Arbres de métropole
139 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) | 456 | 21,9% | 226 | 102,73% | 193 | 112,21% | 199 | 102,58% |
| Sennikov & Kurtto (2017) | 148 | 7,11% | 11 | 5% | 9 | 5,23% | 10 | 5,15% |
| Anonyme (2014) | 147 | 7,06% | 128 | 58,18% | 128 | 74,42% | 108 | 55,67% |
| Fournet (2002) | 96 | 4,61% | 80 | 36,36% | 80 | 46,51% | 76 | 39,18% |
| Linnaeus (1753) | 44 | 2,11% | 29 | 13,18% | 27 | 15,7% | 27 | 13,92% |
| Béguinot (2012) | 35 | 1,68% | 23 | 10,45% | 23 | 13,37% | 15 | 7,73% |
| Hequet & Le Corre (2010) | 33 | 1,59% | 27 | 12,27% | 27 | 15,7% | 24 | 12,37% |
| Hequet et al. (2009) | 33 | 1,59% | 27 | 12,27% | 27 | 15,7% | 24 | 12,37% |
| MacKee (1994) | 33 | 1,59% | 27 | 12,27% | 27 | 15,7% | 24 | 12,37% |
| Miller (1768) | 31 | 1,49% | 9 | 4,09% | 8 | 4,65% | 8 | 4,12% |
| Salisbury (1796) | 27 | 1,3% | 0 | 0% | 0 | 0% | 0 | 0% |
| Schneider (1912) | 18 | 0,86% | 2 | 0,91% | 0 | 0% | 2 | 1,03% |
| Funk et al. (2007) | 17 | 0,82% | 9 | 4,09% | 9 | 5,23% | 9 | 4,64% |
| Delnatte & Meyer (2012) | 16 | 0,77% | 14 | 6,36% | 14 | 8,14% | 14 | 7,22% |
| Rouy (1913) | 12 | 0,58% | 0 | 0% | 0 | 0% | 0 | 0% |
| Euro+Med (2006) | 11 | 0,53% | 0 | 0% | 0 | 0% | 0 | 0% |
| Host (1831) | 11 | 0,53% | 0 | 0% | 0 | 0% | 0 | 0% |
| Wiersema et al. (2018) | 11 | 0,53% | 5 | 2,27% | 5 | 2,91% | 4 | 2,06% |
| Fourdrigniez & Meyer (2008) | 10 | 0,48% | 8 | 3,64% | 8 | 4,65% | 8 | 4,12% |
| Lamarck (1783) | 9 | 0,43% | 0 | 0% | 0 | 0% | 0 | 0% |
| Linnaeus (1753) | 9 | 0,43% | 6 | 2,73% | 6 | 3,49% | 5 | 2,58% |
| Nyman (1882) | 9 | 0,43% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fournier (1934-1940) | 8 | 0,38% | 0 | 0% | 0 | 0% | 0 | 0% |
| Persoon (1807) | 7 | 0,34% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rouy & Foucaud (1897) | 7 | 0,34% | 0 | 0% | 0 | 0% | 0 | 0% |
| Arcangeli (1882) | 6 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
| Grenier & Godron (1856) | 6 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lamarck & Candolle (1805) | 6 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lamarck (1779) | 6 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
| Molino et al. (2009) | 6 | 0,29% | 4 | 1,82% | 4 | 2,33% | 4 | 2,06% |
| Muller et al. (2004) | 6 | 0,29% | 6 | 2,73% | 5 | 2,91% | 5 | 2,58% |
| Bonnier & Layens (1894) | 5 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
| Boullet et al. (2018) | 5 | 0,24% | 5 | 2,27% | 5 | 2,91% | 5 | 2,58% |
| Candolle (1864-1868) | 5 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
| Florence (1997) | 5 | 0,24% | 5 | 2,27% | 5 | 2,91% | 5 | 2,58% |
| Gandoger (1875) | 5 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
| Morat & Veillon (1985) | 5 | 0,24% | 4 | 1,82% | 4 | 2,33% | 4 | 2,06% |
| Scopoli (1771) | 5 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
| Acevedo-Rodríguez & Strong (2012) | 4 | 0,19% | 3 | 1,36% | 3 | 1,74% | 3 | 1,55% |
| Aublet (1775) | 4 | 0,19% | 1 | 0,45% | 1 | 0,58% | 1 | 0,52% |
| Bubani & Penzig (1897) | 4 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gardner et al. (2021) | 4 | 0,19% | 3 | 1,36% | 3 | 1,74% | 3 | 1,55% |
| Grenier & Godron (1850) | 4 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lamarck (1779) | 4 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lavergne (2011) | 4 | 0,19% | 3 | 1,36% | 3 | 1,74% | 3 | 1,55% |
