Espèces végétales exotiques envahissantes
Toutes les Plantes (Plantae) introduites et envahissantes (statut J) dans au moins l'un des territoires français.
260 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) | 745 | 29.98% | 567 | 147.27% | 563 | 156.82% | 543 | 150.42% |
Funk et al. (2007) | 280 | 11.27% | 120 | 31.17% | 118 | 32.87% | 111 | 30.75% |
Tison et al. (2014) | 260 | 10.46% | 139 | 36.1% | 136 | 37.88% | 128 | 35.46% |
MacKee (1994) | 219 | 8.81% | 161 | 41.82% | 158 | 44.01% | 155 | 42.94% |
Hequet & Le Corre (2010) | 207 | 8.33% | 156 | 40.52% | 153 | 42.62% | 150 | 41.55% |
Hequet et al. (2009) | 207 | 8.33% | 156 | 40.52% | 153 | 42.62% | 150 | 41.55% |
Fourdrigniez & Meyer (2008) | 158 | 6.36% | 120 | 31.17% | 115 | 32.03% | 111 | 30.75% |
Molino et al. (2022) | 105 | 4.23% | 8 | 2.08% | 8 | 2.23% | 7 | 1.94% |
Lavergne (2011) | 96 | 3.86% | 81 | 21.04% | 76 | 21.17% | 77 | 21.33% |
Delnatte & Meyer (2012) | 70 | 2.82% | 54 | 14.03% | 54 | 15.04% | 50 | 13.85% |
Meyer et al. (2006) | 64 | 2.58% | 40 | 10.39% | 38 | 10.58% | 38 | 10.53% |
Munzinger et al. (2016) | 58 | 2.33% | 13 | 3.38% | 13 | 3.62% | 12 | 3.32% |
Léotard & Chaline (2013) | 56 | 2.25% | 50 | 12.99% | 48 | 13.37% | 48 | 13.3% |
Acevedo-Rodríguez & Strong (2012) | 52 | 2.09% | 35 | 9.09% | 35 | 9.75% | 30 | 8.31% |
Morat & Veillon (1985) | 49 | 1.97% | 34 | 8.83% | 33 | 9.19% | 30 | 8.31% |
Muller et al. (2004) | 36 | 1.45% | 33 | 8.57% | 31 | 8.64% | 30 | 8.31% |
Morat et al. (2012) | 34 | 1.37% | 12 | 3.12% | 12 | 3.34% | 11 | 3.05% |
Fonseca et al. (2017) | 33 | 1.33% | 1 | 0.26% | 1 | 0.28% | 1 | 0.28% |
Gargominy et al. (1996) | 28 | 1.13% | 21 | 5.45% | 21 | 5.85% | 21 | 5.82% |
Paton et al. (2019) | 28 | 1.13% | 3 | 0.78% | 2 | 0.56% | 2 | 0.55% |
Anonyme (2014) | 27 | 1.09% | 24 | 6.23% | 24 | 6.69% | 20 | 5.54% |
Boullet et al. (2018) | 25 | 1.01% | 24 | 6.23% | 24 | 6.69% | 21 | 5.82% |
Lowe et al. (2007) | 25 | 1.01% | 19 | 4.94% | 18 | 5.01% | 16 | 4.43% |
Molino et al. (2009) | 25 | 1.01% | 22 | 5.71% | 22 | 6.13% | 19 | 5.26% |
Aublet (1775) | 22 | 0.89% | 10 | 2.6% | 9 | 2.51% | 9 | 2.49% |
Baaijens & Veldkamp (1991) | 19 | 0.76% | 1 | 0.26% | 1 | 0.28% | 1 | 0.28% |
Ferlay et al. (2023) | 19 | 0.76% | 19 | 4.94% | 19 | 5.29% | 19 | 5.26% |
Nesom (2009) | 17 | 0.68% | 1 | 0.26% | 1 | 0.28% | 0 | 0% |
Ter Steege et al. (2016) | 15 | 0.6% | 13 | 3.38% | 13 | 3.62% | 12 | 3.32% |
Berg & Roselli (2005) | 13 | 0.52% | 1 | 0.26% | 1 | 0.28% | 1 | 0.28% |
Brandbyge (1986) | 13 | 0.52% | 1 | 0.26% | 1 | 0.28% | 1 | 0.28% |
Cabioc'h & Floc'h (2014) | 13 | 0.52% | 11 | 2.86% | 11 | 3.06% | 11 | 3.05% |
Florence (2004) | 13 | 0.52% | 12 | 3.12% | 11 | 3.06% | 12 | 3.32% |
Wurdack et al. (1993) | 13 | 0.52% | 0 | 0% | 0 | 0% | 0 | 0% |
Barneby & Grimes (1996) | 12 | 0.48% | 0 | 0% | 0 | 0% | 0 | 0% |
Linnaeus (1753) | 12 | 0.48% | 8 | 2.08% | 7 | 1.95% | 7 | 1.94% |
Goulletquer (2016) | 11 | 0.44% | 10 | 2.6% | 10 | 2.79% | 10 | 2.77% |
Lemée (1953) | 11 | 0.44% | 5 | 1.3% | 5 | 1.39% | 5 | 1.39% |
Maddi (2014) | 11 | 0.44% | 6 | 1.56% | 6 | 1.67% | 6 | 1.66% |
Suddee et al. (2004) | 11 | 0.44% | 1 | 0.26% | 1 | 0.28% | 1 | 0.28% |
Copeland (1932) | 9 | 0.36% | 1 | 0.26% | 1 | 0.28% | 1 | 0.28% |
Kyalangalilwa et al. (2013) | 9 | 0.36% | 3 | 0.78% | 2 | 0.56% | 2 | 0.55% |
Linnaeus (1753) | 9 | 0.36% | 5 | 1.3% | 5 | 1.39% | 4 | 1.11% |
Pollard & Paton (2001) | 9 | 0.36% | 0 | 0% | 0 | 0% | 0 | 0% |
Wilmot-Dear & Friis (2013) | 9 | 0.36% | 3 | 0.78% | 2 | 0.56% | 2 | 0.55% |
Guimarães et al. (2019) | 8 | 0.32% | 2 | 0.52% | 2 | 0.56% | 2 | 0.55% |
Kükenthal (1936) | 8 | 0.32% | 2 | 0.52% | 1 | 0.28% | 1 | 0.28% |
Barneby (1991) | 7 | 0.28% | 3 | 0.78% | 2 | 0.56% | 2 | 0.55% |
Burel et al. (2019) | 7 | 0.28% | 6 | 1.56% | 6 | 1.67% | 6 | 1.66% |
Egan & Pan (2015) | 7 | 0.28% | 2 | 0.52% | 1 | 0.28% | 1 | 0.28% |
Evrard et al. (2004) | 7 | 0.28% | 0 | 0% | 0 | 0% | 0 | 0% |
Jeffrey (1980) | 7 | 0.28% | 1 | 0.26% | 1 | 0.28% | 1 | 0.28% |
Judd et al. (2018) | 7 | 0.28% | 1 | 0.26% | 1 | 0.28% | 1 | 0.28% |
Lemée (1955) | 7 | 0.28% | 1 | 0.26% | 1 | 0.28% | 1 | 0.28% |
Moraes et al. (2010) | 7 | 0.28% | 1 | 0.26% | 1 | 0.28% | 1 | 0.28% |
Vorontsova (2022) | 7 | 0.28% | 3 | 0.78% | 3 | 0.84% | 3 | 0.83% |
Bernard (2015) | 6 | 0.24% | 5 | 1.3% | 5 | 1.39% | 5 | 1.39% |
Cremers & Hoff (1994) | 6 | 0.24% | 2 | 0.52% | 2 | 0.56% | 2 | 0.55% |
Oliveira Pellegrini et al. (2016) | 6 | 0.24% | 1 | 0.26% | 1 | 0.28% | 1 | 0.28% |
