Algues marines du Pacifique
Algues marines (sens large) trouvées dans les îles françaises de l'océan Pacifique, c'est-à-dire en Nouvelle-Calédonie (NC), à Wallis-et-Futuna (WF), en Polynésie française (PF) et/ou à Clipperton (CLI) : inclut les espèces strictement marines (habitat 1) ou pouvant également être retrouvées en eau douce (habitat 4 = marin / eau douce), en eau saumâtre (habitat 6) ou à terre (habitat 5 = marin / terrestre).
130 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
| Référence | Total | Valides | Espèces | Taxons terminaux | ||||
|---|---|---|---|---|---|---|---|---|
| nb | % | nb | % | nb | % | nb | % | |
| Payri (2007) | 438 | 11,94% | 359 | 37,32% | 352 | 37,45% | 348 | 36,79% |
| N'Yeurt & Payri (2010) | 196 | 5,34% | 159 | 16,53% | 159 | 16,91% | 159 | 16,81% |
| N'Yeurt & Payri (2004) | 167 | 4,55% | 135 | 14,03% | 133 | 14,15% | 130 | 13,74% |
| Cabioc'h & Floc'h (2014) | 162 | 4,42% | 114 | 11,85% | 114 | 12,13% | 110 | 11,63% |
| Delnatte & Wynne (2016) | 127 | 3,46% | 119 | 12,37% | 116 | 12,34% | 112 | 11,84% |
| Mattio et al. (2015) | 124 | 3,38% | 122 | 12,68% | 119 | 12,66% | 114 | 12,05% |
| Vroman (1968) | 104 | 2,84% | 59 | 6,13% | 59 | 6,28% | 53 | 5,6% |
| Bourmaud (2003) | 98 | 2,67% | 69 | 7,17% | 69 | 7,34% | 65 | 6,87% |
| Payri & N'yeurt (1997) | 96 | 2,62% | 50 | 5,2% | 50 | 5,32% | 49 | 5,18% |
| Silva et al. (1996) | 89 | 2,43% | 67 | 6,96% | 66 | 7,02% | 65 | 6,87% |
| N'Yeurt & Payri (2007) | 77 | 2,1% | 66 | 6,86% | 61 | 6,49% | 59 | 6,24% |
| Rodríguez-Prieto et al. (1999) | 74 | 2,02% | 63 | 6,55% | 61 | 6,49% | 57 | 6,03% |
| Burel et al. (2019) | 69 | 1,88% | 68 | 7,07% | 68 | 7,23% | 66 | 6,98% |
| Payri et al. (2009) | 69 | 1,88% | 58 | 6,03% | 58 | 6,17% | 55 | 5,81% |
| Ricard (1985) | 69 | 1,88% | 39 | 4,05% | 34 | 3,62% | 38 | 4,02% |
| Rapport GIS "Lag-May" & Centre d'Océanologie de Marseille, pour le compte de DAF Mayotte, SPEM & FFEM. 126 pp.">Thomassin et al. (1999) | 58 | 1,58% | 40 | 4,16% | 39 | 4,15% | 39 | 4,12% |
| CEVA (2011) | 37 | 1,01% | 24 | 2,49% | 24 | 2,55% | 22 | 2,33% |
| Mgnify (2018) | 36 | 0,98% | 33 | 3,43% | 33 | 3,51% | 33 | 3,49% |
| Pearman et al. (2020) | 36 | 0,98% | 26 | 2,7% | 26 | 2,77% | 26 | 2,75% |
| Lagourgue et al. (2022) | 30 | 0,82% | 29 | 3,01% | 29 | 3,09% | 29 | 3,07% |
| N'Yeurt & Payri (2006) | 30 | 0,82% | 23 | 2,39% | 23 | 2,45% | 23 | 2,43% |
| Thomassin et al. (1992) | 27 | 0,74% | 12 | 1,25% | 12 | 1,28% | 12 | 1,27% |
| Vieira et al. (2014) | 25 | 0,68% | 24 | 2,49% | 24 | 2,55% | 24 | 2,54% |
| Brugneaux (2012) | 24 | 0,65% | 21 | 2,18% | 21 | 2,23% | 16 | 1,69% |
| Nelson-Smith et al. (2014) | 22 | 0,6% | 13 | 1,35% | 13 | 1,38% | 12 | 1,27% |
| Diaz & Cuzange (2009) | 21 | 0,57% | 20 | 2,08% | 20 | 2,13% | 17 | 1,8% |
| Zubia et al. (2018) | 21 | 0,57% | 20 | 2,08% | 20 | 2,13% | 19 | 2,01% |
| Fukuyo (1981) | 20 | 0,55% | 17 | 1,77% | 17 | 1,81% | 17 | 1,8% |
| Poupin et al. (1999) | 19 | 0,52% | 14 | 1,46% | 14 | 1,49% | 14 | 1,48% |
| Goulletquer (2016) | 18 | 0,49% | 18 | 1,87% | 18 | 1,91% | 17 | 1,8% |
| Payri (comm. pers., 2012) | 18 | 0,49% | 18 | 1,87% | 18 | 1,91% | 18 | 1,9% |
| Guilloux et al. (2013) | 10 | 0,27% | 3 | 0,31% | 3 | 0,32% | 2 | 0,21% |
| Rousseau et al. (2017) | 10 | 0,27% | 8 | 0,83% | 8 | 0,85% | 8 | 0,85% |
| Bijmoer et al. (2021) | 9 | 0,25% | 5 | 0,52% | 5 | 0,53% | 5 | 0,53% |
| Chinain et al. (1999) | 9 | 0,25% | 9 | 0,94% | 9 | 0,96% | 9 | 0,95% |
| Uicn et al. (2019) | 9 | 0,25% | 9 | 0,94% | 9 | 0,96% | 9 | 0,95% |
| Knoepffler et al. (1990) | 8 | 0,22% | 4 | 0,42% | 4 | 0,43% | 4 | 0,42% |
| Segonzac (1984) | 8 | 0,22% | 3 | 0,31% | 3 | 0,32% | 3 | 0,32% |
| Vieira et al. (2019) | 8 | 0,22% | 8 | 0,83% | 8 | 0,85% | 8 | 0,85% |
| Le Gallo (1949) | 7 | 0,19% | 3 | 0,31% | 3 | 0,32% | 3 | 0,32% |
| Litaker et al. (2009) | 7 | 0,19% | 7 | 0,73% | 7 | 0,74% | 7 | 0,74% |
| Nicet & Denis (2011) | 7 | 0,19% | 6 | 0,62% | 6 | 0,64% | 6 | 0,63% |
| Taylor (1973) | 6 | 0,16% | 3 | 0,31% | 2 | 0,21% | 3 | 0,32% |
| Cépède (1914) | 5 | 0,14% | 2 | 0,21% | 2 | 0,21% | 2 | 0,21% |
| Faust et al. (1996) | 5 | 0,14% | 5 | 0,52% | 5 | 0,53% | 5 | 0,53% |
| Lin et al. (2013) | 5 | 0,14% | 5 | 0,52% | 5 | 0,53% | 5 | 0,53% |
| Rignault & Chevallier (2017) | 5 | 0,14% | 5 | 0,52% | 5 | 0,53% | 5 | 0,53% |
| Belton et al. (2013) | 4 | 0,11% | 4 | 0,42% | 4 | 0,43% | 4 | 0,42% |
| Bourdeau et al. (1995) | 4 | 0,11% | 4 | 0,42% | 4 | 0,43% | 4 | 0,42% |
| Chinain et al. (1997) | 4 | 0,11% | 4 | 0,42% | 4 | 0,43% | 4 | 0,42% |
| Couté et al. (2012) | 4 | 0,11% | 4 | 0,42% | 1 | 0,11% | 3 | 0,32% |
| Etcheberry & Abraham (2009) | 4 | 0,11% | 3 | 0,31% | 3 | 0,32% | 3 | 0,32% |
| Fauré-Fremiet & Puigaudeau (1923) | 4 | 0,11% | 2 | 0,21% | 2 | 0,21% | 2 | 0,21% |
| Fourt et al. (2017) | 4 | 0,11% | 4 | 0,42% | 4 | 0,43% | 4 | 0,42% |
| Hollenberg (1967) | 4 | 0,11% | 4 | 0,42% | 4 | 0,43% | 4 | 0,42% |
| Kitayama & Garrigue (1998) | 4 | 0,11% | 4 | 0,42% | 4 | 0,43% | 4 | 0,42% |
| Lagourgue & Payri (2021) | 4 | 0,11% | 4 | 0,42% | 4 | 0,43% | 4 | 0,42% |
| Lopes et al. (2017) | 4 | 0,11% | 4 | 0,42% | 4 | 0,43% | 4 | 0,42% |
| Mattio & Payri (2009) | 4 | 0,11% | 4 | 0,42% | 4 | 0,43% | 4 | 0,42% |
| MGnify (2017) | 4 | 0,11% | 4 | 0,42% | 4 | 0,43% | 4 | 0,42% |
| Payri, N'Yeurt & Orempuller (2000) | 4 | 0,11% | 2 | 0,21% | 2 | 0,21% | 2 | 0,21% |
| Verlaque (2001) | 4 | 0,11% | 4 | 0,42% | 4 | 0,43% | 4 | 0,42% |
| Chomérat et al. (2019) | 3 | 0,08% | 3 | 0,31% | 3 | 0,32% | 3 | 0,32% |
| Dijoux et al. (2012) | 3 | 0,08% | 3 | 0,31% | 3 | 0,32% | 3 | 0,32% |
| Littler & Littler (1992) | 3 | 0,08% | 3 | 0,31% | 3 | 0,32% | 3 | 0,32% |
| Natural History Museum of London (2020) | 3 | 0,08% | 3 | 0,31% | 3 | 0,32% | 3 | 0,32% |
| Pyle et al. (2016) | 3 | 0,08% | 3 | 0,31% | 3 | 0,32% | 3 | 0,32% |
| Vaulot et al. (2004) | 3 | 0,08% | 3 | 0,31% | 3 | 0,32% | 3 | 0,32% |
| , 7(4): 59-81.">Balech (1994) | 2 | 0,05% | 2 | 0,21% | 2 | 0,21% | 2 | 0,21% |
| Brugneaux & Pérès (2006) | 2 | 0,05% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
| Cho et al. (2005) | 2 | 0,05% | 2 | 0,21% | 2 | 0,21% | 2 | 0,21% |
| Couté et al. (2009) | 2 | 0,05% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
| D'archino et al. (2015) | 2 | 0,05% | 2 | 0,21% | 2 | 0,21% | 2 | 0,21% |
| Dragesco (1965) | 2 | 0,05% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
| Fauré-fremiet (1910) | 2 | 0,05% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
| Gabriel et al. (2017) | 2 | 0,05% | 2 | 0,21% | 2 | 0,21% | 2 | 0,21% |
| Grzebyk et al. (1994) | 2 | 0,05% | 2 | 0,21% | 2 | 0,21% | 2 | 0,21% |
| Grzebyk et al. (1998) | 2 | 0,05% | 2 | 0,21% | 2 | 0,21% | 2 | 0,21% |
| Hédouin et al. (2008) | 2 | 0,05% | 2 | 0,21% | 2 | 0,21% | 2 | 0,21% |
| Huisman et al. (2018) | 2 | 0,05% | 2 | 0,21% | 2 | 0,21% | 2 | 0,21% |
| Ifremer (2019) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Maréchal & Trégarot (2012) | 2 | 0,05% | 2 | 0,21% | 2 | 0,21% | 2 | 0,21% |
| Mattio et al. (2008) | 2 | 0,05% | 2 | 0,21% | 2 | 0,21% | 2 | 0,21% |
| Mattio et al. (2013) | 2 | 0,05% | 2 | 0,21% | 2 | 0,21% | 2 | 0,21% |
| Montagne (1840) | 2 | 0,05% | 2 | 0,21% | 2 | 0,21% | 2 | 0,21% |
| Nelson et al. (2013) | 2 | 0,05% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
| Nguyen-ngoc et al. (2021) | 2 | 0,05% | 2 | 0,21% | 2 | 0,21% | 2 | 0,21% |
| N'Yeurt & Payri (2008) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Payri et al. (2002) | 2 | 0,05% | 2 | 0,21% | 2 | 0,21% | 2 | 0,21% |
| Puigaudeau (1923) | 2 | 0,05% | 0 | 0% | 0 | 0% | 0 | 0% |
| Quod et al. (1999) | 2 | 0,05% | 2 | 0,21% | 2 | 0,21% | 2 | 0,21% |
| The Royal Botanic Gardens & Domain Trust (2021) | 2 | 0,05% | 2 | 0,21% | 2 | 0,21% | 2 | 0,21% |
| Tichadou et al. (2010) | 2 | 0,05% | 2 | 0,21% | 2 | 0,21% | 2 | 0,21% |
| Zubia et al. (2012) | 2 | 0,05% | 2 | 0,21% | 2 | 0,21% | 2 | 0,21% |
| Adachi & Fukuyo (1979) | 1 | 0,03% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
| Affe et al. (2019) | 1 | 0,03% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
| Berland & Grzebyk (1991) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Boisseau & Lubet (1955) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Chacana & Silva (2014) | 1 | 0,03% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
| Chomerat et al. (2017) | 1 | 0,03% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
| Cuénot (1890-1891) | 1 | 0,03% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
| Dewarumez et al. (2011) | 1 | 0,03% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
| Earle (1969) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Feldmann (1939) | 1 | 0,03% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
| Feldmann (1954) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Gómez & Artigas (2014) | 1 | 0,03% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
| Grzebyk et al. (1997) | 1 | 0,03% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
| Horellou Arnaud | 1 | 0,03% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
| Hulburt (1957) | 1 | 0,03% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
| Inoue (1983) | 1 | 0,03% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
| Klein & Verlaque (2008) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kraft & Abbott (1998) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Le Duff & Gall (2015) | 1 | 0,03% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
| Levring (1944) | 1 | 0,03% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
| Lizé (2018) | 1 | 0,03% | 1 | 0,1% | 1 | 0,11% | 0 | 0% |
| Lizé (2018) | 1 | 0,03% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
| Lowe et al. (2007) | 1 | 0,03% | 1 | 0,1% | 1 | 0,11% | 0 | 0% |
| Mateo-cid et al. (2014) | 1 | 0,03% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
| Metti (2017) | 1 | 0,03% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
| Müller (2004) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| N’yeurt et al. (1995) | 1 | 0,03% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
| N'Yeurt et al. (2006) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Orrell (2019) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Santiañez et al. (2018) | 1 | 0,03% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
| Schultz et al. (2015) | 1 | 0,03% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
| Ten-Hage et al. (2000) | 1 | 0,03% | 0 | 0% | 0 | 0% | 0 | 0% |
| Tunin‐Ley et al. (2007) | 1 | 0,03% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
| Vacelet (1982) | 1 | 0,03% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
| Vidal et al. (1984) | 1 | 0,03% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
| Vieira et al. (2019) | 1 | 0,03% | 1 | 0,1% | 1 | 0,11% | 1 | 0,11% |
