Gymnospermes
Ginkgoidae, Pinidae, Cycadidae et Gnetidae
78 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
| Référence | Total | Valides | Espèces | Taxons terminaux | ||||
|---|---|---|---|---|---|---|---|---|
| nb | % | nb | % | nb | % | nb | % | |
| Tison et al. (2014) | 515 | 47,55% | 365 | 98,38% | 353 | 113,87% | 301 | 90,66% |
| Munzinger et al. (2016) | 79 | 7,29% | 47 | 12,67% | 47 | 15,16% | 47 | 14,16% |
| Anonyme (2014) | 78 | 7,2% | 70 | 18,87% | 70 | 22,58% | 60 | 18,07% |
| Fournet (2002) | 64 | 5,91% | 56 | 15,09% | 56 | 18,06% | 48 | 14,46% |
| Morat et al. (2012) | 61 | 5,63% | 44 | 11,86% | 44 | 14,19% | 44 | 13,25% |
| Véron et al. (2021) | 50 | 4,62% | 49 | 13,21% | 49 | 15,81% | 49 | 14,76% |
| Linnaeus (1753) | 27 | 2,49% | 17 | 4,58% | 15 | 4,84% | 15 | 4,52% |
| Hequet & Le Corre (2010) | 20 | 1,85% | 14 | 3,77% | 13 | 4,19% | 10 | 3,01% |
| Hequet et al. (2009) | 20 | 1,85% | 14 | 3,77% | 13 | 4,19% | 10 | 3,01% |
| MacKee (1994) | 20 | 1,85% | 14 | 3,77% | 13 | 4,19% | 10 | 3,01% |
| Miller (1768) | 18 | 1,66% | 7 | 1,89% | 6 | 1,94% | 5 | 1,51% |
| Salisbury (1796) | 17 | 1,57% | 0 | 0% | 0 | 0% | 0 | 0% |
| Stevenson & Zanoni (1991) | 12 | 1,11% | 3 | 0,81% | 3 | 0,97% | 3 | 0,9% |
| Funk et al. (2007) | 11 | 1,02% | 4 | 1,08% | 4 | 1,29% | 3 | 0,9% |
| Anonyme (2023) | 8 | 0,74% | 2 | 0,54% | 0 | 0% | 2 | 0,6% |
| Rouy (1913) | 8 | 0,74% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anonyme (1938) | 5 | 0,46% | 2 | 0,54% | 2 | 0,65% | 2 | 0,6% |
| Béguinot (2012) | 5 | 0,46% | 4 | 1,08% | 4 | 1,29% | 3 | 0,9% |
| Fournier (1934-1940) | 5 | 0,46% | 0 | 0% | 0 | 0% | 0 | 0% |
| Moench (1794) | 5 | 0,46% | 1 | 0,27% | 1 | 0,32% | 1 | 0,3% |
| Arcangeli (1882) | 4 | 0,37% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bonnier & Layens (1894) | 4 | 0,37% | 0 | 0% | 0 | 0% | 0 | 0% |
| Grenier & Godron (1856) | 4 | 0,37% | 0 | 0% | 0 | 0% | 0 | 0% |
| Host (1831) | 4 | 0,37% | 2 | 0,54% | 1 | 0,32% | 1 | 0,3% |
| Lebreton et al. (2001) | 4 | 0,37% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lemée (1955) | 4 | 0,37% | 3 | 0,81% | 3 | 0,97% | 3 | 0,9% |
| Nyman (1882) | 4 | 0,37% | 0 | 0% | 0 | 0% | 0 | 0% |
| Shao & Xiang (2015) | 4 | 0,37% | 3 | 0,81% | 1 | 0,32% | 2 | 0,6% |
| Coughlan et al. (2020) | 3 | 0,28% | 3 | 0,81% | 3 | 0,97% | 3 | 0,9% |
| Delnatte & Meyer (2012) | 3 | 0,28% | 2 | 0,54% | 2 | 0,65% | 1 | 0,3% |
| Hou et al. (2015) | 3 | 0,28% | 2 | 0,54% | 2 | 0,65% | 2 | 0,6% |
| Lamarck & Candolle (1805) | 3 | 0,28% | 1 | 0,27% | 1 | 0,32% | 1 | 0,3% |
| Lamarck (1779) | 3 | 0,28% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cariot & Saint-lager (1889) | 2 | 0,18% | 0 | 0% | 0 | 0% | 0 | 0% |
| Couhia & Fleurot (2016) | 2 | 0,18% | 2 | 0,54% | 2 | 0,65% | 2 | 0,6% |
| Ferrer‐gallego & Laguna (2021) | 2 | 0,18% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fourdrigniez & Meyer (2008) | 2 | 0,18% | 2 | 0,54% | 1 | 0,32% | 1 | 0,3% |
| Garland & Moore (2012) | 2 | 0,18% | 2 | 0,54% | 2 | 0,65% | 2 | 0,6% |
| Gussone (1843) | 2 | 0,18% | 1 | 0,27% | 1 | 0,32% | 1 | 0,3% |
| Jordan & Fourreau (1903) | 2 | 0,18% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lamarck (1786) | 2 | 0,18% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lindstrom & Hill (2007) | 2 | 0,18% | 2 | 0,54% | 2 | 0,65% | 2 | 0,6% |
| Linnaeus (1763) | 2 | 0,18% | 0 | 0% | 0 | 0% | 0 | 0% |
| Shao et al. (2019) | 2 | 0,18% | 2 | 0,54% | 1 | 0,32% | 1 | 0,3% |
| Stevenson (1991) | 2 | 0,18% | 2 | 0,54% | 2 | 0,65% | 2 | 0,6% |
| Tenore (1811-1815) | 2 | 0,18% | 2 | 0,54% | 1 | 0,32% | 1 | 0,3% |
| Wiersema et al. (2018) | 2 | 0,18% | 0 | 0% | 0 | 0% | 0 | 0% |
| Brullo et al. (2021) | 1 | 0,09% | 1 | 0,27% | 1 | 0,32% | 0 | 0% |
| Candolle (1815) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Candolle (1864-1868) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Coste (1937) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Duhamel & Monceau (1806) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jolinon (1985) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lamarck (1779) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lapeyrouse (1813) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lapeyrouse (1818) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lavergne (2011) | 1 | 0,09% | 1 | 0,27% | 1 | 0,32% | 1 | 0,3% |
| Léotard & Chaline (2013) | 1 | 0,09% | 1 | 0,27% | 1 | 0,32% | 0 | 0% |
| Linnaeus (1753) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Linnaeus (1771) | 1 | 0,09% | 1 | 0,27% | 1 | 0,32% | 1 | 0,3% |
| Lowe et al. (2007) | 1 | 0,09% | 1 | 0,27% | 1 | 0,32% | 1 | 0,3% |
| Maire (1928) | 1 | 0,09% | 1 | 0,27% | 0 | 0% | 1 | 0,3% |
| Marais (1997) | 1 | 0,09% | 1 | 0,27% | 1 | 0,32% | 1 | 0,3% |
| Meyer et al. (2006) | 1 | 0,09% | 1 | 0,27% | 0 | 0% | 1 | 0,3% |
| Molino et al. (2009) | 1 | 0,09% | 1 | 0,27% | 1 | 0,32% | 0 | 0% |
| Morat & Veillon (1985) | 1 | 0,09% | 1 | 0,27% | 1 | 0,32% | 0 | 0% |
| Nouals & Bariteau (1993) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Orlova et al. (2016) | 1 | 0,09% | 1 | 0,27% | 1 | 0,32% | 1 | 0,3% |
| Persoon (1807) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Presl & Presl (1822) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rabasse et al. (2005) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rivière (2003) | 1 | 0,09% | 1 | 0,27% | 1 | 0,32% | 0 | 0% |
| Scopoli (1771) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sibthorp & Smith (1813-1816) | 1 | 0,09% | 1 | 0,27% | 1 | 0,32% | 1 | 0,3% |
| Sprengel (1826) | 1 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Stevenson (1991) | 1 | 0,09% | 1 | 0,27% | 1 | 0,32% | 0 | 0% |
| Tassin et al. (2006) | 1 | 0,09% | 1 | 0,27% | 1 | 0,32% | 0 | 0% |
| Wilcox & Platt (2002) | 1 | 0,09% | 1 | 0,27% | 1 | 0,32% | 1 | 0,3% |
