Scléractiniaires de Wallis-et-Futuna
83 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) | 176 | 23,66% | 133 | 49,63% | 133 | 50% | 133 | 50% |
Pichon et al. (2007) | 171 | 22,98% | 137 | 51,12% | 137 | 51,5% | 137 | 51,5% |
Pichon & Thomassin (2005) | 135 | 18,15% | 102 | 38,06% | 102 | 38,35% | 102 | 38,35% |
Faure et al. (2008) | 109 | 14,65% | 89 | 33,21% | 89 | 33,46% | 89 | 33,46% |
Glynn et al. (2007) | 100 | 13,44% | 76 | 28,36% | 76 | 28,57% | 76 | 28,57% |
Cairns (1999) | 95 | 12,77% | 88 | 32,84% | 85 | 31,95% | 88 | 33,08% |
Kitahara (2011) | 39 | 5,24% | 38 | 14,18% | 36 | 13,53% | 38 | 14,29% |
Chevalier & Kuhlmann (1983) | 38 | 5,11% | 23 | 8,58% | 23 | 8,65% | 23 | 8,65% |
Dana (1846-1849) | 32 | 4,3% | 2 | 0,75% | 2 | 0,75% | 2 | 0,75% |
Pichon (comm. pers., 2012) | 24 | 3,23% | 20 | 7,46% | 20 | 7,52% | 20 | 7,52% |
Uicn et al. (2020) | 24 | 3,23% | 19 | 7,09% | 19 | 7,14% | 19 | 7,14% |
Sheppard (1987) | 21 | 2,82% | 2 | 0,75% | 2 | 0,75% | 2 | 0,75% |
Flot & Adjeroud (2009) | 12 | 1,61% | 10 | 3,73% | 10 | 3,76% | 10 | 3,76% |
Kitahara & Cairns (2009) | 10 | 1,34% | 10 | 3,73% | 10 | 3,76% | 10 | 3,76% |
Payri et al. (2002) | 10 | 1,34% | 7 | 2,61% | 7 | 2,63% | 7 | 2,63% |
Bosserelle et al. (2014) | 8 | 1,08% | 7 | 2,61% | 7 | 2,63% | 7 | 2,63% |
Fautin (2013) | 8 | 1,08% | 8 | 2,99% | 8 | 3,01% | 7 | 2,63% |
. Rapport GIS "Lag-May" / Conseil Général de Mayotte / Centre d'Océanologie de Marseille. 61 pp.">Thomassin et al. (1998) | 8 | 1,08% | 6 | 2,24% | 6 | 2,26% | 6 | 2,26% |
IUCN (2013) | 7 | 0,94% | 4 | 1,49% | 4 | 1,5% | 4 | 1,5% |
Low & Evenhuis (2013) | 7 | 0,94% | 2 | 0,75% | 2 | 0,75% | 2 | 0,75% |
Moseley ([1880]) | 7 | 0,94% | 2 | 0,75% | 2 | 0,75% | 2 | 0,75% |
Bigot (comm. pers., 2018) | 6 | 0,81% | 6 | 2,24% | 6 | 2,26% | 6 | 2,26% |
Fourt et al. (2017) | 6 | 0,81% | 4 | 1,49% | 4 | 1,5% | 4 | 1,5% |
Gardiner (1899) | 6 | 0,81% | 2 | 0,75% | 2 | 0,75% | 2 | 0,75% |
Quelch (1886) | 6 | 0,81% | 0 | 0% | 0 | 0% | 0 | 0% |
Reveillaud et al. (2008) | 6 | 0,81% | 5 | 1,87% | 5 | 1,88% | 5 | 1,88% |
Fenner & Muir (2008) | 5 | 0,67% | 5 | 1,87% | 5 | 1,88% | 5 | 1,88% |
Kitahara et al. (2010) | 5 | 0,67% | 5 | 1,87% | 5 | 1,88% | 5 | 1,88% |
Milne-Edwards (1848) | 5 | 0,67% | 0 | 0% | 0 | 0% | 0 | 0% |
Pearman et al. (2020) | 5 | 0,67% | 5 | 1,87% | 5 | 1,88% | 5 | 1,88% |
Adjeroud et al. (2012) | 4 | 0,54% | 2 | 0,75% | 2 | 0,75% | 2 | 0,75% |
Benzoni et al. (2010) | 4 | 0,54% | 0 | 0% | 0 | 0% | 0 | 0% |
Ifremer (2009) | 4 | 0,54% | 2 | 0,75% | 2 | 0,75% | 2 | 0,75% |
Kitahara & Cairns (2008) | 4 | 0,54% | 4 | 1,49% | 4 | 1,5% | 4 | 1,5% |
Orrell (2019) | 4 | 0,54% | 0 | 0% | 0 | 0% | 0 | 0% |
Uicn et al. (2019) | 4 | 0,54% | 4 | 1,49% | 4 | 1,5% | 4 | 1,5% |
Chevalier (1971) | 3 | 0,4% | 3 | 1,12% | 3 | 1,13% | 3 | 1,13% |
Martin (2011) | 3 | 0,4% | 1 | 0,37% | 1 | 0,38% | 1 | 0,38% |
National Institute of Water and Atmospheric Research (2016) | 3 | 0,4% | 0 | 0% | 0 | 0% | 0 | 0% |
Zibrowius (1974) | 3 | 0,4% | 1 | 0,37% | 1 | 0,38% | 1 | 0,38% |
AAMP (2010) | 2 | 0,27% | 2 | 0,75% | 2 | 0,75% | 2 | 0,75% |
