Trachéophytes de Saint-Barthélemy
341 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) | 2426 | 49,32% | 1936 | 274,61% | 1928 | 286,05% | 1884 | 278,7% |
| Funk et al. (2007) | 919 | 18,68% | 343 | 48,65% | 339 | 50,3% | 326 | 48,22% |
| Hequet & Le Corre (2010) | 279 | 5,67% | 221 | 31,35% | 218 | 32,34% | 207 | 30,62% |
| Hequet et al. (2009) | 279 | 5,67% | 221 | 31,35% | 218 | 32,34% | 207 | 30,62% |
| MacKee (1994) | 277 | 5,63% | 217 | 30,78% | 214 | 31,75% | 203 | 30,03% |
| Tison et al. (2014) | 263 | 5,35% | 138 | 19,57% | 136 | 20,18% | 131 | 19,38% |
| Molino et al. (2022) | 242 | 4,92% | 17 | 2,41% | 17 | 2,52% | 14 | 2,07% |
| Fourdrigniez & Meyer (2008) | 170 | 3,46% | 136 | 19,29% | 133 | 19,73% | 128 | 18,93% |
| Acevedo-Rodríguez & Strong (2012) | 167 | 3,39% | 114 | 16,17% | 106 | 15,73% | 114 | 16,86% |
| Delnatte & Meyer (2012) | 143 | 2,91% | 117 | 16,6% | 116 | 17,21% | 113 | 16,72% |
| Munzinger et al. (2016) | 117 | 2,38% | 39 | 5,53% | 37 | 5,49% | 37 | 5,47% |
| Paton et al. (2019) | 116 | 2,36% | 2 | 0,28% | 2 | 0,3% | 2 | 0,3% |
| Morat & Veillon (1985) | 83 | 1,69% | 68 | 9,65% | 66 | 9,79% | 62 | 9,17% |
| Morat et al. (2012) | 80 | 1,63% | 40 | 5,67% | 38 | 5,64% | 38 | 5,62% |
| Aublet (1775) | 79 | 1,61% | 34 | 4,82% | 33 | 4,9% | 33 | 4,88% |
| Boullet et al. (2018) | 78 | 1,59% | 71 | 10,07% | 68 | 10,09% | 67 | 9,91% |
| Lemée (1952) | 54 | 1,1% | 35 | 4,96% | 35 | 5,19% | 35 | 5,18% |
| Kuijt (2003) | 53 | 1,08% | 2 | 0,28% | 2 | 0,3% | 2 | 0,3% |
| Léotard & Chaline (2013) | 50 | 1,02% | 46 | 6,52% | 46 | 6,82% | 46 | 6,8% |
| Molino et al. (2009) | 46 | 0,94% | 42 | 5,96% | 42 | 6,23% | 39 | 5,77% |
| Wilmot-Dear & Friis (1996) | 43 | 0,87% | 6 | 0,85% | 6 | 0,89% | 6 | 0,89% |
| Florence (2004) | 42 | 0,85% | 35 | 4,96% | 34 | 5,04% | 34 | 5,03% |
| Ortuño & Borsch (2020) | 40 | 0,81% | 3 | 0,43% | 3 | 0,45% | 3 | 0,44% |
| Ter Steege et al. (2016) | 35 | 0,71% | 31 | 4,4% | 31 | 4,6% | 28 | 4,14% |
| Véron et al. (2021) | 35 | 0,71% | 33 | 4,68% | 33 | 4,9% | 33 | 4,88% |
| Feldmann (2012) | 31 | 0,63% | 28 | 3,97% | 28 | 4,15% | 28 | 4,14% |
| Stace (2010) | 30 | 0,61% | 10 | 1,42% | 6 | 0,89% | 8 | 1,18% |
| Rogers & Appan (1973) | 26 | 0,53% | 1 | 0,14% | 1 | 0,15% | 0 | 0% |
| Anonyme (2014) | 25 | 0,51% | 22 | 3,12% | 22 | 3,26% | 22 | 3,25% |
| Lemée (1955) | 25 | 0,51% | 13 | 1,84% | 13 | 1,93% | 12 | 1,78% |
| 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 | 2,08% | 13 | 1,92% |
| Gargominy et al. (1996) | 21 | 0,43% | 18 | 2,55% | 18 | 2,67% | 17 | 2,51% |
| Lemée (1953) | 21 | 0,43% | 11 | 1,56% | 11 | 1,63% | 11 | 1,63% |
| Cornejo (2020) | 20 | 0,41% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
| Linnaeus (1753) | 20 | 0,41% | 14 | 1,99% | 14 | 2,08% | 12 | 1,78% |
| Linnaeus (1753) | 20 | 0,41% | 15 | 2,13% | 15 | 2,23% | 14 | 2,07% |
| 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% |
| Ståhl (2010) | 18 | 0,37% | 8 | 1,13% | 8 | 1,19% | 8 | 1,18% |
| Wasshausen (2006) | 18 | 0,37% | 4 | 0,57% | 4 | 0,59% | 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 | 0,3% | 7 | 0,99% | 7 | 1,04% | 7 | 1,04% |
| Cremers & Hoff (1994) | 15 | 0,3% | 4 | 0,57% | 4 | 0,59% | 4 | 0,59% |
| Yang et al. (2012) | 15 | 0,3% | 15 | 2,13% | 15 | 2,23% | 15 | 2,22% |
| Berg (1992) | 14 | 0,28% | 5 | 0,71% | 5 | 0,74% | 5 | 0,74% |
| Fryxell (2001) | 14 | 0,28% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
| Jost et al. (2019) | 14 | 0,28% | 12 | 1,7% | 10 | 1,48% | 12 | 1,78% |
| Pool (2014) | 14 | 0,28% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
| Christenhusz (2002) | 13 | 0,26% | 8 | 1,13% | 8 | 1,19% | 8 | 1,18% |
| Cremers & Hoff (1997) | 13 | 0,26% | 3 | 0,43% | 3 | 0,45% | 3 | 0,44% |
| 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% |
| Simões & Staples (2017) | 13 | 0,26% | 5 | 0,71% | 5 | 0,74% | 5 | 0,74% |
| Meyer et al. (2006) | 12 | 0,24% | 9 | 1,28% | 8 | 1,19% | 8 | 1,18% |
| Feldmann (2014) | 11 | 0,22% | 11 | 1,56% | 11 | 1,63% | 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 | 1,18% |
| Salisbury (1796) | 11 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sauer (1964) | 11 | 0,22% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
| Wiersema et al. (2018) | 11 | 0,22% | 3 | 0,43% | 2 | 0,3% | 2 | 0,3% |
| Couté & Garrouste (2009) | 10 | 0,2% | 9 | 1,28% | 8 | 1,19% | 9 | 1,33% |
| Oliveira Pellegrini & Forzza (2017) | 10 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
| 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 | 1,33% |
