Algues vertes marines de métropole
81 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) | 318 | 18,17% | 226 | 75,59% | 226 | 80,14% | 215 | 74,65% |
Burel et al. (2019) | 117 | 6,69% | 113 | 37,79% | 113 | 40,07% | 108 | 37,5% |
Delnatte & Wynne (2016) | 28 | 1,6% | 27 | 9,03% | 27 | 9,57% | 26 | 9,03% |
Vroman (1968) | 20 | 1,14% | 12 | 4,01% | 12 | 4,26% | 11 | 3,82% |
N'Yeurt & Payri (2007) | 17 | 0,97% | 14 | 4,68% | 14 | 4,96% | 12 | 4,17% |
Payri (2007) | 17 | 0,97% | 13 | 4,35% | 13 | 4,61% | 12 | 4,17% |
Rodríguez-Prieto et al. (1999) | 17 | 0,97% | 12 | 4,01% | 12 | 4,26% | 12 | 4,17% |
Nelson-Smith et al. (2014) | 16 | 0,91% | 11 | 3,68% | 11 | 3,9% | 10 | 3,47% |
Knoepffler et al. (1990) | 15 | 0,86% | 9 | 3,01% | 9 | 3,19% | 8 | 2,78% |
Payri & N'yeurt (1997) | 14 | 0,8% | 3 | 1% | 3 | 1,06% | 3 | 1,04% |
MGnify (2017) | 13 | 0,74% | 13 | 4,35% | 13 | 4,61% | 13 | 4,51% |
Silva et al. (1996) | 13 | 0,74% | 8 | 2,68% | 8 | 2,84% | 8 | 2,78% |
Le Gallo (1949) | 10 | 0,57% | 5 | 1,67% | 5 | 1,77% | 4 | 1,39% |
Payri et al. (2009) | 9 | 0,51% | 9 | 3,01% | 9 | 3,19% | 7 | 2,43% |
N'Yeurt & Payri (2004) | 8 | 0,46% | 7 | 2,34% | 7 | 2,48% | 7 | 2,43% |
Pearman et al. (2020) | 8 | 0,46% | 7 | 2,34% | 7 | 2,48% | 6 | 2,08% |
Rapport GIS "Lag-May" & Centre d'Océanologie de Marseille, pour le compte de DAF Mayotte, SPEM & FFEM. 126 pp.">Thomassin et al. (1999) | 8 | 0,46% | 4 | 1,34% | 4 | 1,42% | 4 | 1,39% |
Verlaque (2001) | 8 | 0,46% | 7 | 2,34% | 7 | 2,48% | 6 | 2,08% |
Bijmoer et al. (2021) | 7 | 0,4% | 6 | 2,01% | 5 | 1,77% | 6 | 2,08% |
Goulletquer (2016) | 7 | 0,4% | 6 | 2,01% | 6 | 2,13% | 4 | 1,39% |
Vaulot et al. (2004) | 7 | 0,4% | 7 | 2,34% | 7 | 2,48% | 7 | 2,43% |
Toussaint et al. (2019) | 6 | 0,34% | 0 | 0% | 0 | 0% | 0 | 0% |
Alongi et al. (2014) | 5 | 0,29% | 4 | 1,34% | 3 | 1,06% | 4 | 1,39% |
Bourmaud (2003) | 5 | 0,29% | 2 | 0,67% | 2 | 0,71% | 1 | 0,35% |
Diaz & Cuzange (2009) | 5 | 0,29% | 5 | 1,67% | 5 | 1,77% | 5 | 1,74% |
Lagourgue et al. (2022) | 5 | 0,29% | 4 | 1,34% | 4 | 1,42% | 3 | 1,04% |
Mattio et al. (2015) | 5 | 0,29% | 5 | 1,67% | 5 | 1,77% | 4 | 1,39% |
Rignault & Chevallier (2017) | 5 | 0,29% | 4 | 1,34% | 4 | 1,42% | 4 | 1,39% |
Rimet (2011) | 5 | 0,29% | 3 | 1% | 3 | 1,06% | 3 | 1,04% |
Wynne & Furnari (2014) | 5 | 0,29% | 3 | 1% | 3 | 1,06% | 3 | 1,04% |
Brugneaux (2012) | 4 | 0,23% | 4 | 1,34% | 4 | 1,42% | 4 | 1,39% |
Darienko & Pröschold (2017) | 4 | 0,23% | 4 | 1,34% | 4 | 1,42% | 4 | 1,39% |
Etcheberry & Abraham (2009) | 4 | 0,23% | 3 | 1% | 3 | 1,06% | 2 | 0,69% |
Feldmann (1954) | 4 | 0,23% | 3 | 1% | 3 | 1,06% | 3 | 1,04% |
Fourt et al. (2017) | 4 | 0,23% | 4 | 1,34% | 4 | 1,42% | 4 | 1,39% |
Levring (1944) | 4 | 0,23% | 1 | 0,33% | 1 | 0,35% | 1 | 0,35% |
Buyck et al. (2021) | 3 | 0,17% | 3 | 1% | 3 | 1,06% | 3 | 1,04% |
Cachon & Caram (1979) | 3 | 0,17% | 3 | 1% | 3 | 1,06% | 3 | 1,04% |
Guilloux et al. (2013) | 3 | 0,17% | 3 | 1% | 3 | 1,06% | 3 | 1,04% |
Jacquet et al. (2008) | 3 | 0,17% | 1 | 0,33% | 1 | 0,35% | 1 | 0,35% |
Johns et al. (2022) | 3 | 0,17% | 3 | 1% | 3 | 1,06% | 3 | 1,04% |
Marin et al. (1996) | 3 | 0,17% | 3 | 1% | 3 | 1,06% | 3 | 1,04% |
Breton (2014) | 2 | 0,11% | 2 | 0,67% | 2 | 0,71% | 1 | 0,35% |
Cépède (1914) | 2 | 0,11% | 2 | 0,67% | 2 | 0,71% | 2 | 0,69% |
CEVA (2011) | 2 | 0,11% | 1 | 0,33% | 1 | 0,35% | 1 | 0,35% |
Chrétiennot-Dinet et al. (1995) | 2 | 0,11% | 2 | 0,67% | 2 | 0,71% | 2 | 0,69% |
Dangeard (1965) | 2 | 0,11% | 0 | 0% | 0 | 0% | 0 | 0% |
Dizerbo & Herpe (2007) | 2 | 0,11% | 1 | 0,33% | 1 | 0,35% | 1 | 0,35% |
Fort et al. (2020) | 2 | 0,11% | 1 | 0,33% | 1 | 0,35% | 1 | 0,35% |
Lopes et al. (2017) | 2 | 0,11% | 2 | 0,67% | 2 | 0,71% | 2 | 0,69% |
Mouronval et al. (2015) | 2 | 0,11% | 1 | 0,33% | 1 | 0,35% | 0 | 0% |
Müller (2004) | 2 | 0,11% | 1 | 0,33% | 1 | 0,35% | 1 | 0,35% |
Thomassin et al. (1992) | 2 | 0,11% | 1 | 0,33% | 1 | 0,35% | 1 | 0,35% |
Uicn et al. (2019) | 2 | 0,11% | 1 | 0,33% | 1 | 0,35% | 1 | 0,35% |
Wittrock (1866) | 2 | 0,11% | 2 | 0,67% | 2 | 0,71% | 2 | 0,69% |
Zubia et al. (2018) | 2 | 0,11% | 2 | 0,67% | 2 | 0,71% | 1 | 0,35% |
Androuin et al. (2020) | 1 | 0,06% | 1 | 0,33% | 1 | 0,35% | 1 | 0,35% |
Bárbara et al. (2012) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Comère (1912) | 1 | 0,06% | 1 | 0,33% | 1 | 0,35% | 1 | 0,35% |
Cormaci et al. (2014) | 1 | 0,06% | 1 | 0,33% | 1 | 0,35% | 1 | 0,35% |
Dewarumez et al. (2011) | 1 | 0,06% | 1 | 0,33% | 0 | 0% | 1 | 0,35% |
Guiry (2017) | 1 | 0,06% | 1 | 0,33% | 1 | 0,35% | 1 | 0,35% |
Horellou Arnaud | 1 | 0,06% | 1 | 0,33% | 1 | 0,35% | 1 | 0,35% |
Ifremer (2020) | 1 | 0,06% | 1 | 0,33% | 1 | 0,35% | 1 | 0,35% |
Kitayama & Garrigue (1998) | 1 | 0,06% | 1 | 0,33% | 1 | 0,35% | 1 | 0,35% |
Klein & Verlaque (2008) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Lambert et al. (2013) | 1 | 0,06% | 1 | 0,33% | 1 | 0,35% | 1 | 0,35% |
Lizé (2018) | 1 | 0,06% | 1 | 0,33% | 1 | 0,35% | 1 | 0,35% |
Lowe et al. (2007) | 1 | 0,06% | 1 | 0,33% | 1 | 0,35% | 1 | 0,35% |
Magne (1954) | 1 | 0,06% | 1 | 0,33% | 1 | 0,35% | 1 | 0,35% |
Maréchal & Trégarot (2012) | 1 | 0,06% | 1 | 0,33% | 1 | 0,35% | 1 | 0,35% |
Mgnify (2019) | 1 | 0,06% | 1 | 0,33% | 1 | 0,35% | 1 | 0,35% |
Möbius (1887) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Natural History Museum of London (2020) | 1 | 0,06% | 1 | 0,33% | 1 | 0,35% | 1 | 0,35% |
Orrell (2019) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Provan et al. (2008) | 1 | 0,06% | 1 | 0,33% | 1 | 0,35% | 0 | 0% |
Rossat (1955) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Sellier et al. (2016) | 1 | 0,06% | 1 | 0,33% | 1 | 0,35% | 0 | 0% |
Sir Alister Hardy Foundation for Ocean Science (2018) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Verlaque et al. (2015) | 1 | 0,06% | 1 | 0,33% | 1 | 0,35% | 1 | 0,35% |
Zubia et al. (2012) | 1 | 0,06% | 1 | 0,33% | 1 | 0,35% | 1 | 0,35% |