Ascidies de Martinique
41 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
| Référence | Total | Valides | Espèces | Taxons terminaux | ||||
|---|---|---|---|---|---|---|---|---|
| nb | % | nb | % | nb | % | nb | % | |
| Gravier (1955) | 25 | 8,14% | 12 | 21,82% | 12 | 21,82% | 12 | 21,82% |
| Monniot (2007) | 23 | 7,49% | 14 | 25,45% | 14 | 25,45% | 14 | 25,45% |
| Monniot (2018) | 19 | 6,19% | 18 | 32,73% | 18 | 32,73% | 18 | 32,73% |
| Monniot (1983) | 18 | 5,86% | 9 | 16,36% | 9 | 16,36% | 9 | 16,36% |
| Monniot (1983) | 16 | 5,21% | 12 | 21,82% | 12 | 21,82% | 12 | 21,82% |
| Uicn et al. (2019) | 16 | 5,21% | 15 | 27,27% | 15 | 27,27% | 15 | 27,27% |
| Monniot (1983) | 15 | 4,89% | 12 | 21,82% | 12 | 21,82% | 12 | 21,82% |
| Monniot (2016) | 14 | 4,56% | 12 | 21,82% | 12 | 21,82% | 12 | 21,82% |
| Monniot & Monniot (1987) | 13 | 4,23% | 9 | 16,36% | 9 | 16,36% | 9 | 16,36% |
| Lafargue & Vasseur (1989) | 12 | 3,91% | 8 | 14,55% | 8 | 14,55% | 8 | 14,55% |
| Monniot (2018) | 12 | 3,91% | 12 | 21,82% | 12 | 21,82% | 12 | 21,82% |
| Monniot (2018) | 7 | 2,28% | 7 | 12,73% | 7 | 12,73% | 7 | 12,73% |
| Milne-Edwards (1841) | 6 | 1,95% | 0 | 0% | 0 | 0% | 0 | 0% |
| Monniot & Monniot (1984) | 5 | 1,63% | 1 | 1,82% | 1 | 1,82% | 1 | 1,82% |
| Questel (2020) | 4 | 1,3% | 3 | 5,45% | 3 | 5,45% | 3 | 5,45% |
| Shenkar & Swalla (2010) | 4 | 1,3% | 1 | 1,82% | 1 | 1,82% | 1 | 1,82% |
| Bay-nouailhat & Bay-nouailhat (2020) | 3 | 0,98% | 3 | 5,45% | 3 | 5,45% | 3 | 5,45% |
| Giard (1872) | 3 | 0,98% | 0 | 0% | 0 | 0% | 0 | 0% |
| Monniot (1983) | 3 | 0,98% | 3 | 5,45% | 3 | 5,45% | 3 | 5,45% |
| Monniot (1969) | 2 | 0,65% | 1 | 1,82% | 1 | 1,82% | 1 | 1,82% |
| Monniot (1983) | 2 | 0,65% | 2 | 3,64% | 2 | 3,64% | 2 | 3,64% |
| Monniot (1984) | 2 | 0,65% | 1 | 1,82% | 1 | 1,82% | 1 | 1,82% |
| Monniot (1994) | 2 | 0,65% | 2 | 3,64% | 2 | 3,64% | 2 | 3,64% |
| Monniot (2016) | 2 | 0,65% | 2 | 3,64% | 2 | 3,64% | 2 | 3,64% |
| Nelson-Smith et al. (2014) | 2 | 0,65% | 1 | 1,82% | 1 | 1,82% | 1 | 1,82% |
| Breton (2014) | 1 | 0,33% | 1 | 1,82% | 1 | 1,82% | 1 | 1,82% |
| Brunetti & Mastrototaro (2004) | 1 | 0,33% | 1 | 1,82% | 1 | 1,82% | 1 | 1,82% |
| Dewarumez et al. (2011) | 1 | 0,33% | 1 | 1,82% | 1 | 1,82% | 1 | 1,82% |
| Fougue (1961) | 1 | 0,33% | 1 | 1,82% | 1 | 1,82% | 1 | 1,82% |
| Godet et al. (2010) | 1 | 0,33% | 1 | 1,82% | 1 | 1,82% | 1 | 1,82% |
| Goulletquer (2016) | 1 | 0,33% | 1 | 1,82% | 1 | 1,82% | 1 | 1,82% |
| Harant (1924) | 1 | 0,33% | 0 | 0% | 0 | 0% | 0 | 0% |
| Herdman (1886) | 1 | 0,33% | 0 | 0% | 0 | 0% | 0 | 0% |
| Monniot & Monniot (1987) | 1 | 0,33% | 1 | 1,82% | 1 | 1,82% | 1 | 1,82% |
| Monniot (1978) | 1 | 0,33% | 0 | 0% | 0 | 0% | 0 | 0% |
| Monniot (1983) | 1 | 0,33% | 1 | 1,82% | 1 | 1,82% | 1 | 1,82% |
| Monniot (2016) | 1 | 0,33% | 1 | 1,82% | 1 | 1,82% | 1 | 1,82% |
| Questel & Le Quellec (2012) | 1 | 0,33% | 1 | 1,82% | 1 | 1,82% | 1 | 1,82% |
| Rignault & Chevallier (2017) | 1 | 0,33% | 1 | 1,82% | 1 | 1,82% | 1 | 1,82% |
| Schleyer et al. (2016) | 1 | 0,33% | 0 | 0% | 0 | 0% | 0 | 0% |
| Stimpson (1852) | 1 | 0,33% | 0 | 0% | 0 | 0% | 0 | 0% |
