Ascidies de Nouvelle-Calédonie
84 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
| Référence | Total | Valides | Espèces | Taxons terminaux | ||||
|---|---|---|---|---|---|---|---|---|
| nb | % | nb | % | nb | % | nb | % | |
| Monniot (2007) | 289 | 34,57% | 239 | 77,1% | 238 | 77,02% | 238 | 77,02% |
| Monniot & Monniot (1991) | 66 | 7,89% | 60 | 19,35% | 60 | 19,42% | 60 | 19,42% |
| Monniot & Monniot (1987) | 56 | 6,7% | 48 | 15,48% | 48 | 15,53% | 47 | 15,21% |
| Kott (2001) | 48 | 5,74% | 43 | 13,87% | 43 | 13,92% | 43 | 13,92% |
| Ifremer (2009) | 31 | 3,71% | 30 | 9,68% | 30 | 9,71% | 30 | 9,71% |
| Monniot (1988) | 29 | 3,47% | 22 | 7,1% | 22 | 7,12% | 22 | 7,12% |
| Lafargue & Vasseur (1989) | 25 | 2,99% | 18 | 5,81% | 18 | 5,83% | 18 | 5,83% |
| Uicn et al. (2019) | 22 | 2,63% | 21 | 6,77% | 21 | 6,8% | 15 | 4,85% |
| Milne-Edwards (1841) | 15 | 1,79% | 0 | 0% | 0 | 0% | 0 | 0% |
| Monniot (1989) | 13 | 1,56% | 13 | 4,19% | 13 | 4,21% | 13 | 4,21% |
| Giard (1872) | 11 | 1,32% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gravier (1955) | 11 | 1,32% | 5 | 1,61% | 5 | 1,62% | 4 | 1,29% |
| Monniot (1992) | 10 | 1,2% | 10 | 3,23% | 10 | 3,24% | 10 | 3,24% |
| Monniot (1983) | 9 | 1,08% | 3 | 0,97% | 3 | 0,97% | 3 | 0,97% |
| Monniot (1983) | 9 | 1,08% | 6 | 1,94% | 6 | 1,94% | 5 | 1,62% |
| Bay-nouailhat & Bay-nouailhat (2020) | 8 | 0,96% | 8 | 2,58% | 8 | 2,59% | 8 | 2,59% |
| Monniot & Monniot (2003) | 8 | 0,96% | 8 | 2,58% | 8 | 2,59% | 8 | 2,59% |
| Monniot & Monniot (2008) | 8 | 0,96% | 8 | 2,58% | 8 | 2,59% | 8 | 2,59% |
| Monniot (1983) | 8 | 0,96% | 7 | 2,26% | 7 | 2,27% | 7 | 2,27% |
| Monniot (2021) | 8 | 0,96% | 8 | 2,58% | 8 | 2,59% | 8 | 2,59% |
| Pearman et al. (2020) | 7 | 0,84% | 6 | 1,94% | 5 | 1,62% | 6 | 1,94% |
| Monniot & Monniot (1985) | 6 | 0,72% | 1 | 0,32% | 1 | 0,32% | 1 | 0,32% |
| Monniot (1983) | 6 | 0,72% | 4 | 1,29% | 4 | 1,29% | 4 | 1,29% |
| Monniot (1994) | 6 | 0,72% | 4 | 1,29% | 4 | 1,29% | 4 | 1,29% |
| Monniot (2016) | 6 | 0,72% | 5 | 1,61% | 5 | 1,62% | 5 | 1,62% |
| Monniot (2018) | 6 | 0,72% | 5 | 1,61% | 5 | 1,62% | 5 | 1,62% |
| Monniot (2022) | 5 | 0,6% | 5 | 1,61% | 5 | 1,62% | 5 | 1,62% |
| Monniot & Monniot (1984) | 4 | 0,48% | 3 | 0,97% | 3 | 0,97% | 3 | 0,97% |
| Monniot (1990) | 4 | 0,48% | 4 | 1,29% | 4 | 1,29% | 4 | 1,29% |
| Monniot (2018) | 4 | 0,48% | 4 | 1,29% | 4 | 1,29% | 4 | 1,29% |
| Monniot & Debitus (2015) | 3 | 0,36% | 3 | 0,97% | 3 | 0,97% | 3 | 0,97% |
| Monniot & Monniot (1983) | 3 | 0,36% | 3 | 0,97% | 3 | 0,97% | 3 | 0,97% |
| Monniot (comm. pers., 2012) | 3 | 0,36% | 3 | 0,97% | 3 | 0,97% | 3 | 0,97% |
| Monniot (2018) | 3 | 0,36% | 3 | 0,97% | 3 | 0,97% | 2 | 0,65% |
| Nelson-Smith et al. (2014) | 3 | 0,36% | 1 | 0,32% | 1 | 0,32% | 1 | 0,32% |
| Bouzon et al. (2014) | 2 | 0,24% | 2 | 0,65% | 2 | 0,65% | 2 | 0,65% |
| Godet et al. (2010) | 2 | 0,24% | 2 | 0,65% | 2 | 0,65% | 2 | 0,65% |
| Goulletquer (2016) | 2 | 0,24% | 2 | 0,65% | 2 | 0,65% | 2 | 0,65% |
| Monniot & Monniot (1974) | 2 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
| Monniot & Monniot (1977) | 2 | 0,24% | 2 | 0,65% | 2 | 0,65% | 2 | 0,65% |
| Monniot & Monniot (1984) | 2 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
| Monniot & Monniot (1987) | 2 | 0,24% | 2 | 0,65% | 2 | 0,65% | 2 | 0,65% |
| Monniot & Monniot (1990) | 2 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
| Monniot (1986) | 2 | 0,24% | 2 | 0,65% | 2 | 0,65% | 2 | 0,65% |
| Monniot (1994) | 2 | 0,24% | 2 | 0,65% | 2 | 0,65% | 2 | 0,65% |
| Monniot (2007) | 2 | 0,24% | 2 | 0,65% | 2 | 0,65% | 2 | 0,65% |
| Pruvot-Fol (1929) | 2 | 0,24% | 2 | 0,65% | 2 | 0,65% | 2 | 0,65% |
| Questel (2020) | 2 | 0,24% | 1 | 0,32% | 1 | 0,32% | 1 | 0,32% |
| Rocha & Monniot (1993) | 2 | 0,24% | 2 | 0,65% | 2 | 0,65% | 2 | 0,65% |
| Schleyer et al. (2016) | 2 | 0,24% | 1 | 0,32% | 1 | 0,32% | 1 | 0,32% |
| Sentz‐Braconnot (1966) | 2 | 0,24% | 2 | 0,65% | 2 | 0,65% | 2 | 0,65% |
| Sluiter (1890) | 2 | 0,24% | 2 | 0,65% | 2 | 0,65% | 2 | 0,65% |
| Sluiter (1904) | 2 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
| Traustedt (1882) | 2 | 0,24% | 2 | 0,65% | 2 | 0,65% | 2 | 0,65% |
| Arnaud (1974) | 1 | 0,12% | 1 | 0,32% | 1 | 0,32% | 1 | 0,32% |
| Bishop et al. (2013) | 1 | 0,12% | 1 | 0,32% | 1 | 0,32% | 1 | 0,32% |
| Breton (2005) | 1 | 0,12% | 1 | 0,32% | 1 | 0,32% | 1 | 0,32% |
| Breton (2014) | 1 | 0,12% | 1 | 0,32% | 1 | 0,32% | 1 | 0,32% |
| Dewarumez et al. (2011) | 1 | 0,12% | 1 | 0,32% | 1 | 0,32% | 1 | 0,32% |
| Eldredge (1967) | 1 | 0,12% | 1 | 0,32% | 1 | 0,32% | 1 | 0,32% |
| Fougue (1961) | 1 | 0,12% | 1 | 0,32% | 1 | 0,32% | 1 | 0,32% |
| Harant (1924) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Heller (1878) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Herdman (1882) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Herdman (1886) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kim & Boxshall (2020) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Michaelsen (1921) | 1 | 0,12% | 1 | 0,32% | 1 | 0,32% | 1 | 0,32% |
| Monniot & Monniot (1977) | 1 | 0,12% | 1 | 0,32% | 1 | 0,32% | 1 | 0,32% |
| Monniot & Monniot (1991) | 1 | 0,12% | 1 | 0,32% | 1 | 0,32% | 1 | 0,32% |
| Monniot & Monniot (2001) | 1 | 0,12% | 1 | 0,32% | 1 | 0,32% | 1 | 0,32% |
| Monniot & Monniot (2006) | 1 | 0,12% | 1 | 0,32% | 1 | 0,32% | 1 | 0,32% |
| Monniot & Tatián (2020) | 1 | 0,12% | 1 | 0,32% | 1 | 0,32% | 1 | 0,32% |
| Monniot et al. (1991) | 1 | 0,12% | 1 | 0,32% | 1 | 0,32% | 1 | 0,32% |
| Monniot et al. (2011) | 1 | 0,12% | 1 | 0,32% | 1 | 0,32% | 1 | 0,32% |
| Monniot (1969) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Monniot (1978) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Monniot (1983) | 1 | 0,12% | 1 | 0,32% | 1 | 0,32% | 1 | 0,32% |
| Monniot (1983) | 1 | 0,12% | 1 | 0,32% | 1 | 0,32% | 1 | 0,32% |
| Monniot (1988) | 1 | 0,12% | 1 | 0,32% | 1 | 0,32% | 1 | 0,32% |
| Renier (1804) | 1 | 0,12% | 1 | 0,32% | 1 | 0,32% | 1 | 0,32% |
| Richer de Forges et al. (2005) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Stimpson (1852) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Tokioka (1954) | 1 | 0,12% | 1 | 0,32% | 1 | 0,32% | 1 | 0,32% |
| Van Name (1918) | 1 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
