Espèces exotiques envahissantes (EEE)
Toutes les espèces introduites et envahissantes (J) dans au moins l'un des territoires français.
82 outil(s) de détermination permet(tent) d'identifier des taxons de ce groupe.
Référence | Total | Valides | Espèces | Taxons terminaux | ||||
---|---|---|---|---|---|---|---|---|
nb | % | nb | % | nb | % | nb | % | |
Tison et al. (2014) | 175 | 4.71% | 96 | 15.14% | 93 | 15.58% | 89 | 14.86% |
Aulagnier et al. (2017) | 15 | 0.4% | 13 | 2.05% | 13 | 2.18% | 12 | 2% |
Nelson-Smith et al. (2014) | 15 | 0.4% | 9 | 1.42% | 9 | 1.51% | 9 | 1.5% |
Cabioc'h & Floc'h (2014) | 13 | 0.35% | 11 | 1.74% | 11 | 1.84% | 11 | 1.84% |
Chaezl & Chazel (2011) | 12 | 0.32% | 12 | 1.89% | 12 | 2.01% | 11 | 1.84% |
Muus et al. (2015) | 12 | 0.32% | 3 | 0.47% | 3 | 0.5% | 3 | 0.5% |
Svensson et al. (2023) | 11 | 0.3% | 10 | 1.58% | 10 | 1.68% | 10 | 1.67% |
Delannoye et al. (2015) | 8 | 0.22% | 6 | 0.95% | 6 | 1.01% | 6 | 1% |
Angin et al. (2024) | 7 | 0.19% | 6 | 0.95% | 6 | 1.01% | 5 | 0.83% |
Dewynter et al. (2023) | 7 | 0.19% | 7 | 1.1% | 7 | 1.17% | 6 | 1% |
Folschweiller et al. (2020) | 7 | 0.19% | 7 | 1.1% | 7 | 1.17% | 6 | 1% |
Leraut & Blanchot (2012) | 7 | 0.19% | 6 | 0.95% | 6 | 1.01% | 6 | 1% |
Welter-schultes (2012) | 7 | 0.19% | 6 | 0.95% | 6 | 1.01% | 6 | 1% |
Bay-nouailhat & Bay-nouailhat (2020) | 6 | 0.16% | 6 | 0.95% | 6 | 1.01% | 6 | 1% |
Hullé et al. (2018) | 6 | 0.16% | 6 | 0.95% | 6 | 1.01% | 6 | 1% |
Lebas et al. (2016) | 6 | 0.16% | 6 | 0.95% | 6 | 1.01% | 6 | 1% |
Prié (2017) | 6 | 0.16% | 6 | 0.95% | 5 | 0.84% | 5 | 0.83% |
Sanchez (2020) | 6 | 0.16% | 6 | 0.95% | 6 | 1.01% | 5 | 0.83% |
Dewynter et al. (2022) | 5 | 0.13% | 5 | 0.79% | 5 | 0.84% | 4 | 0.67% |
Dewynter et al. (2023) | 5 | 0.13% | 5 | 0.79% | 5 | 0.84% | 4 | 0.67% |
Martin (2011) | 5 | 0.13% | 3 | 0.47% | 3 | 0.5% | 3 | 0.5% |
Questel et al. (2023) | 5 | 0.13% | 5 | 0.79% | 5 | 0.84% | 4 | 0.67% |
Questel et al. (2023) | 5 | 0.13% | 5 | 0.79% | 5 | 0.84% | 4 | 0.67% |
Arnold & Ovenden (2014) | 4 | 0.11% | 2 | 0.32% | 2 | 0.34% | 0 | 0% |
Dewynter (2021) | 4 | 0.11% | 4 | 0.63% | 4 | 0.67% | 4 | 0.67% |
Fouquet et al. (2024) | 4 | 0.11% | 4 | 0.63% | 4 | 0.67% | 4 | 0.67% |
Kerney & Cameron (1999) | 4 | 0.11% | 3 | 0.47% | 3 | 0.5% | 3 | 0.5% |
Quéré & Louarn (2011) | 4 | 0.11% | 3 | 0.47% | 3 | 0.5% | 3 | 0.5% |
. SFEPM, Bourges. 56 pp. ">Rigaux & Dupasquier (2012) | 4 | 0.11% | 4 | 0.63% | 4 | 0.67% | 4 | 0.67% |
Aubouin et al. (2016) | 3 | 0.08% | 3 | 0.47% | 3 | 0.5% | 3 | 0.5% |
Gerber (2018) | 3 | 0.08% | 3 | 0.47% | 3 | 0.5% | 3 | 0.5% |
Jouveau et al. (2018) | 3 | 0.08% | 0 | 0% | 0 | 0% | 0 | 0% |
Kerney & Cameron (2015) | 3 | 0.08% | 3 | 0.47% | 3 | 0.5% | 3 | 0.5% |
Lamand & Prié (2017) | 3 | 0.08% | 3 | 0.47% | 3 | 0.5% | 2 | 0.33% |
Meynard (2011) | 3 | 0.08% | 2 | 0.32% | 2 | 0.34% | 2 | 0.33% |
Albouy et al. (2017) | 2 | 0.05% | 2 | 0.32% | 2 | 0.34% | 2 | 0.33% |
Barabé & Gibernau (2015) | 2 | 0.05% | 2 | 0.32% | 2 | 0.34% | 2 | 0.33% |
Bellmann (2019) | 2 | 0.05% | 2 | 0.32% | 2 | 0.34% | 1 | 0.17% |
Bochaton et al. (2016) | 2 | 0.05% | 2 | 0.32% | 2 | 0.34% | 2 | 0.33% |
Breuil (2013) | 2 | 0.05% | 1 | 0.16% | 1 | 0.17% | 1 | 0.17% |
Dewynter et al. (2017) | 2 | 0.05% | 2 | 0.32% | 2 | 0.34% | 2 | 0.33% |
Dewynter (2018) | 2 | 0.05% | 2 | 0.32% | 2 | 0.34% | 2 | 0.33% |
Dubos et al. (2023) | 2 | 0.05% | 2 | 0.32% | 2 | 0.34% | 1 | 0.17% |
Gargominy (2011-2023) | 2 | 0.05% | 2 | 0.32% | 2 | 0.34% | 2 | 0.33% |
Leraut (2012) | 2 | 0.05% | 2 | 0.32% | 2 | 0.34% | 2 | 0.33% |
Muratet (2015) | 2 | 0.05% | 2 | 0.32% | 1 | 0.17% | 1 | 0.17% |
Wegnez et al. (2013) | 2 | 0.05% | 2 | 0.32% | 2 | 0.34% | 2 | 0.33% |
Albouy & Richard (2017) | 1 | 0.03% | 1 | 0.16% | 1 | 0.17% | 1 | 0.17% |
Cazals & Dupont (2022) | 1 | 0.03% | 1 | 0.16% | 1 | 0.17% | 1 | 0.17% |
Cheon et al. (2023) | 1 | 0.03% | 1 | 0.16% | 0 | 0% | 1 | 0.17% |
Compte (2025) | 1 | 0.03% | 1 | 0.16% | 1 | 0.17% | 1 | 0.17% |
Cox (1970) | 1 | 0.03% | 1 | 0.16% | 1 | 0.17% | 1 | 0.17% |
de Massary et al. (2015) | 1 | 0.03% | 1 | 0.16% | 1 | 0.17% | 0 | 0% |
Dewynter & Claessens (2020) | 1 | 0.03% | 1 | 0.16% | 1 | 0.17% | 1 | 0.17% |
Dewynter et al. (2019) | 1 | 0.03% | 1 | 0.16% | 1 | 0.17% | 0 | 0% |
Duguet & Melki (2003) | 1 | 0.03% | 1 | 0.16% | 1 | 0.17% | 0 | 0% |
Dusoulier et al. (2025) | 1 | 0.03% | 1 | 0.16% | 1 | 0.17% | 1 | 0.17% |
Dyrynda et al. (2000) | 1 | 0.03% | 1 | 0.16% | 1 | 0.17% | 1 | 0.17% |
Fabre & Orsini (2016) | 1 | 0.03% | 1 | 0.16% | 1 | 0.17% | 1 | 0.17% |
Flores et al. (2024) | 1 | 0.03% | 1 | 0.16% | 1 | 0.17% | 1 | 0.17% |
Flores et al. (2024) | 1 | 0.03% | 1 | 0.16% | 1 | 0.17% | 1 | 0.17% |
Fourt et al. (2017) | 1 | 0.03% | 1 | 0.16% | 1 | 0.17% | 1 | 0.17% |
Gargominy (2016-2025) | 1 | 0.03% | 1 | 0.16% | 1 | 0.17% | 1 | 0.17% |
Hugonnot et al. (2017) | 1 | 0.03% | 1 | 0.16% | 1 | 0.17% | 1 | 0.17% |
Kwet (2009) | 1 | 0.03% | 1 | 0.16% | 1 | 0.17% | 0 | 0% |
Lafranchis (2014) | 1 | 0.03% | 1 | 0.16% | 1 | 0.17% | 1 | 0.17% |
Lafranchis (2016) | 1 | 0.03% | 1 | 0.16% | 1 | 0.17% | 1 | 0.17% |
Leraut (2014) | 1 | 0.03% | 1 | 0.16% | 1 | 0.17% | 1 | 0.17% |
Light (1932) | 1 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Lupoli & Dusoulier (2015) | 1 | 0.03% | 1 | 0.16% | 1 | 0.17% | 1 | 0.17% |
Lupoli (2023) | 1 | 0.03% | 1 | 0.16% | 1 | 0.17% | 1 | 0.17% |
Martiré & Rochat (2008) | 1 | 0.03% | 1 | 0.16% | 1 | 0.17% | 1 | 0.17% |
Mériguet & Zagatti (2016) | 1 | 0.03% | 1 | 0.16% | 1 | 0.17% | 1 | 0.17% |
Probst et al. (1999) | 1 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Rome (2016) | 1 | 0.03% | 1 | 0.16% | 1 | 0.17% | 0 | 0% |
Sant (2022) | 1 | 0.03% | 1 | 0.16% | 1 | 0.17% | 1 | 0.17% |
Serre-collet (2013) | 1 | 0.03% | 1 | 0.16% | 1 | 0.17% | 0 | 0% |
Starace (2013) | 1 | 0.03% | 1 | 0.16% | 1 | 0.17% | 1 | 0.17% |
Thirion & Evrard (2012) | 1 | 0.03% | 1 | 0.16% | 1 | 0.17% | 0 | 0% |
Tolman & Lewington (2015) | 1 | 0.03% | 1 | 0.16% | 1 | 0.17% | 1 | 0.17% |
Tolman & Lewington (2021) | 1 | 0.03% | 1 | 0.16% | 1 | 0.17% | 1 | 0.17% |
Zaremski et al. (2011) | 1 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |