Pinidae et Cupressidae
Pinidae et Cupressidae
71 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) | 492 | 49,5% | 352 | 101,44% | 345 | 119,38% | 290 | 93,55% |
Anonyme (2014) | 78 | 7,85% | 70 | 20,17% | 70 | 24,22% | 60 | 19,35% |
Munzinger et al. (2016) | 77 | 7,75% | 46 | 13,26% | 46 | 15,92% | 46 | 14,84% |
Morat et al. (2012) | 60 | 6,04% | 43 | 12,39% | 43 | 14,88% | 43 | 13,87% |
Véron et al. (2021) | 50 | 5,03% | 49 | 14,12% | 49 | 16,96% | 49 | 15,81% |
Fournet (2002) | 40 | 4,02% | 32 | 9,22% | 32 | 11,07% | 24 | 7,74% |
Linnaeus (1753) | 25 | 2,52% | 15 | 4,32% | 14 | 4,84% | 14 | 4,52% |
Hequet & Le Corre (2010) | 18 | 1,81% | 12 | 3,46% | 11 | 3,81% | 8 | 2,58% |
Hequet et al. (2009) | 18 | 1,81% | 12 | 3,46% | 11 | 3,81% | 8 | 2,58% |
MacKee (1994) | 18 | 1,81% | 12 | 3,46% | 11 | 3,81% | 8 | 2,58% |
Miller (1768) | 18 | 1,81% | 7 | 2,02% | 6 | 2,08% | 5 | 1,61% |
Salisbury (1796) | 17 | 1,71% | 0 | 0% | 0 | 0% | 0 | 0% |
Rouy (1913) | 8 | 0,8% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme (2023) | 7 | 0,7% | 2 | 0,58% | 0 | 0% | 2 | 0,65% |
Anonyme (1938) | 5 | 0,5% | 2 | 0,58% | 2 | 0,69% | 2 | 0,65% |
Béguinot (2012) | 5 | 0,5% | 4 | 1,15% | 4 | 1,38% | 3 | 0,97% |
Moench (1794) | 5 | 0,5% | 1 | 0,29% | 1 | 0,35% | 1 | 0,32% |
Arcangeli (1882) | 4 | 0,4% | 0 | 0% | 0 | 0% | 0 | 0% |
Fournier (1934-1940) | 4 | 0,4% | 0 | 0% | 0 | 0% | 0 | 0% |
Lebreton et al. (2001) | 4 | 0,4% | 0 | 0% | 0 | 0% | 0 | 0% |
Shao & Xiang (2015) | 4 | 0,4% | 3 | 0,86% | 1 | 0,35% | 2 | 0,65% |
Coughlan et al. (2020) | 3 | 0,3% | 3 | 0,86% | 3 | 1,04% | 3 | 0,97% |
Grenier & Godron (1856) | 3 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
Lamarck & Candolle (1805) | 3 | 0,3% | 1 | 0,29% | 1 | 0,35% | 1 | 0,32% |
Lamarck (1779) | 3 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
Nyman (1882) | 3 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
Bonnier & Layens (1894) | 2 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Cariot & Saint-lager (1889) | 2 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Couhia & Fleurot (2016) | 2 | 0,2% | 2 | 0,58% | 2 | 0,69% | 2 | 0,65% |
Delnatte & Meyer (2012) | 2 | 0,2% | 1 | 0,29% | 1 | 0,35% | 0 | 0% |
Ferrer‐gallego & Laguna (2021) | 2 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Fourdrigniez & Meyer (2008) | 2 | 0,2% | 2 | 0,58% | 1 | 0,35% | 1 | 0,32% |
Garland & Moore (2012) | 2 | 0,2% | 2 | 0,58% | 2 | 0,69% | 2 | 0,65% |
Gussone (1843) | 2 | 0,2% | 1 | 0,29% | 1 | 0,35% | 1 | 0,32% |
Jordan & Fourreau (1903) | 2 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Lamarck (1786) | 2 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Linnaeus (1763) | 2 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Shao et al. (2019) | 2 | 0,2% | 2 | 0,58% | 1 | 0,35% | 1 | 0,32% |
Tenore (1811-1815) | 2 | 0,2% | 2 | 0,58% | 1 | 0,35% | 1 | 0,32% |
Wiersema et al. (2018) | 2 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Candolle (1815) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Candolle (1864-1868) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Coste (1937) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Duhamel & Monceau (1806) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Funk et al. (2007) | 1 | 0,1% | 1 | 0,29% | 1 | 0,35% | 0 | 0% |
Host (1831) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Jolinon (1985) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Lamarck (1779) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Lapeyrouse (1813) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Lapeyrouse (1818) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Lavergne (2011) | 1 | 0,1% | 1 | 0,29% | 1 | 0,35% | 1 | 0,32% |
Léotard & Chaline (2013) | 1 | 0,1% | 1 | 0,29% | 1 | 0,35% | 0 | 0% |
Linnaeus (1753) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Lowe et al. (2007) | 1 | 0,1% | 1 | 0,29% | 1 | 0,35% | 1 | 0,32% |
Maire (1928) | 1 | 0,1% | 1 | 0,29% | 0 | 0% | 1 | 0,32% |
Marais (1997) | 1 | 0,1% | 1 | 0,29% | 1 | 0,35% | 1 | 0,32% |
Meyer et al. (2006) | 1 | 0,1% | 1 | 0,29% | 0 | 0% | 1 | 0,32% |
Molino et al. (2009) | 1 | 0,1% | 1 | 0,29% | 1 | 0,35% | 0 | 0% |
Morat & Veillon (1985) | 1 | 0,1% | 1 | 0,29% | 1 | 0,35% | 0 | 0% |
Nouals & Bariteau (1993) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Orlova et al. (2016) | 1 | 0,1% | 1 | 0,29% | 1 | 0,35% | 1 | 0,32% |
Pearman et al. (2020) | 1 | 0,1% | 1 | 0,29% | 1 | 0,35% | 1 | 0,32% |
Persoon (1807) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Presl & Presl (1822) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Rabasse et al. (2005) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Rivière (2003) | 1 | 0,1% | 1 | 0,29% | 1 | 0,35% | 0 | 0% |
Scopoli (1771) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Sibthorp & Smith (1813-1816) | 1 | 0,1% | 1 | 0,29% | 1 | 0,35% | 1 | 0,32% |
Sprengel (1826) | 1 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Stevenson (1991) | 1 | 0,1% | 1 | 0,29% | 1 | 0,35% | 0 | 0% |
Tassin et al. (2006) | 1 | 0,1% | 1 | 0,29% | 1 | 0,35% | 0 | 0% |