Angiospermes des îles Éparses
Magnoliidae des îles Éparses
147 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
Référence | Total | Valides | Espèces | Taxons terminaux | ||||
---|---|---|---|---|---|---|---|---|
nb | % | nb | % | nb | % | nb | % | |
Fournet (2002) | 405 | 24,27% | 316 | 125,4% | 312 | 138,05% | 280 | 122,27% |
Boullet et al. (2018) | 208 | 12,46% | 193 | 76,59% | 177 | 78,32% | 186 | 81,22% |
Funk et al. (2007) | 194 | 11,62% | 79 | 31,35% | 78 | 34,51% | 68 | 29,69% |
Munzinger et al. (2016) | 159 | 9,53% | 50 | 19,84% | 48 | 21,24% | 45 | 19,65% |
Molino et al. (2022) | 93 | 5,57% | 5 | 1,98% | 5 | 2,21% | 4 | 1,75% |
Morat et al. (2012) | 93 | 5,57% | 50 | 19,84% | 48 | 21,24% | 45 | 19,65% |
Hequet & Le Corre (2010) | 87 | 5,21% | 72 | 28,57% | 70 | 30,97% | 62 | 27,07% |
Hequet et al. (2009) | 87 | 5,21% | 72 | 28,57% | 70 | 30,97% | 62 | 27,07% |
MacKee (1994) | 83 | 4,97% | 67 | 26,59% | 65 | 28,76% | 58 | 25,33% |
Tison et al. (2014) | 81 | 4,85% | 51 | 20,24% | 49 | 21,68% | 47 | 20,52% |
Fourdrigniez & Meyer (2008) | 69 | 4,13% | 53 | 21,03% | 51 | 22,57% | 46 | 20,09% |
Morat & Veillon (1985) | 62 | 3,71% | 52 | 20,63% | 50 | 22,12% | 41 | 17,9% |
Acevedo-Rodríguez & Strong (2012) | 44 | 2,64% | 23 | 9,13% | 23 | 10,18% | 16 | 6,99% |
Delnatte & Meyer (2012) | 38 | 2,28% | 30 | 11,9% | 30 | 13,27% | 24 | 10,48% |
Anonyme (2014) | 28 | 1,68% | 22 | 8,73% | 22 | 9,73% | 20 | 8,73% |
Porter-Utley (2014) | 26 | 1,56% | 8 | 3,17% | 8 | 3,54% | 8 | 3,49% |
Rogers & Appan (1973) | 26 | 1,56% | 1 | 0,4% | 1 | 0,44% | 0 | 0% |
Léotard & Chaline (2013) | 22 | 1,32% | 19 | 7,54% | 19 | 8,41% | 16 | 6,99% |
Florence (2004) | 20 | 1,2% | 18 | 7,14% | 17 | 7,52% | 17 | 7,42% |
Orchard (2013) | 20 | 1,2% | 2 | 0,79% | 1 | 0,44% | 1 | 0,44% |
Allem (1994) | 17 | 1,02% | 2 | 0,79% | 1 | 0,44% | 1 | 0,44% |
Véron et al. (2021) | 17 | 1,02% | 16 | 6,35% | 15 | 6,64% | 15 | 6,55% |
Krapovickas (2003) | 16 | 0,96% | 4 | 1,59% | 4 | 1,77% | 4 | 1,75% |
Lemée (1952) | 16 | 0,96% | 10 | 3,97% | 10 | 4,42% | 10 | 4,37% |
Molino et al. (2009) | 16 | 0,96% | 13 | 5,16% | 13 | 5,75% | 11 | 4,8% |
Aublet (1775) | 15 | 0,9% | 9 | 3,57% | 8 | 3,54% | 8 | 3,49% |
Gargominy et al. (1996) | 14 | 0,84% | 13 | 5,16% | 13 | 5,75% | 12 | 5,24% |
Lemée (1955) | 11 | 0,66% | 7 | 2,78% | 7 | 3,1% | 6 | 2,62% |
Linnaeus (1753) | 10 | 0,6% | 7 | 2,78% | 7 | 3,1% | 5 | 2,18% |
Iamonico (2016) | 9 | 0,54% | 0 | 0% | 0 | 0% | 0 | 0% |
Jost et al. (2019) | 9 | 0,54% | 7 | 2,78% | 5 | 2,21% | 7 | 3,06% |
Miller (1768) | 9 | 0,54% | 2 | 0,79% | 2 | 0,88% | 2 | 0,87% |
Stace (2010) | 9 | 0,54% | 3 | 1,19% | 3 | 1,33% | 3 | 1,31% |
Allen et al. (2022) | 8 | 0,48% | 8 | 3,17% | 8 | 3,54% | 8 | 3,49% |
Florence (1997) | 8 | 0,48% | 3 | 1,19% | 3 | 1,33% | 2 | 0,87% |
Meyer et al. (2006) | 8 | 0,48% | 6 | 2,38% | 5 | 2,21% | 4 | 1,75% |
Nepal & Purintun (2021) | 8 | 0,48% | 1 | 0,4% | 1 | 0,44% | 1 | 0,44% |
Sauer (1964) | 8 | 0,48% | 0 | 0% | 0 | 0% | 0 | 0% |
Toutain (1989) | 8 | 0,48% | 8 | 3,17% | 8 | 3,54% | 7 | 3,06% |
Hily et al. (2010) | 7 | 0,42% | 5 | 1,98% | 5 | 2,21% | 5 | 2,18% |
Jeffrey (1980) | 7 | 0,42% | 1 | 0,4% | 1 | 0,44% | 1 | 0,44% |
Lavergne (2011) | 6 | 0,36% | 5 | 1,98% | 4 | 1,77% | 3 | 1,31% |
Bayón (2015) | 5 | 0,3% | 3 | 1,19% | 2 | 0,88% | 2 | 0,87% |
Bouman et al. (2022) | 5 | 0,3% | 3 | 1,19% | 3 | 1,33% | 3 | 1,31% |
Couté & Garrouste (2009) | 5 | 0,3% | 4 | 1,59% | 3 | 1,33% | 4 | 1,75% |
Cremers & Hoff (1997) | 5 | 0,3% | 1 | 0,4% | 1 | 0,44% | 1 | 0,44% |
Linnaeus (1753) | 5 | 0,3% | 3 | 1,19% | 3 | 1,33% | 3 | 1,31% |
Mattio et al. (2015) | 5 | 0,3% | 5 | 1,98% | 5 | 2,21% | 5 | 2,18% |
Ter Steege et al. (2016) | 5 | 0,3% | 2 | 0,79% | 2 | 0,88% | 2 | 0,87% |
Yang et al. (2012) | 5 | 0,3% | 5 | 1,98% | 5 | 2,21% | 5 | 2,18% |
Boggan et al. (1992) | 4 | 0,24% | 1 | 0,4% | 1 | 0,44% | 1 | 0,44% |
Candolle (1849) | 4 | 0,24% | 1 | 0,4% | 1 | 0,44% | 1 | 0,44% |
Christenhusz (2002) | 4 | 0,24% | 3 | 1,19% | 3 | 1,33% | 3 | 1,31% |
Cowan & Lindeman (1989) | 4 | 0,24% | 1 | 0,4% | 1 | 0,44% | 1 | 0,44% |
Fryxell (2001) | 4 | 0,24% | 1 | 0,4% | 1 | 0,44% | 1 | 0,44% |
Gardner et al. (2021) | 4 | 0,24% | 2 | 0,79% | 2 | 0,88% | 2 | 0,87% |
Lamarck (1798) | 4 | 0,24% | 1 | 0,4% | 1 | 0,44% | 1 | 0,44% |
Lemée (1953) | 4 | 0,24% | 2 | 0,79% | 2 | 0,88% | 2 | 0,87% |
Lowe et al. (2007) | 4 | 0,24% | 3 | 1,19% | 2 | 0,88% | 1 | 0,44% |
Pejhanmehr (2022) | 4 | 0,24% | 4 | 1,59% | 4 | 1,77% | 4 | 1,75% |
Wiersema et al. (2018) | 4 | 0,24% | 1 | 0,4% | 1 | 0,44% | 1 | 0,44% |
Cremers & Hoff (1994) | 3 | 0,18% | 2 | 0,79% | 2 | 0,88% | 2 | 0,87% |
Ferlay et al. (2023) | 3 | 0,18% | 3 | 1,19% | 3 | 1,33% | 3 | 1,31% |
Hassemer et al. (2017) | 3 | 0,18% | 3 | 1,19% | 3 | 1,33% | 3 | 1,31% |
Kyalangalilwa et al. (2013) | 3 | 0,18% | 1 | 0,4% | 1 | 0,44% | 1 | 0,44% |
Patchell et al. (2014) | 3 | 0,18% | 2 | 0,79% | 2 | 0,88% | 2 | 0,87% |
Sanders (2006) | 3 | 0,18% | 2 | 0,79% | 1 | 0,44% | 1 | 0,44% |
Sanders (2012) | 3 | 0,18% | 1 | 0,4% | 0 | 0% | 0 | 0% |
Sennen & Frère (1936) | 3 | 0,18% | 0 | 0% | 0 | 0% | 0 | 0% |
Al-Shehbaz et al. (2002) | 2 | 0,12% | 1 | 0,4% | 1 | 0,44% | 1 | 0,44% |
Candolle (1852) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Chemisquy et al. (2010) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Coode 1982 | 2 | 0,12% | 2 | 0,79% | 2 | 0,88% | 2 | 0,87% |
Dorsey et al. (2013) | 2 | 0,12% | 2 | 0,79% | 2 | 0,88% | 2 | 0,87% |
Flora of China (2015-) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Fosberg (1937) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Gagnon et al. (2016) | 2 | 0,12% | 1 | 0,4% | 1 | 0,44% | 1 | 0,44% |
Hendrian & Kondo (2007) | 2 | 0,12% | 1 | 0,4% | 1 | 0,44% | 1 | 0,44% |
Liede‐schumann et al. (2022) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Moench (1794) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Mohamed et al. (2001) | 2 | 0,12% | 1 | 0,4% | 1 | 0,44% | 1 | 0,44% |
Mucina (2017) | 2 | 0,12% | 2 | 0,79% | 2 | 0,88% | 2 | 0,87% |
N'Yeurt & Payri (2004) | 2 | 0,12% | 2 | 0,79% | 2 | 0,88% | 2 | 0,87% |
Peraza et al. (2022) | 2 | 0,12% | 2 | 0,79% | 2 | 0,88% | 2 | 0,87% |
Roalson & Hall (2017) | 2 | 0,12% | 2 | 0,79% | 2 | 0,88% | 2 | 0,87% |
Sachet (1962) | 2 | 0,12% | 2 | 0,79% | 2 | 0,88% | 2 | 0,87% |
Song et al. (2019) | 2 | 0,12% | 2 | 0,79% | 2 | 0,88% | 2 | 0,87% |
Stepansky et al. (1999) | 2 | 0,12% | 2 | 0,79% | 1 | 0,44% | 0 | 0% |
Suessenguth (1936) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
Veldkamp (2014) | 2 | 0,12% | 1 | 0,4% | 1 | 0,44% | 1 | 0,44% |
Wood et al. (2020) | 2 | 0,12% | 2 | 0,79% | 2 | 0,88% | 1 | 0,44% |
Zuloaga et al. (2018) | 2 | 0,12% | 2 | 0,79% | 2 | 0,88% | 2 | 0,87% |
Acevedo-Rodríguez (2012) | 1 | 0,06% | 1 | 0,4% | 1 | 0,44% | 1 | 0,44% |
Alencar et al. (2021) | 1 | 0,06% | 1 | 0,4% | 1 | 0,44% | 1 | 0,44% |
Allorge-Boiteau (2015) | 1 | 0,06% | 1 | 0,4% | 1 | 0,44% | 0 | 0% |
Alvarado-Cárdenas & Ochoterena (2007) | 1 | 0,06% | 1 | 0,4% | 1 | 0,44% | 1 | 0,44% |
Appelhans et al. (2021) | 1 | 0,06% | 1 | 0,4% | 1 | 0,44% | 1 | 0,44% |
Augros et al. (2018) | 1 | 0,06% | 1 | 0,4% | 0 | 0% | 0 | 0% |
Austin & Huáman (1996) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Barthelat (2019) | 1 | 0,06% | 1 | 0,4% | 1 | 0,44% | 1 | 0,44% |
Batianoff et al. (2009) | 1 | 0,06% | 1 | 0,4% | 1 | 0,44% | 1 | 0,44% |
Bell (1982) | 1 | 0,06% | 1 | 0,4% | 1 | 0,44% | 1 | 0,44% |
Béreau (2017) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Bohley et al. (2017) | 1 | 0,06% | 1 | 0,4% | 1 | 0,44% | 0 | 0% |
Bouman et al. (2020) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Bovini (2010) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Candolle (1844) | 1 | 0,06% | 1 | 0,4% | 1 | 0,44% | 1 | 0,44% |
Couhia & Fleurot (2016) | 1 | 0,06% | 1 | 0,4% | 1 | 0,44% | 1 | 0,44% |
Edwards et al. (2018) | 1 | 0,06% | 1 | 0,4% | 1 | 0,44% | 0 | 0% |
Euro+Med (2006) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Fernandes (1984) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Feuillet (2009) | 1 | 0,06% | 1 | 0,4% | 1 | 0,44% | 1 | 0,44% |
Forsskål (1775) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Frenot et al. (2001) | 1 | 0,06% | 1 | 0,4% | 1 | 0,44% | 1 | 0,44% |
Friis & Holt (2016) | 1 | 0,06% | 1 | 0,4% | 1 | 0,44% | 1 | 0,44% |
Granville & Gayot (2014) | 1 | 0,06% | 1 | 0,4% | 1 | 0,44% | 1 | 0,44% |
Guillaumin (1936) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Host (1809) | 1 | 0,06% | 1 | 0,4% | 1 | 0,44% | 1 | 0,44% |
Hullé et al. (2003) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Iamonico et al. (2015) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Iltis (1960) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Jolinon (1985) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Jolinon (1987) | 1 | 0,06% | 1 | 0,4% | 1 | 0,44% | 1 | 0,44% |
Judziewicz (1990) | 1 | 0,06% | 1 | 0,4% | 1 | 0,44% | 1 | 0,44% |
Lamarck (1779) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Lamarck (1783) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Levin et al. (2022) | 1 | 0,06% | 1 | 0,4% | 1 | 0,44% | 1 | 0,44% |
Li et al. (2022) | 1 | 0,06% | 1 | 0,4% | 1 | 0,44% | 1 | 0,44% |
Liu et al. (2004) | 1 | 0,06% | 1 | 0,4% | 1 | 0,44% | 0 | 0% |
Maddi (2014) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Masters et al. (2023) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Meyer (2017) | 1 | 0,06% | 1 | 0,4% | 1 | 0,44% | 1 | 0,44% |
Mohamed (1994) | 1 | 0,06% | 1 | 0,4% | 1 | 0,44% | 1 | 0,44% |
Persoon (1805) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Questel (2023) | 1 | 0,06% | 1 | 0,4% | 1 | 0,44% | 1 | 0,44% |
Richard (1792) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Salisbury (1796) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Sant (2022) | 1 | 0,06% | 1 | 0,4% | 1 | 0,44% | 1 | 0,44% |
Schenck (1905) | 1 | 0,06% | 1 | 0,4% | 1 | 0,44% | 1 | 0,44% |
Schrire et al. (2009) | 1 | 0,06% | 1 | 0,4% | 1 | 0,44% | 1 | 0,44% |
Snak et al. (2016) | 1 | 0,06% | 1 | 0,4% | 1 | 0,44% | 1 | 0,44% |
Soubeyran (2008) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Souza et al. (2021) | 1 | 0,06% | 1 | 0,4% | 1 | 0,44% | 1 | 0,44% |
Sukhorukov et al. (2018) | 1 | 0,06% | 1 | 0,4% | 0 | 0% | 1 | 0,44% |
Sullivan & Short (2023) | 1 | 0,06% | 1 | 0,4% | 1 | 0,44% | 1 | 0,44% |
Webster (1957) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
Welker et al. (2020) | 1 | 0,06% | 1 | 0,4% | 1 | 0,44% | 0 | 0% |