Espèces végétales marines introduites
Plantes marines (au sens large) introduites dans un moins l'un des territoires français. Par marine, on entend : marine (1), marine et d'eau douce (2), marine et terrestre (5) ou d'eau saumâtre (6). Par introduite, on entend : introduites naturalisées (I), invasives (J), introduites non naturalisées (M) ou introduites éteintes (Y) en France métropolitaine et/ou en outre-mer.
77 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
| Référence | Total | Valides | Espèces | Taxons terminaux | ||||
|---|---|---|---|---|---|---|---|---|
| nb | % | nb | % | nb | % | nb | % | |
| Cabioc'h & Floc'h (2014) | 121 | 23,09% | 92 | 80% | 92 | 83,64% | 89 | 79,46% |
| Goulletquer (2016) | 53 | 10,11% | 45 | 39,13% | 45 | 40,91% | 42 | 37,5% |
| Burel et al. (2019) | 43 | 8,21% | 41 | 35,65% | 41 | 37,27% | 39 | 34,82% |
| Rignault & Chevallier (2017) | 28 | 5,34% | 23 | 20% | 23 | 20,91% | 23 | 20,54% |
| Delnatte & Wynne (2016) | 19 | 3,63% | 18 | 15,65% | 18 | 16,36% | 18 | 16,07% |
| Vroman (1968) | 17 | 3,24% | 13 | 11,3% | 13 | 11,82% | 12 | 10,71% |
| Payri (2007) | 16 | 3,05% | 12 | 10,43% | 12 | 10,91% | 11 | 9,82% |
| Rodríguez-Prieto et al. (1999) | 14 | 2,67% | 13 | 11,3% | 13 | 11,82% | 13 | 11,61% |
| Verlaque (2001) | 13 | 2,48% | 11 | 9,57% | 10 | 9,09% | 10 | 8,93% |
| N'Yeurt & Payri (2004) | 10 | 1,91% | 7 | 6,09% | 7 | 6,36% | 7 | 6,25% |
| N'Yeurt & Payri (2010) | 10 | 1,91% | 9 | 7,83% | 9 | 8,18% | 9 | 8,04% |
| Bourmaud (2003) | 9 | 1,72% | 6 | 5,22% | 6 | 5,45% | 5 | 4,46% |
| Mattio et al. (2015) | 8 | 1,53% | 7 | 6,09% | 7 | 6,36% | 7 | 6,25% |
| Dewarumez et al. (2011) | 7 | 1,34% | 6 | 5,22% | 5 | 4,55% | 6 | 5,36% |
| Rapport GIS "Lag-May" & Centre d'Océanologie de Marseille, pour le compte de DAF Mayotte, SPEM & FFEM. 126 pp.">Thomassin et al. (1999) | 7 | 1,34% | 4 | 3,48% | 4 | 3,64% | 4 | 3,57% |
| N'Yeurt & Payri (2007) | 6 | 1,15% | 3 | 2,61% | 3 | 2,73% | 2 | 1,79% |
| Payri et al. (2009) | 6 | 1,15% | 6 | 5,22% | 6 | 5,45% | 5 | 4,46% |
| Silva et al. (1996) | 6 | 1,15% | 5 | 4,35% | 5 | 4,55% | 5 | 4,46% |
| Lagourgue et al. (2022) | 5 | 0,95% | 5 | 4,35% | 5 | 4,55% | 4 | 3,57% |
| Morat et al. (2012) | 5 | 0,95% | 4 | 3,48% | 4 | 3,64% | 4 | 3,57% |
| Munzinger et al. (2016) | 5 | 0,95% | 4 | 3,48% | 4 | 3,64% | 4 | 3,57% |
| Tison et al. (2014) | 5 | 0,95% | 4 | 3,48% | 4 | 3,64% | 4 | 3,57% |
| Verlaque et al. (2015) | 5 | 0,95% | 4 | 3,48% | 4 | 3,64% | 4 | 3,57% |
| CEVA (2011) | 4 | 0,76% | 3 | 2,61% | 3 | 2,73% | 3 | 2,68% |
| Fournet (2002) | 4 | 0,76% | 4 | 3,48% | 4 | 3,64% | 4 | 3,57% |
| Knoepffler et al. (1990) | 4 | 0,76% | 2 | 1,74% | 2 | 1,82% | 2 | 1,79% |
| Uicn et al. (2019) | 4 | 0,76% | 3 | 2,61% | 3 | 2,73% | 3 | 2,68% |
| Brugneaux (2012) | 3 | 0,57% | 2 | 1,74% | 2 | 1,82% | 2 | 1,79% |
| Payri & N'yeurt (1997) | 3 | 0,57% | 0 | 0% | 0 | 0% | 0 | 0% |
| Thomassin et al. (1992) | 3 | 0,57% | 0 | 0% | 0 | 0% | 0 | 0% |
| Willette et al. (2014) | 3 | 0,57% | 3 | 2,61% | 3 | 2,73% | 3 | 2,68% |
| Fourt et al. (2017) | 2 | 0,38% | 2 | 1,74% | 2 | 1,82% | 2 | 1,79% |
| Nelson-Smith et al. (2014) | 2 | 0,38% | 2 | 1,74% | 2 | 1,82% | 1 | 0,89% |
| Pearman et al. (2020) | 2 | 0,38% | 1 | 0,87% | 1 | 0,91% | 1 | 0,89% |
| Plouguerné et al. (2007) | 2 | 0,38% | 2 | 1,74% | 2 | 1,82% | 2 | 1,79% |
| Rousseau et al. (2017) | 2 | 0,38% | 2 | 1,74% | 2 | 1,82% | 2 | 1,79% |
| Verlaque & Riouall (1989) | 2 | 0,38% | 1 | 0,87% | 1 | 0,91% | 1 | 0,89% |
| Verlaque (2002) | 2 | 0,38% | 2 | 1,74% | 2 | 1,82% | 2 | 1,79% |
| Akhani et al. (2014) | 1 | 0,19% | 1 | 0,87% | 1 | 0,91% | 1 | 0,89% |
| Bárbara et al. (2012) | 1 | 0,19% | 1 | 0,87% | 1 | 0,91% | 1 | 0,89% |
| Bijmoer et al. (2021) | 1 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
| Boudouresque et al. (2024) | 1 | 0,19% | 1 | 0,87% | 1 | 0,91% | 1 | 0,89% |
| Cho et al. (2005) | 1 | 0,19% | 1 | 0,87% | 1 | 0,91% | 1 | 0,89% |
| Dauphin (1999) | 1 | 0,19% | 1 | 0,87% | 1 | 0,91% | 1 | 0,89% |
| Diaz & Cuzange (2009) | 1 | 0,19% | 1 | 0,87% | 1 | 0,91% | 1 | 0,89% |
| Etcheberry & Abraham (2009) | 1 | 0,19% | 1 | 0,87% | 1 | 0,91% | 0 | 0% |
| Feldmann (1954) | 1 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
| Fort et al. (2020) | 1 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
| Funk et al. (2007) | 1 | 0,19% | 1 | 0,87% | 1 | 0,91% | 1 | 0,89% |
| Goulletquer et al. (2002) | 1 | 0,19% | 1 | 0,87% | 1 | 0,91% | 1 | 0,89% |
| Gurgel et al. (2018) | 1 | 0,19% | 1 | 0,87% | 1 | 0,91% | 1 | 0,89% |
| Hequet & Le Corre (2010) | 1 | 0,19% | 1 | 0,87% | 1 | 0,91% | 1 | 0,89% |
| Hequet et al. (2009) | 1 | 0,19% | 1 | 0,87% | 1 | 0,91% | 1 | 0,89% |
| Hily et al. (2010) | 1 | 0,19% | 1 | 0,87% | 1 | 0,91% | 1 | 0,89% |
| Klein & Verlaque (2005) | 1 | 0,19% | 1 | 0,87% | 1 | 0,91% | 1 | 0,89% |
| Klein & Verlaque (2008) | 1 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lamarck (1779) | 1 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
| Le Duff & Gall (2015) | 1 | 0,19% | 1 | 0,87% | 1 | 0,91% | 1 | 0,89% |
| Le Gallo (1949) | 1 | 0,19% | 1 | 0,87% | 1 | 0,91% | 0 | 0% |
| Levring (1944) | 1 | 0,19% | 1 | 0,87% | 1 | 0,91% | 1 | 0,89% |
| Linnaeus (1753) | 1 | 0,19% | 1 | 0,87% | 1 | 0,91% | 1 | 0,89% |
| Lizé (2018) | 1 | 0,19% | 1 | 0,87% | 1 | 0,91% | 1 | 0,89% |
| Lizé (2018) | 1 | 0,19% | 1 | 0,87% | 1 | 0,91% | 1 | 0,89% |
| Lizé (2022) | 1 | 0,19% | 1 | 0,87% | 1 | 0,91% | 1 | 0,89% |
| Lowe et al. (2007) | 1 | 0,19% | 1 | 0,87% | 1 | 0,91% | 1 | 0,89% |
| MacKee (1994) | 1 | 0,19% | 1 | 0,87% | 1 | 0,91% | 1 | 0,89% |
| Maréchal et al. (2013) | 1 | 0,19% | 1 | 0,87% | 1 | 0,91% | 1 | 0,89% |
| Mineur et al. (2012) | 1 | 0,19% | 1 | 0,87% | 1 | 0,91% | 1 | 0,89% |
| Moench (1794) | 1 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
| Provan et al. (2008) | 1 | 0,19% | 1 | 0,87% | 1 | 0,91% | 0 | 0% |
| Questel (2017) | 1 | 0,19% | 1 | 0,87% | 1 | 0,91% | 1 | 0,89% |
| Salisbury (1796) | 1 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sellier et al. (2016) | 1 | 0,19% | 1 | 0,87% | 1 | 0,91% | 0 | 0% |
| Sjøtun et al. (2008) | 1 | 0,19% | 0 | 0% | 0 | 0% | 0 | 0% |
| Thibaut et al. (2022) | 1 | 0,19% | 1 | 0,87% | 1 | 0,91% | 1 | 0,89% |
| Thiébaut (2007) | 1 | 0,19% | 1 | 0,87% | 1 | 0,91% | 1 | 0,89% |
| Yamada (1928) | 1 | 0,19% | 1 | 0,87% | 1 | 0,91% | 1 | 0,89% |
