Porifères de Nouvelle-Calédonie
Porifera de Nouvelle-Calédonie
144 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
Référence | Total | Valides | Espèces | Taxons terminaux | ||||
---|---|---|---|---|---|---|---|---|
nb | % | nb | % | nb | % | nb | % | |
Richer de Forges et al. (2005) | 208 | 23,91% | 159 | 37,32% | 159 | 37,5% | 157 | 37,03% |
Hooper & Schlacher-Hoenlinger (2007) | 141 | 16,21% | 129 | 30,28% | 129 | 30,42% | 129 | 30,42% |
Lévi (1993) | 69 | 7,93% | 55 | 12,91% | 55 | 12,97% | 55 | 12,97% |
Tabachnick & Lévi (2004) | 54 | 6,21% | 50 | 11,74% | 48 | 11,32% | 49 | 11,56% |
Lévi & Lévi (1983) | 53 | 6,09% | 43 | 10,09% | 43 | 10,14% | 43 | 10,14% |
Lévi & Lévi (1983b) | 40 | 4,6% | 26 | 6,1% | 25 | 5,9% | 26 | 6,13% |
Desqueyroux-faúndez (1984) | 31 | 3,56% | 25 | 5,87% | 25 | 5,9% | 25 | 5,9% |
Tabachnick & Lévi (2000) | 31 | 3,56% | 25 | 5,87% | 25 | 5,9% | 25 | 5,9% |
Hooper & Levi (1993) | 26 | 2,99% | 22 | 5,16% | 22 | 5,19% | 22 | 5,19% |
Levi (1967) | 20 | 2,3% | 9 | 2,11% | 9 | 2,12% | 9 | 2,12% |
Schlacher-Hoenlinger et al. (2005) | 19 | 2,18% | 19 | 4,46% | 19 | 4,48% | 19 | 4,48% |
Hooper & Lévi (1993) | 17 | 1,95% | 4 | 0,94% | 4 | 0,94% | 4 | 0,94% |
Vacelet (1981) | 16 | 1,84% | 16 | 3,76% | 16 | 3,77% | 16 | 3,77% |
Van et al. (2015) | 13 | 1,49% | 13 | 3,05% | 13 | 3,07% | 13 | 3,07% |
Haeckel (1872) | 11 | 1,26% | 2 | 0,47% | 2 | 0,47% | 2 | 0,47% |
Borojevic & Klautau (2000) | 10 | 1,15% | 9 | 2,11% | 9 | 2,12% | 9 | 2,12% |
Vacelet (2020) | 10 | 1,15% | 7 | 1,64% | 7 | 1,65% | 7 | 1,65% |
Dendy (1905) | 9 | 1,03% | 2 | 0,47% | 2 | 0,47% | 2 | 0,47% |
Vacelet (1977) | 9 | 1,03% | 6 | 1,41% | 6 | 1,42% | 6 | 1,42% |
Hooper & Van Soest (2002) | 8 | 0,92% | 4 | 0,94% | 4 | 0,94% | 4 | 0,94% |
Van Soest et al. (2020) | 8 | 0,92% | 5 | 1,17% | 5 | 1,18% | 5 | 1,18% |
Borojevic (1967) | 7 | 0,8% | 4 | 0,94% | 4 | 0,94% | 4 | 0,94% |
Lévi & Lévi (1982) | 7 | 0,8% | 4 | 0,94% | 4 | 0,94% | 4 | 0,94% |
Bourmaud (2003) | 6 | 0,69% | 4 | 0,94% | 4 | 0,94% | 4 | 0,94% |
Desqueyroux-faúndez (1987) | 6 | 0,69% | 6 | 1,41% | 6 | 1,42% | 6 | 1,42% |
Klautau et al. (2020) | 6 | 0,69% | 6 | 1,41% | 6 | 1,42% | 6 | 1,42% |
Ridley & Dendy (1886) | 6 | 0,69% | 3 | 0,7% | 3 | 0,71% | 3 | 0,71% |
Vacelet (1961) | 5 | 0,57% | 3 | 0,7% | 3 | 0,71% | 3 | 0,71% |
Vacelet (1967) | 5 | 0,57% | 5 | 1,17% | 5 | 1,18% | 5 | 1,18% |
Vacelet (1969) | 5 | 0,57% | 2 | 0,47% | 2 | 0,47% | 2 | 0,47% |
Valderrama et al. (2009) | 5 | 0,57% | 5 | 1,17% | 5 | 1,18% | 5 | 1,18% |
Volkmer-Ribeiro & Rützler (1997) | 5 | 0,57% | 5 | 1,17% | 5 | 1,18% | 5 | 1,18% |
Australian Museum (2020) | 4 | 0,46% | 4 | 0,94% | 4 | 0,94% | 4 | 0,94% |
Barucca et al. (2007) | 4 | 0,46% | 4 | 0,94% | 4 | 0,94% | 4 | 0,94% |
Carter (1885) | 4 | 0,46% | 2 | 0,47% | 2 | 0,47% | 2 | 0,47% |
Ekins et al. (2023) | 4 | 0,46% | 3 | 0,7% | 3 | 0,71% | 3 | 0,71% |
Fourt et al. (2017) | 4 | 0,46% | 4 | 0,94% | 4 | 0,94% | 4 | 0,94% |
Hall et al. (2013) | 4 | 0,46% | 3 | 0,7% | 3 | 0,71% | 3 | 0,71% |
Lage et al. (2018) | 4 | 0,46% | 4 | 0,94% | 4 | 0,94% | 4 | 0,94% |
Laubenfels (1957) | 4 | 0,46% | 0 | 0% | 0 | 0% | 0 | 0% |
Lévi & Lévi (1988) | 4 | 0,46% | 4 | 0,94% | 4 | 0,94% | 4 | 0,94% |
Pérez et al. (2017) | 4 | 0,46% | 4 | 0,94% | 4 | 0,94% | 4 | 0,94% |
Reiswig & Kelly (2016) | 4 | 0,46% | 4 | 0,94% | 4 | 0,94% | 4 | 0,94% |
Sarà (1988) | 4 | 0,46% | 4 | 0,94% | 4 | 0,94% | 4 | 0,94% |
Vacelet (1967) | 4 | 0,46% | 4 | 0,94% | 4 | 0,94% | 4 | 0,94% |
Van Soest et al. (2021) | 4 | 0,46% | 4 | 0,94% | 4 | 0,94% | 4 | 0,94% |
Alcolado & Busutil (2012) | 3 | 0,34% | 3 | 0,7% | 3 | 0,71% | 3 | 0,71% |
Boury-esnault et al. (1982) | 3 | 0,34% | 0 | 0% | 0 | 0% | 0 | 0% |
Transactions of the Linnean Society of London, 18: 1-164.">Dendy (1922) | 3 | 0,34% | 2 | 0,47% | 2 | 0,47% | 2 | 0,47% |
Ekins et al. (2016) | 3 | 0,34% | 3 | 0,7% | 3 | 0,71% | 3 | 0,71% |
Ekins et al. (2018) | 3 | 0,34% | 3 | 0,7% | 3 | 0,71% | 3 | 0,71% |
Keller (1889) | 3 | 0,34% | 0 | 0% | 0 | 0% | 0 | 0% |
Lévi & Lévi (1979) | 3 | 0,34% | 3 | 0,7% | 3 | 0,71% | 3 | 0,71% |
Levi (1983) | 3 | 0,34% | 0 | 0% | 0 | 0% | 0 | 0% |
Poléjaeff (1883) | 3 | 0,34% | 2 | 0,47% | 2 | 0,47% | 2 | 0,47% |
Ridley (1884) | 3 | 0,34% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Tabachnick at al. (2011) | 3 | 0,34% | 3 | 0,7% | 3 | 0,71% | 3 | 0,71% |
Vacelet (1982) | 3 | 0,34% | 3 | 0,7% | 3 | 0,71% | 3 | 0,71% |
Woerheide et al. (2002) | 3 | 0,34% | 3 | 0,7% | 3 | 0,71% | 3 | 0,71% |
Adjeroud (1997) | 2 | 0,23% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Alvarez et al. (2000) | 2 | 0,23% | 2 | 0,47% | 2 | 0,47% | 2 | 0,47% |
Alvarez et al. (2008) | 2 | 0,23% | 2 | 0,47% | 2 | 0,47% | 2 | 0,47% |
Bergquist & Kelly-borges (1991) | 2 | 0,23% | 2 | 0,47% | 2 | 0,47% | 2 | 0,47% |
Bourcier (1988) | 2 | 0,23% | 2 | 0,47% | 2 | 0,47% | 2 | 0,47% |
Carteron & Pouget (2008) | 2 | 0,23% | 2 | 0,47% | 2 | 0,47% | 2 | 0,47% |
Castello-branco & Hajdu (2018) | 2 | 0,23% | 2 | 0,47% | 2 | 0,47% | 2 | 0,47% |
Dendy (192) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Diaz & Cuzange (2009) | 2 | 0,23% | 2 | 0,47% | 2 | 0,47% | 2 | 0,47% |
Duchassaing & Michelotti (1864) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Fontana et al. (2018) | 2 | 0,23% | 2 | 0,47% | 2 | 0,47% | 2 | 0,47% |
Hartman & Goreau (1976) | 2 | 0,23% | 2 | 0,47% | 2 | 0,47% | 2 | 0,47% |
Hartman & Goreau (1975) | 2 | 0,23% | 2 | 0,47% | 2 | 0,47% | 2 | 0,47% |
Hooper & Bergquist (1992) | 2 | 0,23% | 2 | 0,47% | 2 | 0,47% | 2 | 0,47% |
Hooper et al. (1999) | 2 | 0,23% | 2 | 0,47% | 2 | 0,47% | 2 | 0,47% |
Hooper (1991) | 2 | 0,23% | 2 | 0,47% | 2 | 0,47% | 2 | 0,47% |
Kieschnick (1896) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Lister (1900) | 2 | 0,23% | 2 | 0,47% | 2 | 0,47% | 2 | 0,47% |
Little (1968) | 2 | 0,23% | 2 | 0,47% | 2 | 0,47% | 2 | 0,47% |
Questel & Le Quellec (2012) | 2 | 0,23% | 2 | 0,47% | 2 | 0,47% | 2 | 0,47% |
Questel (2020) | 2 | 0,23% | 2 | 0,47% | 2 | 0,47% | 2 | 0,47% |
Row & Hôzawa (1931) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Ruiz et al. (2015) | 2 | 0,23% | 2 | 0,47% | 2 | 0,47% | 2 | 0,47% |
Salvat & Bacchet (2011) | 2 | 0,23% | 2 | 0,47% | 2 | 0,47% | 2 | 0,47% |
Samaai et al. (2006) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Samaai et al. (2009) | 2 | 0,23% | 2 | 0,47% | 2 | 0,47% | 2 | 0,47% |
Sara et al. (1992) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Sarà et al. (2000) | 2 | 0,23% | 2 | 0,47% | 2 | 0,47% | 2 | 0,47% |
Schleyer et al. (2016) | 2 | 0,23% | 2 | 0,47% | 2 | 0,47% | 2 | 0,47% |
Thiele (1898) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Topsent (1890) | 2 | 0,23% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Topsent (1892) | 2 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Vacelet et al. (1992) | 2 | 0,23% | 2 | 0,47% | 2 | 0,47% | 2 | 0,47% |
Woerheide et al. (2002) | 2 | 0,23% | 2 | 0,47% | 2 | 0,47% | 2 | 0,47% |