Toutain (1989) | 6 | 0.24% | 4 | 1.04% | 4 | 1.11% | 4 | 1.11% |
Wasshausen (2006) | 6 | 0.24% | 4 | 1.04% | 4 | 1.11% | 3 | 0.83% |
Bosser & Heine (1988) | 5 | 0.2% | 1 | 0.26% | 1 | 0.28% | 1 | 0.28% |
Euro+Med (2006) | 5 | 0.2% | 0 | 0% | 0 | 0% | 0 | 0% |
Florence (1997) | 5 | 0.2% | 5 | 1.3% | 4 | 1.11% | 4 | 1.11% |
Gagnon et al. (2016) | 5 | 0.2% | 1 | 0.26% | 1 | 0.28% | 1 | 0.28% |
Horn (1994) | 5 | 0.2% | 1 | 0.26% | 1 | 0.28% | 1 | 0.28% |
Hovenkamp & Miyamoto (2005) | 5 | 0.2% | 1 | 0.26% | 1 | 0.28% | 1 | 0.28% |
Maddi (2010) | 5 | 0.2% | 3 | 0.78% | 3 | 0.84% | 3 | 0.83% |
Masters et al. (2023) | 5 | 0.2% | 4 | 1.04% | 4 | 1.11% | 4 | 1.11% |
Moench (1794) | 5 | 0.2% | 0 | 0% | 0 | 0% | 0 | 0% |
Thouvenot & Bardat (2010) | 5 | 0.2% | 1 | 0.26% | 1 | 0.28% | 1 | 0.28% |
Turner (2013) | 5 | 0.2% | 1 | 0.26% | 1 | 0.28% | 1 | 0.28% |
Barneby (1987) | 4 | 0.16% | 2 | 0.52% | 2 | 0.56% | 2 | 0.55% |
Candolle (1845) | 4 | 0.16% | 0 | 0% | 0 | 0% | 0 | 0% |
Cayet et al. (2022) | 4 | 0.16% | 0 | 0% | 0 | 0% | 0 | 0% |
Frenot et al. (2001) | 4 | 0.16% | 3 | 0.78% | 3 | 0.84% | 2 | 0.55% |
Green (1985) | 4 | 0.16% | 1 | 0.26% | 0 | 0% | 1 | 0.28% |
Hassemer (2017) | 4 | 0.16% | 0 | 0% | 0 | 0% | 0 | 0% |
Jolinon (1987) | 4 | 0.16% | 4 | 1.04% | 4 | 1.11% | 4 | 1.11% |
Judziewicz (1990) | 4 | 0.16% | 3 | 0.78% | 3 | 0.84% | 3 | 0.83% |
Lemée (1952) | 4 | 0.16% | 3 | 0.78% | 3 | 0.84% | 3 | 0.83% |
McDonald & Maslin (2000) | 4 | 0.16% | 2 | 0.52% | 2 | 0.56% | 2 | 0.55% |
Miller (1768) | 4 | 0.16% | 0 | 0% | 0 | 0% | 0 | 0% |
Peterson et al. (2014) | 4 | 0.16% | 4 | 1.04% | 4 | 1.11% | 4 | 1.11% |
Philcox (1965) | 4 | 0.16% | 1 | 0.26% | 1 | 0.28% | 1 | 0.28% |
Salisbury (1796) | 4 | 0.16% | 0 | 0% | 0 | 0% | 0 | 0% |
Sanders (2006) | 4 | 0.16% | 3 | 0.78% | 1 | 0.28% | 2 | 0.55% |
Simões & Staples (2017) | 4 | 0.16% | 2 | 0.52% | 2 | 0.56% | 2 | 0.55% |
Wiersema et al. (2018) | 4 | 0.16% | 2 | 0.52% | 1 | 0.28% | 0 | 0% |
Berg (1992) | 3 | 0.12% | 1 | 0.26% | 1 | 0.28% | 1 | 0.28% |
Byng et al. (2016) | 3 | 0.12% | 3 | 0.78% | 3 | 0.84% | 3 | 0.83% |
Carcaillet (1993) | 3 | 0.12% | 3 | 0.78% | 3 | 0.84% | 2 | 0.55% |
Christenhusz (2009) | 3 | 0.12% | 3 | 0.78% | 3 | 0.84% | 3 | 0.83% |
Delnatte & Wynne (2016) | 3 | 0.12% | 3 | 0.78% | 3 | 0.84% | 3 | 0.83% |
Feuillet (2014) | 3 | 0.12% | 3 | 0.78% | 3 | 0.84% | 3 | 0.83% |
Graham (1988) | 3 | 0.12% | 2 | 0.52% | 2 | 0.56% | 2 | 0.55% |
Granville & Gayot (2014) | 3 | 0.12% | 3 | 0.78% | 3 | 0.84% | 3 | 0.83% |
Harley & Pastore (2012) | 3 | 0.12% | 1 | 0.26% | 1 | 0.28% | 1 | 0.28% |
Meyer et al. (2008) | 3 | 0.12% | 3 | 0.78% | 3 | 0.84% | 3 | 0.83% |
Moench (1794) | 3 | 0.12% | 0 | 0% | 0 | 0% | 0 | 0% |
Moonlight et al. (2018) | 3 | 0.12% | 3 | 0.78% | 3 | 0.84% | 2 | 0.55% |
Pellegrini et al. (2018) | 3 | 0.12% | 1 | 0.26% | 1 | 0.28% | 1 | 0.28% |
Sanders (2012) | 3 | 0.12% | 1 | 0.26% | 0 | 0% | 0 | 0% |
Schenck (1906) | 3 | 0.12% | 3 | 0.78% | 3 | 0.84% | 3 | 0.83% |
Wagner et al. (2007) | 3 | 0.12% | 3 | 0.78% | 2 | 0.56% | 1 | 0.28% |
Welker et al. (2020) | 3 | 0.12% | 3 | 0.78% | 3 | 0.84% | 3 | 0.83% |
Willette et al. (2014) | 3 | 0.12% | 3 | 0.78% | 3 | 0.84% | 3 | 0.83% |
Yang et al. (2022) | 3 | 0.12% | 2 | 0.52% | 2 | 0.56% | 2 | 0.55% |
Appelhans et al. (2021) | 2 | 0.08% | 2 | 0.52% | 2 | 0.56% | 2 | 0.55% |
Arcangeli (1882) | 2 | 0.08% | 0 | 0% | 0 | 0% | 0 | 0% |
Barabé & Gibernau (2015) | 2 | 0.08% | 2 | 0.52% | 2 | 0.56% | 2 | 0.55% |
Boggan et al. (1992) | 2 | 0.08% | 2 | 0.52% | 2 | 0.56% | 2 | 0.55% |
Bosser & Heine (2000) | 2 | 0.08% | 2 | 0.52% | 2 | 0.56% | 2 | 0.55% |
Boudrie & Bizot (2006) | 2 | 0.08% | 2 | 0.52% | 2 | 0.56% | 2 | 0.55% |
Candolle (1815) | 2 | 0.08% | 0 | 0% | 0 | 0% | 0 | 0% |
Chemisquy et al. (2010) | 2 | 0.08% | 1 | 0.26% | 1 | 0.28% | 1 | 0.28% |
Fourt et al. (2017) | 2 | 0.08% | 2 | 0.52% | 2 | 0.56% | 2 | 0.55% |
Gray (1821) | 2 | 0.08% | 0 | 0% | 0 | 0% | 0 | 0% |
Hullé et al. (2003) | 2 | 0.08% | 2 | 0.52% | 2 | 0.56% | 2 | 0.55% |
Knapp (2013) | 2 | 0.08% | 2 | 0.52% | 2 | 0.56% | 2 | 0.55% |
Kuntze (1891) | 2 | 0.08% | 0 | 0% | 0 | 0% | 0 | 0% |
Lamarck (1783) | 2 | 0.08% | 1 | 0.26% | 1 | 0.28% | 1 | 0.28% |
Lohmann & Taylor (2014) | 2 | 0.08% | 1 | 0.26% | 1 | 0.28% | 1 | 0.28% |
Moran & Smith (1999) | 2 | 0.08% | 1 | 0.26% | 1 | 0.28% | 1 | 0.28% |
N'Yeurt & Payri (2004) | 2 | 0.08% | 2 | 0.52% | 2 | 0.56% | 2 | 0.55% |
N'Yeurt & Payri (2010) | 2 | 0.08% | 2 | 0.52% | 2 | 0.56% | 2 | 0.55% |
