Arbres de métropole
144 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) | 460 | 21,46% | 220 | 96,49% | 192 | 111,63% | 183 | 92,89% |
Sennikov & Kurtto (2017) | 148 | 6,9% | 11 | 4,82% | 9 | 5,23% | 10 | 5,08% |
Anonyme (2014) | 147 | 6,86% | 127 | 55,7% | 127 | 73,84% | 102 | 51,78% |
Fournet (2002) | 96 | 4,48% | 80 | 35,09% | 80 | 46,51% | 76 | 38,58% |
Linnaeus (1753) | 51 | 2,38% | 35 | 15,35% | 30 | 17,44% | 29 | 14,72% |
Béguinot (2012) | 35 | 1,63% | 23 | 10,09% | 23 | 13,37% | 14 | 7,11% |
Salisbury (1796) | 33 | 1,54% | 0 | 0% | 0 | 0% | 0 | 0% |
Hequet & Le Corre (2010) | 32 | 1,49% | 26 | 11,4% | 26 | 15,12% | 21 | 10,66% |
Hequet et al. (2009) | 32 | 1,49% | 26 | 11,4% | 26 | 15,12% | 21 | 10,66% |
MacKee (1994) | 32 | 1,49% | 26 | 11,4% | 26 | 15,12% | 21 | 10,66% |
Miller (1768) | 32 | 1,49% | 9 | 3,95% | 8 | 4,65% | 7 | 3,55% |
Schneider (1912) | 18 | 0,84% | 2 | 0,88% | 0 | 0% | 2 | 1,02% |
Funk et al. (2007) | 17 | 0,79% | 9 | 3,95% | 9 | 5,23% | 9 | 4,57% |
Delnatte & Meyer (2012) | 16 | 0,75% | 13 | 5,7% | 13 | 7,56% | 13 | 6,6% |
Rouy (1913) | 13 | 0,61% | 0 | 0% | 0 | 0% | 0 | 0% |
Euro+Med (2006) | 11 | 0,51% | 0 | 0% | 0 | 0% | 0 | 0% |
Host (1831) | 11 | 0,51% | 0 | 0% | 0 | 0% | 0 | 0% |
Wiersema et al. (2018) | 11 | 0,51% | 5 | 2,19% | 5 | 2,91% | 3 | 1,52% |
Fourdrigniez & Meyer (2008) | 10 | 0,47% | 8 | 3,51% | 8 | 4,65% | 8 | 4,06% |
Linnaeus (1753) | 10 | 0,47% | 7 | 3,07% | 7 | 4,07% | 6 | 3,05% |
Fournier (1934-1940) | 9 | 0,42% | 0 | 0% | 0 | 0% | 0 | 0% |
Gandoger (1875) | 9 | 0,42% | 0 | 0% | 0 | 0% | 0 | 0% |
Lamarck (1783) | 9 | 0,42% | 0 | 0% | 0 | 0% | 0 | 0% |
Nyman (1882) | 9 | 0,42% | 0 | 0% | 0 | 0% | 0 | 0% |
Persoon (1807) | 8 | 0,37% | 0 | 0% | 0 | 0% | 0 | 0% |
Bonnier & Layens (1894) | 7 | 0,33% | 0 | 0% | 0 | 0% | 0 | 0% |
Rouy & Foucaud (1897) | 7 | 0,33% | 0 | 0% | 0 | 0% | 0 | 0% |
Arcangeli (1882) | 6 | 0,28% | 0 | 0% | 0 | 0% | 0 | 0% |
Grenier & Godron (1856) | 6 | 0,28% | 0 | 0% | 0 | 0% | 0 | 0% |
Lamarck & Candolle (1805) | 6 | 0,28% | 0 | 0% | 0 | 0% | 0 | 0% |
Lamarck (1779) | 6 | 0,28% | 0 | 0% | 0 | 0% | 0 | 0% |
Molino et al. (2009) | 6 | 0,28% | 4 | 1,75% | 4 | 2,33% | 4 | 2,03% |
Muller et al. (2004) | 6 | 0,28% | 6 | 2,63% | 5 | 2,91% | 5 | 2,54% |
Rouy (1910) | 6 | 0,28% | 0 | 0% | 0 | 0% | 0 | 0% |
Boullet et al. (2018) | 5 | 0,23% | 5 | 2,19% | 5 | 2,91% | 5 | 2,54% |
Candolle (1864-1868) | 5 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Florence (1997) | 5 | 0,23% | 5 | 2,19% | 5 | 2,91% | 5 | 2,54% |
Lamarck (1779) | 5 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Morat & Veillon (1985) | 5 | 0,23% | 4 | 1,75% | 4 | 2,33% | 4 | 2,03% |
Scopoli (1771) | 5 | 0,23% | 0 | 0% | 0 | 0% | 0 | 0% |
Acevedo-Rodríguez & Strong (2012) | 4 | 0,19% | 3 | 1,32% | 3 | 1,74% | 3 | 1,52% |
Anonyme (2023) | 4 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Aublet (1775) | 4 | 0,19% | 1 | 0,44% | 1 | 0,58% | 1 | 0,51% |
Bubani & Penzig (1897) | 4 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Gardner et al. (2021) | 4 | 0,19% | 3 | 1,32% | 3 | 1,74% | 3 | 1,52% |
Grenier & Godron (1850) | 4 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Koch (1837) | 4 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Lavergne (2011) | 4 | 0,19% | 3 | 1,32% | 3 | 1,74% | 3 | 1,52% |
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 | 0,44% | 1 | 0,58% | 1 | 0,51% |
Lapeyrouse (1813) | 3 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Léotard & Chaline (2013) | 3 | 0,14% | 3 | 1,32% | 3 | 1,74% | 3 | 1,52% |
Lemée (1952) | 3 | 0,14% | 1 | 0,44% | 1 | 0,58% | 1 | 0,51% |
Loesener (1901) | 3 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Morat et al. (2012) | 3 | 0,14% | 2 | 0,88% | 2 | 1,16% | 2 | 1,02% |
Munzinger et al. (2016) | 3 | 0,14% | 2 | 0,88% | 2 | 1,16% | 2 | 1,02% |
Nepal & Purintun (2021) | 3 | 0,14% | 1 | 0,44% | 1 | 0,58% | 1 | 0,51% |
Ollitrault et al. (2020) | 3 | 0,14% | 2 | 0,88% | 0 | 0% | 2 | 1,02% |
Pigott (2020) | 3 | 0,14% | 3 | 1,32% | 0 | 0% | 3 | 1,52% |
Scopoli (1771) | 3 | 0,14% | 2 | 0,88% | 1 | 0,58% | 1 | 0,51% |
Tassin et al. (2006) | 3 | 0,14% | 3 | 1,32% | 3 | 1,74% | 2 | 1,02% |
Tenore (1811-1815) | 3 | 0,14% | 2 | 0,88% | 1 | 0,58% | 1 | 0,51% |
Ter Steege et al. (2016) | 3 | 0,14% | 2 | 0,88% | 2 | 1,16% | 2 | 1,02% |
. Alger, typographie A. Jourdan ; Paris, librairie F. Savy. 825 pp.">Battandier & Trabut (1890) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Béreau (2017) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Flora iberica | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Florence (2004) | 2 | 0,09% | 2 | 0,88% | 2 | 1,16% | 2 | 1,02% |
Gaertner (1791) | 2 | 0,09% | 1 | 0,44% | 1 | 0,58% | 1 | 0,51% |
Gussone (1843) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Kuntze (1891) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Léveillé (1917) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Marchenko & Kuzovkina (2022) | 2 | 0,09% | 1 | 0,44% | 1 | 0,58% | 1 | 0,51% |
Meyer et al. (2006) | 2 | 0,09% | 1 | 0,44% | 1 | 0,58% | 1 | 0,51% |
Moench (1794) | 2 | 0,09% | 2 | 0,88% | 1 | 0,58% | 1 | 0,51% |
Moench (1794) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Schrank et al. (1789) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Tausch (1829) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Tison et al. (2021) | 2 | 0,09% | 2 | 0,88% | 0 | 0% | 2 | 1,02% |
Weston (1770) | 2 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Allen et al. (2022) | 1 | 0,05% | 1 | 0,44% | 1 | 0,58% | 1 | 0,51% |
