Scléractiniaires d'outre-mer
183 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
| Référence | Total | Valides | Espèces | Taxons terminaux | ||||
|---|---|---|---|---|---|---|---|---|
| nb | % | nb | % | nb | % | nb | % | |
| Pichon (2007) | 313 | 17,99% | 232 | 28,43% | 232 | 28,54% | 232 | 28,54% |
| Pichon & Thomassin (2005) | 202 | 11,61% | 153 | 18,75% | 153 | 18,82% | 153 | 18,82% |
| Pichon et al. (2007) | 171 | 9,83% | 137 | 16,79% | 137 | 16,85% | 137 | 16,85% |
| Faure et al. (2008) | 162 | 9,31% | 133 | 16,3% | 133 | 16,36% | 133 | 16,36% |
| Glynn et al. (2007) | 149 | 8,56% | 117 | 14,34% | 117 | 14,39% | 117 | 14,39% |
| Kitahara (2011) | 119 | 6,84% | 118 | 14,46% | 116 | 14,27% | 118 | 14,51% |
| Tricart & Foubert (2000) | 99 | 5,69% | 82 | 10,05% | 82 | 10,09% | 82 | 10,09% |
| Cairns (1999) | 98 | 5,63% | 91 | 11,15% | 88 | 10,82% | 90 | 11,07% |
| Pichon (comm. pers., 2012) | 82 | 4,71% | 68 | 8,33% | 68 | 8,36% | 68 | 8,36% |
| Uicn et al. (2020) | 66 | 3,79% | 59 | 7,23% | 59 | 7,26% | 59 | 7,26% |
| Questel (2020) | 56 | 3,22% | 53 | 6,5% | 53 | 6,52% | 53 | 6,52% |
| Chevalier & Kuhlmann (1983) | 52 | 2,99% | 31 | 3,8% | 31 | 3,81% | 31 | 3,81% |
| Questel & Le Quellec (2012) | 49 | 2,82% | 41 | 5,02% | 41 | 5,04% | 41 | 5,04% |
| Dana (1846-1849) | 40 | 2,3% | 2 | 0,25% | 2 | 0,25% | 2 | 0,25% |
| Fenner & Muir (2008) | 37 | 2,13% | 31 | 3,8% | 31 | 3,81% | 31 | 3,81% |
| Andouche et al. (2020) | 32 | 1,84% | 31 | 3,8% | 31 | 3,81% | 31 | 3,81% |
| Diaz & Cuzange (2009) | 31 | 1,78% | 24 | 2,94% | 24 | 2,95% | 24 | 2,95% |
| Sheppard (1987) | 30 | 1,72% | 8 | 0,98% | 8 | 0,98% | 8 | 0,98% |
| Bigot (comm. pers., 2018) | 26 | 1,49% | 25 | 3,06% | 25 | 3,08% | 25 | 3,08% |
| Fautin (2013) | 22 | 1,26% | 22 | 2,7% | 21 | 2,58% | 21 | 2,58% |
| IUCN (2013) | 21 | 1,21% | 17 | 2,08% | 17 | 2,09% | 17 | 2,09% |
| Quelch (1886) | 20 | 1,15% | 4 | 0,49% | 4 | 0,49% | 4 | 0,49% |
| Gardiner (1899) | 19 | 1,09% | 9 | 1,1% | 9 | 1,11% | 9 | 1,11% |
| Bosserelle et al. (2014) | 17 | 0,98% | 16 | 1,96% | 16 | 1,97% | 16 | 1,97% |
| Flot & Adjeroud (2009) | 17 | 0,98% | 15 | 1,84% | 15 | 1,85% | 15 | 1,85% |
| AAMP (2010) | 15 | 0,86% | 15 | 1,84% | 14 | 1,72% | 15 | 1,85% |
| Kitahara & Cairns (2009) | 15 | 0,86% | 15 | 1,84% | 15 | 1,85% | 15 | 1,85% |
| Kitahara et al. (2010) | 15 | 0,86% | 15 | 1,84% | 15 | 1,85% | 15 | 1,85% |
| Orrell (2019) | 15 | 0,86% | 10 | 1,23% | 10 | 1,23% | 10 | 1,23% |
| Low & Evenhuis (2013) | 13 | 0,75% | 6 | 0,74% | 6 | 0,74% | 6 | 0,74% |
| Reveillaud et al. (2008) | 13 | 0,75% | 12 | 1,47% | 12 | 1,48% | 11 | 1,35% |
| Moseley ([1880]) | 12 | 0,69% | 5 | 0,61% | 5 | 0,62% | 5 | 0,62% |
| . Rapport GIS "Lag-May" / Conseil Général de Mayotte / Centre d'Océanologie de Marseille. 61 pp.">Thomassin et al. (1998) | 11 | 0,63% | 9 | 1,1% | 9 | 1,11% | 9 | 1,11% |
| National Institute of Water and Atmospheric Research (2016) | 10 | 0,57% | 7 | 0,86% | 7 | 0,86% | 7 | 0,86% |
| Payri et al. (2002) | 10 | 0,57% | 7 | 0,86% | 7 | 0,86% | 7 | 0,86% |
| Adjeroud et al. (2012) | 8 | 0,46% | 5 | 0,61% | 5 | 0,62% | 5 | 0,62% |
| Arrigoni et al. (2016) | 8 | 0,46% | 8 | 0,98% | 8 | 0,98% | 8 | 0,98% |
| Cairns (1989) | 6 | 0,34% | 6 | 0,74% | 6 | 0,74% | 6 | 0,74% |
| Cairns (2000) | 6 | 0,34% | 6 | 0,74% | 6 | 0,74% | 6 | 0,74% |
| Cairns (2004) | 6 | 0,34% | 6 | 0,74% | 6 | 0,74% | 6 | 0,74% |
| Duchassaing et al. (1860) | 6 | 0,34% | 2 | 0,25% | 2 | 0,25% | 2 | 0,25% |
| Fourt et al. (2017) | 6 | 0,34% | 4 | 0,49% | 4 | 0,49% | 4 | 0,49% |
| Kitahara & Cairns (2008) | 6 | 0,34% | 6 | 0,74% | 6 | 0,74% | 6 | 0,74% |
| Milne-Edwards (1848) | 6 | 0,34% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Peralta & Fautin (2013) | 6 | 0,34% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Pourtales (1868) | 6 | 0,34% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pourtalès (1880) | 6 | 0,34% | 4 | 0,49% | 4 | 0,49% | 4 | 0,49% |
| Zibrowius (1974) | 6 | 0,34% | 4 | 0,49% | 4 | 0,49% | 4 | 0,49% |
| Ifremer (2009) | 5 | 0,29% | 3 | 0,37% | 3 | 0,37% | 2 | 0,25% |
| Wells (1968) | 5 | 0,29% | 4 | 0,49% | 4 | 0,49% | 4 | 0,49% |
| Arrigoni et al. (2018) | 4 | 0,23% | 4 | 0,49% | 4 | 0,49% | 4 | 0,49% |
| Arrigoni et al. (2020) | 4 | 0,23% | 4 | 0,49% | 4 | 0,49% | 4 | 0,49% |
| Benzoni et al. (2010) | 4 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Duchassaing et al. (1864) | 4 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Goud et al. (2021) | 4 | 0,23% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Proceedings of the Royal Society of London, 24: 543-569.">Moseley (1876) | 4 | 0,23% | 2 | 0,25% | 2 | 0,25% | 2 | 0,25% |