Amade et al. (1982) | 1 | 0,11% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Arnaud (1974) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Ayling (1982) | 1 | 0,11% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Barboza du Bocage (1869) | 1 | 0,11% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Blainville (1834) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Bowerbank (1873) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Records of the Indian Museum, 30(1): pp. 109-138.">Burton (1928) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Carter (1880) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Carter (1881) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Carter (1882) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Carter (1883) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Dendy & Frederick (1924) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Dendy (1887) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Transactions of the Linnean Society 2nd Ser Zoology London, 16: 1-29.">Dendy (1913) | 1 | 0,11% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Dendy (1924) | 1 | 0,11% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Descatoire (1966) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Ehlers (1872) | 1 | 0,11% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Erpenbeck et al. (2012) | 1 | 0,11% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Esper ([1791]-1794) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Fallon et al. (2005) | 1 | 0,11% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Fromont (1998) | 1 | 0,11% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Goud et al. (2021) | 1 | 0,11% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Hansson (1999) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Higgin (1877) | 1 | 0,11% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Ifremer (2022) | 1 | 0,11% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Janussen & Downey (2021) | 1 | 0,11% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Kelly-Borges & Bergquist (1997) | 1 | 0,11% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Kirkpatrick (1908) | 1 | 0,11% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Kirkpatrick (1910) | 1 | 0,11% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Laubenfels (1936) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Lendenfeld (1887) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Lévi (1956) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Pisera & Vacelet (2011) | 1 | 0,11% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Quod et al. (1995) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Ramsby et al. (2018) | 1 | 0,11% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Reiswig & Kelly (2011) | 1 | 0,11% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Richmond (1997) | 1 | 0,11% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Ridley & Dendy (1886) | 1 | 0,11% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Sim-smith & Kelly (2019) | 1 | 0,11% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Sollas (1908) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Thiele (1899) | 1 | 0,11% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Thiele (1900) | 1 | 0,11% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Tomono et al. (1998) | 1 | 0,11% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Topsent (1891) | 1 | 0,11% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Topsent (1914) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Uicn et al. (2019) | 1 | 0,11% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Vacelet (1984) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Van et al. (2018) | 1 | 0,11% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Voigt et al. (2012) | 1 | 0,11% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
West et al. (2013) | 1 | 0,11% | 1 | 0,23% | 1 | 0,24% | 1 | 0,24% |
Wilson (1902) | 1 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |