Ptéridophytes de Polynésie française
Monilophyta et Lycopodiophyta de Polynésie française
111 références bibliographiques sont utilisées pour les noms de rangs spécifiques de ce groupe.
| Référence | Total | Valides | Espèces | Taxons terminaux | ||||
|---|---|---|---|---|---|---|---|---|
| nb | % | nb | % | nb | % | nb | % | |
| Munzinger et al. (2016) | 242 | 19,1% | 66 | 22,53% | 64 | 23,62% | 59 | 21,38% |
| Copeland (1932) | 172 | 13,58% | 59 | 20,14% | 59 | 21,77% | 52 | 18,84% |
| Morat et al. (2012) | 147 | 11,6% | 63 | 21,5% | 62 | 22,88% | 55 | 19,93% |
| Véron et al. (2021) | 90 | 7,1% | 76 | 25,94% | 76 | 28,04% | 75 | 27,17% |
| Murdock & Smith (2003) | 79 | 6,24% | 52 | 17,75% | 48 | 17,71% | 46 | 16,67% |
| Copeland (1938) | 59 | 4,66% | 14 | 4,78% | 14 | 5,17% | 14 | 5,07% |
| Funk et al. (2007) | 43 | 3,39% | 14 | 4,78% | 13 | 4,8% | 9 | 3,26% |
| Lorence et al. (2011) | 37 | 2,92% | 22 | 7,51% | 22 | 8,12% | 22 | 7,97% |
| Rouhan et al. (2008) | 37 | 2,92% | 27 | 9,22% | 27 | 9,96% | 27 | 9,78% |
| Morat & Veillon (1985) | 31 | 2,45% | 19 | 6,48% | 18 | 6,64% | 15 | 5,43% |
| Moore (1933) | 29 | 2,29% | 4 | 1,37% | 4 | 1,48% | 4 | 1,45% |
| Hovenkamp & Miyamoto (2005) | 27 | 2,13% | 5 | 1,71% | 4 | 1,48% | 3 | 1,09% |
| Reed (1968) | 27 | 2,13% | 7 | 2,39% | 7 | 2,58% | 7 | 2,54% |
| Christenhusz (2009) | 24 | 1,89% | 19 | 6,48% | 18 | 6,64% | 15 | 5,43% |
| Gasper et al. (2016) | 21 | 1,66% | 8 | 2,73% | 8 | 2,95% | 8 | 2,9% |
| Parris (2007) | 18 | 1,42% | 13 | 4,44% | 13 | 4,8% | 13 | 4,71% |
| Bernard (2015) | 16 | 1,26% | 10 | 3,41% | 10 | 3,69% | 7 | 2,54% |
| Ebihara et al. (2006) | 12 | 0,95% | 9 | 3,07% | 9 | 3,32% | 9 | 3,26% |
| Fourdrigniez & Meyer (2008) | 12 | 0,95% | 9 | 3,07% | 9 | 3,32% | 6 | 2,17% |
| Holttum (1977) | 11 | 0,87% | 0 | 0% | 0 | 0% | 0 | 0% |
| Øllgaard et al. (2020) | 10 | 0,79% | 1 | 0,34% | 1 | 0,37% | 1 | 0,36% |
| Tison et al. (2014) | 10 | 0,79% | 8 | 2,73% | 8 | 2,95% | 7 | 2,54% |
| Chambers & Wilson (2019) | 8 | 0,63% | 0 | 0% | 0 | 0% | 0 | 0% |
| Dubuisson et al. (2018) | 8 | 0,63% | 1 | 0,34% | 1 | 0,37% | 1 | 0,36% |
| John (1942) | 8 | 0,63% | 7 | 2,39% | 7 | 2,58% | 7 | 2,54% |
| Øllgaard & Windisch (2016) | 8 | 0,63% | 1 | 0,34% | 1 | 0,37% | 1 | 0,36% |
| Parris (1997) | 8 | 0,63% | 3 | 1,02% | 3 | 1,11% | 3 | 1,09% |
| Cremers & Boudrie (2007) | 7 | 0,55% | 5 | 1,71% | 5 | 1,85% | 1 | 0,36% |
| Nitta et al. (2011) | 7 | 0,55% | 6 | 2,05% | 6 | 2,21% | 6 | 2,17% |
| Holttum (1973) | 6 | 0,47% | 2 | 0,68% | 2 | 0,74% | 2 | 0,72% |
| Parris (2013) | 6 | 0,47% | 4 | 1,37% | 4 | 1,48% | 4 | 1,45% |
| Dubuisson et al. (2021) | 5 | 0,39% | 2 | 0,68% | 2 | 0,74% | 0 | 0% |
| Fawcett & Smith (2021) | 5 | 0,39% | 2 | 0,68% | 2 | 0,74% | 2 | 0,72% |
| Holttum (1966) | 5 | 0,39% | 5 | 1,71% | 5 | 1,85% | 5 | 1,81% |
| Lange & Parris (2019) | 5 | 0,39% | 5 | 1,71% | 5 | 1,85% | 5 | 1,81% |
| Pteridophyte Phylogeny Group (2016) | 5 | 0,39% | 3 | 1,02% | 3 | 1,11% | 3 | 1,09% |
| Badré (2008b) | 4 | 0,32% | 4 | 1,37% | 3 | 1,11% | 2 | 0,72% |
| Holub (1985) | 4 | 0,32% | 1 | 0,34% | 1 | 0,37% | 1 | 0,36% |
| Clausen (1938) | 3 | 0,24% | 2 | 0,68% | 2 | 0,74% | 0 | 0% |
| Ebihara et al. (2009) | 3 | 0,24% | 1 | 0,34% | 1 | 0,37% | 1 | 0,36% |
| Ferlay et al. (2023) | 3 | 0,24% | 3 | 1,02% | 3 | 1,11% | 1 | 0,36% |
| Grangaud (2010) | 3 | 0,24% | 3 | 1,02% | 2 | 0,74% | 1 | 0,36% |
| Hoff & Cremers (2005) | 3 | 0,24% | 2 | 0,68% | 1 | 0,37% | 2 | 0,72% |
| Holttum (1985) | 3 | 0,24% | 3 | 1,02% | 3 | 1,11% | 2 | 0,72% |
| Ke et al. (2022) | 3 | 0,24% | 3 | 1,02% | 3 | 1,11% | 3 | 1,09% |
| Léotard & Chaline (2013) | 3 | 0,24% | 3 | 1,02% | 2 | 0,74% | 2 | 0,72% |
| Linnaeus (1753) | 3 | 0,24% | 1 | 0,34% | 1 | 0,37% | 1 | 0,36% |
| Lorence & Wagner (2019) | 3 | 0,24% | 3 | 1,02% | 3 | 1,11% | 3 | 1,09% |
| Nitta et al. (2018) | 3 | 0,24% | 3 | 1,02% | 3 | 1,11% | 3 | 1,09% |
| Testo et al. (2019) | 3 | 0,24% | 0 | 0% | 0 | 0% | 0 | 0% |
| Wiersema et al. (2018) | 3 | 0,24% | 1 | 0,34% | 1 | 0,37% | 0 | 0% |
| Allen et al. (2022) | 2 | 0,16% | 1 | 0,34% | 1 | 0,37% | 1 | 0,36% |
| Boullet et al. (2018) | 2 | 0,16% | 2 | 0,68% | 2 | 0,74% | 1 | 0,36% |
| Christensen (1934) | 2 | 0,16% | 2 | 0,68% | 2 | 0,74% | 2 | 0,72% |
| Delnatte & Meyer (2012) | 2 | 0,16% | 2 | 0,68% | 2 | 0,74% | 2 | 0,72% |
| Derrick et al. (1987) | 2 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Drake (1890) | 2 | 0,16% | 2 | 0,68% | 2 | 0,74% | 2 | 0,72% |
| Field et al. (2016) | 2 | 0,16% | 1 | 0,34% | 1 | 0,37% | 1 | 0,36% |
| Holttum (1982) | 2 | 0,16% | 2 | 0,68% | 2 | 0,74% | 2 | 0,72% |
| Kuhn (1869) | 2 | 0,16% | 2 | 0,68% | 2 | 0,74% | 2 | 0,72% |
| Maddi (2010) | 2 | 0,16% | 2 | 0,68% | 2 | 0,74% | 2 | 0,72% |
| Moran & Smith (1999) | 2 | 0,16% | 1 | 0,34% | 1 | 0,37% | 1 | 0,36% |
| Parris & Sundue (2020) | 2 | 0,16% | 1 | 0,34% | 1 | 0,37% | 1 | 0,36% |
| Perrie et al. (2021) | 2 | 0,16% | 1 | 0,34% | 1 | 0,37% | 1 | 0,36% |
| Questel (2023) | 2 | 0,16% | 2 | 0,68% | 2 | 0,74% | 1 | 0,36% |
| Schmidt (1924) | 2 | 0,16% | 2 | 0,68% | 2 | 0,74% | 2 | 0,72% |
| Wagner et al. (1984) | 2 | 0,16% | 1 | 0,34% | 1 | 0,37% | 0 | 0% |
| Wang et al. (2010) | 2 | 0,16% | 2 | 0,68% | 2 | 0,74% | 1 | 0,36% |
| Warburg (1900) | 2 | 0,16% | 2 | 0,68% | 2 | 0,74% | 2 | 0,72% |
| Zhang & Zhang (2012) | 2 | 0,16% | 0 | 0% | 0 | 0% | 0 | 0% |
| Almeida et al. (2016) | 1 | 0,08% | 1 | 0,34% | 1 | 0,37% | 1 | 0,36% |
| Anonyme (2023) | 1 | 0,08% | 1 | 0,34% | 0 | 0% | 1 | 0,36% |
| Badré & Lorence (2008) | 1 | 0,08% | 1 | 0,34% | 1 | 0,37% | 1 | 0,36% |
| Baker (1867) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Barthelat (2019) | 1 | 0,08% | 1 | 0,34% | 1 | 0,37% | 0 | 0% |
| Brownsey & Perrie (2016) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Chen et al. (2020) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Crane (1998) | 1 | 0,08% | 1 | 0,34% | 1 | 0,37% | 1 | 0,36% |
| Cremers & Boudrie (2006) | 1 | 0,08% | 1 | 0,34% | 1 | 0,37% | 1 | 0,36% |
| Cremers & Hoff (1990) | 1 | 0,08% | 1 | 0,34% | 1 | 0,37% | 1 | 0,36% |
| Dulac (1867) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Eppo (2011) | 1 | 0,08% | 1 | 0,34% | 1 | 0,37% | 1 | 0,36% |
| Florence & Hallé (1986) | 1 | 0,08% | 1 | 0,34% | 1 | 0,37% | 1 | 0,36% |
| Forsskål (1775) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Kunze (1840) | 1 | 0,08% | 1 | 0,34% | 1 | 0,37% | 1 | 0,36% |
| Labiak et al. (2015) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lamarck (1778) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lavergne (2011) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lehtonen et al. (2010) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Lorence et al. (2019) | 1 | 0,08% | 1 | 0,34% | 1 | 0,37% | 1 | 0,36% |
| Maddi (2014) | 1 | 0,08% | 1 | 0,34% | 1 | 0,37% | 1 | 0,36% |
| Maddi (2014) | 1 | 0,08% | 1 | 0,34% | 1 | 0,37% | 1 | 0,36% |
| Meza-Torres (2015) | 1 | 0,08% | 1 | 0,34% | 1 | 0,37% | 0 | 0% |
| Nooteboom (1997) | 1 | 0,08% | 1 | 0,34% | 1 | 0,37% | 1 | 0,36% |
| Paradis & Miniconi (2011) | 1 | 0,08% | 1 | 0,34% | 1 | 0,37% | 1 | 0,36% |
| Prelli & Boudrie (2021) | 1 | 0,08% | 1 | 0,34% | 1 | 0,37% | 1 | 0,36% |
| Ragavan et al. (2014) | 1 | 0,08% | 1 | 0,34% | 1 | 0,37% | 1 | 0,36% |
| Rouhan et al. (2021) | 1 | 0,08% | 1 | 0,34% | 0 | 0% | 1 | 0,36% |
| Roux (2009) | 1 | 0,08% | 1 | 0,34% | 1 | 0,37% | 1 | 0,36% |
| Saïd et al. (2017) | 1 | 0,08% | 1 | 0,34% | 1 | 0,37% | 1 | 0,36% |
| Salino et al. (2015) | 1 | 0,08% | 1 | 0,34% | 1 | 0,37% | 1 | 0,36% |
| Salisbury (1796) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Sant (2002) | 1 | 0,08% | 1 | 0,34% | 1 | 0,37% | 1 | 0,36% |
| Sant (2002) | 1 | 0,08% | 1 | 0,34% | 1 | 0,37% | 1 | 0,36% |
| Shinohara et al. (2013) | 1 | 0,08% | 1 | 0,34% | 1 | 0,37% | 1 | 0,36% |
| Sykes & Game (1996) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Tsutsumi et al. (2008) | 1 | 0,08% | 1 | 0,34% | 1 | 0,37% | 1 | 0,36% |
| Wilson (2022) | 1 | 0,08% | 0 | 0% | 0 | 0% | 0 | 0% |
| Yahaya et al. (2016) | 1 | 0,08% | 1 | 0,34% | 0 | 0% | 1 | 0,36% |
| Zhang et al. (2007) | 1 | 0,08% | 1 | 0,34% | 1 | 0,37% | 1 | 0,36% |
| Zhang et al. (2013) | 1 | 0,08% | 1 | 0,34% | 1 | 0,37% | 1 | 0,36% |