Oliveira Pellegrini & Forzza (2017) | 2 | 0.08% | 0 | 0% | 0 | 0% | 0 | 0% |
Payri (2007) | 2 | 0.08% | 2 | 0.52% | 2 | 0.56% | 2 | 0.55% |
Pennington & Biggs (2016) | 2 | 0.08% | 2 | 0.52% | 2 | 0.56% | 2 | 0.55% |
Peraza et al. (2022) | 2 | 0.08% | 2 | 0.52% | 2 | 0.56% | 2 | 0.55% |
Pereira et al. (2021) | 2 | 0.08% | 1 | 0.26% | 1 | 0.28% | 1 | 0.28% |
Plouguerné et al. (2007) | 2 | 0.08% | 2 | 0.52% | 2 | 0.56% | 2 | 0.55% |
Richard (1792) | 2 | 0.08% | 1 | 0.26% | 1 | 0.28% | 1 | 0.28% |
Rignault & Chevallier (2017) | 2 | 0.08% | 2 | 0.52% | 2 | 0.56% | 2 | 0.55% |
Rodríguez-Prieto et al. (1999) | 2 | 0.08% | 2 | 0.52% | 2 | 0.56% | 2 | 0.55% |
Rogers & Appan (1973) | 2 | 0.08% | 0 | 0% | 0 | 0% | 0 | 0% |
Rohde et al. (2017) | 2 | 0.08% | 2 | 0.52% | 2 | 0.56% | 2 | 0.55% |
Rouy (1913) | 2 | 0.08% | 0 | 0% | 0 | 0% | 0 | 0% |
Satthaphorn et al. (2023) | 2 | 0.08% | 2 | 0.52% | 2 | 0.56% | 2 | 0.55% |
Schenck (1905) | 2 | 0.08% | 2 | 0.52% | 2 | 0.56% | 2 | 0.55% |
Schrire et al. (2009) | 2 | 0.08% | 2 | 0.52% | 2 | 0.56% | 2 | 0.55% |
Seigler et al. (2014) | 2 | 0.08% | 0 | 0% | 0 | 0% | 0 | 0% |
Song et al. (2019) | 2 | 0.08% | 2 | 0.52% | 2 | 0.56% | 2 | 0.55% |
Sprengel (1826) | 2 | 0.08% | 1 | 0.26% | 1 | 0.28% | 1 | 0.28% |
Tassin et al. (2006) | 2 | 0.08% | 2 | 0.52% | 2 | 0.56% | 2 | 0.55% |
Veldkamp (2014) | 2 | 0.08% | 2 | 0.52% | 2 | 0.56% | 2 | 0.55% |
Yang et al. (2012) | 2 | 0.08% | 2 | 0.52% | 2 | 0.56% | 2 | 0.55% |
Zuntini et al. (2014) | 2 | 0.08% | 1 | 0.26% | 1 | 0.28% | 1 | 0.28% |
Allem (2001) | 1 | 0.04% | 1 | 0.26% | 0 | 0% | 1 | 0.28% |
Allen et al. (2022) | 1 | 0.04% | 0 | 0% | 0 | 0% | 0 | 0% |
Baker (1867) | 1 | 0.04% | 0 | 0% | 0 | 0% | 0 | 0% |
Bell (1982) | 1 | 0.04% | 1 | 0.26% | 1 | 0.28% | 1 | 0.28% |
Berg (1972) | 1 | 0.04% | 1 | 0.26% | 0 | 0% | 1 | 0.28% |
Bernardi (2000) | 1 | 0.04% | 0 | 0% | 0 | 0% | 0 | 0% |
Berry et al. (1999) | 1 | 0.04% | 1 | 0.26% | 1 | 0.28% | 1 | 0.28% |
Berry et al. (2004) | 1 | 0.04% | 0 | 0% | 0 | 0% | 0 | 0% |
Bosser & Heine (2000b) | 1 | 0.04% | 1 | 0.26% | 1 | 0.28% | 1 | 0.28% |
Breton (2014) | 1 | 0.04% | 1 | 0.26% | 1 | 0.28% | 1 | 0.28% |
Brottier et al. (2018) | 1 | 0.04% | 1 | 0.26% | 1 | 0.28% | 1 | 0.28% |
Candolle (1830) | 1 | 0.04% | 0 | 0% | 0 | 0% | 0 | 0% |
Chauvel et al. (2006) | 1 | 0.04% | 1 | 0.26% | 1 | 0.28% | 1 | 0.28% |
Christenhusz (2002) | 1 | 0.04% | 0 | 0% | 0 | 0% | 0 | 0% |
Cremers & Hoff (1998) | 1 | 0.04% | 1 | 0.26% | 1 | 0.28% | 1 | 0.28% |
Cremers & Hoff (2000) | 1 | 0.04% | 1 | 0.26% | 1 | 0.28% | 1 | 0.28% |
Dauphin & Matile-Ferrero (2003) | 1 | 0.04% | 1 | 0.26% | 1 | 0.28% | 1 | 0.28% |
Dehgan (2012) | 1 | 0.04% | 1 | 0.26% | 1 | 0.28% | 1 | 0.28% |
Delnatte et al. (2021) | 1 | 0.04% | 1 | 0.26% | 1 | 0.28% | 1 | 0.28% |
Dewarumez et al. (2011) | 1 | 0.04% | 0 | 0% | 0 | 0% | 0 | 0% |
Don (1831) | 1 | 0.04% | 0 | 0% | 0 | 0% | 0 | 0% |
Dulac (1867) | 1 | 0.04% | 0 | 0% | 0 | 0% | 0 | 0% |
Eppo (2011) | 1 | 0.04% | 1 | 0.26% | 1 | 0.28% | 1 | 0.28% |
Eriksson et al. (1998) | 1 | 0.04% | 0 | 0% | 0 | 0% | 0 | 0% |
Etcheberry & Abraham (2009) | 1 | 0.04% | 0 | 0% | 0 | 0% | 0 | 0% |
Ferrer-Gallego & Boisset (2015) | 1 | 0.04% | 1 | 0.26% | 1 | 0.28% | 1 | 0.28% |
Ferrer-gallego & Laguna (2018) | 1 | 0.04% | 1 | 0.26% | 1 | 0.28% | 1 | 0.28% |
Feuillet (2009) | 1 | 0.04% | 1 | 0.26% | 1 | 0.28% | 0 | 0% |
Flora of North America (1993-) | 1 | 0.04% | 0 | 0% | 0 | 0% | 0 | 0% |
Fournier (1934-1940) | 1 | 0.04% | 0 | 0% | 0 | 0% | 0 | 0% |
Gaertner (1788) | 1 | 0.04% | 1 | 0.26% | 1 | 0.28% | 1 | 0.28% |
Gardner et al. (2021) | 1 | 0.04% | 1 | 0.26% | 1 | 0.28% | 1 | 0.28% |
Gardner et al. (2021) | 1 | 0.04% | 1 | 0.26% | 1 | 0.28% | 0 | 0% |
Geir (2018) | 1 | 0.04% | 1 | 0.26% | 1 | 0.28% | 1 | 0.28% |
Goldberg (1967) | 1 | 0.04% | 1 | 0.26% | 1 | 0.28% | 1 | 0.28% |
González‐Elizondo & Peterson (1997) | 1 | 0.04% | 1 | 0.26% | 1 | 0.28% | 1 | 0.28% |
Greene & Greene (1963) | 1 | 0.04% | 1 | 0.26% | 1 | 0.28% | 1 | 0.28% |
Gurgel et al. (2018) | 1 | 0.04% | 1 | 0.26% | 1 | 0.28% | 1 | 0.28% |
Hassemer et al. (2017) | 1 | 0.04% | 1 | 0.26% | 1 | 0.28% | 1 | 0.28% |
Hébrard (1970) | 1 | 0.04% | 1 | 0.26% | 1 | 0.28% | 1 | 0.28% |
Hily et al. (2010) | 1 | 0.04% | 1 | 0.26% | 1 | 0.28% | 1 | 0.28% |
Hind et al. (1993) | 1 | 0.04% | 1 | 0.26% | 1 | 0.28% | 1 | 0.28% |
Hodgetts et al. (2020) | 1 | 0.04% | 1 | 0.26% | 1 | 0.28% | 1 | 0.28% |
Hugonnot et al. (2017) | 1 | 0.04% | 1 | 0.26% | 1 | 0.28% | 1 | 0.28% |
Jost et al. (2019) | 1 | 0.04% | 1 | 0.26% | 1 | 0.28% | 1 | 0.28% |
Kaehler et al. (2019) | 1 | 0.04% | 1 | 0.26% | 1 | 0.28% | 1 | 0.28% |
Kirschner & Cheek (2000) | 1 | 0.04% | 1 | 0.26% | 1 | 0.28% | 0 | 0% |
Klein & Verlaque (2008) | 1 | 0.04% | 0 | 0% | 0 | 0% | 0 | 0% |
Klonowska et al. (2012) | 1 | 0.04% | 1 | 0.26% | 1 | 0.28% | 1 | 0.28% |
Klonowska et al. (2020) | 1 | 0.04% | 1 | 0.26% | 1 | 0.28% | 1 | 0.28% |
Knoepffler et al. (1990) | 1 | 0.04% | 0 | 0% | 0 | 0% | 0 | 0% |
Lamarck (1779) | 1 | 0.04% | 0 | 0% | 0 | 0% | 0 | 0% |
Larregle et al. (2014) | 1 | 0.04% | 1 | 0.26% | 1 | 0.28% | 1 | 0.28% |
Linnaeus (1759) | 1 | 0.04% | 0 | 0% | 0 | 0% | 0 | 0% |
Linnaeus (1762) | 1 | 0.04% | 1 | 0.26% | 1 | 0.28% | 1 | 0.28% |
Linnaeus (1763) | 1 | 0.04% | 0 | 0% | 0 | 0% | 0 | 0% |
Lizé (2018) | 1 | 0.04% | 1 | 0.26% | 1 | 0.28% | 1 | 0.28% |
Lizé (2018) | 1 | 0.04% | 1 | 0.26% | 1 | 0.28% | 1 | 0.28% |
Lizé (2022) | 1 | 0.04% | 1 | 0.26% | 1 | 0.28% | 1 | 0.28% |
Lowry & Plunkett (2020) | 1 | 0.04% | 1 | 0.26% | 1 | 0.28% | 1 | 0.28% |
Macallister & Marshall (2017) | 1 | 0.04% | 0 | 0% | 0 | 0% | 0 | 0% |
Maddi & Brizard (2010) | 1 | 0.04% | 1 | 0.26% | 1 | 0.28% | 1 | 0.28% |
Maddi (2014) | 1 | 0.04% | 1 | 0.26% | 1 | 0.28% | 1 | 0.28% |
Mandák et al. (2005) | 1 | 0.04% | 1 | 0.26% | 0 | 0% | 1 | 0.28% |
Maréchal et al. (2013) | 1 | 0.04% | 1 | 0.26% | 1 | 0.28% | 1 | 0.28% |
Massé (1982) | 1 | 0.04% | 1 | 0.26% | 1 | 0.28% | 1 | 0.28% |
Mattio et al. (2015) | 1 | 0.04% | 1 | 0.26% | 1 | 0.28% | 1 | 0.28% |
Mazine et al. (2018) | 1 | 0.04% | 1 | 0.26% | 1 | 0.28% | 1 | 0.28% |
Mitchell (1997) | 1 | 0.04% | 1 | 0.26% | 1 | 0.28% | 1 | 0.28% |
Munir (1992) | 1 | 0.04% | 0 | 0% | 0 | 0% | 0 | 0% |
Murdock & Smith (2003) | 1 | 0.04% | 1 | 0.26% | 1 | 0.28% | 1 | 0.28% |
N'Yeurt & Payri (2007) | 1 | 0.04% | 1 | 0.26% | 1 | 0.28% | 1 | 0.28% |
Nyman (1882) | 1 | 0.04% | 0 | 0% | 0 | 0% | 0 | 0% |
Ochyra et al. (2008) | 1 | 0.04% | 1 | 0.26% | 1 | 0.28% | 1 | 0.28% |
O’Shea (2006) | 1 | 0.04% | 1 | 0.26% | 1 | 0.28% | 1 | 0.28% |
Paradis & Miniconi (2011) | 1 | 0.04% | 1 | 0.26% | 1 | 0.28% | 1 | 0.28% |
Pastore et al. (2023) | 1 | 0.04% | 1 | 0.26% | 1 | 0.28% | 1 | 0.28% |
Paton et al. (2018) | 1 | 0.04% | 1 | 0.26% | 1 | 0.28% | 1 | 0.28% |