Carricart-Ganivet & Reyes-Bonilla (1999) | 2 | 0,27% | 1 | 0,37% | 1 | 0,38% | 1 | 0,38% |
Gall (2021) | 2 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Linsley et al. (1999) | 2 | 0,27% | 2 | 0,75% | 2 | 0,75% | 2 | 0,75% |
Proceedings of the Royal Society of London, 24: 543-569.">Moseley (1876) | 2 | 0,27% | 2 | 0,75% | 2 | 0,75% | 2 | 0,75% |
Quelch (1884) | 2 | 0,27% | 2 | 0,75% | 2 | 0,75% | 2 | 0,75% |
Questel & Le Quellec (2012) | 2 | 0,27% | 1 | 0,37% | 1 | 0,38% | 1 | 0,38% |
Questel (2020) | 2 | 0,27% | 2 | 0,75% | 2 | 0,75% | 2 | 0,75% |
Richer de Forges et al. (2005) | 2 | 0,27% | 2 | 0,75% | 2 | 0,75% | 2 | 0,75% |
Tricart & Foubert (2000) | 2 | 0,27% | 2 | 0,75% | 2 | 0,75% | 2 | 0,75% |
Umbgrove (1940) | 2 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Vaughan (1906) | 2 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Wells (1961) | 2 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Arrigoni et al. (2018) | 1 | 0,13% | 1 | 0,37% | 1 | 0,38% | 1 | 0,38% |
Brook (1891) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Brook (1892) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Cairns (1989) | 1 | 0,13% | 1 | 0,37% | 1 | 0,38% | 1 | 0,38% |
Cairns (2000) | 1 | 0,13% | 1 | 0,37% | 1 | 0,38% | 1 | 0,38% |
Cambert et al. (2011) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Devantier et al. (2008) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Devantier et al. (2014) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
deVantier et al. (2014) | 1 | 0,13% | 1 | 0,37% | 1 | 0,38% | 1 | 0,38% |
deVantier et al. (2014) | 1 | 0,13% | 1 | 0,37% | 1 | 0,38% | 1 | 0,38% |
Gardiner (1897) | 1 | 0,13% | 1 | 0,37% | 1 | 0,38% | 1 | 0,38% |
Goud et al. (2021) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Hoeksema et al. (2014) | 1 | 0,13% | 1 | 0,37% | 1 | 0,38% | 1 | 0,38% |
Hoeksema et al. (2014) | 1 | 0,13% | 1 | 0,37% | 1 | 0,38% | 1 | 0,38% |
Hoeksema et al. (2014) | 1 | 0,13% | 1 | 0,37% | 1 | 0,38% | 1 | 0,38% |
Hoeksema et al. (2014) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Hoffmeister (1929) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Kitahara (2005) | 1 | 0,13% | 1 | 0,37% | 1 | 0,38% | 1 | 0,38% |
Linnaeus (1758) | 1 | 0,13% | 1 | 0,37% | 1 | 0,38% | 1 | 0,38% |
Owens (1994) | 1 | 0,13% | 1 | 0,37% | 1 | 0,38% | 1 | 0,38% |
Peralta & Fautin (2013) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Pourtales (1868) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Pyle et al. (2016) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Richards et al. (2014) | 1 | 0,13% | 1 | 0,37% | 1 | 0,38% | 1 | 0,38% |
Vaga et al. (2023) | 1 | 0,13% | 1 | 0,37% | 1 | 0,38% | 1 | 0,38% |
Veron et al. (1977) | 1 | 0,13% | 1 | 0,37% | 1 | 0,38% | 1 | 0,38% |
Verrill (1864) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
Zibrowius (1968) | 1 | 0,13% | 1 | 0,37% | 1 | 0,38% | 1 | 0,38% |
Zibrowius (1980) | 1 | 0,13% | 1 | 0,37% | 1 | 0,38% | 1 | 0,38% |
Zibrowius (1982) | 1 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |