Espèces végétales introduites naturalisées ou invasives
836 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) | 4205 | 17.92% | 3406 | 97.09% | 3402 | 109.95% | 3121 | 97.81% |
Tison et al. (2014) | 3477 | 14.82% | 1876 | 53.48% | 1701 | 54.98% | 1658 | 51.96% |
Funk et al. (2007) | 1655 | 7.05% | 625 | 17.82% | 601 | 19.42% | 559 | 17.52% |
Hequet & Le Corre (2010) | 990 | 4.22% | 781 | 22.26% | 769 | 24.85% | 710 | 22.25% |
Hequet et al. (2009) | 989 | 4.22% | 780 | 22.23% | 768 | 24.82% | 709 | 22.22% |
MacKee (1994) | 989 | 4.22% | 775 | 22.09% | 763 | 24.66% | 707 | 22.16% |
Fourdrigniez & Meyer (2008) | 623 | 2.66% | 489 | 13.94% | 454 | 14.67% | 436 | 13.66% |
Munzinger et al. (2016) | 416 | 1.77% | 133 | 3.79% | 128 | 4.14% | 115 | 3.6% |
Molino et al. (2022) | 341 | 1.45% | 27 | 0.77% | 27 | 0.87% | 26 | 0.81% |
Delnatte & Meyer (2012) | 338 | 1.44% | 266 | 7.58% | 262 | 8.47% | 238 | 7.46% |
Morat et al. (2012) | 258 | 1.1% | 131 | 3.73% | 127 | 4.1% | 112 | 3.51% |
Acevedo-Rodríguez & Strong (2012) | 230 | 0.98% | 152 | 4.33% | 150 | 4.85% | 132 | 4.14% |
Léotard & Chaline (2013) | 204 | 0.87% | 166 | 4.73% | 157 | 5.07% | 151 | 4.73% |
Morat & Veillon (1985) | 193 | 0.82% | 150 | 4.28% | 148 | 4.78% | 126 | 3.95% |
Linnaeus (1753) | 158 | 0.67% | 110 | 3.14% | 98 | 3.17% | 91 | 2.85% |
Linnaeus (1753) | 149 | 0.64% | 98 | 2.79% | 92 | 2.97% | 85 | 2.66% |
Florence (2004) | 135 | 0.58% | 117 | 3.34% | 102 | 3.3% | 114 | 3.57% |
Paton et al. (2019) | 130 | 0.55% | 4 | 0.11% | 3 | 0.1% | 3 | 0.09% |
Boullet et al. (2018) | 122 | 0.52% | 109 | 3.11% | 99 | 3.2% | 101 | 3.17% |
Cabioc'h & Floc'h (2014) | 121 | 0.52% | 92 | 2.62% | 92 | 2.97% | 89 | 2.79% |
Anonyme (2014) | 113 | 0.48% | 96 | 2.74% | 96 | 3.1% | 84 | 2.63% |
Aublet (1775) | 103 | 0.44% | 45 | 1.28% | 44 | 1.42% | 41 | 1.28% |
Lavergne (2011) | 99 | 0.42% | 82 | 2.34% | 77 | 2.49% | 75 | 2.35% |
Molino et al. (2009) | 88 | 0.38% | 76 | 2.17% | 76 | 2.46% | 70 | 2.19% |
Wiersema et al. (2018) | 71 | 0.3% | 27 | 0.77% | 26 | 0.84% | 20 | 0.63% |
Costea et al. (2001) | 66 | 0.28% | 8 | 0.23% | 6 | 0.19% | 7 | 0.22% |
Meyer et al. (2006) | 66 | 0.28% | 40 | 1.14% | 38 | 1.23% | 38 | 1.19% |
Salisbury (1796) | 66 | 0.28% | 0 | 0% | 0 | 0% | 0 | 0% |
Nesom (2009) | 65 | 0.28% | 3 | 0.09% | 3 | 0.1% | 2 | 0.06% |
Frenot et al. (2001) | 64 | 0.27% | 56 | 1.6% | 54 | 1.75% | 48 | 1.5% |
Ter Steege et al. (2016) | 58 | 0.25% | 53 | 1.51% | 53 | 1.71% | 49 | 1.54% |
Lemée (1952) | 56 | 0.24% | 39 | 1.11% | 39 | 1.26% | 32 | 1% |
Gargominy et al. (1996) | 54 | 0.23% | 40 | 1.14% | 40 | 1.29% | 37 | 1.16% |
Krapovickas (2003) | 54 | 0.23% | 11 | 0.31% | 11 | 0.36% | 11 | 0.34% |
Ferlay et al. (2023) | 53 | 0.23% | 53 | 1.51% | 53 | 1.71% | 49 | 1.54% |
Goulletquer (2016) | 53 | 0.23% | 45 | 1.28% | 45 | 1.45% | 42 | 1.32% |
Wasshausen (2006) | 52 | 0.22% | 13 | 0.37% | 13 | 0.42% | 12 | 0.38% |
Lemée (1953) | 51 | 0.22% | 25 | 0.71% | 25 | 0.81% | 24 | 0.75% |
Wilmot-Dear & Friis (2013) | 51 | 0.22% | 10 | 0.29% | 3 | 0.1% | 8 | 0.25% |
Florence (1997) | 46 | 0.2% | 34 | 0.97% | 31 | 1% | 32 | 1% |
Lemée (1955) | 46 | 0.2% | 21 | 0.6% | 20 | 0.65% | 20 | 0.63% |
Burel et al. (2019) | 43 | 0.18% | 41 | 1.17% | 41 | 1.33% | 39 | 1.22% |
Muller et al. (2004) | 43 | 0.18% | 37 | 1.05% | 35 | 1.13% | 33 | 1.03% |
Jolinon (1987) | 42 | 0.18% | 37 | 1.05% | 37 | 1.2% | 30 | 0.94% |
Bayón (2015) | 41 | 0.17% | 8 | 0.23% | 3 | 0.1% | 4 | 0.13% |
Miller (1768) | 41 | 0.17% | 8 | 0.23% | 7 | 0.23% | 7 | 0.22% |
Carcaillet (1993) | 40 | 0.17% | 37 | 1.05% | 36 | 1.16% | 30 | 0.94% |
Euro+Med (2006) | 40 | 0.17% | 1 | 0.03% | 1 | 0.03% | 0 | 0% |
Moench (1794) | 40 | 0.17% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Chew (1969) | 37 | 0.16% | 2 | 0.06% | 2 | 0.06% | 2 | 0.06% |
Fischer et al. (2013) | 36 | 0.15% | 9 | 0.26% | 9 | 0.29% | 9 | 0.28% |
Fournier (1934-1940) | 34 | 0.14% | 0 | 0% | 0 | 0% | 0 | 0% |
Fonseca et al. (2017) | 33 | 0.14% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Bell (1982) | 32 | 0.14% | 25 | 0.71% | 24 | 0.78% | 19 | 0.6% |
Frajman et al. (2013) | 31 | 0.13% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Hullé et al. (2003) | 31 | 0.13% | 29 | 0.83% | 29 | 0.94% | 21 | 0.66% |
Toutain (1989) | 30 | 0.13% | 21 | 0.6% | 21 | 0.68% | 18 | 0.56% |
Wurdack et al. (1993) | 30 | 0.13% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Béguinot (2012) | 29 | 0.12% | 25 | 0.71% | 25 | 0.81% | 20 | 0.63% |
Dickoré & Kasperek (2010) | 29 | 0.12% | 9 | 0.26% | 9 | 0.29% | 9 | 0.28% |
Baaijens & Veldkamp (1991) | 28 | 0.12% | 3 | 0.09% | 3 | 0.1% | 3 | 0.09% |
Rignault & Chevallier (2017) | 28 | 0.12% | 23 | 0.66% | 23 | 0.74% | 23 | 0.72% |
Rogers & Appan (1973) | 28 | 0.12% | 1 | 0.03% | 1 | 0.03% | 0 | 0% |
Sennikov & Kurtto (2017) | 27 | 0.12% | 3 | 0.09% | 3 | 0.1% | 3 | 0.09% |
Zuloaga (2022) | 27 | 0.12% | 2 | 0.06% | 2 | 0.06% | 1 | 0.03% |
Freire-Fierro (2002) | 26 | 0.11% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Guimarães et al. (2019) | 26 | 0.11% | 5 | 0.14% | 5 | 0.16% | 5 | 0.16% |
Lowe et al. (2007) | 26 | 0.11% | 20 | 0.57% | 19 | 0.61% | 16 | 0.5% |
Souza & Giulietti (2009) | 26 | 0.11% | 5 | 0.14% | 5 | 0.16% | 5 | 0.16% |
Wood et al. (2020) | 25 | 0.11% | 17 | 0.48% | 16 | 0.52% | 15 | 0.47% |
Raynal (1974) | 24 | 0.1% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Schenck (1906) | 23 | 0.1% | 20 | 0.57% | 20 | 0.65% | 16 | 0.5% |
Yang et al. (2012) | 23 | 0.1% | 23 | 0.66% | 23 | 0.74% | 21 | 0.66% |
Candolle (1849) | 22 | 0.09% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Kükenthal (1936) | 22 | 0.09% | 2 | 0.06% | 1 | 0.03% | 1 | 0.03% |
Etcheberry & Abraham (2009) | 21 | 0.09% | 17 | 0.48% | 17 | 0.55% | 14 | 0.44% |
Kuntze (1891) | 21 | 0.09% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Nyman (1882) | 21 | 0.09% | 0 | 0% | 0 | 0% | 0 | 0% |
Simões & Staples (2017) | 21 | 0.09% | 9 | 0.26% | 9 | 0.29% | 7 | 0.22% |
Bubani & Penzig (1897) | 20 | 0.09% | 0 | 0% | 0 | 0% | 0 | 0% |
Philcox (1970) | 20 | 0.09% | 3 | 0.09% | 3 | 0.1% | 3 | 0.09% |
Suddee et al. (2004) | 20 | 0.09% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Welker et al. (2020) | 20 | 0.09% | 19 | 0.54% | 19 | 0.61% | 18 | 0.56% |
Delnatte & Wynne (2016) | 19 | 0.08% | 18 | 0.51% | 18 | 0.58% | 18 | 0.56% |
Du Puy et al. (1993) | 19 | 0.08% | 2 | 0.06% | 2 | 0.06% | 2 | 0.06% |
Fourreau (1869) | 19 | 0.08% | 0 | 0% | 0 | 0% | 0 | 0% |
Maas (1985) | 19 | 0.08% | 3 | 0.09% | 3 | 0.1% | 3 | 0.09% |
Sambin (2020) | 19 | 0.08% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Andersson (1981) | 18 | 0.08% | 3 | 0.09% | 3 | 0.1% | 3 | 0.09% |
Boggan et al. (1992) | 18 | 0.08% | 9 | 0.26% | 8 | 0.26% | 8 | 0.25% |
Cambecèdes et al. (2012) | 18 | 0.08% | 15 | 0.43% | 14 | 0.45% | 13 | 0.41% |
Mitchell & Daly (2015) | 18 | 0.08% | 2 | 0.06% | 2 | 0.06% | 2 | 0.06% |
Moench (1794) | 18 | 0.08% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Rouy (1908) | 18 | 0.08% | 0 | 0% | 0 | 0% | 0 | 0% |
Allem (1994) | 17 | 0.07% | 2 | 0.06% | 1 | 0.03% | 1 | 0.03% |
Drew et al. (2017) | 17 | 0.07% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Goldblatt & Snow (1991) | 17 | 0.07% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Gray (1821) | 17 | 0.07% | 0 | 0% | 0 | 0% | 0 | 0% |
Judziewicz (1990) | 17 | 0.07% | 16 | 0.46% | 16 | 0.52% | 15 | 0.47% |
Lewis (2000) | 17 | 0.07% | 4 | 0.11% | 4 | 0.13% | 4 | 0.13% |
Satthaphorn et al. (2023) | 17 | 0.07% | 16 | 0.46% | 16 | 0.52% | 16 | 0.5% |
Wilmot-Dear & Friis (1996) | 17 | 0.07% | 6 | 0.17% | 6 | 0.19% | 6 | 0.19% |
