Espèces végétales introduites en Guyane
Plantes introduites au sens large en Guyane française, c'est-à-dire introduites naturalisées (I), invasives (J), introduites non naturalisées (M) ou introduites éteintes (Y)
442 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) | 2830 | 46,34% | 2269 | 201,69% | 2265 | 215,1% | 2171 | 204,81% |
Funk et al. (2007) | 938 | 15,36% | 415 | 36,89% | 399 | 37,89% | 382 | 36,04% |
Hequet & Le Corre (2010) | 545 | 8,92% | 423 | 37,6% | 419 | 39,79% | 397 | 37,45% |
Hequet et al. (2009) | 545 | 8,92% | 423 | 37,6% | 419 | 39,79% | 397 | 37,45% |
MacKee (1994) | 541 | 8,86% | 416 | 36,98% | 412 | 39,13% | 391 | 36,89% |
Delnatte & Meyer (2012) | 444 | 7,27% | 358 | 31,82% | 354 | 33,62% | 347 | 32,74% |
Tison et al. (2014) | 383 | 6,27% | 224 | 19,91% | 219 | 20,8% | 200 | 18,87% |
Fourdrigniez & Meyer (2008) | 277 | 4,54% | 213 | 18,93% | 207 | 19,66% | 197 | 18,58% |
Léotard & Chaline (2013) | 210 | 3,44% | 170 | 15,11% | 161 | 15,29% | 162 | 15,28% |
Munzinger et al. (2016) | 175 | 2,87% | 49 | 4,36% | 49 | 4,65% | 43 | 4,06% |
Acevedo-Rodríguez & Strong (2012) | 157 | 2,57% | 103 | 9,16% | 95 | 9,02% | 96 | 9,06% |
Paton et al. (2019) | 148 | 2,42% | 9 | 0,8% | 7 | 0,66% | 7 | 0,66% |
Molino et al. (2022) | 139 | 2,28% | 13 | 1,16% | 13 | 1,23% | 12 | 1,13% |
Morat et al. (2012) | 104 | 1,7% | 52 | 4,62% | 52 | 4,94% | 44 | 4,15% |
Morat & Veillon (1985) | 96 | 1,57% | 76 | 6,76% | 75 | 7,12% | 64 | 6,04% |
Molino et al. (2009) | 85 | 1,39% | 74 | 6,58% | 74 | 7,03% | 70 | 6,6% |
Aublet (1775) | 79 | 1,29% | 40 | 3,56% | 39 | 3,7% | 37 | 3,49% |
Boullet et al. (2018) | 65 | 1,06% | 56 | 4,98% | 55 | 5,22% | 51 | 4,81% |
Anonyme (2014) | 63 | 1,03% | 53 | 4,71% | 53 | 5,03% | 51 | 4,81% |
Florence (2004) | 60 | 0,98% | 50 | 4,44% | 47 | 4,46% | 50 | 4,72% |
Wasshausen (2006) | 55 | 0,9% | 16 | 1,42% | 15 | 1,42% | 14 | 1,32% |
Ter Steege et al. (2016) | 50 | 0,82% | 47 | 4,18% | 47 | 4,46% | 38 | 3,58% |
Lemée (1955) | 40 | 0,65% | 16 | 1,42% | 16 | 1,52% | 15 | 1,42% |
Pennington (1990) | 39 | 0,64% | 4 | 0,36% | 4 | 0,38% | 4 | 0,38% |
Florence (1997) | 37 | 0,61% | 23 | 2,04% | 23 | 2,18% | 21 | 1,98% |
Lemée (1952) | 35 | 0,57% | 23 | 2,04% | 23 | 2,18% | 21 | 1,98% |
Lavergne (2011) | 32 | 0,52% | 26 | 2,31% | 23 | 2,18% | 24 | 2,26% |
Swenson et al. (2023) | 32 | 0,52% | 4 | 0,36% | 4 | 0,38% | 4 | 0,38% |
Linnaeus (1753) | 31 | 0,51% | 22 | 1,96% | 21 | 1,99% | 19 | 1,79% |
Gargominy et al. (1996) | 29 | 0,47% | 23 | 2,04% | 23 | 2,18% | 22 | 2,08% |
Lemée (1953) | 29 | 0,47% | 15 | 1,33% | 15 | 1,42% | 15 | 1,42% |
Rogers & Appan (1973) | 28 | 0,46% | 1 | 0,09% | 1 | 0,09% | 0 | 0% |
Linnaeus (1753) | 27 | 0,44% | 19 | 1,69% | 19 | 1,8% | 18 | 1,7% |
Meyer et al. (2006) | 26 | 0,43% | 16 | 1,42% | 15 | 1,42% | 15 | 1,42% |
Souza & Giulietti (2009) | 25 | 0,41% | 4 | 0,36% | 4 | 0,38% | 4 | 0,38% |
Korotkova et al. (2017) | 23 | 0,38% | 3 | 0,27% | 3 | 0,28% | 3 | 0,28% |
Cremers & Hoff (1997) | 22 | 0,36% | 3 | 0,27% | 3 | 0,28% | 3 | 0,28% |
Ferlay et al. (2023) | 21 | 0,34% | 21 | 1,87% | 21 | 1,99% | 19 | 1,79% |
Fischer et al. (2013) | 21 | 0,34% | 7 | 0,62% | 7 | 0,66% | 7 | 0,66% |
Stace (2010) | 21 | 0,34% | 6 | 0,53% | 5 | 0,47% | 5 | 0,47% |
Welker et al. (2020) | 21 | 0,34% | 20 | 1,78% | 20 | 1,9% | 18 | 1,7% |
Cremers & Hoff (1994) | 20 | 0,33% | 6 | 0,53% | 6 | 0,57% | 6 | 0,57% |
Suddee et al. (2004) | 20 | 0,33% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Barneby & Grimes (1996) | 19 | 0,31% | 3 | 0,27% | 3 | 0,28% | 3 | 0,28% |
Bayón (2015) | 19 | 0,31% | 3 | 0,27% | 2 | 0,19% | 1 | 0,09% |
Hovenkamp & Miyamoto (2005) | 19 | 0,31% | 3 | 0,27% | 3 | 0,28% | 2 | 0,19% |
Sambin (2020) | 19 | 0,31% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Granville & Gayot (2014) | 18 | 0,29% | 18 | 1,6% | 18 | 1,71% | 17 | 1,6% |
Salisbury (1796) | 18 | 0,29% | 0 | 0% | 0 | 0% | 0 | 0% |
Allem (1994) | 17 | 0,28% | 2 | 0,18% | 1 | 0,09% | 1 | 0,09% |
Drew et al. (2017) | 17 | 0,28% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Goldblatt & Snow (1991) | 17 | 0,28% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Guimarães et al. (2019) | 17 | 0,28% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Miller (1768) | 17 | 0,28% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Nesom (2009) | 17 | 0,28% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Christenhusz (2009) | 16 | 0,26% | 13 | 1,16% | 11 | 1,04% | 11 | 1,04% |
Lewis (2000) | 16 | 0,26% | 3 | 0,27% | 3 | 0,28% | 3 | 0,28% |
Mitchell & Daly (2015) | 16 | 0,26% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Toutain (1989) | 16 | 0,26% | 12 | 1,07% | 12 | 1,14% | 11 | 1,04% |
Wiersema et al. (2018) | 16 | 0,26% | 5 | 0,44% | 5 | 0,47% | 5 | 0,47% |
Mora & Clark (2016) | 15 | 0,25% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Philcox (1970) | 15 | 0,25% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Plowman et al. (1998) | 15 | 0,25% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Boggan et al. (1992) | 14 | 0,23% | 8 | 0,71% | 8 | 0,76% | 7 | 0,66% |
Christenhusz (2002) | 14 | 0,23% | 11 | 0,98% | 9 | 0,85% | 10 | 0,94% |
Hassemer (2017) | 13 | 0,21% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Webster (1956) | 13 | 0,21% | 3 | 0,27% | 1 | 0,09% | 2 | 0,19% |
Wood et al. (2020) | 13 | 0,21% | 11 | 0,98% | 10 | 0,95% | 10 | 0,94% |
Manzitto‐Tripp & Daniel (2023) | 12 | 0,2% | 12 | 1,07% | 12 | 1,14% | 12 | 1,13% |
Oliveira Pellegrini & Forzza (2017) | 12 | 0,2% | 0 | 0% | 0 | 0% | 0 | 0% |
Veldkamp (1991) | 12 | 0,2% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Zerega et al. (2005) | 12 | 0,2% | 4 | 0,36% | 4 | 0,38% | 4 | 0,38% |
Candolle (1849) | 11 | 0,18% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Croat & Delannay (2017) | 11 | 0,18% | 3 | 0,27% | 3 | 0,28% | 3 | 0,28% |
Graham (2017) | 11 | 0,18% | 3 | 0,27% | 3 | 0,28% | 3 | 0,28% |
Hunt (1986) | 11 | 0,18% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Kyalangalilwa et al. (2013) | 11 | 0,18% | 4 | 0,36% | 3 | 0,28% | 3 | 0,28% |
Marhold et al. (2016) | 11 | 0,18% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Skog & Feuillet (2008) | 11 | 0,18% | 3 | 0,27% | 3 | 0,28% | 3 | 0,28% |
Béreau (2017) | 10 | 0,16% | 7 | 0,62% | 7 | 0,66% | 6 | 0,57% |
Bernard (2015) | 10 | 0,16% | 7 | 0,62% | 7 | 0,66% | 6 | 0,57% |
Hoff & Cremers (2005) | 10 | 0,16% | 9 | 0,8% | 6 | 0,57% | 9 | 0,85% |
Lukhoba & Paton (2003) | 10 | 0,16% | 1 | 0,09% | 1 | 0,09% | 0 | 0% |
Patchell et al. (2014) | 10 | 0,16% | 6 | 0,53% | 6 | 0,57% | 6 | 0,57% |
Satthaphorn et al. (2023) | 10 | 0,16% | 10 | 0,89% | 10 | 0,95% | 10 | 0,94% |
Webster (2003) | 10 | 0,16% | 4 | 0,36% | 1 | 0,09% | 3 | 0,28% |
Acevedo-Rodríguez (2012) | 9 | 0,15% | 5 | 0,44% | 5 | 0,47% | 5 | 0,47% |
Armada & Barra (1992) | 9 | 0,15% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Borchsenius et al. (2012) | 9 | 0,15% | 4 | 0,36% | 4 | 0,38% | 4 | 0,38% |
Bouman et al. (2022) | 9 | 0,15% | 6 | 0,53% | 6 | 0,57% | 4 | 0,38% |
Feldmann (2012) | 9 | 0,15% | 9 | 0,8% | 9 | 0,85% | 9 | 0,85% |
Gentry (1980) | 9 | 0,15% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Iamonico (2016) | 9 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Judziewicz (1990) | 9 | 0,15% | 8 | 0,71% | 8 | 0,76% | 8 | 0,75% |
Kükenthal (1936) | 9 | 0,15% | 2 | 0,18% | 1 | 0,09% | 1 | 0,09% |
Maddi (2014) | 9 | 0,15% | 6 | 0,53% | 6 | 0,57% | 6 | 0,57% |
Pollard & Paton (2001) | 9 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Soto Arenas & Cribb (2010) | 9 | 0,15% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Véron et al. (2021) | 9 | 0,15% | 8 | 0,71% | 8 | 0,76% | 8 | 0,75% |
Yang et al. (2012) | 9 | 0,15% | 9 | 0,8% | 9 | 0,85% | 8 | 0,75% |
Bouman et al. (2020) | 8 | 0,13% | 2 | 0,18% | 2 | 0,19% | 0 | 0% |
Cardiel et al. (2022) | 8 | 0,13% | 6 | 0,53% | 6 | 0,57% | 6 | 0,57% |
Du Puy et al. (1993) | 8 | 0,13% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Handlos (1975) | 8 | 0,13% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Hassemer et al. (2017) | 8 | 0,13% | 8 | 0,71% | 8 | 0,76% | 7 | 0,66% |
Jost et al. (2019) | 8 | 0,13% | 6 | 0,53% | 5 | 0,47% | 6 | 0,57% |
Maas et al. (2023) | 8 | 0,13% | 4 | 0,36% | 4 | 0,38% | 4 | 0,38% |
Masters et al. (2023) | 8 | 0,13% | 7 | 0,62% | 7 | 0,66% | 7 | 0,66% |
Mitchell (1997) | 8 | 0,13% | 5 | 0,44% | 5 | 0,47% | 5 | 0,47% |
Smith & Downs (1979) | 8 | 0,13% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Arriagada (2003) | 7 | 0,11% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Aurore et al. (2014) | 7 | 0,11% | 3 | 0,27% | 3 | 0,28% | 3 | 0,28% |
Copeland (1932) | 7 | 0,11% | 5 | 0,44% | 5 | 0,47% | 2 | 0,19% |
Egan & Pan (2015) | 7 | 0,11% | 2 | 0,18% | 1 | 0,09% | 1 | 0,09% |
Mori et al. (2002) | 7 | 0,11% | 6 | 0,53% | 6 | 0,57% | 6 | 0,57% |
Vorontsova (2022) | 7 | 0,11% | 3 | 0,27% | 3 | 0,28% | 3 | 0,28% |
Barabé & Gibernau (2015) | 6 | 0,1% | 4 | 0,36% | 4 | 0,38% | 4 | 0,38% |
Barneby (1991) | 6 | 0,1% | 0 | 0% | 0 | 0% | 0 | 0% |
Barrett et al. (2017) | 6 | 0,1% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Barthelat (2019) | 6 | 0,1% | 6 | 0,53% | 6 | 0,57% | 5 | 0,47% |
Colletta et al. (2020) | 6 | 0,1% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
David & Thiebaut (2013) | 6 | 0,1% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Dehgan (2012) | 6 | 0,1% | 5 | 0,44% | 5 | 0,47% | 5 | 0,47% |
Dorsey et al. (2013) | 6 | 0,1% | 6 | 0,53% | 6 | 0,57% | 5 | 0,47% |
Feuillet & Poncy (1998) | 6 | 0,1% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Lowe et al. (2007) | 6 | 0,1% | 4 | 0,36% | 3 | 0,28% | 3 | 0,28% |
Oliveira Pellegrini et al. (2016) | 6 | 0,1% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Pfeifer (1966) | 6 | 0,1% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Prévoteau (2012) | 6 | 0,1% | 6 | 0,53% | 5 | 0,47% | 6 | 0,57% |
Rainer (2007) | 6 | 0,1% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Rivera et al. (2013) | 6 | 0,1% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Roalson & Hall (2017) | 6 | 0,1% | 4 | 0,36% | 3 | 0,28% | 3 | 0,28% |
Scatigna et al. (2022) | 6 | 0,1% | 6 | 0,53% | 6 | 0,57% | 6 | 0,57% |
Simões & Staples (2017) | 6 | 0,1% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Thulin et al. (2016) | 6 | 0,1% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Allen et al. (2022) | 5 | 0,08% | 5 | 0,44% | 5 | 0,47% | 5 | 0,47% |
Berton (2020) | 5 | 0,08% | 5 | 0,44% | 5 | 0,47% | 5 | 0,47% |
Bosser & Heine (1988) | 5 | 0,08% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Byng et al. (2016) | 5 | 0,08% | 5 | 0,44% | 5 | 0,47% | 5 | 0,47% |
Costea et al. (2001) | 5 | 0,08% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Couté & Garrouste (2009) | 5 | 0,08% | 4 | 0,36% | 4 | 0,38% | 4 | 0,38% |
Fournier (1934-1940) | 5 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Gandoger (1875) | 5 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Graham (1988) | 5 | 0,08% | 4 | 0,36% | 4 | 0,38% | 4 | 0,38% |
Hullé et al. (2003) | 5 | 0,08% | 4 | 0,36% | 4 | 0,38% | 2 | 0,19% |
Kress et al. (2005) | 5 | 0,08% | 5 | 0,44% | 5 | 0,47% | 5 | 0,47% |
Larridon et al. (2014) | 5 | 0,08% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Levin et al. (2022) | 5 | 0,08% | 5 | 0,44% | 5 | 0,47% | 5 | 0,47% |
Linnaeus (1759) | 5 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Moench (1794) | 5 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Murdock & Smith (2003) | 5 | 0,08% | 5 | 0,44% | 5 | 0,47% | 3 | 0,28% |
Pennington & Biggs (2016) | 5 | 0,08% | 4 | 0,36% | 4 | 0,38% | 4 | 0,38% |
Questel (2023) | 5 | 0,08% | 5 | 0,44% | 5 | 0,47% | 4 | 0,38% |
Sachet (1962) | 5 | 0,08% | 4 | 0,36% | 4 | 0,38% | 4 | 0,38% |
Soto Arenas & Dressler (2010) | 5 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
Turner (2013) | 5 | 0,08% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Andersson (1981) | 4 | 0,07% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Appelhans et al. (2021) | 4 | 0,07% | 4 | 0,36% | 4 | 0,38% | 4 | 0,38% |
Baaijens & Veldkamp (1991) | 4 | 0,07% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Bell (1982) | 4 | 0,07% | 4 | 0,36% | 4 | 0,38% | 3 | 0,28% |
Chemisquy et al. (2010) | 4 | 0,07% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Coode 1982 | 4 | 0,07% | 4 | 0,36% | 4 | 0,38% | 4 | 0,38% |
Cowan & Lindeman (1989) | 4 | 0,07% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Cuatrecasas (1964) | 4 | 0,07% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Feldmann (2014) | 4 | 0,07% | 4 | 0,36% | 4 | 0,38% | 4 | 0,38% |
Feuillet (2009) | 4 | 0,07% | 4 | 0,36% | 4 | 0,38% | 2 | 0,19% |
Frenot et al. (2001) | 4 | 0,07% | 4 | 0,36% | 4 | 0,38% | 4 | 0,38% |
Fryxell (2001) | 4 | 0,07% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Gardner et al. (2021) | 4 | 0,07% | 4 | 0,36% | 4 | 0,38% | 4 | 0,38% |
Grether (2000) | 4 | 0,07% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Harley & Pastore (2012) | 4 | 0,07% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Iles et al. (2017) | 4 | 0,07% | 4 | 0,36% | 4 | 0,38% | 4 | 0,38% |
Jolinon (1987) | 4 | 0,07% | 3 | 0,27% | 3 | 0,28% | 1 | 0,09% |
Kuntze (1891) | 4 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Lamarck (1779) | 4 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Lamarck (1783) | 4 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Lemée (1956) | 4 | 0,07% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Lohmann & Taylor (2014) | 4 | 0,07% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
McDonald & Maslin (2000) | 4 | 0,07% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Moench (1794) | 4 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Zornia". Webbia, 16(1): 1-141.">Mohlenbrock (1961) | 4 | 0,07% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Moore (1933) | 4 | 0,07% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Ocampo & Columbus (2012) | 4 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
O'Leary et al. (2016) | 4 | 0,07% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Paton et al. (2018) | 4 | 0,07% | 4 | 0,36% | 4 | 0,38% | 3 | 0,28% |
Peterson et al. (2014) | 4 | 0,07% | 4 | 0,36% | 4 | 0,38% | 4 | 0,38% |
Philcox (1965) | 4 | 0,07% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Richard (1792) | 4 | 0,07% | 1 | 0,09% | 1 | 0,09% | 0 | 0% |
Rouy (1908) | 4 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Sakuragui et al. (2018) | 4 | 0,07% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Schaefer & Renner (2011) | 4 | 0,07% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Silva et al. (2017) | 4 | 0,07% | 4 | 0,36% | 4 | 0,38% | 4 | 0,38% |
Tareau (2015) | 4 | 0,07% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Tippery et al. (2024) | 4 | 0,07% | 4 | 0,36% | 4 | 0,38% | 4 | 0,38% |
Béguinot (2012) | 3 | 0,05% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Bosser & Heine (2000b) | 3 | 0,05% | 3 | 0,27% | 3 | 0,28% | 2 | 0,19% |
Bubani & Penzig (1897) | 3 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Candolle (1828) | 3 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Candolle (1830) | 3 | 0,05% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Carcaillet (1993) | 3 | 0,05% | 3 | 0,27% | 3 | 0,28% | 2 | 0,19% |
Cochrane & Iltis (2014) | 3 | 0,05% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Crantz (1766) | 3 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Cremers & Boudrie (2007) | 3 | 0,05% | 2 | 0,18% | 2 | 0,19% | 1 | 0,09% |
Cremers & Hoff (1998) | 3 | 0,05% | 1 | 0,09% | 1 | 0,09% | 0 | 0% |
Dumbardon-Martial & Delblond (2019) | 3 | 0,05% | 3 | 0,27% | 3 | 0,28% | 3 | 0,28% |
Grose & Olmstead (2007) | 3 | 0,05% | 3 | 0,27% | 3 | 0,28% | 3 | 0,28% |
Iltis & Cochrane (2007) | 3 | 0,05% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Iltis (1960) | 3 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Jordan & Fourreau (1866) | 3 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Kocyan et al. (2011) | 3 | 0,05% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Lamarck & Candolle (1805) | 3 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Lamarck (1779) | 3 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Lamarck (1789) | 3 | 0,05% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Lorence et al. (2007) | 3 | 0,05% | 3 | 0,27% | 3 | 0,28% | 3 | 0,28% |
Maas (1985) | 3 | 0,05% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Mabberley (2018) | 3 | 0,05% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Margońska (2019) | 3 | 0,05% | 3 | 0,27% | 3 | 0,28% | 3 | 0,28% |
Montero et al. (2018) | 3 | 0,05% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Moonlight et al. (2018) | 3 | 0,05% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Ollitrault et al. (2020) | 3 | 0,05% | 2 | 0,18% | 0 | 0% | 2 | 0,19% |
Pearman et al. (2020) | 3 | 0,05% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Persoon (1805) | 3 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Pteridophyte Phylogeny Group (2016) | 3 | 0,05% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Sanders (2006) | 3 | 0,05% | 2 | 0,18% | 1 | 0,09% | 1 | 0,09% |
Sanders (2012) | 3 | 0,05% | 1 | 0,09% | 0 | 0% | 0 | 0% |
Schrire et al. (2009) | 3 | 0,05% | 3 | 0,27% | 3 | 0,28% | 3 | 0,28% |
Small (2015) | 3 | 0,05% | 1 | 0,09% | 0 | 0% | 1 | 0,09% |
Souza et al. (2021) | 3 | 0,05% | 3 | 0,27% | 3 | 0,28% | 3 | 0,28% |
Souza et al. (2022) | 3 | 0,05% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Sprague (1928) | 3 | 0,05% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Tassin et al. (2006) | 3 | 0,05% | 3 | 0,27% | 3 | 0,28% | 3 | 0,28% |
Teres (2006) | 3 | 0,05% | 3 | 0,27% | 3 | 0,28% | 3 | 0,28% |
Thellung (1912) | 3 | 0,05% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Verdcourt (1970) | 3 | 0,05% | 3 | 0,27% | 1 | 0,09% | 2 | 0,19% |
Walter et al. (2015) | 3 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Webster (1957) | 3 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Wood et al. (2015) | 3 | 0,05% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Yang et al. (2022) | 3 | 0,05% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Acevedo-Rodríguez & Strong (2005) | 2 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Allorge-Boiteau (2015) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Augros et al. (2018) | 2 | 0,03% | 2 | 0,18% | 1 | 0,09% | 1 | 0,09% |
Berg (1992) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Berry et al. (1999) | 2 | 0,03% | 2 | 0,18% | 1 | 0,09% | 1 | 0,09% |
Boggan et al. (1997) | 2 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Borchsenius & Bernal (1996) | 2 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Bosser & Heine (2000) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Boudrie & Bizot (2006) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Candolle (1852) | 2 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Capellari Jr. (2000) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Cariot & Saint-lager (1889) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Chevalier (1936) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Chukr & Giulietti (2008) | 2 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Couhia & Fleurot (2016) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Crantz (1766) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
DeFilipps (1992) | 2 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Espírito Santo et al. (2019) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Euro+Med (2006) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Ferrer-gallego et al. (2019) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Filipowicz et al. (2014) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Fortuna-Perez (2009) | 2 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Foster (1962) | 2 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Fried & Dumbardon‑Martial (2015) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Fryxell (1988) | 2 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Gagnon et al. (2016) | 2 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Garcia-Mendoza & Chiang (2003) | 2 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Görts-van Rijn (2007) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Gray (1821) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Hollowell et al. (2001) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Joe et al. (2016) | 2 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Knapp (2013) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Linnaeus (1762) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Linnaeus (1763) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Maas (1985) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Maddi (2010) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Mapaya (2017) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Mazine et al. (2018) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Mcclintock (1957) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Meyer et al. (2008) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Moraes (2012) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Moran & Smith (1999) | 2 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Muller et al. (2004) | 2 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Orejuela et al. (2017) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Peraza et al. (2022) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Polhill (1990) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Prance et al. (2007) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Reed (1968) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Ridsdale (1974) | 2 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Rohde et al. (2017) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Rome & Coppens d'Eeckenbrugge (2023) | 2 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Rudd (1955) | 2 | 0,03% | 2 | 0,18% | 1 | 0,09% | 1 | 0,09% |
Samson (2005) | 2 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Seigler et al. (2014) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Snak et al. (2016) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Soares Neto et al. (2018) | 2 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Soares Netoet al. (2017) | 2 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Song et al. (2019) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Suessenguth (1936) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Veldkamp (2014) | 2 | 0,03% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Webster (1957) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Willdenow (1800) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Zakardjian et al. (2020) | 2 | 0,03% | 2 | 0,18% | 2 | 0,19% | 2 | 0,19% |
Alencar et al. (2021) | 1 | 0,02% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Allem (2001) | 1 | 0,02% | 1 | 0,09% | 0 | 0% | 1 | 0,09% |
Almeida et al. (2016) | 1 | 0,02% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Alvarado-Cárdenas & Ochoterena (2007) | 1 | 0,02% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Arcangeli (1882) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Aubert de la Rüe (1932) | 1 | 0,02% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Austin & Huáman (1996) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Bacon & Baker (2011) | 1 | 0,02% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Badré (2008b) | 1 | 0,02% | 1 | 0,09% | 1 | 0,09% | 0 | 0% |
Baker (1867) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Berg (2007) | 1 | 0,02% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Berry et al. (2001) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Bikaeff (2002) | 1 | 0,02% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Blake (1917) | 1 | 0,02% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Bossa‐Castro et al. (2024) | 1 | 0,02% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Bovini (2010) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Brenan (1994) | 1 | 0,02% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Breton (2014) | 1 | 0,02% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Brottier et al. (2018) | 1 | 0,02% | 1 | 0,09% | 1 | 0,09% | 0 | 0% |
Bryson et al. (1997) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Bubani & Penzig (1901) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Cafferty et al. (2000) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Calviño et al. (2008) | 1 | 0,02% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Candolle (1844) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Candolle (1845) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Christenhusz et al. (2018) | 1 | 0,02% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Cohen & Ackerman (2009) | 1 | 0,02% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Colli-Silva et al. (2024) | 1 | 0,02% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Cramer (1978) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Cremers & Boudrie (2006) | 1 | 0,02% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Cremers & Hoff (1993) | 1 | 0,02% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Daniel & Mcdade (2014) | 1 | 0,02% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Danin et al. (2012) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Don (1831) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Don (1834) | 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% |
Eppo (2011) | 1 | 0,02% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Ezcurra & Daniel (2007) | 1 | 0,02% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Fedde (1939) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Fernandes (1984) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Feuillet (2014) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Filipowicz & Renner (2012) | 1 | 0,02% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Flora of North America (1993-) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Forsskål (1775) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Fosberg & Sachet (1975) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Fosberg (1937) | 1 | 0,02% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Freitas et al. (2016) | 1 | 0,02% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Gaertner (1788) | 1 | 0,02% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Gardner et al. (2021) | 1 | 0,02% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Grangaud (2010) | 1 | 0,02% | 1 | 0,09% | 1 | 0,09% | 0 | 0% |
Grayum et al. (2012) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Gregório et al. (2023) | 1 | 0,02% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Grenand et al. (2004) | 1 | 0,02% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Guillaumin (1936) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Epidendrum". Icones Orchidacearum, 8: i-xi + pl. 801-900.">Hágsater (2006) | 1 | 0,02% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Hillig (2005) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Hodel et al. (2021) | 1 | 0,02% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Hoehne (1944) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Iamonico et al. (2015) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Jolinon (1985) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Kaastra (1982) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Karsch (1853) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Kennedy (1978) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Klonowska et al. (2012) | 1 | 0,02% | 1 | 0,09% | 1 | 0,09% | 0 | 0% |
Klonowska et al. (2020) | 1 | 0,02% | 1 | 0,09% | 1 | 0,09% | 0 | 0% |
Laguna (2006) | 1 | 0,02% | 1 | 0,09% | 0 | 0% | 1 | 0,09% |
Lamarck & Candolle (1805) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Lambinon & Worm (1993) | 1 | 0,02% | 1 | 0,09% | 0 | 0% | 1 | 0,09% |
Landrum (1986) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Laubengayer et al. (2012) | 1 | 0,02% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Leuenberger (1997) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Li et al. (2021) | 1 | 0,02% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Lieutard (1893) | 1 | 0,02% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Lindstrom & Hill (2007) | 1 | 0,02% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Linné (1766) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Liu et al. (2004) | 1 | 0,02% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Maas & de Rooij (1979) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Maas & Westra (1992) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Maas (1985) | 1 | 0,02% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Maddi (2014) | 1 | 0,02% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Majure et al. (2012) | 1 | 0,02% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Maya-Lastra & Steinmann (2018) | 1 | 0,02% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Mestier et al. (2022) | 1 | 0,02% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Meyer (2017) | 1 | 0,02% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Michelangeli et al. (2013) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Mori et al. (1997) | 1 | 0,02% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Mori et al. (2002) | 1 | 0,02% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Mosyakin & Clemants (2002) | 1 | 0,02% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Munir (1992) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Nitta et al. (2011) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Nyman (1882) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Oldeman (1968) | 1 | 0,02% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
O'Leary & Múlgura (2012) | 1 | 0,02% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Ortuño & Borsch (2020) | 1 | 0,02% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Paradis & Miniconi (2011) | 1 | 0,02% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Peck et al. (2014) | 1 | 0,02% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Pedersen (2000) | 1 | 0,02% | 1 | 0,09% | 0 | 0% | 1 | 0,09% |
Peichoto (2010) | 1 | 0,02% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Pellegrini et al. (2018) | 1 | 0,02% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Persoon (1807) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Portères (1955) | 1 | 0,02% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Prelli & Boudrie (2021) | 1 | 0,02% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Ravenna (1984) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Raz (2016) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Rivière (2003) | 1 | 0,02% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Rome & Coppens d'Eeckenbrugge (2016) | 1 | 0,02% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Rouy (1909) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Sagot (1881) | 1 | 0,02% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Scopoli (1771) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Scopoli (1771) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Sherff (1937) | 1 | 0,02% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Soubeyran (2008) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Specht & Stevenson (2006) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Stafleu & Cowan (1983) | 1 | 0,02% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Stehlé & Stehlé (1958) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Stepansky et al. (1999) | 1 | 0,02% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Stevenson (1991) | 1 | 0,02% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Stevenson (1991) | 1 | 0,02% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Tamboli et al. (2016) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Tareau (2019) | 1 | 0,02% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Tenore (1811-1815) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Tison et al. (2021) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Tripp et al. (2013) | 1 | 0,02% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Turner & Veldkamp (2009) | 1 | 0,02% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Türpe (1984) | 1 | 0,02% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Van Andel (2010) | 1 | 0,02% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Vanhöffen (1912) | 1 | 0,02% | 1 | 0,09% | 1 | 0,09% | 0 | 0% |
Veldkamp (2002) | 1 | 0,02% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Villanueva-almanza et al. (2021) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Webster (1957) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Wiersema & Dahlberg (2007) | 1 | 0,02% | 1 | 0,09% | 0 | 0% | 1 | 0,09% |
Willdenow (1799) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Willdenow (1799) | 1 | 0,02% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Wilson (2022) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Wood (2008) | 1 | 0,02% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Wörz (2005) | 1 | 0,02% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Wurdack et al. (1993) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Yahaya et al. (2016) | 1 | 0,02% | 1 | 0,09% | 0 | 0% | 1 | 0,09% |
Yuan et al. (2010) | 1 | 0,02% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |
Ziffer-Berger et al. (2015) | 1 | 0,02% | 1 | 0,09% | 1 | 0,09% | 1 | 0,09% |