Angiospermes de Saint-Barthélemy
Magnoliidae de Saint-Barthélemy
352 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) | 2414 | 49,21% | 1932 | 274,82% | 1924 | 286,74% | 1876 | 278,75% |
Funk et al. (2007) | 915 | 18,65% | 342 | 48,65% | 337 | 50,22% | 324 | 48,14% |
Hequet & Le Corre (2010) | 277 | 5,65% | 221 | 31,44% | 218 | 32,49% | 206 | 30,61% |
Hequet et al. (2009) | 277 | 5,65% | 221 | 31,44% | 218 | 32,49% | 206 | 30,61% |
MacKee (1994) | 275 | 5,61% | 217 | 30,87% | 214 | 31,89% | 202 | 30,01% |
Tison et al. (2014) | 262 | 5,34% | 139 | 19,77% | 137 | 20,42% | 130 | 19,32% |
Molino et al. (2022) | 242 | 4,93% | 17 | 2,42% | 17 | 2,53% | 14 | 2,08% |
Fourdrigniez & Meyer (2008) | 168 | 3,42% | 135 | 19,2% | 132 | 19,67% | 126 | 18,72% |
Acevedo-Rodríguez & Strong (2012) | 167 | 3,4% | 114 | 16,22% | 106 | 15,8% | 114 | 16,94% |
Delnatte & Meyer (2012) | 142 | 2,89% | 116 | 16,5% | 115 | 17,14% | 111 | 16,49% |
Paton et al. (2019) | 116 | 2,36% | 2 | 0,28% | 2 | 0,3% | 2 | 0,3% |
Munzinger et al. (2016) | 114 | 2,32% | 38 | 5,41% | 36 | 5,37% | 35 | 5,2% |
Morat & Veillon (1985) | 81 | 1,65% | 67 | 9,53% | 65 | 9,69% | 60 | 8,92% |
Aublet (1775) | 79 | 1,61% | 34 | 4,84% | 33 | 4,92% | 33 | 4,9% |
Boullet et al. (2018) | 78 | 1,59% | 71 | 10,1% | 68 | 10,13% | 67 | 9,96% |
Morat et al. (2012) | 78 | 1,59% | 39 | 5,55% | 37 | 5,51% | 36 | 5,35% |
Lemée (1952) | 54 | 1,1% | 35 | 4,98% | 35 | 5,22% | 35 | 5,2% |
Kuijt (2003) | 53 | 1,08% | 2 | 0,28% | 2 | 0,3% | 2 | 0,3% |
Léotard & Chaline (2013) | 50 | 1,02% | 46 | 6,54% | 46 | 6,86% | 45 | 6,69% |
Molino et al. (2009) | 46 | 0,94% | 42 | 5,97% | 42 | 6,26% | 39 | 5,79% |
Wilmot-Dear & Friis (1996) | 43 | 0,88% | 6 | 0,85% | 6 | 0,89% | 6 | 0,89% |
Florence (2004) | 42 | 0,86% | 35 | 4,98% | 34 | 5,07% | 34 | 5,05% |
Ortuño & Borsch (2020) | 40 | 0,82% | 3 | 0,43% | 3 | 0,45% | 3 | 0,45% |
Ter Steege et al. (2016) | 35 | 0,71% | 31 | 4,41% | 31 | 4,62% | 28 | 4,16% |
Véron et al. (2021) | 35 | 0,71% | 33 | 4,69% | 33 | 4,92% | 33 | 4,9% |
Feldmann (2012) | 31 | 0,63% | 28 | 3,98% | 28 | 4,17% | 28 | 4,16% |
Stace (2010) | 30 | 0,61% | 10 | 1,42% | 6 | 0,89% | 8 | 1,19% |
Rogers & Appan (1973) | 26 | 0,53% | 1 | 0,14% | 1 | 0,15% | 0 | 0% |
Anonyme (2014) | 25 | 0,51% | 22 | 3,13% | 22 | 3,28% | 22 | 3,27% |
Lemée (1955) | 25 | 0,51% | 13 | 1,85% | 13 | 1,94% | 12 | 1,78% |
Linnaeus (1753) | 25 | 0,51% | 19 | 2,7% | 19 | 2,83% | 17 | 2,53% |
Krapovickas (2003) | 24 | 0,49% | 9 | 1,28% | 9 | 1,34% | 9 | 1,34% |
Baaijens & Veldkamp (1991) | 23 | 0,47% | 2 | 0,28% | 2 | 0,3% | 2 | 0,3% |
Bauters et al. (2019) | 23 | 0,47% | 2 | 0,28% | 1 | 0,15% | 1 | 0,15% |
Florence (1997) | 22 | 0,45% | 14 | 1,99% | 14 | 2,09% | 13 | 1,93% |
Gargominy et al. (1996) | 21 | 0,43% | 18 | 2,56% | 18 | 2,68% | 17 | 2,53% |
Lemée (1953) | 21 | 0,43% | 11 | 1,56% | 11 | 1,64% | 11 | 1,63% |
Linnaeus (1753) | 21 | 0,43% | 17 | 2,42% | 16 | 2,38% | 15 | 2,23% |
Cornejo (2020) | 20 | 0,41% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Suddee et al. (2004) | 20 | 0,41% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Korotkova et al. (2017) | 19 | 0,39% | 3 | 0,43% | 3 | 0,45% | 2 | 0,3% |
Porter-Utley (2014) | 18 | 0,37% | 6 | 0,85% | 6 | 0,89% | 6 | 0,89% |
Ståhl (2010) | 18 | 0,37% | 8 | 1,14% | 8 | 1,19% | 8 | 1,19% |
Wasshausen (2006) | 18 | 0,37% | 4 | 0,57% | 4 | 0,6% | 4 | 0,59% |
Allem (1994) | 17 | 0,35% | 2 | 0,28% | 1 | 0,15% | 1 | 0,15% |
