Angiospermes de Saint-Pierre-et-Miquelon
Magnoliidae de Saint-Pierre-et-Miquelon
205 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) | 1059 | 11,43% | 494 | 61,9% | 448 | 67,98% | 415 | 61,39% |
| Fournet (2002) | 147 | 1,59% | 128 | 16,04% | 128 | 19,42% | 112 | 16,57% |
| Linnaeus (1753) | 64 | 0,69% | 44 | 5,51% | 40 | 6,07% | 35 | 5,18% |
| Etcheberry & Abraham (2009) | 54 | 0,58% | 37 | 4,64% | 37 | 5,61% | 30 | 4,44% |
| MacKee (1994) | 53 | 0,57% | 43 | 5,39% | 43 | 6,53% | 39 | 5,77% |
| Hequet & Le Corre (2010) | 52 | 0,56% | 42 | 5,26% | 42 | 6,37% | 38 | 5,62% |
| Hequet et al. (2009) | 52 | 0,56% | 42 | 5,26% | 42 | 6,37% | 38 | 5,62% |
| Frenot et al. (2001) | 36 | 0,39% | 32 | 4,01% | 31 | 4,7% | 26 | 3,85% |
| Wiersema et al. (2018) | 32 | 0,35% | 10 | 1,25% | 10 | 1,52% | 7 | 1,04% |
| Jolinon (1987) | 28 | 0,3% | 25 | 3,13% | 25 | 3,79% | 22 | 3,25% |
| Linnaeus (1753) | 28 | 0,3% | 22 | 2,76% | 21 | 3,19% | 19 | 2,81% |
| Béguinot (2012) | 27 | 0,29% | 18 | 2,26% | 18 | 2,73% | 11 | 1,63% |
| Euro+Med (2006) | 26 | 0,28% | 1 | 0,13% | 1 | 0,15% | 0 | 0% |
| Carcaillet (1993) | 24 | 0,26% | 23 | 2,88% | 22 | 3,34% | 19 | 2,81% |
| Hullé et al. (2003) | 21 | 0,23% | 20 | 2,51% | 20 | 3,03% | 17 | 2,51% |
| Bell (1982) | 20 | 0,22% | 17 | 2,13% | 17 | 2,58% | 16 | 2,37% |
| Fourdrigniez & Meyer (2008) | 18 | 0,19% | 16 | 2,01% | 15 | 2,28% | 15 | 2,22% |
| Schenck (1906) | 18 | 0,19% | 16 | 2,01% | 16 | 2,43% | 12 | 1,78% |
| Funk et al. (2007) | 16 | 0,17% | 9 | 1,13% | 9 | 1,37% | 6 | 0,89% |
| Gray (1821) | 16 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rouy (1908) | 15 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Flora of North America (1993-) | 14 | 0,15% | 2 | 0,25% | 1 | 0,15% | 2 | 0,3% |
| Host (1831) | 14 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
| Moench (1794) | 14 | 0,15% | 1 | 0,13% | 1 | 0,15% | 0 | 0% |
| Munzinger et al. (2016) | 13 | 0,14% | 8 | 1% | 8 | 1,21% | 7 | 1,04% |
| Salisbury (1796) | 13 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Nyman (1882) | 12 | 0,13% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hoff (2021) | 11 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lamarck (1779) | 11 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Molina et al. (2008) | 11 | 0,12% | 1 | 0,13% | 1 | 0,15% | 1 | 0,15% |
| Morat et al. (2012) | 11 | 0,12% | 8 | 1% | 8 | 1,21% | 7 | 1,04% |
| Bourzat & Monie (1977) | 10 | 0,11% | 6 | 0,75% | 6 | 0,91% | 6 | 0,89% |
| Bubani & Penzig (1897) | 9 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fournier (1934-1940) | 9 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dulac (1867) | 8 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sennikov & Kurtto (2017) | 8 | 0,09% | 1 | 0,13% | 1 | 0,15% | 1 | 0,15% |
| Boreau (1857) | 7 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Arcangeli (1882) | 6 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Aublet (1775) | 6 | 0,06% | 4 | 0,5% | 4 | 0,61% | 4 | 0,59% |
| Cambecèdes et al. (2012) | 6 | 0,06% | 5 | 0,63% | 5 | 0,76% | 4 | 0,59% |
| Candolle (1815) | 6 | 0,06% | 1 | 0,13% | 1 | 0,15% | 1 | 0,15% |
| Fourreau (1869) | 6 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| González‐Elizondo & Peterson (1997) | 6 | 0,06% | 6 | 0,75% | 6 | 0,91% | 6 | 0,89% |
| Koch (1837) | 6 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lamarck & Candolle (1805) | 6 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lavergne (2011) | 6 | 0,06% | 5 | 0,63% | 5 | 0,76% | 3 | 0,44% |
| Rouy (1909) | 6 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Schenck (1905) | 6 | 0,06% | 6 | 0,75% | 6 | 0,91% | 4 | 0,59% |
| Breton (2014) | 5 | 0,05% | 5 | 0,63% | 5 | 0,76% | 5 | 0,74% |
| Bubani & Penzig (1900) | 5 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dumortier (1827) | 5 | 0,05% | 2 | 0,25% | 1 | 0,15% | 1 | 0,15% |
| Mennema (1989) | 5 | 0,05% | 1 | 0,13% | 1 | 0,15% | 1 | 0,15% |
| Miller (1768) | 5 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Moench (1794) | 5 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Muller et al. (2004) | 5 | 0,05% | 2 | 0,25% | 2 | 0,3% | 2 | 0,3% |
| Roalson et al. (2010) | 5 | 0,05% | 5 | 0,63% | 5 | 0,76% | 5 | 0,74% |
| Scopoli (1771) | 5 | 0,05% | 1 | 0,13% | 1 | 0,15% | 0 | 0% |
| Young (1970) | 5 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anonyme (2014) | 4 | 0,04% | 4 | 0,5% | 4 | 0,61% | 3 | 0,44% |
| Catalán et al. (2012) | 4 | 0,04% | 1 | 0,13% | 1 | 0,15% | 1 | 0,15% |
| Gandoger (1875) | 4 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gandoger (1876) | 4 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gandoger (1884) | 4 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Grenier & Godron (1850) | 4 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jordan (1864) | 4 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Persoon (1805) | 4 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Reichenbach (1830-1832) | 4 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rouy (1899) | 4 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bonnier & Layens (1894) | 3 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Couté & Garrouste (2009) | 3 | 0,03% | 1 | 0,13% | 1 | 0,15% | 1 | 0,15% |
| Davies, L. & Greene, S.W. (1976) | 3 | 0,03% | 3 | 0,38% | 3 | 0,46% | 3 | 0,44% |
| Don (1834) | 3 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Florence (2004) | 3 | 0,03% | 3 | 0,38% | 2 | 0,3% | 2 | 0,3% |
| Fourreau (1868) | 3 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gargominy et al. (1996) | 3 | 0,03% | 3 | 0,38% | 3 | 0,46% | 3 | 0,44% |
| Jolinon (1985) | 3 | 0,03% | 2 | 0,25% | 2 | 0,3% | 1 | 0,15% |
| Lamarck (1779) | 3 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Link (1821) | 3 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Muller et al. (2012) | 3 | 0,03% | 2 | 0,25% | 2 | 0,3% | 2 | 0,3% |
| Schur (1866) | 3 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Schuster et al. (2015) | 3 | 0,03% | 1 | 0,13% | 1 | 0,15% | 1 | 0,15% |
| Young (1971) | 3 | 0,03% | 3 | 0,38% | 3 | 0,46% | 3 | 0,44% |
| Zika & Tucker (2017) | 3 | 0,03% | 2 | 0,25% | 1 | 0,15% | 1 | 0,15% |
| Anonyme & Bosch (1950) | 2 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ascherson & Graebner (1897) | 2 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bobrov et al. (2022) | 2 | 0,02% | 2 | 0,25% | 2 | 0,3% | 2 | 0,3% |
| Candolle (1824) | 2 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Carine et al. (2003) | 2 | 0,02% | 1 | 0,13% | 1 | 0,15% | 1 | 0,15% |
| Carine et al. (2004) | 2 | 0,02% | 1 | 0,13% | 1 | 0,15% | 1 | 0,15% |
| Cariot & Saint-lager (1889) | 2 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Chaix (1785) | 2 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Coulot & Rabaute (2016) | 2 | 0,02% | 1 | 0,13% | 1 | 0,15% | 1 | 0,15% |
| Crantz (1766) | 2 | 0,02% | 1 | 0,13% | 1 | 0,15% | 1 | 0,15% |
| Drapikowska et al. (2012) | 2 | 0,02% | 1 | 0,13% | 1 | 0,15% | 1 | 0,15% |
| Ferlay et al. (2023) | 2 | 0,02% | 2 | 0,25% | 2 | 0,3% | 2 | 0,3% |
| Fiori (1925) | 2 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fujii et al. (2019) | 2 | 0,02% | 1 | 0,13% | 1 | 0,15% | 1 | 0,15% |
| Greene & Greene (1963) | 2 | 0,02% | 2 | 0,25% | 2 | 0,3% | 1 | 0,15% |
| Große-veldmann (2017) | 2 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hill (1768) | 2 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Husnot (1908) | 2 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kirschner (1990) | 2 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lansdown (2022) | 2 | 0,02% | 2 | 0,25% | 2 | 0,3% | 2 | 0,3% |
| Lejeune & Courtois (1831) | 2 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lemée (1953) | 2 | 0,02% | 2 | 0,25% | 2 | 0,3% | 2 | 0,3% |
| Lemée (1955) | 2 | 0,02% | 2 | 0,25% | 2 | 0,3% | 2 | 0,3% |
| Léveillé (1917) | 2 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Linnaeus (1759) | 2 | 0,02% | 2 | 0,25% | 2 | 0,3% | 2 | 0,3% |
| Lowe et al. (2007) | 2 | 0,02% | 1 | 0,13% | 1 | 0,15% | 1 | 0,15% |
| Massé (1982) | 2 | 0,02% | 2 | 0,25% | 1 | 0,15% | 2 | 0,3% |
| Meyer (1819) | 2 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Persoon (1807) | 2 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Peterson et al. (2014) | 2 | 0,02% | 2 | 0,25% | 2 | 0,3% | 2 | 0,3% |
| Pimentel & Sahuquillo (2008) | 2 | 0,02% | 1 | 0,13% | 1 | 0,15% | 1 | 0,15% |
| Reveal et al. (1991) | 2 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Riina et al. (2013) | 2 | 0,02% | 2 | 0,25% | 2 | 0,3% | 2 | 0,3% |
| Rouy (1913) | 2 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sennen & Frère (1936) | 2 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sprengel (1825) | 2 | 0,02% | 2 | 0,25% | 2 | 0,3% | 2 | 0,3% |
| Sprengel (1826) | 2 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Stefanovic et al. (2003) | 2 | 0,02% | 1 | 0,13% | 1 | 0,15% | 1 | 0,15% |
| Steudel (1841) | 2 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Van Der Putten et al. (2010) | 2 | 0,02% | 2 | 0,25% | 2 | 0,3% | 1 | 0,15% |
| Walters (1953) | 2 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| Abbayes (1931) | 1 | 0,01% | 1 | 0,13% | 1 | 0,15% | 1 | 0,15% |
| Acevedo-Rodríguez & Strong (2012) | 1 | 0,01% | 1 | 0,13% | 1 | 0,15% | 1 | 0,15% |
| Akhani et al. (2014) | 1 | 0,01% | 1 | 0,13% | 1 | 0,15% | 1 | 0,15% |
| Allioni (1785) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Anonyme. (2002) | 1 | 0,01% | 1 | 0,13% | 1 | 0,15% | 1 | 0,15% |
| Ascherson & Graebner (1910) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Aubert de la Rüe (1932) | 1 | 0,01% | 1 | 0,13% | 1 | 0,15% | 1 | 0,15% |
| Barker et al. (2012) | 1 | 0,01% | 1 | 0,13% | 1 | 0,15% | 1 | 0,15% |
| . Alger, typographie A. Jourdan ; Paris, librairie F. Savy. 825 pp.">Battandier & Trabut (1890) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bayón (2015) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Berton (2020) | 1 | 0,01% | 1 | 0,13% | 1 | 0,15% | 1 | 0,15% |
| Boreau (1849) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Boullet et al. (2018) | 1 | 0,01% | 1 | 0,13% | 1 | 0,15% | 1 | 0,15% |
| Braun-blanquet (1933) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bubani & Penzig (1901) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Candolle (1830) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Candolle (1838-1839) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Candolle (1848) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Candolle (1864-1868) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Chauvel et al. (2006) | 1 | 0,01% | 1 | 0,13% | 1 | 0,15% | 1 | 0,15% |
| Cheek (2016) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Correa & Silva (2005) | 1 | 0,01% | 1 | 0,13% | 1 | 0,15% | 1 | 0,15% |
| Coste (1937) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Costea et al. (2001) | 1 | 0,01% | 1 | 0,13% | 1 | 0,15% | 1 | 0,15% |
| Crantz (1766) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cremers & Hoff (1997) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dauphin (1999) | 1 | 0,01% | 1 | 0,13% | 1 | 0,15% | 0 | 0% |
| Delnatte & Meyer (2012) | 1 | 0,01% | 1 | 0,13% | 1 | 0,15% | 1 | 0,15% |
| Don (1832) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Eaton (1922) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ehrhart (1780) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Felber-girard et al. (1996) | 1 | 0,01% | 1 | 0,13% | 1 | 0,15% | 1 | 0,15% |
| Fleischmann & Gonella (2020) | 1 | 0,01% | 1 | 0,13% | 1 | 0,15% | 1 | 0,15% |
| Flora iberica | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fournier (1928) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gaertner (1791) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Greuter & Raus (2002) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Grisebach (1866) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gussone (1843) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hartman (1820) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hassemer et al. (2017) | 1 | 0,01% | 1 | 0,13% | 1 | 0,15% | 1 | 0,15% |
| Hemsley (1885) | 1 | 0,01% | 1 | 0,13% | 1 | 0,15% | 1 | 0,15% |
| Hoffmann (1804) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ito et al. (2015) | 1 | 0,01% | 1 | 0,13% | 1 | 0,15% | 1 | 0,15% |
| Jordan & Fourreau (1868) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Karsch (1853) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Knapp (2013) | 1 | 0,01% | 1 | 0,13% | 1 | 0,15% | 1 | 0,15% |
| Koch (1844) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kuntze (1891) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lamarck & Candolle (1805) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lansdown & Jarvis (2004) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Léotard & Chaline (2013) | 1 | 0,01% | 1 | 0,13% | 1 | 0,15% | 1 | 0,15% |
| Ledebour (1851) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Link (1829) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Linnaeus (1762) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mady et al. (2016) | 1 | 0,01% | 1 | 0,13% | 1 | 0,15% | 1 | 0,15% |
| Mandák et al. (2005) | 1 | 0,01% | 1 | 0,13% | 0 | 0% | 1 | 0,15% |
| Manns & Anderberg (2009) | 1 | 0,01% | 1 | 0,13% | 1 | 0,15% | 1 | 0,15% |
| Meyer et al. (2006) | 1 | 0,01% | 1 | 0,13% | 1 | 0,15% | 1 | 0,15% |
| Miégeville (1863) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Morat & Veillon (1985) | 1 | 0,01% | 1 | 0,13% | 1 | 0,15% | 1 | 0,15% |
| Munzinger & Lebigre (2007) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Nelson-Smith et al. (2014) | 1 | 0,01% | 1 | 0,13% | 1 | 0,15% | 1 | 0,15% |
| Reichardt (1871) | 1 | 0,01% | 1 | 0,13% | 1 | 0,15% | 1 | 0,15% |
| Rouy & Camus (1901) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rouy & Foucaud (1896) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Schaefer et al. (2012) | 1 | 0,01% | 1 | 0,13% | 1 | 0,15% | 1 | 0,15% |
| Schreber (1771) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Scopoli (1771) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Scopoli (1786) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sennen (1928) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sweet (1826) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Timaná et al. (2019) | 1 | 0,01% | 1 | 0,13% | 1 | 0,15% | 1 | 0,15% |
| Urtubey et al. (2016) | 1 | 0,01% | 1 | 0,13% | 1 | 0,15% | 1 | 0,15% |
| Villars (1779) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Villars (1789) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Walthers (1802) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Wiggers (1780) | 1 | 0,01% | 1 | 0,13% | 1 | 0,15% | 1 | 0,15% |
| Willdenow (1799) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Wilson (2017) | 1 | 0,01% | 1 | 0,13% | 1 | 0,15% | 1 | 0,15% |
| Zhang et al. (2008) | 1 | 0,01% | 1 | 0,13% | 1 | 0,15% | 1 | 0,15% |