| Iamonico (2016) | 9 | 0,18% | 0 | 0% | 0 | 0% | 0 | 0% |
| Miller (1768) | 9 | 0,18% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
| Candolle (1849) | 8 | 0,16% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
| Ferlay et al. (2023) | 8 | 0,16% | 8 | 1,13% | 8 | 1,19% | 8 | 1,18% |
| Mitchell & Daly (2015) | 8 | 0,16% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
| Staples (2007) | 8 | 0,16% | 4 | 0,57% | 4 | 0,59% | 4 | 0,59% |
| Werkhoven (1986) | 8 | 0,16% | 4 | 0,57% | 4 | 0,59% | 4 | 0,59% |
| Borchsenius et al. (2012) | 7 | 0,14% | 4 | 0,57% | 4 | 0,59% | 4 | 0,59% |
| Graham (1988) | 7 | 0,14% | 7 | 0,99% | 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 | 0,59% | 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 | 0,74% | 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 | 0,74% | 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 | 0,59% | 4 | 0,59% |
| 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 | 0,74% | 5 | 0,74% |
| Appelhans et al. (2021) | 5 | 0,1% | 4 | 0,57% | 4 | 0,59% | 4 | 0,59% |
| 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% |
| Franck et al. (2019) | 5 | 0,1% | 5 | 0,71% | 5 | 0,74% | 5 | 0,74% |
| Gagnon et al. (2016) | 5 | 0,1% | 3 | 0,43% | 3 | 0,45% | 3 | 0,44% |
| Hullé et al. (2003) | 5 | 0,1% | 4 | 0,57% | 4 | 0,59% | 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 | 0,44% |
| Moench (1794) | 5 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mori et al. (2002) | 5 | 0,1% | 4 | 0,57% | 4 | 0,59% | 4 | 0,59% |
| Patchell et al. (2014) | 5 | 0,1% | 5 | 0,71% | 5 | 0,74% | 5 | 0,74% |
| Toutain (1989) | 5 | 0,1% | 5 | 0,71% | 5 | 0,74% | 5 | 0,74% |
| Andersson (1981) | 4 | 0,08% | 2 | 0,28% | 2 | 0,3% | 2 | 0,3% |
| Bell (1982) | 4 | 0,08% | 4 | 0,57% | 4 | 0,59% | 3 | 0,44% |
| 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 | 0,59% | 3 | 0,44% |
| 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 | 0,59% | 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% |
| 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 | 0,44% |
| Barthelat (2019) | 3 | 0,06% | 3 | 0,43% | 3 | 0,45% | 3 | 0,44% |
| 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% |
| Fournier (1934-1940) | 3 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| 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 | 0,44% |
| 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 | 0,44% |
| 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% |
| 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 | 0,44% |
| 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 | 0,44% |
| 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% |
| Bernard (2015) | 2 | 0,04% | 2 | 0,28% | 2 | 0,3% | 2 | 0,3% |
| Boggan et al. (1997) | 2 | 0,04% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
| 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% |
| Carcaillet (1993) | 2 | 0,04% | 2 | 0,28% | 2 | 0,3% | 1 | 0,15% |
| Chiron & Bellone (2005) | 2 | 0,04% | 2 | 0,28% | 2 | 0,3% | 2 | 0,3% |
| Christenhusz (2009) | 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% |
| Copeland (1932) | 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% |
| Lamarck (1779) | 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% |
| Linnaeus (1762) | 2 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
| 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% |
| 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% |
| Murdock & Smith (2003) | 2 | 0,04% | 2 | 0,28% | 2 | 0,3% | 2 | 0,3% |
| 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% |
| 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 (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% |
| 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% |
| 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% |
| Kerguélen & Bock (2011) | 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% |
| 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% |
| Lindstrom & Hill (2007) | 1 | 0,02% | 1 | 0,14% | 1 | 0,15% | 1 | 0,15% |
| Linnaeus (1759) | 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% |
| Moench (1794) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
| 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% |
| 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% |
| 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% |
| Stevenson (1991) | 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% |
| Verdcourt (1970) | 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% |
