Hydrozoaires de Nouvelle-Calédonie
97 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
Référence | Total | Valides | Espèces | Taxons terminaux | ||||
---|---|---|---|---|---|---|---|---|
nb | % | nb | % | nb | % | nb | % | |
Cairns (2015) | 162 | 27,93% | 158 | 43,77% | 158 | 43,77% | 158 | 43,77% |
Gravier-Bonnet (2007) | 101 | 17,41% | 86 | 23,82% | 86 | 23,82% | 86 | 23,82% |
Vervoort (1993) | 98 | 16,9% | 87 | 24,1% | 87 | 24,1% | 87 | 24,1% |
Ifremer (2009) | 80 | 13,79% | 75 | 20,78% | 75 | 20,78% | 75 | 20,78% |
Galea & Schuchert (2019) | 53 | 9,14% | 52 | 14,4% | 52 | 14,4% | 52 | 14,4% |
Galea (2016) | 51 | 8,79% | 51 | 14,13% | 51 | 14,13% | 51 | 14,13% |
Gravier-Bonnet et al. (2007) | 40 | 6,9% | 30 | 8,31% | 30 | 8,31% | 30 | 8,31% |
Pena et al. (2010) | 33 | 5,69% | 33 | 9,14% | 33 | 9,14% | 33 | 9,14% |
Bourmaud (2003) | 21 | 3,62% | 16 | 4,43% | 16 | 4,43% | 16 | 4,43% |
Lindner (2007) | 21 | 3,62% | 19 | 5,26% | 19 | 5,26% | 19 | 5,26% |
Galea (2015) | 18 | 3,1% | 18 | 4,99% | 18 | 4,99% | 18 | 4,99% |
Galea (2020) | 18 | 3,1% | 17 | 4,71% | 17 | 4,71% | 17 | 4,71% |
Gravier-Bonnet & Bourmaud (2005) | 15 | 2,59% | 12 | 3,32% | 12 | 3,32% | 12 | 3,32% |
Postaire et al. (2016) | 15 | 2,59% | 12 | 3,32% | 12 | 3,32% | 12 | 3,32% |
Galea (2013) | 14 | 2,41% | 14 | 3,88% | 14 | 3,88% | 14 | 3,88% |
Galea & Maggioni (2020) | 13 | 2,24% | 13 | 3,6% | 13 | 3,6% | 13 | 3,6% |
Cantero (2020) | 12 | 2,07% | 12 | 3,32% | 12 | 3,32% | 12 | 3,32% |
Mackay (2014) | 12 | 2,07% | 10 | 2,77% | 10 | 2,77% | 10 | 2,77% |
Ansín Agís et al. (2014) | 10 | 1,72% | 8 | 2,22% | 8 | 2,22% | 8 | 2,22% |
Vervoort & Vasseur (1977) | 10 | 1,72% | 6 | 1,66% | 6 | 1,66% | 6 | 1,66% |
Ansín Agís et al. (2009) | 9 | 1,55% | 7 | 1,94% | 7 | 1,94% | 7 | 1,94% |
Ansín Agís et al. (2016) | 9 | 1,55% | 9 | 2,49% | 9 | 2,49% | 9 | 2,49% |
Galea et al. (2021) | 8 | 1,38% | 8 | 2,22% | 8 | 2,22% | 8 | 2,22% |
Galea et al. (2022) | 8 | 1,38% | 5 | 1,39% | 5 | 1,39% | 5 | 1,39% |
Totton (1930) | 8 | 1,38% | 3 | 0,83% | 3 | 0,83% | 3 | 0,83% |
Bedot (1910) | 7 | 1,21% | 5 | 1,39% | 5 | 1,39% | 5 | 1,39% |
Galea (2008) | 7 | 1,21% | 7 | 1,94% | 7 | 1,94% | 7 | 1,94% |
Bedot (1914) | 6 | 1,03% | 3 | 0,83% | 3 | 0,83% | 3 | 0,83% |
Galea (2010) | 6 | 1,03% | 6 | 1,66% | 6 | 1,66% | 6 | 1,66% |
Nelson-Smith et al. (2014) | 6 | 1,03% | 5 | 1,39% | 5 | 1,39% | 5 | 1,39% |
Allman (1888) | 5 | 0,86% | 2 | 0,55% | 2 | 0,55% | 2 | 0,55% |
Billard (1919) | 5 | 0,86% | 2 | 0,55% | 2 | 0,55% | 2 | 0,55% |
Gravier-Bonnet & Bourmaud (2006) | 5 | 0,86% | 4 | 1,11% | 4 | 1,11% | 4 | 1,11% |
Lamouroux (1816) | 5 | 0,86% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
Lindner et al. (2014) | 5 | 0,86% | 4 | 1,11% | 4 | 1,11% | 4 | 1,11% |
Galea & Maggioni (2021) | 4 | 0,69% | 4 | 1,11% | 4 | 1,11% | 4 | 1,11% |
Andouche et al. (2020) | 3 | 0,52% | 3 | 0,83% | 3 | 0,83% | 3 | 0,83% |
Bale (1888) | 3 | 0,52% | 0 | 0% | 0 | 0% | 0 | 0% |
Archives de zoologie expérimentale et générale, 57: 21-27.">Billard (1918) | 3 | 0,52% | 2 | 0,55% | 2 | 0,55% | 2 | 0,55% |
Fenner & Muir (2008) | 3 | 0,52% | 3 | 0,83% | 3 | 0,83% | 3 | 0,83% |
Galea & Ferry (2015) | 3 | 0,52% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
Godet et al. (2010) | 3 | 0,52% | 2 | 0,55% | 2 | 0,55% | 2 | 0,55% |
Linnaeus (1758) | 3 | 0,52% | 0 | 0% | 0 | 0% | 0 | 0% |
Millard (1977) | 3 | 0,52% | 2 | 0,55% | 2 | 0,55% | 2 | 0,55% |
Vervoort & Watson (2003) | 3 | 0,52% | 2 | 0,55% | 2 | 0,55% | 2 | 0,55% |
Ansin et al. (2004) | 2 | 0,34% | 2 | 0,55% | 2 | 0,55% | 2 | 0,55% |
Bale (1924) | 2 | 0,34% | 0 | 0% | 0 | 0% | 0 | 0% |
Bulletin de la Société zoologique de France, 45: 144-147.">Billard (1920) | 2 | 0,34% | 2 | 0,55% | 2 | 0,55% | 2 | 0,55% |
Breton (2014) | 2 | 0,34% | 2 | 0,55% | 2 | 0,55% | 2 | 0,55% |