Nesom (2009) | 17 | 0,35% | 1 | 0,14% | 1 | 0,15% | 0 | 0% |
Boggan et al. (1992) | 15 | 0,31% | 7 | 1% | 7 | 1,04% | 7 | 1,04% |
Cremers & Hoff (1994) | 15 | 0,31% | 4 | 0,57% | 4 | 0,6% | 4 | 0,59% |
Miller (1768) | 15 | 0,31% | 2 | 0,28% | 2 | 0,3% | 2 | 0,3% |
Yang et al. (2012) | 15 | 0,31% | 15 | 2,13% | 15 | 2,24% | 15 | 2,23% |
Berg (1992) | 14 | 0,29% | 5 | 0,71% | 5 | 0,75% | 5 | 0,74% |
Fryxell (2001) | 14 | 0,29% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Jost et al. (2019) | 14 | 0,29% | 12 | 1,71% | 10 | 1,49% | 12 | 1,78% |
Pool (2014) | 14 | 0,29% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Christenhusz (2002) | 13 | 0,26% | 8 | 1,14% | 8 | 1,19% | 8 | 1,19% |
Cremers & Hoff (1997) | 13 | 0,26% | 3 | 0,43% | 3 | 0,45% | 3 | 0,45% |
D'arcy (1987) | 13 | 0,26% | 0 | 0% | 0 | 0% | 0 | 0% |
Kükenthal (1936) | 13 | 0,26% | 0 | 0% | 0 | 0% | 0 | 0% |
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% |
Pejhanmehr (2022) | 13 | 0,26% | 12 | 1,71% | 12 | 1,79% | 12 | 1,78% |
Salisbury (1796) | 13 | 0,26% | 0 | 0% | 0 | 0% | 0 | 0% |
Simões & Staples (2017) | 13 | 0,26% | 5 | 0,71% | 5 | 0,75% | 5 | 0,74% |
Meyer et al. (2006) | 12 | 0,24% | 9 | 1,28% | 8 | 1,19% | 8 | 1,19% |
Feldmann (2014) | 11 | 0,22% | 11 | 1,56% | 11 | 1,64% | 11 | 1,63% |
Hunt (1986) | 11 | 0,22% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Lavergne (2011) | 11 | 0,22% | 10 | 1,42% | 9 | 1,34% | 8 | 1,19% |
Sauer (1964) | 11 | 0,22% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Couté & Garrouste (2009) | 10 | 0,2% | 9 | 1,28% | 8 | 1,19% | 9 | 1,34% |
Oliveira Pellegrini & Forzza (2017) | 10 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Wiersema et al. (2018) | 10 | 0,2% | 2 | 0,28% | 2 | 0,3% | 2 | 0,3% |
Carvalho (1997) | 9 | 0,18% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Hassemer et al. (2017) | 9 | 0,18% | 9 | 1,28% | 9 | 1,34% | 9 | 1,34% |
Iamonico (2016) | 9 | 0,18% | 0 | 0% | 0 | 0% | 0 | 0% |
Candolle (1849) | 8 | 0,16% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Ferlay et al. (2023) | 8 | 0,16% | 8 | 1,14% | 8 | 1,19% | 8 | 1,19% |
Mitchell & Daly (2015) | 8 | 0,16% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Staples (2007) | 8 | 0,16% | 4 | 0,57% | 4 | 0,6% | 4 | 0,59% |
Werkhoven (1986) | 8 | 0,16% | 4 | 0,57% | 4 | 0,6% | 4 | 0,59% |
Borchsenius et al. (2012) | 7 | 0,14% | 4 | 0,57% | 4 | 0,6% | 4 | 0,59% |
Graham (1988) | 7 | 0,14% | 7 | 1% | 7 | 1,04% | 7 | 1,04% |
Kuijt (2007) | 7 | 0,14% | 2 | 0,28% | 2 | 0,3% | 2 | 0,3% |
Plowman et al. (1998) | 7 | 0,14% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Sachet (1962) | 7 | 0,14% | 6 | 0,85% | 6 | 0,89% | 6 | 0,89% |
Zerega et al. (2005) | 7 | 0,14% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Acevedo-Rodríguez (2012) | 6 | 0,12% | 4 | 0,57% | 4 | 0,6% | 4 | 0,59% |
Barrett et al. (2017) | 6 | 0,12% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Biral 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% |
Feuillet (2009) | 6 | 0,12% | 5 | 0,71% | 5 | 0,75% | 4 | 0,59% |
Krings (2011) | 6 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Kyalangalilwa et al. (2013) | 6 | 0,12% | 2 | 0,28% | 2 | 0,3% | 2 | 0,3% |
Mazine et al. (2018) | 6 | 0,12% | 6 | 0,85% | 6 | 0,89% | 6 | 0,89% |
Noguera-savelli (2010) | 6 | 0,12% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Paudyal et al. (2018) | 6 | 0,12% | 5 | 0,71% | 5 | 0,75% | 5 | 0,74% |
Peterson et al. (2014) | 6 | 0,12% | 6 | 0,85% | 6 | 0,89% | 6 | 0,89% |
Silva et al. (2019) | 6 | 0,12% | 4 | 0,57% | 4 | 0,6% | 4 | 0,59% |
Welker et al. (2020) | 6 | 0,12% | 6 | 0,85% | 6 | 0,89% | 5 | 0,74% |
Wood et al. (2020) | 6 | 0,12% | 6 | 0,85% | 6 | 0,89% | 5 | 0,74% |
Allen et al. (2022) | 5 | 0,1% | 5 | 0,71% | 5 | 0,75% | 5 | 0,74% |
Cornejo & Iltis (2007) | 5 | 0,1% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
David & Thiebaut (2013) | 5 | 0,1% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Fournier (1934-1940) | 5 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Franck et al. (2019) | 5 | 0,1% | 5 | 0,71% | 5 | 0,75% | 5 | 0,74% |
Gagnon et al. (2016) | 5 | 0,1% | 3 | 0,43% | 3 | 0,45% | 3 | 0,45% |
Hullé et al. (2003) | 5 | 0,1% | 4 | 0,57% | 4 | 0,6% | 4 | 0,59% |
Jeffrey (1980) | 5 | 0,1% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Mitchell (1997) | 5 | 0,1% | 3 | 0,43% | 3 | 0,45% | 3 | 0,45% |
Moench (1794) | 5 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Mori et al. (2002) | 5 | 0,1% | 4 | 0,57% | 4 | 0,6% | 4 | 0,59% |
Patchell et al. (2014) | 5 | 0,1% | 5 | 0,71% | 5 | 0,75% | 5 | 0,74% |
Toutain (1989) | 5 | 0,1% | 5 | 0,71% | 5 | 0,75% | 5 | 0,74% |
Andersson (1981) | 4 | 0,08% | 2 | 0,28% | 2 | 0,3% | 2 | 0,3% |
Appelhans et al. (2021) | 4 | 0,08% | 4 | 0,57% | 4 | 0,6% | 4 | 0,59% |
Bell (1982) | 4 | 0,08% | 4 | 0,57% | 4 | 0,6% | 3 | 0,45% |
Candolle (1828) | 4 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Cowan & Lindeman (1989) | 4 | 0,08% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Dorsey et al. (2013) | 4 | 0,08% | 4 | 0,57% | 4 | 0,6% | 3 | 0,45% |
Fader et al. (2016) | 4 | 0,08% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Judziewicz (1990) | 4 | 0,08% | 4 | 0,57% | 4 | 0,6% | 4 | 0,59% |
Kuntze (1891) | 4 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Lamarck (1783) | 4 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Lohmann & Taylor (2014) | 4 | 0,08% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Manzitto‐Tripp & Daniel (2023) | 4 | 0,08% | 4 | 0,57% | 4 | 0,6% | 4 | 0,59% |
Ocampo & Columbus (2012) | 4 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Orchard (2013) | 4 | 0,08% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Sauleda (1988) | 4 | 0,08% | 3 | 0,43% | 3 | 0,45% | 3 | 0,45% |
Barthelat (2019) | 3 | 0,06% | 3 | 0,43% | 3 | 0,45% | 3 | 0,45% |
Bayón (2015) | 3 | 0,06% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Bouman et al. (2022) | 3 | 0,06% | 2 | 0,28% | 2 | 0,3% | 2 | 0,3% |
Cochrane & Iltis (2014) | 3 | 0,06% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Frenot et al. (2001) | 3 | 0,06% | 3 | 0,43% | 3 | 0,45% | 2 | 0,3% |
Friis (1993) | 3 | 0,06% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Fryxell (1988) | 3 | 0,06% | 2 | 0,28% | 2 | 0,3% | 2 | 0,3% |
Granville & Gayot (2014) | 3 | 0,06% | 3 | 0,43% | 3 | 0,45% | 3 | 0,45% |
Hassemer (2017) | 3 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Hily et al. (2010) | 3 | 0,06% | 3 | 0,43% | 3 | 0,45% | 3 | 0,45% |
Jolinon (1987) | 3 | 0,06% | 2 | 0,28% | 2 | 0,3% | 2 | 0,3% |
Lamarck (1779) | 3 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Lamarck (1779) | 3 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Lima et al. (2012) | 3 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Lowe et al. (2007) | 3 | 0,06% | 3 | 0,43% | 2 | 0,3% | 2 | 0,3% |
Lowry et al. (2019) | 3 | 0,06% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Maas (1985) | 3 | 0,06% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Pool (2007) | 3 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Richard (1792) | 3 | 0,06% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Small (2015) | 3 | 0,06% | 1 | 0,14% | 0 | 0% | 1 | 0,15% |
Souza et al. (2021) | 3 | 0,06% | 3 | 0,43% | 3 | 0,45% | 3 | 0,45% |
Verdcourt (1970) | 3 | 0,06% | 3 | 0,43% | 1 | 0,15% | 2 | 0,3% |
Walter et al. (2015) | 3 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Willette et al. (2014) | 3 | 0,06% | 3 | 0,43% | 3 | 0,45% | 3 | 0,45% |
Ackerman & Galarza-perez (1991) | 2 | 0,04% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Allorge-Boiteau (2015) | 2 | 0,04% | 2 | 0,28% | 2 | 0,3% | 2 | 0,3% |
Aurore et al. (2014) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Bauters et al. (2016) | 2 | 0,04% | 2 | 0,28% | 2 | 0,3% | 0 | 0% |
Béreau (2017) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Boggan et al. (1997) | 2 | 0,04% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Bonnier & Layens (1894) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Bouman et al. (2020) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Bubani & Penzig (1897) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Candolle (1824) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Candolle (1852) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Carcaillet (1993) | 2 | 0,04% | 2 | 0,28% | 2 | 0,3% | 1 | 0,15% |
Cardiel et al. (2022) | 2 | 0,04% | 2 | 0,28% | 2 | 0,3% | 2 | 0,3% |
Chiron & Bellone (2005) | 2 | 0,04% | 2 | 0,28% | 2 | 0,3% | 2 | 0,3% |
Coode 1982 | 2 | 0,04% | 2 | 0,28% | 2 | 0,3% | 2 | 0,3% |
Coppens d'Eeckenbrugge & Govaerts (2015) | 2 | 0,04% | 2 | 0,28% | 1 | 0,15% | 1 | 0,15% |
Crantz (1766) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Dehgan (2012) | 2 | 0,04% | 2 | 0,28% | 2 | 0,3% | 2 | 0,3% |
Delnatte & Wynne (2016) | 2 | 0,04% | 2 | 0,28% | 2 | 0,3% | 2 | 0,3% |
Dumbardon-Martial & Delblond (2019) | 2 | 0,04% | 2 | 0,28% | 2 | 0,3% | 2 | 0,3% |
Duss (1897) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Feldmann & Barré (2001) | 2 | 0,04% | 2 | 0,28% | 2 | 0,3% | 2 | 0,3% |
Feuillet (2020) | 2 | 0,04% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Gentry (1980) | 2 | 0,04% | 2 | 0,28% | 2 | 0,3% | 2 | 0,3% |
Goldberg (1967) | 2 | 0,04% | 2 | 0,28% | 2 | 0,3% | 2 | 0,3% |
Görts-van Rijn (2007) | 2 | 0,04% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Hoff & Cremers (2005) | 2 | 0,04% | 2 | 0,28% | 2 | 0,3% | 1 | 0,15% |
Hollowell et al. (2001) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
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% |
Johnston (1935) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Lemée (1956) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Leuenberger (1997) | 2 | 0,04% | 2 | 0,28% | 2 | 0,3% | 1 | 0,15% |
Levin et al. (2022) | 2 | 0,04% | 2 | 0,28% | 2 | 0,3% | 2 | 0,3% |
Linnaeus (1759) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Linnaeus (1762) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Maas et al. (2023) | 2 | 0,04% | 2 | 0,28% | 2 | 0,3% | 2 | 0,3% |
Maas (1985) | 2 | 0,04% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Mapaya (2017) | 2 | 0,04% | 2 | 0,28% | 2 | 0,3% | 2 | 0,3% |
Masters et al. (2023) | 2 | 0,04% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Moench (1794) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Moore (1933) | 2 | 0,04% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
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 | 0,28% | 2 | 0,3% | 2 | 0,3% |
Paula-Souza & Ballard (2014) | 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 | 0,28% | 2 | 0,3% | 2 | 0,3% |
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% |
Rudge (1805) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Sant (2022) | 2 | 0,04% | 2 | 0,28% | 2 | 0,3% | 1 | 0,15% |
Schrire et al. (2009) | 2 | 0,04% | 2 | 0,28% | 2 | 0,3% | 2 | 0,3% |
Seigler et al. (2014) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Skog & Feuillet (2008) | 2 | 0,04% | 2 | 0,28% | 2 | 0,3% | 2 | 0,3% |
Snak et al. (2016) | 2 | 0,04% | 2 | 0,28% | 2 | 0,3% | 2 | 0,3% |
Song et al. (2019) | 2 | 0,04% | 2 | 0,28% | 2 | 0,3% | 2 | 0,3% |
Souza & Giulietti (2009) | 2 | 0,04% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Suessenguth (1936) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Teres (2006) | 2 | 0,04% | 2 | 0,28% | 2 | 0,3% | 2 | 0,3% |
Thellung (1912) | 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% |
Allioni (1785) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Alvarado-Cárdenas & Ochoterena (2007) | 1 | 0,02% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Arcangeli (1882) | 1 | 0,02% | 1 | 0,14% | 0 | 0% | 1 | 0,15% |
Armbruster et al. (2009) | 1 | 0,02% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Barabé & Gibernau (2015) | 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% |
Bernard et al. (2014) | 1 | 0,02% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Berry et al. (1997) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Berry et al. (1999) | 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% |
Berton (2020) | 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% |
Bosser & Heine (2000) | 1 | 0,02% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Breuil (2001) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Brottier et al. (2018) | 1 | 0,02% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Bubani & Penzig (1900) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Bubani & Penzig (1901) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Byng et al. (2016) | 1 | 0,02% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Cafferty et al. (2000) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Candolle (1844) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Candolle (1845) | 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% |
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% |
Cremers & Hoff (1998) | 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% |
Descoings (2011) | 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% |
Dumortier (1827) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Etcheberry & Abraham (2009) | 1 | 0,02% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
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% |
Feuillet (2008) | 1 | 0,02% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Feuillet (2014) | 1 | 0,02% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Filipowicz & Renner (2012) | 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% |
Gillespie & Armbruster (1997) | 1 | 0,02% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
González‐Elizondo & Peterson (1997) | 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% |
Hillig (2005) | 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% |
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% |
Laguna (2006) | 1 | 0,02% | 1 | 0,14% | 0 | 0% | 1 | 0,15% |
Lamarck (1789) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Landrum (1986) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Li et al. (2021) | 1 | 0,02% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
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 (1763) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Liu et al. (2004) | 1 | 0,02% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Longhi-Wagner et al. (2010) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Lorence et al. (2007) | 1 | 0,02% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Maddi (2014) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Manzitto‐Tripp et al. (2021) | 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% |
Mestier et al. (2022) | 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% |
Moonlight et al. (2018) | 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% |
Mori et al. (2002) | 1 | 0,02% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
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% |
Oldeman (1968) | 1 | 0,02% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
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% |
Polhill (1990) | 1 | 0,02% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Questel (2017) | 1 | 0,02% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Questel (2020) | 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% |
Roalson et al. (2010) | 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% |
Rome & Coppens d'Eeckenbrugge (2023) | 1 | 0,02% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Rouy (1912) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Rudd (1955) | 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% |
Samarakoon (2015) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
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% |
Sanders (2012) | 1 | 0,02% | 1 | 0,14% | 0 | 0% | 0 | 0% |
Scatigna et al. (2022) | 1 | 0,02% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Schenck (1905) | 1 | 0,02% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Scopoli (1771) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
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% |
Soubeyran (2008) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
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% |
Stepansky et al. (1999) | 1 | 0,02% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
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% |
Thulin et al. (2016) | 1 | 0,02% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Tison et al. (2014) | 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% |
Uicn et al. (2022) | 1 | 0,02% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Veldkamp (2002) | 1 | 0,02% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Veldkamp (2014) | 1 | 0,02% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
Webster (1957) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Webster (1957) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
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% |
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% |
Ziffer-Berger et al. (2015) | 1 | 0,02% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |