Trachéophytes signalées par erreur de métropole
167 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) | 740 | 25,37% | 466 | 72,36% | 348 | 63,74% | 375 | 67,69% |
| Fournet (2002) | 40 | 1,37% | 36 | 5,59% | 32 | 5,86% | 20 | 3,61% |
| Funk et al. (2007) | 32 | 1,1% | 10 | 1,55% | 8 | 1,47% | 8 | 1,44% |
| Euro+Med (2006) | 25 | 0,86% | 7 | 1,09% | 6 | 1,1% | 6 | 1,08% |
| Krapovickas (2003) | 22 | 0,75% | 4 | 0,62% | 4 | 0,73% | 4 | 0,72% |
| Linnaeus (1753) | 22 | 0,75% | 16 | 2,48% | 15 | 2,75% | 9 | 1,62% |
| Linnaeus (1753) | 20 | 0,69% | 12 | 1,86% | 12 | 2,2% | 4 | 0,72% |
| Nyman (1882) | 19 | 0,65% | 0 | 0% | 0 | 0% | 0 | 0% |
| Coulomb (2000) | 17 | 0,58% | 2 | 0,31% | 2 | 0,37% | 1 | 0,18% |
| Rojas-Andrés et al. (2016) | 15 | 0,51% | 3 | 0,47% | 2 | 0,37% | 1 | 0,18% |
| Buttler et al. (2008) | 12 | 0,41% | 2 | 0,31% | 1 | 0,18% | 1 | 0,18% |
| Hequet & Le Corre (2010) | 12 | 0,41% | 9 | 1,4% | 8 | 1,47% | 7 | 1,26% |
| Hequet et al. (2009) | 12 | 0,41% | 9 | 1,4% | 8 | 1,47% | 7 | 1,26% |
| Wiersema et al. (2018) | 11 | 0,38% | 6 | 0,93% | 6 | 1,1% | 1 | 0,18% |
| MacKee (1994) | 10 | 0,34% | 8 | 1,24% | 7 | 1,28% | 6 | 1,08% |
| Moore & Dillenberger (2017) | 10 | 0,34% | 2 | 0,31% | 2 | 0,37% | 2 | 0,36% |
| Veldkamp (1990) | 10 | 0,34% | 1 | 0,16% | 1 | 0,18% | 1 | 0,18% |
| Caković et al. (2021) | 9 | 0,31% | 1 | 0,16% | 1 | 0,18% | 0 | 0% |
| Dillenberger & Kadereit (2015) | 8 | 0,27% | 2 | 0,31% | 2 | 0,37% | 2 | 0,36% |
| Christenhusz et al. (2019) | 7 | 0,24% | 1 | 0,16% | 1 | 0,18% | 1 | 0,18% |
| Flora iberica | 7 | 0,24% | 2 | 0,31% | 1 | 0,18% | 2 | 0,36% |
| Fournier (1934-1940) | 7 | 0,24% | 1 | 0,16% | 1 | 0,18% | 1 | 0,18% |
| Devesa et al. (2013) | 6 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
| Evrard et al. (2004) | 6 | 0,21% | 2 | 0,31% | 2 | 0,37% | 2 | 0,36% |
| Komarov (1960) | 6 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
| Morat et al. (2012) | 6 | 0,21% | 3 | 0,47% | 3 | 0,55% | 3 | 0,54% |
| Salisbury (1796) | 6 | 0,21% | 0 | 0% | 0 | 0% | 0 | 0% |
| Tison & de Foucault (2015) | 6 | 0,21% | 4 | 0,62% | 4 | 0,73% | 3 | 0,54% |
| Aublet (1775) | 5 | 0,17% | 3 | 0,47% | 2 | 0,37% | 1 | 0,18% |
| Dulac (1867) | 5 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fourdrigniez & Meyer (2008) | 5 | 0,17% | 2 | 0,31% | 1 | 0,18% | 0 | 0% |
| Haynes & Holm-nielsen (2009) | 5 | 0,17% | 2 | 0,31% | 1 | 0,18% | 1 | 0,18% |
| Morat & Veillon (1985) | 5 | 0,17% | 4 | 0,62% | 3 | 0,55% | 3 | 0,54% |
| Prelli & Boudrie (2021) | 5 | 0,17% | 5 | 0,78% | 4 | 0,73% | 4 | 0,72% |
| Acevedo-Rodríguez & Strong (2012) | 4 | 0,14% | 3 | 0,47% | 3 | 0,55% | 3 | 0,54% |
| Banfi et al. (2022) | 4 | 0,14% | 2 | 0,31% | 2 | 0,37% | 2 | 0,36% |
| Klak et al. (2007) | 4 | 0,14% | 2 | 0,31% | 2 | 0,37% | 2 | 0,36% |
| Lavergne (2011) | 4 | 0,14% | 4 | 0,62% | 3 | 0,55% | 1 | 0,18% |
| Lemée (1953) | 4 | 0,14% | 2 | 0,31% | 2 | 0,37% | 2 | 0,36% |
| Moench (1794) | 4 | 0,14% | 1 | 0,16% | 1 | 0,18% | 0 | 0% |
| Munzinger et al. (2016) | 4 | 0,14% | 2 | 0,31% | 2 | 0,37% | 2 | 0,36% |
| Riina et al. (2013) | 4 | 0,14% | 4 | 0,62% | 4 | 0,73% | 3 | 0,54% |
| Arcangeli (1882) | 3 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Béguinot (2012) | 3 | 0,1% | 3 | 0,47% | 3 | 0,55% | 0 | 0% |
| Bonnier & Layens (1894) | 3 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bubani & Penzig (1897) | 3 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cambecèdes et al. (2012) | 3 | 0,1% | 1 | 0,16% | 1 | 0,18% | 0 | 0% |
| Hoff (2021) | 3 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Koch (1844) | 3 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kuntze (1891) | 3 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lamarck (1779) | 3 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Linnaeus (1759) | 3 | 0,1% | 3 | 0,47% | 2 | 0,37% | 2 | 0,36% |
| Meyer et al. (2006) | 3 | 0,1% | 3 | 0,47% | 2 | 0,37% | 2 | 0,36% |
| Miller (1768) | 3 | 0,1% | 1 | 0,16% | 1 | 0,18% | 1 | 0,18% |
| Moench (1794) | 3 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Prieto et al. (2012) | 3 | 0,1% | 1 | 0,16% | 1 | 0,18% | 1 | 0,18% |
| Reichenbach (1830-1832) | 3 | 0,1% | 1 | 0,16% | 1 | 0,18% | 1 | 0,18% |
| Richter (1890) | 3 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rostański & Verloove (2015) | 3 | 0,1% | 1 | 0,16% | 1 | 0,18% | 1 | 0,18% |
| Rouy (1909) | 3 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Schur (1866) | 3 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| André et al. (2020) | 2 | 0,07% | 2 | 0,31% | 2 | 0,37% | 2 | 0,36% |
| Anonyme (2014) | 2 | 0,07% | 2 | 0,31% | 2 | 0,37% | 0 | 0% |
| Boullet et al. (2018) | 2 | 0,07% | 2 | 0,31% | 2 | 0,37% | 1 | 0,18% |
| Candolle (1824) | 2 | 0,07% | 1 | 0,16% | 1 | 0,18% | 1 | 0,18% |
| Chaix (1785) | 2 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cires & Prieto (2015) | 2 | 0,07% | 1 | 0,16% | 1 | 0,18% | 1 | 0,18% |
| Del et al. (2020) | 2 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Delnatte & Meyer (2012) | 2 | 0,07% | 2 | 0,31% | 2 | 0,37% | 1 | 0,18% |
| Díaz et al. (1996) | 2 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dunkel (2014) | 2 | 0,07% | 1 | 0,16% | 1 | 0,18% | 1 | 0,18% |
| Dunkel (2018) | 2 | 0,07% | 1 | 0,16% | 1 | 0,18% | 1 | 0,18% |
| Fiori (1925) | 2 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Flora of North America (1993-) | 2 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fourreau (1869) | 2 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Friis (1989) | 2 | 0,07% | 2 | 0,31% | 2 | 0,37% | 2 | 0,36% |
| Gray (1821) | 2 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gussone (1827) | 2 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Haynes & Holm-nielsen (1994) | 2 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Koch (1837) | 2 | 0,07% | 2 | 0,31% | 2 | 0,37% | 2 | 0,36% |
| Lansdown (2022) | 2 | 0,07% | 2 | 0,31% | 2 | 0,37% | 2 | 0,36% |
| Link (1829) | 2 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Linnaeus (1762) | 2 | 0,07% | 2 | 0,31% | 2 | 0,37% | 2 | 0,36% |
| Lowe et al. (2007) | 2 | 0,07% | 1 | 0,16% | 0 | 0% | 0 | 0% |
| Mosyakin & Lange (2018) | 2 | 0,07% | 2 | 0,31% | 2 | 0,37% | 2 | 0,36% |
| Peterson et al. (2014) | 2 | 0,07% | 2 | 0,31% | 2 | 0,37% | 2 | 0,36% |
| Presl & Presl (1822) | 2 | 0,07% | 1 | 0,16% | 1 | 0,18% | 1 | 0,18% |
| Rouy (1913) | 2 | 0,07% | 2 | 0,31% | 1 | 0,18% | 1 | 0,18% |
| Sanders (2006) | 2 | 0,07% | 2 | 0,31% | 0 | 0% | 1 | 0,18% |
| Sanders (2012) | 2 | 0,07% | 1 | 0,16% | 0 | 0% | 0 | 0% |
| Scopoli (1771) | 2 | 0,07% | 1 | 0,16% | 1 | 0,18% | 1 | 0,18% |
| Sennen & Frère (1902) | 2 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sennen & Frère (1936) | 2 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sibthorp & Smith (1806-1809) | 2 | 0,07% | 1 | 0,16% | 1 | 0,18% | 1 | 0,18% |
| Spach (1838) | 2 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sprengel (1826) | 2 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Thellung (1912) | 2 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
| Toutain (1989) | 2 | 0,07% | 1 | 0,16% | 1 | 0,18% | 1 | 0,18% |
| Anonyme. (2002) | 1 | 0,03% | 1 | 0,16% | 1 | 0,18% | 1 | 0,18% |
| Anonyme (2023) | 1 | 0,03% | 1 | 0,16% | 1 | 0,18% | 1 | 0,18% |
| Bock & Tison (2012) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bosser (1997) | 1 | 0,03% | 1 | 0,16% | 1 | 0,18% | 1 | 0,18% |
| Bourzat & Monie (1977) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Brunton & Rumsey (2021) | 1 | 0,03% | 1 | 0,16% | 1 | 0,18% | 1 | 0,18% |
| Bubani & Penzig (1900) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Candolle (1813) | 1 | 0,03% | 1 | 0,16% | 1 | 0,18% | 1 | 0,18% |
| Candolle (1845) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Candolle (1848) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Candolle (1849) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Candolle (1864-1868) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Carcaillet (1993) | 1 | 0,03% | 1 | 0,16% | 1 | 0,18% | 0 | 0% |
| Cariot & Saint-lager (1889) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Chinnock (2010) | 1 | 0,03% | 1 | 0,16% | 1 | 0,18% | 1 | 0,18% |
| Desfontaines (1798) | 1 | 0,03% | 1 | 0,16% | 1 | 0,18% | 1 | 0,18% |
| Desfontaines (1798) | 1 | 0,03% | 1 | 0,16% | 1 | 0,18% | 1 | 0,18% |
| Ferlay et al. (2023) | 1 | 0,03% | 1 | 0,16% | 1 | 0,18% | 1 | 0,18% |
| Fiori (1929) | 1 | 0,03% | 1 | 0,16% | 1 | 0,18% | 1 | 0,18% |
| Florence (2004) | 1 | 0,03% | 1 | 0,16% | 1 | 0,18% | 0 | 0% |
| Fourreau (1868) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Frenot et al. (2001) | 1 | 0,03% | 1 | 0,16% | 1 | 0,18% | 0 | 0% |
| Gargominy et al. (1996) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gussone (1843) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gutermannn (2019) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hardion et al. (2020) | 1 | 0,03% | 1 | 0,16% | 0 | 0% | 1 | 0,18% |
| Harpke et al. (2014) | 1 | 0,03% | 1 | 0,16% | 1 | 0,18% | 1 | 0,18% |
| Hoffmann (1804) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Host (1831) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hullé et al. (2003) | 1 | 0,03% | 1 | 0,16% | 1 | 0,18% | 0 | 0% |
| Jolinon (1987) | 1 | 0,03% | 1 | 0,16% | 1 | 0,18% | 0 | 0% |
| Lamarck & Candolle (1805) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lamarck (1779) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lamarck (1783) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lamarck (1789) | 1 | 0,03% | 1 | 0,16% | 1 | 0,18% | 1 | 0,18% |
| Lapeyrouse (1813) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lemée (1955) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Leuenberger (1997) | 1 | 0,03% | 1 | 0,16% | 1 | 0,18% | 1 | 0,18% |
| Maddi (2014) | 1 | 0,03% | 1 | 0,16% | 1 | 0,18% | 0 | 0% |
| Martínez-azorín et al. (2022) | 1 | 0,03% | 1 | 0,16% | 1 | 0,18% | 1 | 0,18% |
| Martínez-Azorín et al. (2023) | 1 | 0,03% | 1 | 0,16% | 1 | 0,18% | 1 | 0,18% |
| Meyer et al. (2008) | 1 | 0,03% | 1 | 0,16% | 1 | 0,18% | 1 | 0,18% |
| Mitchell (1997) | 1 | 0,03% | 1 | 0,16% | 1 | 0,18% | 1 | 0,18% |
| Pejhanmehr (2022) | 1 | 0,03% | 1 | 0,16% | 1 | 0,18% | 1 | 0,18% |
| Pérez et al. (2021) | 1 | 0,03% | 1 | 0,16% | 0 | 0% | 1 | 0,18% |
| Proćków & Drábková (2023) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Reichert et al. (2018) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Reveal et al. (1991) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rouy & Foucaud (1893) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rouy & Foucaud (1895) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rouy & Foucaud (1897) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rouy (1912) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Schenck (1905) | 1 | 0,03% | 1 | 0,16% | 1 | 0,18% | 0 | 0% |
| Schenck (1906) | 1 | 0,03% | 1 | 0,16% | 1 | 0,18% | 0 | 0% |
| Schur (1885) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Siadati et al. (2018) | 1 | 0,03% | 1 | 0,16% | 1 | 0,18% | 1 | 0,18% |
| Snogerup (1993) | 1 | 0,03% | 1 | 0,16% | 1 | 0,18% | 1 | 0,18% |
| Sweet (1830) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Tremetsberger et al. (2002) | 1 | 0,03% | 1 | 0,16% | 1 | 0,18% | 0 | 0% |
| Uicn et al. (2012) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Van Der Putten et al. (2010) | 1 | 0,03% | 1 | 0,16% | 1 | 0,18% | 1 | 0,18% |
| Véron et al. (2021) | 1 | 0,03% | 1 | 0,16% | 1 | 0,18% | 1 | 0,18% |
| Villars (1789) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Vollmann (1914) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Willdenow (1799) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Willkomm & Lange (1870) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Yang et al. (2012) | 1 | 0,03% | 1 | 0,16% | 1 | 0,18% | 1 | 0,18% |
| Záveská et al. (2013) | 1 | 0,03% | 1 | 0,16% | 1 | 0,18% | 1 | 0,18% |
| Zeltner (1970) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
