Espèces végétales introduites en métropole
Plantes introduites au sens large en France métropolitaine, c'est-à-dire introduites naturalisées (I), invasives (J), introduites non naturalisées (M) ou introduites éteintes (Y)
630 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
Référence | Total | Valides | Espèces | Taxons terminaux | ||||
---|---|---|---|---|---|---|---|---|
nb | % | nb | % | nb | % | nb | % | |
Tison et al. (2014) | 5697 | 33.76% | 4044 | 103.03% | 3724 | 109.14% | 3655 | 102.12% |
Fournet (2002) | 1256 | 7.44% | 1018 | 25.94% | 1014 | 29.72% | 911 | 25.45% |
Hequet & Le Corre (2010) | 369 | 2.19% | 290 | 7.39% | 288 | 8.44% | 243 | 6.79% |
Hequet et al. (2009) | 369 | 2.19% | 290 | 7.39% | 288 | 8.44% | 243 | 6.79% |
MacKee (1994) | 363 | 2.15% | 284 | 7.24% | 282 | 8.26% | 238 | 6.65% |
Funk et al. (2007) | 335 | 1.99% | 125 | 3.18% | 123 | 3.6% | 114 | 3.19% |
Linnaeus (1753) | 177 | 1.05% | 125 | 3.18% | 111 | 3.25% | 103 | 2.88% |
Linnaeus (1753) | 163 | 0.97% | 99 | 2.52% | 94 | 2.75% | 85 | 2.37% |
Cabioc'h & Floc'h (2014) | 121 | 0.72% | 92 | 2.34% | 92 | 2.7% | 89 | 2.49% |
Fourdrigniez & Meyer (2008) | 118 | 0.7% | 88 | 2.24% | 86 | 2.52% | 77 | 2.15% |
Dickoré & Kasperek (2010) | 110 | 0.65% | 36 | 0.92% | 36 | 1.06% | 36 | 1.01% |
Wiersema et al. (2018) | 83 | 0.49% | 36 | 0.92% | 35 | 1.03% | 27 | 0.75% |
Anonyme (2014) | 82 | 0.49% | 71 | 1.81% | 71 | 2.08% | 58 | 1.62% |
Munzinger et al. (2016) | 82 | 0.49% | 24 | 0.61% | 23 | 0.67% | 22 | 0.61% |
Delnatte & Meyer (2012) | 80 | 0.47% | 68 | 1.73% | 67 | 1.96% | 62 | 1.73% |
Costea et al. (2001) | 73 | 0.43% | 9 | 0.23% | 7 | 0.21% | 8 | 0.22% |
Miller (1768) | 67 | 0.4% | 24 | 0.61% | 23 | 0.67% | 21 | 0.59% |
Nesom (2009) | 65 | 0.39% | 3 | 0.08% | 3 | 0.09% | 2 | 0.06% |
Salisbury (1796) | 63 | 0.37% | 0 | 0% | 0 | 0% | 0 | 0% |
Acevedo-Rodríguez & Strong (2012) | 60 | 0.36% | 38 | 0.97% | 38 | 1.11% | 32 | 0.89% |
Flora of China (2015-) | 57 | 0.34% | 13 | 0.33% | 7 | 0.21% | 13 | 0.36% |
Goulletquer (2016) | 53 | 0.31% | 45 | 1.15% | 45 | 1.32% | 42 | 1.17% |
Morat et al. (2012) | 48 | 0.28% | 24 | 0.61% | 24 | 0.7% | 21 | 0.59% |
Muller et al. (2004) | 45 | 0.27% | 38 | 0.97% | 36 | 1.06% | 34 | 0.95% |
Burel et al. (2019) | 43 | 0.25% | 41 | 1.04% | 41 | 1.2% | 39 | 1.09% |
Fici (2014) | 43 | 0.25% | 8 | 0.2% | 1 | 0.03% | 5 | 0.14% |
Euro+Med (2006) | 42 | 0.25% | 2 | 0.05% | 1 | 0.03% | 2 | 0.06% |
Aublet (1775) | 41 | 0.24% | 27 | 0.69% | 26 | 0.76% | 25 | 0.7% |
Moench (1794) | 38 | 0.23% | 3 | 0.08% | 3 | 0.09% | 3 | 0.08% |
Florence (2004) | 36 | 0.21% | 32 | 0.82% | 32 | 0.94% | 30 | 0.84% |
Bayón (2015) | 34 | 0.2% | 10 | 0.25% | 6 | 0.18% | 6 | 0.17% |
Fonseca et al. (2017) | 33 | 0.2% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Wilmot-Dear & Friis (1996) | 32 | 0.19% | 5 | 0.13% | 5 | 0.15% | 5 | 0.14% |
Léotard & Chaline (2013) | 31 | 0.18% | 28 | 0.71% | 28 | 0.82% | 26 | 0.73% |
Boullet et al. (2018) | 30 | 0.18% | 28 | 0.71% | 27 | 0.79% | 25 | 0.7% |
Kuntze (1891) | 30 | 0.18% | 5 | 0.13% | 5 | 0.15% | 4 | 0.11% |
Morat & Veillon (1985) | 30 | 0.18% | 28 | 0.71% | 27 | 0.79% | 26 | 0.73% |
Fournier (1934-1940) | 29 | 0.17% | 1 | 0.03% | 0 | 0% | 1 | 0.03% |
Rignault & Chevallier (2017) | 28 | 0.17% | 23 | 0.59% | 23 | 0.67% | 23 | 0.64% |
Thellung (1912) | 28 | 0.17% | 15 | 0.38% | 12 | 0.35% | 15 | 0.42% |
Zuloaga (2022) | 27 | 0.16% | 2 | 0.05% | 2 | 0.06% | 1 | 0.03% |
Linnaeus (1759) | 26 | 0.15% | 12 | 0.31% | 12 | 0.35% | 12 | 0.34% |
Lavergne (2011) | 25 | 0.15% | 20 | 0.51% | 18 | 0.53% | 17 | 0.47% |
Baaijens & Veldkamp (1991) | 23 | 0.14% | 2 | 0.05% | 2 | 0.06% | 2 | 0.06% |
Moench (1794) | 23 | 0.14% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Candolle (1849) | 21 | 0.12% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Chew (1969) | 21 | 0.12% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Lemée (1955) | 21 | 0.12% | 10 | 0.25% | 10 | 0.29% | 10 | 0.28% |
Nyman (1882) | 21 | 0.12% | 0 | 0% | 0 | 0% | 0 | 0% |
André et al. (2020) | 19 | 0.11% | 19 | 0.48% | 19 | 0.56% | 19 | 0.53% |
Anonyme (2023) | 19 | 0.11% | 4 | 0.1% | 0 | 0% | 4 | 0.11% |
Lamarck (1783) | 19 | 0.11% | 6 | 0.15% | 5 | 0.15% | 5 | 0.14% |
Cambecèdes et al. (2012) | 18 | 0.11% | 16 | 0.41% | 16 | 0.47% | 12 | 0.34% |
Delnatte & Wynne (2016) | 18 | 0.11% | 17 | 0.43% | 17 | 0.5% | 17 | 0.47% |
Dillenberger & Kadereit (2014) | 18 | 0.11% | 4 | 0.1% | 3 | 0.09% | 3 | 0.08% |
Gargominy et al. (1996) | 17 | 0.1% | 11 | 0.28% | 11 | 0.32% | 10 | 0.28% |
Payri (2007) | 16 | 0.09% | 12 | 0.31% | 12 | 0.35% | 11 | 0.31% |
Fischer et al. (2013) | 15 | 0.09% | 2 | 0.05% | 2 | 0.06% | 2 | 0.06% |
Rojas-Andrés et al. (2016) | 15 | 0.09% | 4 | 0.1% | 2 | 0.06% | 2 | 0.06% |
Vroman (1968) | 15 | 0.09% | 11 | 0.28% | 11 | 0.32% | 10 | 0.28% |
Yang et al. (2012) | 15 | 0.09% | 15 | 0.38% | 15 | 0.44% | 14 | 0.39% |
Calviño et al. (2008) | 14 | 0.08% | 14 | 0.36% | 14 | 0.41% | 13 | 0.36% |
Candolle (1824) | 14 | 0.08% | 4 | 0.1% | 4 | 0.12% | 4 | 0.11% |
Godron (1853) | 14 | 0.08% | 5 | 0.13% | 5 | 0.15% | 5 | 0.14% |
Rodríguez-Prieto et al. (1999) | 14 | 0.08% | 13 | 0.33% | 13 | 0.38% | 13 | 0.36% |
Meyer et al. (2006) | 13 | 0.08% | 7 | 0.18% | 6 | 0.18% | 6 | 0.17% |
Verlaque (2001) | 13 | 0.08% | 11 | 0.28% | 10 | 0.29% | 10 | 0.28% |
Wood et al. (2020) | 13 | 0.08% | 6 | 0.15% | 6 | 0.18% | 6 | 0.17% |
Arcangeli (1882) | 12 | 0.07% | 1 | 0.03% | 0 | 0% | 1 | 0.03% |
Cremers & Hoff (1998) | 12 | 0.07% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Gardner et al. (2021) | 12 | 0.07% | 8 | 0.2% | 8 | 0.23% | 8 | 0.22% |
Giacò et al. (2021) | 12 | 0.07% | 2 | 0.05% | 2 | 0.06% | 2 | 0.06% |
Lemée (1952) | 12 | 0.07% | 7 | 0.18% | 7 | 0.21% | 7 | 0.2% |
Lowe et al. (2007) | 12 | 0.07% | 9 | 0.23% | 8 | 0.23% | 6 | 0.17% |
Oliveira Pellegrini & Forzza (2017) | 12 | 0.07% | 0 | 0% | 0 | 0% | 0 | 0% |
Frenot et al. (2001) | 11 | 0.07% | 9 | 0.23% | 9 | 0.26% | 5 | 0.14% |
Lamarck (1779) | 11 | 0.07% | 0 | 0% | 0 | 0% | 0 | 0% |
Lamarck (1789) | 11 | 0.07% | 7 | 0.18% | 7 | 0.21% | 5 | 0.14% |
Linnaeus (1762) | 11 | 0.07% | 7 | 0.18% | 6 | 0.18% | 6 | 0.17% |
Marhold et al. (2016) | 11 | 0.07% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Nepal & Purintun (2021) | 11 | 0.07% | 2 | 0.05% | 2 | 0.06% | 2 | 0.06% |
Urtubey et al. (2016) | 11 | 0.07% | 2 | 0.05% | 2 | 0.06% | 2 | 0.06% |
Bonnier & Layens (1894) | 10 | 0.06% | 0 | 0% | 0 | 0% | 0 | 0% |
Don (1831) | 10 | 0.06% | 2 | 0.05% | 2 | 0.06% | 2 | 0.06% |
Etcheberry & Abraham (2009) | 10 | 0.06% | 6 | 0.15% | 6 | 0.18% | 3 | 0.08% |
Florence (1997) | 10 | 0.06% | 6 | 0.15% | 6 | 0.18% | 6 | 0.17% |
Gallo (2020) | 10 | 0.06% | 1 | 0.03% | 0 | 0% | 1 | 0.03% |
Heywood (1971) | 10 | 0.06% | 2 | 0.05% | 2 | 0.06% | 2 | 0.06% |
Jolinon (1987) | 10 | 0.06% | 9 | 0.23% | 9 | 0.26% | 3 | 0.08% |
Lemée (1953) | 10 | 0.06% | 6 | 0.15% | 6 | 0.18% | 6 | 0.17% |
N'Yeurt & Payri (2004) | 10 | 0.06% | 7 | 0.18% | 7 | 0.21% | 7 | 0.2% |
N'Yeurt & Payri (2010) | 10 | 0.06% | 9 | 0.23% | 9 | 0.26% | 9 | 0.25% |
Peterson et al. (2014) | 10 | 0.06% | 10 | 0.25% | 10 | 0.29% | 10 | 0.28% |
Rouy (1909) | 10 | 0.06% | 0 | 0% | 0 | 0% | 0 | 0% |
Al-Saghir & Porter (2012) | 9 | 0.05% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Appelhans et al. (2021) | 9 | 0.05% | 8 | 0.2% | 8 | 0.23% | 8 | 0.22% |
Armada & Barra (1992) | 9 | 0.05% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Barker et al. (2012) | 9 | 0.05% | 5 | 0.13% | 4 | 0.12% | 4 | 0.11% |
Blake (1914) | 9 | 0.05% | 2 | 0.05% | 1 | 0.03% | 1 | 0.03% |
Bourmaud (2003) | 9 | 0.05% | 6 | 0.15% | 6 | 0.18% | 5 | 0.14% |
Flora of North America (1993-) | 9 | 0.05% | 3 | 0.08% | 1 | 0.03% | 3 | 0.08% |
Gladis & Hammer (2003) | 9 | 0.05% | 3 | 0.08% | 0 | 0% | 3 | 0.08% |
Iamonico (2016) | 9 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
Lamarck (1798) | 9 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
Toutain (1989) | 9 | 0.05% | 6 | 0.15% | 6 | 0.18% | 5 | 0.14% |
Béguinot (2012) | 8 | 0.05% | 6 | 0.15% | 6 | 0.18% | 1 | 0.03% |
Béreau (2017) | 8 | 0.05% | 3 | 0.08% | 3 | 0.09% | 3 | 0.08% |
Bubani & Penzig (1897) | 8 | 0.05% | 0 | 0% | 0 | 0% | 0 | 0% |
Candolle (1830) | 8 | 0.05% | 3 | 0.08% | 3 | 0.09% | 3 | 0.08% |
Dewarumez et al. (2011) | 8 | 0.05% | 6 | 0.15% | 5 | 0.15% | 6 | 0.17% |
Drew et al. (2017) | 8 | 0.05% | 4 | 0.1% | 4 | 0.12% | 4 | 0.11% |
Hoff et al. (2016) | 8 | 0.05% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Hovenkamp & Miyamoto (2005) | 8 | 0.05% | 2 | 0.05% | 1 | 0.03% | 1 | 0.03% |
Mattio et al. (2015) | 8 | 0.05% | 7 | 0.18% | 7 | 0.21% | 7 | 0.2% |
Molino et al. (2009) | 8 | 0.05% | 5 | 0.13% | 5 | 0.15% | 5 | 0.14% |
Wahlsteen & Tyler (2019) | 8 | 0.05% | 3 | 0.08% | 1 | 0.03% | 2 | 0.06% |
. Alger, typographie A. Jourdan ; Paris, librairie F. Savy. 825 pp.">Battandier & Trabut (1890) | 7 | 0.04% | 1 | 0.03% | 0 | 0% | 1 | 0.03% |
Bell (1982) | 7 | 0.04% | 5 | 0.13% | 5 | 0.15% | 0 | 0% |
Cecchi & Selvi (2015) | 7 | 0.04% | 2 | 0.05% | 1 | 0.03% | 1 | 0.03% |
Christenhusz (2002) | 7 | 0.04% | 5 | 0.13% | 5 | 0.15% | 4 | 0.11% |
Cremers & Hoff (1994) | 7 | 0.04% | 3 | 0.08% | 3 | 0.09% | 3 | 0.08% |
Domina et al. (2021) | 7 | 0.04% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Evrard et al. (2004) | 7 | 0.04% | 0 | 0% | 0 | 0% | 0 | 0% |
Ferlay et al. (2023) | 7 | 0.04% | 7 | 0.18% | 7 | 0.21% | 7 | 0.2% |
Flora iberica | 7 | 0.04% | 1 | 0.03% | 0 | 0% | 1 | 0.03% |
Hassemer (2017) | 7 | 0.04% | 0 | 0% | 0 | 0% | 0 | 0% |
Hoff & Cremers (2005) | 7 | 0.04% | 7 | 0.18% | 4 | 0.12% | 6 | 0.17% |
Host (1831) | 7 | 0.04% | 0 | 0% | 0 | 0% | 0 | 0% |
Hullé et al. (2003) | 7 | 0.04% | 5 | 0.13% | 5 | 0.15% | 2 | 0.06% |
Lamarck (1779) | 7 | 0.04% | 0 | 0% | 0 | 0% | 0 | 0% |
Link (1821) | 7 | 0.04% | 5 | 0.13% | 4 | 0.12% | 4 | 0.11% |
Persoon (1805) | 7 | 0.04% | 0 | 0% | 0 | 0% | 0 | 0% |
Persoon (1807) | 7 | 0.04% | 1 | 0.03% | 0 | 0% | 1 | 0.03% |
Scopoli (1771) | 7 | 0.04% | 2 | 0.05% | 1 | 0.03% | 1 | 0.03% |
Tenore (1811-1815) | 7 | 0.04% | 4 | 0.1% | 3 | 0.09% | 3 | 0.08% |
Rapport GIS "Lag-May" & Centre d'Océanologie de Marseille, pour le compte de DAF Mayotte, SPEM & FFEM. 126 pp.">Thomassin et al. (1999) | 7 | 0.04% | 4 | 0.1% | 4 | 0.12% | 4 | 0.11% |
Tison et al. (2021) | 7 | 0.04% | 5 | 0.13% | 2 | 0.06% | 5 | 0.14% |
Zuloaga et al. (2018) | 7 | 0.04% | 7 | 0.18% | 7 | 0.21% | 4 | 0.11% |
Berg et al. (2006) | 6 | 0.04% | 0 | 0% | 0 | 0% | 0 | 0% |
Boggan et al. (1992) | 6 | 0.04% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Candolle (1828) | 6 | 0.04% | 4 | 0.1% | 4 | 0.12% | 4 | 0.11% |
Candolle (1845) | 6 | 0.04% | 0 | 0% | 0 | 0% | 0 | 0% |
Candolle (1846) | 6 | 0.04% | 2 | 0.05% | 2 | 0.06% | 2 | 0.06% |
Christenhusz et al. (2019) | 6 | 0.04% | 1 | 0.03% | 1 | 0.03% | 0 | 0% |
Desfontaines (1798) | 6 | 0.04% | 2 | 0.05% | 2 | 0.06% | 2 | 0.06% |
Desfontaines (1798) | 6 | 0.04% | 5 | 0.13% | 5 | 0.15% | 5 | 0.14% |
Gray (1821) | 6 | 0.04% | 0 | 0% | 0 | 0% | 0 | 0% |
Hassemer et al. (2017) | 6 | 0.04% | 6 | 0.15% | 6 | 0.18% | 5 | 0.14% |
Lamarck (1786) | 6 | 0.04% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Medina et al. (2015) | 6 | 0.04% | 2 | 0.05% | 0 | 0% | 2 | 0.06% |
Mosyakin & Clemants (2002) | 6 | 0.04% | 6 | 0.15% | 6 | 0.18% | 6 | 0.17% |
Mosyakin (1996) | 6 | 0.04% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
N'Yeurt & Payri (2007) | 6 | 0.04% | 3 | 0.08% | 3 | 0.09% | 2 | 0.06% |
Ollitrault et al. (2020) | 6 | 0.04% | 5 | 0.13% | 1 | 0.03% | 5 | 0.14% |
Payri et al. (2009) | 6 | 0.04% | 6 | 0.15% | 6 | 0.18% | 5 | 0.14% |
Prelli & Boudrie (2021) | 6 | 0.04% | 6 | 0.15% | 5 | 0.15% | 6 | 0.17% |
Riina et al. (2013) | 6 | 0.04% | 6 | 0.15% | 6 | 0.18% | 6 | 0.17% |
Rivera et al. (2013) | 6 | 0.04% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Rouy (1912) | 6 | 0.04% | 0 | 0% | 0 | 0% | 0 | 0% |
Sachet (1962) | 6 | 0.04% | 5 | 0.13% | 5 | 0.15% | 5 | 0.14% |
Silva et al. (1996) | 6 | 0.04% | 5 | 0.13% | 5 | 0.15% | 5 | 0.14% |
Small (2015) | 6 | 0.04% | 2 | 0.05% | 0 | 0% | 2 | 0.06% |
Anonyme (1938) | 5 | 0.03% | 2 | 0.05% | 2 | 0.06% | 2 | 0.06% |
Berg (1992) | 5 | 0.03% | 2 | 0.05% | 2 | 0.06% | 2 | 0.06% |
Carcaillet (1993) | 5 | 0.03% | 5 | 0.13% | 5 | 0.15% | 1 | 0.03% |
Crantz (1766) | 5 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Dakskobler et al. (2011) | 5 | 0.03% | 2 | 0.05% | 2 | 0.06% | 2 | 0.06% |
Fiori (1925) | 5 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Forsskål (1775) | 5 | 0.03% | 2 | 0.05% | 2 | 0.06% | 2 | 0.06% |
Fuentes-bazan et al. (2012) | 5 | 0.03% | 3 | 0.08% | 3 | 0.09% | 3 | 0.08% |
Gaertner (1788) | 5 | 0.03% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Horn (1994) | 5 | 0.03% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Knapp (2013) | 5 | 0.03% | 2 | 0.05% | 2 | 0.06% | 2 | 0.06% |
Lehtonen et al. (2016) | 5 | 0.03% | 5 | 0.13% | 5 | 0.15% | 3 | 0.08% |
Mosyakin & Walter (2018) | 5 | 0.03% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Reichenbach (1830-1832) | 5 | 0.03% | 3 | 0.08% | 3 | 0.09% | 3 | 0.08% |
Schneider (1912) | 5 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Sibthorp & Smith (1806-1809) | 5 | 0.03% | 3 | 0.08% | 3 | 0.09% | 3 | 0.08% |
Sprengel (1825) | 5 | 0.03% | 3 | 0.08% | 3 | 0.09% | 3 | 0.08% |
Tassin et al. (2006) | 5 | 0.03% | 5 | 0.13% | 5 | 0.15% | 3 | 0.08% |
Thouvenot & Bardat (2010) | 5 | 0.03% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Verlaque et al. (2015) | 5 | 0.03% | 4 | 0.1% | 4 | 0.12% | 4 | 0.11% |
Welker et al. (2020) | 5 | 0.03% | 5 | 0.13% | 5 | 0.15% | 4 | 0.11% |
Allioni (1785) | 4 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Banfi et al. (2005) | 4 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Bernard (2015) | 4 | 0.02% | 3 | 0.08% | 3 | 0.09% | 3 | 0.08% |
Candolle (1815) | 4 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Candolle (1825) | 4 | 0.02% | 1 | 0.03% | 0 | 0% | 1 | 0.03% |
Cecchi et al. (2014) | 4 | 0.02% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
CEVA (2011) | 4 | 0.02% | 3 | 0.08% | 3 | 0.09% | 3 | 0.08% |
Christenhusz (2009) | 4 | 0.02% | 2 | 0.05% | 2 | 0.06% | 2 | 0.06% |
Derrick et al. (1987) | 4 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Don (1834) | 4 | 0.02% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Donnell et al. (2012) | 4 | 0.02% | 4 | 0.1% | 4 | 0.12% | 4 | 0.11% |
Dulac (1867) | 4 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Dumortier (1827) | 4 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Ferrer-Gallego & Güemes (2020) | 4 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Fourreau (1869) | 4 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Gaertner (1791) | 4 | 0.02% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Göktürk & Sümbül (2014) | 4 | 0.02% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Grace et al. (2013) | 4 | 0.02% | 4 | 0.1% | 2 | 0.06% | 4 | 0.11% |
Green (1985) | 4 | 0.02% | 1 | 0.03% | 0 | 0% | 1 | 0.03% |
Hodgetts et al. (2020) | 4 | 0.02% | 4 | 0.1% | 4 | 0.12% | 4 | 0.11% |
Hunt (1981) | 4 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Ito et al. (2017) | 4 | 0.02% | 4 | 0.1% | 4 | 0.12% | 4 | 0.11% |
Jiménez-lópez et al. (2022) | 4 | 0.02% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Jolinon (1985) | 4 | 0.02% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Jost et al. (2019) | 4 | 0.02% | 4 | 0.1% | 4 | 0.12% | 3 | 0.08% |
Judziewicz (1990) | 4 | 0.02% | 4 | 0.1% | 4 | 0.12% | 3 | 0.08% |
Knoepffler et al. (1990) | 4 | 0.02% | 2 | 0.05% | 2 | 0.06% | 2 | 0.06% |
Kyalangalilwa et al. (2013) | 4 | 0.02% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Lamarck & Candolle (1805) | 4 | 0.02% | 2 | 0.05% | 2 | 0.06% | 2 | 0.06% |
Linnaeus (1763) | 4 | 0.02% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Maddi (2014) | 4 | 0.02% | 3 | 0.08% | 3 | 0.09% | 3 | 0.08% |
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 | 0.05% | 2 | 0.06% | 2 | 0.06% |
Quere & Geslin (2016) | 4 | 0.02% | 4 | 0.1% | 4 | 0.12% | 4 | 0.11% |
Rico et al. (2006) | 4 | 0.02% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Sennen & Frère (1936) | 4 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Sennikov (2011) | 4 | 0.02% | 2 | 0.05% | 2 | 0.06% | 2 | 0.06% |
Shao & Xiang (2015) | 4 | 0.02% | 3 | 0.08% | 1 | 0.03% | 2 | 0.06% |
Sherff (1937) | 4 | 0.02% | 4 | 0.1% | 4 | 0.12% | 4 | 0.11% |
Siadati et al. (2018) | 4 | 0.02% | 4 | 0.1% | 3 | 0.09% | 3 | 0.08% |
Sweet (1830) | 4 | 0.02% | 3 | 0.08% | 3 | 0.09% | 3 | 0.08% |
Thiébaut & Tison (2016) | 4 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Thulin et al. (2016) | 4 | 0.02% | 4 | 0.1% | 4 | 0.12% | 4 | 0.11% |
Tison et al. (2014) | 4 | 0.02% | 4 | 0.1% | 4 | 0.12% | 4 | 0.11% |
Willdenow (1800) | 4 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Yang et al. (2022) | 4 | 0.02% | 2 | 0.05% | 2 | 0.06% | 2 | 0.06% |
Bouman et al. (2022) | 3 | 0.02% | 2 | 0.05% | 2 | 0.06% | 2 | 0.06% |
Brugneaux (2012) | 3 | 0.02% | 2 | 0.05% | 2 | 0.06% | 2 | 0.06% |
Candolle (1837) | 3 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Candolle (1838-1839) | 3 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Candolle (1848) | 3 | 0.02% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Carine & Robba (2010) | 3 | 0.02% | 1 | 0.03% | 0 | 0% | 1 | 0.03% |
Chaix (1785) | 3 | 0.02% | 1 | 0.03% | 1 | 0.03% | 0 | 0% |
Coughlan et al. (2020) | 3 | 0.02% | 3 | 0.08% | 3 | 0.09% | 3 | 0.08% |
Coulot & Rabaute (2016) | 3 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Crantz (1766) | 3 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Cremers & Hoff (1997) | 3 | 0.02% | 2 | 0.05% | 2 | 0.06% | 2 | 0.06% |
Don (1838) | 3 | 0.02% | 2 | 0.05% | 2 | 0.06% | 2 | 0.06% |
Gagnon et al. (2016) | 3 | 0.02% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Gardner et al. (2021) | 3 | 0.02% | 2 | 0.05% | 2 | 0.06% | 2 | 0.06% |
González‐Elizondo & Peterson (1997) | 3 | 0.02% | 3 | 0.08% | 3 | 0.09% | 3 | 0.08% |
Grenier & Godron (1856) | 3 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Gussone (1827) | 3 | 0.02% | 2 | 0.05% | 2 | 0.06% | 2 | 0.06% |
IPNI (2000-) | 3 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Jordan (1864) | 3 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Kearney (1949) | 3 | 0.02% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Koch (1837) | 3 | 0.02% | 1 | 0.03% | 0 | 0% | 1 | 0.03% |
Krebs (1994) | 3 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Laguna et al. (2013) | 3 | 0.02% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Linnaeus (1771) | 3 | 0.02% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Maas (1985) | 3 | 0.02% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Mabberley (2011) | 3 | 0.02% | 2 | 0.05% | 2 | 0.06% | 2 | 0.06% |
Maddi (2010) | 3 | 0.02% | 2 | 0.05% | 2 | 0.06% | 2 | 0.06% |
Mesterházy et al. (2021) | 3 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Murdock & Smith (2003) | 3 | 0.02% | 3 | 0.08% | 3 | 0.09% | 2 | 0.06% |
Murray (1784) | 3 | 0.02% | 3 | 0.08% | 3 | 0.09% | 3 | 0.08% |
Payri & N'yeurt (1997) | 3 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Reduron (2007) | 3 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Roalson et al. (2010) | 3 | 0.02% | 3 | 0.08% | 3 | 0.09% | 3 | 0.08% |
Rouy & Foucaud (1897) | 3 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Rouy (1910) | 3 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Schuster et al. (2015) | 3 | 0.02% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Scopoli (1771) | 3 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Sprengel (1826) | 3 | 0.02% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Stackpole et al. (2013) | 3 | 0.02% | 3 | 0.08% | 3 | 0.09% | 3 | 0.08% |
Stepansky et al. (1999) | 3 | 0.02% | 3 | 0.08% | 1 | 0.03% | 1 | 0.03% |
Ter Steege et al. (2016) | 3 | 0.02% | 2 | 0.05% | 2 | 0.06% | 2 | 0.06% |
Thomassin et al. (1992) | 3 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Turner & Tanaka (2024) | 3 | 0.02% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Uicn et al. (2019) | 3 | 0.02% | 2 | 0.05% | 2 | 0.06% | 2 | 0.06% |
Wagner et al. (2007) | 3 | 0.02% | 3 | 0.08% | 2 | 0.06% | 1 | 0.03% |
Ward (2012) | 3 | 0.02% | 2 | 0.05% | 2 | 0.06% | 2 | 0.06% |
Willdenow (1798) | 3 | 0.02% | 2 | 0.05% | 2 | 0.06% | 2 | 0.06% |
Willdenow (1799) | 3 | 0.02% | 0 | 0% | 0 | 0% | 0 | 0% |
Willdenow (1799) | 3 | 0.02% | 2 | 0.05% | 2 | 0.06% | 1 | 0.03% |
Willette et al. (2014) | 3 | 0.02% | 3 | 0.08% | 3 | 0.09% | 3 | 0.08% |
Allioni (1785) | 2 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Anonyme (2015) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Badré (2008b) | 2 | 0.01% | 2 | 0.05% | 1 | 0.03% | 1 | 0.03% |
Banfi et al. (2022) | 2 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Barabé & Gibernau (2015) | 2 | 0.01% | 2 | 0.05% | 2 | 0.06% | 2 | 0.06% |
Bigazzi & Raffaelli (2000) | 2 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Boissier (1845) | 2 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Boreau (1857) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Bouman et al. (2020) | 2 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Breton (2014) | 2 | 0.01% | 2 | 0.05% | 2 | 0.06% | 2 | 0.06% |
Caillon & Lavoué (2016) | 2 | 0.01% | 2 | 0.05% | 2 | 0.06% | 2 | 0.06% |
Candolle (1813) | 2 | 0.01% | 1 | 0.03% | 1 | 0.03% | 0 | 0% |
Candolle (1821) | 2 | 0.01% | 1 | 0.03% | 1 | 0.03% | 0 | 0% |
Cecchi & Selvi (2015) | 2 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Compton et al. (2019) | 2 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Cosson (1859) | 2 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Cosson (1864) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Coste (1937) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Coulot et al. (2021) | 2 | 0.01% | 2 | 0.05% | 2 | 0.06% | 2 | 0.06% |
Couté & Garrouste (2009) | 2 | 0.01% | 2 | 0.05% | 2 | 0.06% | 1 | 0.03% |
Das (2012) | 2 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Demoly (1996) | 2 | 0.01% | 2 | 0.05% | 2 | 0.06% | 2 | 0.06% |
Don (1832) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Flora of Australia Online (1982) | 2 | 0.01% | 1 | 0.03% | 0 | 0% | 1 | 0.03% |
Fourt et al. (2017) | 2 | 0.01% | 2 | 0.05% | 2 | 0.06% | 2 | 0.06% |
Freire et al. (2021) | 2 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Garland & Moore (2012) | 2 | 0.01% | 2 | 0.05% | 2 | 0.06% | 2 | 0.06% |
Grangaud (2010) | 2 | 0.01% | 2 | 0.05% | 1 | 0.03% | 1 | 0.03% |
Gray (1997) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Grenier & Godron (1848) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Grenier (1857) | 2 | 0.01% | 2 | 0.05% | 2 | 0.06% | 2 | 0.06% |
Haworth (1803) | 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% |
Hoff (2021) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Hugonnot et al. (2017) | 2 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Inocencio et al. (2006) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Kilian et al. (2011) | 2 | 0.01% | 2 | 0.05% | 0 | 0% | 2 | 0.06% |
Klak et al. (2007) | 2 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Lagourgue et al. (2022) | 2 | 0.01% | 2 | 0.05% | 2 | 0.06% | 1 | 0.03% |
Lambinon & Worm (1993) | 2 | 0.01% | 2 | 0.05% | 0 | 0% | 2 | 0.06% |
Lassen (1987) | 2 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Lespinasse & Theveneau (1859) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Linnaeus (1767) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Linné (1771) | 2 | 0.01% | 2 | 0.05% | 1 | 0.03% | 1 | 0.03% |
Majure et al. (2017) | 2 | 0.01% | 2 | 0.05% | 1 | 0.03% | 1 | 0.03% |
Mandák et al. (2005) | 2 | 0.01% | 2 | 0.05% | 0 | 0% | 2 | 0.06% |
Manning et al. (2014) | 2 | 0.01% | 2 | 0.05% | 2 | 0.06% | 2 | 0.06% |
Mcclintock (1957) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Mitka et al. (2021) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
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 | 0.05% | 2 | 0.06% | 1 | 0.03% |
Nesom (2022) | 2 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Pejhanmehr (2022) | 2 | 0.01% | 2 | 0.05% | 2 | 0.06% | 2 | 0.06% |
Peraza et al. (2022) | 2 | 0.01% | 2 | 0.05% | 2 | 0.06% | 2 | 0.06% |
Pereira et al. (2021) | 2 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Peterson et al. (2012) | 2 | 0.01% | 1 | 0.03% | 1 | 0.03% | 0 | 0% |
Philcox (1965) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Plouguerné et al. (2007) | 2 | 0.01% | 2 | 0.05% | 2 | 0.06% | 2 | 0.06% |
Prévention de l'introduction et de la propagation des espèces végétales exotiques envahissantes sur le territoire de La Réunion | 2 | 0.01% | 2 | 0.05% | 2 | 0.06% | 2 | 0.06% |
Rafinesque Schmaltz (1810) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Richter (1890) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Roemer & Schultes (1819) | 2 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Ros et al. (2013) | 2 | 0.01% | 2 | 0.05% | 2 | 0.06% | 2 | 0.06% |
Rousseau et al. (2017) | 2 | 0.01% | 2 | 0.05% | 2 | 0.06% | 2 | 0.06% |
Samson (2005) | 2 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Sanders (2006) | 2 | 0.01% | 2 | 0.05% | 0 | 0% | 1 | 0.03% |
Sanders (2012) | 2 | 0.01% | 1 | 0.03% | 0 | 0% | 0 | 0% |
Sant (2002) | 2 | 0.01% | 2 | 0.05% | 2 | 0.06% | 2 | 0.06% |
Sant (2002) | 2 | 0.01% | 2 | 0.05% | 2 | 0.06% | 2 | 0.06% |
Satthaphorn et al. (2023) | 2 | 0.01% | 2 | 0.05% | 2 | 0.06% | 2 | 0.06% |
Schaefer et al. (2012) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Schneeweiss et al. (2004) | 2 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Schrank et al. (1789) | 2 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Schreber (1771) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Shao et al. (2019) | 2 | 0.01% | 2 | 0.05% | 1 | 0.03% | 1 | 0.03% |
Sherff (1937) | 2 | 0.01% | 2 | 0.05% | 2 | 0.06% | 1 | 0.03% |
Sibthorp & Smith (1813-1816) | 2 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Smith et al. (2020) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Snow & Peterson (2012) | 2 | 0.01% | 2 | 0.05% | 0 | 0% | 2 | 0.06% |
Song et al. (2019) | 2 | 0.01% | 2 | 0.05% | 2 | 0.06% | 2 | 0.06% |
Sun et al. (2017) | 2 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Tropicos (1980-) | 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 | 0.05% | 2 | 0.06% | 2 | 0.06% |
Véron et al. (2021) | 2 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Vorontsova et al. (2016) | 2 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Wilson (2017) | 2 | 0.01% | 1 | 0.03% | 1 | 0.03% | 0 | 0% |
Zieliński et al. (2004) | 2 | 0.01% | 1 | 0.03% | 0 | 0% | 1 | 0.03% |
Abbayes (1931) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Acevedo-Rodríguez (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Acta Plantarum (2007-) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Adeux et al. (2022) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Albert & Jahandiez (1908) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Allen et al. (2022) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Almeida et al. (2016) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Anonyme (1809) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Anonyme (1846) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Applequist (2019) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 0 | 0% |
Austin et al. (2014) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Bacchetta et al. (2011) | 1 | 0.01% | 1 | 0.03% | 0 | 0% | 1 | 0.03% |
Ball (1878) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Bárbara et al. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Barthelat (2019) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Bean (1919) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Bernard et al. (2014) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Berton (2020) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Bijmoer et al. (2021) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Bock & Tison (2012) | 1 | 0.01% | 1 | 0.03% | 0 | 0% | 1 | 0.03% |
Bock (2011) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Boenninghausen (1824) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Boissier (1844) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Bolòs & Vigo (1974) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Bonnier (1912) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Borkhausen (1793) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Bosser & Heine (2000) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Bourzat & Monie (1977) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 0 | 0% |
Briquet (1895) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Brown et al. (2009) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Bubani & Penzig (1900) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Bubani & Penzig (1901) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Bubani & Penzig (1902) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Cafferty et al. (2000) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Candolle (1844) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Candolle (1852) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Charpin & Salanon (1985) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Chauvel et al. (2006) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Chemisquy et al. (2010) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Chevalier (1936) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Chew (1965) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Cho et al. (2005) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Choo et al. (2020) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Christenhusz et al. (2018) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Collectif (1823) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Coode 1982 | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Copeland (1932) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 0 | 0% |
Coste (1937) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Coulot & Rabaute (2013) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Couté, Noël & Perrette (2017) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Crantz (1769) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Cremers & Boudrie (2006) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Cremers & Boudrie (2007) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 0 | 0% |
Cremers & Hoff (2000) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Dauphin & Matile-Ferrero (2003) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Delaunay (2015) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Dentant et al. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Desjardins et al. (2015) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Diaz & Cuzange (2009) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Döll (1843) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Dorsey et al. (2013) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Eaton (1922) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Ebihara et al. (2017) | 1 | 0.01% | 1 | 0.03% | 0 | 0% | 1 | 0.03% |
Edgar (1995) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Emil et al. (2016) | 1 | 0.01% | 1 | 0.03% | 0 | 0% | 1 | 0.03% |
Engelmann (1873) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Eppo (2011) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Eppo (2011) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Eppo (2013) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Eriksson et al. (1998) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Essi et al. (2017) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Faden & Hunt (1987) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Ferrer-Gallego & Boisset (2015) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Ferrer-gallego & Laguna (2018) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Fischer & Meyer (1835) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Focke (1910) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Fort et al. (2020) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Fried (2011) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Fryer & Hylmö (2009) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Gandhi et al. (2020) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Gaudefroy & Mouillefarine (1871) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Geir (2018) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
German & Al-shehbaz (2015) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Gmelin (1791) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Goldblatt (2011) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Goulletquer et al. (2002) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Graham et al. (2021) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Granville & Gayot (2014) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Grayum et al. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Grenier et Godron (1856) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Grenier (1859) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Greuter & Raus (1989) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Grisebach (1864) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Grolle & Long (2000) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Grulich (1984) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Guinet (1936) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Gurgel et al. (2018) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Gutermannn (2019) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Harpke et al. (2014) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Haworth (1812) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Hébrard (1970) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Heylen et al. (2021) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Hill et al. (2006) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Hill (1768) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Hillig (2005) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Hily et al. (2010) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Hodgetts & Lockhart (2020) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Hohenacker (1838) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Holub (1993) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Huet (1889) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Iamonico et al. (2015) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Iltis & Cochrane (2007) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Jacobs (2001) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Jacques (1859) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Jahandiez (1928) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Janchen (1977) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Janczewski (1906) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Jordan & Fourreau (1869-1903) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Jussieu (1825) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Kaehler et al. (2019) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Karsch (1853) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Kerguélen & Bock (2011) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Klein & Verlaque (2005) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Klein & Verlaque (2008) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Knox (2014) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Lack (2019) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Laguna (2006) | 1 | 0.01% | 1 | 0.03% | 0 | 0% | 1 | 0.03% |
Lamarck & Candolle (1805) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Lamarck (1799) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Lapeyrouse (1818) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Larregle et al. (2014) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Le Duff & Gall (2015) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Les & Crawford (1999) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Leuenberger (1997) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Léveillé (1911) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Léveillé (1917) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Levring (1944) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Lewis (2000) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Li et al. (2021) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 0 | 0% |
Lieutard (1893) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 0 | 0% |
Link (1829) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Linné (1766) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Liu et al. (2004) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 0 | 0% |
Lizé (2018) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Lizé (2018) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Lizé (2022) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Loiseleur-deslongchamps (1806) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Maddi (2014) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Mady et al. (2016) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Manning (1960) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Manns & Anderberg (2009) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Marais (1997) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Maréchal et al. (2013) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Martínez-Azorín et al. (2023) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Mazine et al. (2018) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Melnikov (2016) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Merino (1909) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Meyer et al. (2008) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Mineur et al. (2012) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Moreno et al. (2018) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Moreno (1993) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Mori et al. (2002) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Mori et al. (2002) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Morren & Decaisne (1836) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Moura-Júnior et al. (2016) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Muhlenberg (1813) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Niebler, F. et al. (2021) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Nikulin et al. (2016) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Nouals & Bariteau (1993) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Novikoff & Hurdu (2015) | 1 | 0.01% | 1 | 0.03% | 0 | 0% | 1 | 0.03% |
Ochyra et al. (2008) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Orlova et al. (2016) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
O’Shea (2006) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Pallas (1773) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Paradis & Miniconi (2011) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Pastore et al. (2023) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Patchell et al. (2014) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Pax (2018) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Pennington & Biggs (2016) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Petelczyc et al. (2006) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 0 | 0% |
Pigott (2020) | 1 | 0.01% | 1 | 0.03% | 0 | 0% | 1 | 0.03% |
Pócs (2022) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Polhill (1990) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Portal & Tort (2014) | 1 | 0.01% | 1 | 0.03% | 0 | 0% | 1 | 0.03% |
Prain (1913) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Prance et al. (2007) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Prelli (2015) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Prévention de l'introduction et de la propagation des espèces végétales exotiques envahissantes sur le territoire de la Guadeloupe | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Provan et al. (2008) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 0 | 0% |
Questel (2017) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Questel (2023) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Rabasse et al. (2005) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Rabaute & Coulot (2015) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Reduron (2006) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Rehder (1920) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Richard (1792) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Risso (1826) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Rivière (2003) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 0 | 0% |
Rohde et al. (2017) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Rojas-andrés & Martínez-ortega (2016) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Rouy & Foucaud (1893) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Rouy & Foucaud (1896) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Rouy (1899) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Rouy (1903) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Rouy (1908) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Ruiz & Pavon (1794) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Sant (2022) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Sargent (1911) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Scatigna et al. (2022) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Schenck (1906) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 0 | 0% |
Scott (1981) | 1 | 0.01% | 1 | 0.03% | 0 | 0% | 1 | 0.03% |
Sellier et al. (2016) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 0 | 0% |
Selvi et al. (2009) | 1 | 0.01% | 1 | 0.03% | 0 | 0% | 1 | 0.03% |
Seringe (1815) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Shrestha et al. (2003) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Silva et al. (1922) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Sjøtun et al. (2008) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Soubeyran (2008) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Speta (1998) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Stace (2019) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Stefanovic & Dickinson (2007) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Steudel (1821) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Steudel (1841) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Stevenson (1991) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Stevenson (1991) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Sudhakaran & Ganapathi (2008) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Sweet (1826) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Tchichatscheff (1860) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Terrin et al. (2014) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Thibaut et al. (2022) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Thiébaut (2007) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Thomson et al. (2023) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Tison & de Foucault (2015) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Toussaint et al. (2013) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Uotila et al. (2021) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Van et al. (2022) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Vanhöffen (1912) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 0 | 0% |
Vaquer (1988) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Veldkamp (2002) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 0 | 0% |
Verloove & Lambinon (2011) | 1 | 0.01% | 1 | 0.03% | 0 | 0% | 1 | 0.03% |
Villanueva-almanza et al. (2021) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Villars (1787) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Vorontsova et al. (2023) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Waldstein & Kitaibel (1802) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Ward & Wiersema (2008) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Webster (1956) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Webster (1957) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Webster (1957) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Wells et al. (2021) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Whittier (1976) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Willdenow (1797) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Wilson (2017) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Wilson (2017) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Wilson (2022) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Wood & Scotland (2017) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Wörz (2005) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Yamada (1928) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Zakardjian et al. (2020) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 1 | 0.03% |
Zeng (2009) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
Ziffer-Berger et al. (2015) | 1 | 0.01% | 1 | 0.03% | 1 | 0.03% | 0 | 0% |