Scléractiniaires de la Réunion
74 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) | 170 | 26,6% | 131 | 61,79% | 131 | 61,79% | 131 | 61,79% |
Faure et al. (2008) | 162 | 25,35% | 133 | 62,74% | 133 | 62,74% | 133 | 62,74% |
Pichon & Thomassin (2005) | 145 | 22,69% | 114 | 53,77% | 114 | 53,77% | 114 | 53,77% |
Pichon et al. (2007) | 118 | 18,47% | 95 | 44,81% | 95 | 44,81% | 95 | 44,81% |
Glynn et al. (2007) | 114 | 17,84% | 89 | 41,98% | 89 | 41,98% | 89 | 41,98% |
Chevalier & Kuhlmann (1983) | 45 | 7,04% | 26 | 12,26% | 26 | 12,26% | 26 | 12,26% |
Dana (1846-1849) | 35 | 5,48% | 2 | 0,94% | 2 | 0,94% | 2 | 0,94% |
Uicn et al. (2020) | 35 | 5,48% | 30 | 14,15% | 30 | 14,15% | 30 | 14,15% |
Sheppard (1987) | 30 | 4,69% | 8 | 3,77% | 8 | 3,77% | 8 | 3,77% |
Pichon (comm. pers., 2012) | 27 | 4,23% | 23 | 10,85% | 23 | 10,85% | 23 | 10,85% |
Quelch (1886) | 12 | 1,88% | 0 | 0% | 0 | 0% | 0 | 0% |
Flot & Adjeroud (2009) | 11 | 1,72% | 9 | 4,25% | 9 | 4,25% | 9 | 4,25% |
Bigot (comm. pers., 2018) | 10 | 1,56% | 10 | 4,72% | 10 | 4,72% | 10 | 4,72% |
Bosserelle et al. (2014) | 10 | 1,56% | 9 | 4,25% | 9 | 4,25% | 9 | 4,25% |
IUCN (2013) | 8 | 1,25% | 4 | 1,89% | 4 | 1,89% | 4 | 1,89% |
Fenner & Muir (2008) | 7 | 1,1% | 7 | 3,3% | 7 | 3,3% | 7 | 3,3% |
Adjeroud et al. (2012) | 6 | 0,94% | 3 | 1,42% | 3 | 1,42% | 3 | 1,42% |
Payri et al. (2002) | 6 | 0,94% | 3 | 1,42% | 3 | 1,42% | 3 | 1,42% |
. Rapport GIS "Lag-May" / Conseil Général de Mayotte / Centre d'Océanologie de Marseille. 61 pp.">Thomassin et al. (1998) | 5 | 0,78% | 5 | 2,36% | 5 | 2,36% | 5 | 2,36% |
Benzoni et al. (2010) | 4 | 0,63% | 0 | 0% | 0 | 0% | 0 | 0% |
Uicn et al. (2019) | 4 | 0,63% | 4 | 1,89% | 4 | 1,89% | 4 | 1,89% |
Vaughan (1906) | 4 | 0,63% | 0 | 0% | 0 | 0% | 0 | 0% |
Chevalier (1971) | 3 | 0,47% | 3 | 1,42% | 3 | 1,42% | 3 | 1,42% |
Hoffmeister (1929) | 3 | 0,47% | 0 | 0% | 0 | 0% | 0 | 0% |
National Institute of Water and Atmospheric Research (2016) | 3 | 0,47% | 0 | 0% | 0 | 0% | 0 | 0% |
Orrell (2019) | 3 | 0,47% | 0 | 0% | 0 | 0% | 0 | 0% |
Arrigoni et al. (2016) | 2 | 0,31% | 2 | 0,94% | 2 | 0,94% | 2 | 0,94% |
Brook (1892) | 2 | 0,31% | 0 | 0% | 0 | 0% | 0 | 0% |
Carricart-Ganivet & Reyes-Bonilla (1999) | 2 | 0,31% | 1 | 0,47% | 1 | 0,47% | 1 | 0,47% |
Gall (2021) | 2 | 0,31% | 0 | 0% | 0 | 0% | 0 | 0% |
Gardiner (1899) | 2 | 0,31% | 0 | 0% | 0 | 0% | 0 | 0% |
Linsley et al. (1999) | 2 | 0,31% | 2 | 0,94% | 2 | 0,94% | 2 | 0,94% |
Sheppard et al. (2008) | 2 | 0,31% | 2 | 0,94% | 2 | 0,94% | 2 | 0,94% |
Umbgrove (1940) | 2 | 0,31% | 0 | 0% | 0 | 0% | 0 | 0% |
Wells (1961) | 2 | 0,31% | 0 | 0% | 0 | 0% | 0 | 0% |
Arrigoni et al. (2018) | 1 | 0,16% | 1 | 0,47% | 1 | 0,47% | 1 | 0,47% |
Bernard (1896) | 1 | 0,16% | 1 | 0,47% | 1 | 0,47% | 1 | 0,47% |
Brook (1891) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Cairns (1999) | 1 | 0,16% | 1 | 0,47% | 1 | 0,47% | 1 | 0,47% |
Cambert et al. (2011) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Devantier et al. (2008) | 1 | 0,16% | 1 | 0,47% | 1 | 0,47% | 1 | 0,47% |
Devantier et al. (2008) | 1 | 0,16% | 1 | 0,47% | 1 | 0,47% | 1 | 0,47% |
Devantier et al. (2008) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
deVantier et al. (2008) | 1 | 0,16% | 1 | 0,47% | 1 | 0,47% | 1 | 0,47% |
deVantier et al. (2008) | 1 | 0,16% | 1 | 0,47% | 1 | 0,47% | 1 | 0,47% |
Devantier et al. (2014) | 1 | 0,16% | 1 | 0,47% | 1 | 0,47% | 1 | 0,47% |
Devantier et al. (2014) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
deVantier et al. (2014) | 1 | 0,16% | 1 | 0,47% | 1 | 0,47% | 1 | 0,47% |
deVantier et al. (2014) | 1 | 0,16% | 1 | 0,47% | 1 | 0,47% | 1 | 0,47% |
deVantier et al. (2014) | 1 | 0,16% | 1 | 0,47% | 1 | 0,47% | 1 | 0,47% |
Duncan (1889) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Gardiner (1897) | 1 | 0,16% | 1 | 0,47% | 1 | 0,47% | 1 | 0,47% |
Goud et al. (2021) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Gravier (1910) | 1 | 0,16% | 1 | 0,47% | 1 | 0,47% | 1 | 0,47% |
Head (1978) | 1 | 0,16% | 1 | 0,47% | 1 | 0,47% | 1 | 0,47% |
Hoeksema et al. (2014) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Kitahara (2011) | 1 | 0,16% | 1 | 0,47% | 1 | 0,47% | 1 | 0,47% |
Klunzinger (1879) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Milne & Edwards (1860) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Milne et al. (1857) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Pyle et al. (2016) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Questel & Le Quellec (2012) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Questel (2020) | 1 | 0,16% | 1 | 0,47% | 1 | 0,47% | 1 | 0,47% |
Richards et al. (2008) | 1 | 0,16% | 1 | 0,47% | 1 | 0,47% | 1 | 0,47% |
Richards et al. (2014) | 1 | 0,16% | 1 | 0,47% | 1 | 0,47% | 1 | 0,47% |
Sheppard et al. (2008) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Tricart & Foubert (2000) | 1 | 0,16% | 1 | 0,47% | 1 | 0,47% | 1 | 0,47% |
Turak et al. (2008) | 1 | 0,16% | 1 | 0,47% | 1 | 0,47% | 1 | 0,47% |
Van et al. (2008) | 1 | 0,16% | 1 | 0,47% | 1 | 0,47% | 1 | 0,47% |
Vaughan (1907) | 1 | 0,16% | 1 | 0,47% | 1 | 0,47% | 1 | 0,47% |
Veron et al. (1977) | 1 | 0,16% | 1 | 0,47% | 1 | 0,47% | 1 | 0,47% |
Verrill (1864) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Wells (1968) | 1 | 0,16% | 1 | 0,47% | 1 | 0,47% | 1 | 0,47% |
Zibrowius & Arnaud (1995) | 1 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |