Trachéophytes des îles Eparses
Trachéophyta des îles Eparses
163 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 | 23,3% | 316 | 119,7% | 312 | 131,09% | 280 | 116,18% |
| Boullet et al. (2018) | 216 | 12,43% | 200 | 75,76% | 184 | 77,31% | 193 | 80,08% |
| Funk et al. (2007) | 200 | 11,51% | 82 | 31,06% | 81 | 34,03% | 71 | 29,46% |
| Munzinger et al. (2016) | 173 | 9,95% | 54 | 20,45% | 52 | 21,85% | 49 | 20,33% |
| Morat et al. (2012) | 99 | 5,7% | 53 | 20,08% | 51 | 21,43% | 48 | 19,92% |
| Molino et al. (2022) | 93 | 5,35% | 5 | 1,89% | 5 | 2,1% | 4 | 1,66% |
| Hequet & Le Corre (2010) | 87 | 5,01% | 72 | 27,27% | 70 | 29,41% | 62 | 25,73% |
| Hequet et al. (2009) | 87 | 5,01% | 72 | 27,27% | 70 | 29,41% | 62 | 25,73% |
| MacKee (1994) | 83 | 4,78% | 67 | 25,38% | 65 | 27,31% | 58 | 24,07% |
| Tison et al. (2014) | 81 | 4,66% | 51 | 19,32% | 49 | 20,59% | 47 | 19,5% |
| Fourdrigniez & Meyer (2008) | 69 | 3,97% | 53 | 20,08% | 51 | 21,43% | 46 | 19,09% |
| Morat & Veillon (1985) | 65 | 3,74% | 55 | 20,83% | 53 | 22,27% | 44 | 18,26% |
| Acevedo-Rodríguez & Strong (2012) | 44 | 2,53% | 23 | 8,71% | 23 | 9,66% | 16 | 6,64% |
| Delnatte & Meyer (2012) | 38 | 2,19% | 30 | 11,36% | 30 | 12,61% | 24 | 9,96% |
| Anonyme (2014) | 28 | 1,61% | 22 | 8,33% | 22 | 9,24% | 20 | 8,3% |
| Porter-Utley (2014) | 26 | 1,5% | 8 | 3,03% | 8 | 3,36% | 8 | 3,32% |
| Rogers & Appan (1973) | 26 | 1,5% | 1 | 0,38% | 1 | 0,42% | 0 | 0% |
| Léotard & Chaline (2013) | 22 | 1,27% | 19 | 7,2% | 19 | 7,98% | 16 | 6,64% |
| Florence (2004) | 20 | 1,15% | 18 | 6,82% | 17 | 7,14% | 17 | 7,05% |
| Orchard (2013) | 20 | 1,15% | 2 | 0,76% | 1 | 0,42% | 1 | 0,41% |
| Allem (1994) | 17 | 0,98% | 2 | 0,76% | 1 | 0,42% | 1 | 0,41% |
| Véron et al. (2021) | 17 | 0,98% | 16 | 6,06% | 15 | 6,3% | 15 | 6,22% |
| Krapovickas (2003) | 16 | 0,92% | 4 | 1,52% | 4 | 1,68% | 4 | 1,66% |
| Lemée (1952) | 16 | 0,92% | 10 | 3,79% | 10 | 4,2% | 10 | 4,15% |
| Molino et al. (2009) | 16 | 0,92% | 13 | 4,92% | 13 | 5,46% | 11 | 4,56% |
| Aublet (1775) | 15 | 0,86% | 9 | 3,41% | 8 | 3,36% | 8 | 3,32% |
| Gargominy et al. (1996) | 14 | 0,81% | 13 | 4,92% | 13 | 5,46% | 12 | 4,98% |
| Hovenkamp & Miyamoto (2005) | 12 | 0,69% | 1 | 0,38% | 1 | 0,42% | 1 | 0,41% |
| Lemée (1955) | 11 | 0,63% | 7 | 2,65% | 7 | 2,94% | 6 | 2,49% |
| Linnaeus (1753) | 10 | 0,58% | 7 | 2,65% | 7 | 2,94% | 5 | 2,07% |
| Iamonico (2016) | 9 | 0,52% | 0 | 0% | 0 | 0% | 0 | 0% |
| Jost et al. (2019) | 9 | 0,52% | 7 | 2,65% | 5 | 2,1% | 7 | 2,9% |
| Miller (1768) | 9 | 0,52% | 2 | 0,76% | 2 | 0,84% | 2 | 0,83% |
| Stace (2010) | 9 | 0,52% | 3 | 1,14% | 3 | 1,26% | 3 | 1,24% |
| Allen et al. (2022) | 8 | 0,46% | 8 | 3,03% | 8 | 3,36% | 8 | 3,32% |
| Florence (1997) | 8 | 0,46% | 3 | 1,14% | 3 | 1,26% | 2 | 0,83% |
| Meyer et al. (2006) | 8 | 0,46% | 6 | 2,27% | 5 | 2,1% | 4 | 1,66% |
| Nepal & Purintun (2021) | 8 | 0,46% | 1 | 0,38% | 1 | 0,42% | 1 | 0,41% |
| Sauer (1964) | 8 | 0,46% | 0 | 0% | 0 | 0% | 0 | 0% |
| Toutain (1989) | 8 | 0,46% | 8 | 3,03% | 8 | 3,36% | 7 | 2,9% |
| Hily et al. (2010) | 7 | 0,4% | 5 | 1,89% | 5 | 2,1% | 5 | 2,07% |
| Jeffrey (1980) | 7 | 0,4% | 1 | 0,38% | 1 | 0,42% | 1 | 0,41% |
| Lavergne (2011) | 6 | 0,35% | 5 | 1,89% | 4 | 1,68% | 3 | 1,24% |
| Bayón (2015) | 5 | 0,29% | 3 | 1,14% | 2 | 0,84% | 2 | 0,83% |
| Bouman et al. (2022) | 5 | 0,29% | 3 | 1,14% | 3 | 1,26% | 3 | 1,24% |
| Christenhusz (2009) | 5 | 0,29% | 4 | 1,52% | 4 | 1,68% | 4 | 1,66% |
| Couté & Garrouste (2009) | 5 | 0,29% | 4 | 1,52% | 3 | 1,26% | 4 | 1,66% |
| Cremers & Hoff (1997) | 5 | 0,29% | 1 | 0,38% | 1 | 0,42% | 1 | 0,41% |
| Linnaeus (1753) | 5 | 0,29% | 3 | 1,14% | 3 | 1,26% | 3 | 1,24% |
| Mattio et al. (2015) | 5 | 0,29% | 5 | 1,89% | 5 | 2,1% | 5 | 2,07% |
| Ter Steege et al. (2016) | 5 | 0,29% | 2 | 0,76% | 2 | 0,84% | 2 | 0,83% |
| Yang et al. (2012) | 5 | 0,29% | 5 | 1,89% | 5 | 2,1% | 5 | 2,07% |
| Bernard (2015) | 4 | 0,23% | 3 | 1,14% | 3 | 1,26% | 3 | 1,24% |
| Boggan et al. (1992) | 4 | 0,23% | 1 | 0,38% | 1 | 0,42% | 1 | 0,41% |
| Candolle (1849) | 4 | 0,23% | 1 | 0,38% | 1 | 0,42% | 1 | 0,41% |
| Christenhusz (2002) | 4 | 0,23% | 3 | 1,14% | 3 | 1,26% | 3 | 1,24% |
| Copeland (1932) | 4 | 0,23% | 4 | 1,52% | 4 | 1,68% | 4 | 1,66% |
| Cowan & Lindeman (1989) | 4 | 0,23% | 1 | 0,38% | 1 | 0,42% | 1 | 0,41% |
| Fryxell (2001) | 4 | 0,23% | 1 | 0,38% | 1 | 0,42% | 1 | 0,41% |
| Gardner et al. (2021) | 4 | 0,23% | 2 | 0,76% | 2 | 0,84% | 2 | 0,83% |
| Lamarck (1798) | 4 | 0,23% | 1 | 0,38% | 1 | 0,42% | 1 | 0,41% |
| Lemée (1953) | 4 | 0,23% | 2 | 0,76% | 2 | 0,84% | 2 | 0,83% |
| Lowe et al. (2007) | 4 | 0,23% | 3 | 1,14% | 2 | 0,84% | 1 | 0,41% |
| Murdock & Smith (2003) | 4 | 0,23% | 4 | 1,52% | 4 | 1,68% | 4 | 1,66% |
| Pejhanmehr (2022) | 4 | 0,23% | 4 | 1,52% | 4 | 1,68% | 4 | 1,66% |
| Wiersema et al. (2018) | 4 | 0,23% | 1 | 0,38% | 1 | 0,42% | 1 | 0,41% |
| Cremers & Boudrie (2007) | 3 | 0,17% | 1 | 0,38% | 1 | 0,42% | 1 | 0,41% |
| Cremers & Hoff (1994) | 3 | 0,17% | 2 | 0,76% | 2 | 0,84% | 2 | 0,83% |
| Ferlay et al. (2023) | 3 | 0,17% | 3 | 1,14% | 3 | 1,26% | 3 | 1,24% |
| Hassemer et al. (2017) | 3 | 0,17% | 3 | 1,14% | 3 | 1,26% | 3 | 1,24% |
| Kyalangalilwa et al. (2013) | 3 | 0,17% | 1 | 0,38% | 1 | 0,42% | 1 | 0,41% |
| Patchell et al. (2014) | 3 | 0,17% | 2 | 0,76% | 2 | 0,84% | 2 | 0,83% |
| Sanders (2006) | 3 | 0,17% | 2 | 0,76% | 1 | 0,42% | 1 | 0,41% |
| Sanders (2012) | 3 | 0,17% | 1 | 0,38% | 0 | 0% | 0 | 0% |
| Sennen & Frère (1936) | 3 | 0,17% | 0 | 0% | 0 | 0% | 0 | 0% |
| Al-Shehbaz et al. (2002) | 2 | 0,12% | 1 | 0,38% | 1 | 0,42% | 1 | 0,41% |
| Barthelat (2019) | 2 | 0,12% | 2 | 0,76% | 2 | 0,84% | 2 | 0,83% |
| 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 | 0,76% | 2 | 0,84% | 2 | 0,83% |
| Dorsey et al. (2013) | 2 | 0,12% | 2 | 0,76% | 2 | 0,84% | 2 | 0,83% |
| Flora of China (2015-) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Forsskål (1775) | 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 | 0,38% | 1 | 0,42% | 1 | 0,41% |
| Grangaud (2010) | 2 | 0,12% | 2 | 0,76% | 2 | 0,84% | 2 | 0,83% |
| Hendrian & Kondo (2007) | 2 | 0,12% | 1 | 0,38% | 1 | 0,42% | 1 | 0,41% |
| 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 | 0,38% | 1 | 0,42% | 1 | 0,41% |
| Mucina (2017) | 2 | 0,12% | 2 | 0,76% | 2 | 0,84% | 2 | 0,83% |
| N'Yeurt & Payri (2004) | 2 | 0,12% | 2 | 0,76% | 2 | 0,84% | 2 | 0,83% |
| Peraza et al. (2022) | 2 | 0,12% | 2 | 0,76% | 2 | 0,84% | 2 | 0,83% |
| Questel (2023) | 2 | 0,12% | 2 | 0,76% | 2 | 0,84% | 2 | 0,83% |
| Ragavan et al. (2014) | 2 | 0,12% | 2 | 0,76% | 2 | 0,84% | 2 | 0,83% |
| Roalson & Hall (2017) | 2 | 0,12% | 2 | 0,76% | 2 | 0,84% | 2 | 0,83% |
| Sachet (1962) | 2 | 0,12% | 2 | 0,76% | 2 | 0,84% | 2 | 0,83% |
| Song et al. (2019) | 2 | 0,12% | 2 | 0,76% | 2 | 0,84% | 2 | 0,83% |
| Stepansky et al. (1999) | 2 | 0,12% | 2 | 0,76% | 1 | 0,42% | 0 | 0% |
| Suessenguth (1936) | 2 | 0,12% | 0 | 0% | 0 | 0% | 0 | 0% |
| Veldkamp (2014) | 2 | 0,12% | 1 | 0,38% | 1 | 0,42% | 1 | 0,41% |
| Wood et al. (2020) | 2 | 0,12% | 2 | 0,76% | 2 | 0,84% | 1 | 0,41% |
| Zhang et al. (2013) | 2 | 0,12% | 2 | 0,76% | 2 | 0,84% | 2 | 0,83% |
| Zuloaga et al. (2018) | 2 | 0,12% | 2 | 0,76% | 2 | 0,84% | 2 | 0,83% |
| Acevedo-Rodríguez (2012) | 1 | 0,06% | 1 | 0,38% | 1 | 0,42% | 1 | 0,41% |
| Alencar et al. (2021) | 1 | 0,06% | 1 | 0,38% | 1 | 0,42% | 1 | 0,41% |
| Allorge-Boiteau (2015) | 1 | 0,06% | 1 | 0,38% | 1 | 0,42% | 0 | 0% |
| Almeida et al. (2016) | 1 | 0,06% | 1 | 0,38% | 1 | 0,42% | 1 | 0,41% |
| Alvarado-Cárdenas & Ochoterena (2007) | 1 | 0,06% | 1 | 0,38% | 1 | 0,42% | 1 | 0,41% |
| Appelhans et al. (2021) | 1 | 0,06% | 1 | 0,38% | 1 | 0,42% | 1 | 0,41% |
| Augros et al. (2018) | 1 | 0,06% | 1 | 0,38% | 0 | 0% | 0 | 0% |
| Austin & Huáman (1996) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Badré (2008b) | 1 | 0,06% | 1 | 0,38% | 1 | 0,42% | 1 | 0,41% |
| Batianoff et al. (2009) | 1 | 0,06% | 1 | 0,38% | 1 | 0,42% | 1 | 0,41% |
| Bell (1982) | 1 | 0,06% | 1 | 0,38% | 1 | 0,42% | 1 | 0,41% |
| Béreau (2017) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Bohley et al. (2017) | 1 | 0,06% | 1 | 0,38% | 1 | 0,42% | 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 | 0,38% | 1 | 0,42% | 1 | 0,41% |
| Couhia & Fleurot (2016) | 1 | 0,06% | 1 | 0,38% | 1 | 0,42% | 1 | 0,41% |
| Cremers & Boudrie (2006) | 1 | 0,06% | 1 | 0,38% | 1 | 0,42% | 1 | 0,41% |
| Cremers & Hoff (1990) | 1 | 0,06% | 1 | 0,38% | 1 | 0,42% | 1 | 0,41% |
| Edwards et al. (2018) | 1 | 0,06% | 1 | 0,38% | 1 | 0,42% | 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 | 0,38% | 1 | 0,42% | 1 | 0,41% |
| Frenot et al. (2001) | 1 | 0,06% | 1 | 0,38% | 1 | 0,42% | 1 | 0,41% |
| Friis & Holt (2016) | 1 | 0,06% | 1 | 0,38% | 1 | 0,42% | 1 | 0,41% |
| Granville & Gayot (2014) | 1 | 0,06% | 1 | 0,38% | 1 | 0,42% | 1 | 0,41% |
| Guillaumin (1936) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Host (1809) | 1 | 0,06% | 1 | 0,38% | 1 | 0,42% | 1 | 0,41% |
| 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 | 0,38% | 1 | 0,42% | 1 | 0,41% |
| Judziewicz (1990) | 1 | 0,06% | 1 | 0,38% | 1 | 0,42% | 1 | 0,41% |
| 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 | 0,38% | 1 | 0,42% | 1 | 0,41% |
| Li et al. (2022) | 1 | 0,06% | 1 | 0,38% | 1 | 0,42% | 1 | 0,41% |
| Liu et al. (2004) | 1 | 0,06% | 1 | 0,38% | 1 | 0,42% | 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 | 0,38% | 1 | 0,42% | 1 | 0,41% |
| Mohamed (1994) | 1 | 0,06% | 1 | 0,38% | 1 | 0,42% | 1 | 0,41% |
| Persoon (1805) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Prelli & Boudrie (2021) | 1 | 0,06% | 1 | 0,38% | 1 | 0,42% | 1 | 0,41% |
| Pteridophyte Phylogeny Group (2016) | 1 | 0,06% | 1 | 0,38% | 1 | 0,42% | 1 | 0,41% |
| Richard (1792) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Rouy (1913) | 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 | 0,38% | 1 | 0,42% | 1 | 0,41% |
| Schenck (1905) | 1 | 0,06% | 1 | 0,38% | 1 | 0,42% | 1 | 0,41% |
| Schrire et al. (2009) | 1 | 0,06% | 1 | 0,38% | 1 | 0,42% | 1 | 0,41% |
| Snak et al. (2016) | 1 | 0,06% | 1 | 0,38% | 1 | 0,42% | 1 | 0,41% |
| Soubeyran (2008) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Souza et al. (2021) | 1 | 0,06% | 1 | 0,38% | 1 | 0,42% | 1 | 0,41% |
| Sukhorukov et al. (2018) | 1 | 0,06% | 1 | 0,38% | 0 | 0% | 1 | 0,41% |
| Sullivan & Short (2023) | 1 | 0,06% | 1 | 0,38% | 1 | 0,42% | 1 | 0,41% |
| Webster (1957) | 1 | 0,06% | 0 | 0% | 0 | 0% | 0 | 0% |
| Welker et al. (2020) | 1 | 0,06% | 1 | 0,38% | 1 | 0,42% | 0 | 0% |