Christenhusz (2009) | 16 | 0.07% | 12 | 0.34% | 12 | 0.39% | 11 | 0.34% |
Copeland (1932) | 16 | 0.07% | 5 | 0.14% | 5 | 0.16% | 3 | 0.09% |
Cremers & Hoff (1997) | 16 | 0.07% | 3 | 0.09% | 3 | 0.1% | 3 | 0.09% |
Flora of China (2015-) | 16 | 0.07% | 3 | 0.09% | 2 | 0.06% | 3 | 0.09% |
Host (1831) | 16 | 0.07% | 0 | 0% | 0 | 0% | 0 | 0% |
Jost et al. (2019) | 16 | 0.07% | 14 | 0.4% | 12 | 0.39% | 13 | 0.41% |
Kyalangalilwa et al. (2013) | 16 | 0.07% | 7 | 0.2% | 6 | 0.19% | 6 | 0.19% |
Payri (2007) | 16 | 0.07% | 12 | 0.34% | 12 | 0.39% | 11 | 0.34% |
Peterson et al. (2014) | 16 | 0.07% | 16 | 0.46% | 16 | 0.52% | 16 | 0.5% |
Soto Arenas & Cribb (2010) | 16 | 0.07% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Vroman (1968) | 16 | 0.07% | 12 | 0.34% | 12 | 0.39% | 11 | 0.34% |
André et al. (2020) | 15 | 0.06% | 15 | 0.43% | 15 | 0.48% | 15 | 0.47% |
Berg (1992) | 15 | 0.06% | 6 | 0.17% | 6 | 0.19% | 6 | 0.19% |
Bernard (2015) | 15 | 0.06% | 12 | 0.34% | 12 | 0.39% | 11 | 0.34% |
Lamarck (1779) | 15 | 0.06% | 0 | 0% | 0 | 0% | 0 | 0% |
Lamarck (1783) | 15 | 0.06% | 2 | 0.06% | 2 | 0.06% | 2 | 0.06% |
Linnaeus (1759) | 15 | 0.06% | 4 | 0.11% | 4 | 0.13% | 4 | 0.13% |
Rojas-Andrés et al. (2016) | 15 | 0.06% | 4 | 0.11% | 2 | 0.06% | 2 | 0.06% |
Arcangeli (1882) | 14 | 0.06% | 1 | 0.03% | 0 | 0% | 1 | 0.03% |
Christenhusz (2002) | 14 | 0.06% | 11 | 0.31% | 11 | 0.36% | 10 | 0.31% |
Gardner et al. (2021) | 14 | 0.06% | 10 | 0.29% | 10 | 0.32% | 9 | 0.28% |
Desmodium incanum and Fall of D. canum (Fabaceae). Taxon, 27(4): 365-370.">Nicolson (1978) | 14 | 0.06% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Rodríguez-Prieto et al. (1999) | 14 | 0.06% | 13 | 0.37% | 13 | 0.42% | 13 | 0.41% |
Barabé & Gibernau (2015) | 13 | 0.06% | 10 | 0.29% | 10 | 0.32% | 10 | 0.31% |
Barneby (1991) | 13 | 0.06% | 3 | 0.09% | 2 | 0.06% | 2 | 0.06% |
Berg & Roselli (2005) | 13 | 0.06% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Brandbyge (1986) | 13 | 0.06% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Feldmann (2012) | 13 | 0.06% | 12 | 0.34% | 12 | 0.39% | 12 | 0.38% |
Hovenkamp & Miyamoto (2005) | 13 | 0.06% | 3 | 0.09% | 2 | 0.06% | 2 | 0.06% |
Maddi (2014) | 13 | 0.06% | 8 | 0.23% | 8 | 0.26% | 8 | 0.25% |
Mora & Clark (2016) | 13 | 0.06% | 2 | 0.06% | 2 | 0.06% | 2 | 0.06% |
Stace (2010) | 13 | 0.06% | 4 | 0.11% | 4 | 0.13% | 4 | 0.13% |
Thulin et al. (2016) | 13 | 0.06% | 8 | 0.23% | 8 | 0.26% | 8 | 0.25% |
Verlaque (2001) | 13 | 0.06% | 11 | 0.31% | 10 | 0.32% | 10 | 0.31% |
Webster (1956) | 13 | 0.06% | 3 | 0.09% | 1 | 0.03% | 2 | 0.06% |
Barneby & Grimes (1996) | 12 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
Bonnier & Layens (1894) | 12 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
Bouman et al. (2022) | 12 | 0.05% | 8 | 0.23% | 8 | 0.26% | 7 | 0.22% |
Couté & Garrouste (2009) | 12 | 0.05% | 9 | 0.26% | 8 | 0.26% | 8 | 0.25% |
Gagnon et al. (2016) | 12 | 0.05% | 4 | 0.11% | 4 | 0.13% | 4 | 0.13% |
Harley & Pastore (2012) | 12 | 0.05% | 3 | 0.09% | 3 | 0.1% | 3 | 0.09% |
Hassemer et al. (2017) | 12 | 0.05% | 12 | 0.34% | 12 | 0.39% | 11 | 0.34% |
Oliveira Pellegrini & Forzza (2017) | 12 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
Urtubey et al. (2016) | 12 | 0.05% | 3 | 0.09% | 3 | 0.1% | 3 | 0.09% |
Veldkamp (1991) | 12 | 0.05% | 2 | 0.06% | 2 | 0.06% | 2 | 0.06% |
Véron et al. (2021) | 12 | 0.05% | 8 | 0.23% | 8 | 0.26% | 8 | 0.25% |
Zerega et al. (2005) | 12 | 0.05% | 4 | 0.11% | 4 | 0.13% | 4 | 0.13% |
Acevedo-Rodríguez (2012) | 11 | 0.05% | 7 | 0.2% | 7 | 0.23% | 7 | 0.22% |
Candolle (1824) | 11 | 0.05% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Dumortier (1827) | 11 | 0.05% | 4 | 0.11% | 3 | 0.1% | 3 | 0.09% |
Graham (2017) | 11 | 0.05% | 3 | 0.09% | 3 | 0.1% | 3 | 0.09% |
Granville & Gayot (2014) | 11 | 0.05% | 11 | 0.31% | 11 | 0.36% | 10 | 0.31% |
Lohmann & Taylor (2014) | 11 | 0.05% | 4 | 0.11% | 4 | 0.13% | 4 | 0.13% |
Marhold et al. (2016) | 11 | 0.05% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Nepal & Purintun (2021) | 11 | 0.05% | 2 | 0.06% | 2 | 0.06% | 2 | 0.06% |
Pejhanmehr (2022) | 11 | 0.05% | 11 | 0.31% | 11 | 0.36% | 11 | 0.34% |
Turner (2013) | 11 | 0.05% | 2 | 0.06% | 2 | 0.06% | 1 | 0.03% |
Bourzat & Monie (1977) | 10 | 0.04% | 6 | 0.17% | 6 | 0.19% | 5 | 0.16% |
Cremers & Hoff (1994) | 10 | 0.04% | 5 | 0.14% | 5 | 0.16% | 5 | 0.16% |
Heywood (1971) | 10 | 0.04% | 2 | 0.06% | 2 | 0.06% | 2 | 0.06% |
Hoff & Cremers (2005) | 10 | 0.04% | 9 | 0.26% | 7 | 0.23% | 7 | 0.22% |
Lamarck (1779) | 10 | 0.04% | 0 | 0% | 0 | 0% | 0 | 0% |
Manzitto‐Tripp & Daniel (2023) | 10 | 0.04% | 10 | 0.29% | 10 | 0.32% | 10 | 0.31% |
Moonlight et al. (2018) | 10 | 0.04% | 8 | 0.23% | 8 | 0.26% | 6 | 0.19% |
N'Yeurt & Payri (2004) | 10 | 0.04% | 7 | 0.2% | 7 | 0.23% | 7 | 0.22% |
N'Yeurt & Payri (2010) | 10 | 0.04% | 9 | 0.26% | 9 | 0.29% | 9 | 0.28% |
Pennington (1990) | 10 | 0.04% | 4 | 0.11% | 4 | 0.13% | 4 | 0.13% |
Armada & Barra (1992) | 9 | 0.04% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Blake (1914) | 9 | 0.04% | 2 | 0.06% | 1 | 0.03% | 1 | 0.03% |
Bourmaud (2003) | 9 | 0.04% | 6 | 0.17% | 6 | 0.19% | 5 | 0.16% |
Breton (2014) | 9 | 0.04% | 9 | 0.26% | 9 | 0.29% | 9 | 0.28% |
Croat & Delannay (2017) | 9 | 0.04% | 2 | 0.06% | 2 | 0.06% | 2 | 0.06% |
Gandoger (1884) | 9 | 0.04% | 0 | 0% | 0 | 0% | 0 | 0% |
Hoff (2021) | 9 | 0.04% | 0 | 0% | 0 | 0% | 0 | 0% |
Iamonico (2016) | 9 | 0.04% | 0 | 0% | 0 | 0% | 0 | 0% |
Jiménez-lópez et al. (2022) | 9 | 0.04% | 2 | 0.06% | 2 | 0.06% | 2 | 0.06% |
Murdock & Smith (2003) | 9 | 0.04% | 9 | 0.26% | 9 | 0.29% | 7 | 0.22% |
Persoon (1805) | 9 | 0.04% | 0 | 0% | 0 | 0% | 0 | 0% |
Pollard & Paton (2001) | 9 | 0.04% | 0 | 0% | 0 | 0% | 0 | 0% |
Reichenbach (1830-1832) | 9 | 0.04% | 2 | 0.06% | 2 | 0.06% | 2 | 0.06% |
Sachet (1962) | 9 | 0.04% | 8 | 0.23% | 8 | 0.26% | 8 | 0.25% |
. Alger, typographie A. Jourdan ; Paris, librairie F. Savy. 825 pp.">Battandier & Trabut (1890) | 8 | 0.03% | 1 | 0.03% | 0 | 0% | 1 | 0.03% |
Béreau (2017) | 8 | 0.03% | 4 | 0.11% | 4 | 0.13% | 4 | 0.13% |
Candolle (1815) | 8 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Cardiel et al. (2022) | 8 | 0.03% | 4 | 0.11% | 4 | 0.13% | 4 | 0.13% |
Dewarumez et al. (2011) | 8 | 0.03% | 6 | 0.17% | 5 | 0.16% | 6 | 0.19% |
Don (1831) | 8 | 0.03% | 2 | 0.06% | 2 | 0.06% | 2 | 0.06% |
Giacò et al. (2021) | 8 | 0.03% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Lamarck & Candolle (1805) | 8 | 0.03% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Lamarck (1789) | 8 | 0.03% | 3 | 0.09% | 3 | 0.1% | 3 | 0.09% |
Maddi (2010) | 8 | 0.03% | 6 | 0.17% | 6 | 0.19% | 6 | 0.19% |
Masters et al. (2023) | 8 | 0.03% | 7 | 0.2% | 7 | 0.23% | 7 | 0.22% |
Mattio et al. (2015) | 8 | 0.03% | 7 | 0.2% | 7 | 0.23% | 7 | 0.22% |
Moore (1933) | 8 | 0.03% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Patchell et al. (2014) | 8 | 0.03% | 6 | 0.17% | 6 | 0.19% | 6 | 0.19% |
Plowman et al. (1998) | 8 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Proćków & Drábková (2023) | 8 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Schuster et al. (2015) | 8 | 0.03% | 3 | 0.09% | 3 | 0.1% | 3 | 0.09% |
Skog & Feuillet (2008) | 8 | 0.03% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Staples (2007) | 8 | 0.03% | 4 | 0.11% | 4 | 0.13% | 4 | 0.13% |
Thellung (1912) | 8 | 0.03% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Wahlsteen & Tyler (2019) | 8 | 0.03% | 3 | 0.09% | 1 | 0.03% | 2 | 0.06% |
Allen et al. (2022) | 7 | 0.03% | 6 | 0.17% | 6 | 0.19% | 6 | 0.19% |
Appelhans et al. (2021) | 7 | 0.03% | 6 | 0.17% | 6 | 0.19% | 6 | 0.19% |
Aurore et al. (2014) | 7 | 0.03% | 3 | 0.09% | 3 | 0.1% | 3 | 0.09% |
Barthelat (2019) | 7 | 0.03% | 7 | 0.2% | 7 | 0.23% | 7 | 0.22% |
Boreau (1857) | 7 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Cariot & Saint-lager (1889) | 7 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Cecchi & Selvi (2015) | 7 | 0.03% | 2 | 0.06% | 1 | 0.03% | 1 | 0.03% |
Chemisquy et al. (2010) | 7 | 0.03% | 2 | 0.06% | 2 | 0.06% | 2 | 0.06% |
Crantz (1766) | 7 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Domina et al. (2021) | 7 | 0.03% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Dulac (1867) | 7 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Egan & Pan (2015) | 7 | 0.03% | 2 | 0.06% | 1 | 0.03% | 1 | 0.03% |
Evrard et al. (2004) | 7 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Graham (1988) | 7 | 0.03% | 6 | 0.17% | 6 | 0.19% | 6 | 0.19% |
Hassemer (2017) | 7 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Jeffrey (1980) | 7 | 0.03% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Jolinon (1985) | 7 | 0.03% | 4 | 0.11% | 4 | 0.13% | 3 | 0.09% |
Judd et al. (2018) | 7 | 0.03% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Mitchell (1997) | 7 | 0.03% | 5 | 0.14% | 5 | 0.16% | 5 | 0.16% |
Moraes et al. (2010) | 7 | 0.03% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Mori et al. (2002) | 7 | 0.03% | 6 | 0.17% | 6 | 0.19% | 6 | 0.19% |
Polhill (1990) | 7 | 0.03% | 7 | 0.2% | 7 | 0.23% | 6 | 0.19% |
Rico et al. (2006) | 7 | 0.03% | 3 | 0.09% | 3 | 0.1% | 3 | 0.09% |
Rouy (1909) | 7 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Sant (2022) | 7 | 0.03% | 6 | 0.17% | 6 | 0.19% | 5 | 0.16% |
Scatigna et al. (2022) | 7 | 0.03% | 7 | 0.2% | 7 | 0.23% | 7 | 0.22% |
Schenck (1905) | 7 | 0.03% | 7 | 0.2% | 7 | 0.23% | 5 | 0.16% |
Soto Arenas & Dressler (2010) | 7 | 0.03% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Rapport GIS "Lag-May" & Centre d'Océanologie de Marseille, pour le compte de DAF Mayotte, SPEM & FFEM. 126 pp.">Thomassin et al. (1999) | 7 | 0.03% | 4 | 0.11% | 4 | 0.13% | 4 | 0.13% |
Vorontsova (2022) | 7 | 0.03% | 3 | 0.09% | 3 | 0.1% | 3 | 0.09% |
Wagner et al. (2007) | 7 | 0.03% | 7 | 0.2% | 5 | 0.16% | 5 | 0.16% |
Yang et al. (2022) | 7 | 0.03% | 4 | 0.11% | 4 | 0.13% | 4 | 0.13% |
Zuloaga et al. (2018) | 7 | 0.03% | 7 | 0.2% | 7 | 0.23% | 6 | 0.19% |
Barrett et al. (2017) | 6 | 0.03% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Berg et al. (2006) | 6 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Bouman et al. (2020) | 6 | 0.03% | 1 | 0.03% | 1 | 0.03% | 0 | 0% |
Byng et al. (2016) | 6 | 0.03% | 6 | 0.17% | 6 | 0.19% | 6 | 0.19% |
Candolle (1845) | 6 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Colletta et al. (2020) | 6 | 0.03% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Dehgan (2012) | 6 | 0.03% | 5 | 0.14% | 5 | 0.16% | 5 | 0.16% |
Feldmann (2014) | 6 | 0.03% | 6 | 0.17% | 6 | 0.19% | 6 | 0.19% |
Fernandes (1984) | 6 | 0.03% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Feuillet (2009) | 6 | 0.03% | 6 | 0.17% | 6 | 0.19% | 5 | 0.16% |
Fiaschi et al. (2020) | 6 | 0.03% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Fourreau (1868) | 6 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Gladis & Hammer (2003) | 6 | 0.03% | 1 | 0.03% | 0 | 0% | 1 | 0.03% |
Knapp (2013) | 6 | 0.03% | 3 | 0.09% | 3 | 0.1% | 3 | 0.09% |
Maas et al. (1994) | 6 | 0.03% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Mennema (1989) | 6 | 0.03% | 2 | 0.06% | 2 | 0.06% | 2 | 0.06% |
N'Yeurt & Payri (2007) | 6 | 0.03% | 3 | 0.09% | 3 | 0.1% | 2 | 0.06% |
Oliveira Pellegrini et al. (2016) | 6 | 0.03% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Payri et al. (2009) | 6 | 0.03% | 6 | 0.17% | 6 | 0.19% | 5 | 0.16% |
Rivera et al. (2013) | 6 | 0.03% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Rouy (1913) | 6 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Sennen & Frère (1936) | 6 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Silva et al. (1996) | 6 | 0.03% | 5 | 0.14% | 5 | 0.16% | 5 | 0.16% |
Berton (2020) | 5 | 0.02% | 5 | 0.14% | 5 | 0.16% | 5 | 0.16% |
Bosser & Heine (1988) | 5 | 0.02% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Candolle (1830) | 5 | 0.02% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Christenhusz et al. (2018) | 5 | 0.02% | 2 | 0.06% | 2 | 0.06% | 2 | 0.06% |
Coode 1982 | 5 | 0.02% | 5 | 0.14% | 5 | 0.16% | 5 | 0.16% |
David & Thiebaut (2013) | 5 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Derrick et al. (1987) | 5 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Dorsey et al. (2013) | 5 | 0.02% | 5 | 0.14% | 5 | 0.16% | 5 | 0.16% |
Fici (2014) | 5 | 0.02% | 4 | 0.11% | 1 | 0.03% | 2 | 0.06% |
Gaertner (1791) | 5 | 0.02% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Gandoger (1875) | 5 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Gardner et al. (2021) | 5 | 0.02% | 4 | 0.11% | 4 | 0.13% | 4 | 0.13% |
González‐Elizondo & Peterson (1997) | 5 | 0.02% | 5 | 0.14% | 5 | 0.16% | 5 | 0.16% |
Grenier & Godron (1850) | 5 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Horn (1994) | 5 | 0.02% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Iles et al. (2017) | 5 | 0.02% | 5 | 0.14% | 5 | 0.16% | 5 | 0.16% |
Ito et al. (2017) | 5 | 0.02% | 5 | 0.14% | 5 | 0.16% | 3 | 0.09% |
Karremans et al. (2020) | 5 | 0.02% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Korotkova et al. (2017) | 5 | 0.02% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Lagourgue et al. (2022) | 5 | 0.02% | 5 | 0.14% | 5 | 0.16% | 4 | 0.13% |
Lamarck (1798) | 5 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Larridon et al. (2014) | 5 | 0.02% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Lemée (1956) | 5 | 0.02% | 2 | 0.06% | 2 | 0.06% | 2 | 0.06% |
Link (1821) | 5 | 0.02% | 3 | 0.09% | 2 | 0.06% | 2 | 0.06% |
Linnaeus (1762) | 5 | 0.02% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Lowry & Plunkett (2020) | 5 | 0.02% | 3 | 0.09% | 2 | 0.06% | 2 | 0.06% |
Maas (1985) | 5 | 0.02% | 2 | 0.06% | 2 | 0.06% | 2 | 0.06% |
Madhani et al. (2018) | 5 | 0.02% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Meyer & Lavergne (2004) | 5 | 0.02% | 5 | 0.14% | 5 | 0.16% | 5 | 0.16% |
Nicolson & Sivadasan (1981) | 5 | 0.02% | 4 | 0.11% | 4 | 0.13% | 4 | 0.13% |
Pennington & Biggs (2016) | 5 | 0.02% | 4 | 0.11% | 4 | 0.13% | 4 | 0.13% |
Persoon (1807) | 5 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Prévoteau (2012) | 5 | 0.02% | 5 | 0.14% | 4 | 0.13% | 5 | 0.16% |
Richter (1890) | 5 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Roalson & Hall (2017) | 5 | 0.02% | 3 | 0.09% | 2 | 0.06% | 2 | 0.06% |
Roalson et al. (2010) | 5 | 0.02% | 5 | 0.14% | 5 | 0.16% | 5 | 0.16% |
Schrire et al. (2009) | 5 | 0.02% | 5 | 0.14% | 5 | 0.16% | 5 | 0.16% |
Scopoli (1771) | 5 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Smith & Downs (1979) | 5 | 0.02% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Song et al. (2019) | 5 | 0.02% | 4 | 0.11% | 4 | 0.13% | 3 | 0.09% |
Souza et al. (2021) | 5 | 0.02% | 5 | 0.14% | 5 | 0.16% | 5 | 0.16% |
Sprague (1928) | 5 | 0.02% | 2 | 0.06% | 2 | 0.06% | 2 | 0.06% |
Suessenguth (1936) | 5 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Tassin et al. (2006) | 5 | 0.02% | 5 | 0.14% | 5 | 0.16% | 5 | 0.16% |
Thouvenot & Bardat (2010) | 5 | 0.02% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Tison et al. (2021) | 5 | 0.02% | 4 | 0.11% | 2 | 0.06% | 4 | 0.13% |
Verlaque et al. (2015) | 5 | 0.02% | 4 | 0.11% | 4 | 0.13% | 4 | 0.13% |
Anonyme (2023) | 4 | 0.02% | 2 | 0.06% | 0 | 0% | 2 | 0.06% |
Barneby (1987) | 4 | 0.02% | 2 | 0.06% | 2 | 0.06% | 2 | 0.06% |
Brottier et al. (2018) | 4 | 0.02% | 4 | 0.11% | 4 | 0.13% | 3 | 0.09% |
Candolle (1828) | 4 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Cayet et al. (2022) | 4 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Cecchi et al. (2014) | 4 | 0.02% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
CEVA (2011) | 4 | 0.02% | 3 | 0.09% | 3 | 0.1% | 3 | 0.09% |
Couhia & Fleurot (2016) | 4 | 0.02% | 4 | 0.11% | 4 | 0.13% | 4 | 0.13% |
Cowan & Lindeman (1989) | 4 | 0.02% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Cremers & Hoff (1998) | 4 | 0.02% | 2 | 0.06% | 2 | 0.06% | 1 | 0.03% |
Cuatrecasas (1964) | 4 | 0.02% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Davies, L. & Greene, S.W. (1976) | 4 | 0.02% | 4 | 0.11% | 4 | 0.13% | 4 | 0.13% |
Dumbardon-Martial & Delblond (2019) | 4 | 0.02% | 4 | 0.11% | 4 | 0.13% | 3 | 0.09% |
Ferrer-Gallego & Güemes (2020) | 4 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Feuillet (2014) | 4 | 0.02% | 3 | 0.09% | 3 | 0.1% | 3 | 0.09% |
Fiori (1925) | 4 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Fryxell (1988) | 4 | 0.02% | 3 | 0.09% | 3 | 0.1% | 3 | 0.09% |
Fryxell (2001) | 4 | 0.02% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Gandoger (1875) | 4 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Görts-van Rijn (2007) | 4 | 0.02% | 3 | 0.09% | 3 | 0.1% | 3 | 0.09% |
Green (1985) | 4 | 0.02% | 1 | 0.03% | 0 | 0% | 1 | 0.03% |
Green (1995) | 4 | 0.02% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Grenier & Godron (1856) | 4 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Grether (2000) | 4 | 0.02% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Hammel & Grayum (2011) | 4 | 0.02% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Hodgetts et al. (2020) | 4 | 0.02% | 4 | 0.11% | 4 | 0.13% | 4 | 0.13% |
Knoepffler et al. (1990) | 4 | 0.02% | 2 | 0.06% | 2 | 0.06% | 2 | 0.06% |
Koch (1837) | 4 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Koehne (1877) | 4 | 0.02% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Levin et al. (2022) | 4 | 0.02% | 4 | 0.11% | 4 | 0.13% | 4 | 0.13% |
Manns & Anderberg (2007) | 4 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
McDonald & Maslin (2000) | 4 | 0.02% | 2 | 0.06% | 2 | 0.06% | 2 | 0.06% |
Zornia". Webbia, 16(1): 1-141.">Mohlenbrock (1961) | 4 | 0.02% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Ocampo & Columbus (2012) | 4 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
O'Leary et al. (2016) | 4 | 0.02% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Pellegrini et al. (2018) | 4 | 0.02% | 2 | 0.06% | 2 | 0.06% | 2 | 0.06% |
Peraza et al. (2022) | 4 | 0.02% | 4 | 0.11% | 4 | 0.13% | 4 | 0.13% |
Philcox (1965) | 4 | 0.02% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Richard (1792) | 4 | 0.02% | 1 | 0.03% | 1 | 0.03% | 0 | 0% |
Rico et al. (2006) | 4 | 0.02% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Rohde et al. (2017) | 4 | 0.02% | 2 | 0.06% | 2 | 0.06% | 2 | 0.06% |
Rouy & Foucaud (1897) | 4 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Rouy (1899) | 4 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Rouy (1912) | 4 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Rudge (1805) | 4 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Sanders (2006) | 4 | 0.02% | 3 | 0.09% | 1 | 0.03% | 2 | 0.06% |
Schur (1866) | 4 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Scopoli (1771) | 4 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Tenore (1811-1815) | 4 | 0.02% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Thomson et al. (2022) | 4 | 0.02% | 4 | 0.11% | 4 | 0.13% | 4 | 0.13% |
Tippery et al. (2024) | 4 | 0.02% | 4 | 0.11% | 4 | 0.13% | 4 | 0.13% |
Uicn et al. (2019) | 4 | 0.02% | 3 | 0.09% | 3 | 0.1% | 3 | 0.09% |
Verdcourt (1970) | 4 | 0.02% | 4 | 0.11% | 1 | 0.03% | 3 | 0.09% |
Villars (1787) | 4 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Wood et al. (2015) | 4 | 0.02% | 2 | 0.06% | 2 | 0.06% | 2 | 0.06% |
Brugneaux (2012) | 3 | 0.01% | 2 | 0.06% | 2 | 0.06% | 2 | 0.06% |
Bubani & Penzig (1901) | 3 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Calviño et al. (2008) | 3 | 0.01% | 3 | 0.09% | 3 | 0.1% | 3 | 0.09% |
Candolle (1844) | 3 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Candolle (1846) | 3 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Carine & Robba (2010) | 3 | 0.01% | 1 | 0.03% | 0 | 0% | 1 | 0.03% |
Cochrane & Iltis (2014) | 3 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Coste (1937) | 3 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Crantz (1766) | 3 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Desjardins et al. (2015) | 3 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Dillenberger & Kadereit (2022) | 3 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Flora iberica | 3 | 0.01% | 1 | 0.03% | 0 | 0% | 1 | 0.03% |
Flora of North America (1993-) | 3 | 0.01% | 1 | 0.03% | 0 | 0% | 1 | 0.03% |
Forsskål (1775) | 3 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Friis (1993) | 3 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Fuentes-bazan et al. (2012) | 3 | 0.01% | 3 | 0.09% | 3 | 0.1% | 3 | 0.09% |
Giraldo-Cañas (2012) | 3 | 0.01% | 3 | 0.09% | 3 | 0.1% | 3 | 0.09% |
Goldblatt & Mabberley (2005) | 3 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Hill (1768) | 3 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Hoffmann (1791) | 3 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Iltis (1960) | 3 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Jordan & Fourreau (1866) | 3 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Klak et al. (2007) | 3 | 0.01% | 2 | 0.06% | 2 | 0.06% | 2 | 0.06% |
Kocyan et al. (2011) | 3 | 0.01% | 2 | 0.06% | 2 | 0.06% | 2 | 0.06% |
Kress et al. (2005) | 3 | 0.01% | 3 | 0.09% | 3 | 0.1% | 3 | 0.09% |
Laguna et al. (2013) | 3 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Lima et al. (2012) | 3 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Linnaeus (1763) | 3 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Lorence et al. (2007) | 3 | 0.01% | 3 | 0.09% | 3 | 0.1% | 3 | 0.09% |
Madison (1981) | 3 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Manns & Anderberg (2009) | 3 | 0.01% | 3 | 0.09% | 3 | 0.1% | 3 | 0.09% |
Mapaya (2017) | 3 | 0.01% | 3 | 0.09% | 3 | 0.1% | 2 | 0.06% |
Margońska (2019) | 3 | 0.01% | 3 | 0.09% | 3 | 0.1% | 3 | 0.09% |
Mazine et al. (2018) | 3 | 0.01% | 3 | 0.09% | 3 | 0.1% | 3 | 0.09% |
Meyer et al. (2008) | 3 | 0.01% | 3 | 0.09% | 3 | 0.1% | 3 | 0.09% |
Moraes (2012) | 3 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Moraes (2018) | 3 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Mosyakin & Clemants (2002) | 3 | 0.01% | 3 | 0.09% | 3 | 0.1% | 3 | 0.09% |
Ollitrault et al. (2020) | 3 | 0.01% | 2 | 0.06% | 0 | 0% | 2 | 0.06% |
Payri & N'yeurt (1997) | 3 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Questel (2023) | 3 | 0.01% | 3 | 0.09% | 3 | 0.1% | 2 | 0.06% |
Riina et al. (2013) | 3 | 0.01% | 3 | 0.09% | 3 | 0.1% | 3 | 0.09% |
Roemer & Schultes (1819) | 3 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Rouy & Foucaud (1896) | 3 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Rudd (1955) | 3 | 0.01% | 3 | 0.09% | 2 | 0.06% | 2 | 0.06% |
Ruiz-Sanchez et al. (2019) | 3 | 0.01% | 3 | 0.09% | 3 | 0.1% | 3 | 0.09% |
Sanders (2012) | 3 | 0.01% | 1 | 0.03% | 0 | 0% | 0 | 0% |
Sherff (1937) | 3 | 0.01% | 3 | 0.09% | 3 | 0.1% | 3 | 0.09% |
Small (2015) | 3 | 0.01% | 1 | 0.03% | 0 | 0% | 1 | 0.03% |
Thomassin et al. (1992) | 3 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Veldkamp (2014) | 3 | 0.01% | 2 | 0.06% | 2 | 0.06% | 2 | 0.06% |
Verdcourt (1987) | 3 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Vorontsova et al. (2023) | 3 | 0.01% | 2 | 0.06% | 2 | 0.06% | 2 | 0.06% |
Walter et al. (2015) | 3 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Willdenow (1799) | 3 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Willdenow (1799) | 3 | 0.01% | 2 | 0.06% | 2 | 0.06% | 2 | 0.06% |
Willette et al. (2014) | 3 | 0.01% | 3 | 0.09% | 3 | 0.1% | 3 | 0.09% |
Young (1971) | 3 | 0.01% | 3 | 0.09% | 3 | 0.1% | 3 | 0.09% |
Abbayes (1931) | 2 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Allorge-Boiteau (2015) | 2 | 0.01% | 2 | 0.06% | 2 | 0.06% | 1 | 0.03% |
Aubert de la Rüe (1932) | 2 | 0.01% | 2 | 0.06% | 2 | 0.06% | 1 | 0.03% |
Augros et al. (2018) | 2 | 0.01% | 2 | 0.06% | 1 | 0.03% | 1 | 0.03% |
Badré (2008b) | 2 | 0.01% | 2 | 0.06% | 1 | 0.03% | 1 | 0.03% |
Barker et al. (2012) | 2 | 0.01% | 2 | 0.06% | 2 | 0.06% | 2 | 0.06% |
Berry et al. (1999) | 2 | 0.01% | 2 | 0.06% | 1 | 0.03% | 1 | 0.03% |
Bikaeff (2002) | 2 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Boggan et al. (1997) | 2 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Borchsenius et al. (2012) | 2 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Boreau (1849) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Bossa‐Castro et al. (2024) | 2 | 0.01% | 2 | 0.06% | 2 | 0.06% | 2 | 0.06% |
Bosser & Heine (2000) | 2 | 0.01% | 2 | 0.06% | 2 | 0.06% | 2 | 0.06% |
Bosser & Heine (2000b) | 2 | 0.01% | 2 | 0.06% | 2 | 0.06% | 2 | 0.06% |
Boudrie & Bizot (2006) | 2 | 0.01% | 2 | 0.06% | 2 | 0.06% | 2 | 0.06% |
Bubani & Penzig (1902) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Candolle (1848) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Carine et al. (2003) | 2 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Carine et al. (2004) | 2 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Cecchi & Selvi (2015) | 2 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Chaix (1785) | 2 | 0.01% | 1 | 0.03% | 1 | 0.03% | 0 | 0% |
Chen et al. (2011) | 2 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Chew (1965) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Chukr & Giulietti (2008) | 2 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Coppens d'Eeckenbrugge & Govaerts (2015) | 2 | 0.01% | 2 | 0.06% | 1 | 0.03% | 1 | 0.03% |
Coste (1937) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Coulot & Rabaute (2016) | 2 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Cristóbal (1976) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Delgado-Salinas et al. (2011) | 2 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Don (1834) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Don (1838) | 2 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Donnell et al. (2012) | 2 | 0.01% | 2 | 0.06% | 2 | 0.06% | 2 | 0.06% |
Ferrer-gallego et al. (2019) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Filipowicz et al. (2014) | 2 | 0.01% | 2 | 0.06% | 2 | 0.06% | 2 | 0.06% |
Fortuna-Perez (2009) | 2 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Fourt et al. (2017) | 2 | 0.01% | 2 | 0.06% | 2 | 0.06% | 2 | 0.06% |
Freire et al. (2021) | 2 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Fried & Dumbardon‑Martial (2015) | 2 | 0.01% | 2 | 0.06% | 2 | 0.06% | 2 | 0.06% |
Garcia-Mendoza & Chiang (2003) | 2 | 0.01% | 1 | 0.03% | 1 | 0.03% | 0 | 0% |
Gaudin (1828) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Gentry (1980) | 2 | 0.01% | 2 | 0.06% | 2 | 0.06% | 2 | 0.06% |
Goldberg (1967) | 2 | 0.01% | 2 | 0.06% | 1 | 0.03% | 1 | 0.03% |
Grace et al. (2013) | 2 | 0.01% | 2 | 0.06% | 1 | 0.03% | 1 | 0.03% |
Graham et al. (2021) | 2 | 0.01% | 2 | 0.06% | 2 | 0.06% | 2 | 0.06% |
Grangaud (2010) | 2 | 0.01% | 2 | 0.06% | 1 | 0.03% | 1 | 0.03% |
Gray (1997) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Greene & Greene (1963) | 2 | 0.01% | 2 | 0.06% | 2 | 0.06% | 1 | 0.03% |
Grenier & Godron (1848) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Grose & Olmstead (2007) | 2 | 0.01% | 2 | 0.06% | 2 | 0.06% | 2 | 0.06% |
Große-veldmann (2017) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Gussone (1827) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Hipp et al. (2019) | 2 | 0.01% | 1 | 0.03% | 1 | 0.03% | 0 | 0% |
Hirschegger et al. (2010) | 2 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Hodge (1941) | 2 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Houlès et al. (2022) | 2 | 0.01% | 2 | 0.06% | 2 | 0.06% | 2 | 0.06% |
Hugonnot et al. (2017) | 2 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Husnot (1908) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Kaehler et al. (2019) | 2 | 0.01% | 2 | 0.06% | 2 | 0.06% | 2 | 0.06% |
Kirschner (1990) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Kirschner (2002) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Koch et al. (2013) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Lambinon & Worm (1993) | 2 | 0.01% | 2 | 0.06% | 0 | 0% | 2 | 0.06% |
Linné (1771) | 2 | 0.01% | 2 | 0.06% | 1 | 0.03% | 1 | 0.03% |
Lourteig (1985) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Majure et al. (2017) | 2 | 0.01% | 2 | 0.06% | 1 | 0.03% | 1 | 0.03% |
Mandák et al. (2005) | 2 | 0.01% | 2 | 0.06% | 0 | 0% | 2 | 0.06% |
Massé (1982) | 2 | 0.01% | 2 | 0.06% | 1 | 0.03% | 2 | 0.06% |
Mcclintock (1957) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Meyer (1819) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Michelangeli et al. (2013) | 2 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Montero et al. (2018) | 2 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Moran & Smith (1999) | 2 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Muhlenberg (1817) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Nelson-Smith et al. (2014) | 2 | 0.01% | 2 | 0.06% | 2 | 0.06% | 1 | 0.03% |
Pastore et al. (2023) | 2 | 0.01% | 2 | 0.06% | 2 | 0.06% | 2 | 0.06% |
Paton et al. (2018) | 2 | 0.01% | 2 | 0.06% | 2 | 0.06% | 2 | 0.06% |
Pereira et al. (2021) | 2 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Philcox (1965) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Plouguerné et al. (2007) | 2 | 0.01% | 2 | 0.06% | 2 | 0.06% | 2 | 0.06% |
Prance et al. (2007) | 2 | 0.01% | 2 | 0.06% | 2 | 0.06% | 2 | 0.06% |
Presl & Presl (1822) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Pteridophyte Phylogeny Group (2016) | 2 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Quere & Geslin (2016) | 2 | 0.01% | 2 | 0.06% | 2 | 0.06% | 2 | 0.06% |
Reed (1968) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Reveal et al. (1991) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Ros et al. (2013) | 2 | 0.01% | 2 | 0.06% | 2 | 0.06% | 2 | 0.06% |
Rousseau et al. (2017) | 2 | 0.01% | 2 | 0.06% | 2 | 0.06% | 2 | 0.06% |
Rouy & Foucaud (1893) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Rouy (1910) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Rudd (1965) | 2 | 0.01% | 2 | 0.06% | 2 | 0.06% | 2 | 0.06% |
Schaefer et al. (2012) | 2 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Schrank et al. (1789) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Schreber (1771) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Scott (1981) | 2 | 0.01% | 2 | 0.06% | 1 | 0.03% | 2 | 0.06% |
Seigler et al. (2014) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Sennen (1926) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Sherff (1937) | 2 | 0.01% | 2 | 0.06% | 2 | 0.06% | 1 | 0.03% |
Smith et al. (2020) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Snak et al. (2016) | 2 | 0.01% | 2 | 0.06% | 2 | 0.06% | 2 | 0.06% |
Soares Neto et al. (2018) | 2 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Sprengel (1826) | 2 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Stafleu & Cowan (1983) | 2 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Stefanovic et al. (2003) | 2 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Stepansky et al. (1999) | 2 | 0.01% | 2 | 0.06% | 1 | 0.03% | 0 | 0% |
Steudel (1821) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Sweet (1830) | 2 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Swenson et al. (2023) | 2 | 0.01% | 2 | 0.06% | 2 | 0.06% | 2 | 0.06% |
Teres (2006) | 2 | 0.01% | 2 | 0.06% | 2 | 0.06% | 2 | 0.06% |
Tippery & Sokolik (2020) | 2 | 0.01% | 2 | 0.06% | 2 | 0.06% | 2 | 0.06% |
Tippery et al. (2018) | 2 | 0.01% | 2 | 0.06% | 2 | 0.06% | 2 | 0.06% |
Tutin et al. (1972) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Véla et al. (2021) | 2 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Verlaque & Riouall (1989) | 2 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Verlaque (2002) | 2 | 0.01% | 2 | 0.06% | 2 | 0.06% | 2 | 0.06% |
Verwijs et al. (2019) | 2 | 0.01% | 2 | 0.06% | 2 | 0.06% | 2 | 0.06% |
Vorontsova et al. (2016) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Webster (1957) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Webster (1957) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Wells et al. (2021) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Willdenow (1798) | 2 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Willdenow (1800) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Witono & Kondo (2007) | 2 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Zakardjian et al. (2020) | 2 | 0.01% | 2 | 0.06% | 2 | 0.06% | 2 | 0.06% |
Zardini & Raven (1991) | 2 | 0.01% | 2 | 0.06% | 2 | 0.06% | 2 | 0.06% |
Zuntini et al. (2014) | 2 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Acta Plantarum (2007-) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Adeux et al. (2022) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Akhani et al. (2014) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Alencar et al. (2021) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Allem (2001) | 1 | 0% | 1 | 0.03% | 0 | 0% | 1 | 0.03% |
Allioni (1785) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Allioni (1785) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Almeida et al. (2016) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Alvarado-Cárdenas & Ochoterena (2007) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Applequist (2019) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Ascherson & Graebner (1910) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Austin & Huáman (1996) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Bacchetta et al. (2011) | 1 | 0% | 1 | 0.03% | 0 | 0% | 1 | 0.03% |
Badré & Lorence (2008) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Baker (1867) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Bárbara et al. (2012) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Bean (1919) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Berg (1972) | 1 | 0% | 1 | 0.03% | 0 | 0% | 1 | 0.03% |
Bernardi (2000) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Berry et al. (1997) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Berry et al. (2004) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Bijmoer et al. (2021) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Blake (1924) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Boissier (1845) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Bolòs & Vigo (1974) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Bonnier (1912) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Boreau (1853) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Bovini (2010) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Brenan (1994) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Brown et al. (2009) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Bryson et al. (1997) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Bubani & Penzig (1900) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Cafferty et al. (2000) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Candolle (1852) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Chauvel et al. (2006) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Chevalier (1936) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Cho et al. (2005) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Choo et al. (2020) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Cohen & Ackerman (2009) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Collectif (1823) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Colli-Silva et al. (2024) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Coulot et al. (2021) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Couté, Noël & Perrette (2017) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Craig (1918) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Cremers & Boudrie (2006) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Cremers & Boudrie (2007) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 0 | 0% |
Cremers & Hoff (1995) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Cremers & Hoff (2000) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Daniel & Mcdade (2014) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Danin et al. (2012) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Dauphin & Matile-Ferrero (2003) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Delaunay (2015) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Delnatte et al. (2021) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Delprete (2015) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Denham (2005) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Dentant et al. (2012) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Descoings (2011) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Desfontaines (1798) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Desportes (1838) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Diaz & Cuzange (2009) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Don (1832) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Duhamel & Monceau (1806) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Dumortier (1865) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Eaton (1922) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Ebihara et al. (2017) | 1 | 0% | 1 | 0.03% | 0 | 0% | 1 | 0.03% |
Edgar (1995) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Ehrhart (1780) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Emil et al. (2016) | 1 | 0% | 1 | 0.03% | 0 | 0% | 1 | 0.03% |
Engelmann (1873) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Eppo (2011) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Eppo (2011) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Eppo (2013) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Eriksson et al. (1998) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Espírito Santo et al. (2019) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Ezcurra & Daniel (2007) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Fedde (1939) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Ferrer-Gallego & Boisset (2015) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Ferrer-gallego & Laguna (2018) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Feuillet (2010) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Filipowicz & Renner (2012) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Fort et al. (2020) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Fosberg & Sachet (1975) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Fosberg (1937) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Foster (1962) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Fournier (1928) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Fried (2011) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Gaertner (1788) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Gandoger (1876) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Gaudefroy & Mouillefarine (1871) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Geir (2018) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Gmelin (1791) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Gouan (1773) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Goulletquer et al. (2002) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Gregório et al. (2023) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 0 | 0% |
Grenand et al. (2004) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Greuter & Raus (1989) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Greuter (1995) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Grisebach (1864) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Grisebach (1866) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Grolle & Long (2000) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Guillaumin (1936) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Guinet (1936) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Gurgel et al. (2018) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Gussone (1843) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Gustafsson (1998) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Hartman (1820) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Haworth (1803) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Haynes & Holm-Nielsen (2009) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Hébrard (1970) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Hemsley (1885) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Heylen et al. (2021) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Hill et al. (2006) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Hillig (2005) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Hily et al. (2010) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Hind et al. (1993) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Hodgetts & Lockhart (2020) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Hoehne (1944) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Hollowell et al. (2001) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Holub (1993) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Host (1809) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Huet (1889) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Huygh et al. (2010) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Iamonico et al. (2015) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Iltis & Cochrane (2007) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Irwin & Barneby (1982) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Jacobs (2001) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Jansen (1985) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Jordan & Fourreau (1868) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Jordan & Fourreau (1869-1903) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Kaastra (1982) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Karsch (1853) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Kerguélen & Bock (2011) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Kirschner & Cheek (2000) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 0 | 0% |
Klein & Verlaque (2005) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Klein & Verlaque (2008) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Klonowska et al. (2012) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 0 | 0% |
Klonowska et al. (2020) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 0 | 0% |
Koch (1844) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Kok (2007) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Krebs et al. (2004) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Laguna (2006) | 1 | 0% | 1 | 0.03% | 0 | 0% | 1 | 0.03% |
Lamarck & Candolle (1805) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Lamarck & Candolle (1805) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Lamarck (1778) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Lamarck (1786) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Lamarck (1799) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Landrum (1986) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Lansdown (2022) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Lapeyrouse (1813) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Larregle et al. (2014) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Le Duff & Gall (2015) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Ledebour (1851) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Lehtonen et al. (2016) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 0 | 0% |
Lejeune & Courtois (1831) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Les & Crawford (1999) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Levring (1944) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Li et al. (2021) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Lieutard (1893) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 0 | 0% |
Lima et al. (2014) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Linnaeus (1767) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Linnaeus (1771) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Linné (1766) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Liu et al. (2004) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 0 | 0% |
Lizé (2018) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Lizé (2018) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Lizé (2022) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Lowden (1986) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Mabberley (2017) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 0 | 0% |
Macallister & Marshall (2017) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Maddi & Brizard (2010) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Maddi (2014) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Manning (1960) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Marais (1990) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 0 | 0% |
Marais (1997) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Maréchal et al. (2013) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Maya-Lastra & Steinmann (2018) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Mestier et al. (2022) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Meyer (1836) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Meyer (2017) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Miégeville (1863) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Mineur et al. (2012) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Moraes et al. (2013) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Moraes et al. (2014) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Catalogue of Brazilian plants collected by Prince Maximilian of Wied". Plant Ecology and Evolution, 149(3): 308-315.">Moraes et al. (2016) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Mori et al. (2002) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Mosyakin & Iamonico (2018) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Moura-Júnior et al. (2016) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Muhlenberg (1813) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Munir (1992) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Murray (1784) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Mutel (1834) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Nesom (2022) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Niebler, F. et al. (2021) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Nitta et al. (2011) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Ochyra et al. (2008) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Oldeman (1968) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Oliveira et al. (2019) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Ortuño & Borsch (2020) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
O’Shea (2006) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Paradis & Miniconi (2011) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Pax (2018) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Peck et al. (2014) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Peichoto (2010) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Pelletier (1998) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Petelczyc et al. (2006) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 0 | 0% |
Pócs (2022) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Portal & Tort (2014) | 1 | 0% | 1 | 0.03% | 0 | 0% | 1 | 0.03% |
Prelli & Boudrie (2021) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Provan et al. (2008) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 0 | 0% |
Pruski & Robinson (2018) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Pulle (1906) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Questel (2017) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Rabasse et al. (2005) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Rabaute & Coulot (2015) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Rahiminejad & Gornall (2004) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Raimondo (2011) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Rankin Rodríguez & Greuter (2001) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Reichardt (1871) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Ridley (2022) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Rivière (2003) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Robyns (1963) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Rojas-andrés & Martínez-ortega (2016) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Rome & Coppens d'Eeckenbrugge (2016) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Rouy & Camus (1901) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Sagot (1881) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Sambin & Chiron (2017) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Sant (2002) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Sant (2002) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Scopoli (1786) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Scott (1994a) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Sellier et al. (2016) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 0 | 0% |
Selvi et al. (2009) | 1 | 0% | 1 | 0.03% | 0 | 0% | 1 | 0.03% |
Sennen (1928) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Shen & Gao (2020) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Shrestha et al. (2003) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Shrestha et al. (2005) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Sibthorp & Smith (1806-1809) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Sjøtun et al. (2008) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Soares et al. (2021) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Soderstrom & Zuloaga (1989) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Soubeyran (2008) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Specht & Stevenson (2006) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Sprengel (1825) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Staples et al. (2012) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Stefanovic & Dickinson (2007) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Steudel (1841) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Stevenson (1991) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 0 | 0% |
Sweet (1826) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Tamboli et al. (2016) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Tareau (2015) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Terrin et al. (2014) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Thibaut et al. (2022) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Thiébaut (2007) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Timaná et al. (2019) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Tison & de Foucault (2015) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Tison et al. (2014) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Toussaint et al. (2013) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Tripp et al. (2013) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Tropicos (1980-) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Tumino (2010) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Turner & Veldkamp (2009) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Türpe (1984) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Uotila et al. (2021) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Vanhöffen (1912) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 0 | 0% |
Vaquer (1988) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Veldkamp (2002) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 0 | 0% |
Verloove & Lambinon (2011) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Villanueva-almanza et al. (2021) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Villars (1779) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Villars (1789) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Vollmann (1904) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Waldstein & Kitaibel (1802) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Webster (1957) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Werkhoven (1986) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Whitlock & Hale (2011) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Whittier (1976) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Wiersema & Dahlberg (2007) | 1 | 0% | 1 | 0.03% | 0 | 0% | 1 | 0.03% |
Wiggers (1780) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Willdenow (1797) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Wilson (2017) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Wilson (2017) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Wilson (2017) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Wilson (2022) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Witono et al. (2002) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Wood & Scotland (2017) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Wörz (2005) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Yahaya et al. (2016) | 1 | 0% | 1 | 0.03% | 0 | 0% | 1 | 0.03% |
Yamada (1928) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Zeng (2009) | 1 | 0% | 0 | 0% | 0 | 0% | 0 | 0% |
Zhang et al. (2008) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Ziffer-Berger et al. (2015) | 1 | 0% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |