Trachéophytes des îles subantarctiques
Trachéophyta des îles subantarctiques
171 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) | 445 | 11% | 197 | 86,78% | 192 | 86,88% | 189 | 85,52% |
Fournet (2002) | 135 | 3,34% | 120 | 52,86% | 120 | 54,3% | 120 | 54,3% |
Frenot et al. (2001) | 68 | 1,68% | 60 | 26,43% | 58 | 26,24% | 60 | 27,15% |
Hequet & Le Corre (2010) | 46 | 1,14% | 39 | 17,18% | 39 | 17,65% | 38 | 17,19% |
Hequet et al. (2009) | 46 | 1,14% | 39 | 17,18% | 39 | 17,65% | 38 | 17,19% |
MacKee (1994) | 46 | 1,14% | 39 | 17,18% | 39 | 17,65% | 38 | 17,19% |
Jolinon (1987) | 45 | 1,11% | 39 | 17,18% | 39 | 17,65% | 39 | 17,65% |
Carcaillet (1993) | 43 | 1,06% | 39 | 17,18% | 38 | 17,19% | 38 | 17,19% |
Hullé et al. (2003) | 43 | 1,06% | 38 | 16,74% | 38 | 17,19% | 36 | 16,29% |
Bell (1982) | 35 | 0,86% | 28 | 12,33% | 27 | 12,22% | 28 | 12,67% |
Linnaeus (1753) | 28 | 0,69% | 20 | 8,81% | 20 | 9,05% | 20 | 9,05% |
Schenck (1906) | 28 | 0,69% | 23 | 10,13% | 23 | 10,41% | 22 | 9,95% |
Wiersema et al. (2018) | 23 | 0,57% | 7 | 3,08% | 7 | 3,17% | 7 | 3,17% |
Linnaeus (1753) | 22 | 0,54% | 13 | 5,73% | 13 | 5,88% | 12 | 5,43% |
Van Der Putten et al. (2010) | 22 | 0,54% | 20 | 8,81% | 20 | 9,05% | 20 | 9,05% |
Fourdrigniez & Meyer (2008) | 18 | 0,44% | 14 | 6,17% | 14 | 6,33% | 14 | 6,33% |
Nesom (2009) | 17 | 0,42% | 1 | 0,44% | 1 | 0,45% | 1 | 0,45% |
UICN Comité français et al. (2024) | 15 | 0,37% | 14 | 6,17% | 14 | 6,33% | 13 | 5,88% |
Funk et al. (2007) | 14 | 0,35% | 7 | 3,08% | 7 | 3,17% | 7 | 3,17% |
Hemsley (1885) | 14 | 0,35% | 7 | 3,08% | 7 | 3,17% | 7 | 3,17% |
Munzinger et al. (2016) | 13 | 0,32% | 6 | 2,64% | 6 | 2,71% | 6 | 2,71% |
Euro+Med (2006) | 12 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
Rouy (1908) | 11 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Bourzat & Monie (1977) | 10 | 0,25% | 6 | 2,64% | 6 | 2,71% | 6 | 2,71% |
Etcheberry & Abraham (2009) | 10 | 0,25% | 8 | 3,52% | 8 | 3,62% | 8 | 3,62% |
Jolinon (1985) | 10 | 0,25% | 6 | 2,64% | 6 | 2,71% | 6 | 2,71% |
Cambecèdes et al. (2012) | 8 | 0,2% | 6 | 2,64% | 5 | 2,26% | 6 | 2,71% |
Reichardt (1871) | 8 | 0,2% | 6 | 2,64% | 6 | 2,71% | 6 | 2,71% |
Gray (1821) | 7 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Morat et al. (2012) | 7 | 0,17% | 5 | 2,2% | 5 | 2,26% | 5 | 2,26% |
Salisbury (1796) | 7 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
Schenck (1905) | 7 | 0,17% | 7 | 3,08% | 7 | 3,17% | 7 | 3,17% |
Béguinot (2012) | 6 | 0,15% | 5 | 2,2% | 5 | 2,26% | 5 | 2,26% |
Chapuis et al. (2004) | 6 | 0,15% | 6 | 2,64% | 6 | 2,71% | 6 | 2,71% |
Fourreau (1869) | 6 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Gandoger (1884) | 6 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Lavergne (2011) | 6 | 0,15% | 5 | 2,2% | 5 | 2,26% | 5 | 2,26% |
Nyman (1882) | 6 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Proćków & Drábková (2023) | 6 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Schenck (1905) | 6 | 0,15% | 3 | 1,32% | 3 | 1,36% | 3 | 1,36% |
Timaná et al. (2019) | 6 | 0,15% | 6 | 2,64% | 6 | 2,71% | 6 | 2,71% |
Fournier (1934-1940) | 5 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Jiménez-lópez et al. (2022) | 5 | 0,12% | 1 | 0,44% | 1 | 0,45% | 1 | 0,45% |
Mennema (1989) | 5 | 0,12% | 1 | 0,44% | 1 | 0,45% | 1 | 0,45% |
Perrie & Parris (2012) | 5 | 0,12% | 2 | 0,88% | 2 | 0,9% | 2 | 0,9% |
Acevedo-Rodríguez & Strong (2012) | 4 | 0,1% | 1 | 0,44% | 1 | 0,45% | 1 | 0,45% |
Davies, L. & Greene, S.W. (1976) | 4 | 0,1% | 4 | 1,76% | 4 | 1,81% | 4 | 1,81% |
Gandoger (1875) | 4 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Hooker (1875) | 4 | 0,1% | 2 | 0,88% | 2 | 0,9% | 2 | 0,9% |
Moench (1794) | 4 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Rouy (1899) | 4 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Arcangeli (1882) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
. Alger, typographie A. Jourdan ; Paris, librairie F. Savy. 825 pp.">Battandier & Trabut (1890) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Boullet et al. (2018) | 3 | 0,07% | 3 | 1,32% | 3 | 1,36% | 3 | 1,36% |
Candolle (1815) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Chau et al. (2020) | 3 | 0,07% | 3 | 1,32% | 3 | 1,36% | 3 | 1,36% |
Dillenberger & Kadereit (2022) | 3 | 0,07% | 1 | 0,44% | 1 | 0,45% | 1 | 0,45% |
Dulac (1867) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Ferlay et al. (2023) | 3 | 0,07% | 2 | 0,88% | 2 | 0,9% | 2 | 0,9% |
Gargominy et al. (1996) | 3 | 0,07% | 3 | 1,32% | 3 | 1,36% | 3 | 1,36% |
Gasper et al. (2016) | 3 | 0,07% | 1 | 0,44% | 1 | 0,45% | 1 | 0,45% |
Presl & Presl (1822) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Scopoli (1771) | 3 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Sundue et al. (2010) | 3 | 0,07% | 3 | 1,32% | 3 | 1,36% | 3 | 1,36% |
Young (1971) | 3 | 0,07% | 3 | 1,32% | 3 | 1,36% | 3 | 1,36% |
Anonyme (2014) | 2 | 0,05% | 1 | 0,44% | 1 | 0,45% | 1 | 0,45% |
Aubert de la Rüe (1932) | 2 | 0,05% | 2 | 0,88% | 2 | 0,9% | 2 | 0,9% |
Aublet (1775) | 2 | 0,05% | 2 | 0,88% | 2 | 0,9% | 2 | 0,9% |
Boreau (1857) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Bubani & Penzig (1901) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Coulot & Rabaute (2016) | 2 | 0,05% | 1 | 0,44% | 1 | 0,45% | 1 | 0,45% |
Delarue (1988) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Döll (1843) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Fuentes-bazan et al. (2012) | 2 | 0,05% | 2 | 0,88% | 2 | 0,9% | 2 | 0,9% |
Gaudin (1828) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Greene & Greene (1963) | 2 | 0,05% | 2 | 0,88% | 2 | 0,9% | 2 | 0,9% |
Grenier & Godron (1850) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Hoff & Cremers (2005) | 2 | 0,05% | 2 | 0,88% | 2 | 0,9% | 2 | 0,9% |
Hoffmann (1791) | 2 | 0,05% | 1 | 0,44% | 1 | 0,45% | 1 | 0,45% |
Husnot (1908) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Kirschner (1990) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Kuntze (1891) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Lamarck (1779) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Lamarck (1779) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Léotard & Chaline (2013) | 2 | 0,05% | 2 | 0,88% | 2 | 0,9% | 2 | 0,9% |
Lemée (1953) | 2 | 0,05% | 2 | 0,88% | 2 | 0,9% | 2 | 0,9% |
Manns & Anderberg (2007) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Massé (1982) | 2 | 0,05% | 2 | 0,88% | 1 | 0,45% | 2 | 0,9% |
Meyer (1819) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Miller (1768) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Morat & Veillon (1985) | 2 | 0,05% | 2 | 0,88% | 2 | 0,9% | 2 | 0,9% |
Peterson et al. (2014) | 2 | 0,05% | 2 | 0,88% | 2 | 0,9% | 2 | 0,9% |
Reveal et al. (1991) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Rouhan et al. (2004) | 2 | 0,05% | 2 | 0,88% | 2 | 0,9% | 2 | 0,9% |
Rouy & Foucaud (1897) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Siljak-Yakovlev et al. (2020) | 2 | 0,05% | 2 | 0,88% | 2 | 0,9% | 2 | 0,9% |
Abbayes (1931) | 1 | 0,02% | 1 | 0,44% | 1 | 0,45% | 1 | 0,45% |
Allioni (1785) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Badré & Deschâtres (1979) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Banfi et al. (2022) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Berton (2020) | 1 | 0,02% | 1 | 0,44% | 1 | 0,45% | 1 | 0,45% |
Bonnier & Layens (1894) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Boreau (1849) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Breton (2014) | 1 | 0,02% | 1 | 0,44% | 1 | 0,45% | 1 | 0,45% |
Bubani & Penzig (1897) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Bubani & Penzig (1902) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Candolle (1824) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Candolle (1844) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Candolle (1848) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Cariot & Saint-lager (1889) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Crantz (1766) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Crantz (1766) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Cremers & Hoff (1997) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Delnatte & Meyer (2012) | 1 | 0,02% | 1 | 0,44% | 1 | 0,45% | 1 | 0,45% |
Derrick et al. (1987) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Desportes (1838) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Don (1831) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Don (1834) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Dumortier (1827) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Flora iberica | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Florence (2004) | 1 | 0,02% | 1 | 0,44% | 1 | 0,45% | 1 | 0,45% |
Fourreau (1868) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Global Carex Group (2015) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Grisebach (1866) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Heylen et al. (2021) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Hoffmann (1804) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Jordan & Fourreau (1868) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Karsch (1853) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Koch (1837) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Lamarck & Candolle (1805) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Lamarck & Candolle (1805) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Lamarck (1778) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Lamarck (1786) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Lamarck (1789) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Lansdown (2022) | 1 | 0,02% | 1 | 0,44% | 1 | 0,45% | 1 | 0,45% |
Li et al. (2021) | 1 | 0,02% | 1 | 0,44% | 1 | 0,45% | 1 | 0,45% |
Lieutard (1893) | 1 | 0,02% | 1 | 0,44% | 1 | 0,45% | 1 | 0,45% |
Manns & Anderberg (2009) | 1 | 0,02% | 1 | 0,44% | 1 | 0,45% | 1 | 0,45% |
Massé et al. (1982) | 1 | 0,02% | 1 | 0,44% | 1 | 0,45% | 1 | 0,45% |
Meyer et al. (2006) | 1 | 0,02% | 1 | 0,44% | 1 | 0,45% | 1 | 0,45% |
Meyer (1836) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Miégeville (1863) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Moench (1794) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Monod & Dollfus (1932) | 1 | 0,02% | 1 | 0,44% | 1 | 0,45% | 1 | 0,45% |
Muller et al. (2004) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Mutel (1834) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Pelletier (1998) | 1 | 0,02% | 1 | 0,44% | 1 | 0,45% | 1 | 0,45% |
Persoon (1805) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Pteridophyte Phylogeny Group (2016) | 1 | 0,02% | 1 | 0,44% | 1 | 0,45% | 1 | 0,45% |
Rouhan (2005) | 1 | 0,02% | 1 | 0,44% | 1 | 0,45% | 1 | 0,45% |
Rouy & Foucaud (1893) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Rouy & Foucaud (1896) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Rouy (1909) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Rouy (1912) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Rouy (1913) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Schaefer et al. (2012) | 1 | 0,02% | 1 | 0,44% | 1 | 0,45% | 1 | 0,45% |
Schrank et al. (1789) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Schur (1866) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Scopoli (1771) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Sennen (1926) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Timaná (2018) | 1 | 0,02% | 1 | 0,44% | 1 | 0,45% | 1 | 0,45% |
Vanhöffen (1912) | 1 | 0,02% | 1 | 0,44% | 1 | 0,45% | 1 | 0,45% |
Viane (2021) | 1 | 0,02% | 1 | 0,44% | 1 | 0,45% | 1 | 0,45% |
Viane (2021) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Villars (1779) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Villars (1787) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Villars (1789) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Vollmann (1904) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Wiggers (1780) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Wilson (2017) | 1 | 0,02% | 1 | 0,44% | 1 | 0,45% | 1 | 0,45% |
Ziffer-Berger et al. (2015) | 1 | 0,02% | 1 | 0,44% | 1 | 0,45% | 1 | 0,45% |