| Quelch (1884) | 4 | 0,23% | 2 | 0,25% | 2 | 0,25% | 2 | 0,25% |
| Uicn et al. (2019) | 4 | 0,23% | 4 | 0,49% | 4 | 0,49% | 4 | 0,49% |
| Vaughan (1906) | 4 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Volpi & Benvenuti (2003) | 4 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
| Zibrowius (1968) | 4 | 0,23% | 4 | 0,49% | 4 | 0,49% | 4 | 0,49% |
| Carricart-Ganivet & Reyes-Bonilla (1999) | 3 | 0,17% | 2 | 0,25% | 2 | 0,25% | 2 | 0,25% |
| Chevalier (1971) | 3 | 0,17% | 3 | 0,37% | 3 | 0,37% | 3 | 0,37% |
| Devantier et al. (2008) | 3 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Devantier et al. (2014) | 3 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gall (2021) | 3 | 0,17% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Gardiner (1897) | 3 | 0,17% | 3 | 0,37% | 3 | 0,37% | 3 | 0,37% |
| Harvard University Museum & Morris P.J. (2020) | 3 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hoffmeister (1929) | 3 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Impact-Mer et al. (2011) | 3 | 0,17% | 3 | 0,37% | 3 | 0,37% | 3 | 0,37% |
| Johnston & Burgess (2023) | 3 | 0,17% | 3 | 0,37% | 3 | 0,37% | 3 | 0,37% |
| Martin (2011) | 3 | 0,17% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Vaughan (1907) | 3 | 0,17% | 3 | 0,37% | 3 | 0,37% | 3 | 0,37% |
| Tijdschrift der Nederlandse Dierkundige Vereeniging (Ser. 2), 7: 89-115.">Alcock (1902) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Benzoni & Pichon (2004) | 2 | 0,11% | 2 | 0,25% | 2 | 0,25% | 2 | 0,25% |
| Benzoni et al. (2014) | 2 | 0,11% | 2 | 0,25% | 2 | 0,25% | 2 | 0,25% |
| Benzoni (2013) | 2 | 0,11% | 2 | 0,25% | 2 | 0,25% | 2 | 0,25% |
| Brook (1892) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Brugneaux & Pérès (2006) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cairns (1977) | 2 | 0,11% | 2 | 0,25% | 2 | 0,25% | 2 | 0,25% |
| Cairns (1979) | 2 | 0,11% | 2 | 0,25% | 1 | 0,12% | 2 | 0,25% |
| Cairns (1995) | 2 | 0,11% | 2 | 0,25% | 2 | 0,25% | 2 | 0,25% |
| Duchassaing & Fonbressin (1870) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gardiner (1900) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ifremer (2020) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Le Sueur (1817) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lindström (1877) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Linsley et al. (1999) | 2 | 0,11% | 2 | 0,25% | 2 | 0,25% | 2 | 0,25% |
| Mckenna et al. (2009) | 2 | 0,11% | 2 | 0,25% | 2 | 0,25% | 2 | 0,25% |
| Richer de Forges et al. (2005) | 2 | 0,11% | 2 | 0,25% | 2 | 0,25% | 2 | 0,25% |
| Sheppard et al. (2008) | 2 | 0,11% | 2 | 0,25% | 2 | 0,25% | 2 | 0,25% |
| Turak et al. (2008) | 2 | 0,11% | 2 | 0,25% | 2 | 0,25% | 2 | 0,25% |
| Turak et al. (2014) | 2 | 0,11% | 2 | 0,25% | 2 | 0,25% | 2 | 0,25% |
| Umbgrove (1940) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Veron (2000) | 2 | 0,11% | 2 | 0,25% | 2 | 0,25% | 2 | 0,25% |
| Wells (1961) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
| Wijsman-Best (1970) | 2 | 0,11% | 2 | 0,25% | 2 | 0,25% | 2 | 0,25% |
| Yiu & Qiu (2022) | 2 | 0,11% | 2 | 0,25% | 2 | 0,25% | 2 | 0,25% |
| Zibrowius (1980) | 2 | 0,11% | 2 | 0,25% | 2 | 0,25% | 2 | 0,25% |
| Aronson et al. (2008) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Aronson et al. (2008) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Aronson et al. (2008) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Aronson et al. (2008) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Aronson et al. (2008) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Aronson et al. (2008) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Aronson et al. (2008) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Arrigoni et al. (2016) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Australian Museum (2020) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Bernard (1896) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Bernard (1897) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Bernard (1897) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Bourcier (1988) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Brook (1891) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cairns (1979) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Cairns (1998) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cambert et al. (2011) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cuif et al. (2003) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Dennant (1904) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Devantier et al. (2008) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Devantier et al. (2008) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Devantier et al. (2008) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Devantier et al. (2008) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| deVantier et al. (2008) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| deVantier et al. (2008) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Devantier et al. (2014) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Devantier et al. (2014) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| deVantier et al. (2014) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| deVantier et al. (2014) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| deVantier et al. (2014) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| deVantier et al. (2014) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Duchassaing & Fontbressin (1850) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Duncan (1865) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Duncan (1876) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Duncan (1889) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ellis & Solander (1786) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| European Nucleotide Archive (2019) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Gardiner (1898) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Gravier (1910) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Gregory (1895) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Head (1978) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Hoeksema et al. (2014) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Hoeksema et al. (2014) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Hoeksema et al. (2014) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Hoeksema et al. (2014) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Hoeksema et al. (2014) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hoeksema (2012) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Hourigan (2020) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| ICZN (2011) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ifremer (2021) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| IUCN (2014) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Kitahara (2005) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Klunzinger (1879) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Linnaeus (1758) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Mckenna et al. (2011) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Milne & Edwards (1860) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Milne et al. (1857) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Nemenzo (1976) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Owens (1994) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Payri et al. (2016) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Pichon et al. (2020) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Pourtalès (1874) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Pyle et al. (2016) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Questel (2022) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Richards et al. (2008) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Richards et al. (2014) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Sheppard et al. (2008) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sheppard et al. (2014) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Turak et al. (2008) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Vaga et al. (2023) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Van et al. (2008) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Veron & Wallace (1984) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Veron et al. (1977) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Veron (1985) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Veron (1985) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Verrill (1864) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Verrill (1872) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Verrill (1901) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Wallace & Wolstenholme (1998) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Wallace (1994) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Wallace (1999) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Yabe & Sugiyama (1937) | 1 | 0,06% | 1 | 0,12% | 1 | 0,12% | 1 | 0,12% |
| Zibrowius & Arnaud (1995) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Zibrowius (1982) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
