Trachéophytes de Saint-Pierre-et-Miquelon
Trachéophyta de Saint-Pierre-et-Miquelon
235 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) | 1142 | 11,52% | 535 | 61,99% | 488 | 68,25% | 445 | 60,79% |
Fournet (2002) | 147 | 1,48% | 128 | 14,83% | 128 | 17,9% | 112 | 15,3% |
Christenhusz et al. (2019) | 88 | 0,89% | 3 | 0,35% | 3 | 0,42% | 2 | 0,27% |
Linnaeus (1753) | 67 | 0,68% | 44 | 5,1% | 40 | 5,59% | 35 | 4,78% |
Linnaeus (1753) | 59 | 0,6% | 32 | 3,71% | 30 | 4,2% | 27 | 3,69% |
Etcheberry & Abraham (2009) | 54 | 0,54% | 37 | 4,29% | 37 | 5,17% | 30 | 4,1% |
MacKee (1994) | 53 | 0,53% | 43 | 4,98% | 43 | 6,01% | 39 | 5,33% |
Hequet & Le Corre (2010) | 52 | 0,52% | 42 | 4,87% | 42 | 5,87% | 38 | 5,19% |
Hequet et al. (2009) | 52 | 0,52% | 42 | 4,87% | 42 | 5,87% | 38 | 5,19% |
Frenot et al. (2001) | 36 | 0,36% | 32 | 3,71% | 31 | 4,34% | 26 | 3,55% |
Wiersema et al. (2018) | 34 | 0,34% | 11 | 1,27% | 11 | 1,54% | 8 | 1,09% |
Béguinot (2012) | 28 | 0,28% | 19 | 2,2% | 19 | 2,66% | 11 | 1,5% |
Gray (1821) | 28 | 0,28% | 0 | 0% | 0 | 0% | 0 | 0% |
Jolinon (1987) | 28 | 0,28% | 25 | 2,9% | 25 | 3,5% | 22 | 3,01% |
Derrick et al. (1987) | 27 | 0,27% | 0 | 0% | 0 | 0% | 0 | 0% |
Euro+Med (2006) | 26 | 0,26% | 1 | 0,12% | 1 | 0,14% | 0 | 0% |
Salisbury (1796) | 26 | 0,26% | 0 | 0% | 0 | 0% | 0 | 0% |
Carcaillet (1993) | 24 | 0,24% | 23 | 2,67% | 22 | 3,08% | 19 | 2,6% |
Hullé et al. (2003) | 21 | 0,21% | 20 | 2,32% | 20 | 2,8% | 17 | 2,32% |
Bell (1982) | 20 | 0,2% | 17 | 1,97% | 17 | 2,38% | 16 | 2,19% |
Funk et al. (2007) | 19 | 0,19% | 10 | 1,16% | 10 | 1,4% | 7 | 0,96% |
Dulac (1867) | 18 | 0,18% | 0 | 0% | 0 | 0% | 0 | 0% |
Fourdrigniez & Meyer (2008) | 18 | 0,18% | 16 | 1,85% | 15 | 2,1% | 15 | 2,05% |
Schenck (1906) | 18 | 0,18% | 16 | 1,85% | 16 | 2,24% | 12 | 1,64% |
Flora of North America (1993-) | 16 | 0,16% | 2 | 0,23% | 1 | 0,14% | 2 | 0,27% |
Moench (1794) | 15 | 0,15% | 2 | 0,23% | 2 | 0,28% | 1 | 0,14% |
Munzinger et al. (2016) | 15 | 0,15% | 9 | 1,04% | 9 | 1,26% | 8 | 1,09% |
Rouy (1908) | 15 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Host (1831) | 14 | 0,14% | 0 | 0% | 0 | 0% | 0 | 0% |
Lamarck (1779) | 12 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Morat et al. (2012) | 12 | 0,12% | 9 | 1,04% | 9 | 1,26% | 8 | 1,09% |
Nyman (1882) | 12 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Fournier (1934-1940) | 11 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Hoff (2021) | 11 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Molina et al. (2008) | 11 | 0,11% | 1 | 0,12% | 1 | 0,14% | 1 | 0,14% |
Bourzat & Monie (1977) | 10 | 0,1% | 6 | 0,7% | 6 | 0,84% | 6 | 0,82% |
Arcangeli (1882) | 9 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Bubani & Penzig (1897) | 9 | 0,09% | 0 | 0% | 0 | 0% | 0 | 0% |
Döll (1843) | 8 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Lamarck (1778) | 8 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Rouy (1913) | 8 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Savulescu (1952) | 8 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Sennikov & Kurtto (2017) | 8 | 0,08% | 1 | 0,12% | 1 | 0,14% | 1 | 0,14% |
Anonyme (2014) | 7 | 0,07% | 7 | 0,81% | 7 | 0,98% | 5 | 0,68% |
Boreau (1857) | 7 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Gandoger (1884) | 7 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Miller (1768) | 7 | 0,07% | 1 | 0,12% | 1 | 0,14% | 0 | 0% |
Schur (1866) | 7 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Aublet (1775) | 6 | 0,06% | 4 | 0,46% | 4 | 0,56% | 4 | 0,55% |
Cambecèdes et al. (2012) | 6 | 0,06% | 5 | 0,58% | 5 | 0,7% | 4 | 0,55% |
Candolle (1815) | 6 | 0,06% | 1 | 0,12% | 1 | 0,14% | 1 | 0,14% |
Fourreau (1869) | 6 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
González‐Elizondo & Peterson (1997) | 6 | 0,06% | 6 | 0,7% | 6 | 0,84% | 6 | 0,82% |
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 | 0,58% | 5 | 0,7% | 3 | 0,41% |
Rouy (1909) | 6 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Schenck (1905) | 6 | 0,06% | 6 | 0,7% | 6 | 0,84% | 4 | 0,55% |
Bonnier & Layens (1894) | 5 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Breton (2014) | 5 | 0,05% | 5 | 0,58% | 5 | 0,7% | 5 | 0,68% |
Bubani & Penzig (1900) | 5 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Dumortier (1827) | 5 | 0,05% | 2 | 0,23% | 1 | 0,14% | 1 | 0,14% |
Greuter & Troia (2015) | 5 | 0,05% | 1 | 0,12% | 1 | 0,14% | 1 | 0,14% |
Kuntze (1891) | 5 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Mennema (1989) | 5 | 0,05% | 1 | 0,12% | 1 | 0,14% | 1 | 0,14% |
Moench (1794) | 5 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Muller et al. (2004) | 5 | 0,05% | 2 | 0,23% | 2 | 0,28% | 2 | 0,27% |
Roalson et al. (2010) | 5 | 0,05% | 5 | 0,58% | 5 | 0,7% | 5 | 0,68% |
Scopoli (1771) | 5 | 0,05% | 1 | 0,12% | 1 | 0,14% | 0 | 0% |
Young (1970) | 5 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Catalán et al. (2012) | 4 | 0,04% | 1 | 0,12% | 1 | 0,14% | 1 | 0,14% |
Gandoger (1875) | 4 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Gandoger (1876) | 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% |
Muller et al. (2012) | 4 | 0,04% | 2 | 0,23% | 2 | 0,28% | 2 | 0,27% |
Persoon (1805) | 4 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Prelli & Boudrie (2021) | 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% |
Anonyme (2023) | 3 | 0,03% | 2 | 0,23% | 1 | 0,14% | 2 | 0,27% |
Cariot & Saint-lager (1889) | 3 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Couté & Garrouste (2009) | 3 | 0,03% | 1 | 0,12% | 1 | 0,14% | 1 | 0,14% |
Davies, L. & Greene, S.W. (1976) | 3 | 0,03% | 3 | 0,35% | 3 | 0,42% | 3 | 0,41% |
Don (1834) | 3 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Florence (2004) | 3 | 0,03% | 3 | 0,35% | 2 | 0,28% | 2 | 0,27% |
Fourreau (1868) | 3 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Gargominy et al. (1996) | 3 | 0,03% | 3 | 0,35% | 3 | 0,42% | 3 | 0,41% |
Hassler & Schmitt (2018) | 3 | 0,03% | 2 | 0,23% | 1 | 0,14% | 2 | 0,27% |
Jolinon (1985) | 3 | 0,03% | 2 | 0,23% | 2 | 0,28% | 1 | 0,14% |
Lamarck (1779) | 3 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Link (1821) | 3 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Persoon (1807) | 3 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Schuster et al. (2015) | 3 | 0,03% | 1 | 0,12% | 1 | 0,14% | 1 | 0,14% |
Young (1971) | 3 | 0,03% | 3 | 0,35% | 3 | 0,42% | 3 | 0,41% |
Zika & Tucker (2017) | 3 | 0,03% | 2 | 0,23% | 1 | 0,14% | 1 | 0,14% |
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 | 0,23% | 2 | 0,28% | 2 | 0,27% |
Bubani & Penzig (1902) | 2 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Candolle (1824) | 2 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Carine et al. (2003) | 2 | 0,02% | 1 | 0,12% | 1 | 0,14% | 1 | 0,14% |
Carine et al. (2004) | 2 | 0,02% | 1 | 0,12% | 1 | 0,14% | 1 | 0,14% |
Chaix (1785) | 2 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Coulot & Rabaute (2016) | 2 | 0,02% | 1 | 0,12% | 1 | 0,14% | 1 | 0,14% |
Crantz (1766) | 2 | 0,02% | 1 | 0,12% | 1 | 0,14% | 1 | 0,14% |
Drapikowska et al. (2012) | 2 | 0,02% | 1 | 0,12% | 1 | 0,14% | 1 | 0,14% |
Elven & Murray (2008) | 2 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Ferlay et al. (2023) | 2 | 0,02% | 2 | 0,23% | 2 | 0,28% | 2 | 0,27% |
Fiori (1925) | 2 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Fujii et al. (2019) | 2 | 0,02% | 1 | 0,12% | 1 | 0,14% | 1 | 0,14% |
Greene & Greene (1963) | 2 | 0,02% | 2 | 0,23% | 2 | 0,28% | 1 | 0,14% |
Große-veldmann (2017) | 2 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Hauk et al. (2003) | 2 | 0,02% | 1 | 0,12% | 1 | 0,14% | 1 | 0,14% |
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 | 0,23% | 2 | 0,28% | 2 | 0,27% |
Lejeune & Courtois (1831) | 2 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Lemée (1953) | 2 | 0,02% | 2 | 0,23% | 2 | 0,28% | 2 | 0,27% |
Lemée (1955) | 2 | 0,02% | 2 | 0,23% | 2 | 0,28% | 2 | 0,27% |
Léveillé (1917) | 2 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Linnaeus (1759) | 2 | 0,02% | 2 | 0,23% | 2 | 0,28% | 2 | 0,27% |
Lowe et al. (2007) | 2 | 0,02% | 1 | 0,12% | 1 | 0,14% | 1 | 0,14% |
Massé (1982) | 2 | 0,02% | 2 | 0,23% | 1 | 0,14% | 2 | 0,27% |
Meyer (1819) | 2 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Peterson et al. (2014) | 2 | 0,02% | 2 | 0,23% | 2 | 0,28% | 2 | 0,27% |
Pimentel & Sahuquillo (2008) | 2 | 0,02% | 1 | 0,12% | 1 | 0,14% | 1 | 0,14% |
Pteridophyte Phylogeny Group (2016) | 2 | 0,02% | 2 | 0,23% | 2 | 0,28% | 2 | 0,27% |
Reveal et al. (1991) | 2 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Riina et al. (2013) | 2 | 0,02% | 2 | 0,23% | 2 | 0,28% | 2 | 0,27% |
Sennen & Frère (1936) | 2 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Sprengel (1825) | 2 | 0,02% | 2 | 0,23% | 2 | 0,28% | 2 | 0,27% |
Sprengel (1826) | 2 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Stefanovic et al. (2003) | 2 | 0,02% | 1 | 0,12% | 1 | 0,14% | 1 | 0,14% |
Steudel (1841) | 2 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Van Der Putten et al. (2010) | 2 | 0,02% | 2 | 0,23% | 2 | 0,28% | 1 | 0,14% |
Villars (1786) | 2 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Walters (1953) | 2 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Abbayes (1931) | 1 | 0,01% | 1 | 0,12% | 1 | 0,14% | 1 | 0,14% |
Acevedo-Rodríguez & Strong (2012) | 1 | 0,01% | 1 | 0,12% | 1 | 0,14% | 1 | 0,14% |
Akhani et al. (2014) | 1 | 0,01% | 1 | 0,12% | 1 | 0,14% | 1 | 0,14% |
Allioni (1785) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme. (2002) | 1 | 0,01% | 1 | 0,12% | 1 | 0,14% | 1 | 0,14% |
Ascherson & Graebner (1910) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Aubert de la Rüe (1932) | 1 | 0,01% | 1 | 0,12% | 1 | 0,14% | 1 | 0,14% |
Badré & Deschâtres (1979) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Barker et al. (2012) | 1 | 0,01% | 1 | 0,12% | 1 | 0,14% | 1 | 0,14% |
. 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% |
Bernard (2015) | 1 | 0,01% | 1 | 0,12% | 1 | 0,14% | 1 | 0,14% |
Berton (2020) | 1 | 0,01% | 1 | 0,12% | 1 | 0,14% | 1 | 0,14% |
Boreau (1849) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Boullet et al. (2018) | 1 | 0,01% | 1 | 0,12% | 1 | 0,14% | 1 | 0,14% |
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 | 0,12% | 1 | 0,14% | 1 | 0,14% |
Cheek (2016) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Christenhusz (2009) | 1 | 0,01% | 1 | 0,12% | 1 | 0,14% | 1 | 0,14% |
Correa & Silva (2005) | 1 | 0,01% | 1 | 0,12% | 1 | 0,14% | 1 | 0,14% |
Coste (1937) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Costea et al. (2001) | 1 | 0,01% | 1 | 0,12% | 1 | 0,14% | 1 | 0,14% |
Coughlan et al. (2020) | 1 | 0,01% | 1 | 0,12% | 1 | 0,14% | 1 | 0,14% |
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 | 0,12% | 1 | 0,14% | 0 | 0% |
Delnatte & Meyer (2012) | 1 | 0,01% | 1 | 0,12% | 1 | 0,14% | 1 | 0,14% |
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% |
Ekrt et al. (2022) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Etcheberry (1998) | 1 | 0,01% | 1 | 0,12% | 1 | 0,14% | 0 | 0% |
Fawcett & Smith (2021) | 1 | 0,01% | 1 | 0,12% | 0 | 0% | 1 | 0,14% |
Felber-girard et al. (1996) | 1 | 0,01% | 1 | 0,12% | 1 | 0,14% | 1 | 0,14% |
Fleischmann & Gonella (2020) | 1 | 0,01% | 1 | 0,12% | 1 | 0,14% | 1 | 0,14% |
Flora iberica | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Fournier (1928) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Fuchs (1974) | 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 | 0,12% | 1 | 0,14% | 1 | 0,14% |
Hemsley (1885) | 1 | 0,01% | 1 | 0,12% | 1 | 0,14% | 1 | 0,14% |
Hoffmann (1796) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Hoffmann (1804) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Holub (1969) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Ito et al. (2015) | 1 | 0,01% | 1 | 0,12% | 1 | 0,14% | 1 | 0,14% |
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 | 0,12% | 1 | 0,14% | 1 | 0,14% |
Koch (1844) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Koch (1845) | 1 | 0,01% | 1 | 0,12% | 1 | 0,14% | 1 | 0,14% |
Lamarck & Candolle (1805) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Lansdown & Jarvis (2004) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Lapeyrouse (1813) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Léotard & Chaline (2013) | 1 | 0,01% | 1 | 0,12% | 1 | 0,14% | 1 | 0,14% |
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 | 0,12% | 1 | 0,14% | 1 | 0,14% |
Mandák et al. (2005) | 1 | 0,01% | 1 | 0,12% | 0 | 0% | 1 | 0,14% |
Manns & Anderberg (2009) | 1 | 0,01% | 1 | 0,12% | 1 | 0,14% | 1 | 0,14% |
Meyer et al. (2006) | 1 | 0,01% | 1 | 0,12% | 1 | 0,14% | 1 | 0,14% |
Miégeville (1863) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Morat & Veillon (1985) | 1 | 0,01% | 1 | 0,12% | 1 | 0,14% | 1 | 0,14% |
Munzinger & Lebigre (2007) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Murray (1784) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Nelson-Smith et al. (2014) | 1 | 0,01% | 1 | 0,12% | 1 | 0,14% | 1 | 0,14% |
Øllgaard et al. (2020) | 1 | 0,01% | 1 | 0,12% | 1 | 0,14% | 1 | 0,14% |
Reichardt (1871) | 1 | 0,01% | 1 | 0,12% | 1 | 0,14% | 1 | 0,14% |
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 | 0,12% | 1 | 0,14% | 1 | 0,14% |
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% |
Sessa (2024) | 1 | 0,01% | 1 | 0,12% | 0 | 0% | 1 | 0,14% |
Sweet (1826) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Thomson (2004) | 1 | 0,01% | 1 | 0,12% | 0 | 0% | 1 | 0,14% |
Timaná et al. (2019) | 1 | 0,01% | 1 | 0,12% | 1 | 0,14% | 1 | 0,14% |
Urtubey et al. (2016) | 1 | 0,01% | 1 | 0,12% | 1 | 0,14% | 1 | 0,14% |
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 | 0,12% | 1 | 0,14% | 1 | 0,14% |
Willdenow (1799) | 1 | 0,01% | 0 | 0% | 0 | 0% | 0 | 0% |
Wilson (2017) | 1 | 0,01% | 1 | 0,12% | 1 | 0,14% | 1 | 0,14% |
Zhang et al. (2008) | 1 | 0,01% | 1 | 0,12% | 1 | 0,14% | 1 | 0,14% |