Ascidies de Guadeloupe et de Martinique
52 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) | 35 | 7,48% | 25 | 21,37% | 25 | 21,55% | 24 | 20,69% |
| Gravier (1955) | 31 | 6,62% | 17 | 14,53% | 17 | 14,66% | 17 | 14,66% |
| Monniot (1983) | 28 | 5,98% | 16 | 13,68% | 16 | 13,79% | 16 | 13,79% |
| Monniot & Monniot (1987) | 24 | 5,13% | 20 | 17,09% | 20 | 17,24% | 19 | 16,38% |
| Uicn et al. (2019) | 22 | 4,7% | 21 | 17,95% | 21 | 18,1% | 20 | 17,24% |
| Monniot (1983) | 20 | 4,27% | 17 | 14,53% | 17 | 14,66% | 17 | 14,66% |
| Monniot (2016) | 20 | 4,27% | 17 | 14,53% | 17 | 14,66% | 17 | 14,66% |
| Monniot (2018) | 19 | 4,06% | 18 | 15,38% | 18 | 15,52% | 18 | 15,52% |
| Monniot (1983) | 18 | 3,85% | 17 | 14,53% | 17 | 14,66% | 16 | 13,79% |
| Monniot (1983) | 17 | 3,63% | 13 | 11,11% | 13 | 11,21% | 13 | 11,21% |
| Lafargue & Vasseur (1989) | 15 | 3,21% | 11 | 9,4% | 11 | 9,48% | 9 | 7,76% |
| Monniot (1983) | 13 | 2,78% | 13 | 11,11% | 13 | 11,21% | 13 | 11,21% |
| Monniot & Monniot (1984) | 12 | 2,56% | 8 | 6,84% | 8 | 6,9% | 8 | 6,9% |
| Monniot (2018) | 12 | 2,56% | 12 | 10,26% | 12 | 10,34% | 12 | 10,34% |
| Bay-nouailhat & Bay-nouailhat (2020) | 9 | 1,92% | 9 | 7,69% | 9 | 7,76% | 9 | 7,76% |
| Monniot (1984) | 9 | 1,92% | 8 | 6,84% | 6 | 5,17% | 8 | 6,9% |
| Monniot (1983) | 7 | 1,5% | 6 | 5,13% | 6 | 5,17% | 6 | 5,17% |
| Monniot (2018) | 7 | 1,5% | 7 | 5,98% | 7 | 6,03% | 7 | 6,03% |
| Questel (2020) | 7 | 1,5% | 6 | 5,13% | 6 | 5,17% | 6 | 5,17% |
| Milne-Edwards (1841) | 6 | 1,28% | 0 | 0% | 0 | 0% | 0 | 0% |
| Giard (1872) | 5 | 1,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Goulletquer (2016) | 4 | 0,85% | 4 | 3,42% | 4 | 3,45% | 4 | 3,45% |
| Shenkar & Swalla (2010) | 4 | 0,85% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Monniot & Monniot (1987) | 3 | 0,64% | 3 | 2,56% | 3 | 2,59% | 3 | 2,59% |
| Nelson-Smith et al. (2014) | 3 | 0,64% | 2 | 1,71% | 2 | 1,72% | 2 | 1,72% |
| Ordóñez et al. (2016) | 3 | 0,64% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Breton (2014) | 2 | 0,43% | 2 | 1,71% | 2 | 1,72% | 2 | 1,72% |
| Millar & Goodbody (1974) | 2 | 0,43% | 2 | 1,71% | 2 | 1,72% | 2 | 1,72% |
| Monniot (1969) | 2 | 0,43% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Monniot (1986) | 2 | 0,43% | 2 | 1,71% | 2 | 1,72% | 2 | 1,72% |
| Monniot (1994) | 2 | 0,43% | 2 | 1,71% | 2 | 1,72% | 2 | 1,72% |
| Monniot (2016) | 2 | 0,43% | 2 | 1,71% | 2 | 1,72% | 2 | 1,72% |
| Pineda et al. (2011) | 2 | 0,43% | 2 | 1,71% | 2 | 1,72% | 2 | 1,72% |
| Questel & Le Quellec (2012) | 2 | 0,43% | 2 | 1,71% | 2 | 1,72% | 2 | 1,72% |
| Sluiter (1890) | 2 | 0,43% | 2 | 1,71% | 2 | 1,72% | 2 | 1,72% |
| Traustedt (1882) | 2 | 0,43% | 2 | 1,71% | 2 | 1,72% | 2 | 1,72% |
| Brunetti & Mastrototaro (2004) | 1 | 0,21% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Dewarumez et al. (2011) | 1 | 0,21% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Fougue (1961) | 1 | 0,21% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Godet et al. (2010) | 1 | 0,21% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Harant (1924) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
| Herdman (1886) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lafargue (1968) | 1 | 0,21% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Lizé (2019) | 1 | 0,21% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Monniot (1978) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
| Monniot (2007) | 1 | 0,21% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Monniot (2016) | 1 | 0,21% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Rignault & Chevallier (2017) | 1 | 0,21% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
| Salfi (1929) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
| Schleyer et al. (2016) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
| Stimpson (1852) | 1 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ulman et al. (2017) | 1 | 0,21% | 1 | 0,85% | 1 | 0,86% | 1 | 0,86% |