| Anonyme (2023) | 3 | 0,14% | 1 | 0,45% | 1 | 0,58% | 1 | 0,52% |
| Boreau (1857) | 3 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Chaix (1785) | 3 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gray (1821) | 3 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hoffmann (1791) | 3 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kyalangalilwa et al. (2013) | 3 | 0,14% | 1 | 0,45% | 1 | 0,58% | 1 | 0,52% |
| Lapeyrouse (1813) | 3 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Léotard & Chaline (2013) | 3 | 0,14% | 3 | 1,36% | 3 | 1,74% | 3 | 1,55% |
| Lemée (1952) | 3 | 0,14% | 1 | 0,45% | 1 | 0,58% | 1 | 0,52% |
| Loesener (1901) | 3 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Morat et al. (2012) | 3 | 0,14% | 2 | 0,91% | 2 | 1,16% | 2 | 1,03% |
| Munzinger et al. (2016) | 3 | 0,14% | 2 | 0,91% | 2 | 1,16% | 2 | 1,03% |
| Nepal & Purintun (2021) | 3 | 0,14% | 1 | 0,45% | 1 | 0,58% | 1 | 0,52% |
| Ollitrault et al. (2020) | 3 | 0,14% | 2 | 0,91% | 0 | 0% | 2 | 1,03% |
| Pigott (2020) | 3 | 0,14% | 3 | 1,36% | 0 | 0% | 3 | 1,55% |
| Scopoli (1771) | 3 | 0,14% | 2 | 0,91% | 1 | 0,58% | 1 | 0,52% |
| Tassin et al. (2006) | 3 | 0,14% | 3 | 1,36% | 3 | 1,74% | 2 | 1,03% |
| Tenore (1811-1815) | 3 | 0,14% | 1 | 0,45% | 1 | 0,58% | 0 | 0% |
| Ter Steege et al. (2016) | 3 | 0,14% | 2 | 0,91% | 2 | 1,16% | 2 | 1,03% |
| Béreau (2017) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Flora iberica | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Florence (2004) | 2 | 0,1% | 2 | 0,91% | 2 | 1,16% | 2 | 1,03% |
| Gaertner (1791) | 2 | 0,1% | 1 | 0,45% | 1 | 0,58% | 1 | 0,52% |
| Gussone (1843) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Koch (1837) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Léveillé (1917) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Meyer et al. (2006) | 2 | 0,1% | 1 | 0,45% | 1 | 0,58% | 1 | 0,52% |
| Moench (1794) | 2 | 0,1% | 2 | 0,91% | 1 | 0,58% | 1 | 0,52% |
| Tausch (1829) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Tison et al. (2021) | 2 | 0,1% | 2 | 0,91% | 0 | 0% | 2 | 1,03% |
| Weston (1770) | 2 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Allen et al. (2022) | 1 | 0,05% | 1 | 0,45% | 1 | 0,58% | 1 | 0,52% |
| Appelhans et al. (2021) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| . Alger, typographie A. Jourdan ; Paris, librairie F. Savy. 825 pp.">Battandier & Trabut (1890) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Björk & Goward (2022) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Boreau (1849) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bosser & Heine (2000) | 1 | 0,05% | 1 | 0,45% | 1 | 0,58% | 1 | 0,52% |
| Bouman et al. (2020) | 1 | 0,05% | 1 | 0,45% | 1 | 0,58% | 1 | 0,52% |
| Bouman et al. (2022) | 1 | 0,05% | 1 | 0,45% | 1 | 0,58% | 1 | 0,52% |
| Candolle (1813) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Candolle (1815) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Candolle (1824) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Candolle (1825) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Candolle (1845) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Don (1831) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dulac (1867) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fourreau (1868) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gaertner (1788) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gardner et al. (2021) | 1 | 0,05% | 1 | 0,45% | 1 | 0,58% | 1 | 0,52% |
