Espèces animales introduites dans l'océan Indien
Animaux introduits au sens large dans l'océan Indien, c'est-à-dire introduits établis (I), invasifs (J), introduits non établis (M) ou introduits éteints (Y). Par "océan Indien" on entend: la Réunion, Mayotte et les îles Éparses.
76 outil(s) de détermination permet(tent) d'identifier des taxons de ce groupe.
Référence | Total | Valides | Espèces | Taxons terminaux | ||||
---|---|---|---|---|---|---|---|---|
nb | % | nb | % | nb | % | nb | % | |
Welter-schultes (2012) | 18 | 0.56% | 13 | 1.69% | 13 | 1.78% | 13 | 1.75% |
Lebas et al. (2016) | 17 | 0.53% | 15 | 1.96% | 15 | 2.05% | 15 | 2.02% |
Sanchez (2020) | 17 | 0.53% | 17 | 2.22% | 17 | 2.32% | 15 | 2.02% |
Kerney & Cameron (1999) | 15 | 0.47% | 11 | 1.43% | 11 | 1.5% | 11 | 1.48% |
Martiré & Rochat (2008) | 13 | 0.4% | 10 | 1.3% | 8 | 1.09% | 10 | 1.34% |
Albouy & Richard (2017) | 12 | 0.37% | 11 | 1.43% | 11 | 1.5% | 10 | 1.34% |
Delannoye et al. (2015) | 11 | 0.34% | 7 | 0.91% | 7 | 0.96% | 7 | 0.94% |
Aulagnier et al. (2017) | 10 | 0.31% | 10 | 1.3% | 10 | 1.37% | 9 | 1.21% |
Chaezl & Chazel (2011) | 8 | 0.25% | 8 | 1.04% | 8 | 1.09% | 7 | 0.94% |
Hullé et al. (2018) | 8 | 0.25% | 8 | 1.04% | 8 | 1.09% | 8 | 1.08% |
Gargominy (2011-2023) | 7 | 0.22% | 7 | 0.91% | 7 | 0.96% | 7 | 0.94% |
Gargominy (2016-2025) | 6 | 0.19% | 6 | 0.78% | 6 | 0.82% | 6 | 0.81% |
Albouy et al. (2017) | 5 | 0.16% | 5 | 0.65% | 5 | 0.68% | 4 | 0.54% |
Dewynter et al. (2022) | 5 | 0.16% | 5 | 0.65% | 5 | 0.68% | 3 | 0.4% |
Dewynter et al. (2023) | 5 | 0.16% | 5 | 0.65% | 5 | 0.68% | 3 | 0.4% |
Questel et al. (2023) | 5 | 0.16% | 5 | 0.65% | 5 | 0.68% | 3 | 0.4% |
Questel et al. (2023) | 5 | 0.16% | 5 | 0.65% | 5 | 0.68% | 3 | 0.4% |
Bellmann (2019) | 4 | 0.12% | 4 | 0.52% | 4 | 0.55% | 3 | 0.4% |
Leraut (2014) | 4 | 0.12% | 4 | 0.52% | 4 | 0.55% | 4 | 0.54% |
Maran & Frétey (2023) | 4 | 0.12% | 4 | 0.52% | 4 | 0.55% | 4 | 0.54% |
Mériguet & Zagatti (2016) | 4 | 0.12% | 4 | 0.52% | 4 | 0.55% | 3 | 0.4% |
de Massary et al. (2015) | 3 | 0.09% | 3 | 0.39% | 3 | 0.41% | 2 | 0.27% |
Dewynter et al. (2023) | 3 | 0.09% | 3 | 0.39% | 3 | 0.41% | 1 | 0.13% |
Gerber (2018) | 3 | 0.09% | 3 | 0.39% | 3 | 0.41% | 3 | 0.4% |
Muratet (2015) | 3 | 0.09% | 2 | 0.26% | 1 | 0.14% | 1 | 0.13% |
. SFEPM, Bourges. 56 pp. ">Rigaux & Dupasquier (2012) | 3 | 0.09% | 3 | 0.39% | 3 | 0.41% | 2 | 0.27% |
Arnold & Ovenden (2014) | 2 | 0.06% | 2 | 0.26% | 2 | 0.27% | 1 | 0.13% |
Aubouin et al. (2016) | 2 | 0.06% | 2 | 0.26% | 2 | 0.27% | 2 | 0.27% |
Breuil (2013) | 2 | 0.06% | 1 | 0.13% | 1 | 0.14% | 0 | 0% |
Dubos et al. (2023) | 2 | 0.06% | 2 | 0.26% | 2 | 0.27% | 1 | 0.13% |
Gabriac et al. (2024) | 2 | 0.06% | 2 | 0.26% | 2 | 0.27% | 2 | 0.27% |
Heidemann & Seidenbusch (2002) | 2 | 0.06% | 1 | 0.13% | 1 | 0.14% | 1 | 0.13% |
Le Coeur et al. (2023) | 2 | 0.06% | 2 | 0.26% | 2 | 0.27% | 1 | 0.13% |
Leraut (2012) | 2 | 0.06% | 1 | 0.13% | 1 | 0.14% | 0 | 0% |
Lichtenfels et al. (1994) | 2 | 0.06% | 2 | 0.26% | 2 | 0.27% | 2 | 0.27% |
Light (1932) | 2 | 0.06% | 0 | 0% | 0 | 0% | 0 | 0% |
Meurgey & Picard (2011) | 2 | 0.06% | 2 | 0.26% | 2 | 0.27% | 2 | 0.27% |
Nelson-Smith et al. (2014) | 2 | 0.06% | 2 | 0.26% | 2 | 0.27% | 2 | 0.27% |
Roberts (2014) | 2 | 0.06% | 0 | 0% | 0 | 0% | 0 | 0% |
Zaremski et al. (2011) | 2 | 0.06% | 1 | 0.13% | 1 | 0.14% | 1 | 0.13% |
Bochaton et al. (2016) | 1 | 0.03% | 1 | 0.13% | 1 | 0.14% | 0 | 0% |
Cazals & Dupont (2022) | 1 | 0.03% | 1 | 0.13% | 1 | 0.14% | 1 | 0.13% |
Chalumeau (1983) | 1 | 0.03% | 1 | 0.13% | 1 | 0.14% | 1 | 0.13% |
Cheon et al. (2023) | 1 | 0.03% | 1 | 0.13% | 0 | 0% | 1 | 0.13% |
Cochard et al. (2021) | 1 | 0.03% | 1 | 0.13% | 1 | 0.14% | 1 | 0.13% |
Csősz et al. (2023) | 1 | 0.03% | 1 | 0.13% | 1 | 0.14% | 1 | 0.13% |
Denys et al. (2024) | 1 | 0.03% | 1 | 0.13% | 1 | 0.14% | 1 | 0.13% |
Dewynter & Claessens (2020) | 1 | 0.03% | 1 | 0.13% | 1 | 0.14% | 1 | 0.13% |
Dewynter et al. (2019) | 1 | 0.03% | 1 | 0.13% | 1 | 0.14% | 0 | 0% |
Dewynter et al. (2020) | 1 | 0.03% | 1 | 0.13% | 1 | 0.14% | 1 | 0.13% |
Dijkstra et al. (2015) | 1 | 0.03% | 1 | 0.13% | 1 | 0.14% | 1 | 0.13% |
Doucet (2016) | 1 | 0.03% | 1 | 0.13% | 1 | 0.14% | 1 | 0.13% |
Dusoulier et al. (2025) | 1 | 0.03% | 1 | 0.13% | 1 | 0.14% | 1 | 0.13% |
Fabre & Orsini (2016) | 1 | 0.03% | 1 | 0.13% | 1 | 0.14% | 1 | 0.13% |
Flores et al. (2024) | 1 | 0.03% | 1 | 0.13% | 1 | 0.14% | 1 | 0.13% |
Furminieux (2019) | 1 | 0.03% | 1 | 0.13% | 1 | 0.14% | 1 | 0.13% |
Grand & Boudot (2007) | 1 | 0.03% | 1 | 0.13% | 1 | 0.14% | 1 | 0.13% |
Grand et al. (2014) | 1 | 0.03% | 1 | 0.13% | 1 | 0.14% | 1 | 0.13% |
Grech-Angelini et al. (2019) | 1 | 0.03% | 1 | 0.13% | 1 | 0.14% | 1 | 0.13% |
Iorio et al. (2022) | 1 | 0.03% | 1 | 0.13% | 1 | 0.14% | 1 | 0.13% |
Jacquiet et al. (1997) | 1 | 0.03% | 1 | 0.13% | 1 | 0.14% | 1 | 0.13% |
Johnson et al. (2021) | 1 | 0.03% | 1 | 0.13% | 1 | 0.14% | 1 | 0.13% |
Jouveau et al. (2018) | 1 | 0.03% | 1 | 0.13% | 1 | 0.14% | 0 | 0% |
Lafranchis (2014) | 1 | 0.03% | 1 | 0.13% | 1 | 0.14% | 1 | 0.13% |
Lafranchis (2016) | 1 | 0.03% | 1 | 0.13% | 1 | 0.14% | 1 | 0.13% |
Lehrter et al. (2016) | 1 | 0.03% | 1 | 0.13% | 1 | 0.14% | 1 | 0.13% |
Lü & Zhou (2012) | 1 | 0.03% | 1 | 0.13% | 1 | 0.14% | 1 | 0.13% |
Lupoli & Dusoulier (2015) | 1 | 0.03% | 1 | 0.13% | 1 | 0.14% | 1 | 0.13% |
Lupoli (2023) | 1 | 0.03% | 1 | 0.13% | 1 | 0.14% | 1 | 0.13% |
Martin (2011) | 1 | 0.03% | 1 | 0.13% | 1 | 0.14% | 1 | 0.13% |
Probst et al. (1999) | 1 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Sardet et al. (2015) | 1 | 0.03% | 1 | 0.13% | 1 | 0.14% | 1 | 0.13% |
Skrjabin (1942) | 1 | 0.03% | 0 | 0% | 0 | 0% | 0 | 0% |
Souza et al. (2019) | 1 | 0.03% | 1 | 0.13% | 1 | 0.14% | 1 | 0.13% |
Wallach (2020) | 1 | 0.03% | 1 | 0.13% | 1 | 0.14% | 1 | 0.13% |
Yadav et al. (2021) | 1 | 0.03% | 1 | 0.13% | 1 | 0.14% | 1 | 0.13% |