Scléractiniaires de Nouvelle-Calédonie
132 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 | 23,27% | 232 | 37,66% | 232 | 37,79% | 232 | 37,79% |
| Pichon & Thomassin (2005) | 186 | 13,83% | 141 | 22,89% | 141 | 22,96% | 141 | 22,96% |
| Pichon et al. (2007) | 170 | 12,64% | 136 | 22,08% | 136 | 22,15% | 136 | 22,15% |
| Faure et al. (2008) | 144 | 10,71% | 116 | 18,83% | 116 | 18,89% | 116 | 18,89% |
| Glynn et al. (2007) | 140 | 10,41% | 110 | 17,86% | 110 | 17,92% | 110 | 17,92% |
| Kitahara (2011) | 119 | 8,85% | 118 | 19,16% | 116 | 18,89% | 118 | 19,22% |
| Pichon (comm. pers., 2012) | 76 | 5,65% | 63 | 10,23% | 63 | 10,26% | 63 | 10,26% |
| Cairns (1999) | 74 | 5,5% | 71 | 11,53% | 68 | 11,07% | 71 | 11,56% |
| Chevalier & Kuhlmann (1983) | 49 | 3,64% | 30 | 4,87% | 30 | 4,89% | 30 | 4,89% |
| Uicn et al. (2020) | 47 | 3,49% | 41 | 6,66% | 41 | 6,68% | 41 | 6,68% |
| Dana (1846-1849) | 39 | 2,9% | 2 | 0,32% | 2 | 0,33% | 2 | 0,33% |
| Fenner & Muir (2008) | 37 | 2,75% | 31 | 5,03% | 31 | 5,05% | 31 | 5,05% |
| Andouche et al. (2020) | 32 | 2,38% | 31 | 5,03% | 31 | 5,05% | 31 | 5,05% |
| Sheppard (1987) | 25 | 1,86% | 4 | 0,65% | 4 | 0,65% | 4 | 0,65% |
| Bigot (comm. pers., 2018) | 20 | 1,49% | 19 | 3,08% | 19 | 3,09% | 19 | 3,09% |
| Gardiner (1899) | 19 | 1,41% | 9 | 1,46% | 9 | 1,47% | 9 | 1,47% |
| Quelch (1886) | 16 | 1,19% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kitahara & Cairns (2009) | 15 | 1,12% | 15 | 2,44% | 15 | 2,44% | 15 | 2,44% |
| Kitahara et al. (2010) | 15 | 1,12% | 15 | 2,44% | 15 | 2,44% | 15 | 2,44% |
| Bosserelle et al. (2014) | 14 | 1,04% | 13 | 2,11% | 13 | 2,12% | 13 | 2,12% |
| Flot & Adjeroud (2009) | 13 | 0,97% | 11 | 1,79% | 11 | 1,79% | 11 | 1,79% |
| IUCN (2013) | 13 | 0,97% | 9 | 1,46% | 9 | 1,47% | 9 | 1,47% |
| Fautin (2013) | 12 | 0,89% | 12 | 1,95% | 12 | 1,95% | 11 | 1,79% |
| Low & Evenhuis (2013) | 12 | 0,89% | 6 | 0,97% | 6 | 0,98% | 6 | 0,98% |
| Moseley ([1880]) | 11 | 0,82% | 5 | 0,81% | 5 | 0,81% | 5 | 0,81% |
| Payri et al. (2002) | 10 | 0,74% | 7 | 1,14% | 7 | 1,14% | 7 | 1,14% |
| . Rapport GIS "Lag-May" / Conseil Général de Mayotte / Centre d'Océanologie de Marseille. 61 pp.">Thomassin et al. (1998) | 10 | 0,74% | 8 | 1,3% | 8 | 1,3% | 8 | 1,3% |
| National Institute of Water and Atmospheric Research (2016) | 9 | 0,67% | 6 | 0,97% | 6 | 0,98% | 6 | 0,98% |
| Orrell (2019) | 9 | 0,67% | 4 | 0,65% | 4 | 0,65% | 4 | 0,65% |
| Adjeroud et al. (2012) | 8 | 0,59% | 5 | 0,81% | 5 | 0,81% | 5 | 0,81% |
| Arrigoni et al. (2016) | 8 | 0,59% | 8 | 1,3% | 8 | 1,3% | 8 | 1,3% |
| Cairns (1989) | 6 | 0,45% | 6 | 0,97% | 6 | 0,98% | 6 | 0,98% |
| Cairns (2004) | 6 | 0,45% | 6 | 0,97% | 6 | 0,98% | 6 | 0,98% |
| Kitahara & Cairns (2008) | 6 | 0,45% | 6 | 0,97% | 6 | 0,98% | 6 | 0,98% |
| Milne-Edwards (1848) | 6 | 0,45% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Reveillaud et al. (2008) | 6 | 0,45% | 6 | 0,97% | 6 | 0,98% | 6 | 0,98% |
| Pearman et al. (2020) | 5 | 0,37% | 5 | 0,81% | 5 | 0,81% | 5 | 0,81% |
| Wells (1968) | 5 | 0,37% | 4 | 0,65% | 4 | 0,65% | 4 | 0,65% |
| Benzoni et al. (2010) | 4 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fourt et al. (2017) | 4 | 0,3% | 4 | 0,65% | 4 | 0,65% | 4 | 0,65% |
| Goud et al. (2021) | 4 | 0,3% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Pourtales (1868) | 4 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
| Uicn et al. (2019) | 4 | 0,3% | 4 | 0,65% | 4 | 0,65% | 4 | 0,65% |
| Vaughan (1906) | 4 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
| Zibrowius (1974) | 4 | 0,3% | 3 | 0,49% | 3 | 0,49% | 3 | 0,49% |
| AAMP (2010) | 3 | 0,22% | 3 | 0,49% | 3 | 0,49% | 3 | 0,49% |
| Carricart-Ganivet & Reyes-Bonilla (1999) | 3 | 0,22% | 2 | 0,32% | 2 | 0,33% | 2 | 0,33% |
| Chevalier (1971) | 3 | 0,22% | 3 | 0,49% | 3 | 0,49% | 3 | 0,49% |
| Devantier et al. (2014) | 3 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gardiner (1897) | 3 | 0,22% | 3 | 0,49% | 3 | 0,49% | 3 | 0,49% |
| Questel & Le Quellec (2012) | 3 | 0,22% | 2 | 0,32% | 2 | 0,33% | 2 | 0,33% |
| Questel (2020) | 3 | 0,22% | 3 | 0,49% | 3 | 0,49% | 3 | 0,49% |
| Tricart & Foubert (2000) | 3 | 0,22% | 3 | 0,49% | 3 | 0,49% | 3 | 0,49% |
| Tijdschrift der Nederlandse Dierkundige Vereeniging (Ser. 2), 7: 89-115.">Alcock (1902) | 2 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
| Arrigoni et al. (2020) | 2 | 0,15% | 2 | 0,32% | 2 | 0,33% | 2 | 0,33% |
| Benzoni & Pichon (2004) | 2 | 0,15% | 2 | 0,32% | 2 | 0,33% | 2 | 0,33% |
| Benzoni et al. (2014) | 2 | 0,15% | 2 | 0,32% | 2 | 0,33% | 2 | 0,33% |
| Benzoni (2013) | 2 | 0,15% | 2 | 0,32% | 2 | 0,33% | 2 | 0,33% |
| Cairns (1995) | 2 | 0,15% | 2 | 0,32% | 2 | 0,33% | 2 | 0,33% |
| Gall (2021) | 2 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gardiner (1900) | 2 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ifremer (2009) | 2 | 0,15% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Linsley et al. (1999) | 2 | 0,15% | 2 | 0,32% | 2 | 0,33% | 2 | 0,33% |