Chevalier & Kuhlmann (1983) | 2 | 0,34% | 2 | 0,55% | 2 | 0,55% | 2 | 0,55% |
Forsskål (1775) | 2 | 0,34% | 2 | 0,55% | 2 | 0,55% | 2 | 0,55% |
Galea et al. (2018) | 2 | 0,34% | 2 | 0,55% | 2 | 0,55% | 2 | 0,55% |
Galea et al. (2020) | 2 | 0,34% | 2 | 0,55% | 2 | 0,55% | 2 | 0,55% |
Galea (2021) | 2 | 0,34% | 2 | 0,55% | 2 | 0,55% | 2 | 0,55% |
Gravier-Bonnet et al. (2009) | 2 | 0,34% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
Gray (1860) | 2 | 0,34% | 2 | 0,55% | 2 | 0,55% | 2 | 0,55% |
Mccrady (1859) | 2 | 0,34% | 0 | 0% | 0 | 0% | 0 | 0% |
Millard (1957) | 2 | 0,34% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
Peña Cantero & Vervoort (2003) | 2 | 0,34% | 2 | 0,55% | 2 | 0,55% | 2 | 0,55% |
Stechow (1923) | 2 | 0,34% | 2 | 0,55% | 2 | 0,55% | 2 | 0,55% |
Alder (1856) | 1 | 0,17% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
Ansin Agis et al. (2001) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Memoirs of the Museum of Comparative Zoology at Harvard College Cambridge, 37: 1-243.">Bigelow (1909) | 1 | 0,17% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
Boissin et al. (2019) | 1 | 0,17% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
Brugneaux & Pérès (2005) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Cauvin (2010) | 1 | 0,17% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
Dana (1846-1849) | 1 | 0,17% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
Diaz & Cuzange (2009) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Flot & Adjeroud (2009) | 1 | 0,17% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
Fraser (1948) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Gmelin (1791) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Goud et al. (2021) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Gravier-Bonnet et al. (2022) | 1 | 0,17% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
Gu et al. (2022) | 1 | 0,17% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
Harvard University Museum & Morris P.J. (2020) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Hassall (1848) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Hincks (1866) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Proceedings of the Zoological Society of London, 1907: 1035-1037.">Hopkinson (1907) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Impact-Mer et al. (2011) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Kayal & Kayal (2017) | 1 | 0,17% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
Kousteni et al. (2019) | 1 | 0,17% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
Lamarck (1816) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Nicet & Denis (2011) | 1 | 0,17% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
Nutting (1905) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Orrell (2019) | 1 | 0,17% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
Pearman et al. (2020) | 1 | 0,17% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
Peralta & Fautin (2013) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Questel & Le Quellec (2012) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Questel (2020) | 1 | 0,17% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
Questel (2022) | 1 | 0,17% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
Redier (1971) | 1 | 0,17% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
Richer de Forges et al. (2005) | 1 | 0,17% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
Sauvage (1886) | 1 | 0,17% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
Stechow (1932) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Svoboda & Cornelius (1991) | 1 | 0,17% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |
Trebilcock (1928) | 1 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Watson (2003) | 1 | 0,17% | 1 | 0,28% | 1 | 0,28% | 1 | 0,28% |