Espèces introduites naturalisées voire invasives en métropole
Toutes les espèces introduites et établies/naturalisées (I), voire envahissantes (J) en France métropolitaine
75 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) | 1497 | 11.76% | 894 | 31.66% | 807 | 31.03% | 777 | 29.49% |
| Cabioc'h & Floc'h (2014) | 121 | 0.95% | 92 | 3.26% | 92 | 3.54% | 89 | 3.38% |
| Nelson-Smith et al. (2014) | 38 | 0.3% | 25 | 0.89% | 25 | 0.96% | 24 | 0.91% |
| Welter-schultes (2012) | 24 | 0.19% | 18 | 0.64% | 18 | 0.69% | 14 | 0.53% |
| Aulagnier et al. (2017) | 18 | 0.14% | 18 | 0.64% | 18 | 0.69% | 13 | 0.49% |
| Arnold & Ovenden (2014) | 14 | 0.11% | 9 | 0.32% | 9 | 0.35% | 2 | 0.08% |
| Gargominy (2011-2023) | 13 | 0.1% | 13 | 0.46% | 8 | 0.31% | 13 | 0.49% |
| Kerney & Cameron (1999) | 13 | 0.1% | 10 | 0.35% | 10 | 0.38% | 6 | 0.23% |
| Leraut (2014) | 13 | 0.1% | 12 | 0.42% | 12 | 0.46% | 12 | 0.46% |
| Prié (2017) | 11 | 0.09% | 11 | 0.39% | 9 | 0.35% | 9 | 0.34% |
| Albouy & Richard (2017) | 10 | 0.08% | 9 | 0.32% | 9 | 0.35% | 9 | 0.34% |
| Bay-nouailhat & Bay-nouailhat (2020) | 10 | 0.08% | 10 | 0.35% | 10 | 0.38% | 10 | 0.38% |
| Gerber (2018) | 8 | 0.06% | 7 | 0.25% | 7 | 0.27% | 6 | 0.23% |
| Hullé et al. (2018) | 8 | 0.06% | 8 | 0.28% | 8 | 0.31% | 7 | 0.27% |
| Martin (2011) | 8 | 0.06% | 6 | 0.21% | 6 | 0.23% | 6 | 0.23% |
| André et al. (2020) | 7 | 0.05% | 7 | 0.25% | 7 | 0.27% | 7 | 0.27% |
| Lebas et al. (2016) | 6 | 0.05% | 6 | 0.21% | 6 | 0.23% | 6 | 0.23% |
| Martiré & Rochat (2008) | 6 | 0.05% | 5 | 0.18% | 5 | 0.19% | 5 | 0.19% |
| Albouy et al. (2017) | 5 | 0.04% | 5 | 0.18% | 5 | 0.19% | 5 | 0.19% |
| de Massary et al. (2015) | 5 | 0.04% | 5 | 0.18% | 5 | 0.19% | 1 | 0.04% |
| Delannoye et al. (2015) | 5 | 0.04% | 3 | 0.11% | 3 | 0.12% | 3 | 0.11% |
| Meynard (2011) | 5 | 0.04% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Muratet (2015) | 5 | 0.04% | 5 | 0.18% | 3 | 0.12% | 3 | 0.11% |
| Aubouin et al. (2016) | 4 | 0.03% | 4 | 0.14% | 4 | 0.15% | 2 | 0.08% |
| Duguet & Melki (2003) | 4 | 0.03% | 3 | 0.11% | 3 | 0.12% | 0 | 0% |
| Iorio et al. (2022) | 4 | 0.03% | 4 | 0.14% | 4 | 0.15% | 4 | 0.15% |
| Jouveau et al. (2018) | 4 | 0.03% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
| Maran & Frétey (2023) | 4 | 0.03% | 4 | 0.14% | 3 | 0.12% | 2 | 0.08% |
| Sardet et al. (2015) | 4 | 0.03% | 3 | 0.11% | 3 | 0.12% | 3 | 0.11% |
| Séguy (1944) | 4 | 0.03% | 3 | 0.11% | 3 | 0.12% | 1 | 0.04% |
| Bellmann (2019) | 3 | 0.02% | 3 | 0.11% | 3 | 0.12% | 2 | 0.08% |
| Kwet (2009) | 3 | 0.02% | 3 | 0.11% | 3 | 0.12% | 0 | 0% |
| Leraut (2012) | 3 | 0.02% | 3 | 0.11% | 3 | 0.12% | 3 | 0.11% |
| Mériguet & Zagatti (2016) | 3 | 0.02% | 3 | 0.11% | 3 | 0.12% | 3 | 0.11% |
| Serre-collet (2013) | 3 | 0.02% | 3 | 0.11% | 3 | 0.12% | 0 | 0% |
| Thirion & Evrard (2012) | 3 | 0.02% | 3 | 0.11% | 3 | 0.12% | 0 | 0% |
| Bonadona (1981) | 2 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
| Hugonnot et al. (2017) | 2 | 0.02% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
| Lafranchis (2016) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 2 | 0.08% |
| Miaud & Muratet (2018) | 2 | 0.02% | 2 | 0.07% | 2 | 0.08% | 0 | 0% |
| Amoros (1980) | 1 | 0.01% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
| Anderson (1949) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cazals & Dupont (2022) | 1 | 0.01% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
| Chalumeau (1983) | 1 | 0.01% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
| Cheon et al. (2023) | 1 | 0.01% | 1 | 0.04% | 0 | 0% | 1 | 0.04% |
| D'Aguilar & Martinez (1979) | 1 | 0.01% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
| Dewynter et al. (2019) | 1 | 0.01% | 1 | 0.04% | 1 | 0.04% | 0 | 0% |
| Dewynter et al. (2022) | 1 | 0.01% | 1 | 0.04% | 1 | 0.04% | 0 | 0% |
| Dewynter et al. (2023) | 1 | 0.01% | 1 | 0.04% | 1 | 0.04% | 0 | 0% |
| Dewynter et al. (2023) | 1 | 0.01% | 1 | 0.04% | 1 | 0.04% | 0 | 0% |
| Ducarme (2023) | 1 | 0.01% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
| Dyrynda et al. (2000) | 1 | 0.01% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
| Fourt et al. (2017) | 1 | 0.01% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
| Furminieux (2019) | 1 | 0.01% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
| Gouillieux (2018) | 1 | 0.01% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
| Greigert et al. (2019) | 1 | 0.01% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
| Grisebach (1864) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Halstead & Green (1979) | 1 | 0.01% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
| Halstead (1973) | 1 | 0.01% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
| Herrmann & Hava (2006) | 1 | 0.01% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
| Huchet & Labatut (2022) | 1 | 0.01% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
| Kadej et al. (2013) | 1 | 0.01% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
| Koch (1837) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kurochkin (2005) | 1 | 0.01% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
| Lafranchis (2014) | 1 | 0.01% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
| Latry et al. (2024) | 1 | 0.01% | 1 | 0.04% | 0 | 0% | 1 | 0.04% |
| Lupoli & Dusoulier (2015) | 1 | 0.01% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
| Majka et al. (2009) | 1 | 0.01% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
| Peacock (1976) | 1 | 0.01% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
| Questel et al. (2023) | 1 | 0.01% | 1 | 0.04% | 1 | 0.04% | 0 | 0% |
| Questel et al. (2023) | 1 | 0.01% | 1 | 0.04% | 1 | 0.04% | 0 | 0% |
| Rome (2016) | 1 | 0.01% | 1 | 0.04% | 1 | 0.04% | 0 | 0% |
| Sant (2022) | 1 | 0.01% | 0 | 0% | 0 | 0% | 0 | 0% |
| Secq et al. (2023) | 1 | 0.01% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
| Yadav et al. (2021) | 1 | 0.01% | 1 | 0.04% | 1 | 0.04% | 1 | 0.04% |