| Mckenna et al. (2009) | 2 | 0,15% | 2 | 0,32% | 2 | 0,33% | 2 | 0,33% |
| Proceedings of the Royal Society of London, 24: 543-569.">Moseley (1876) | 2 | 0,15% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Quelch (1884) | 2 | 0,15% | 2 | 0,32% | 2 | 0,33% | 2 | 0,33% |
| Richer de Forges et al. (2005) | 2 | 0,15% | 2 | 0,32% | 2 | 0,33% | 2 | 0,33% |
| Turak et al. (2008) | 2 | 0,15% | 2 | 0,32% | 2 | 0,33% | 2 | 0,33% |
| Umbgrove (1940) | 2 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
| Vaughan (1907) | 2 | 0,15% | 2 | 0,32% | 2 | 0,33% | 2 | 0,33% |
| Wells (1961) | 2 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
| Wijsman-Best (1970) | 2 | 0,15% | 2 | 0,32% | 2 | 0,33% | 2 | 0,33% |
| Yiu & Qiu (2022) | 2 | 0,15% | 2 | 0,32% | 2 | 0,33% | 2 | 0,33% |
| Zibrowius (1968) | 2 | 0,15% | 2 | 0,32% | 2 | 0,33% | 2 | 0,33% |
| Arrigoni et al. (2018) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Australian Museum (2020) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Bernard (1896) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Bernard (1897) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Bernard (1897) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Brook (1891) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Brook (1892) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cairns (1998) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cairns (2000) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Cambert et al. (2011) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dennant (1904) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Devantier et al. (2008) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Devantier et al. (2008) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Devantier et al. (2008) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| deVantier et al. (2008) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| deVantier et al. (2008) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Devantier et al. (2014) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Devantier et al. (2014) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| deVantier et al. (2014) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| deVantier et al. (2014) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| deVantier et al. (2014) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| deVantier et al. (2014) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Duncan (1865) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Duncan (1876) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| European Nucleotide Archive (2019) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Gardiner (1898) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Harvard University Museum & Morris P.J. (2020) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hoeksema et al. (2014) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Hoeksema et al. (2014) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Hoeksema et al. (2014) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hoeksema et al. (2014) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Hoeksema et al. (2014) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Hoffmeister (1929) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| ICZN (2011) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kitahara (2005) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Linnaeus (1758) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Martin (2011) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Mckenna et al. (2011) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Milne & Edwards (1860) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Milne et al. (1857) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Nemenzo (1976) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Payri et al. (2016) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Peralta & Fautin (2013) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pyle et al. (2016) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Richards et al. (2014) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Sheppard et al. (2014) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Turak et al. (2008) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Veron & Wallace (1984) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Veron et al. (1977) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Veron (1985) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Veron (1985) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Verrill (1864) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Wallace & Wolstenholme (1998) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Wallace (1994) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Yabe & Sugiyama (1937) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Zibrowius & Arnaud (1995) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Zibrowius (1980) | 1 | 0,07% | 1 | 0,16% | 1 | 0,16% | 1 | 0,16% |
| Zibrowius (1982) | 1 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
