Angiospermes de Saint-Martin
Magnoliidae de Saint-Martin
358 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
Référence | Total | Valides | Espèces | Taxons terminaux | ||||
---|---|---|---|---|---|---|---|---|
nb | % | nb | % | nb | % | nb | % | |
Fournet (2002) | 2367 | 46,55% | 1870 | 271,01% | 1862 | 285,58% | 1806 | 276,15% |
Funk et al. (2007) | 937 | 18,43% | 333 | 48,26% | 326 | 50% | 309 | 47,25% |
Molino et al. (2022) | 564 | 11,09% | 25 | 3,62% | 25 | 3,83% | 22 | 3,36% |
Hequet & Le Corre (2010) | 248 | 4,88% | 194 | 28,12% | 190 | 29,14% | 179 | 27,37% |
Hequet et al. (2009) | 248 | 4,88% | 194 | 28,12% | 190 | 29,14% | 179 | 27,37% |
MacKee (1994) | 246 | 4,84% | 189 | 27,39% | 185 | 28,37% | 175 | 26,76% |
Tison et al. (2014) | 233 | 4,58% | 117 | 16,96% | 114 | 17,48% | 109 | 16,67% |
Acevedo-Rodríguez & Strong (2012) | 164 | 3,23% | 104 | 15,07% | 92 | 14,11% | 102 | 15,6% |
Fourdrigniez & Meyer (2008) | 145 | 2,85% | 116 | 16,81% | 114 | 17,48% | 107 | 16,36% |
Delnatte & Meyer (2012) | 126 | 2,48% | 101 | 14,64% | 99 | 15,18% | 98 | 14,98% |
Paton et al. (2019) | 116 | 2,28% | 2 | 0,29% | 2 | 0,31% | 2 | 0,31% |
Munzinger et al. (2016) | 111 | 2,18% | 34 | 4,93% | 31 | 4,75% | 32 | 4,89% |
Morat & Veillon (1985) | 78 | 1,53% | 60 | 8,7% | 58 | 8,9% | 54 | 8,26% |
Aublet (1775) | 76 | 1,49% | 28 | 4,06% | 27 | 4,14% | 27 | 4,13% |
Morat et al. (2012) | 76 | 1,49% | 35 | 5,07% | 32 | 4,91% | 32 | 4,89% |
Boullet et al. (2018) | 66 | 1,3% | 57 | 8,26% | 55 | 8,44% | 51 | 7,8% |
Molino et al. (2009) | 51 | 1% | 47 | 6,81% | 47 | 7,21% | 44 | 6,73% |
Léotard & Chaline (2013) | 50 | 0,98% | 42 | 6,09% | 42 | 6,44% | 41 | 6,27% |
Ter Steege et al. (2016) | 45 | 0,88% | 43 | 6,23% | 43 | 6,6% | 39 | 5,96% |
Ortuño & Borsch (2020) | 40 | 0,79% | 3 | 0,43% | 3 | 0,46% | 3 | 0,46% |
Florence (2004) | 39 | 0,77% | 34 | 4,93% | 34 | 5,21% | 33 | 5,05% |
Lemée (1952) | 38 | 0,75% | 25 | 3,62% | 25 | 3,83% | 25 | 3,82% |
Feldmann (2012) | 35 | 0,69% | 32 | 4,64% | 32 | 4,91% | 32 | 4,89% |
Fonseca et al. (2017) | 33 | 0,65% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Véron et al. (2021) | 33 | 0,65% | 29 | 4,2% | 29 | 4,45% | 29 | 4,43% |
Porter-Utley (2014) | 31 | 0,61% | 10 | 1,45% | 6 | 0,92% | 4 | 0,61% |
Ståhl (2010) | 31 | 0,61% | 10 | 1,45% | 10 | 1,53% | 10 | 1,53% |
Kuijt (2003) | 29 | 0,57% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Lemée (1953) | 28 | 0,55% | 15 | 2,17% | 15 | 2,3% | 15 | 2,29% |
Korotkova et al. (2017) | 27 | 0,53% | 4 | 0,58% | 4 | 0,61% | 3 | 0,46% |
Lemée (1955) | 26 | 0,51% | 13 | 1,88% | 13 | 1,99% | 13 | 1,99% |
Stace (2010) | 26 | 0,51% | 9 | 1,3% | 5 | 0,77% | 7 | 1,07% |
Linnaeus (1753) | 24 | 0,47% | 15 | 2,17% | 15 | 2,3% | 14 | 2,14% |
Baaijens & Veldkamp (1991) | 23 | 0,45% | 2 | 0,29% | 2 | 0,31% | 2 | 0,31% |
Anonyme (2014) | 22 | 0,43% | 19 | 2,75% | 19 | 2,91% | 18 | 2,75% |
Gargominy et al. (1996) | 22 | 0,43% | 17 | 2,46% | 17 | 2,61% | 17 | 2,6% |
Krapovickas (2003) | 22 | 0,43% | 4 | 0,58% | 4 | 0,61% | 4 | 0,61% |
Cornejo (2020) | 20 | 0,39% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Suddee et al. (2004) | 20 | 0,39% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Florence (1997) | 19 | 0,37% | 12 | 1,74% | 12 | 1,84% | 12 | 1,83% |
Sambin (2020) | 19 | 0,37% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Cremers & Hoff (1997) | 18 | 0,35% | 3 | 0,43% | 3 | 0,46% | 3 | 0,46% |
Nesom (2009) | 17 | 0,33% | 1 | 0,14% | 1 | 0,15% | 0 | 0% |
Linnaeus (1753) | 16 | 0,31% | 13 | 1,88% | 12 | 1,84% | 11 | 1,68% |
Webster & Armbruster (1991) | 15 | 0,29% | 2 | 0,29% | 1 | 0,15% | 1 | 0,15% |
Fryxell (2001) | 14 | 0,28% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Howard (1973) | 14 | 0,28% | 0 | 0% | 0 | 0% | 0 | 0% |
Mathias & Theobald (1981) | 14 | 0,28% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Meyer et al. (2006) | 14 | 0,28% | 9 | 1,3% | 8 | 1,23% | 7 | 1,07% |
Miller (1768) | 14 | 0,28% | 2 | 0,29% | 2 | 0,31% | 2 | 0,31% |
Pool (2014) | 14 | 0,28% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Cremers & Hoff (1994) | 13 | 0,26% | 3 | 0,43% | 3 | 0,46% | 3 | 0,46% |
D'arcy (1987) | 13 | 0,26% | 0 | 0% | 0 | 0% | 0 | 0% |
Görts-van Rijn (2007) | 13 | 0,26% | 3 | 0,43% | 3 | 0,46% | 3 | 0,46% |
Kükenthal (1936) | 13 | 0,26% | 0 | 0% | 0 | 0% | 0 | 0% |
Lavergne (2011) | 13 | 0,26% | 11 | 1,59% | 10 | 1,53% | 9 | 1,38% |
Desmodium incanum and Fall of D. canum (Fabaceae). Taxon, 27(4): 365-370.">Nicolson (1978) | 13 | 0,26% | 1 | 0,14% | 1 | 0,15% | 0 | 0% |
Taylor (1994) | 13 | 0,26% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Boggan et al. (1992) | 12 | 0,24% | 7 | 1,01% | 7 | 1,07% | 7 | 1,07% |
Feldmann (2014) | 12 | 0,24% | 12 | 1,74% | 12 | 1,84% | 12 | 1,83% |
Jeffrey (1980) | 12 | 0,24% | 2 | 0,29% | 2 | 0,31% | 2 | 0,31% |
Salisbury (1796) | 12 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
Feuillet (2020) | 11 | 0,22% | 4 | 0,58% | 4 | 0,61% | 4 | 0,61% |
Hunt (1986) | 11 | 0,22% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Jost et al. (2019) | 11 | 0,22% | 9 | 1,3% | 8 | 1,23% | 9 | 1,38% |
Werkhoven (1986) | 11 | 0,22% | 6 | 0,87% | 6 | 0,92% | 6 | 0,92% |
Christenhusz (2002) | 10 | 0,2% | 6 | 0,87% | 6 | 0,92% | 6 | 0,92% |
Couté & Garrouste (2009) | 10 | 0,2% | 9 | 1,3% | 8 | 1,23% | 9 | 1,38% |
Ferlay et al. (2023) | 10 | 0,2% | 10 | 1,45% | 10 | 1,53% | 10 | 1,53% |
Oliveira Pellegrini & Forzza (2017) | 10 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Simões & Staples (2017) | 10 | 0,2% | 4 | 0,58% | 4 | 0,61% | 4 | 0,61% |
Iamonico (2016) | 9 | 0,18% | 0 | 0% | 0 | 0% | 0 | 0% |
Yang et al. (2012) | 9 | 0,18% | 9 | 1,3% | 9 | 1,38% | 9 | 1,38% |
Gagnon et al. (2016) | 8 | 0,16% | 4 | 0,58% | 4 | 0,61% | 4 | 0,61% |
Sauer (1964) | 8 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
Acevedo-Rodríguez (2012) | 7 | 0,14% | 3 | 0,43% | 3 | 0,46% | 2 | 0,31% |
Berg & Roselli (2005) | 7 | 0,14% | 6 | 0,87% | 3 | 0,46% | 3 | 0,46% |
Berg (1992) | 7 | 0,14% | 3 | 0,43% | 3 | 0,46% | 3 | 0,46% |
Borchsenius et al. (2012) | 7 | 0,14% | 4 | 0,58% | 4 | 0,61% | 4 | 0,61% |
Candolle (1849) | 7 | 0,14% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
David & Thiebaut (2013) | 7 | 0,14% | 2 | 0,29% | 2 | 0,31% | 2 | 0,31% |
Hassemer et al. (2017) | 7 | 0,14% | 7 | 1,01% | 7 | 1,07% | 7 | 1,07% |
Patchell et al. (2014) | 7 | 0,14% | 6 | 0,87% | 6 | 0,92% | 6 | 0,92% |
Pejhanmehr (2022) | 7 | 0,14% | 7 | 1,01% | 7 | 1,07% | 7 | 1,07% |
Questel (2023) | 7 | 0,14% | 6 | 0,87% | 6 | 0,92% | 5 | 0,76% |
Vorontsova et al. (2023) | 7 | 0,14% | 4 | 0,58% | 4 | 0,61% | 4 | 0,61% |
Wasshausen (2006) | 7 | 0,14% | 2 | 0,29% | 2 | 0,31% | 2 | 0,31% |
Wood et al. (2020) | 7 | 0,14% | 7 | 1,01% | 6 | 0,92% | 5 | 0,76% |
Zerega et al. (2005) | 7 | 0,14% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Barrett et al. (2017) | 6 | 0,12% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Bovini (2010) | 6 | 0,12% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Bunting (1960) | 6 | 0,12% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Espinoza et al. (2018) | 6 | 0,12% | 3 | 0,43% | 3 | 0,46% | 3 | 0,46% |
Feuillet & Poncy (1998) | 6 | 0,12% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Judziewicz (1990) | 6 | 0,12% | 6 | 0,87% | 6 | 0,92% | 6 | 0,92% |
Krings (2011) | 6 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Kuijt (2007) | 6 | 0,12% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Noguera-savelli (2010) | 6 | 0,12% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Peterson et al. (2014) | 6 | 0,12% | 6 | 0,87% | 6 | 0,92% | 6 | 0,92% |
Pfeifer (1966) | 6 | 0,12% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Silva et al. (2019) | 6 | 0,12% | 4 | 0,58% | 4 | 0,61% | 4 | 0,61% |
Toutain (1989) | 6 | 0,12% | 6 | 0,87% | 6 | 0,92% | 5 | 0,76% |
Turner (2013) | 6 | 0,12% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Welker et al. (2020) | 6 | 0,12% | 6 | 0,87% | 6 | 0,92% | 5 | 0,76% |
Allen et al. (2022) | 5 | 0,1% | 5 | 0,72% | 5 | 0,77% | 5 | 0,76% |
Cornejo & Iltis (2007) | 5 | 0,1% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Feuillet (2020) | 5 | 0,1% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Franck et al. (2019) | 5 | 0,1% | 5 | 0,72% | 5 | 0,77% | 5 | 0,76% |
Horn (1994) | 5 | 0,1% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Lowe et al. (2007) | 5 | 0,1% | 4 | 0,58% | 3 | 0,46% | 3 | 0,46% |
Maddi (2014) | 5 | 0,1% | 2 | 0,29% | 2 | 0,31% | 2 | 0,31% |
Mazine et al. (2018) | 5 | 0,1% | 5 | 0,72% | 5 | 0,77% | 5 | 0,76% |
Moench (1794) | 5 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Wiersema et al. (2018) | 5 | 0,1% | 2 | 0,29% | 2 | 0,31% | 2 | 0,31% |
Zuloaga et al. (2018) | 5 | 0,1% | 5 | 0,72% | 5 | 0,77% | 5 | 0,76% |
Andersson (1981) | 4 | 0,08% | 2 | 0,29% | 2 | 0,31% | 2 | 0,31% |
Candolle (1828) | 4 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Candolle (1845) | 4 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Cowan & Lindeman (1989) | 4 | 0,08% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Dehgan (2012) | 4 | 0,08% | 3 | 0,43% | 3 | 0,46% | 3 | 0,46% |
Dorsey et al. (2013) | 4 | 0,08% | 4 | 0,58% | 4 | 0,61% | 3 | 0,46% |
Feuillet (2009) | 4 | 0,08% | 4 | 0,58% | 4 | 0,61% | 3 | 0,46% |
Feuillet (2019) | 4 | 0,08% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Fournier (1934-1940) | 4 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Freire-Fierro (2002) | 4 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Epidendrum". Icones Orchidacearum, 11: pls. 1101-1200.">Hágsater (2008) | 4 | 0,08% | 2 | 0,29% | 1 | 0,15% | 1 | 0,15% |
Hauenschild et al. (2016) | 4 | 0,08% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Hily et al. (2010) | 4 | 0,08% | 4 | 0,58% | 4 | 0,61% | 4 | 0,61% |
Manzitto‐Tripp & Daniel (2023) | 4 | 0,08% | 4 | 0,58% | 4 | 0,61% | 4 | 0,61% |
Mori et al. (2002) | 4 | 0,08% | 3 | 0,43% | 3 | 0,46% | 3 | 0,46% |
Ocampo & Columbus (2012) | 4 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Paudyal et al. (2018) | 4 | 0,08% | 3 | 0,43% | 3 | 0,46% | 3 | 0,46% |
Sachet (1962) | 4 | 0,08% | 4 | 0,58% | 4 | 0,61% | 4 | 0,61% |
Sant (2022) | 4 | 0,08% | 4 | 0,58% | 4 | 0,61% | 3 | 0,46% |
Sauleda (1988) | 4 | 0,08% | 3 | 0,43% | 3 | 0,46% | 3 | 0,46% |
Silva et al. (2015) | 4 | 0,08% | 2 | 0,29% | 2 | 0,31% | 2 | 0,31% |
Thulin et al. (2016) | 4 | 0,08% | 3 | 0,43% | 3 | 0,46% | 3 | 0,46% |
Appelhans et al. (2021) | 3 | 0,06% | 3 | 0,43% | 3 | 0,46% | 3 | 0,46% |
Bayón (2015) | 3 | 0,06% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Bouman et al. (2022) | 3 | 0,06% | 2 | 0,29% | 2 | 0,31% | 2 | 0,31% |
Chiron & Bellone (2005) | 3 | 0,06% | 3 | 0,43% | 3 | 0,46% | 3 | 0,46% |
Cochrane & Iltis (2014) | 3 | 0,06% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Delnatte & Wynne (2016) | 3 | 0,06% | 3 | 0,43% | 3 | 0,46% | 3 | 0,46% |
Feuillet (2014) | 3 | 0,06% | 3 | 0,43% | 3 | 0,46% | 1 | 0,15% |
Frenot et al. (2001) | 3 | 0,06% | 3 | 0,43% | 3 | 0,46% | 2 | 0,31% |
Fritsch (2003) | 3 | 0,06% | 3 | 0,43% | 3 | 0,46% | 3 | 0,46% |
Gillespie & Armbruster (1997) | 3 | 0,06% | 3 | 0,43% | 2 | 0,31% | 2 | 0,31% |
Granville & Gayot (2014) | 3 | 0,06% | 3 | 0,43% | 3 | 0,46% | 3 | 0,46% |
Hassemer (2017) | 3 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Hullé et al. (2003) | 3 | 0,06% | 2 | 0,29% | 2 | 0,31% | 2 | 0,31% |
Lamarck (1783) | 3 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Lima et al. (2012) | 3 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Maas (1985) | 3 | 0,06% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Masters et al. (2023) | 3 | 0,06% | 2 | 0,29% | 2 | 0,31% | 2 | 0,31% |
Mestier et al. (2022) | 3 | 0,06% | 3 | 0,43% | 3 | 0,46% | 3 | 0,46% |
Moore (1933) | 3 | 0,06% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Pellegrini et al. (2018) | 3 | 0,06% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Polhill (1990) | 3 | 0,06% | 3 | 0,43% | 3 | 0,46% | 3 | 0,46% |
Small (2015) | 3 | 0,06% | 1 | 0,14% | 0 | 0% | 1 | 0,15% |
Verdcourt (1970) | 3 | 0,06% | 3 | 0,43% | 1 | 0,15% | 2 | 0,31% |
Walter et al. (2015) | 3 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Willette et al. (2014) | 3 | 0,06% | 3 | 0,43% | 3 | 0,46% | 3 | 0,46% |
Ackerman & Galarza-perez (1991) | 2 | 0,04% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Allorge-Boiteau (2015) | 2 | 0,04% | 2 | 0,29% | 2 | 0,31% | 2 | 0,31% |
Armbruster et al. (2009) | 2 | 0,04% | 2 | 0,29% | 2 | 0,31% | 1 | 0,15% |
Arriagada (2003) | 2 | 0,04% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Aurore et al. (2014) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Béreau (2017) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Bikaeff (2002) | 2 | 0,04% | 2 | 0,29% | 2 | 0,31% | 2 | 0,31% |
Boggan et al. (1997) | 2 | 0,04% | 2 | 0,29% | 2 | 0,31% | 2 | 0,31% |
Bouman et al. (2020) | 2 | 0,04% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Bubani & Penzig (1897) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Campbell et al. (2019) | 2 | 0,04% | 2 | 0,29% | 2 | 0,31% | 2 | 0,31% |
Carcaillet (1993) | 2 | 0,04% | 2 | 0,29% | 2 | 0,31% | 1 | 0,15% |
Cardiel et al. (2022) | 2 | 0,04% | 2 | 0,29% | 2 | 0,31% | 2 | 0,31% |
Chemisquy et al. (2010) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Coppens d'Eeckenbrugge & Govaerts (2015) | 2 | 0,04% | 2 | 0,29% | 1 | 0,15% | 1 | 0,15% |
Crantz (1766) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Duss (1897) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Feldmann & Barré (2001) | 2 | 0,04% | 2 | 0,29% | 2 | 0,31% | 2 | 0,31% |
Fryxell (1988) | 2 | 0,04% | 2 | 0,29% | 2 | 0,31% | 2 | 0,31% |
Garcia-Mendoza & Chiang (2003) | 2 | 0,04% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Gentry (1980) | 2 | 0,04% | 2 | 0,29% | 2 | 0,31% | 2 | 0,31% |
Goldberg (1967) | 2 | 0,04% | 2 | 0,29% | 2 | 0,31% | 2 | 0,31% |
González‐Elizondo & Peterson (1997) | 2 | 0,04% | 2 | 0,29% | 2 | 0,31% | 2 | 0,31% |
Graham (1988) | 2 | 0,04% | 2 | 0,29% | 2 | 0,31% | 2 | 0,31% |
Hoff & Cremers (2005) | 2 | 0,04% | 2 | 0,29% | 2 | 0,31% | 2 | 0,31% |
Iltis & Cochrane (2014) | 2 | 0,04% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Iltis (1960) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Jolinon (1987) | 2 | 0,04% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Külkamp et al. (2023) | 2 | 0,04% | 2 | 0,29% | 2 | 0,31% | 2 | 0,31% |
Kyalangalilwa et al. (2013) | 2 | 0,04% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Lamarck (1779) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Lamarck (1779) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Leuenberger (1997) | 2 | 0,04% | 2 | 0,29% | 2 | 0,31% | 1 | 0,15% |
Levin et al. (2022) | 2 | 0,04% | 2 | 0,29% | 2 | 0,31% | 2 | 0,31% |
Linnaeus (1763) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Maas et al. (2023) | 2 | 0,04% | 2 | 0,29% | 2 | 0,31% | 2 | 0,31% |
Maas (1985) | 2 | 0,04% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Maddi (2010) | 2 | 0,04% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Melo & Semir (2009) | 2 | 0,04% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Mitchell (1997) | 2 | 0,04% | 2 | 0,29% | 2 | 0,31% | 2 | 0,31% |
Moench (1794) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Morillo (2012) | 2 | 0,04% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Muhlenberg (1817) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Ollitrault et al. (2020) | 2 | 0,04% | 1 | 0,14% | 0 | 0% | 1 | 0,15% |
Paton et al. (2018) | 2 | 0,04% | 2 | 0,29% | 2 | 0,31% | 2 | 0,31% |
Pearman et al. (2020) | 2 | 0,04% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Pedersen (1980) | 2 | 0,04% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Peraza et al. (2022) | 2 | 0,04% | 2 | 0,29% | 2 | 0,31% | 2 | 0,31% |
Peterson et al. (2012) | 2 | 0,04% | 1 | 0,14% | 1 | 0,15% | 0 | 0% |
Prado et al. (2013) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Raz (2016) | 2 | 0,04% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Richard (1792) | 2 | 0,04% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Roalson et al. (2010) | 2 | 0,04% | 2 | 0,29% | 2 | 0,31% | 2 | 0,31% |
Rome & Coppens d'Eeckenbrugge (2023) | 2 | 0,04% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Rudge (1805) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Samarakoon (2015) | 2 | 0,04% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Sanders (2012) | 2 | 0,04% | 1 | 0,14% | 0 | 0% | 0 | 0% |
Skog & Feuillet (2008) | 2 | 0,04% | 2 | 0,29% | 2 | 0,31% | 2 | 0,31% |
Soares Neto et al. (2018) | 2 | 0,04% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Souza et al. (2021) | 2 | 0,04% | 2 | 0,29% | 2 | 0,31% | 2 | 0,31% |
Staples (2007) | 2 | 0,04% | 2 | 0,29% | 2 | 0,31% | 2 | 0,31% |
Teres (2006) | 2 | 0,04% | 2 | 0,29% | 2 | 0,31% | 2 | 0,31% |
Thellung (1912) | 2 | 0,04% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Urtubey et al. (2016) | 2 | 0,04% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Veldkamp (1978) | 2 | 0,04% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Wagner et al. (2007) | 2 | 0,04% | 2 | 0,29% | 2 | 0,31% | 2 | 0,31% |
Zardini & Raven (1991) | 2 | 0,04% | 2 | 0,29% | 2 | 0,31% | 2 | 0,31% |
Arcangeli (1882) | 1 | 0,02% | 1 | 0,14% | 0 | 0% | 1 | 0,15% |
Barabé & Gibernau (2015) | 1 | 0,02% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Barthelat (2019) | 1 | 0,02% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Béguinot (2012) | 1 | 0,02% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Bell (1982) | 1 | 0,02% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Bernard et al. (2014) | 1 | 0,02% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Berry et al. (2001) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Berry et al. (2005) | 1 | 0,02% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Bohley et al. (2017) | 1 | 0,02% | 1 | 0,14% | 1 | 0,15% | 0 | 0% |
Bos et al. (2018) | 1 | 0,02% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Bosser & Heine (2000) | 1 | 0,02% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Bubani & Penzig (1901) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Burkart (1971) | 1 | 0,02% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Byng et al. (2016) | 1 | 0,02% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Calviño et al. (2008) | 1 | 0,02% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Candolle (1824) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Candolle (1844) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Candolle (1852) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Candolle (1869) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Cardinal-McTeague & Gillespie (2016) | 1 | 0,02% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Christenhusz et al. (2018) | 1 | 0,02% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Cohen & Ackerman (2009) | 1 | 0,02% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Coode 1982 | 1 | 0,02% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Crantz (1766) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Cremers & Hoff (1995) | 1 | 0,02% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Danin et al. (2012) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Delprete & Kirkbride (2015) | 1 | 0,02% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Delprete (2015) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Den et al. (2020) | 1 | 0,02% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Don (1831) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Dulac (1867) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Dumbardon-Martial & Delblond (2019) | 1 | 0,02% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Etcheberry & Abraham (2009) | 1 | 0,02% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Euro+Med (2006) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Fernandes (1984) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Feuillet (2008) | 1 | 0,02% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Flora of North America (1993-) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Fosberg & Sachet (1975) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Fourreau (1869) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Fuentes-bazan et al. (2012) | 1 | 0,02% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Gardner et al. (2021) | 1 | 0,02% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Graham et al. (2021) | 1 | 0,02% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Gray (1821) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Gregório et al. (2023) | 1 | 0,02% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Greuter & Rankin‐Rodríguez (2021) | 1 | 0,02% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Grose & Olmstead (2007) | 1 | 0,02% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Guillaumin (1936) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Harrington & Gadek (2009) | 1 | 0,02% | 1 | 0,14% | 0 | 0% | 1 | 0,15% |
Harrington (2008) | 1 | 0,02% | 1 | 0,14% | 0 | 0% | 1 | 0,15% |
Hillig (2005) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Hollowell et al. (2001) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Huygh et al. (2010) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Iamonico et al. (2015) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Iles et al. (2017) | 1 | 0,02% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Jolinon (1985) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Kaastra (1982) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Kaehler et al. (2019) | 1 | 0,02% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Klonowska et al. (2012) | 1 | 0,02% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Klonowska et al. (2020) | 1 | 0,02% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Kuntze (1891) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Lamarck (1789) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Landrum (1986) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Lemée (1956) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Li et al. (2022) | 1 | 0,02% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Lieutard (1893) | 1 | 0,02% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Lima et al. (2014) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Linnaeus (1759) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Linnaeus (1762) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Mabberley (2017) | 1 | 0,02% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Manzitto‐Tripp et al. (2021) | 1 | 0,02% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Mapaya (2017) | 1 | 0,02% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Maréchal et al. (2013) | 1 | 0,02% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Méndez Santos (2001) | 1 | 0,02% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Meyer et al. (2008) | 1 | 0,02% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Montero et al. (2018) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Moonen (2013) | 1 | 0,02% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Moraes et al. (2013) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Moraes et al. (2014) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Mosyakin & Clemants (2002) | 1 | 0,02% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Muhlenberg (1813) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Muller et al. (2004) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Nesom (2008) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Peck et al. (2014) | 1 | 0,02% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Pedersen (2000) | 1 | 0,02% | 1 | 0,14% | 0 | 0% | 1 | 0,15% |
Pennington & Biggs (2016) | 1 | 0,02% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Pennington (1990) | 1 | 0,02% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Persoon (1805) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Persoon (1807) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Questel (2017) | 1 | 0,02% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Questel (2022) | 1 | 0,02% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Rignault & Chevallier (2017) | 1 | 0,02% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Roalson & Hall (2017) | 1 | 0,02% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Rome & Coppens d'Eeckenbrugge (2016) | 1 | 0,02% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Sagot (1881) | 1 | 0,02% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Sambin & Aucourd (2020) | 1 | 0,02% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Samson (2005) | 1 | 0,02% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Sanders (2006) | 1 | 0,02% | 1 | 0,14% | 0 | 0% | 0 | 0% |
Schenck (1905) | 1 | 0,02% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Schrire et al. (2009) | 1 | 0,02% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Scopoli (1771) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Sherff (1937) | 1 | 0,02% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Shrestha et al. (2003) | 1 | 0,02% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Silva et al. (2020) | 1 | 0,02% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Sleumer (1980) | 1 | 0,02% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Snak et al. (2016) | 1 | 0,02% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Snow & Peterson (2012) | 1 | 0,02% | 1 | 0,14% | 0 | 0% | 1 | 0,15% |
Song et al. (2019) | 1 | 0,02% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Sprengel (1825) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Stafleu & Cowan (1983) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Staples et al. (2012) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Sukhorukov et al. (2018) | 1 | 0,02% | 1 | 0,14% | 0 | 0% | 1 | 0,15% |
Sweet (1826) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Tamboli et al. (2016) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Tareau (2015) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Taylor et al. (2017) | 1 | 0,02% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Thibaut et al. (2022) | 1 | 0,02% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Tison et al. (2021) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Tripp et al. (2013) | 1 | 0,02% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Trofimov et al. (2016) | 1 | 0,02% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Uicn et al. (2022) | 1 | 0,02% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Veldkamp (2014) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Webster (1957) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Webster (1958) | 1 | 0,02% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Willdenow (1799) | 1 | 0,02% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Willdenow (1800) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Wörz (2005) | 1 | 0,02% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Yuan et al. (2010) | 1 | 0,02% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Zakardjian et al. (2020) | 1 | 0,02% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Zuloaga et al. (2011) | 1 | 0,02% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |