Trachéophytes aquatiques de France
Trachéophytes aquatiques au sens large (eau douce ou eau saumâtre ou marin ou eau douce/terrestre ou marin/terrestre ou eau douce/marin)
236 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) | 371 | 13,87% | 217 | 43,93% | 198 | 43,61% | 199 | 42,98% |
Munzinger et al. (2016) | 266 | 9,94% | 133 | 26,92% | 120 | 26,43% | 131 | 28,29% |
Funk et al. (2007) | 257 | 9,61% | 88 | 17,81% | 87 | 19,16% | 82 | 17,71% |
Fournet (2002) | 216 | 8,07% | 180 | 36,44% | 180 | 39,65% | 168 | 36,29% |
Morat et al. (2012) | 214 | 8% | 141 | 28,54% | 129 | 28,41% | 128 | 27,65% |
Véron et al. (2021) | 63 | 2,36% | 62 | 12,55% | 57 | 12,56% | 60 | 12,96% |
Royen (1951) | 35 | 1,31% | 25 | 5,06% | 23 | 5,07% | 24 | 5,18% |
Raynal (1974) | 32 | 1,2% | 2 | 0,4% | 2 | 0,44% | 2 | 0,43% |
Philbrick et al. (2016) | 31 | 1,16% | 5 | 1,01% | 5 | 1,1% | 5 | 1,08% |
Larridon et al. (2011) | 27 | 1,01% | 1 | 0,2% | 1 | 0,22% | 1 | 0,22% |
Horn (1994) | 23 | 0,86% | 4 | 0,81% | 4 | 0,88% | 4 | 0,86% |
Pellegrini et al. (2018) | 21 | 0,79% | 9 | 1,82% | 9 | 1,98% | 9 | 1,94% |
Molino et al. (2022) | 20 | 0,75% | 2 | 0,4% | 2 | 0,44% | 2 | 0,43% |
Hily et al. (2010) | 19 | 0,71% | 17 | 3,44% | 17 | 3,74% | 17 | 3,67% |
Wiersema et al. (2008) | 18 | 0,67% | 3 | 0,61% | 3 | 0,66% | 3 | 0,65% |
Li et al. (2022) | 17 | 0,64% | 14 | 2,83% | 14 | 3,08% | 14 | 3,02% |
Linnaeus (1753) | 17 | 0,64% | 14 | 2,83% | 14 | 3,08% | 13 | 2,81% |
Rouy & Foucaud (1893) | 17 | 0,64% | 0 | 0% | 0 | 0% | 0 | 0% |
Linnaeus (1753) | 16 | 0,6% | 14 | 2,83% | 13 | 2,86% | 13 | 2,81% |
Hequet & Le Corre (2010) | 15 | 0,56% | 11 | 2,23% | 11 | 2,42% | 11 | 2,38% |
Hequet et al. (2009) | 15 | 0,56% | 11 | 2,23% | 11 | 2,42% | 11 | 2,38% |
González‐Elizondo & Peterson (1997) | 14 | 0,52% | 12 | 2,43% | 12 | 2,64% | 12 | 2,59% |
MacKee (1994) | 14 | 0,52% | 10 | 2,02% | 10 | 2,2% | 10 | 2,16% |
Padgett (2007) | 14 | 0,52% | 3 | 0,61% | 3 | 0,66% | 3 | 0,65% |
Echternacht (2012) | 13 | 0,49% | 1 | 0,2% | 1 | 0,22% | 1 | 0,22% |
Evrard et al. (2004) | 13 | 0,49% | 2 | 0,4% | 2 | 0,44% | 2 | 0,43% |
Lansdown (2022) | 13 | 0,49% | 12 | 2,43% | 10 | 2,2% | 9 | 1,94% |
Roalson et al. (2010) | 13 | 0,49% | 13 | 2,63% | 13 | 2,86% | 12 | 2,59% |
Breton (2014) | 12 | 0,45% | 12 | 2,43% | 12 | 2,64% | 12 | 2,59% |
Fourdrigniez & Meyer (2008) | 12 | 0,45% | 5 | 1,01% | 4 | 0,88% | 4 | 0,86% |
Grenier & Godron (1848) | 12 | 0,45% | 0 | 0% | 0 | 0% | 0 | 0% |
Muller et al. (2004) | 12 | 0,45% | 11 | 2,23% | 10 | 2,2% | 9 | 1,94% |
Nyman (1882) | 12 | 0,45% | 0 | 0% | 0 | 0% | 0 | 0% |
Schnell (1969) | 12 | 0,45% | 10 | 2,02% | 10 | 2,2% | 10 | 2,16% |
Maddi (2010) | 10 | 0,37% | 8 | 1,62% | 8 | 1,76% | 8 | 1,73% |
Bobrov et al. (2022) | 9 | 0,34% | 7 | 1,42% | 7 | 1,54% | 7 | 1,51% |
Boullet et al. (2018) | 9 | 0,34% | 8 | 1,62% | 8 | 1,76% | 6 | 1,3% |
Ito et al. (2017) | 9 | 0,34% | 9 | 1,82% | 9 | 1,98% | 7 | 1,51% |
Lemée (1955) | 9 | 0,34% | 7 | 1,42% | 7 | 1,54% | 6 | 1,3% |
Bonnier & Layens (1894) | 7 | 0,26% | 0 | 0% | 0 | 0% | 0 | 0% |
Ferlay et al. (2023) | 7 | 0,26% | 7 | 1,42% | 7 | 1,54% | 7 | 1,51% |
Morat & Veillon (1985) | 7 | 0,26% | 7 | 1,42% | 7 | 1,54% | 4 | 0,86% |
Barabé & Gibernau (2015) | 6 | 0,22% | 6 | 1,21% | 6 | 1,32% | 6 | 1,3% |
Bernard (2015) | 6 | 0,22% | 6 | 1,21% | 6 | 1,32% | 6 | 1,3% |
Delnatte & Wynne (2016) | 6 | 0,22% | 6 | 1,21% | 6 | 1,32% | 6 | 1,3% |
Gray (1821) | 6 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Haynes & Holm-Nielsen (1992) | 6 | 0,22% | 1 | 0,2% | 1 | 0,22% | 1 | 0,22% |
Hopkins et al. (2014) | 6 | 0,22% | 6 | 1,21% | 6 | 1,32% | 6 | 1,3% |
Lamarck (1779) | 6 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Richter (1890) | 6 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Acevedo-Rodríguez & Strong (2012) | 5 | 0,19% | 3 | 0,61% | 3 | 0,66% | 3 | 0,65% |
Barrett et al. (2019) | 5 | 0,19% | 4 | 0,81% | 4 | 0,88% | 4 | 0,86% |
Christenhusz (2009) | 5 | 0,19% | 3 | 0,61% | 3 | 0,66% | 3 | 0,65% |
Couté & Garrouste (2009) | 5 | 0,19% | 2 | 0,4% | 2 | 0,44% | 2 | 0,43% |
Florence (2004) | 5 | 0,19% | 4 | 0,81% | 4 | 0,88% | 3 | 0,65% |
Kuntze (1891) | 5 | 0,19% | 1 | 0,2% | 1 | 0,22% | 1 | 0,22% |
Maddi (2014) | 5 | 0,19% | 3 | 0,61% | 3 | 0,66% | 3 | 0,65% |
Mattio et al. (2015) | 5 | 0,19% | 5 | 1,01% | 5 | 1,1% | 5 | 1,08% |
Ørgaard (1991) | 5 | 0,19% | 1 | 0,2% | 1 | 0,22% | 1 | 0,22% |
Tippery et al. (2018) | 5 | 0,19% | 5 | 1,01% | 5 | 1,1% | 5 | 1,08% |
Triest (1987) | 5 | 0,19% | 2 | 0,4% | 2 | 0,44% | 2 | 0,43% |
Van Der Putten et al. (2010) | 5 | 0,19% | 5 | 1,01% | 5 | 1,1% | 4 | 0,86% |
Wagner et al. (2007) | 5 | 0,19% | 5 | 1,01% | 3 | 0,66% | 3 | 0,65% |
Anonyme (2023) | 4 | 0,15% | 1 | 0,2% | 0 | 0% | 1 | 0,22% |
Euro+Med (2006) | 4 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Fournier (1928) | 4 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Fournier (1934-1940) | 4 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Léotard & Chaline (2013) | 4 | 0,15% | 4 | 0,81% | 4 | 0,88% | 4 | 0,86% |
Lowden (1986) | 4 | 0,15% | 3 | 0,61% | 3 | 0,66% | 3 | 0,65% |
Rouy (1912) | 4 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Ter Steege et al. (2016) | 4 | 0,15% | 3 | 0,61% | 3 | 0,66% | 2 | 0,43% |
Tippery & Sokolik (2020) | 4 | 0,15% | 4 | 0,81% | 4 | 0,88% | 4 | 0,86% |
Tippery et al. (2024) | 4 | 0,15% | 4 | 0,81% | 4 | 0,88% | 4 | 0,86% |
Wiersema (1987) | 4 | 0,15% | 4 | 0,81% | 3 | 0,66% | 3 | 0,65% |
Anonyme (2014) | 3 | 0,11% | 3 | 0,61% | 3 | 0,66% | 2 | 0,43% |
Arcangeli (1882) | 3 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Boggan et al. (1992) | 3 | 0,11% | 2 | 0,4% | 2 | 0,44% | 2 | 0,43% |
Boreau (1857) | 3 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Bosser (1997) | 3 | 0,11% | 2 | 0,4% | 1 | 0,22% | 1 | 0,22% |
Bubani & Penzig (1902) | 3 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Candolle (1815) | 3 | 0,11% | 1 | 0,2% | 1 | 0,22% | 1 | 0,22% |
Den et al. (2020) | 3 | 0,11% | 3 | 0,61% | 3 | 0,66% | 3 | 0,65% |
Derrick et al. (1987) | 3 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Dulac (1867) | 3 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Haynes & Holm-Nielsen (2009) | 3 | 0,11% | 2 | 0,4% | 2 | 0,44% | 2 | 0,43% |
Jérémie et al. (2001) | 3 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Lamarck (1783) | 3 | 0,11% | 1 | 0,2% | 1 | 0,22% | 1 | 0,22% |
Lamarck (1789) | 3 | 0,11% | 1 | 0,2% | 1 | 0,22% | 1 | 0,22% |
Meyer et al. (2006) | 3 | 0,11% | 1 | 0,2% | 1 | 0,22% | 1 | 0,22% |
Moench (1794) | 3 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Mori et al. (2002) | 3 | 0,11% | 3 | 0,61% | 3 | 0,66% | 3 | 0,65% |
Nelson-Smith et al. (2014) | 3 | 0,11% | 1 | 0,2% | 1 | 0,22% | 0 | 0% |
N'Yeurt & Payri (2004) | 3 | 0,11% | 3 | 0,61% | 3 | 0,66% | 3 | 0,65% |
Rouy (1909) | 3 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Royen (1953) | 3 | 0,11% | 1 | 0,2% | 1 | 0,22% | 1 | 0,22% |
Salisbury (1796) | 3 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Walters (1953) | 3 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Willette et al. (2014) | 3 | 0,11% | 3 | 0,61% | 3 | 0,66% | 3 | 0,65% |
Yang et al. (2012) | 3 | 0,11% | 3 | 0,61% | 3 | 0,66% | 3 | 0,65% |
Yuncker (1937) | 3 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Zuloaga et al. (2018) | 3 | 0,11% | 3 | 0,61% | 3 | 0,66% | 3 | 0,65% |
Ascherson & Graebner (1897) | 2 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Aublet (1775) | 2 | 0,07% | 2 | 0,4% | 2 | 0,44% | 1 | 0,22% |
Candolle (1821) | 2 | 0,07% | 1 | 0,2% | 1 | 0,22% | 1 | 0,22% |
Candolle (1830) | 2 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Cariot & Saint-lager (1889) | 2 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Delnatte & Meyer (2012) | 2 | 0,07% | 1 | 0,2% | 1 | 0,22% | 1 | 0,22% |
Dumortier (1827) | 2 | 0,07% | 1 | 0,2% | 1 | 0,22% | 1 | 0,22% |
Etcheberry & Abraham (2009) | 2 | 0,07% | 2 | 0,4% | 2 | 0,44% | 1 | 0,22% |
Flora of North America (1993-) | 2 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Fourreau (1869) | 2 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Gandoger (1884) | 2 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Gatignol & Zunino (2019) | 2 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Grenier & Godron (1856) | 2 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Judziewicz (1990) | 2 | 0,07% | 2 | 0,4% | 2 | 0,44% | 2 | 0,43% |
Kirschner (2002) | 2 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Lavergne (2011) | 2 | 0,07% | 1 | 0,2% | 1 | 0,22% | 1 | 0,22% |
Lemée (1953) | 2 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Martínez-y-Pérez et al. (2008) | 2 | 0,07% | 2 | 0,4% | 2 | 0,44% | 2 | 0,43% |
Miller (1768) | 2 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Moench (1794) | 2 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Moran & Smith (1999) | 2 | 0,07% | 1 | 0,2% | 1 | 0,22% | 1 | 0,22% |
Mucina (2017) | 2 | 0,07% | 2 | 0,4% | 2 | 0,44% | 2 | 0,43% |
Oliveira & Bove (2015) | 2 | 0,07% | 1 | 0,2% | 1 | 0,22% | 1 | 0,22% |
Persoon (1805) | 2 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Royen (1954) | 2 | 0,07% | 1 | 0,2% | 1 | 0,22% | 1 | 0,22% |
Scatigna et al. (2022) | 2 | 0,07% | 2 | 0,4% | 2 | 0,44% | 2 | 0,43% |
Schultz (1848) | 2 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Scopoli (1771) | 2 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Sullivan & Short (2023) | 2 | 0,07% | 2 | 0,4% | 2 | 0,44% | 2 | 0,43% |
Willdenow (1799) | 2 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Zardini & Raven (1991) | 2 | 0,07% | 1 | 0,2% | 1 | 0,22% | 1 | 0,22% |
Zuloaga et al. (2010) | 2 | 0,07% | 1 | 0,2% | 1 | 0,22% | 1 | 0,22% |
Zuloaga (2022) | 2 | 0,07% | 1 | 0,2% | 1 | 0,22% | 1 | 0,22% |
Akhani et al. (2014) | 1 | 0,04% | 1 | 0,2% | 1 | 0,22% | 1 | 0,22% |
Allen et al. (2022) | 1 | 0,04% | 1 | 0,2% | 1 | 0,22% | 0 | 0% |
Allioni (1785) | 1 | 0,04% | 1 | 0,2% | 1 | 0,22% | 1 | 0,22% |
Anonyme. (2002) | 1 | 0,04% | 1 | 0,2% | 1 | 0,22% | 1 | 0,22% |
Anonyme. (2002) | 1 | 0,04% | 1 | 0,2% | 1 | 0,22% | 1 | 0,22% |
Anonyme. (2002) | 1 | 0,04% | 1 | 0,2% | 1 | 0,22% | 1 | 0,22% |
Batista et al. (2011) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Bock (2011) | 1 | 0,04% | 1 | 0,2% | 1 | 0,22% | 1 | 0,22% |
Bohley et al. (2017) | 1 | 0,04% | 1 | 0,2% | 1 | 0,22% | 0 | 0% |
Bonnier (1912) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Bubani & Penzig (1901) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Butaud (2015) | 1 | 0,04% | 1 | 0,2% | 0 | 0% | 1 | 0,22% |
Carrijo et al. (2012) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Chaix (1785) | 1 | 0,04% | 1 | 0,2% | 1 | 0,22% | 0 | 0% |
Champeau et al. (1991) | 1 | 0,04% | 1 | 0,2% | 1 | 0,22% | 1 | 0,22% |
Chau et al. (2020) | 1 | 0,04% | 1 | 0,2% | 1 | 0,22% | 1 | 0,22% |
Christenhusz et al. (2018) | 1 | 0,04% | 1 | 0,2% | 1 | 0,22% | 1 | 0,22% |
Copeland (1932) | 1 | 0,04% | 1 | 0,2% | 1 | 0,22% | 1 | 0,22% |
Couhia & Fleurot (2016) | 1 | 0,04% | 1 | 0,2% | 1 | 0,22% | 1 | 0,22% |
Cremers & Boudrie (2007) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Cremers & Hoff (1990) | 1 | 0,04% | 1 | 0,2% | 1 | 0,22% | 1 | 0,22% |
Cremers & Hoff (1994) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Cremers & Hoff (1997) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Cremers & Hoff (2000) | 1 | 0,04% | 1 | 0,2% | 1 | 0,22% | 1 | 0,22% |
Dauphin (1999) | 1 | 0,04% | 1 | 0,2% | 1 | 0,22% | 1 | 0,22% |
Delnatte et al. (2021) | 1 | 0,04% | 1 | 0,2% | 1 | 0,22% | 1 | 0,22% |
Don (1834) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Emig (2007) | 1 | 0,04% | 1 | 0,2% | 1 | 0,22% | 1 | 0,22% |
Eppo (2011) | 1 | 0,04% | 1 | 0,2% | 1 | 0,22% | 1 | 0,22% |
Eppo (2011) | 1 | 0,04% | 1 | 0,2% | 1 | 0,22% | 1 | 0,22% |
Fedde (1939) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Florence (1996) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Florence (1997) | 1 | 0,04% | 1 | 0,2% | 0 | 0% | 1 | 0,22% |
Friis & Holt (2016) | 1 | 0,04% | 1 | 0,2% | 1 | 0,22% | 1 | 0,22% |
Gaertner (1788) | 1 | 0,04% | 1 | 0,2% | 1 | 0,22% | 1 | 0,22% |
Gagnon et al. (2016) | 1 | 0,04% | 1 | 0,2% | 1 | 0,22% | 1 | 0,22% |
Gaudin (1828) | 1 | 0,04% | 1 | 0,2% | 1 | 0,22% | 1 | 0,22% |
Geir (2018) | 1 | 0,04% | 1 | 0,2% | 1 | 0,22% | 1 | 0,22% |
Graham et al. (2021) | 1 | 0,04% | 1 | 0,2% | 1 | 0,22% | 1 | 0,22% |
Gray (1821) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Hoff (2021) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Hoffmann (1804) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Host (1831) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Jost et al. (2019) | 1 | 0,04% | 1 | 0,2% | 1 | 0,22% | 1 | 0,22% |
Koch (1837) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Lamarck & Candolle (1805) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Lamarck (1779) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Lansdown & Jarvis (2004) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Les & Crawford (1999) | 1 | 0,04% | 1 | 0,2% | 1 | 0,22% | 1 | 0,22% |
Les (1986) | 1 | 0,04% | 1 | 0,2% | 1 | 0,22% | 0 | 0% |
Linnaeus (1763) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Linnaeus (1771) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Longhi-Wagner et al. (2010) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Lowe et al. (2007) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Maddi & Brizard (2010) | 1 | 0,04% | 1 | 0,2% | 1 | 0,22% | 1 | 0,22% |
Maddi (2014) | 1 | 0,04% | 1 | 0,2% | 1 | 0,22% | 1 | 0,22% |
Maréchal et al. (2013) | 1 | 0,04% | 1 | 0,2% | 1 | 0,22% | 1 | 0,22% |
Molino et al. (2009) | 1 | 0,04% | 1 | 0,2% | 1 | 0,22% | 1 | 0,22% |
Moore (1933) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Murdock & Smith (2003) | 1 | 0,04% | 1 | 0,2% | 1 | 0,22% | 1 | 0,22% |
Niebler, F. et al. (2021) | 1 | 0,04% | 1 | 0,2% | 1 | 0,22% | 1 | 0,22% |
Paradis & Miniconi (2011) | 1 | 0,04% | 1 | 0,2% | 1 | 0,22% | 1 | 0,22% |
Persoon (1807) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Petelczyc et al. (2006) | 1 | 0,04% | 1 | 0,2% | 1 | 0,22% | 0 | 0% |
Philbrick & Bove (2019) | 1 | 0,04% | 1 | 0,2% | 1 | 0,22% | 1 | 0,22% |
Pignal et al. (2022) | 1 | 0,04% | 1 | 0,2% | 1 | 0,22% | 1 | 0,22% |
Piirainen et al. (2017) | 1 | 0,04% | 1 | 0,2% | 1 | 0,22% | 1 | 0,22% |
Presl & Presl (1822) | 1 | 0,04% | 1 | 0,2% | 1 | 0,22% | 1 | 0,22% |
Prévention de l'introduction et de la propagation des espèces végétales exotiques envahissantes sur le territoire de la Guadeloupe | 1 | 0,04% | 1 | 0,2% | 1 | 0,22% | 1 | 0,22% |
Proćków & Drábková (2023) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Questel (2017) | 1 | 0,04% | 1 | 0,2% | 1 | 0,22% | 1 | 0,22% |
Ragavan et al. (2014) | 1 | 0,04% | 1 | 0,2% | 1 | 0,22% | 1 | 0,22% |
Reichenbach (1830-1832) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Ricketson & Pipoly (2010) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Rignault & Chevallier (2017) | 1 | 0,04% | 1 | 0,2% | 1 | 0,22% | 1 | 0,22% |
Rouy & Camus (1901) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Rudge (1805) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Sant (2022) | 1 | 0,04% | 1 | 0,2% | 1 | 0,22% | 1 | 0,22% |
Schenck (1905) | 1 | 0,04% | 1 | 0,2% | 1 | 0,22% | 1 | 0,22% |
Schur (1866) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Sennikov (2016) | 1 | 0,04% | 1 | 0,2% | 1 | 0,22% | 1 | 0,22% |
Sibthorp & Smith (1806-1809) | 1 | 0,04% | 1 | 0,2% | 1 | 0,22% | 1 | 0,22% |
Siljak-Yakovlev et al. (2020) | 1 | 0,04% | 1 | 0,2% | 1 | 0,22% | 1 | 0,22% |
Sramkó et al. (2016) | 1 | 0,04% | 1 | 0,2% | 1 | 0,22% | 1 | 0,22% |
Sukhorukov et al. (2018) | 1 | 0,04% | 1 | 0,2% | 0 | 0% | 1 | 0,22% |
Sweet (1826) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Takács et al. (2017) | 1 | 0,04% | 1 | 0,2% | 1 | 0,22% | 1 | 0,22% |
Taylor (1989) | 1 | 0,04% | 1 | 0,2% | 1 | 0,22% | 1 | 0,22% |
Tenore (1811-1815) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Thibaut et al. (2022) | 1 | 0,04% | 1 | 0,2% | 1 | 0,22% | 1 | 0,22% |
Thiébaut (2007) | 1 | 0,04% | 1 | 0,2% | 1 | 0,22% | 1 | 0,22% |
Toutain (1989) | 1 | 0,04% | 1 | 0,2% | 1 | 0,22% | 1 | 0,22% |
Van et al. (2022) | 1 | 0,04% | 1 | 0,2% | 1 | 0,22% | 1 | 0,22% |
Villars (1787) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Werkhoven (1986) | 1 | 0,04% | 1 | 0,2% | 1 | 0,22% | 1 | 0,22% |
Wiersema et al. (2018) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Wiggers (1780) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Wilson (2021) | 1 | 0,04% | 1 | 0,2% | 1 | 0,22% | 1 | 0,22% |
Wilson (2022) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Wood et al. (2020) | 1 | 0,04% | 1 | 0,2% | 1 | 0,22% | 1 | 0,22% |
Zhang et al. (2008) | 1 | 0,04% | 1 | 0,2% | 1 | 0,22% | 1 | 0,22% |
Zhang et al. (2013) | 1 | 0,04% | 1 | 0,2% | 1 | 0,22% | 1 | 0,22% |