| Gargominy et al. (1996) | 1 | 0,05% | 1 | 0,45% | 1 | 0,58% | 1 | 0,52% |
| Garland & Moore (2012) | 1 | 0,05% | 1 | 0,45% | 1 | 0,58% | 1 | 0,52% |
| Granville & Gayot (2014) | 1 | 0,05% | 1 | 0,45% | 1 | 0,58% | 1 | 0,52% |
| Green (1988) | 1 | 0,05% | 1 | 0,45% | 1 | 0,58% | 1 | 0,52% |
| Hayne (1822) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hoff (2021) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| IPNI (2000-) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jolinon (1985) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Krebs et al. (2004) | 1 | 0,05% | 1 | 0,45% | 1 | 0,58% | 1 | 0,52% |
| Kuntze (1891) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lamarck (1786) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lamarck (1799) | 1 | 0,05% | 1 | 0,45% | 1 | 0,58% | 1 | 0,52% |
| Lapeyrouse (1818) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lavallée (1877) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Linnaeus (1763) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lowe et al. (2007) | 1 | 0,05% | 1 | 0,45% | 1 | 0,58% | 1 | 0,52% |
| Manning (1960) | 1 | 0,05% | 1 | 0,45% | 1 | 0,58% | 1 | 0,52% |
| Marais (1997) | 1 | 0,05% | 1 | 0,45% | 1 | 0,58% | 1 | 0,52% |
| Meyer et al. (2008) | 1 | 0,05% | 1 | 0,45% | 1 | 0,58% | 1 | 0,52% |
| Moench (1794) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Nouals & Bariteau (1993) | 1 | 0,05% | 1 | 0,45% | 0 | 0% | 1 | 0,52% |
| Pennington & Biggs (2016) | 1 | 0,05% | 1 | 0,45% | 1 | 0,58% | 1 | 0,52% |
| Prance et al. (2007) | 1 | 0,05% | 1 | 0,45% | 1 | 0,58% | 1 | 0,52% |
| Presl & Presl (1822) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rabasse et al. (2005) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Reichenbach (1830-1832) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Richard (1792) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rivière (2003) | 1 | 0,05% | 1 | 0,45% | 1 | 0,58% | 0 | 0% |
| Rouy (1903) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rouy (1910) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rouy (1912) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Schrank et al. (1789) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sennen & Frère (1936) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Seringe (1815) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Song et al. (2019) | 1 | 0,05% | 1 | 0,45% | 1 | 0,58% | 1 | 0,52% |
| Soubeyran (2008) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Stafleu & Cowan (1983) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Stevenson (1991) | 1 | 0,05% | 1 | 0,45% | 1 | 0,58% | 1 | 0,52% |
| Tison & de Foucault (2015) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Vázquez & Coombes (2017) | 1 | 0,05% | 1 | 0,45% | 1 | 0,58% | 1 | 0,52% |
| Villanueva-almanza et al. (2021) | 1 | 0,05% | 1 | 0,45% | 1 | 0,58% | 1 | 0,52% |
| Webster (1956) | 1 | 0,05% | 1 | 0,45% | 1 | 0,58% | 1 | 0,52% |
| Webster (1957) | 1 | 0,05% | 1 | 0,45% | 1 | 0,58% | 1 | 0,52% |
| Zakardjian et al. (2020) | 1 | 0,05% | 1 | 0,45% | 1 | 0,58% | 1 | 0,52% |
| (2008) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
