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)
237 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) | 388 | 14,42% | 226 | 46,5% | 203 | 46,03% | 206 | 45,47% |
Munzinger et al. (2016) | 267 | 9,93% | 134 | 27,57% | 121 | 27,44% | 132 | 29,14% |
Funk et al. (2007) | 257 | 9,55% | 89 | 18,31% | 88 | 19,95% | 83 | 18,32% |
Fournet (2002) | 216 | 8,03% | 184 | 37,86% | 184 | 41,72% | 172 | 37,97% |
Morat et al. (2012) | 215 | 7,99% | 142 | 29,22% | 130 | 29,48% | 129 | 28,48% |
Véron et al. (2021) | 64 | 2,38% | 63 | 12,96% | 58 | 13,15% | 61 | 13,47% |
Royen (1951) | 35 | 1,3% | 25 | 5,14% | 23 | 5,22% | 24 | 5,3% |
Raynal (1974) | 32 | 1,19% | 2 | 0,41% | 2 | 0,45% | 2 | 0,44% |
Philbrick et al. (2016) | 31 | 1,15% | 5 | 1,03% | 5 | 1,13% | 5 | 1,1% |
Larridon et al. (2011) | 27 | 1% | 1 | 0,21% | 1 | 0,23% | 1 | 0,22% |
Horn (1994) | 23 | 0,86% | 4 | 0,82% | 4 | 0,91% | 4 | 0,88% |
Pellegrini et al. (2018) | 21 | 0,78% | 9 | 1,85% | 9 | 2,04% | 9 | 1,99% |
Molino et al. (2022) | 20 | 0,74% | 2 | 0,41% | 2 | 0,45% | 2 | 0,44% |
Hily et al. (2010) | 19 | 0,71% | 18 | 3,7% | 18 | 4,08% | 18 | 3,97% |
Wiersema et al. (2008) | 18 | 0,67% | 3 | 0,62% | 3 | 0,68% | 3 | 0,66% |
Rouy & Foucaud (1893) | 17 | 0,63% | 0 | 0% | 0 | 0% | 0 | 0% |
Li et al. (2022) | 16 | 0,59% | 13 | 2,67% | 13 | 2,95% | 13 | 2,87% |
Linnaeus (1753) | 16 | 0,59% | 13 | 2,67% | 13 | 2,95% | 12 | 2,65% |
Linnaeus (1753) | 16 | 0,59% | 14 | 2,88% | 13 | 2,95% | 13 | 2,87% |
Hequet & Le Corre (2010) | 15 | 0,56% | 11 | 2,26% | 11 | 2,49% | 11 | 2,43% |
Hequet et al. (2009) | 15 | 0,56% | 11 | 2,26% | 11 | 2,49% | 11 | 2,43% |
González‐Elizondo & Peterson (1997) | 14 | 0,52% | 12 | 2,47% | 12 | 2,72% | 12 | 2,65% |
MacKee (1994) | 14 | 0,52% | 10 | 2,06% | 10 | 2,27% | 10 | 2,21% |
Padgett (2007) | 14 | 0,52% | 3 | 0,62% | 3 | 0,68% | 3 | 0,66% |
Echternacht (2012) | 13 | 0,48% | 1 | 0,21% | 1 | 0,23% | 1 | 0,22% |
Evrard et al. (2004) | 13 | 0,48% | 2 | 0,41% | 2 | 0,45% | 2 | 0,44% |
Grenier & Godron (1848) | 13 | 0,48% | 0 | 0% | 0 | 0% | 0 | 0% |
Lansdown (2022) | 13 | 0,48% | 12 | 2,47% | 10 | 2,27% | 9 | 1,99% |
Roalson et al. (2010) | 13 | 0,48% | 13 | 2,67% | 13 | 2,95% | 12 | 2,65% |
Breton (2014) | 12 | 0,45% | 12 | 2,47% | 12 | 2,72% | 12 | 2,65% |
Fourdrigniez & Meyer (2008) | 12 | 0,45% | 6 | 1,23% | 5 | 1,13% | 5 | 1,1% |
Muller et al. (2004) | 12 | 0,45% | 12 | 2,47% | 11 | 2,49% | 10 | 2,21% |
Nyman (1882) | 12 | 0,45% | 0 | 0% | 0 | 0% | 0 | 0% |
Schnell (1969) | 12 | 0,45% | 10 | 2,06% | 10 | 2,27% | 10 | 2,21% |
Maddi (2010) | 10 | 0,37% | 8 | 1,65% | 8 | 1,81% | 8 | 1,77% |
Bobrov et al. (2022) | 9 | 0,33% | 7 | 1,44% | 7 | 1,59% | 7 | 1,55% |
Boullet et al. (2018) | 9 | 0,33% | 8 | 1,65% | 8 | 1,81% | 6 | 1,32% |
Ito et al. (2017) | 9 | 0,33% | 9 | 1,85% | 9 | 2,04% | 7 | 1,55% |
Lemée (1955) | 9 | 0,33% | 7 | 1,44% | 7 | 1,59% | 6 | 1,32% |
Euro+Med (2006) | 8 | 0,3% | 0 | 0% | 0 | 0% | 0 | 0% |
Bonnier & Layens (1894) | 7 | 0,26% | 0 | 0% | 0 | 0% | 0 | 0% |
Ferlay et al. (2023) | 7 | 0,26% | 7 | 1,44% | 7 | 1,59% | 7 | 1,55% |
Morat & Veillon (1985) | 7 | 0,26% | 7 | 1,44% | 7 | 1,59% | 4 | 0,88% |
Barabé & Gibernau (2015) | 6 | 0,22% | 6 | 1,23% | 6 | 1,36% | 6 | 1,32% |
Bernard (2015) | 6 | 0,22% | 6 | 1,23% | 6 | 1,36% | 6 | 1,32% |
Delnatte & Wynne (2016) | 6 | 0,22% | 6 | 1,23% | 6 | 1,36% | 6 | 1,32% |
Gray (1821) | 6 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Haynes & Holm-Nielsen (1992) | 6 | 0,22% | 1 | 0,21% | 1 | 0,23% | 1 | 0,22% |
Hopkins et al. (2014) | 6 | 0,22% | 6 | 1,23% | 6 | 1,36% | 6 | 1,32% |
Lamarck (1779) | 6 | 0,22% | 0 | 0% | 0 | 0% | 0 | 0% |
Acevedo-Rodríguez & Strong (2012) | 5 | 0,19% | 3 | 0,62% | 3 | 0,68% | 3 | 0,66% |
Barrett et al. (2019) | 5 | 0,19% | 4 | 0,82% | 4 | 0,91% | 4 | 0,88% |
Christenhusz (2009) | 5 | 0,19% | 3 | 0,62% | 3 | 0,68% | 3 | 0,66% |
Couté & Garrouste (2009) | 5 | 0,19% | 2 | 0,41% | 2 | 0,45% | 2 | 0,44% |
Florence (2004) | 5 | 0,19% | 4 | 0,82% | 4 | 0,91% | 3 | 0,66% |
Kuntze (1891) | 5 | 0,19% | 1 | 0,21% | 1 | 0,23% | 1 | 0,22% |
Maddi (2014) | 5 | 0,19% | 3 | 0,62% | 3 | 0,68% | 3 | 0,66% |
Mattio et al. (2015) | 5 | 0,19% | 5 | 1,03% | 5 | 1,13% | 5 | 1,1% |
Ørgaard (1991) | 5 | 0,19% | 1 | 0,21% | 1 | 0,23% | 1 | 0,22% |
Richter (1890) | 5 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
Tippery et al. (2018) | 5 | 0,19% | 5 | 1,03% | 5 | 1,13% | 5 | 1,1% |
Triest (1987) | 5 | 0,19% | 2 | 0,41% | 2 | 0,45% | 2 | 0,44% |
Van Der Putten et al. (2010) | 5 | 0,19% | 5 | 1,03% | 5 | 1,13% | 4 | 0,88% |
Wagner et al. (2007) | 5 | 0,19% | 5 | 1,03% | 3 | 0,68% | 3 | 0,66% |
Anonyme (2023) | 4 | 0,15% | 1 | 0,21% | 0 | 0% | 1 | 0,22% |
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 | 0,82% | 4 | 0,91% | 4 | 0,88% |
Lowden (1986) | 4 | 0,15% | 3 | 0,62% | 3 | 0,68% | 3 | 0,66% |
Rouy (1912) | 4 | 0,15% | 0 | 0% | 0 | 0% | 0 | 0% |
Ter Steege et al. (2016) | 4 | 0,15% | 3 | 0,62% | 3 | 0,68% | 2 | 0,44% |
Tippery & Sokolik (2020) | 4 | 0,15% | 4 | 0,82% | 4 | 0,91% | 4 | 0,88% |
Tippery et al. (2024) | 4 | 0,15% | 4 | 0,82% | 4 | 0,91% | 4 | 0,88% |
Wiersema (1987) | 4 | 0,15% | 4 | 0,82% | 3 | 0,68% | 3 | 0,66% |
Anonyme (2014) | 3 | 0,11% | 3 | 0,62% | 3 | 0,68% | 2 | 0,44% |
Arcangeli (1882) | 3 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Boggan et al. (1992) | 3 | 0,11% | 2 | 0,41% | 2 | 0,45% | 2 | 0,44% |
Boreau (1857) | 3 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Bosser (1997) | 3 | 0,11% | 2 | 0,41% | 1 | 0,23% | 1 | 0,22% |
Bubani & Penzig (1902) | 3 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Candolle (1815) | 3 | 0,11% | 1 | 0,21% | 1 | 0,23% | 1 | 0,22% |
Den et al. (2020) | 3 | 0,11% | 2 | 0,41% | 2 | 0,45% | 2 | 0,44% |
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 | 0,41% | 2 | 0,45% | 2 | 0,44% |
Jérémie et al. (2001) | 3 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Lamarck (1783) | 3 | 0,11% | 1 | 0,21% | 1 | 0,23% | 1 | 0,22% |
Lamarck (1789) | 3 | 0,11% | 1 | 0,21% | 1 | 0,23% | 1 | 0,22% |
Meyer et al. (2006) | 3 | 0,11% | 1 | 0,21% | 1 | 0,23% | 1 | 0,22% |
Moench (1794) | 3 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Mori et al. (2002) | 3 | 0,11% | 3 | 0,62% | 3 | 0,68% | 3 | 0,66% |
Nelson-Smith et al. (2014) | 3 | 0,11% | 1 | 0,21% | 1 | 0,23% | 0 | 0% |
N'Yeurt & Payri (2004) | 3 | 0,11% | 3 | 0,62% | 3 | 0,68% | 3 | 0,66% |
Rouy (1909) | 3 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Royen (1953) | 3 | 0,11% | 1 | 0,21% | 1 | 0,23% | 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 | 0,62% | 3 | 0,68% | 3 | 0,66% |
Yang et al. (2012) | 3 | 0,11% | 3 | 0,62% | 3 | 0,68% | 3 | 0,66% |
Yuncker (1937) | 3 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Zuloaga et al. (2018) | 3 | 0,11% | 3 | 0,62% | 3 | 0,68% | 3 | 0,66% |
Ascherson & Graebner (1897) | 2 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Aublet (1775) | 2 | 0,07% | 2 | 0,41% | 2 | 0,45% | 1 | 0,22% |
Candolle (1821) | 2 | 0,07% | 1 | 0,21% | 1 | 0,23% | 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 | 0,21% | 1 | 0,23% | 1 | 0,22% |
Dumortier (1827) | 2 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Etcheberry & Abraham (2009) | 2 | 0,07% | 2 | 0,41% | 2 | 0,45% | 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 | 0,41% | 2 | 0,45% | 2 | 0,44% |
Kirschner (2002) | 2 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Lavergne (2011) | 2 | 0,07% | 1 | 0,21% | 1 | 0,23% | 1 | 0,22% |
Lemée (1953) | 2 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Martínez-y-Pérez et al. (2008) | 2 | 0,07% | 2 | 0,41% | 2 | 0,45% | 2 | 0,44% |
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 | 0,21% | 1 | 0,23% | 1 | 0,22% |
Mucina (2017) | 2 | 0,07% | 2 | 0,41% | 2 | 0,45% | 2 | 0,44% |
Oliveira & Bove (2015) | 2 | 0,07% | 1 | 0,21% | 1 | 0,23% | 1 | 0,22% |
Persoon (1805) | 2 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Royen (1954) | 2 | 0,07% | 1 | 0,21% | 1 | 0,23% | 1 | 0,22% |
Scatigna et al. (2022) | 2 | 0,07% | 2 | 0,41% | 2 | 0,45% | 2 | 0,44% |
Schultz (1848) | 2 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Scopoli (1771) | 2 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Willdenow (1799) | 2 | 0,07% | 0 | 0% | 0 | 0% | 0 | 0% |
Zardini & Raven (1991) | 2 | 0,07% | 1 | 0,21% | 1 | 0,23% | 1 | 0,22% |
Zuloaga et al. (2010) | 2 | 0,07% | 1 | 0,21% | 1 | 0,23% | 1 | 0,22% |
Zuloaga (2022) | 2 | 0,07% | 1 | 0,21% | 1 | 0,23% | 1 | 0,22% |
Akhani et al. (2014) | 1 | 0,04% | 1 | 0,21% | 1 | 0,23% | 1 | 0,22% |
Allen et al. (2022) | 1 | 0,04% | 1 | 0,21% | 1 | 0,23% | 0 | 0% |
Allioni (1785) | 1 | 0,04% | 1 | 0,21% | 1 | 0,23% | 1 | 0,22% |
Anonyme. (2002) | 1 | 0,04% | 1 | 0,21% | 1 | 0,23% | 1 | 0,22% |
Anonyme. (2002) | 1 | 0,04% | 1 | 0,21% | 1 | 0,23% | 1 | 0,22% |
Anonyme. (2002) | 1 | 0,04% | 1 | 0,21% | 1 | 0,23% | 1 | 0,22% |
Anonyme (2019) | 1 | 0,04% | 1 | 0,21% | 1 | 0,23% | 1 | 0,22% |
Batista et al. (2011) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Bock (2011) | 1 | 0,04% | 1 | 0,21% | 1 | 0,23% | 1 | 0,22% |
Bohley et al. (2017) | 1 | 0,04% | 1 | 0,21% | 1 | 0,23% | 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 | 0,21% | 0 | 0% | 1 | 0,22% |
Carrijo et al. (2012) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Chaix (1785) | 1 | 0,04% | 1 | 0,21% | 1 | 0,23% | 0 | 0% |
Champeau et al. (1991) | 1 | 0,04% | 1 | 0,21% | 1 | 0,23% | 1 | 0,22% |
Chau et al. (2020) | 1 | 0,04% | 1 | 0,21% | 1 | 0,23% | 1 | 0,22% |
Christenhusz et al. (2018) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Copeland (1932) | 1 | 0,04% | 1 | 0,21% | 1 | 0,23% | 1 | 0,22% |
Couhia & Fleurot (2016) | 1 | 0,04% | 1 | 0,21% | 1 | 0,23% | 1 | 0,22% |
Cremers & Boudrie (2007) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Cremers & Hoff (1990) | 1 | 0,04% | 1 | 0,21% | 1 | 0,23% | 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 | 0,21% | 1 | 0,23% | 1 | 0,22% |
Dauphin (1999) | 1 | 0,04% | 1 | 0,21% | 1 | 0,23% | 1 | 0,22% |
Delnatte et al. (2021) | 1 | 0,04% | 1 | 0,21% | 1 | 0,23% | 1 | 0,22% |
Don (1834) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Dunkel (2018) | 1 | 0,04% | 1 | 0,21% | 1 | 0,23% | 1 | 0,22% |
Emig (2007) | 1 | 0,04% | 1 | 0,21% | 1 | 0,23% | 1 | 0,22% |
Eppo (2011) | 1 | 0,04% | 1 | 0,21% | 1 | 0,23% | 1 | 0,22% |
Eppo (2011) | 1 | 0,04% | 1 | 0,21% | 1 | 0,23% | 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 | 0,21% | 0 | 0% | 1 | 0,22% |
Friis & Holt (2016) | 1 | 0,04% | 1 | 0,21% | 1 | 0,23% | 1 | 0,22% |
Gaertner (1788) | 1 | 0,04% | 1 | 0,21% | 1 | 0,23% | 1 | 0,22% |
Gagnon et al. (2016) | 1 | 0,04% | 1 | 0,21% | 1 | 0,23% | 1 | 0,22% |
Gaudin (1828) | 1 | 0,04% | 1 | 0,21% | 1 | 0,23% | 1 | 0,22% |
Geir (2018) | 1 | 0,04% | 1 | 0,21% | 1 | 0,23% | 1 | 0,22% |
Graham et al. (2021) | 1 | 0,04% | 1 | 0,21% | 1 | 0,23% | 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 | 0,21% | 1 | 0,23% | 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 | 0,21% | 1 | 0,23% | 1 | 0,22% |
Les (1986) | 1 | 0,04% | 1 | 0,21% | 1 | 0,23% | 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 | 0,21% | 1 | 0,23% | 1 | 0,22% |
Maddi (2014) | 1 | 0,04% | 1 | 0,21% | 1 | 0,23% | 1 | 0,22% |
Maréchal et al. (2013) | 1 | 0,04% | 1 | 0,21% | 1 | 0,23% | 1 | 0,22% |
Molino et al. (2009) | 1 | 0,04% | 1 | 0,21% | 1 | 0,23% | 1 | 0,22% |
Moore (1933) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Murdock & Smith (2003) | 1 | 0,04% | 1 | 0,21% | 1 | 0,23% | 1 | 0,22% |
Niebler, F. et al. (2021) | 1 | 0,04% | 1 | 0,21% | 1 | 0,23% | 1 | 0,22% |
Paradis & Miniconi (2011) | 1 | 0,04% | 1 | 0,21% | 1 | 0,23% | 1 | 0,22% |
Persoon (1807) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Petelczyc et al. (2006) | 1 | 0,04% | 1 | 0,21% | 1 | 0,23% | 0 | 0% |
Philbrick & Bove (2019) | 1 | 0,04% | 1 | 0,21% | 1 | 0,23% | 1 | 0,22% |
Pignal et al. (2022) | 1 | 0,04% | 1 | 0,21% | 1 | 0,23% | 1 | 0,22% |
Piirainen et al. (2017) | 1 | 0,04% | 1 | 0,21% | 1 | 0,23% | 1 | 0,22% |
Presl & Presl (1822) | 1 | 0,04% | 1 | 0,21% | 1 | 0,23% | 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 | 0,21% | 1 | 0,23% | 1 | 0,22% |
Proćków & Drábková (2023) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Questel (2017) | 1 | 0,04% | 1 | 0,21% | 1 | 0,23% | 1 | 0,22% |
Ragavan et al. (2014) | 1 | 0,04% | 1 | 0,21% | 1 | 0,23% | 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 | 0,21% | 1 | 0,23% | 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 | 0,21% | 1 | 0,23% | 1 | 0,22% |
Schenck (1905) | 1 | 0,04% | 1 | 0,21% | 1 | 0,23% | 1 | 0,22% |
Schur (1866) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Sennikov (2016) | 1 | 0,04% | 1 | 0,21% | 1 | 0,23% | 1 | 0,22% |
Sibthorp & Smith (1806-1809) | 1 | 0,04% | 1 | 0,21% | 1 | 0,23% | 1 | 0,22% |
Siljak-Yakovlev et al. (2020) | 1 | 0,04% | 1 | 0,21% | 1 | 0,23% | 1 | 0,22% |
Sramkó et al. (2016) | 1 | 0,04% | 1 | 0,21% | 1 | 0,23% | 1 | 0,22% |
Sukhorukov et al. (2018) | 1 | 0,04% | 1 | 0,21% | 0 | 0% | 1 | 0,22% |
Sweet (1826) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Takács et al. (2017) | 1 | 0,04% | 1 | 0,21% | 1 | 0,23% | 1 | 0,22% |
Taylor (1989) | 1 | 0,04% | 1 | 0,21% | 1 | 0,23% | 1 | 0,22% |
Tenore (1811-1815) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Thibaut et al. (2022) | 1 | 0,04% | 1 | 0,21% | 1 | 0,23% | 1 | 0,22% |
Thiébaut (2007) | 1 | 0,04% | 1 | 0,21% | 1 | 0,23% | 1 | 0,22% |
Toutain (1989) | 1 | 0,04% | 1 | 0,21% | 1 | 0,23% | 1 | 0,22% |
Van et al. (2022) | 1 | 0,04% | 1 | 0,21% | 1 | 0,23% | 1 | 0,22% |
Villars (1787) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Werkhoven (1986) | 1 | 0,04% | 1 | 0,21% | 1 | 0,23% | 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 | 0,21% | 1 | 0,23% | 1 | 0,22% |
Wilson (2022) | 1 | 0,04% | 0 | 0% | 0 | 0% | 0 | 0% |
Wood et al. (2020) | 1 | 0,04% | 1 | 0,21% | 1 | 0,23% | 1 | 0,22% |
Zhang et al. (2008) | 1 | 0,04% | 1 | 0,21% | 1 | 0,23% | 1 | 0,22% |
Zhang et al. (2013) | 1 | 0,04% | 1 | 0,21% | 1 | 0,23% | 1 | 0,22% |