Amphibiens exotiques envahissants
Tous les Amphibiens (Amphibia) introduits et envahissants (statut J) dans au moins l'un des territoires français.
146 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
| Référence | Total | Valides | Espèces | Taxons terminaux | ||||
|---|---|---|---|---|---|---|---|---|
| nb | % | nb | % | nb | % | nb | % | |
| Henderson & Breuil (2012) | 8 | 28,57% | 8 | 72,73% | 8 | 80% | 8 | 80% |
| Powell & Henderson (2023) | 5 | 17,86% | 4 | 36,36% | 4 | 40% | 4 | 40% |
| Breuil & Ibéné (2008) | 4 | 14,29% | 4 | 36,36% | 4 | 40% | 4 | 40% |
| Dewynter et al. (2019) | 4 | 14,29% | 4 | 36,36% | 4 | 40% | 4 | 40% |
| Dewynter et al. (2023) | 4 | 14,29% | 4 | 36,36% | 4 | 40% | 4 | 40% |
| Dewynter (2021) | 4 | 14,29% | 4 | 36,36% | 4 | 40% | 4 | 40% |
| González-sánchez et al. (2021) | 4 | 14,29% | 2 | 18,18% | 2 | 20% | 1 | 10% |
| Lescure & Marty (2000) | 4 | 14,29% | 3 | 27,27% | 3 | 30% | 3 | 30% |
| Lescure et al. (2012) | 4 | 14,29% | 2 | 18,18% | 1 | 10% | 1 | 10% |
| Lescure et al. (2022) | 4 | 14,29% | 4 | 36,36% | 4 | 40% | 4 | 40% |
| Uicn et al. (2017) | 4 | 14,29% | 4 | 36,36% | 4 | 40% | 4 | 40% |
| Arnold & Ovenden (2014) | 3 | 10,71% | 1 | 9,09% | 1 | 10% | 0 | 0% |
| Breuil (2009) | 3 | 10,71% | 2 | 18,18% | 2 | 20% | 2 | 20% |
| Easteal (1981) | 3 | 10,71% | 3 | 27,27% | 3 | 30% | 3 | 30% |
| Yokoyama (2013) | 3 | 10,71% | 2 | 18,18% | 2 | 20% | 2 | 20% |
| Altamirano-Benavides & Woolrich-Piña (2023) | 2 | 7,14% | 2 | 18,18% | 2 | 20% | 2 | 20% |
| Altamirano-benavides & Woolrich-piña (2023) | 2 | 7,14% | 2 | 18,18% | 2 | 20% | 2 | 20% |
| Bour et al. (2008) | 2 | 7,14% | 1 | 9,09% | 1 | 10% | 0 | 0% |
| Dewynter et al. (2017) | 2 | 7,14% | 2 | 18,18% | 2 | 20% | 2 | 20% |
| Dewynter et al. (2022) | 2 | 7,14% | 2 | 18,18% | 2 | 20% | 2 | 20% |
| Dewynter (2018) | 2 | 7,14% | 2 | 18,18% | 2 | 20% | 2 | 20% |
| Doniol-valcroze et al. (2021) | 2 | 7,14% | 2 | 18,18% | 2 | 20% | 2 | 20% |
| Dubois et al. (2021) | 2 | 7,14% | 2 | 18,18% | 2 | 20% | 2 | 20% |
| Ficetola & Scali (2010) | 2 | 7,14% | 1 | 9,09% | 1 | 10% | 0 | 0% |
| Hedges (2022) | 2 | 7,14% | 2 | 18,18% | 2 | 20% | 2 | 20% |
| Hill et al. (2020) | 2 | 7,14% | 2 | 18,18% | 2 | 20% | 0 | 0% |
| Ineich et al. (2015) | 2 | 7,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kruger et al. (2019) | 2 | 7,14% | 1 | 9,09% | 1 | 10% | 0 | 0% |
| Lowe et al. (2007) | 2 | 7,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Massary et al. (2019) | 2 | 7,14% | 1 | 9,09% | 1 | 10% | 0 | 0% |
| Massary et al. (2021) | 2 | 7,14% | 2 | 18,18% | 2 | 20% | 2 | 20% |
| Nicolas et al. (2015) | 2 | 7,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ouellet et al. (2012) | 2 | 7,14% | 1 | 9,09% | 1 | 10% | 0 | 0% |
| Speare (1990) | 2 | 7,14% | 0 | 0% | 0 | 0% | 0 | 0% |
| Yokoyama (2012) | 2 | 7,14% | 1 | 9,09% | 1 | 10% | 1 | 10% |
| Alfaia et al. (2020) | 1 | 3,57% | 0 | 0% | 0 | 0% | 0 | 0% |
| Alvarez-berríos et al. (2016) | 1 | 3,57% | 1 | 9,09% | 1 | 10% | 1 | 10% |
| Anderson et al. (2024) | 1 | 3,57% | 1 | 9,09% | 1 | 10% | 0 | 0% |
| Andino et al. (2024) | 1 | 3,57% | 1 | 9,09% | 1 | 10% | 0 | 0% |
| Andreone et al. (1987) | 1 | 3,57% | 0 | 0% | 0 | 0% | 0 | 0% |
| Araujo-vieira et al. (2020) | 1 | 3,57% | 0 | 0% | 0 | 0% | 0 | 0% |
| Augustine & Neff (2016) | 1 | 3,57% | 0 | 0% | 0 | 0% | 0 | 0% |
| Barbour (1914) | 1 | 3,57% | 1 | 9,09% | 1 | 10% | 1 | 10% |
| Bauer & Sadlier (2000) | 1 | 3,57% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bauer et al. (1997) | 1 | 3,57% | 0 | 0% | 0 | 0% | 0 | 0% |
| Béguin & Michelin (2012) | 1 | 3,57% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ben Hassine & Nouira (2009) | 1 | 3,57% | 1 | 9,09% | 1 | 10% | 1 | 10% |
| Bourgade (2020) | 1 | 3,57% | 1 | 9,09% | 1 | 10% | 1 | 10% |
| Bucol & Bucol (2019) | 1 | 3,57% | 0 | 0% | 0 | 0% | 0 | 0% |
| Cabana & Fernández (2010) | 1 | 3,57% | 0 | 0% | 0 | 0% | 0 | 0% |
| Castro et al. (2018) | 1 | 3,57% | 1 | 9,09% | 1 | 10% | 1 | 10% |
| CEN Nouvelle-Calédonie (2021) | 1 | 3,57% | 1 | 9,09% | 1 | 10% | 1 | 10% |
| Cope (1862) | 1 | 3,57% | 0 | 0% | 0 | 0% | 0 | 0% |
| Courant et al. (2018) | 1 | 3,57% | 1 | 9,09% | 1 | 10% | 0 | 0% |
| Courant et al. (2018) | 1 | 3,57% | 1 | 9,09% | 1 | 10% | 0 | 0% |
| Cubillos-abrahams et al. (2021) | 1 | 3,57% | 0 | 0% | 0 | 0% | 0 | 0% |
| Daly et al. (2023) | 1 | 3,57% | 0 | 0% | 0 | 0% | 0 | 0% |
| Daudin (1803) | 1 | 3,57% | 0 | 0% | 0 | 0% | 0 | 0% |
| Détaint & Coïc (2003) | 1 | 3,57% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dewynter et al. (2023) | 1 | 3,57% | 1 | 9,09% | 1 | 10% | 1 | 10% |
| Donini & Doody (2021) | 1 | 3,57% | 1 | 9,09% | 1 | 10% | 1 | 10% |
| Dória et al. (2015) | 1 | 3,57% | 1 | 9,09% | 1 | 10% | 1 | 10% |
| Driouche & Ziane (2022) | 1 | 3,57% | 1 | 9,09% | 1 | 10% | 1 | 10% |
| Dubois & Frétey (2016) | 1 | 3,57% | 1 | 9,09% | 1 | 10% | 1 | 10% |
| Dufresnes et al. (2024) | 1 | 3,57% | 1 | 9,09% | 1 | 10% | 1 | 10% |
| Dufresnes et al. (2024) | 1 | 3,57% | 1 | 9,09% | 1 | 10% | 1 | 10% |
| Duguet & Melki (2003) | 1 | 3,57% | 1 | 9,09% | 1 | 10% | 0 | 0% |
| Ernetti et al. (2024) | 1 | 3,57% | 1 | 9,09% | 1 | 10% | 1 | 10% |
| Ferrante et al. (2017) | 1 | 3,57% | 0 | 0% | 0 | 0% | 0 | 0% |
| Flechas et al. (2018) | 1 | 3,57% | 1 | 9,09% | 1 | 10% | 1 | 10% |
| Fraga & Carvalho (2021) | 1 | 3,57% | 1 | 9,09% | 1 | 10% | 1 | 10% |
| García-padrón & Quevedo (2022) | 1 | 3,57% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gargominy et al. (1996) | 1 | 3,57% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gérard et al. (2016) | 1 | 3,57% | 1 | 9,09% | 1 | 10% | 1 | 10% |
| Gill (1995) | 1 | 3,57% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ginal et al. (2021) | 1 | 3,57% | 1 | 9,09% | 1 | 10% | 0 | 0% |
| Girard (2007) | 1 | 3,57% | 1 | 9,09% | 1 | 10% | 1 | 10% |
| Gould et al. (2023) | 1 | 3,57% | 0 | 0% | 0 | 0% | 0 | 0% |
| Grano & Cattaneo (2014) | 1 | 3,57% | 0 | 0% | 0 | 0% | 0 | 0% |
| Grant-mackie et al. (2003) | 1 | 3,57% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hartert (1913) | 1 | 3,57% | 0 | 0% | 0 | 0% | 0 | 0% |
| Holsbeek et al. (2008) | 1 | 3,57% | 1 | 9,09% | 1 | 10% | 1 | 10% |
| Hong et al. (2022) | 1 | 3,57% | 0 | 0% | 0 | 0% | 0 | 0% |
| Horseman et al. (1976) | 1 | 3,57% | 0 | 0% | 0 | 0% | 0 | 0% |
| Hudson et al. (2018) | 1 | 3,57% | 1 | 9,09% | 1 | 10% | 1 | 10% |
| Hudson et al. (2021) | 1 | 3,57% | 1 | 9,09% | 1 | 10% | 1 | 10% |
| Kaiser & Hardy (1994) | 1 | 3,57% | 1 | 9,09% | 1 | 10% | 1 | 10% |
| Kirbiš et al. (2016) | 1 | 3,57% | 0 | 0% | 0 | 0% | 0 | 0% |
| Koch & Audebaud (2012) | 1 | 3,57% | 1 | 9,09% | 1 | 10% | 0 | 0% |
| Koch & Audebaud (2012) | 1 | 3,57% | 1 | 9,09% | 1 | 10% | 0 | 0% |
| Koo & Choe (2021) | 1 | 3,57% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kusrini et al. (2021) | 1 | 3,57% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kwet (2009) | 1 | 3,57% | 1 | 9,09% | 1 | 10% | 0 | 0% |
| Laurenti (1768) | 1 | 3,57% | 0 | 0% | 0 | 0% | 0 | 0% |
| Leonhardt et al. (2019) | 1 | 3,57% | 1 | 9,09% | 1 | 10% | 1 | 10% |
| Leonhardt et al. (2022) | 1 | 3,57% | 1 | 9,09% | 1 | 10% | 1 | 10% |
| Lesson (1830) | 1 | 3,57% | 0 | 0% | 0 | 0% | 0 | 0% |
| Linnaeus (1758) | 1 | 3,57% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lorrain-soligon & Secondi (2022) | 1 | 3,57% | 1 | 9,09% | 1 | 10% | 0 | 0% |
| Massary et al. (2017) | 1 | 3,57% | 1 | 9,09% | 1 | 10% | 1 | 10% |
| Massary et al. (2018) | 1 | 3,57% | 1 | 9,09% | 1 | 10% | 1 | 10% |
| Merlet & Trochet (2021) | 1 | 3,57% | 1 | 9,09% | 1 | 10% | 0 | 0% |
| Merlet & Trochet (2021) | 1 | 3,57% | 0 | 0% | 0 | 0% | 0 | 0% |
| Michelin & Béguin (2012) | 1 | 3,57% | 0 | 0% | 0 | 0% | 0 | 0% |
| Mo & Mo (2023) | 1 | 3,57% | 0 | 0% | 0 | 0% | 0 | 0% |
| Moravec et al. (2020) | 1 | 3,57% | 1 | 9,09% | 1 | 10% | 1 | 10% |
| Neveu (1997) | 1 | 3,57% | 0 | 0% | 0 | 0% | 0 | 0% |
| Ouellet (2008) | 1 | 3,57% | 0 | 0% | 0 | 0% | 0 | 0% |
| Park et al. (2022) | 1 | 3,57% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pauwels et al. (2023) | 1 | 3,57% | 1 | 9,09% | 1 | 10% | 0 | 0% |
| Pereira (2023) | 1 | 3,57% | 1 | 9,09% | 1 | 10% | 1 | 10% |
| Petit et al. (2021) | 1 | 3,57% | 0 | 0% | 0 | 0% | 0 | 0% |
| Pettit et al. (2021) | 1 | 3,57% | 1 | 9,09% | 1 | 10% | 1 | 10% |
| Pizzuti Piccoli & Cattaneo (2008) | 1 | 3,57% | 0 | 0% | 0 | 0% | 0 | 0% |
| Plötner et al. (2012) | 1 | 3,57% | 1 | 9,09% | 1 | 10% | 1 | 10% |
| Prado et al. (2023) | 1 | 3,57% | 1 | 9,09% | 1 | 10% | 1 | 10% |
| Questel & Le Quellec (2012) | 1 | 3,57% | 1 | 9,09% | 1 | 10% | 1 | 10% |
| Questel et al. (2023) | 1 | 3,57% | 1 | 9,09% | 1 | 10% | 1 | 10% |
| Questel et al. (2023) | 1 | 3,57% | 1 | 9,09% | 1 | 10% | 1 | 10% |
| Questel (2020) | 1 | 3,57% | 1 | 9,09% | 1 | 10% | 1 | 10% |
| Roux (1913) | 1 | 3,57% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sanz et al. (2023) | 1 | 3,57% | 0 | 0% | 0 | 0% | 0 | 0% |
| Saucedo et al. (2019) | 1 | 3,57% | 0 | 0% | 0 | 0% | 0 | 0% |
| Serre-collet (2013) | 1 | 3,57% | 1 | 9,09% | 1 | 10% | 0 | 0% |
| Shaw (1802) | 1 | 3,57% | 0 | 0% | 0 | 0% | 0 | 0% |
| Shine et al. (2021) | 1 | 3,57% | 1 | 9,09% | 1 | 10% | 1 | 10% |
| Shine (2010) | 1 | 3,57% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sonnini & Latreille (1801) | 1 | 3,57% | 0 | 0% | 0 | 0% | 0 | 0% |
| Spix (1824) | 1 | 3,57% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sy & Ibañes (2020) | 1 | 3,57% | 0 | 0% | 0 | 0% | 0 | 0% |
| Teunissen & Peters (2022) | 1 | 3,57% | 1 | 9,09% | 1 | 10% | 1 | 10% |
| Thirion & Evrard (2012) | 1 | 3,57% | 1 | 9,09% | 1 | 10% | 0 | 0% |
| Thirion & Fouquet (2003) | 1 | 3,57% | 1 | 9,09% | 1 | 10% | 0 | 0% |
| Touratier (1992) | 1 | 3,57% | 0 | 0% | 0 | 0% | 0 | 0% |
| Touratier (1992) | 1 | 3,57% | 0 | 0% | 0 | 0% | 0 | 0% |
| Urbina et al. (2018) | 1 | 3,57% | 0 | 0% | 0 | 0% | 0 | 0% |
| Valencia-zuleta et al. (2024) | 1 | 3,57% | 0 | 0% | 0 | 0% | 0 | 0% |
| van Doorn et al. (2022) | 1 | 3,57% | 1 | 9,09% | 1 | 10% | 0 | 0% |
| Vannini et al. (2015) | 1 | 3,57% | 0 | 0% | 0 | 0% | 0 | 0% |
| Vera-pérez et al. (2021) | 1 | 3,57% | 1 | 9,09% | 1 | 10% | 1 | 10% |
| Vieira (2022) | 1 | 3,57% | 1 | 9,09% | 1 | 10% | 1 | 10% |
| Vimercati et al. (2021) | 1 | 3,57% | 1 | 9,09% | 1 | 10% | 0 | 0% |
| Webb & Waddle (2022) | 1 | 3,57% | 0 | 0% | 0 | 0% | 0 | 0% |
| Yasumiba et al. (2015) | 1 | 3,57% | 1 | 9,09% | 1 | 10% | 1 | 10% |
| Yuan et al. (2022) | 1 | 3,57% | 1 | 9,09% | 1 | 10% | 1 | 10% |
| Zug & Zug (1979) | 1 | 3,57% | 0 | 0% | 0 | 0% | 0 | 0% |