Allioni (1785) | 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 | 0,44% | 1 | 0,58% | 1 | 0,51% |
Bouman et al. (2020) | 1 | 0,05% | 1 | 0,44% | 1 | 0,58% | 1 | 0,51% |
Bouman et al. (2022) | 1 | 0,05% | 1 | 0,44% | 1 | 0,58% | 1 | 0,51% |
Bubani & Penzig (1900) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
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% |
Dumortier (1827) | 1 | 0,05% | 1 | 0,44% | 0 | 0% | 1 | 0,51% |
Fourreau (1868) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Gaertner (1788) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Gandoger (1876) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Gardner et al. (2021) | 1 | 0,05% | 1 | 0,44% | 1 | 0,58% | 1 | 0,51% |
Gargominy et al. (1996) | 1 | 0,05% | 1 | 0,44% | 1 | 0,58% | 1 | 0,51% |
Garland & Moore (2012) | 1 | 0,05% | 1 | 0,44% | 1 | 0,58% | 1 | 0,51% |
Granville & Gayot (2014) | 1 | 0,05% | 1 | 0,44% | 1 | 0,58% | 1 | 0,51% |
Green (1988) | 1 | 0,05% | 1 | 0,44% | 1 | 0,58% | 1 | 0,51% |
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 | 0,44% | 1 | 0,58% | 1 | 0,51% |
Lamarck (1786) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Lamarck (1799) | 1 | 0,05% | 1 | 0,44% | 1 | 0,58% | 1 | 0,51% |
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 | 0,44% | 1 | 0,58% | 1 | 0,51% |
Manning (1960) | 1 | 0,05% | 1 | 0,44% | 1 | 0,58% | 1 | 0,51% |
Marais (1997) | 1 | 0,05% | 1 | 0,44% | 1 | 0,58% | 1 | 0,51% |
Meyer et al. (2008) | 1 | 0,05% | 1 | 0,44% | 1 | 0,58% | 1 | 0,51% |
Nouals & Bariteau (1993) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Pearman et al. (2020) | 1 | 0,05% | 1 | 0,44% | 1 | 0,58% | 1 | 0,51% |
Pennington & Biggs (2016) | 1 | 0,05% | 1 | 0,44% | 1 | 0,58% | 1 | 0,51% |
Prance et al. (2007) | 1 | 0,05% | 1 | 0,44% | 1 | 0,58% | 1 | 0,51% |
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 | 0,44% | 1 | 0,58% | 0 | 0% |
Rouy (1903) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Rouy (1912) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Schur (1866) | 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 | 0,44% | 1 | 0,58% | 1 | 0,51% |
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 | 0,44% | 1 | 0,58% | 1 | 0,51% |
Tison & de Foucault (2015) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Vázquez & Coombes (2017) | 1 | 0,05% | 1 | 0,44% | 1 | 0,58% | 1 | 0,51% |
Villanueva-almanza et al. (2021) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Webster (1956) | 1 | 0,05% | 1 | 0,44% | 1 | 0,58% | 1 | 0,51% |
Webster (1957) | 1 | 0,05% | 1 | 0,44% | 1 | 0,58% | 1 | 0,51% |
Zakardjian et al. (2020) | 1 | 0,05% | 1 | 0,44% | 1 | 0,58% | 1 | 0,51% |
(2008) | 1 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |