Algues rouges marines de France
Rhodophytes marines de France (métropole et outre-mer) : inclut les espèces strictement marines ainsi que celles pouvant également être trouvées en eau douce, en eau saumâtre ou à terre.
130 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) | 915 | 14,33% | 689 | 44,6% | 689 | 46,12% | 663 | 43,94% |
Burel et al. (2019) | 406 | 6,36% | 379 | 24,53% | 379 | 25,37% | 358 | 23,72% |
Payri (2007) | 212 | 3,32% | 168 | 10,87% | 168 | 11,24% | 163 | 10,8% |
N'Yeurt & Payri (2010) | 200 | 3,13% | 162 | 10,49% | 162 | 10,84% | 153 | 10,14% |
Delnatte & Wynne (2016) | 173 | 2,71% | 160 | 10,36% | 157 | 10,51% | 149 | 9,87% |
Silva et al. (1996) | 128 | 2,01% | 112 | 7,25% | 99 | 6,63% | 105 | 6,96% |
N'Yeurt & Payri (2004) | 118 | 1,85% | 90 | 5,83% | 90 | 6,02% | 87 | 5,77% |
Vroman (1968) | 93 | 1,46% | 55 | 3,56% | 55 | 3,68% | 52 | 3,45% |
Mattio et al. (2015) | 84 | 1,32% | 80 | 5,18% | 80 | 5,35% | 77 | 5,1% |
Rodríguez-Prieto et al. (1999) | 79 | 1,24% | 61 | 3,95% | 61 | 4,08% | 57 | 3,78% |
Bourmaud (2003) | 53 | 0,83% | 32 | 2,07% | 32 | 2,14% | 30 | 1,99% |
Rapport GIS "Lag-May" & Centre d'Océanologie de Marseille, pour le compte de DAF Mayotte, SPEM & FFEM. 126 pp.">Thomassin et al. (1999) | 53 | 0,83% | 37 | 2,39% | 37 | 2,48% | 35 | 2,32% |
Féral et al. (2021) | 52 | 0,81% | 50 | 3,24% | 50 | 3,35% | 50 | 3,31% |
Goulletquer (2016) | 50 | 0,78% | 41 | 2,65% | 41 | 2,74% | 39 | 2,58% |
Levring (1944) | 48 | 0,75% | 32 | 2,07% | 32 | 2,14% | 32 | 2,12% |
Payri & N'yeurt (1997) | 47 | 0,74% | 25 | 1,62% | 25 | 1,67% | 24 | 1,59% |
Nelson-Smith et al. (2014) | 46 | 0,72% | 27 | 1,75% | 27 | 1,81% | 22 | 1,46% |
Payri et al. (2009) | 40 | 0,63% | 32 | 2,07% | 32 | 2,14% | 32 | 2,12% |
Thomassin et al. (1992) | 37 | 0,58% | 19 | 1,23% | 19 | 1,27% | 18 | 1,19% |
CEVA (2011) | 23 | 0,36% | 14 | 0,91% | 14 | 0,94% | 13 | 0,86% |
Natural History Museum of London (2020) | 22 | 0,34% | 18 | 1,17% | 18 | 1,2% | 18 | 1,19% |
Rignault & Chevallier (2017) | 22 | 0,34% | 18 | 1,17% | 18 | 1,2% | 18 | 1,19% |
Brugneaux (2012) | 17 | 0,27% | 13 | 0,84% | 13 | 0,87% | 9 | 0,6% |
Zubia et al. (2018) | 16 | 0,25% | 16 | 1,04% | 15 | 1% | 16 | 1,06% |
Bijmoer et al. (2021) | 15 | 0,23% | 10 | 0,65% | 10 | 0,67% | 10 | 0,66% |
Nicet & Denis (2011) | 14 | 0,22% | 12 | 0,78% | 12 | 0,8% | 12 | 0,8% |
Rousseau et al. (2017) | 14 | 0,22% | 13 | 0,84% | 13 | 0,87% | 12 | 0,8% |
Segonzac (1984) | 13 | 0,2% | 3 | 0,19% | 3 | 0,2% | 3 | 0,2% |
Verlaque (2001) | 12 | 0,19% | 9 | 0,58% | 8 | 0,54% | 9 | 0,6% |
Mgnify (2018) | 11 | 0,17% | 11 | 0,71% | 11 | 0,74% | 11 | 0,73% |
Diaz & Cuzange (2009) | 9 | 0,14% | 6 | 0,39% | 6 | 0,4% | 6 | 0,4% |
MGnify (2017) | 9 | 0,14% | 9 | 0,58% | 9 | 0,6% | 9 | 0,6% |
Payri (comm. pers., 2012) | 8 | 0,13% | 8 | 0,52% | 8 | 0,54% | 8 | 0,53% |
Boudouresque et al. (2022) | 7 | 0,11% | 5 | 0,32% | 5 | 0,33% | 5 | 0,33% |
Orrell (2019) | 7 | 0,11% | 7 | 0,45% | 6 | 0,4% | 7 | 0,46% |
Dewarumez et al. (2011) | 6 | 0,09% | 5 | 0,32% | 5 | 0,33% | 5 | 0,33% |
Dizerbo & Herpe (2007) | 6 | 0,09% | 5 | 0,32% | 5 | 0,33% | 5 | 0,33% |
Fourt et al. (2017) | 6 | 0,09% | 4 | 0,26% | 4 | 0,27% | 4 | 0,27% |
Bressan & Cabioch (2004) | 5 | 0,08% | 4 | 0,26% | 4 | 0,27% | 4 | 0,27% |
Lin et al. (2013) | 5 | 0,08% | 5 | 0,32% | 5 | 0,33% | 5 | 0,33% |
Feldmann (1954) | 4 | 0,06% | 3 | 0,19% | 3 | 0,2% | 3 | 0,2% |
Hollenberg (1967) | 4 | 0,06% | 4 | 0,26% | 4 | 0,27% | 4 | 0,27% |
Piñeiro-corbeira et al. (2020) | 4 | 0,06% | 4 | 0,26% | 4 | 0,27% | 4 | 0,27% |
Verlaque et al. (2015) | 4 | 0,06% | 3 | 0,19% | 3 | 0,2% | 3 | 0,2% |
Beauchamp (1914) | 3 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
Boo et al. (2016) | 3 | 0,05% | 2 | 0,13% | 2 | 0,13% | 2 | 0,13% |
Bourcier (1988) | 3 | 0,05% | 2 | 0,13% | 2 | 0,13% | 1 | 0,07% |
Brugneaux & Pérès (2006) | 3 | 0,05% | 2 | 0,13% | 2 | 0,13% | 2 | 0,13% |
Cho et al. (2005) | 3 | 0,05% | 3 | 0,19% | 3 | 0,2% | 3 | 0,2% |
Payri, N'Yeurt & Orempuller (2000) | 3 | 0,05% | 1 | 0,06% | 1 | 0,07% | 1 | 0,07% |
Pearman et al. (2020) | 3 | 0,05% | 2 | 0,13% | 2 | 0,13% | 2 | 0,13% |
Bárbara et al. (2012) | 2 | 0,03% | 2 | 0,13% | 2 | 0,13% | 2 | 0,13% |
Caragnano et al. (2020) | 2 | 0,03% | 2 | 0,13% | 2 | 0,13% | 2 | 0,13% |
Crouan & Crouan (1858) | 2 | 0,03% | 1 | 0,06% | 1 | 0,07% | 1 | 0,07% |
D'archino et al. (2015) | 2 | 0,03% | 2 | 0,13% | 2 | 0,13% | 2 | 0,13% |
Diaz-Tapia et al. (2013) | 2 | 0,03% | 2 | 0,13% | 2 | 0,13% | 2 | 0,13% |
Etcheberry & Abraham (2009) | 2 | 0,03% | 2 | 0,13% | 2 | 0,13% | 2 | 0,13% |
Gabriel et al. (2017) | 2 | 0,03% | 2 | 0,13% | 2 | 0,13% | 2 | 0,13% |
Gall & Saunders (2010) | 2 | 0,03% | 2 | 0,13% | 2 | 0,13% | 2 | 0,13% |
Jeong et al. (2021) | 2 | 0,03% | 2 | 0,13% | 2 | 0,13% | 2 | 0,13% |
Klein & Verlaque (2011) | 2 | 0,03% | 2 | 0,13% | 2 | 0,13% | 2 | 0,13% |
L'hardy-halos & Maggs (1991) | 2 | 0,03% | 2 | 0,13% | 2 | 0,13% | 2 | 0,13% |
Montagne (1840) | 2 | 0,03% | 2 | 0,13% | 2 | 0,13% | 2 | 0,13% |
Nelson et al. (2013) | 2 | 0,03% | 1 | 0,06% | 1 | 0,07% | 1 | 0,07% |
N'Yeurt & Payri (2008) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Plouguerné et al. (2007) | 2 | 0,03% | 2 | 0,13% | 2 | 0,13% | 2 | 0,13% |
Rodríguez-prieto et al. (2018) | 2 | 0,03% | 2 | 0,13% | 2 | 0,13% | 2 | 0,13% |
Rodríguez-prieto et al. (2019) | 2 | 0,03% | 2 | 0,13% | 2 | 0,13% | 2 | 0,13% |
Rodríguez-prieto et al. (2020) | 2 | 0,03% | 2 | 0,13% | 2 | 0,13% | 2 | 0,13% |
Salomaki et al. (2014) | 2 | 0,03% | 2 | 0,13% | 2 | 0,13% | 2 | 0,13% |
Taylor (1973) | 2 | 0,03% | 1 | 0,06% | 1 | 0,07% | 1 | 0,07% |
The International Barcode of Life Consortium (2016) | 2 | 0,03% | 2 | 0,13% | 2 | 0,13% | 2 | 0,13% |
The Royal Botanic Gardens & Domain Trust (2021) | 2 | 0,03% | 2 | 0,13% | 2 | 0,13% | 2 | 0,13% |
Verlaque & Riouall (1989) | 2 | 0,03% | 1 | 0,06% | 1 | 0,07% | 1 | 0,07% |
Verlaque (2002) | 2 | 0,03% | 2 | 0,13% | 2 | 0,13% | 2 | 0,13% |
Zinoun et al. (1993) | 2 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
Aguirre et al. (2012) | 1 | 0,02% | 1 | 0,06% | 1 | 0,07% | 1 | 0,07% |
Arnaud (1964) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Augier et al. (1971) | 1 | 0,02% | 1 | 0,06% | 1 | 0,07% | 1 | 0,07% |
Baez et al. (2005) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Billard & Gayral (1972) | 1 | 0,02% | 1 | 0,06% | 1 | 0,07% | 1 | 0,07% |
Bottalico et al. (2015) | 1 | 0,02% | 1 | 0,06% | 1 | 0,07% | 1 | 0,07% |
Breton (2014) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Cabioch & Mendoza (2003) | 1 | 0,02% | 1 | 0,06% | 1 | 0,07% | 1 | 0,07% |
Chiasson & Vis (2014) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Coppejans (1979) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Cremades et al. (2011) | 1 | 0,02% | 1 | 0,06% | 1 | 0,07% | 1 | 0,07% |
European Nucleotide Archive (2019) | 1 | 0,02% | 1 | 0,06% | 1 | 0,07% | 1 | 0,07% |
Feldmann (1939) | 1 | 0,02% | 1 | 0,06% | 1 | 0,07% | 1 | 0,07% |
Feldmann (1943) | 1 | 0,02% | 1 | 0,06% | 1 | 0,07% | 1 | 0,07% |
Gall et al. (2018) | 1 | 0,02% | 1 | 0,06% | 1 | 0,07% | 1 | 0,07% |
Goulletquer et al. (2002) | 1 | 0,02% | 1 | 0,06% | 1 | 0,07% | 1 | 0,07% |
Gurgel et al. (2018) | 1 | 0,02% | 1 | 0,06% | 1 | 0,07% | 1 | 0,07% |
Hernandez-Kantun et al. (2015) | 1 | 0,02% | 1 | 0,06% | 1 | 0,07% | 1 | 0,07% |
Hughey et al. (2020) | 1 | 0,02% | 1 | 0,06% | 1 | 0,07% | 1 | 0,07% |
Ifremer (2020) | 1 | 0,02% | 1 | 0,06% | 1 | 0,07% | 1 | 0,07% |
Ifremer (2023) | 1 | 0,02% | 1 | 0,06% | 1 | 0,07% | 1 | 0,07% |
Kitayama & Garrigue (1998) | 1 | 0,02% | 1 | 0,06% | 1 | 0,07% | 1 | 0,07% |
Klein & Verlaque (2005) | 1 | 0,02% | 1 | 0,06% | 1 | 0,07% | 1 | 0,07% |
Kraft & Abbott (1998) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Le Duff & Gall (2015) | 1 | 0,02% | 1 | 0,06% | 1 | 0,07% | 1 | 0,07% |
Lee & Kim (2018) | 1 | 0,02% | 1 | 0,06% | 1 | 0,07% | 1 | 0,07% |
Lizé (2018) | 1 | 0,02% | 1 | 0,06% | 1 | 0,07% | 1 | 0,07% |
Lizé (2022) | 1 | 0,02% | 1 | 0,06% | 1 | 0,07% | 1 | 0,07% |
Manghisi et al. (2019) | 1 | 0,02% | 1 | 0,06% | 1 | 0,07% | 1 | 0,07% |
Maréchal & Trégarot (2012) | 1 | 0,02% | 1 | 0,06% | 1 | 0,07% | 1 | 0,07% |
Mateo-cid et al. (2014) | 1 | 0,02% | 1 | 0,06% | 1 | 0,07% | 1 | 0,07% |
Metti (2017) | 1 | 0,02% | 1 | 0,06% | 1 | 0,07% | 1 | 0,07% |
Mgnify (2019) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Mineur et al. (2012) | 1 | 0,02% | 1 | 0,06% | 1 | 0,07% | 1 | 0,07% |
Montagne (1838) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Müller (2004) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Muñoz et al. (2018) | 1 | 0,02% | 1 | 0,06% | 1 | 0,07% | 1 | 0,07% |
N’yeurt et al. (1995) | 1 | 0,02% | 1 | 0,06% | 1 | 0,07% | 1 | 0,07% |
N'Yeurt et al. (2006) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Payri et al. (2002) | 1 | 0,02% | 1 | 0,06% | 1 | 0,07% | 1 | 0,07% |
Peña et al. (2014) | 1 | 0,02% | 1 | 0,06% | 1 | 0,07% | 1 | 0,07% |
Peña et al. (2015) | 1 | 0,02% | 1 | 0,06% | 1 | 0,07% | 1 | 0,07% |
Pérez (1931) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Pestana et al. (2021) | 1 | 0,02% | 1 | 0,06% | 1 | 0,07% | 1 | 0,07% |
Pyle et al. (2016) | 1 | 0,02% | 1 | 0,06% | 1 | 0,07% | 1 | 0,07% |
Robuchon et al. (2014) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Rölsler et al. (2016) | 1 | 0,02% | 1 | 0,06% | 1 | 0,07% | 1 | 0,07% |
Sales & Ballesteros (2010) | 1 | 0,02% | 1 | 0,06% | 1 | 0,07% | 1 | 0,07% |
Saunders et al. (2017) | 1 | 0,02% | 1 | 0,06% | 1 | 0,07% | 1 | 0,07% |
Sjøtun et al. (2008) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Uicn et al. (2019) | 1 | 0,02% | 1 | 0,06% | 1 | 0,07% | 1 | 0,07% |
Vergés et al. (2014) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Verlaque et al. (1977) | 1 | 0,02% | 0 | 0% | 0 | 0% | 0 | 0% |
Yamada (1928) | 1 | 0,02% | 1 | 0,06% | 1 | 0,07% | 1 | 0,07% |