Payri & N'yeurt (1997) | 1 | 0.04% | 0 | 0% | 0 | 0% | 0 | 0% |
Pejhanmehr (2022) | 1 | 0.04% | 1 | 0.26% | 1 | 0.28% | 1 | 0.28% |
Persoon (1807) | 1 | 0.04% | 0 | 0% | 0 | 0% | 0 | 0% |
Petelczyc et al. (2006) | 1 | 0.04% | 1 | 0.26% | 1 | 0.28% | 0 | 0% |
Pócs (2022) | 1 | 0.04% | 1 | 0.26% | 1 | 0.28% | 1 | 0.28% |
Polhill (1990) | 1 | 0.04% | 1 | 0.26% | 1 | 0.28% | 1 | 0.28% |
Provan et al. (2008) | 1 | 0.04% | 1 | 0.26% | 1 | 0.28% | 1 | 0.28% |
Questel (2017) | 1 | 0.04% | 1 | 0.26% | 1 | 0.28% | 1 | 0.28% |
Rankin Rodríguez & Greuter (2001) | 1 | 0.04% | 0 | 0% | 0 | 0% | 0 | 0% |
Roalson et al. (2010) | 1 | 0.04% | 1 | 0.26% | 1 | 0.28% | 1 | 0.28% |
Rome & Coppens d'Eeckenbrugge (2016) | 1 | 0.04% | 1 | 0.26% | 1 | 0.28% | 1 | 0.28% |
Rouy & Camus (1901) | 1 | 0.04% | 0 | 0% | 0 | 0% | 0 | 0% |
Rudd (1955) | 1 | 0.04% | 1 | 0.26% | 1 | 0.28% | 1 | 0.28% |
Sant (2022) | 1 | 0.04% | 1 | 0.26% | 1 | 0.28% | 1 | 0.28% |
Scopoli (1771) | 1 | 0.04% | 0 | 0% | 0 | 0% | 0 | 0% |
Scott (1981) | 1 | 0.04% | 1 | 0.26% | 0 | 0% | 1 | 0.28% |
Sellier et al. (2016) | 1 | 0.04% | 1 | 0.26% | 1 | 0.28% | 1 | 0.28% |
Sherff (1937) | 1 | 0.04% | 1 | 0.26% | 1 | 0.28% | 1 | 0.28% |
Shrestha et al. (2003) | 1 | 0.04% | 1 | 0.26% | 1 | 0.28% | 1 | 0.28% |
Sjøtun et al. (2008) | 1 | 0.04% | 0 | 0% | 0 | 0% | 0 | 0% |
Soubeyran (2008) | 1 | 0.04% | 0 | 0% | 0 | 0% | 0 | 0% |
Souza et al. (2021) | 1 | 0.04% | 1 | 0.26% | 1 | 0.28% | 1 | 0.28% |
Stafleu & Cowan (1983) | 1 | 0.04% | 0 | 0% | 0 | 0% | 0 | 0% |
Stevenson (1991) | 1 | 0.04% | 1 | 0.26% | 1 | 0.28% | 0 | 0% |
Tareau (2015) | 1 | 0.04% | 0 | 0% | 0 | 0% | 0 | 0% |
Terrin et al. (2014) | 1 | 0.04% | 1 | 0.26% | 1 | 0.28% | 1 | 0.28% |
Thibaut et al. (2022) | 1 | 0.04% | 1 | 0.26% | 1 | 0.28% | 1 | 0.28% |
Véron et al. (2021) | 1 | 0.04% | 0 | 0% | 0 | 0% | 0 | 0% |
Vorontsova et al. (2023) | 1 | 0.04% | 1 | 0.26% | 1 | 0.28% | 1 | 0.28% |
Vroman (1968) | 1 | 0.04% | 1 | 0.26% | 1 | 0.28% | 1 | 0.28% |
Whittier (1976) | 1 | 0.04% | 1 | 0.26% | 1 | 0.28% | 1 | 0.28% |
Willdenow (1799) | 1 | 0.04% | 0 | 0% | 0 | 0% | 0 | 0% |
Wilson (2022) | 1 | 0.04% | 0 | 0% | 0 | 0% | 0 | 0% |
Wood et al. (2020) | 1 | 0.04% | 1 | 0.26% | 1 | 0.28% | 1 | 0.28% |