Hydrozoaires de Mayotte
65 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
Référence | Total | Valides | Espèces | Taxons terminaux | ||||
---|---|---|---|---|---|---|---|---|
nb | % | nb | % | nb | % | nb | % | |
Gravier-Bonnet et al. (2007) | 74 | 25,87% | 57 | 64,77% | 57 | 64,77% | 57 | 64,77% |
Bourmaud (2003) | 32 | 11,19% | 25 | 28,41% | 25 | 28,41% | 25 | 28,41% |
Gravier-Bonnet (2007) | 29 | 10,14% | 24 | 27,27% | 24 | 27,27% | 24 | 27,27% |
Gravier-Bonnet & Bourmaud (2005) | 23 | 8,04% | 17 | 19,32% | 17 | 19,32% | 17 | 19,32% |
Galea (2013) | 21 | 7,34% | 20 | 22,73% | 20 | 22,73% | 20 | 22,73% |
Galea (2008) | 12 | 4,2% | 12 | 13,64% | 12 | 13,64% | 12 | 13,64% |
Gravier-Bonnet et al. (2009) | 12 | 4,2% | 11 | 12,5% | 11 | 12,5% | 11 | 12,5% |
Vervoort & Vasseur (1977) | 12 | 4,2% | 7 | 7,95% | 7 | 7,95% | 7 | 7,95% |
Galea (2010) | 10 | 3,5% | 8 | 9,09% | 8 | 9,09% | 8 | 9,09% |
Postaire et al. (2016) | 10 | 3,5% | 7 | 7,95% | 7 | 7,95% | 7 | 7,95% |
Galea et al. (2021) | 9 | 3,15% | 9 | 10,23% | 9 | 10,23% | 9 | 10,23% |
Ifremer (2009) | 9 | 3,15% | 6 | 6,82% | 6 | 6,82% | 6 | 6,82% |
Gravier-Bonnet & Bourmaud (2006) | 7 | 2,45% | 6 | 6,82% | 6 | 6,82% | 6 | 6,82% |
Lamouroux (1816) | 7 | 2,45% | 2 | 2,27% | 2 | 2,27% | 2 | 2,27% |
Bedot (1914) | 4 | 1,4% | 3 | 3,41% | 3 | 3,41% | 3 | 3,41% |
Galea & Ferry (2015) | 4 | 1,4% | 2 | 2,27% | 2 | 2,27% | 2 | 2,27% |
Galea et al. (2022) | 4 | 1,4% | 1 | 1,14% | 1 | 1,14% | 1 | 1,14% |
Mccrady (1859) | 4 | 1,4% | 0 | 0% | 0 | 0% | 0 | 0% |
Ansín Agís et al. (2009) | 3 | 1,05% | 3 | 3,41% | 3 | 3,41% | 3 | 3,41% |
Breton (2014) | 3 | 1,05% | 3 | 3,41% | 3 | 3,41% | 3 | 3,41% |
Fenner & Muir (2008) | 3 | 1,05% | 3 | 3,41% | 3 | 3,41% | 3 | 3,41% |
Nelson-Smith et al. (2014) | 3 | 1,05% | 3 | 3,41% | 3 | 3,41% | 3 | 3,41% |
Vervoort (1993) | 3 | 1,05% | 3 | 3,41% | 3 | 3,41% | 3 | 3,41% |
Ansín Agís et al. (2014) | 2 | 0,7% | 2 | 2,27% | 2 | 2,27% | 2 | 2,27% |
Bale (1888) | 2 | 0,7% | 0 | 0% | 0 | 0% | 0 | 0% |
Bedot (1910) | 2 | 0,7% | 1 | 1,14% | 1 | 1,14% | 1 | 1,14% |
Chevalier & Kuhlmann (1983) | 2 | 0,7% | 2 | 2,27% | 2 | 2,27% | 2 | 2,27% |
Forsskål (1775) | 2 | 0,7% | 2 | 2,27% | 2 | 2,27% | 2 | 2,27% |
Galea (2016) | 2 | 0,7% | 2 | 2,27% | 2 | 2,27% | 2 | 2,27% |
Ifremer (2022) | 2 | 0,7% | 1 | 1,14% | 1 | 1,14% | 1 | 1,14% |
Linnaeus (1758) | 2 | 0,7% | 0 | 0% | 0 | 0% | 0 | 0% |
Nicet & Denis (2011) | 2 | 0,7% | 2 | 2,27% | 2 | 2,27% | 2 | 2,27% |
Questel & Le Quellec (2012) | 2 | 0,7% | 2 | 2,27% | 2 | 2,27% | 2 | 2,27% |
Questel (2020) | 2 | 0,7% | 2 | 2,27% | 2 | 2,27% | 2 | 2,27% |
Tricart & Foubert (2000) | 2 | 0,7% | 2 | 2,27% | 2 | 2,27% | 2 | 2,27% |
Alder (1856) | 1 | 0,35% | 1 | 1,14% | 1 | 1,14% | 1 | 1,14% |
Allman (1888) | 1 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
Andouche et al. (2020) | 1 | 0,35% | 1 | 1,14% | 1 | 1,14% | 1 | 1,14% |
Bale (1924) | 1 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
Billard (1919) | 1 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
Boissin et al. (2019) | 1 | 0,35% | 1 | 1,14% | 1 | 1,14% | 1 | 1,14% |
Brugneaux & Pérès (2005) | 1 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
Caziot (1921) | 1 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
Dana (1846-1849) | 1 | 0,35% | 1 | 1,14% | 1 | 1,14% | 1 | 1,14% |
Deuss et al. (2013) | 1 | 0,35% | 1 | 1,14% | 1 | 1,14% | 1 | 1,14% |
Eschscholtz (1829) | 1 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
Flot & Adjeroud (2009) | 1 | 0,35% | 1 | 1,14% | 1 | 1,14% | 1 | 1,14% |
Fraser (1948) | 1 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
Galea & Maggioni (2024) | 1 | 0,35% | 1 | 1,14% | 1 | 1,14% | 1 | 1,14% |
Gmelin (1791) | 1 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
Godet et al. (2010) | 1 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
Goulletquer (2016) | 1 | 0,35% | 1 | 1,14% | 1 | 1,14% | 1 | 1,14% |
Harvard University Museum & Morris P.J. (2020) | 1 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
Hassall (1848) | 1 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
Hincks (1866) | 1 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
Proceedings of the Zoological Society of London, 1907: 1035-1037.">Hopkinson (1907) | 1 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
Kayal & Kayal (2017) | 1 | 0,35% | 1 | 1,14% | 1 | 1,14% | 1 | 1,14% |
Lamarck (1816) | 1 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
Millard (1957) | 1 | 0,35% | 1 | 1,14% | 1 | 1,14% | 1 | 1,14% |
Motz-Kossowska (1910) | 1 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
Peralta & Fautin (2013) | 1 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
Questel (2022) | 1 | 0,35% | 1 | 1,14% | 1 | 1,14% | 1 | 1,14% |
Rignault & Chevallier (2017) | 1 | 0,35% | 1 | 1,14% | 1 | 1,14% | 1 | 1,14% |
Telenius & Shah (2019) | 1 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |
Totton (1930) | 1 | 0,35% | 0 | 0% | 0 | 0% | 0 | 0% |