM. 126 pp.">Thomassin et al. (1999) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Thomson et al. (1909) | 1 | 0,1% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Tricart & Foubert (2000) | 1 | 0,1% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
Valenciennes (1846) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Volpi & Benvenuti (2003) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Weinberg (1978) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |